ClinVar Miner

List of variants in gene ATP2A2 reported as uncertain significance for not provided

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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_170665.4(ATP2A2):c.94C>T (p.Leu32Phe) rs141335001 0.00048
NM_170665.4(ATP2A2):c.3064A>G (p.Ile1022Val) rs140234740 0.00033
NM_170665.4(ATP2A2):c.1096A>G (p.Met366Val) rs199776454 0.00017
NM_170665.4(ATP2A2):c.2797G>A (p.Val933Met) rs372102705 0.00008
NM_170665.4(ATP2A2):c.2281C>T (p.Arg761Cys) rs770065068 0.00001
NM_170665.4(ATP2A2):c.2777C>G (p.Pro926Arg) rs1879821773 0.00001
NM_170665.4(ATP2A2):c.1037C>T (p.Ser346Phe)
NM_170665.4(ATP2A2):c.1058C>G (p.Thr353Ser)
NM_170665.4(ATP2A2):c.105A>T (p.Arg35Ser) rs779082834
NM_170665.4(ATP2A2):c.1061G>A (p.Gly354Asp)
NM_170665.4(ATP2A2):c.1282A>C (p.Asn428His)
NM_170665.4(ATP2A2):c.1312G>A (p.Gly438Arg)
NM_170665.4(ATP2A2):c.131A>G (p.Glu44Gly) rs386352281
NM_170665.4(ATP2A2):c.1352A>T (p.Lys451Met)
NM_170665.4(ATP2A2):c.1384C>T (p.Leu462Phe)
NM_170665.4(ATP2A2):c.1399C>T (p.Arg467Cys)
NM_170665.4(ATP2A2):c.1466G>A (p.Arg489His)
NM_170665.4(ATP2A2):c.1522A>G (p.Met508Val) rs772144757
NM_170665.4(ATP2A2):c.1622_1633del (p.Lys541_Ile544del)
NM_170665.4(ATP2A2):c.1676G>A (p.Arg559Gln)
NM_170665.4(ATP2A2):c.1761G>A (p.Glu587=)
NM_170665.4(ATP2A2):c.220G>C (p.Val74Leu)
NM_170665.4(ATP2A2):c.2212_2214del (p.Asn738del)
NM_170665.4(ATP2A2):c.2216T>A (p.Phe739Tyr) rs2137861544
NM_170665.4(ATP2A2):c.2321T>A (p.Ile774Asn)
NM_170665.4(ATP2A2):c.2353G>T (p.Ala785Ser) rs2137864685
NM_170665.4(ATP2A2):c.2384A>G (p.Asn795Ser) rs1057520789
NM_170665.4(ATP2A2):c.2387T>C (p.Leu796Pro) rs1592864875
NM_170665.4(ATP2A2):c.2488G>A (p.Gly830Arg)
NM_170665.4(ATP2A2):c.2788A>G (p.Ile930Val)
NM_170665.4(ATP2A2):c.2860-3C>G
NM_170665.4(ATP2A2):c.2926G>A (p.Val976Met)
NM_170665.4(ATP2A2):c.323A>C (p.Gln108Pro)
NM_170665.4(ATP2A2):c.371C>T (p.Pro124Leu)
NM_170665.4(ATP2A2):c.392G>T (p.Arg131Leu)
NM_170665.4(ATP2A2):c.484G>A (p.Asp162Asn)
NM_170665.4(ATP2A2):c.545-12C>G rs1064796802
NM_170665.4(ATP2A2):c.545-7C>A
NM_170665.4(ATP2A2):c.547G>A (p.Glu183Lys)
NM_170665.4(ATP2A2):c.704T>A (p.Ile235Asn)
NM_170665.4(ATP2A2):c.710A>G (p.Asp237Gly)
NM_170665.4(ATP2A2):c.908C>T (p.Ala303Val)

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