ClinVar Miner

List of variants in gene ATP6V0A2 reported as likely benign by Invitae

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Total variants: 31
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HGVS dbSNP
NM_012463.4(ATP6V0A2):c.1065A>G (p.Ser355=) rs1593910063
NM_012463.4(ATP6V0A2):c.1069A>T (p.Met357Leu) rs146967928
NM_012463.4(ATP6V0A2):c.1164C>T (p.Val388=) rs757645572
NM_012463.4(ATP6V0A2):c.1326+7_1326+15dup rs1593910803
NM_012463.4(ATP6V0A2):c.1458G>A (p.Ser486=) rs146156426
NM_012463.4(ATP6V0A2):c.1665C>T (p.Ser555=) rs373155729
NM_012463.4(ATP6V0A2):c.1848C>T (p.Thr616=) rs776365183
NM_012463.4(ATP6V0A2):c.18G>A (p.Arg6=)
NM_012463.4(ATP6V0A2):c.1926C>T (p.Tyr642=) rs1593915216
NM_012463.4(ATP6V0A2):c.1936-7C>T rs370135665
NM_012463.4(ATP6V0A2):c.2043C>T (p.Phe681=) rs202084330
NM_012463.4(ATP6V0A2):c.2220C>T (p.Ile740=) rs770098416
NM_012463.4(ATP6V0A2):c.2250C>T (p.Thr750=)
NM_012463.4(ATP6V0A2):c.2274G>A (p.Ala758=) rs1308437998
NM_012463.4(ATP6V0A2):c.2294-6T>C rs756082099
NM_012463.4(ATP6V0A2):c.234C>T (p.Pro78=) rs375372808
NM_012463.4(ATP6V0A2):c.2358C>T (p.Gly786=) rs199720540
NM_012463.4(ATP6V0A2):c.237T>C (p.Leu79=) rs369978210
NM_012463.4(ATP6V0A2):c.2382C>T (p.Ile794=) rs1390474120
NM_012463.4(ATP6V0A2):c.2384C>T (p.Ala795Val) rs139509075
NM_012463.4(ATP6V0A2):c.2556C>T (p.Asp852=) rs762290613
NM_012463.4(ATP6V0A2):c.2559C>T (p.Asp853=) rs1032324166
NM_012463.4(ATP6V0A2):c.264G>A (p.Ala88=) rs139785866
NM_012463.4(ATP6V0A2):c.264G>C (p.Ala88=) rs139785866
NM_012463.4(ATP6V0A2):c.312C>T (p.Leu104=) rs563333869
NM_012463.4(ATP6V0A2):c.33C>T (p.Cys11=) rs1485624455
NM_012463.4(ATP6V0A2):c.522-9G>A rs189175284
NM_012463.4(ATP6V0A2):c.614C>T (p.Ala205Val) rs143802431
NM_012463.4(ATP6V0A2):c.773A>G (p.Glu258Gly) rs141467923
NM_012463.4(ATP6V0A2):c.840C>T (p.Thr280=) rs139680786
NM_012463.4(ATP6V0A2):c.954C>T (p.Asp318=) rs75746974

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