ClinVar Miner

List of variants in gene ATP1A2 reported by Ambry Genetics

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Total variants: 35
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HGVS dbSNP
NM_000702.4(ATP1A2):c.1018-5A>G
NM_000702.4(ATP1A2):c.1043G>A (p.Arg348His)
NM_000702.4(ATP1A2):c.1074C>T (p.Asn358=) rs1558005822
NM_000702.4(ATP1A2):c.1119G>A (p.Ser373=) rs1063125
NM_000702.4(ATP1A2):c.1125G>A (p.Lys375=) rs61734526
NM_000702.4(ATP1A2):c.1284C>T (p.Arg428=) rs752479774
NM_000702.4(ATP1A2):c.129G>A (p.Lys43=) rs61734527
NM_000702.4(ATP1A2):c.1332C>T (p.Asp444=)
NM_000702.4(ATP1A2):c.1368G>A (p.Lys456=) rs369226331
NM_000702.4(ATP1A2):c.1470C>T (p.Ile490=) rs111405592
NM_000702.4(ATP1A2):c.152G>A (p.Arg51His) rs144106169
NM_000702.4(ATP1A2):c.1704C>T (p.Phe568=) rs17846714
NM_000702.4(ATP1A2):c.1710G>A (p.Thr570=) rs536168465
NM_000702.4(ATP1A2):c.1761T>C (p.Ser587=) rs199621678
NM_000702.4(ATP1A2):c.1778G>A (p.Arg593Gln) rs1553245178
NM_000702.4(ATP1A2):c.1928C>G (p.Ala643Gly)
NM_000702.4(ATP1A2):c.1980C>T (p.Cys660=) rs61734529
NM_000702.4(ATP1A2):c.19C>T (p.Arg7Cys)
NM_000702.4(ATP1A2):c.2008A>G (p.Met670Val) rs1184210055
NM_000702.4(ATP1A2):c.2136G>A (p.Thr712=) rs760213030
NM_000702.4(ATP1A2):c.2259C>T (p.Ala753=) rs17846715
NM_000702.4(ATP1A2):c.2273G>C (p.Gly758Ala) rs147183887
NM_000702.4(ATP1A2):c.2563+4C>T rs3747626
NM_000702.4(ATP1A2):c.25T>A (p.Tyr9Asn) rs55858252
NM_000702.4(ATP1A2):c.2810G>A (p.Arg937His) rs1553245943
NM_000702.4(ATP1A2):c.2961C>T (p.Cys987=) rs74123254
NM_000702.4(ATP1A2):c.2967C>T (p.Phe989=) rs138826759
NM_000702.4(ATP1A2):c.2973C>T (p.Tyr991=) rs149286529
NM_000702.4(ATP1A2):c.339C>T (p.Tyr113=) rs148929192
NM_000702.4(ATP1A2):c.340G>A (p.Gly114Ser) rs116711766
NM_000702.4(ATP1A2):c.660G>A (p.Ser220=) rs564452950
NM_000702.4(ATP1A2):c.712C>T (p.Arg238Cys) rs1558004341
NM_000702.4(ATP1A2):c.736A>G (p.Asn246Asp) rs764917849
NM_000702.4(ATP1A2):c.879C>G (p.Ile293Met) rs1553244746
NM_000702.4(ATP1A2):c.969C>T (p.Ile323=)

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