ClinVar Miner

List of variants in gene ATP6V0A2 reported as uncertain significance by GeneDx

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Total variants: 20
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HGVS dbSNP
NM_012463.4(ATP6V0A2):c.1018C>T (p.Arg340Trp) rs781305219
NM_012463.4(ATP6V0A2):c.1069A>T (p.Met357Leu) rs146967928
NM_012463.4(ATP6V0A2):c.1096C>T (p.Pro366Ser) rs372416067
NM_012463.4(ATP6V0A2):c.1457C>T (p.Ser486Leu) rs201271558
NM_012463.4(ATP6V0A2):c.1766C>T (p.Pro589Leu) rs149700024
NM_012463.4(ATP6V0A2):c.1852A>G (p.Arg618Gly) rs1057518488
NM_012463.4(ATP6V0A2):c.1970C>T (p.Ala657Val) rs147641581
NM_012463.4(ATP6V0A2):c.2005C>G (p.Leu669Val) rs374410950
NM_012463.4(ATP6V0A2):c.2030G>A (p.Gly677Glu) rs1555299234
NM_012463.4(ATP6V0A2):c.2246A>G (p.Asn749Ser) rs941238473
NM_012463.4(ATP6V0A2):c.309G>T (p.Lys103Asn) rs144499089
NM_012463.4(ATP6V0A2):c.388C>T (p.His130Tyr) rs199801221
NM_012463.4(ATP6V0A2):c.422G>T (p.Arg141Leu) rs143509747
NM_012463.4(ATP6V0A2):c.515A>G (p.Lys172Arg) rs142935490
NM_012463.4(ATP6V0A2):c.588C>G (p.Cys196Trp) rs940128206
NM_012463.4(ATP6V0A2):c.604G>A (p.Val202Met) rs776619252
NM_012463.4(ATP6V0A2):c.614C>T (p.Ala205Val) rs143802431
NM_012463.4(ATP6V0A2):c.764C>T (p.Thr255Ile) rs369952560
NM_012463.4(ATP6V0A2):c.779G>A (p.Arg260Lys) rs199578524
NM_012463.4(ATP6V0A2):c.968G>A (p.Cys323Tyr) rs775855556

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