ClinVar Miner

List of variants in gene ATP6V0A2 reported as benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_012463.4(ATP6V0A2):c.*1064G>A
NM_012463.4(ATP6V0A2):c.*1122A>G
NM_012463.4(ATP6V0A2):c.*1128T>C rs10744162
NM_012463.4(ATP6V0A2):c.*1205C>G rs6488903
NM_012463.4(ATP6V0A2):c.*1600G>A rs58028686
NM_012463.4(ATP6V0A2):c.*1645G>A
NM_012463.4(ATP6V0A2):c.*1693C>G rs10846553
NM_012463.4(ATP6V0A2):c.*1731C>T
NM_012463.4(ATP6V0A2):c.*1837T>C
NM_012463.4(ATP6V0A2):c.*2329G>A
NM_012463.4(ATP6V0A2):c.*2353G>T rs74386589
NM_012463.4(ATP6V0A2):c.*2357C>T
NM_012463.4(ATP6V0A2):c.*2646A>G rs77292614
NM_012463.4(ATP6V0A2):c.*2710G>A
NM_012463.4(ATP6V0A2):c.*2877T>A rs77765053
NM_012463.4(ATP6V0A2):c.*3000G>A rs183891010
NM_012463.4(ATP6V0A2):c.*3167G>A
NM_012463.4(ATP6V0A2):c.*3227C>G rs111540619
NM_012463.4(ATP6V0A2):c.*3235A>G rs7310965
NM_012463.4(ATP6V0A2):c.*3357G>C
NM_012463.4(ATP6V0A2):c.*3425G>A rs2333834
NM_012463.4(ATP6V0A2):c.*3553G>A rs73420351
NM_012463.4(ATP6V0A2):c.*3603G>A rs73420352
NM_012463.4(ATP6V0A2):c.*3654A>G
NM_012463.4(ATP6V0A2):c.*574C>T rs112521789
NM_012463.4(ATP6V0A2):c.1016G>A (p.Arg339His) rs74922060
NM_012463.4(ATP6V0A2):c.1039-14T>C rs115569365
NM_012463.4(ATP6V0A2):c.1121A>G (p.Lys374Arg) rs79134187
NM_012463.4(ATP6V0A2):c.117+14G>A rs144930749
NM_012463.4(ATP6V0A2):c.1515T>C (p.Asn505=) rs7135542
NM_012463.4(ATP6V0A2):c.1590C>T (p.Pro530=) rs80355657
NM_012463.4(ATP6V0A2):c.1606-12G>A rs112415338
NM_012463.4(ATP6V0A2):c.1872G>A (p.Leu624=) rs73420342
NM_012463.4(ATP6V0A2):c.2054G>A (p.Arg685Gln) rs7969410
NM_012463.4(ATP6V0A2):c.2438C>T (p.Ala813Val) rs17883456
NM_012463.4(ATP6V0A2):c.2549A>G (p.Asn850Ser) rs75279884
NM_012463.4(ATP6V0A2):c.426T>C (p.Asn142=) rs1139789
NM_012463.4(ATP6V0A2):c.432+14C>T rs11837144
NM_012463.4(ATP6V0A2):c.471T>C (p.Ser157=) rs1399961
NM_012463.4(ATP6V0A2):c.777G>A (p.Arg259=) rs73420336

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