@molgenis/vip-report-template 4.0.0 → 5.1.0

This diff represents the content of publicly available package versions that have been released to one of the supported registries. The information contained in this diff is provided for informational purposes only and reflects changes between package versions as they appear in their respective public registries.
Files changed (32) hide show
  1. package/.travis.yml +3 -1
  2. package/package.json +3 -3
  3. package/src/components/GenomeBrowser.tsx +1 -1
  4. package/src/components/VariantSampleTable.tsx +4 -2
  5. package/src/components/VariantsSampleTable.tsx +113 -7
  6. package/src/components/filter/Filter.tsx +31 -22
  7. package/src/components/filter/FilterAllelicBalance.tsx +75 -0
  8. package/src/components/filter/FilterCategorical.tsx +3 -2
  9. package/src/components/filter/FilterIntegerDp.tsx +19 -4
  10. package/src/components/filter/FilterIntegerGq.tsx +32 -0
  11. package/src/components/filter/FilterIntegerVid.tsx +13 -3
  12. package/src/components/filter/FilterIntegerVim.tsx +13 -3
  13. package/src/components/filter/Filters.tsx +7 -8
  14. package/src/components/filter/InfoFilter.tsx +10 -4
  15. package/src/components/filter/InfoFilters.tsx +1 -1
  16. package/src/components/filter/SampleFilters.tsx +16 -19
  17. package/src/components/filter/SamplesFilters.tsx +10 -8
  18. package/src/components/record/Format.tsx +2 -2
  19. package/src/components/record/format/GenotypeField.tsx +11 -10
  20. package/src/mocks/GRCh37/genes.gff.gz.blob +0 -0
  21. package/src/mocks/GRCh37/static.ts +75 -1
  22. package/src/mocks/GRCh37/vcf/family.vcf.blob +31 -30
  23. package/src/mocks/GRCh38/genes.gff.gz.blob +0 -0
  24. package/src/mocks/GRCh38/static.ts +1 -1
  25. package/src/mocks/GRCh38/vcf/family.vcf.blob +25 -24
  26. package/src/mocks/MockApiClient.ts +2 -1
  27. package/src/store/index.tsx +14 -15
  28. package/src/views/SampleVariants.tsx +47 -24
  29. package/src/views/VariantConsequence.tsx +44 -37
  30. package/src/views/Variants.tsx +3 -3
  31. package/src/mocks/GRCh37/genes.txt.gz.blob +0 -0
  32. package/src/mocks/GRCh38/genes.txt.gz.blob +0 -0
package/src/mocks/GRCh38/vcf/family.vcf.blob CHANGED
@@ -7,6 +7,7 @@
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  ##CAPICE_CL=CAPICE classification
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  ##CAPICE_SC=CAPICE score
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  ##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth (reads with MQ=255 or with bad mates are filtered)">
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+ ##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
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  ##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
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  ##FORMAT=<ID=VI,Number=.,Type=String,Description="An enumeration of possible inheritance modes.">
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  ##FORMAT=<ID=VIC,Number=1,Type=String,Description="Possible Compound hetrozygote variants.">
@@ -244,27 +245,27 @@
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  ##fileDate=20200320
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  ##reference=/vip/resources/GRCh38/GCA_000001405.15_GRCh38_no_alt_analysis_set.fna.gz
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  #CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Father MotherHasQuiteALongName Nephew Patient Sister Unrelated
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- chr1 9982480 . C T . PASS CSQ=T|missense_variant|MODERATE|NMNAT1|64802|Transcript|NM_001297778.1|protein_coding|5/5||NM_001297778.1:c.619C>T|NP_001284707.1:p.Arg207Trp|778/3796|619/840|207/279|R/W|Cgg/Tgg|rs142968179&CM127756|1||1|||EntrezGene|||||0.04|0.08||pathogenic||1&1||||||||0|-36|-16|17|0.00|0.00|0.00|0.00|NMNAT1|VUS|0.16328752|||AR|LP||||chr1:9982480-9982480|3.94519e-05|0|P|filter&vkgl&exit_p|,T|downstream_gene_variant|MODIFIER|NMNAT1|64802|Transcript|NM_001297779.2|protein_coding||||||||||rs142968179&CM127756|1|714|1|||EntrezGene||||||||pathogenic||1&1||||||||0|-36|-16|17|0.00|0.00|0.00|0.00|NMNAT1|VUS|0.030009428|||AR|LP||||chr1:9982480-9982480|3.94519e-05|0|P|filter&vkgl&exit_p|,T|missense_variant|MODERATE|NMNAT1|64802|Transcript|NM_022787.4|protein_coding|5/5||NM_022787.4:c.619C>T|NP_073624.2:p.Arg207Trp|716/3734|619/840|207/279|R/W|Cgg/Tgg|rs142968179&CM127756|1||1||1|EntrezGene|||||0.04|0.08||pathogenic||1&1||||||||0|-36|-16|17|0.00|0.00|0.00|0.00|NMNAT1|VUS|0.16328752|||AR|LP||||chr1:9982480-9982480|3.94519e-05|0|P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIM 0|0:10:.:.:.:. 0|0:50:.:.:.:. 0|0:50:.:.:.:. 1|0:50:AD:.:1:0 0|0:50:.:.:.:. 0|0:50:.:.:.:.
248
- chr1 152548312 symbolic1 A <DEL> . PASS CSQ=deletion|transcript_ablation|HIGH|LCE3D|84648|Transcript|NM_032563.2|protein_coding|||||||||||1||-1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|upstream_gene_variant|MODIFIER|LCE3C|353144|Transcript|NM_178434.3|protein_coding|||||||||||1|2608|1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|transcript_ablation|HIGH|LCE3E|353145|Transcript|NM_178435.4|protein_coding|||||||||||1||-1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000372937||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000013752||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000372939||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000372940||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001171682||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000254476||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000931036||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001171683||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00191731851||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00189591243||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00078414360||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00078058090||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00000257725||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;SVLEN=-49314;SVTYPE=DEL GT:DP:VI:VIC:VID:VIM:VIS 0|0:10:.:.:.:.:. 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:. 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:.
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- chr2 47408528 symbolic2 G <INS> . PASS CSQ=insertion|splice_polypyrimidine_tract_variant&coding_sequence_variant&intron_variant&feature_elongation|LOW|MSH2|4436|Transcript|NM_000251.3|protein_coding|2-8/16|2-8/15|||376-?/3115|340-?/2805|114-?/934||||1||1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|splice_polypyrimidine_tract_variant&coding_sequence_variant&intron_variant&feature_elongation|LOW|MSH2|4436|Transcript|NM_001258281.1|protein_coding|3-9/17|3-9/16|||281-?/3025|142-?/2607|48-?/868||||1||1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001031132||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000605106||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001031134||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000605107||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000605109||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001031136||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000605111||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00526224866||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00200869503||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00037157434||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00211420385||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00211397893||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00191281526||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00524206131||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00191128737||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00523779682||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00523716616||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00524736808||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00522488084||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00522348227||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00189912570||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00151154280||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00521803756||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00525714757||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00522888937||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00003947213||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00190965228||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00189989760||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00190028111||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00525662463||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00190489771||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00524615628||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00000366692||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00208026052||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;SVLEN=-49314;SVTYPE=INS GT:DP:VI:VIC:VID:VIM:VIS 0|0:10:.:.:.:.:. 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:. 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:.
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- chr4 105399137 . G A . PASS CSQ=A|missense_variant|MODERATE|PPA2|27068|Transcript|NM_006903.4|protein_coding|7/11||NM_006903.4:c.596C>T|NP_008834.3:p.Pro199Leu|616/1586|596/918|199/305|P/L|cCg/cTg|rs138215926&CM1610192|1||-1|||EntrezGene|||||0|0.985||pathogenic||1&1||||||||-34|27|-2|-43|0.00|0.00|0.00|0.00|PPA2|VUS|0.79802734|||AR|LP||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&exit_p|,A|missense_variant|MODERATE|PPA2|27068|Transcript|NM_176866.2|protein_coding|4/8||NM_176866.2:c.377C>T|NP_789842.2:p.Pro126Leu|397/1367|377/699|126/232|P/L|cCg/cTg|rs138215926&CM1610192|1||-1|||EntrezGene|||||0|0.992||pathogenic||1&1||||||||-34|27|-2|-43|0.00|0.00|0.00|0.00|PPA2|VUS|0.76154137|||AR|LP||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&exit_p|,A|missense_variant|MODERATE|PPA2|27068|Transcript|NM_176867.3|protein_coding|2/6||NM_176867.3:c.185C>T|NP_789843.2:p.Pro62Leu|205/1175|185/507|62/168|P/L|cCg/cTg|rs138215926&CM1610192|1||-1|||EntrezGene|||||0|0.995||pathogenic||1&1||||||||-34|27|-2|-43|0.00|0.00|0.00|0.00|PPA2|VUS|0.7596747|||AR|LP||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&exit_p|,A|missense_variant|MODERATE|PPA2|27068|Transcript|NM_176869.3|protein_coding|8/12||NM_176869.3:c.683C>T|NP_789845.1:p.Pro228Leu|695/1665|683/1005|228/334|P/L|cCg/cTg|rs138215926&CM1610192|1||-1||1|EntrezGene|||||0|0.993||pathogenic||1&1||||||||-34|27|-2|-43|0.00|0.00|0.00|0.00|PPA2|VUS|0.7574089|||AR|LP||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&exit_p|,A|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001252884|enhancer||||||||||rs138215926&CM1610192|1|||||||||||||pathogenic||1&1||||||||||||||||||||||||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&clinVar&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:AR,AD:chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:27068:1:AR_C 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
251
- chr7 41977712 single_breakend_nation C C. . PASS CSQ=BND|coding_sequence_variant|MODIFIER|GLI3|2737|Transcript|NM_000168.6|protein_coding|12/15||||1938/8405|1657/4743|553/1580||||1||-1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000823237||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000325885||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;SVTYPE=BND GT:DP:VI:VIC:VID:VIM:VIS 0|0:10:.:.:.:.:. 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:. 1|0:50:AR,AD:chr4_105399137_G_A,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chr7_42025358_GACTC_G,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:.
