ClinVar Miner

List of variants in gene ATP6V0A4 reported as benign for auditory system disease

Included ClinVar conditions (549):
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Gene type:
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Total variants: 26
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HGVS dbSNP
NM_020632.3(ATP6V0A4):c.*111C>A rs75920897
NM_020632.3(ATP6V0A4):c.*162C>T rs55832008
NM_020632.3(ATP6V0A4):c.*239G>A rs8846
NM_020632.3(ATP6V0A4):c.*73C>T rs78419825
NM_020632.3(ATP6V0A4):c.-25C>G rs35301422
NM_020632.3(ATP6V0A4):c.1029+5G>A
NM_020632.3(ATP6V0A4):c.1033C>A (p.Leu345Ile) rs61747674
NM_020632.3(ATP6V0A4):c.1155C>T (p.Val385=) rs58568563
NM_020632.3(ATP6V0A4):c.1181-4G>A rs189734354
NM_020632.3(ATP6V0A4):c.1498A>G (p.Ser500Gly) rs142818468
NM_020632.3(ATP6V0A4):c.1557G>A (p.Pro519=) rs74921348
NM_020632.3(ATP6V0A4):c.1641G>A (p.Leu547=) rs61747675
NM_020632.3(ATP6V0A4):c.1662C>T (p.Phe554=) rs1026435
NM_020632.3(ATP6V0A4):c.1739T>C (p.Met580Thr) rs3807153
NM_020632.3(ATP6V0A4):c.1812T>C (p.His604=) rs3807154
NM_020632.3(ATP6V0A4):c.1848C>T (p.Phe616=) rs143883618
NM_020632.3(ATP6V0A4):c.1888G>A (p.Ala630Thr) rs73730479
NM_020632.3(ATP6V0A4):c.1956G>A (p.Pro652=) rs141411124
NM_020632.3(ATP6V0A4):c.2035G>T (p.Asp679Tyr) rs150777839
NM_020632.3(ATP6V0A4):c.2306C>T (p.Thr769Met) rs61747678
NM_020632.3(ATP6V0A4):c.2307G>A (p.Thr769=) rs61747677
NM_020632.3(ATP6V0A4):c.417+14G>C
NM_020632.3(ATP6V0A4):c.512+4A>G rs78194949
NM_020632.3(ATP6V0A4):c.5T>C (p.Val2Ala) rs10258719
NM_020632.3(ATP6V0A4):c.735T>C (p.Thr245=) rs77328827
NM_020632.3(ATP6V0A4):c.755C>G (p.Pro252Arg) rs61747681

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