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Variants search result for Homo sapiens
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27 records found for search term Atp1b2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155972388CV2334328single nucleotide variantNM_001678.5(ATP1B2):c.227G>A (p.Arg76Gln)not specified [RCV004188307]uncertain significance1776534887653488Humanname
598223706CV3924045single nucleotide variantNM_001678.5(ATP1B2):c.157G>A (p.Ala53Thr)not specified [RCV005293995]uncertain significance1776534187653418Humanname
8636375CV91598single nucleotide variantNM_001678.4(ATP1B2):c.205C>T (p.His69Tyr)Malignant melanoma [RCV000071696]not provided1776534667653466Humanname
155981628CV2272878single nucleotide variantNM_001678.5(ATP1B2):c.554T>C (p.Val185Ala)not specified [RCV004135778]uncertain significance1776546297654629Humanname
156169530CV2273318single nucleotide variantNM_001678.5(ATP1B2):c.352A>C (p.Asn118His)not specified [RCV004132107]uncertain significance1776540577654057Humanname
156184988CV2335768single nucleotide variantNM_001678.5(ATP1B2):c.634G>A (p.Gly212Ser)not specified [RCV004193960]uncertain significance1776555517655551Humanname
155922363CV2340609single nucleotide variantNM_001678.5(ATP1B2):c.538A>C (p.Ile180Leu)not specified [RCV004197317]uncertain significance1776542437654243Humanname
156119085CV2354020single nucleotide variantNM_001678.5(ATP1B2):c.406G>A (p.Glu136Lys)not specified [RCV004204451]uncertain significance1776541117654111Humanname
156392197CV2378377single nucleotide variantNM_001678.5(ATP1B2):c.388C>T (p.Arg130Cys)not specified [RCV004226398]uncertain significance1776540937654093Humanname
401719820CV2675693single nucleotide variantNM_001678.5(ATP1B2):c.472G>A (p.Gly158Ser)not specified [RCV004287944]uncertain significance1776541777654177Humanname
401779097CV2702150single nucleotide variantNM_001678.5(ATP1B2):c.623C>T (p.Ala208Val)not specified [RCV004314502]uncertain significance1776555407655540Humanname
401757345CV2734962single nucleotide variantNM_001678.5(ATP1B2):c.488T>C (p.Ile163Thr)not specified [RCV004333668]uncertain significance1776541937654193Humanname
405704347CV3301268single nucleotide variantNM_001678.5(ATP1B2):c.349T>A (p.Tyr117Asn)not specified [RCV004425866]uncertain significance1776540547654054Humanname
405704356CV3301269single nucleotide variantNM_001678.5(ATP1B2):c.566A>G (p.Tyr189Cys)not specified [RCV004425867]uncertain significance1776546417654641Humanname
405704368CV3301270single nucleotide variantNM_001678.5(ATP1B2):c.838C>T (p.Arg280Cys)not specified [RCV004425868]uncertain significance1776558607655860Humanname
407461298CV3492530single nucleotide variantNM_001678.5(ATP1B2):c.443G>A (p.Arg148His)not specified [RCV004687618]uncertain significance1776541487654148Humanname
407521834CV3492539single nucleotide variantNM_001678.5(ATP1B2):c.371A>G (p.Gln124Arg)not specified [RCV004677446]uncertain significance1776540767654076Humanname
407521858CV3492549single nucleotide variantNM_001678.5(ATP1B2):c.611G>A (p.Arg204Gln)not specified [RCV004677456]uncertain significance1776555287655528Humanname
407521886CV3492560single nucleotide variantNM_001678.5(ATP1B2):c.452A>G (p.Gln151Arg)not specified [RCV004677466]uncertain significance1776541577654157Humanname
597762563CV3616370single nucleotide variantNM_001678.5(ATP1B2):c.389G>A (p.Arg130His)not specified [RCV004869659]uncertain significance1776540947654094Humanname
597762612CV3616380single nucleotide variantNM_001678.5(ATP1B2):c.839G>A (p.Arg280His)not specified [RCV004869669]uncertain significance1776558617655861Humanname
597762644CV3616388single nucleotide variantNM_001678.5(ATP1B2):c.459C>G (p.Asn153Lys)not specified [RCV004869676]uncertain significance1776541647654164Humanname
597762661CV3616397single nucleotide variantNM_001678.5(ATP1B2):c.791A>C (p.Asn264Thr)not specified [RCV004869680]uncertain significance1776558137655813Humanname
597762706CV3616407single nucleotide variantNM_001678.5(ATP1B2):c.688T>C (p.Tyr230His)not specified [RCV004869690]uncertain significance1776556057655605Humanname
597762755CV3616418single nucleotide variantNM_001678.5(ATP1B2):c.500C>T (p.Thr167Ile)not specified [RCV004869701]uncertain significance1776542057654205Humanname
598223615CV3924025single nucleotide variantNM_001678.5(ATP1B2):c.323A>T (p.Gln108Leu)not specified [RCV005293981]uncertain significance1776539227653922Humanname
598223653CV3924034single nucleotide variantNM_001678.5(ATP1B2):c.560A>C (p.Asn187Thr)not specified [RCV005293987]uncertain significance1776546357654635Humanname