252
- chr7 42025358 . GACTC G . PASS CSQ=-|frameshift_variant|HIGH|GLI3|2737|Transcript|NM_000168.6|protein_coding|9/15||NM_000168.6:c.1258_1261del|NP_000159.3:p.Glu420LeufsTer3|1539-1542/8405|1258-1261/4743|420-421/1580|ES/X|GAGTct/ct||1||-1||1|EntrezGene||||||||||||||||||18|21|-40|6|0.00|0.00|0.00|0.00|GLI3|VUS|0.98730624||1|AD|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:AR,AD:chr7_41977712_C_:1:2737:1:AR_C 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
253
- chr8 60852584 breakend1 G ]11:134014225]G . PASS BND_DEPTH=26;CSQ=BND|intron_variant|MODIFIER|CHD7|55636|Transcript|NM_001316690.1|protein_coding||2/4|||||||||1||1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|coding_sequence_variant|MODIFIER|CHD7|55636|Transcript|NM_017780.4|protein_coding|30/38||||6499/11606|5982/8994|1994/2997||||1||1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001138764||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;MATEID=breakend2;MATE_BND_DEPTH=39;SVTYPE=BND GT:DP:VI:VIC:VID:VIM:VIS 0|0:10:.:.:.:.:. 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:. 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:.
254
- chr8 144085597 . CAG C . PASS CSQ=-|frameshift_variant|HIGH|GPAA1|8733|Transcript|NM_003801.4|protein_coding|11/12||NM_003801.4:c.1477_1478del|NP_003792.1:p.Arg493GlyfsTer152|1574-1575/2054|1477-1478/1866|493/621|R/X|AGg/g|rs782339984|1||1||1|EntrezGene||||||||pathogenic||1||||||||-15|-8|12|-21|0.02|0.00|0.00|0.00|GPAA1|VUS|0.99313146|||AR|LP||||chr8:144085598-144085600|0.000144549|0|P|filter&vkgl&exit_p|,-|downstream_gene_variant|MODIFIER|EXOSC4|54512|Transcript|NM_019037.3|protein_coding||||||||||rs782339984|1|4950|1|||EntrezGene||||||||pathogenic||1||||||||-15|-8|12|-21|0.02|0.00|0.00|0.00|GPAA1|VUS|0.0936931||||||||chr8:144085598-144085600|0.000144549|0|P|filter&vkgl&clinVar&exit_p| GT:DP:VI:VIC:VID:VIM 0|0:10:.:.:.:. 0|0:50:.:.:.:. 0|0:50:.:.:.:. 1|0:50:AD:.:1:0 0|0:50:.:.:.:. 0|0:50:.:.:.:.
255
- chr9 104784352 . AAAGAT A . PASS CSQ=-|frameshift_variant|HIGH|ABCA1|19|Transcript|NM_005502.4|protein_coding|50/50||NM_005502.4:c.6744_6748del|NP_005493.2:p.Phe2250ThrfsTer3|7057-7061/10408|6744-6748/6786|2248-2250/2261|TSF/TX|acATCTTtt/actt||1||-1||1|EntrezGene|||||||||||||||||||||||||||VUS|0.983508|HP:0000951||AD&AR||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,-|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000889339|promoter_flanking_region|||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:AR,AD:chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:19:1:AR_C 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
256
- chr10 124402930 . G C . PASS CSQ=C|stop_gained|HIGH|OAT|4942|Transcript|NM_000274.4|protein_coding|7/10||NM_000274.4:c.897C>G|NP_000265.1:p.Tyr299Ter|977/2039|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1||1|EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.98058724|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001171814.2|protein_coding|6/9||NM_001171814.2:c.483C>G|NP_001165285.1:p.Tyr161Ter|749/1811|483/906|161/301|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9785161|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322965.2|protein_coding|7/10||NM_001322965.2:c.897C>G|NP_001309894.1:p.Tyr299Ter|972/2034|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.98058724|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322966.2|protein_coding|8/11||NM_001322966.2:c.897C>G|NP_001309895.1:p.Tyr299Ter|1292/2354|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9811948|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322967.2|protein_coding|8/11||NM_001322967.2:c.897C>G|NP_001309896.1:p.Tyr299Ter|1097/2159|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9812247|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322968.2|protein_coding|9/12||NM_001322968.2:c.897C>G|NP_001309897.1:p.Tyr299Ter|1184/2246|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9810348|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322969.2|protein_coding|8/11||NM_001322969.2:c.897C>G|NP_001309898.1:p.Tyr299Ter|1064/2126|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.98210436|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322970.2|protein_coding|9/12||NM_001322970.2:c.897C>G|NP_001309899.1:p.Tyr299Ter|1280/2342|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9811948|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322971.2|protein_coding|5/8||NM_001322971.2:c.576C>G|NP_001309900.1:p.Tyr192Ter|656/1718|576/999|192/332|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9727213|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322974.2|protein_coding|7/10||NM_001322974.2:c.297C>G|NP_001309903.1:p.Tyr99Ter|863/1925|297/720|99/239|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.974531|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIM 0|0:10:.:.:.:. 0|0:50:.:.:.:. 0|0:50:.:.:.:. 1|0:50:AD:.:1:0 0|0:50:.:.:.:. 0|0:50:.:.:.:.
257
- chr11 134144330 breakend2 G G[8:61765143[ . PASS BND_DEPTH=39;CSQ=BND|intron_variant|MODIFIER|JAM3|83700|Transcript|NM_001205329.2|protein_coding||3/7|||||||||1||1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|coding_sequence_variant|MODIFIER|JAM3|83700|Transcript|NM_032801.5|protein_coding|4/9||||359/3765|347/933|116/310||||1||1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;MATEID=breakend1;MATE_BND_DEPTH=26;SVTYPE=BND GT:DP:VI:VIC:VID:VIM 0|0:10:.:.:.:. 0|0:50:.:.:.:. 0|0:50:.:.:.:. 1|0:50:AD:.:1:0 0|0:50:.:.:.:. 0|0:50:.:.:.:.
258
- chr13 76995993 . G A . PASS CSQ=A|missense_variant|MODERATE|CLN5|1203|Transcript|NM_001366624.2|protein_coding|3/5||NM_001366624.2:c.431G>A|NP_001353553.1:p.Cys144Tyr|449/5286|431/594|144/197|C/Y|tGt/tAt|rs1566219136|1||1|||EntrezGene|||||0|0.995||pathogenic||1||||||||-27|-43|-27|-1|0.00|0.00|0.01|0.00|CLN5|VUS|0.82795596|||AR|LP|||||||P|filter&vkgl&exit_p|,A|missense_variant|MODERATE|CLN5|1203|Transcript|NM_006493.4|protein_coding|3/4||NM_006493.4:c.431G>A|NP_006484.2:p.Cys144Tyr|449/5243|431/1077|144/358|C/Y|tGt/tAt|rs1566219136|1||1||1|EntrezGene|||||0|0.999||pathogenic||1||||||||-27|-43|-27|-1|0.00|0.00|0.01|0.00|CLN5|VUS|0.8734921|||AR|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIM 0|0:10:.:.:.:. 0|0:50:.:.:.:. 0|0:50:.:.:.:. 1|0:50:AD:.:1:0 0|0:50:.:.:.:. 0|0:50:.:.:.:.
259
- chr14 88870063 . TG T . PASS CSQ=-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001288781.1|protein_coding|12/16||NM_001288781.1:c.963del|NP_001275710.1:p.Met321IlefsTer15|1159/2378|963/1596|321/531|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.9879852|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001288782.1|protein_coding|10/14||NM_001288782.1:c.321del|NP_001275711.1:p.Met107IlefsTer15|1079/2298|321/954|107/317|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.985551|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001288783.1|protein_coding|11/15||NM_001288783.1:c.198del|NP_001275712.1:p.Met66IlefsTer15|1051/2270|198/831|66/276|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.98350626|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001366535.2|protein_coding|10/13||NM_001366535.2:c.885del|NP_001353464.1:p.Met295IlefsTer15|942/5160|885/1434|295/477|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.9825065|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001366536.2|protein_coding|9/12||NM_001366536.2:c.795del|NP_001353465.1:p.Met265IlefsTer15|852/5070|795/1344|265/447|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.9880476|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_144596.4|protein_coding|11/15||NM_144596.4:c.915del|NP_653197.2:p.Met305IlefsTer15|972/2183|915/1548|305/515|M/X|atG/at|rs1431207606|1||1||1|EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.97812086|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_198309.3|protein_coding|11/15||NM_198309.3:c.885del|NP_938051.1:p.Met295IlefsTer15|1081/2300|885/1518|295/505|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.9879701|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_198310.3|protein_coding|10/14||NM_198310.3:c.795del|NP_938052.1:p.Met265IlefsTer15|991/2210|795/1428|265/475|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.98293847|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|non_coding_transcript_exon_variant|MODIFIER|TTC8|123016|Transcript|NR_159362.2|misc_RNA|11/15||NR_159362.2:n.1002del||1002/5304|||||rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.20394427|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIM 0|0:10:.:.:.:. 0|0:50:.:.:.:. 0|0:50:.:.:.:. 1|0:50:AD:.:1:0 0|0:50:.:.:.:. 0|0:50:.:.:.:.
260
- chr14 104701523 . T G . PASS CSQ=G|missense_variant|MODERATE|INF2|64423|Transcript|NM_001031714.4|protein_coding|2/22||NM_001031714.4:c.158T>G|NP_001026884.3:p.Leu53Arg|289/7566|158/3723|53/1240|L/R|cTg/cGg||1||1|||EntrezGene|||||0|0.999||||||||||||-28|-2|37|-2|0.00|0.00|0.00|0.00|INF2|VUS|0.89743406|||AD|LP|||||||P|filter&vkgl&exit_p|,G|missense_variant|MODERATE|INF2|64423|Transcript|NM_022489.4|protein_coding|2/23||NM_022489.4:c.158T>G|NP_071934.3:p.Leu53Arg|289/7623|158/3750|53/1249|L/R|cTg/cGg||1||1||1|EntrezGene|||||0|0.999||||||||||||-28|-2|37|-2|0.00|0.00|0.00|0.00|INF2|VUS|0.89743406|||AD|LP|||||||P|filter&vkgl&exit_p|,G|missense_variant|MODERATE|INF2|64423|Transcript|NM_032714.3|protein_coding|2/5||NM_032714.3:c.158T>G|NP_116103.1:p.Leu53Arg|289/1692|158/705|53/234|L/R|cTg/cGg||1||1|||EntrezGene|||||0|0.999||||||||||||-28|-2|37|-2|0.00|0.00|0.00|0.00|INF2|VUS|0.89743406|||AD|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIG:VIM 0|0:10:.:.:.:.:. 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:. 1|0:50:AD:.:1:64423:1 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:.
