ClinVar Miner

List of variants in gene ATP6V0A2 reported as likely benign for not specified

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Total variants: 35
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HGVS dbSNP
NM_012463.4(ATP6V0A2):c.1039-13G>T rs375793162
NM_012463.4(ATP6V0A2):c.117+14G>A rs144930749
NM_012463.4(ATP6V0A2):c.117+17_117+20delinsTCT rs1555295264
NM_012463.4(ATP6V0A2):c.1189+12G>T rs377235629
NM_012463.4(ATP6V0A2):c.1215G>A (p.Pro405=) rs1171365721
NM_012463.4(ATP6V0A2):c.1258G>T (p.Val420Leu) rs138716143
NM_012463.4(ATP6V0A2):c.1327-16G>A rs149092701
NM_012463.4(ATP6V0A2):c.1452C>T (p.Asn484=) rs567406924
NM_012463.4(ATP6V0A2):c.1485C>T (p.Pro495=) rs759980365
NM_012463.4(ATP6V0A2):c.1486G>A (p.Ala496Thr) rs143142641
NM_012463.4(ATP6V0A2):c.1590C>T (p.Pro530=) rs80355657
NM_012463.4(ATP6V0A2):c.1698A>G (p.Gly566=) rs2271659
NM_012463.4(ATP6V0A2):c.1724+20T>A rs778282853
NM_012463.4(ATP6V0A2):c.196+15T>G rs1404046246
NM_012463.4(ATP6V0A2):c.2014T>C (p.Leu672=) rs367950442
NM_012463.4(ATP6V0A2):c.2056-14C>G rs375232199
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.2308C>T (p.Leu770=) rs149439834
NM_012463.4(ATP6V0A2):c.2340C>T (p.Arg780=) rs201694504
NM_012463.4(ATP6V0A2):c.2367A>G (p.Leu789=) rs142041624
NM_012463.4(ATP6V0A2):c.2384C>T (p.Ala795Val) rs139509075
NM_012463.4(ATP6V0A2):c.2469A>G (p.Val823=) rs775830030
NM_012463.4(ATP6V0A2):c.264G>A (p.Ala88=) rs139785866
NM_012463.4(ATP6V0A2):c.264G>T (p.Ala88=) rs139785866
NM_012463.4(ATP6V0A2):c.295-17C>A rs1555296412
NM_012463.4(ATP6V0A2):c.521+14C>G rs747194853
NM_012463.4(ATP6V0A2):c.521+17G>A rs192339944
NM_012463.4(ATP6V0A2):c.522-13del rs140638516
NM_012463.4(ATP6V0A2):c.732-3C>T rs1371899202
NM_012463.4(ATP6V0A2):c.768C>T (p.Ala256=) rs373419502
NM_012463.4(ATP6V0A2):c.795G>A (p.Gly265=) rs754399086
NM_012463.4(ATP6V0A2):c.840C>A (p.Thr280=) rs139680786
NM_012463.4(ATP6V0A2):c.853A>C (p.Arg285=) rs776563027
NM_012463.4(ATP6V0A2):c.993C>T (p.Pro331=) rs367873118

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