ClinVar Miner

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

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Total variants: 91
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HGVS dbSNP
NM_000702.4(ATP1A2):c.*6T>C rs796052273
NM_000702.4(ATP1A2):c.-14C>G rs756960901
NM_000702.4(ATP1A2):c.-30G>A rs759542448
NM_000702.4(ATP1A2):c.-31C>G rs192111085
NM_000702.4(ATP1A2):c.-33C>A rs1323771499
NM_000702.4(ATP1A2):c.1017+9G>T rs1057521623
NM_000702.4(ATP1A2):c.1018-15_1018-13del rs1064795923
NM_000702.4(ATP1A2):c.108G>A (p.Glu36=) rs1553244021
NM_000702.4(ATP1A2):c.1110C>T (p.Thr370=) rs747219922
NM_000702.4(ATP1A2):c.1155C>A (p.Thr385=) rs759207376
NM_000702.4(ATP1A2):c.1158C>T (p.Val386=) rs752381925
NM_000702.4(ATP1A2):c.1182A>G (p.Gln394=) rs1553244893
NM_000702.4(ATP1A2):c.1203C>T (p.Thr401=) rs547954866
NM_000702.4(ATP1A2):c.1216+12C>T rs748392461
NM_000702.4(ATP1A2):c.1251G>A (p.Thr417=) rs142309356
NM_000702.4(ATP1A2):c.1251G>C (p.Thr417=) rs142309356
NM_000702.4(ATP1A2):c.1263A>G (p.Arg421=) rs1057523616
NM_000702.4(ATP1A2):c.1311C>T (p.Asn437=) rs1057521266
NM_000702.4(ATP1A2):c.1326+8del rs763762298
NM_000702.4(ATP1A2):c.1327-12C>G rs903572955
NM_000702.4(ATP1A2):c.1368G>A (p.Lys456=) rs369226331
NM_000702.4(ATP1A2):c.1461+5G>A rs199906945
NM_000702.4(ATP1A2):c.1462-5T>A rs796052272
NM_000702.4(ATP1A2):c.1473C>T (p.His491=) rs768902765
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.1590G>A (p.Glu530=) rs1042062045
NM_000702.4(ATP1A2):c.1647G>T (p.Val549=) rs1553245135
NM_000702.4(ATP1A2):c.1652-6C>T rs768543626
NM_000702.4(ATP1A2):c.1652-8C>T rs370023134
NM_000702.4(ATP1A2):c.1666A>T (p.Asn556Tyr) rs141467566
NM_000702.4(ATP1A2):c.1710G>A (p.Thr570=) rs536168465
NM_000702.4(ATP1A2):c.1740T>G (p.Leu580=) rs978157409
NM_000702.4(ATP1A2):c.1761T>C (p.Ser587=) rs199621678
NM_000702.4(ATP1A2):c.177+20G>C rs1475100565
NM_000702.4(ATP1A2):c.1815C>T (p.Ser605=) rs771651622
NM_000702.4(ATP1A2):c.1827+134A>G
NM_000702.4(ATP1A2):c.1827+38C>T
NM_000702.4(ATP1A2):c.1959C>T (p.Asn653=)
NM_000702.4(ATP1A2):c.1962C>G (p.Pro654=) rs1057523083
NM_000702.4(ATP1A2):c.1964+14A>G rs201131020
NM_000702.4(ATP1A2):c.1965-130G>T
NM_000702.4(ATP1A2):c.2016G>A (p.Ser672=) rs762744089
NM_000702.4(ATP1A2):c.2088C>T (p.Leu696=) rs151052102
NM_000702.4(ATP1A2):c.2103A>T (p.Gly701=) rs963491650
NM_000702.4(ATP1A2):c.2115+15G>A rs769939965
NM_000702.4(ATP1A2):c.2115+19G>A rs375635569
NM_000702.4(ATP1A2):c.2116-14C>T rs748188822
NM_000702.4(ATP1A2):c.2130C>T (p.Ala710=) rs374749325
NM_000702.4(ATP1A2):c.2136G>A (p.Thr712=) rs760213030
NM_000702.4(ATP1A2):c.2142C>T (p.Asp714=) rs139022921
NM_000702.4(ATP1A2):c.2148G>A (p.Val716=) rs1057523552
NM_000702.4(ATP1A2):c.2427G>A (p.Leu809=) rs369916877
NM_000702.4(ATP1A2):c.2439+13G>A rs1038003940
NM_000702.4(ATP1A2):c.2440-14C>T rs200630442
NM_000702.4(ATP1A2):c.2440-26C>T
NM_000702.4(ATP1A2):c.2562C>T (p.Ile854=) rs371086182
NM_000702.4(ATP1A2):c.2563+17G>A rs1553245863
NM_000702.4(ATP1A2):c.2564-8A>G rs554846350
NM_000702.4(ATP1A2):c.2589C>T (p.Phe863=) rs760872961
NM_000702.4(ATP1A2):c.25T>A (p.Tyr9Asn) rs55858252
NM_000702.4(ATP1A2):c.2709+17A>G rs961165805
NM_000702.4(ATP1A2):c.2710-19C>G rs757662486
NM_000702.4(ATP1A2):c.2790C>T (p.Asp930=) rs376259974
NM_000702.4(ATP1A2):c.2840+36G>A
NM_000702.4(ATP1A2):c.2841-7C>T rs1057521032
NM_000702.4(ATP1A2):c.2895C>G (p.Leu965=) rs200706103
NM_000702.4(ATP1A2):c.291G>T (p.Gly97=) rs759566498
NM_000702.4(ATP1A2):c.2942+16G>A rs776114360
NM_000702.4(ATP1A2):c.2942+19C>T rs187187416
NM_000702.4(ATP1A2):c.2943-75C>G
NM_000702.4(ATP1A2):c.2973C>T (p.Tyr991=) rs149286529
NM_000702.4(ATP1A2):c.3035-284A>T
NM_000702.4(ATP1A2):c.3035-286G>A
NM_000702.4(ATP1A2):c.340G>A (p.Gly114Ser) rs116711766
NM_000702.4(ATP1A2):c.36C>T (p.Ala12=) rs767913105
NM_000702.4(ATP1A2):c.381+12C>T rs368856029
NM_000702.4(ATP1A2):c.381+13G>A
NM_000702.4(ATP1A2):c.381+13G>T rs772082739
NM_000702.4(ATP1A2):c.495+9G>T rs1057522630
NM_000702.4(ATP1A2):c.496-15T>C rs1057522605
NM_000702.4(ATP1A2):c.513G>A (p.Arg171=) rs770882300
NM_000702.4(ATP1A2):c.631-16A>G rs571618030
NM_000702.4(ATP1A2):c.631-231T>G
NM_000702.4(ATP1A2):c.660G>A (p.Ser220=) rs564452950
NM_000702.4(ATP1A2):c.705G>A (p.Leu235=) rs1019036534
NM_000702.4(ATP1A2):c.789G>A (p.Thr263=) rs748890267
NM_000702.4(ATP1A2):c.836G>A (p.Arg279Gln) rs373178892
NM_000702.4(ATP1A2):c.8G>A (p.Arg3His) rs781687346
NM_000702.4(ATP1A2):c.987C>T (p.Asn329=) rs770381135

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