261
- chr17 31229046 . AC A . PASS CSQ=-|frameshift_variant|HIGH|NF1|4763|Transcript|NM_000267.3|protein_coding|21/57||NM_000267.3:c.2433del|NP_000258.1:p.Ile812LeufsTer9|2816/12362|2433/8457|811/2818|T/X|acC/ac||1||1|||EntrezGene|||||||1|||||||||||-22|-11|12|25|0.00|0.00|0.00|0.00|NF1|VUS|0.9921835|HP:0000951|1|AD|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|NF1|4763|Transcript|NM_001042492.3|protein_coding|21/58||NM_001042492.3:c.2433del|NP_001035957.1:p.Ile812LeufsTer9|2766/12373|2433/8520|811/2839|T/X|acC/ac||1||1||1|EntrezGene|||||||1|||||||||||-22|-11|12|25|0.00|0.00|0.00|0.00|NF1|VUS|0.99201524|HP:0000951|1|AD|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:AR,AD:chr17_31336861_T_G:1:4763:1:AR_C 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
262
- chr17 31336861 . T G . PASS CSQ=G|missense_variant|MODERATE|NF1|4763|Transcript|NM_000267.3|protein_coding|41/57||NM_000267.3:c.6311T>G|NP_000258.1:p.Leu2104Arg|6694/12362|6311/8457|2104/2818|L/R|cTg/cGg|CM143458&CM141499|1||1|||EntrezGene|||||0|0.994||||1&1||||||||-42|41|-34|8|0.00|0.00|0.00|0.00|NF1|VUS|0.80934244|HP:0000951|1|AD|LP|||||||P|filter&vkgl&exit_p|,G|missense_variant|MODERATE|NF1|4763|Transcript|NM_001042492.3|protein_coding|42/58||NM_001042492.3:c.6374T>G|NP_001035957.1:p.Leu2125Arg|6707/12373|6374/8520|2125/2839|L/R|cTg/cGg|CM143458&CM141499|1||1||1|EntrezGene|||||0|0.993||||1&1||||||||-42|41|-34|8|0.00|0.00|0.00|0.00|NF1|VUS|0.80934244|HP:0000951|1|AD|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:AR,AD:chr17_31229046_AC_A:1:4763:1:AR_C 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
263
- chr19 11105470 . C G . PASS CSQ=G|stop_gained|HIGH|LDLR|3949|Transcript|NM_000527.5|protein_coding|4/18||NM_000527.5:c.564C>G|NP_000518.1:p.Tyr188Ter|650/5173|564/2583|188/860|Y/*|taC/taG|rs121908034&CM920416|1||1||1|EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.97251827|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|stop_gained|HIGH|LDLR|3949|Transcript|NM_001195798.2|protein_coding|4/18||NM_001195798.2:c.564C>G|NP_001182727.1:p.Tyr188Ter|650/5167|564/2577|188/858|Y/*|taC/taG|rs121908034&CM920416|1||1|||EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.97251827|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|stop_gained|HIGH|LDLR|3949|Transcript|NM_001195799.2|protein_coding|3/17||NM_001195799.2:c.441C>G|NP_001182728.1:p.Tyr147Ter|527/5050|441/2460|147/819|Y/*|taC/taG|rs121908034&CM920416|1||1|||EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.9850093|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|intron_variant|MODIFIER|LDLR|3949|Transcript|NM_001195800.2|protein_coding||3/15|NM_001195800.2:c.314-1922C>G|||||||rs121908034&CM920416|1||1|||EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.006388327|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|intron_variant|MODIFIER|LDLR|3949|Transcript|NM_001195803.2|protein_coding||3/15|NM_001195803.2:c.314-1095C>G|||||||rs121908034&CM920416|1||1|||EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.006388327|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001219902|promoter_flanking_region||||||||||rs121908034&CM920416|1|||||||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803||||||||||||||||||||||||||||P|filter&vkgl&clinVar&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:3949:1:AR_C 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
264
- chr19 17341188 . GA G . PASS CSQ=-|frameshift_variant|HIGH|GTPBP3|84705|Transcript|NM_001128855.3|protein_coding|8/9||NM_001128855.3:c.1058del|NP_001122327.1:p.Asn353ThrfsTer26|1117/2503|1058/1416|353/471|N/X|aAc/ac||1||1|||EntrezGene|||||||1|||||||||||34|33|-7|33|0.01|0.00|0.00|0.00|GTPBP3|VUS|0.9901776|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|GTPBP3|84705|Transcript|NM_001195422.1|protein_coding|8/9||NM_001195422.1:c.1187del|NP_001182351.1:p.Asn396ThrfsTer26|1209/2595|1187/1545|396/514|N/X|aAc/ac||1||1|||EntrezGene|||||||1|||||||||||34|33|-7|33|0.01|0.00|0.00|0.00|GTPBP3|VUS|0.9913974|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|GTPBP3|84705|Transcript|NM_032620.4|protein_coding|8/9||NM_032620.4:c.1121del|NP_116009.2:p.Asn374ThrfsTer26|1180/2566|1121/1479|374/492|N/X|aAc/ac||1||1||1|EntrezGene|||||||1|||||||||||34|33|-7|33|0.01|0.00|0.00|0.00|GTPBP3|VUS|0.99110925|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|GTPBP3|84705|Transcript|NM_133644.4|protein_coding|7/8||NM_133644.4:c.1217del|NP_598399.2:p.Asn406ThrfsTer26|1276/2662|1217/1575|406/524|N/X|aAc/ac||1||1|||EntrezGene|||||||1|||||||||||34|33|-7|33|0.01|0.00|0.00|0.00|GTPBP3|VUS|0.9916678|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000586166|promoter|||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,-|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001022836|CTCF_binding_site|||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,-|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00000278460||||||||||||1||1||||||||||||||||ENSPFM0305|8|N||HOXB2::ELF1||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:84705:1:AR_C 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
265
- chr20 63695639 . C T . PASS CSQ=T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001134758.4|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267544.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267545.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267546.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267547.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267548.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267549.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|missense_variant|MODERATE|RTEL1|51750|Transcript|NM_001283009.2|protein_coding|34/35||NM_001283009.2:c.3811C>T|NP_001269938.1:p.Arg1271Trp|4136/4615|3811/3903|1271/1300|R/W|Cgg/Tgg|rs993254667|1||1||1|EntrezGene|||||0.16|0.003||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1|VUS|0.0055121304|HP:0000951||AD&AR|||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&exit_p|,T|intron_variant|MODIFIER|RTEL1|51750|Transcript|NM_001283010.1|protein_coding||33/33|NM_001283010.1:c.2984-139C>T|||||||rs993254667|1||1|||EntrezGene||||||||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1|VUS|0.002660127|HP:0000951||AD&AR|||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_003224.6|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|upstream_gene_variant|MODIFIER|TNFRSF6B|8771|Transcript|NM_003823.4|protein_coding||||||||||rs993254667|1|1013|1|||EntrezGene|||||||||||||||||||||||||||VUS|0.0115982685||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|intron_variant|MODIFIER|RTEL1|51750|Transcript|NM_016434.4|protein_coding||34/34|NM_016434.4:c.3653-139C>T|||||||rs993254667|1||1|||EntrezGene||||||||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1|VUS|0.002660127|HP:0000951||AD&AR|||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|intron_variant|MODIFIER|RTEL1|51750|Transcript|NM_032957.5|protein_coding||34/34|NM_032957.5:c.3725-139C>T|||||||rs993254667|1||1|||EntrezGene||||||||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1|VUS|0.002660127|HP:0000951||AD&AR|||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|non_coding_transcript_exon_variant|MODIFIER|RTEL1-TNFRSF6B|100533107|Transcript|NR_037882.1|lncRNA|34/38||NR_037882.1:n.4638C>T||4638/5772|||||rs993254667|1||1|||EntrezGene||||||||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1-TNFRSF6B|VUS|0.039789375||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051954.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051955.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051956.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051957.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051958.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000657794|CTCF_binding_site||||||||||rs993254667|1|||||||||||||||||||||||||||||||||||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_:1:51750:1:AR_C 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
266
- chr22 50189164 . C CTG . PASS CSQ=TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_001320484.2|protein_coding||1/9|NM_001320484.2:c.-35+3188_-35+3189insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_001320485.2|protein_coding||1/9|NM_001320485.2:c.-35+3188_-35+3189insTG||||||||1||1||1|EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|upstream_gene_variant|MODIFIER|TRABD|80305|Transcript|NM_001320487.2|protein_coding|||||||||||1|1422|1|||EntrezGene|||||||||||||||||||||||||||VUS|0.25514466|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|upstream_gene_variant|MODIFIER|TRABD|80305|Transcript|NM_001320488.2|protein_coding|||||||||||1|1422|1|||EntrezGene|||||||||||||||||||||||||||VUS|0.25514466|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_001378762.1|protein_coding||1/9|NM_001378762.1:c.-35+3119_-35+3120insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_001378765.1|protein_coding||1/10|NM_001378765.1:c.-35+3159_-35+3160insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_025204.4|protein_coding||1/9|NM_025204.4:c.-35+3163_-35+3164insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant&non_coding_transcript_variant|MODIFIER|TRABD|80305|Transcript|NR_135275.2|misc_RNA||1/9|NR_135275.2:n.64+3188_64+3189insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.015001616|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000147690|promoter|||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIM:VIS 0|0:10:.:.:.:.:. 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:. 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chrM_15325_A_G,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C 0|0:50:.:.:.:.:. 0|0:50:.:.:.:.:.
