ClinVar Miner

List of variants in gene ATP1A2 reported as likely benign by Invitae

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Total variants: 31
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HGVS dbSNP
NM_000702.4(ATP1A2):c.1018-4C>T rs1553244873
NM_000702.4(ATP1A2):c.1128G>A (p.Thr376=) rs374374188
NM_000702.4(ATP1A2):c.1216+7G>T rs962782746
NM_000702.4(ATP1A2):c.1284C>T (p.Arg428=) rs752479774
NM_000702.4(ATP1A2):c.1462-10G>C rs1409479382
NM_000702.4(ATP1A2):c.1500C>T (p.His500=) rs140480795
NM_000702.4(ATP1A2):c.1578G>A (p.Pro526=) rs376128790
NM_000702.4(ATP1A2):c.1581C>G (p.Leu527=) rs371520433
NM_000702.4(ATP1A2):c.1652-7C>A rs200102433
NM_000702.4(ATP1A2):c.1779G>A (p.Arg593=) rs1553245179
NM_000702.4(ATP1A2):c.1806G>A (p.Lys602=) rs1553245180
NM_000702.4(ATP1A2):c.2070G>A (p.Thr690=) rs142865268
NM_000702.4(ATP1A2):c.2088C>T (p.Leu696=) rs151052102
NM_000702.4(ATP1A2):c.2130C>T (p.Ala710=) rs374749325
NM_000702.4(ATP1A2):c.2142C>T (p.Asp714=) rs139022921
NM_000702.4(ATP1A2):c.2440-6A>C rs1553245840
NM_000702.4(ATP1A2):c.2514G>A (p.Thr838=) rs140646289
NM_000702.4(ATP1A2):c.25T>A (p.Tyr9Asn) rs55858252
NM_000702.4(ATP1A2):c.2742G>T (p.Thr914=) rs201215311
NM_000702.4(ATP1A2):c.2790C>T (p.Asp930=) rs376259974
NM_000702.4(ATP1A2):c.2841-8C>T rs1553246128
NM_000702.4(ATP1A2):c.2880G>T (p.Ala960=) rs762969049
NM_000702.4(ATP1A2):c.2895C>G (p.Leu965=) rs200706103
NM_000702.4(ATP1A2):c.340G>A (p.Gly114Ser) rs116711766
NM_000702.4(ATP1A2):c.495+10C>G rs1226066700
NM_000702.4(ATP1A2):c.495+7T>C rs377435696
NM_000702.4(ATP1A2):c.600C>T (p.Asp200=) rs1060504129
NM_000702.4(ATP1A2):c.627T>C (p.Cys209=) rs139229302
NM_000702.4(ATP1A2):c.836G>A (p.Arg279Gln) rs373178892
NM_000702.4(ATP1A2):c.987C>T (p.Asn329=) rs770381135
NM_000702.4(ATP1A2):c.993T>G (p.Pro331=) rs773614984

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