ClinVar Miner

List of variants in gene ATP6V0A2 reported as uncertain significance for not provided

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Total variants: 43
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HGVS dbSNP
NM_012463.4(ATP6V0A2):c.1014G>A (p.Leu338=) rs917452697
NM_012463.4(ATP6V0A2):c.1018C>T (p.Arg340Trp) rs781305219
NM_012463.4(ATP6V0A2):c.1048G>A (p.Gly350Ser) rs768141782
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.1165G>A (p.Gly389Arg)
NM_012463.4(ATP6V0A2):c.118-7_118-3del rs777322469
NM_012463.4(ATP6V0A2):c.1430A>T (p.Asn477Ile) rs532258057
NM_012463.4(ATP6V0A2):c.1457C>T (p.Ser486Leu) rs201271558
NM_012463.4(ATP6V0A2):c.1458G>A (p.Ser486=) rs146156426
NM_012463.4(ATP6V0A2):c.1486G>A (p.Ala496Thr) rs143142641
NM_012463.4(ATP6V0A2):c.1495A>G (p.Lys499Glu) rs1240866102
NM_012463.4(ATP6V0A2):c.1521C>T (p.Ser507=) rs142454880
NM_012463.4(ATP6V0A2):c.1526T>G (p.Val509Gly) rs760212304
NM_012463.4(ATP6V0A2):c.1666G>A (p.Val556Met)
NM_012463.4(ATP6V0A2):c.1766C>T (p.Pro589Leu) rs149700024
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.2116G>A (p.Asp706Asn)
NM_012463.4(ATP6V0A2):c.2229T>C (p.Cys743=) rs150508296
NM_012463.4(ATP6V0A2):c.2238C>T (p.Cys746=) rs138886791
NM_012463.4(ATP6V0A2):c.2314G>C (p.Ala772Pro)
NM_012463.4(ATP6V0A2):c.2320C>T (p.Leu774=) rs1337898685
NM_012463.4(ATP6V0A2):c.2338C>T (p.Arg780Cys) rs768609186
NM_012463.4(ATP6V0A2):c.264G>T (p.Ala88=) rs139785866
NM_012463.4(ATP6V0A2):c.26C>T (p.Thr9Ile) rs752689489
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.482T>G (p.Leu161Trp) rs750042310
NM_012463.4(ATP6V0A2):c.515A>G (p.Lys172Arg) rs142935490
NM_012463.4(ATP6V0A2):c.522-9G>A rs189175284
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.652G>A (p.Glu218Lys) rs759593402
NM_012463.4(ATP6V0A2):c.65C>T (p.Ala22Val)
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.840C>T (p.Thr280=) rs139680786
NM_012463.4(ATP6V0A2):c.892C>T (p.Arg298Cys) rs1217674662
NM_012463.4(ATP6V0A2):c.954C>T (p.Asp318=) rs75746974
NM_012463.4(ATP6V0A2):c.968G>A (p.Cys323Tyr) rs775855556

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