267
- chr22 50283117 . C T . PASS CSQ=T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376864.1|protein_coding|17/37||NM_001376864.1:c.2749G>A|NP_001363793.1:p.Gly917Ser|2881/6611|2749/5754|917/1917|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376865.1|protein_coding|18/38||NM_001376865.1:c.2818G>A|NP_001363794.1:p.Gly940Ser|2898/6391|2818/5586|940/1861|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376866.1|protein_coding|17/37||NM_001376866.1:c.2749G>A|NP_001363795.1:p.Gly917Ser|2909/6402|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376867.1|protein_coding|18/38||NM_001376867.1:c.2749G>A|NP_001363796.1:p.Gly917Ser|2969/6462|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376868.1|protein_coding|18/38||NM_001376868.1:c.2749G>A|NP_001363797.1:p.Gly917Ser|2962/6455|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376869.1|protein_coding|16/36||NM_001376869.1:c.2749G>A|NP_001363798.1:p.Gly917Ser|2856/6349|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376870.1|protein_coding|17/37||NM_001376870.1:c.2749G>A|NP_001363799.1:p.Gly917Ser|2881/6374|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376871.1|protein_coding|17/37||NM_001376871.1:c.2749G>A|NP_001363800.1:p.Gly917Ser|2874/6367|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376872.1|protein_coding|19/39||NM_001376872.1:c.2749G>A|NP_001363801.1:p.Gly917Ser|3066/6559|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376873.1|protein_coding|18/38||NM_001376873.1:c.2749G>A|NP_001363802.1:p.Gly917Ser|3218/6711|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376874.1|protein_coding|18/38||NM_001376874.1:c.2749G>A|NP_001363803.1:p.Gly917Ser|2934/6427|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376875.1|protein_coding|16/36||NM_001376875.1:c.2749G>A|NP_001363804.1:p.Gly917Ser|2933/6426|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376876.1|protein_coding|18/38||NM_001376876.1:c.2749G>A|NP_001363805.1:p.Gly917Ser|2927/6420|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376877.1|protein_coding|18/38||NM_001376877.1:c.2749G>A|NP_001363806.1:p.Gly917Ser|3198/6691|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376878.1|protein_coding|16/36||NM_001376878.1:c.2749G>A|NP_001363807.1:p.Gly917Ser|2821/6314|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376879.1|protein_coding|19/39||NM_001376879.1:c.2749G>A|NP_001363808.1:p.Gly917Ser|3101/6594|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376880.1|protein_coding|17/37||NM_001376880.1:c.2749G>A|NP_001363809.1:p.Gly917Ser|2991/6484|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376881.1|protein_coding|18/38||NM_001376881.1:c.2749G>A|NP_001363810.1:p.Gly917Ser|3046/6539|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376882.1|protein_coding|17/37||NM_001376882.1:c.2749G>A|NP_001363811.1:p.Gly917Ser|3165/6658|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376883.1|protein_coding|17/37||NM_001376883.1:c.2749G>A|NP_001363812.1:p.Gly917Ser|2881/6350|2749/5493|917/1830|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376884.1|protein_coding|16/36||NM_001376884.1:c.2749G>A|NP_001363813.1:p.Gly917Ser|2821/6236|2749/5439|917/1812|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376885.1|protein_coding|17/37||NM_001376885.1:c.2749G>A|NP_001363814.1:p.Gly917Ser|2909/6324|2749/5439|917/1812|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376886.1|protein_coding|17/37||NM_001376886.1:c.2656G>A|NP_001363815.1:p.Gly886Ser|2876/6369|2656/5424|886/1807|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_012401.4|protein_coding|17/37||NM_012401.4:c.2749G>A|NP_036533.2:p.Gly917Ser|2916/6409|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1||1|EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp| GT:DP:VI:VIC:VID:VIM 0|0:10:.:.:.:. 0|0:50:.:.:.:. 0|0:50:.:.:.:. 1|0:50:AD:.:1:0 0|0:50:.:.:.:. 0|0:50:.:.:.:.
268
- chrX 49075362 x_chrom A T . PASS CSQ=T|splice_donor_variant|HIGH|WDR45|11152|Transcript|NM_001029896.2|protein_coding||9/10|NM_001029896.2:c.827+2T>A|||||||CS135341|1||-1||1|EntrezGene||||||||||1||||||||27|28|-2|2|0.02|0.00|0.01|0.99|WDR45|VUS|0.98327905|HP:0000951||XL|LP|||||||P|filter&vkgl&exit_p|,T|splice_donor_variant|HIGH|WDR45|11152|Transcript|NM_007075.4|protein_coding||10/11|NM_007075.4:c.830+2T>A|||||||CS135341|1||-1|||EntrezGene||||||||||1||||||||27|28|-2|2|0.02|0.00|0.01|0.99|WDR45|VUS|0.98327905|HP:0000951||XL|LP|||||||P|filter&vkgl&exit_p|,T|upstream_gene_variant|MODIFIER|PRAF2|11230|Transcript|NM_007213.3|protein_coding||||||||||CS135341|1|1360|-1|||EntrezGene||||||||||1||||||||27|28|-2|2|0.02|0.00|0.01|0.99|WDR45|VUS|0.0113522755|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&exit_p|,T|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000906841|CTCF_binding_site||||||||||CS135341|1|||||||||||||||1|||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS 0|0:10:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:. 1|0:50:XLD,XL,XLR:.:1:11152:1:XLD,XLR 0|0:50:.:.:.:.:.:. 0|0:50:.:.:.:.:.:.
269
- chrY 2787600 y_chrom G A . PASS CSQ=A|stop_gained|HIGH|SRY|6736|Transcript|NM_003140.3|protein_coding|1/1||NM_003140.3:c.4C>T|NP_003131.1:p.Gln2Ter|83/828|4/615|2/204|Q/*|Caa/Taa|rs104894977&CM981858|1||-1||1|EntrezGene||||||||pathogenic||1&1|2401216&9443877|||||||-26|-50|2|-4|0.01|0.00|0.00|0.00|SRY|VUS|0.92795527|||||||||||P|filter&vkgl&clinVar&exit_p| GT:DP:VIC:VID:VIM 0:10:.:.:. .:.:.:.:. 1:50:.:.:. 1:50:.:1:0 .:.:.:.:. 1:50:.:.:.
270
- chrM 15325 mt_chrom A G . PASS CSQ=G|intergenic_variant|MODIFIER|||||||||||||||rs1556424568|1||||1||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VIC:VID:VIM 0|0:10:.:.:. 0|0:50:.:.:. 0|0:50:.:.:. 1|0:50:.:1:0 0|0:50:.:.:. 0|0:50:.:.:.
248
+ chr1 9982480 . C T . PASS CSQ=T|missense_variant|MODERATE|NMNAT1|64802|Transcript|NM_001297778.1|protein_coding|5/5||NM_001297778.1:c.619C>T|NP_001284707.1:p.Arg207Trp|778/3796|619/840|207/279|R/W|Cgg/Tgg|rs142968179&CM127756|1||1|||EntrezGene|||||0.04|0.08||pathogenic||1&1||||||||0|-36|-16|17|0.00|0.00|0.00|0.00|NMNAT1|VUS|0.16328752|||AR|LP||||chr1:9982480-9982480|3.94519e-05|0|P|filter&vkgl&exit_p|,T|downstream_gene_variant|MODIFIER|NMNAT1|64802|Transcript|NM_001297779.2|protein_coding||||||||||rs142968179&CM127756|1|714|1|||EntrezGene||||||||pathogenic||1&1||||||||0|-36|-16|17|0.00|0.00|0.00|0.00|NMNAT1|VUS|0.030009428|||AR|LP||||chr1:9982480-9982480|3.94519e-05|0|P|filter&vkgl&exit_p|,T|missense_variant|MODERATE|NMNAT1|64802|Transcript|NM_022787.4|protein_coding|5/5||NM_022787.4:c.619C>T|NP_073624.2:p.Arg207Trp|716/3734|619/840|207/279|R/W|Cgg/Tgg|rs142968179&CM127756|1||1||1|EntrezGene|||||0.04|0.08||pathogenic||1&1||||||||0|-36|-16|17|0.00|0.00|0.00|0.00|NMNAT1|VUS|0.16328752|||AR|LP||||chr1:9982480-9982480|3.94519e-05|0|P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIM:GQ 0|0:10:.:.:.:.:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50 1|0:50:AD:.:1:0:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50
249
+ chr1 152548312 symbolic1 A <DEL> . PASS CSQ=deletion|transcript_ablation|HIGH|LCE3D|84648|Transcript|NM_032563.2|protein_coding|||||||||||1||-1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|upstream_gene_variant|MODIFIER|LCE3C|353144|Transcript|NM_178434.3|protein_coding|||||||||||1|2608|1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|transcript_ablation|HIGH|LCE3E|353145|Transcript|NM_178435.4|protein_coding|||||||||||1||-1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000372937||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000013752||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000372939||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000372940||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001171682||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000254476||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000931036||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|regulatory_region_ablation&regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001171683||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00191731851||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00189591243||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00078414360||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00078058090||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,deletion|TFBS_ablation&TF_binding_site_variant|MODERATE|||MotifFeature|ENSM00000257725||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;SVLEN=-49314;SVTYPE=DEL GT:DP:VI:VIC:VID:VIM:VIS:GQ 0|0:10:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C:10 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50
250
+ chr2 47408528 symbolic2 G <INS> . PASS CSQ=insertion|splice_polypyrimidine_tract_variant&coding_sequence_variant&intron_variant&feature_elongation|LOW|MSH2|4436|Transcript|NM_000251.3|protein_coding|2-8/16|2-8/15|||376-?/3115|340-?/2805|114-?/934||||1||1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|splice_polypyrimidine_tract_variant&coding_sequence_variant&intron_variant&feature_elongation|LOW|MSH2|4436|Transcript|NM_001258281.1|protein_coding|3-9/17|3-9/16|||281-?/3025|142-?/2607|48-?/868||||1||1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001031132||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000605106||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001031134||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000605107||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000605109||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001031136||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000605111||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00526224866||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00200869503||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00037157434||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00211420385||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00211397893||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00191281526||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00524206131||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00191128737||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00523779682||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00523716616||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00524736808||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00522488084||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00522348227||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00189912570||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00151154280||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00521803756||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00525714757||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00522888937||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00003947213||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00190965228||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00189989760||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00190028111||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00525662463||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00190489771||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00524615628||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00000366692||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,insertion|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00208026052||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;SVLEN=-49314;SVTYPE=INS GT:DP:VI:VIC:VID:VIM:VIS:GQ 0|0:10:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50
