ClinVar Miner

List of variants in gene ATP1A3 studied for not specified

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_152296.5(ATP1A3):c.666T>G (p.Thr222=) rs2217342 0.93139
NM_152296.5(ATP1A3):c.994-20T>G rs138485069 0.01603
NM_152296.5(ATP1A3):c.2319T>C (p.Asn773=) rs61733017 0.01238
NM_152296.5(ATP1A3):c.2264-16C>T rs149116776 0.01189
NM_152296.5(ATP1A3):c.2487G>A (p.Pro829=) rs45606534 0.00759
NM_152296.5(ATP1A3):c.154-5C>G rs191645384 0.00188
NM_152296.5(ATP1A3):c.816G>A (p.Thr272=) rs149898088 0.00140
NM_152296.5(ATP1A3):c.1387C>T (p.Arg463Cys) rs150785666 0.00050
NM_152296.5(ATP1A3):c.147T>C (p.Cys49=) rs376960579 0.00011
NM_152296.5(ATP1A3):c.2489G>A (p.Arg830Gln) rs368371895 0.00010
NM_152296.5(ATP1A3):c.191G>A (p.Arg64Gln) rs201573515 0.00006
NM_152296.5(ATP1A3):c.2886C>T (p.Pro962=) rs141412861 0.00006
NM_152296.5(ATP1A3):c.739G>A (p.Val247Met) rs782227665 0.00006
NM_152296.5(ATP1A3):c.2885C>A (p.Pro962His) rs145179304 0.00004
NM_152296.5(ATP1A3):c.207A>T (p.Ala69=) rs200616931 0.00002
NM_152296.5(ATP1A3):c.2973C>T (p.Tyr991=) rs372919447 0.00002
NM_152296.5(ATP1A3):c.1027C>T (p.Arg343Trp) rs782423325 0.00001
NM_152296.5(ATP1A3):c.2523C>T (p.Ser841=) rs1236093021 0.00001
NM_152296.5(ATP1A3):c.274A>G (p.Ile92Val) rs933392084 0.00001
NM_152296.5(ATP1A3):c.363C>T (p.Tyr121=) rs373180830 0.00001
NM_152296.5(ATP1A3):c.1323G>A (p.Ala441=) rs34578730
NM_152296.5(ATP1A3):c.1549G>C (p.Glu517Gln) rs782583311
NM_152296.5(ATP1A3):c.1721G>A (p.Cys574Tyr) rs1555862110
NM_152296.5(ATP1A3):c.1806+3G>A rs2145964767
NM_152296.5(ATP1A3):c.2267G>A (p.Arg756His) rs606231435
NM_152296.5(ATP1A3):c.2443G>A (p.Glu815Lys) rs387907281
NM_152296.5(ATP1A3):c.2648G>A (p.Arg883His)
NM_152296.5(ATP1A3):c.2953A>G (p.Ser985Gly) rs1599702734
NM_152296.5(ATP1A3):c.760C>T (p.Arg254Cys)
NM_152296.5(ATP1A3):c.910G>A (p.Gly304Arg) rs1032312899

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