ClinVar Miner

List of variants in gene ATP1A2 reported as uncertain significance for not provided

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Total variants: 73
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HGVS dbSNP
NM_000702.4(ATP1A2):c.1092G>A (p.Thr364=) rs55741021
NM_000702.4(ATP1A2):c.1282C>T (p.Arg428Cys) rs779985796
NM_000702.4(ATP1A2):c.1283G>A (p.Arg428His) rs746478136
NM_000702.4(ATP1A2):c.128A>G (p.Lys43Arg) rs796052281
NM_000702.4(ATP1A2):c.1318G>A (p.Val440Met) rs768088341
NM_000702.4(ATP1A2):c.1410C>G (p.Asp470Glu) rs533400580
NM_000702.4(ATP1A2):c.1415A>G (p.Asn472Ser) rs529607288
NM_000702.4(ATP1A2):c.1432A>G (p.Ile478Val) rs1553245013
NM_000702.4(ATP1A2):c.1474G>A (p.Glu492Lys) rs142348542
NM_000702.4(ATP1A2):c.152G>T (p.Arg51Leu) rs144106169
NM_000702.4(ATP1A2):c.1540C>T (p.Arg514Trp) rs781474239
NM_000702.4(ATP1A2):c.1541G>A (p.Arg514Gln) rs748654627
NM_000702.4(ATP1A2):c.1582G>A (p.Asp528Asn) rs374501280
NM_000702.4(ATP1A2):c.1652-8C>T rs370023134
NM_000702.4(ATP1A2):c.1661A>T (p.Gln554Leu) rs199749129
NM_000702.4(ATP1A2):c.1666A>T (p.Asn556Tyr) rs141467566
NM_000702.4(ATP1A2):c.1690C>T (p.Arg564Trp) rs762330744
NM_000702.4(ATP1A2):c.1691G>A (p.Arg564Gln) rs765936799
NM_000702.4(ATP1A2):c.1714G>A (p.Glu572Lys) rs1553245166
NM_000702.4(ATP1A2):c.1821C>T (p.Gly607=) rs771085157
NM_000702.4(ATP1A2):c.1859C>G (p.Thr620Arg) rs1057521886
NM_000702.4(ATP1A2):c.1888A>G (p.Ile630Val) rs1382260409
NM_000702.4(ATP1A2):c.1891A>G (p.Ile631Val) rs201977531
NM_000702.4(ATP1A2):c.192G>T (p.Gln64His) rs796052282
NM_000702.4(ATP1A2):c.193C>T (p.Arg65Trp) rs121918619
NM_000702.4(ATP1A2):c.194G>T (p.Arg65Leu) rs187733403
NM_000702.4(ATP1A2):c.1990G>A (p.Gly664Ser) rs1483366741
NM_000702.4(ATP1A2):c.205G>A (p.Val69Ile) rs558323868
NM_000702.4(ATP1A2):c.2093T>C (p.Ile698Thr) rs1553245737
NM_000702.4(ATP1A2):c.2115+16G>T rs1426409869
NM_000702.4(ATP1A2):c.2128G>A (p.Ala710Thr) rs1553245764
NM_000702.4(ATP1A2):c.2187T>C (p.Ile729=) rs751808345
NM_000702.4(ATP1A2):c.2212G>A (p.Val738Ile) rs1558008569
NM_000702.4(ATP1A2):c.2230G>A (p.Asp744Asn) rs1131691922
NM_000702.4(ATP1A2):c.2271G>A (p.Thr757=) rs202094576
NM_000702.4(ATP1A2):c.2273G>C (p.Gly758Ala) rs147183887
NM_000702.4(ATP1A2):c.2374A>G (p.Ile792Val) rs758749177
NM_000702.4(ATP1A2):c.2412C>T (p.Ile804=) rs143969080
NM_000702.4(ATP1A2):c.2517C>G (p.Asp839Glu) rs752471668
NM_000702.4(ATP1A2):c.2520G>A (p.Lys840=) rs587780283
NM_000702.4(ATP1A2):c.2554G>C (p.Gly852Arg) rs1553245853
NM_000702.4(ATP1A2):c.2564-7C>T rs1558009070
NM_000702.4(ATP1A2):c.2622T>C (p.Gly874=) rs886043454
NM_000702.4(ATP1A2):c.2675T>C (p.Met892Thr) rs794727222
NM_000702.4(ATP1A2):c.2680G>T (p.Asp894Tyr) rs1553245907
NM_000702.4(ATP1A2):c.2722C>T (p.Arg908Trp) rs758772895
NM_000702.4(ATP1A2):c.274C>T (p.Arg92Cys) rs796052278
NM_000702.4(ATP1A2):c.2751G>A (p.Thr917=) rs146839867
NM_000702.4(ATP1A2):c.275G>A (p.Arg92His) rs774275559
NM_000702.4(ATP1A2):c.2770G>A (p.Val924Met) rs373276446
NM_000702.4(ATP1A2):c.280C>T (p.Leu94Phe) rs950102855
NM_000702.4(ATP1A2):c.2850C>G (p.Ile950Met) rs1553246129
NM_000702.4(ATP1A2):c.2887G>A (p.Ala963Thr) rs1057523245
NM_000702.4(ATP1A2):c.2969C>T (p.Pro990Leu) rs775974337
NM_000702.4(ATP1A2):c.2973C>T (p.Tyr991=) rs149286529
NM_000702.4(ATP1A2):c.2977C>T (p.Leu993Phe) rs1303848624
NM_000702.4(ATP1A2):c.2993A>G (p.Tyr998Cys) rs1085307501
NM_000702.4(ATP1A2):c.29C>T (p.Ser10Leu) rs762611119
NM_000702.4(ATP1A2):c.3014T>C (p.Ile1005Thr)
NM_000702.4(ATP1A2):c.3034+6C>A rs574788908
NM_000702.4(ATP1A2):c.44C>T (p.Thr15Met) rs371257019
NM_000702.4(ATP1A2):c.481A>G (p.Asn161Asp) rs796052279
NM_000702.4(ATP1A2):c.56G>T (p.Gly19Val) rs757373744
NM_000702.4(ATP1A2):c.619C>T (p.His207Tyr) rs1057523810
NM_000702.4(ATP1A2):c.736A>G (p.Asn246Asp) rs764917849
NM_000702.4(ATP1A2):c.799C>T (p.Arg267Cys) rs1399834873
NM_000702.4(ATP1A2):c.836G>A (p.Arg279Gln) rs373178892
NM_000702.4(ATP1A2):c.841C>T (p.Pro281Ser)
NM_000702.4(ATP1A2):c.848C>T (p.Ala283Val) rs1553244740
NM_000702.4(ATP1A2):c.862C>T (p.His288Tyr) rs754699681
NM_000702.4(ATP1A2):c.889G>A (p.Ala297Thr) rs181618883
NM_000702.4(ATP1A2):c.909C>T (p.Ser303=) rs1422290691
NM_000702.4(ATP1A2):c.982G>A (p.Ala328Thr) rs1064796371

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