251
+ chr4 105399137 . G A . PASS CSQ=A|missense_variant|MODERATE|PPA2|27068|Transcript|NM_006903.4|protein_coding|7/11||NM_006903.4:c.596C>T|NP_008834.3:p.Pro199Leu|616/1586|596/918|199/305|P/L|cCg/cTg|rs138215926&CM1610192|1||-1|||EntrezGene|||||0|0.985||pathogenic||1&1||||||||-34|27|-2|-43|0.00|0.00|0.00|0.00|PPA2|VUS|0.79802734|||AR|LP||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&exit_p|,A|missense_variant|MODERATE|PPA2|27068|Transcript|NM_176866.2|protein_coding|4/8||NM_176866.2:c.377C>T|NP_789842.2:p.Pro126Leu|397/1367|377/699|126/232|P/L|cCg/cTg|rs138215926&CM1610192|1||-1|||EntrezGene|||||0|0.992||pathogenic||1&1||||||||-34|27|-2|-43|0.00|0.00|0.00|0.00|PPA2|VUS|0.76154137|||AR|LP||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&exit_p|,A|missense_variant|MODERATE|PPA2|27068|Transcript|NM_176867.3|protein_coding|2/6||NM_176867.3:c.185C>T|NP_789843.2:p.Pro62Leu|205/1175|185/507|62/168|P/L|cCg/cTg|rs138215926&CM1610192|1||-1|||EntrezGene|||||0|0.995||pathogenic||1&1||||||||-34|27|-2|-43|0.00|0.00|0.00|0.00|PPA2|VUS|0.7596747|||AR|LP||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&exit_p|,A|missense_variant|MODERATE|PPA2|27068|Transcript|NM_176869.3|protein_coding|8/12||NM_176869.3:c.683C>T|NP_789845.1:p.Pro228Leu|695/1665|683/1005|228/334|P/L|cCg/cTg|rs138215926&CM1610192|1||-1||1|EntrezGene|||||0|0.993||pathogenic||1&1||||||||-34|27|-2|-43|0.00|0.00|0.00|0.00|PPA2|VUS|0.7574089|||AR|LP||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&exit_p|,A|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001252884|enhancer||||||||||rs138215926&CM1610192|1|||||||||||||pathogenic||1&1||||||||||||||||||||||||||chr4:105399137-105399137|0.000434159|0|P|filter&vkgl&clinVar&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:50:AR,AD:chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:27068:1:AR_C:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
252
+ chr7 41977712 single_breakend_nation C C. . PASS CSQ=BND|coding_sequence_variant|MODIFIER|GLI3|2737|Transcript|NM_000168.6|protein_coding|12/15||||1938/8405|1657/4743|553/1580||||1||-1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000823237||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000325885||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;SVTYPE=BND GT:DP:VI:VIC:VID:VIM:VIS:GQ 0|0:10:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 1|0:50:AR,AD:chr4_105399137_G_A,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chr7_42025358_GACTC_G,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50
253
+ chr7 42025358 . GACTC G . PASS CSQ=-|frameshift_variant|HIGH|GLI3|2737|Transcript|NM_000168.6|protein_coding|9/15||NM_000168.6:c.1258_1261del|NP_000159.3:p.Glu420LeufsTer3|1539-1542/8405|1258-1261/4743|420-421/1580|ES/X|GAGTct/ct||1||-1||1|EntrezGene||||||||||||||||||18|21|-40|6|0.00|0.00|0.00|0.00|GLI3|VUS|0.98730624||1|AD|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:50:AR,AD:chr7_41977712_C_:1:2737:1:AR_C:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
254
+ chr8 60852584 breakend1 G ]11:134014225]G . PASS BND_DEPTH=26;CSQ=BND|intron_variant|MODIFIER|CHD7|55636|Transcript|NM_001316690.1|protein_coding||2/4|||||||||1||1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|coding_sequence_variant|MODIFIER|CHD7|55636|Transcript|NM_017780.4|protein_coding|30/38||||6499/11606|5982/8994|1994/2997||||1||1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001138764||||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;MATEID=breakend2;MATE_BND_DEPTH=39;SVTYPE=BND GT:DP:VI:VIC:VID:VIM:VIS:GQ 0|0:10:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50
255
+ chr8 144085597 . CAG C . PASS CSQ=-|frameshift_variant|HIGH|GPAA1|8733|Transcript|NM_003801.4|protein_coding|11/12||NM_003801.4:c.1477_1478del|NP_003792.1:p.Arg493GlyfsTer152|1574-1575/2054|1477-1478/1866|493/621|R/X|AGg/g|rs782339984|1||1||1|EntrezGene||||||||pathogenic||1||||||||-15|-8|12|-21|0.02|0.00|0.00|0.00|GPAA1|VUS|0.99313146|||AR|LP||||chr8:144085598-144085600|0.000144549|0|P|filter&vkgl&exit_p|,-|downstream_gene_variant|MODIFIER|EXOSC4|54512|Transcript|NM_019037.3|protein_coding||||||||||rs782339984|1|4950|1|||EntrezGene||||||||pathogenic||1||||||||-15|-8|12|-21|0.02|0.00|0.00|0.00|GPAA1|VUS|0.0936931||||||||chr8:144085598-144085600|0.000144549|0|P|filter&vkgl&clinVar&exit_p| GT:DP:VI:VIC:VID:VIM:GQ 0|0:10:.:.:.:.:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50 1|0:50:AD:.:1:0:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50
256
+ chr9 104784352 . AAAGAT A . PASS CSQ=-|frameshift_variant|HIGH|ABCA1|19|Transcript|NM_005502.4|protein_coding|50/50||NM_005502.4:c.6744_6748del|NP_005493.2:p.Phe2250ThrfsTer3|7057-7061/10408|6744-6748/6786|2248-2250/2261|TSF/TX|acATCTTtt/actt||1||-1||1|EntrezGene|||||||||||||||||||||||||||VUS|0.983508|HP:0000951||AD&AR||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,-|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000889339|promoter_flanking_region|||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:50:AR,AD:chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:19:1:AR_C:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
257
+ chr10 124402930 . G C . PASS CSQ=C|stop_gained|HIGH|OAT|4942|Transcript|NM_000274.4|protein_coding|7/10||NM_000274.4:c.897C>G|NP_000265.1:p.Tyr299Ter|977/2039|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1||1|EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.98058724|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001171814.2|protein_coding|6/9||NM_001171814.2:c.483C>G|NP_001165285.1:p.Tyr161Ter|749/1811|483/906|161/301|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9785161|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322965.2|protein_coding|7/10||NM_001322965.2:c.897C>G|NP_001309894.1:p.Tyr299Ter|972/2034|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.98058724|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322966.2|protein_coding|8/11||NM_001322966.2:c.897C>G|NP_001309895.1:p.Tyr299Ter|1292/2354|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9811948|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322967.2|protein_coding|8/11||NM_001322967.2:c.897C>G|NP_001309896.1:p.Tyr299Ter|1097/2159|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9812247|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322968.2|protein_coding|9/12||NM_001322968.2:c.897C>G|NP_001309897.1:p.Tyr299Ter|1184/2246|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9810348|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322969.2|protein_coding|8/11||NM_001322969.2:c.897C>G|NP_001309898.1:p.Tyr299Ter|1064/2126|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.98210436|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322970.2|protein_coding|9/12||NM_001322970.2:c.897C>G|NP_001309899.1:p.Tyr299Ter|1280/2342|897/1320|299/439|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9811948|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322971.2|protein_coding|5/8||NM_001322971.2:c.576C>G|NP_001309900.1:p.Tyr192Ter|656/1718|576/999|192/332|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.9727213|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p|,C|stop_gained|HIGH|OAT|4942|Transcript|NM_001322974.2|protein_coding|7/10||NM_001322974.2:c.297C>G|NP_001309903.1:p.Tyr99Ter|863/1925|297/720|99/239|Y/*|taC/taG|rs121965057&CM920525|1||-1|||EntrezGene||||||||likely_pathogenic&pathogenic||1&1|1737786&23076989&1609808&22674428|||||||-1|-3|-3|4|0.00|0.00|0.00|0.00|OAT|VUS|0.974531|||AR|LP||||chr10:124402930-124402930|2.6295e-05|0|P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIM:GQ 0|0:10:.:.:.:.:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50 1|0:50:AD:.:1:0:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50
258
+ chr11 134144330 breakend2 G G[8:61765143[ . PASS BND_DEPTH=39;CSQ=BND|intron_variant|MODIFIER|JAM3|83700|Transcript|NM_001205329.2|protein_coding||3/7|||||||||1||1|||EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,BND|coding_sequence_variant|MODIFIER|JAM3|83700|Transcript|NM_032801.5|protein_coding|4/9||||359/3765|347/933|116/310||||1||1||1|EntrezGene|||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|;MATEID=breakend1;MATE_BND_DEPTH=26;SVTYPE=BND GT:DP:VI:VIC:VID:VIM:GQ 0|0:10:.:.:.:.:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50 1|0:50:AD:.:1:0:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50
259
+ chr13 76995993 . G A . PASS CSQ=A|missense_variant|MODERATE|CLN5|1203|Transcript|NM_001366624.2|protein_coding|3/5||NM_001366624.2:c.431G>A|NP_001353553.1:p.Cys144Tyr|449/5286|431/594|144/197|C/Y|tGt/tAt|rs1566219136|1||1|||EntrezGene|||||0|0.995||pathogenic||1||||||||-27|-43|-27|-1|0.00|0.00|0.01|0.00|CLN5|VUS|0.82795596|||AR|LP|||||||P|filter&vkgl&exit_p|,A|missense_variant|MODERATE|CLN5|1203|Transcript|NM_006493.4|protein_coding|3/4||NM_006493.4:c.431G>A|NP_006484.2:p.Cys144Tyr|449/5243|431/1077|144/358|C/Y|tGt/tAt|rs1566219136|1||1||1|EntrezGene|||||0|0.999||pathogenic||1||||||||-27|-43|-27|-1|0.00|0.00|0.01|0.00|CLN5|VUS|0.8734921|||AR|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIM:GQ 0|0:10:.:.:.:.:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50 1|0:50:AD:.:1:0:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50
