ClinVar Miner

List of variants in gene ATP1A2 reported as uncertain significance by Invitae

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Total variants: 56
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HGVS dbSNP
NM_000702.4(ATP1A2):c.1017+7G>A
NM_000702.4(ATP1A2):c.1028C>T (p.Thr343Ile) rs1553244875
NM_000702.4(ATP1A2):c.1043G>A (p.Arg348His)
NM_000702.4(ATP1A2):c.1097G>A (p.Gly366Asp)
NM_000702.4(ATP1A2):c.1133C>T (p.Thr378Ile) rs28934002
NM_000702.4(ATP1A2):c.1150A>G (p.Met384Val)
NM_000702.4(ATP1A2):c.1216+5T>C rs780155641
NM_000702.4(ATP1A2):c.1244C>T (p.Thr415Met) rs121918618
NM_000702.4(ATP1A2):c.1262G>A (p.Arg421Gln) rs139499540
NM_000702.4(ATP1A2):c.1285G>A (p.Ala429Thr)
NM_000702.4(ATP1A2):c.1288G>A (p.Val430Ile)
NM_000702.4(ATP1A2):c.1382C>T (p.Ser461Phe) rs751491994
NM_000702.4(ATP1A2):c.1474G>A (p.Glu492Lys) rs142348542
NM_000702.4(ATP1A2):c.149G>T (p.Gly50Val)
NM_000702.4(ATP1A2):c.1514A>C (p.Lys505Thr)
NM_000702.4(ATP1A2):c.1528C>T (p.Arg510Cys)
NM_000702.4(ATP1A2):c.152G>A (p.Arg51His) rs144106169
NM_000702.4(ATP1A2):c.1541G>A (p.Arg514Gln) rs748654627
NM_000702.4(ATP1A2):c.1550C>A (p.Thr517Asn)
NM_000702.4(ATP1A2):c.1582G>A (p.Asp528Asn) rs374501280
NM_000702.4(ATP1A2):c.1652-3T>C rs1553245152
NM_000702.4(ATP1A2):c.1666A>T (p.Asn556Tyr) rs141467566
NM_000702.4(ATP1A2):c.1691G>A (p.Arg564Gln) rs765936799
NM_000702.4(ATP1A2):c.1735A>G (p.Lys579Glu)
NM_000702.4(ATP1A2):c.1778G>T (p.Arg593Leu)
NM_000702.4(ATP1A2):c.1811G>A (p.Arg604Gln)
NM_000702.4(ATP1A2):c.1821C>T (p.Gly607=) rs771085157
NM_000702.4(ATP1A2):c.1827+3A>G rs377238291
NM_000702.4(ATP1A2):c.1859C>G (p.Thr620Arg) rs1057521886
NM_000702.4(ATP1A2):c.1881C>T (p.Gly627=)
NM_000702.4(ATP1A2):c.192G>T (p.Gln64His) rs796052282
NM_000702.4(ATP1A2):c.1930C>T (p.Arg644Trp)
NM_000702.4(ATP1A2):c.2062G>T (p.Ala688Ser)
NM_000702.4(ATP1A2):c.2123T>A (p.Ile708Asn) rs1341609289
NM_000702.4(ATP1A2):c.2131G>A (p.Val711Met) rs1282248061
NM_000702.4(ATP1A2):c.2263A>G (p.Ile755Val)
NM_000702.4(ATP1A2):c.2275G>T (p.Val759Leu) rs1553245779
NM_000702.4(ATP1A2):c.2285G>C (p.Gly762Ala) rs1461860929
NM_000702.4(ATP1A2):c.2374A>G (p.Ile792Val) rs758749177
NM_000702.4(ATP1A2):c.2424C>G (p.Asp808Glu)
NM_000702.4(ATP1A2):c.2426T>G (p.Leu809Arg) rs1553245805
NM_000702.4(ATP1A2):c.2636G>A (p.Arg879Gln) rs761597771
NM_000702.4(ATP1A2):c.2770G>A (p.Val924Met) rs373276446
NM_000702.4(ATP1A2):c.280C>A (p.Leu94Ile)
NM_000702.4(ATP1A2):c.335C>A (p.Ala112Asp) rs878854140
NM_000702.4(ATP1A2):c.381T>C (p.Asn127=) rs139243866
NM_000702.4(ATP1A2):c.512G>A (p.Arg171Gln) rs1553244392
NM_000702.4(ATP1A2):c.586C>T (p.Arg196Cys)
NM_000702.4(ATP1A2):c.58G>A (p.Gly20Ser) rs1558002462
NM_000702.4(ATP1A2):c.607A>C (p.Ile203Leu)
NM_000702.4(ATP1A2):c.664C>T (p.Pro222Ser)
NM_000702.4(ATP1A2):c.674G>A (p.Arg225His)
NM_000702.4(ATP1A2):c.889G>A (p.Ala297Thr) rs181618883
NM_000702.4(ATP1A2):c.892G>C (p.Val298Leu) rs757867108
NM_000702.4(ATP1A2):c.8G>A (p.Arg3His) rs781687346
NM_000702.4(ATP1A2):c.970G>A (p.Gly324Ser)

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