ClinVar Miner

List of variants in gene ATP1A2 reported as likely benign by Ambry Genetics

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Total variants: 15
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HGVS dbSNP
NM_000702.3(ATP1A2):c.1074C>T (p.Asn358=)
NM_000702.3(ATP1A2):c.1284C>T (p.Arg428=) rs752479774
NM_000702.3(ATP1A2):c.1332C>T (p.Asp444=)
NM_000702.3(ATP1A2):c.1368G>A (p.Lys456=) rs369226331
NM_000702.3(ATP1A2):c.1470C>T (p.Ile490=) rs111405592
NM_000702.3(ATP1A2):c.152G>A (p.Arg51His) rs144106169
NM_000702.3(ATP1A2):c.1710G>A (p.Thr570=) rs536168465
NM_000702.3(ATP1A2):c.1761T>C (p.Ser587=) rs199621678
NM_000702.3(ATP1A2):c.1928C>G (p.Ala643Gly)
NM_000702.3(ATP1A2):c.2136G>A (p.Thr712=) rs760213030
NM_000702.3(ATP1A2):c.2967C>T (p.Phe989=) rs138826759
NM_000702.3(ATP1A2):c.2973C>T (p.Tyr991=) rs149286529
NM_000702.3(ATP1A2):c.339C>T (p.Tyr113=) rs148929192
NM_000702.3(ATP1A2):c.660G>A (p.Ser220=) rs564452950
NM_000702.3(ATP1A2):c.969C>T (p.Ile323=)

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