260
+ chr14 88870063 . TG T . PASS CSQ=-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001288781.1|protein_coding|12/16||NM_001288781.1:c.963del|NP_001275710.1:p.Met321IlefsTer15|1159/2378|963/1596|321/531|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.9879852|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001288782.1|protein_coding|10/14||NM_001288782.1:c.321del|NP_001275711.1:p.Met107IlefsTer15|1079/2298|321/954|107/317|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.985551|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001288783.1|protein_coding|11/15||NM_001288783.1:c.198del|NP_001275712.1:p.Met66IlefsTer15|1051/2270|198/831|66/276|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.98350626|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001366535.2|protein_coding|10/13||NM_001366535.2:c.885del|NP_001353464.1:p.Met295IlefsTer15|942/5160|885/1434|295/477|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.9825065|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_001366536.2|protein_coding|9/12||NM_001366536.2:c.795del|NP_001353465.1:p.Met265IlefsTer15|852/5070|795/1344|265/447|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.9880476|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_144596.4|protein_coding|11/15||NM_144596.4:c.915del|NP_653197.2:p.Met305IlefsTer15|972/2183|915/1548|305/515|M/X|atG/at|rs1431207606|1||1||1|EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.97812086|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_198309.3|protein_coding|11/15||NM_198309.3:c.885del|NP_938051.1:p.Met295IlefsTer15|1081/2300|885/1518|295/505|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.9879701|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|TTC8|123016|Transcript|NM_198310.3|protein_coding|10/14||NM_198310.3:c.795del|NP_938052.1:p.Met265IlefsTer15|991/2210|795/1428|265/475|M/X|atG/at|rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.98293847|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|non_coding_transcript_exon_variant|MODIFIER|TTC8|123016|Transcript|NR_159362.2|misc_RNA|11/15||NR_159362.2:n.1002del||1002/5304|||||rs1431207606|1||1|||EntrezGene||||||||likely_pathogenic||1||||||||18|-4|-9|-4|0.00|0.16|0.00|0.00|TTC8|VUS|0.20394427|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIM:GQ 0|0:10:.:.:.:.:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50 1|0:50:AD:.:1:0:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50
261
+ chr14 104701523 . T G . PASS CSQ=G|missense_variant|MODERATE|INF2|64423|Transcript|NM_001031714.4|protein_coding|2/22||NM_001031714.4:c.158T>G|NP_001026884.3:p.Leu53Arg|289/7566|158/3723|53/1240|L/R|cTg/cGg||1||1|||EntrezGene|||||0|0.999||||||||||||-28|-2|37|-2|0.00|0.00|0.00|0.00|INF2|VUS|0.89743406|||AD|LP|||||||P|filter&vkgl&exit_p|,G|missense_variant|MODERATE|INF2|64423|Transcript|NM_022489.4|protein_coding|2/23||NM_022489.4:c.158T>G|NP_071934.3:p.Leu53Arg|289/7623|158/3750|53/1249|L/R|cTg/cGg||1||1||1|EntrezGene|||||0|0.999||||||||||||-28|-2|37|-2|0.00|0.00|0.00|0.00|INF2|VUS|0.89743406|||AD|LP|||||||P|filter&vkgl&exit_p|,G|missense_variant|MODERATE|INF2|64423|Transcript|NM_032714.3|protein_coding|2/5||NM_032714.3:c.158T>G|NP_116103.1:p.Leu53Arg|289/1692|158/705|53/234|L/R|cTg/cGg||1||1|||EntrezGene|||||0|0.999||||||||||||-28|-2|37|-2|0.00|0.00|0.00|0.00|INF2|VUS|0.89743406|||AD|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:GQ 0|0:10:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 1|0:50:AD:.:1:64423:1:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50
262
+ chr17 31229046 . AC A . PASS CSQ=-|frameshift_variant|HIGH|NF1|4763|Transcript|NM_000267.3|protein_coding|21/57||NM_000267.3:c.2433del|NP_000258.1:p.Ile812LeufsTer9|2816/12362|2433/8457|811/2818|T/X|acC/ac||1||1|||EntrezGene|||||||1|||||||||||-22|-11|12|25|0.00|0.00|0.00|0.00|NF1|VUS|0.9921835|HP:0000951|1|AD|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|NF1|4763|Transcript|NM_001042492.3|protein_coding|21/58||NM_001042492.3:c.2433del|NP_001035957.1:p.Ile812LeufsTer9|2766/12373|2433/8520|811/2839|T/X|acC/ac||1||1||1|EntrezGene|||||||1|||||||||||-22|-11|12|25|0.00|0.00|0.00|0.00|NF1|VUS|0.99201524|HP:0000951|1|AD|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:9:AR,AD:chr17_31336861_T_G:1:4763:1:AR_C:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
263
+ chr17 31336861 . T G . PASS CSQ=G|missense_variant|MODERATE|NF1|4763|Transcript|NM_000267.3|protein_coding|41/57||NM_000267.3:c.6311T>G|NP_000258.1:p.Leu2104Arg|6694/12362|6311/8457|2104/2818|L/R|cTg/cGg|CM143458&CM141499|1||1|||EntrezGene|||||0|0.994||||1&1||||||||-42|41|-34|8|0.00|0.00|0.00|0.00|NF1|VUS|0.80934244|HP:0000951|1|AD|LP|||||||P|filter&vkgl&exit_p|,G|missense_variant|MODERATE|NF1|4763|Transcript|NM_001042492.3|protein_coding|42/58||NM_001042492.3:c.6374T>G|NP_001035957.1:p.Leu2125Arg|6707/12373|6374/8520|2125/2839|L/R|cTg/cGg|CM143458&CM141499|1||1||1|EntrezGene|||||0|0.993||||1&1||||||||-42|41|-34|8|0.00|0.00|0.00|0.00|NF1|VUS|0.80934244|HP:0000951|1|AD|LP|||||||P|filter&vkgl&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:50:AR,AD:chr17_31229046_AC_A:1:4763:1:AR_C:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
264
+ chr19 11105470 . C G . PASS CSQ=G|stop_gained|HIGH|LDLR|3949|Transcript|NM_000527.5|protein_coding|4/18||NM_000527.5:c.564C>G|NP_000518.1:p.Tyr188Ter|650/5173|564/2583|188/860|Y/*|taC/taG|rs121908034&CM920416|1||1||1|EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.97251827|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|stop_gained|HIGH|LDLR|3949|Transcript|NM_001195798.2|protein_coding|4/18||NM_001195798.2:c.564C>G|NP_001182727.1:p.Tyr188Ter|650/5167|564/2577|188/858|Y/*|taC/taG|rs121908034&CM920416|1||1|||EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.97251827|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|stop_gained|HIGH|LDLR|3949|Transcript|NM_001195799.2|protein_coding|3/17||NM_001195799.2:c.441C>G|NP_001182728.1:p.Tyr147Ter|527/5050|441/2460|147/819|Y/*|taC/taG|rs121908034&CM920416|1||1|||EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.9850093|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|intron_variant|MODIFIER|LDLR|3949|Transcript|NM_001195800.2|protein_coding||3/15|NM_001195800.2:c.314-1922C>G|||||||rs121908034&CM920416|1||1|||EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.006388327|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|intron_variant|MODIFIER|LDLR|3949|Transcript|NM_001195803.2|protein_coding||3/15|NM_001195803.2:c.314-1095C>G|||||||rs121908034&CM920416|1||1|||EntrezGene||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803|||||||1|11|0|-14|0.00|0.00|0.00|0.00|LDLR|VUS|0.006388327|HP:0000951||AD&AR|LP|||||||P|filter&vkgl&exit_p|,G|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001219902|promoter_flanking_region||||||||||rs121908034&CM920416|1|||||||||||||pathogenic/likely_pathogenic&pathogenic||1&1|25741868&27765764&17142622&20809525&8882879&1734722&10422803||||||||||||||||||||||||||||P|filter&vkgl&clinVar&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:3949:1:AR_C:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
265
+ chr19 17341188 . GA G . PASS CSQ=-|frameshift_variant|HIGH|GTPBP3|84705|Transcript|NM_001128855.3|protein_coding|8/9||NM_001128855.3:c.1058del|NP_001122327.1:p.Asn353ThrfsTer26|1117/2503|1058/1416|353/471|N/X|aAc/ac||1||1|||EntrezGene|||||||1|||||||||||34|33|-7|33|0.01|0.00|0.00|0.00|GTPBP3|VUS|0.9901776|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|GTPBP3|84705|Transcript|NM_001195422.1|protein_coding|8/9||NM_001195422.1:c.1187del|NP_001182351.1:p.Asn396ThrfsTer26|1209/2595|1187/1545|396/514|N/X|aAc/ac||1||1|||EntrezGene|||||||1|||||||||||34|33|-7|33|0.01|0.00|0.00|0.00|GTPBP3|VUS|0.9913974|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|GTPBP3|84705|Transcript|NM_032620.4|protein_coding|8/9||NM_032620.4:c.1121del|NP_116009.2:p.Asn374ThrfsTer26|1180/2566|1121/1479|374/492|N/X|aAc/ac||1||1||1|EntrezGene|||||||1|||||||||||34|33|-7|33|0.01|0.00|0.00|0.00|GTPBP3|VUS|0.99110925|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|frameshift_variant|HIGH|GTPBP3|84705|Transcript|NM_133644.4|protein_coding|7/8||NM_133644.4:c.1217del|NP_598399.2:p.Asn406ThrfsTer26|1276/2662|1217/1575|406/524|N/X|aAc/ac||1||1|||EntrezGene|||||||1|||||||||||34|33|-7|33|0.01|0.00|0.00|0.00|GTPBP3|VUS|0.9916678|HP:0000951||AR|LP|||||||P|filter&vkgl&exit_p|,-|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000586166|promoter|||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,-|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00001022836|CTCF_binding_site|||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,-|TF_binding_site_variant|MODIFIER|||MotifFeature|ENSM00000278460||||||||||||1||1||||||||||||||||ENSPFM0305|8|N||HOXB2::ELF1||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:84705:1:AR_C:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
266
+ chr20 63695639 . C T . PASS CSQ=T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001134758.4|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267544.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267545.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267546.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267547.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267548.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_001267549.3|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|missense_variant|MODERATE|RTEL1|51750|Transcript|NM_001283009.2|protein_coding|34/35||NM_001283009.2:c.3811C>T|NP_001269938.1:p.Arg1271Trp|4136/4615|3811/3903|1271/1300|R/W|Cgg/Tgg|rs993254667|1||1||1|EntrezGene|||||0.16|0.003||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1|VUS|0.0055121304|HP:0000951||AD&AR|||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&exit_p|,T|intron_variant|MODIFIER|RTEL1|51750|Transcript|NM_001283010.1|protein_coding||33/33|NM_001283010.1:c.2984-139C>T|||||||rs993254667|1||1|||EntrezGene||||||||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1|VUS|0.002660127|HP:0000951||AD&AR|||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NM_003224.6|protein_coding||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|upstream_gene_variant|MODIFIER|TNFRSF6B|8771|Transcript|NM_003823.4|protein_coding||||||||||rs993254667|1|1013|1|||EntrezGene|||||||||||||||||||||||||||VUS|0.0115982685||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|intron_variant|MODIFIER|RTEL1|51750|Transcript|NM_016434.4|protein_coding||34/34|NM_016434.4:c.3653-139C>T|||||||rs993254667|1||1|||EntrezGene||||||||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1|VUS|0.002660127|HP:0000951||AD&AR|||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|intron_variant|MODIFIER|RTEL1|51750|Transcript|NM_032957.5|protein_coding||34/34|NM_032957.5:c.3725-139C>T|||||||rs993254667|1||1|||EntrezGene||||||||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1|VUS|0.002660127|HP:0000951||AD&AR|||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|non_coding_transcript_exon_variant|MODIFIER|RTEL1-TNFRSF6B|100533107|Transcript|NR_037882.1|lncRNA|34/38||NR_037882.1:n.4638C>T||4638/5772|||||rs993254667|1||1|||EntrezGene||||||||||||||||||12|-21|44|11|0.00|0.00|0.00|0.09|RTEL1-TNFRSF6B|VUS|0.039789375||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051954.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051955.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051956.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051957.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|downstream_gene_variant|MODIFIER|ARFRP1|10139|Transcript|NR_051958.3|misc_RNA||||||||||rs993254667|1|3008|-1|||EntrezGene|||||||||||||||||||||||||||VUS|0.017016819||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,T|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000657794|CTCF_binding_site||||||||||rs993254667|1|||||||||||||||||||||||||||||||||||||||||chr20:63695639-63695639|1.97117e-05|0|P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chrM_15325_A_G,chr22_50189164_C_CTG,chr1_152548312_A_,chr2_47408528_G_:1:51750:1:AR_C:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
267
+ chr22 50189164 . C CTG . PASS CSQ=TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_001320484.2|protein_coding||1/9|NM_001320484.2:c.-35+3188_-35+3189insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_001320485.2|protein_coding||1/9|NM_001320485.2:c.-35+3188_-35+3189insTG||||||||1||1||1|EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|upstream_gene_variant|MODIFIER|TRABD|80305|Transcript|NM_001320487.2|protein_coding|||||||||||1|1422|1|||EntrezGene|||||||||||||||||||||||||||VUS|0.25514466|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|upstream_gene_variant|MODIFIER|TRABD|80305|Transcript|NM_001320488.2|protein_coding|||||||||||1|1422|1|||EntrezGene|||||||||||||||||||||||||||VUS|0.25514466|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_001378762.1|protein_coding||1/9|NM_001378762.1:c.-35+3119_-35+3120insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_001378765.1|protein_coding||1/10|NM_001378765.1:c.-35+3159_-35+3160insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant|MODIFIER|TRABD|80305|Transcript|NM_025204.4|protein_coding||1/9|NM_025204.4:c.-35+3163_-35+3164insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.014847702|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|intron_variant&non_coding_transcript_variant|MODIFIER|TRABD|80305|Transcript|NR_135275.2|misc_RNA||1/9|NR_135275.2:n.64+3188_64+3189insTG||||||||1||1|||EntrezGene|||||||||||||||||||||||||||VUS|0.015001616|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p|,TG|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000147690|promoter|||||||||||1||||||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIM:VIS:GQ 0|0:10:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50 1|0:50:AR,AD:chr4_105399137_G_A,chr7_41977712_C_,chr19_11105470_C_G,chr19_17341188_GA_G,chr9_104784352_AAAGAT_A,chr8_60852584_G_,chrM_15325_A_G,chr1_152548312_A_,chr2_47408528_G_,chr20_63695639_C_T,chrX_49075362_A_T:1:0:AR_C:50 0|0:50:.:.:.:.:.:50 0|0:50:.:.:.:.:.:50
268
+ chr22 50283117 . C T . PASS CSQ=T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376864.1|protein_coding|17/37||NM_001376864.1:c.2749G>A|NP_001363793.1:p.Gly917Ser|2881/6611|2749/5754|917/1917|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376865.1|protein_coding|18/38||NM_001376865.1:c.2818G>A|NP_001363794.1:p.Gly940Ser|2898/6391|2818/5586|940/1861|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376866.1|protein_coding|17/37||NM_001376866.1:c.2749G>A|NP_001363795.1:p.Gly917Ser|2909/6402|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376867.1|protein_coding|18/38||NM_001376867.1:c.2749G>A|NP_001363796.1:p.Gly917Ser|2969/6462|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376868.1|protein_coding|18/38||NM_001376868.1:c.2749G>A|NP_001363797.1:p.Gly917Ser|2962/6455|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376869.1|protein_coding|16/36||NM_001376869.1:c.2749G>A|NP_001363798.1:p.Gly917Ser|2856/6349|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376870.1|protein_coding|17/37||NM_001376870.1:c.2749G>A|NP_001363799.1:p.Gly917Ser|2881/6374|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376871.1|protein_coding|17/37||NM_001376871.1:c.2749G>A|NP_001363800.1:p.Gly917Ser|2874/6367|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376872.1|protein_coding|19/39||NM_001376872.1:c.2749G>A|NP_001363801.1:p.Gly917Ser|3066/6559|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376873.1|protein_coding|18/38||NM_001376873.1:c.2749G>A|NP_001363802.1:p.Gly917Ser|3218/6711|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376874.1|protein_coding|18/38||NM_001376874.1:c.2749G>A|NP_001363803.1:p.Gly917Ser|2934/6427|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376875.1|protein_coding|16/36||NM_001376875.1:c.2749G>A|NP_001363804.1:p.Gly917Ser|2933/6426|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376876.1|protein_coding|18/38||NM_001376876.1:c.2749G>A|NP_001363805.1:p.Gly917Ser|2927/6420|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376877.1|protein_coding|18/38||NM_001376877.1:c.2749G>A|NP_001363806.1:p.Gly917Ser|3198/6691|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376878.1|protein_coding|16/36||NM_001376878.1:c.2749G>A|NP_001363807.1:p.Gly917Ser|2821/6314|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376879.1|protein_coding|19/39||NM_001376879.1:c.2749G>A|NP_001363808.1:p.Gly917Ser|3101/6594|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376880.1|protein_coding|17/37||NM_001376880.1:c.2749G>A|NP_001363809.1:p.Gly917Ser|2991/6484|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376881.1|protein_coding|18/38||NM_001376881.1:c.2749G>A|NP_001363810.1:p.Gly917Ser|3046/6539|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376882.1|protein_coding|17/37||NM_001376882.1:c.2749G>A|NP_001363811.1:p.Gly917Ser|3165/6658|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376883.1|protein_coding|17/37||NM_001376883.1:c.2749G>A|NP_001363812.1:p.Gly917Ser|2881/6350|2749/5493|917/1830|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376884.1|protein_coding|16/36||NM_001376884.1:c.2749G>A|NP_001363813.1:p.Gly917Ser|2821/6236|2749/5439|917/1812|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376885.1|protein_coding|17/37||NM_001376885.1:c.2749G>A|NP_001363814.1:p.Gly917Ser|2909/6324|2749/5439|917/1812|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_001376886.1|protein_coding|17/37||NM_001376886.1:c.2656G>A|NP_001363815.1:p.Gly886Ser|2876/6369|2656/5424|886/1807|G/S|Ggc/Agc|rs1377653283|1||-1|||EntrezGene||||||||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.15048689||||||||chr22:50283117-50283117|6.57263e-06|0|P|filter&vkgl&clinVar&gnomad&effect&sift&polyphen&impact&exit_p|,T|missense_variant|MODERATE|PLXNB2|23654|Transcript|NM_012401.4|protein_coding|17/37||NM_012401.4:c.2749G>A|NP_036533.2:p.Gly917Ser|2916/6409|2749/5517|917/1838|G/S|Ggc/Agc|rs1377653283|1||-1||1|EntrezGene|||||0|1||||||||||||-2|36|-32|-38|0.05|0.00|0.00|0.00|PLXNB2|VUS|0.94078785||||||||chr22:50283117-50283117|6.57263e-06|0|LP|filter&vkgl&clinVar&gnomad&effect&sift&exit_lp| GT:DP:VI:VIC:VID:VIM:GQ 0|0:10:.:.:.:.:50 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50 1|0:50:AD:.:1:0 0|0:50:.:.:.:.:50 0|0:50:.:.:.:.:50
269
+ chrX 49075362 x_chrom A T . PASS CSQ=T|splice_donor_variant|HIGH|WDR45|11152|Transcript|NM_001029896.2|protein_coding||9/10|NM_001029896.2:c.827+2T>A|||||||CS135341|1||-1||1|EntrezGene||||||||||1||||||||27|28|-2|2|0.02|0.00|0.01|0.99|WDR45|VUS|0.98327905|HP:0000951||XL|LP|||||||P|filter&vkgl&exit_p|,T|splice_donor_variant|HIGH|WDR45|11152|Transcript|NM_007075.4|protein_coding||10/11|NM_007075.4:c.830+2T>A|||||||CS135341|1||-1|||EntrezGene||||||||||1||||||||27|28|-2|2|0.02|0.00|0.01|0.99|WDR45|VUS|0.98327905|HP:0000951||XL|LP|||||||P|filter&vkgl&exit_p|,T|upstream_gene_variant|MODIFIER|PRAF2|11230|Transcript|NM_007213.3|protein_coding||||||||||CS135341|1|1360|-1|||EntrezGene||||||||||1||||||||27|28|-2|2|0.02|0.00|0.01|0.99|WDR45|VUS|0.0113522755|||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&exit_p|,T|regulatory_region_variant|MODIFIER|||RegulatoryFeature|ENSR00000906841|CTCF_binding_site||||||||||CS135341|1|||||||||||||||1|||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VI:VIC:VID:VIG:VIM:VIS:GQ 0|0:10:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50 1|0:50:XLD,XL,XLR:.:1:11152:1:XLD,XLR:50 0|0:50:.:.:.:.:.:.:50 0|0:50:.:.:.:.:.:.:50
270
+ chrY 2787600 y_chrom G A . PASS CSQ=A|stop_gained|HIGH|SRY|6736|Transcript|NM_003140.3|protein_coding|1/1||NM_003140.3:c.4C>T|NP_003131.1:p.Gln2Ter|83/828|4/615|2/204|Q/*|Caa/Taa|rs104894977&CM981858|1||-1||1|EntrezGene||||||||pathogenic||1&1|2401216&9443877|||||||-26|-50|2|-4|0.01|0.00|0.00|0.00|SRY|VUS|0.92795527|||||||||||P|filter&vkgl&clinVar&exit_p| GT:DP:VIC:VID:VIM:GQ 0:10:.:.:.:50 .:.:.:.:.:50 1:50:.:.:.:50 1:50:.:1:0:50 .:.:.:.:.:50 1:50:.:.:.:50
271
+ chrM 15325 mt_chrom A G . PASS CSQ=G|intergenic_variant|MODIFIER|||||||||||||||rs1556424568|1||||1||||||||||||||||||||||||||||||||||||||||P|filter&vkgl&clinVar&gnomad&effect&spliceAI&annotSV&impact&exit_p| GT:DP:VIC:VID:VIM:GQ 0|0:10:.:.:.:50 0|0:50:.:.:.:50 0|0:50:.:.:.:50 1|0:50:.:1:0:50 0|0:50:.:.:.:50 0|0:50:.:.:.:50
package/src/mocks/MockApiClient.ts CHANGED
@@ -26,6 +26,7 @@ import {
26
26
  vcfSamples0 as vcfSamples0GRCh37,
27
27
  vcfSamples1 as vcfSamples1GRCh37,
28
28
  vcfSamples100 as vcfSamples100GRCh37,
29
+ samplesFamilyDuoPlusSister as samplesFamilyDuoPlusSisterGRCh37,
29
30
  } from "./GRCh37/static";
30
31
  import {
31
32
  cram as cramGRCh38,
@@ -156,7 +157,7 @@ export class MockApiClient implements Api {
156
157
  genomeAssembly: "GRCh37",
157
158
  },
158
159
  } as Metadata,
159
- data: samplesFamilyGRCh37,
160
+ data: samplesFamilyDuoPlusSisterGRCh37,
160
161
  binary: {
161
162
  vcf: vcfNoVepGRCh37,
162
163
  fastaGz: fastaGzGRCh37,
package/src/store/index.tsx CHANGED
@@ -1,10 +1,9 @@
1
1
  import { hashIntegration, Router } from "solid-app-router";
2
2
  import { Context, createContext, ParentComponent, useContext } from "solid-js";
3
3
  import { createStore } from "solid-js/store";
4
- import { Item, QueryClause, Sample, Selector, SortOrder } from "@molgenis/vip-report-api/src/Api";
5
- import { selectorKey } from "../utils/query";
4
+ import { Item, Query, Sample, SortOrder } from "@molgenis/vip-report-api/src/Api";
6
5
 
7
- export type FilterQueries = { [key: string]: QueryClause | undefined };
6
+ export type FilterQueries = { [key: string]: Query | undefined };
8
7
 
9
8
  type AppStateVariants = {
10
9
  page?: number;
@@ -33,14 +32,14 @@ export type AppActions = {
33
32
  setVariantsPage(page: number): void;
34
33
  setVariantsPageSize(pageSize: number): void;
35
34
  setVariantsSearchQuery(searchQuery: string): void;
36
- setVariantsFilterQuery(query: QueryClause): void;
37
- clearVariantsFilterQuery(selector: Selector): void;
35
+ setVariantsFilterQuery(query: Query, key: string): void;
36
+ clearVariantsFilterQuery(key: string): void;
38
37
  setVariantsSort(sort: SortOrder | null): void;
39
38
  setSampleVariantsPage(sample: Item<Sample>, page: number): void;
40
39
  setSampleVariantsPageSize(sample: Item<Sample>, pageSize: number): void;
41
40
  setSampleVariantsSearchQuery(sample: Item<Sample>, searchQuery: string): void;
42
- setSampleVariantsFilterQuery(sample: Item<Sample>, query: QueryClause): void;
43
- clearSampleVariantsFilterQuery(sample: Item<Sample>, selector: Selector): void;
41
+ setSampleVariantsFilterQuery(sample: Item<Sample>, query: Query, key: string): void;
42
+ clearSampleVariantsFilterQuery(sample: Item<Sample>, key: string): void;
44
43
  setSampleVariantsSort(sample: Item<Sample>, sort: SortOrder | null): void;
45
44
  setSamplePage(page: number): void;
46
45
  setSampleSearchQuery(searchQuery: string): void;
@@ -73,19 +72,19 @@ export const Provider: ParentComponent = (props) => {
73
72
  setVariantsSearchQuery(searchQuery: string) {
74
73
  setState({ variants: { ...(state.variants || {}), searchQuery } });
75
74
  },
76
- setVariantsFilterQuery(query: QueryClause) {
75
+ setVariantsFilterQuery(query: Query, key: string) {
77
76
  setState({
78
77
  variants: {
79
78
  ...(state.variants || {}),
80
- filterQueries: { ...(state.variants?.filterQueries || {}), [selectorKey(query.selector)]: query },
79
+ filterQueries: { ...(state.variants?.filterQueries || {}), [key]: query },
81
80
  },
82
81
  });
83
82
  },
84
- clearVariantsFilterQuery(selector: Selector) {
83
+ clearVariantsFilterQuery(key: string) {
85
84
  setState({
86
85
  variants: {
87
86
  ...(state.variants || {}),
88
- filterQueries: { ...(state.variants?.filterQueries || {}), [selectorKey(selector)]: undefined },
87
+ filterQueries: { ...(state.variants?.filterQueries || {}), [key]: undefined },
89
88
  },
90
89
  });
91
90
  },
@@ -121,7 +120,7 @@ export const Provider: ParentComponent = (props) => {
121
120
  },
122
121
  });
123
122
  },
124
- setSampleVariantsFilterQuery(sample: Item<Sample>, query: QueryClause) {
123
+ setSampleVariantsFilterQuery(sample: Item<Sample>, query: Query, key: string) {
125
124
  const variants = getVariants(sample);
126
125
  setState({
127
126
  sampleVariants: {
@@ -129,14 +128,14 @@ export const Provider: ParentComponent = (props) => {
129
128
  [sample.id]: {
130
129
  variants: {
131
130
  ...variants,
132
- filterQueries: { ...(variants.filterQueries || {}), [selectorKey(query.selector)]: query },
131
+ filterQueries: { ...(variants.filterQueries || {}), [key]: query },
133
132
  page: undefined,
134
133
  },
135
134
  },
136
135
  },
137
136
  });
138
137
  },
139
- clearSampleVariantsFilterQuery(sample: Item<Sample>, selector: Selector) {
138
+ clearSampleVariantsFilterQuery(sample: Item<Sample>, key: string) {
140
139
  const variants = getVariants(sample);
141
140
  setState({
142
141
  sampleVariants: {
@@ -144,7 +143,7 @@ export const Provider: ParentComponent = (props) => {
144
143
  [sample.id]: {
145
144
  variants: {
146
145
  ...getVariants(sample),
147
- filterQueries: { ...(variants.filterQueries || {}), [selectorKey(selector)]: undefined },
146
+ filterQueries: { ...(variants.filterQueries || {}), [key]: undefined },
148
147
  page: undefined,
149
148
  },
150
149
  },
package/src/views/SampleVariants.tsx CHANGED
@@ -6,7 +6,7 @@ import { SearchBox } from "../components/SearchBox";
6
6
  import { Sort, SortEvent } from "../components/Sort";
7
7
  import { Pager } from "../components/record/Pager";
8
8
  import { RecordDownload } from "../components/record/RecordDownload";
9
- import { createSampleQuery, infoSelector, infoSortPath, sampleSelector } from "../utils/query";
9
+ import { createSampleQuery, infoSelector, infoSortPath, sampleSelector, selector, selectorKey } from "../utils/query";
10
10
  import { VariantsSampleTable } from "../components/VariantsSampleTable";
11
11
  import {
12
12
  fetchHtsFileMetadata,
@@ -17,14 +17,14 @@ import {
17
17
  } from "../utils/ApiUtils";
18
18
  import { Breadcrumb } from "../components/Breadcrumb";
19
19
  import { FieldMetadata } from "@molgenis/vip-report-vcf/src/MetadataParser";
20
- import { Filters } from "../components/filter/Filters";
20
+ import { FilterChangeEvent, FilterClearEvent, Filters } from "../components/filter/Filters";
21
21
  import { DIRECTION_ASCENDING, DIRECTION_DESCENDING } from "../utils/sortUtils";
22
22
  import { SampleRouteData } from "./data/SampleData";
23
23
  import { useStore } from "../store";
24
24
  import { Metadata } from "@molgenis/vip-report-vcf/src/Vcf";
25
25
  import { getSampleLabel } from "../utils/sample";
26
- import { FilterChangeEvent, FilterClearEvent } from "../components/filter/Filter";
27
26
  import { arrayEquals } from "../utils/utils";
27
+ import { getAllelicBalanceQuery } from "../components/filter/FilterAllelicBalance";
28
28
 
29
29
  export const SampleVariantsView: Component = () => {
30
30
  const { sample } = useRouteData<SampleRouteData>();
@@ -80,28 +80,51 @@ export const SampleVariants: Component<{
80
80
  if (getStateVariants()?.filterQueries === undefined) {
81
81
  const hpoField = props.recordsMeta.info?.CSQ?.nested?.items?.find((field) => field.id === "HPO");
82
82
  if (hpoField && props.samplePhenotypes.length > 0) {
83
- actions.setSampleVariantsFilterQuery(props.sample, {
84
- selector: infoSelector(hpoField),
85
- operator: "any_has_any",
86
- args: props.samplePhenotypes.map((phenotype) => phenotype.type.id),
87
- });
83
+ const selectorHpo = infoSelector(hpoField);
84
+ actions.setSampleVariantsFilterQuery(
85
+ props.sample,
86
+ {
87
+ selector: selectorHpo,
88
+ operator: "any_has_any",
89
+ args: props.samplePhenotypes.map((phenotype) => phenotype.type.id),
90
+ },
91
+ selectorKey(selectorHpo)
92
+ );
88
93
  }
89
94
 
90
95
  const vimField = props.recordsMeta.format?.VIM;
91
96
  if (vimField) {
92
- actions.setSampleVariantsFilterQuery(props.sample, {
93
- selector: sampleSelector(props.sample, vimField),
94
- operator: "==",
95
- args: 1,
96
- });
97
+ const selectorVim = sampleSelector(props.sample, vimField);
98
+ actions.setSampleVariantsFilterQuery(
99
+ props.sample,
100
+ {
101
+ selector: selectorVim,
102
+ operator: "==",
103
+ args: 1,
104
+ },
105
+ selectorKey(selectorVim)
106
+ );
97
107
  }
98
- const dpField = props.recordsMeta.format?.DP;
99
- if (dpField) {
100
- actions.setSampleVariantsFilterQuery(props.sample, {
101
- selector: sampleSelector(props.sample, dpField),
102
- operator: ">=",
103
- args: 20,
104
- });
108
+ const gqField = props.recordsMeta.format?.GQ;
109
+ if (gqField) {
110
+ const selectorGq = sampleSelector(props.sample, gqField);
111
+ actions.setSampleVariantsFilterQuery(
112
+ props.sample,
113
+ {
114
+ selector: selectorGq,
115
+ operator: ">=",
116
+ args: 20,
117
+ },
118
+ selectorKey(selectorGq)
119
+ );
120
+ }
121
+ const viabField = props.recordsMeta.format?.VIAB;
122
+ if (viabField) {
123
+ actions.setSampleVariantsFilterQuery(
124
+ props.sample,
125
+ getAllelicBalanceQuery(props.sample.id),
126
+ selectorKey(["s", props.sample.data.index, ...selector(viabField)])
127
+ );
105
128
  }
106
129
  }
107
130
 
@@ -143,7 +166,7 @@ export const SampleVariants: Component<{
143
166
 
144
167
  const formatFields = createMemo(() => {
145
168
  const formatFieldMap = props.recordsMeta.format;
146
- const includedFields = ["VIM", "VID", "DP"];
169
+ const includedFields = ["VIM", "VID", "GQ", "VIAB", "GT", "DP"];
147
170
  return formatFieldMap
148
171
  ? includedFields.map((fieldId) => formatFieldMap[fieldId]).filter((field) => field !== undefined)
149
172
  : [];
@@ -157,9 +180,9 @@ export const SampleVariants: Component<{
157
180
 
158
181
  const onPageChange = (page: number) => actions.setSampleVariantsPage(props.sample, page);
159
182
  const onSearchChange = (search: string) => actions.setSampleVariantsSearchQuery(props.sample, search);
160
- const onFilterChange = (event: FilterChangeEvent) => actions.setSampleVariantsFilterQuery(props.sample, event.query);
161
- const onFilterClear = (event: FilterClearEvent) =>
162
- actions.clearSampleVariantsFilterQuery(props.sample, event.selector);
183
+ const onFilterChange = (event: FilterChangeEvent) =>
184
+ actions.setSampleVariantsFilterQuery(props.sample, event.query, event.key);
185
+ const onFilterClear = (event: FilterClearEvent) => actions.clearSampleVariantsFilterQuery(props.sample, event.key);
163
186
  const onSortChange = (event: SortEvent) => actions.setSampleVariantsSort(props.sample, event.order);
164
187
  const onSortClear = () => actions.setSampleVariantsSort(props.sample, null);
165
188