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Variants search result for Homo sapiens
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20 records found for search term Nck2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597648742CV3562425single nucleotide variantNM_003581.5(NCK2):c.156G>A (p.Pro52=)not specified [RCV004826600]likely benign2105855219105855219Humanname
405789783CV3336820single nucleotide variantNM_003581.5(NCK2):c.64G>A (p.Asp22Asn)not specified [RCV004473699]uncertain significance2105855127105855127Humanname
156241532CV2246118single nucleotide variantNM_003581.5(NCK2):c.289G>A (p.Ala97Thr)not specified [RCV004114020]uncertain significance2105881390105881390Humanname
156099551CV2392876single nucleotide variantNM_003581.5(NCK2):c.284C>T (p.Thr95Met)not specified [RCV004247228]uncertain significance2105881385105881385Humanname
597648889CV3562423single nucleotide variantNM_003581.5(NCK2):c.130G>A (p.Ala44Thr)not specified [RCV004826598]uncertain significance2105855193105855193Humanname
597648734CV3562424single nucleotide variantNM_003581.5(NCK2):c.121G>C (p.Val41Leu)not specified [RCV004826599]uncertain significance2105855184105855184Humanname
597648749CV3562426single nucleotide variantNM_003581.5(NCK2):c.173G>A (p.Arg58Gln)not specified [RCV004826601]uncertain significance2105855236105855236Humanname
598217064CV3983776single nucleotide variantNM_003581.5(NCK2):c.155C>T (p.Pro52Leu)not specified [RCV005379003]uncertain significance2105855218105855218Humanname
156097142CV2310244single nucleotide variantNM_003581.5(NCK2):c.556G>T (p.Ala186Ser)not specified [RCV004163342]uncertain significance2105881657105881657Humanname
156152223CV2377609single nucleotide variantNM_003581.5(NCK2):c.767G>A (p.Ser256Asn)not specified [RCV004227798]uncertain significance2105881868105881868Humanname
329395829CV2454633single nucleotide variantNM_003581.5(NCK2):c.832G>A (p.Gly278Arg)not specified [RCV004268092]uncertain significance2105881933105881933Humanname
401888843CV2764978single nucleotide variantNM_003581.5(NCK2):c.746A>G (p.Lys249Arg)not specified [RCV004335057]uncertain significance2105881847105881847Humanname
405789710CV3336801single nucleotide variantNM_003581.5(NCK2):c.312C>A (p.Ser104Arg)not specified [RCV004473680]uncertain significance2105881413105881413Humanname
405789726CV3336805single nucleotide variantNM_003581.5(NCK2):c.332A>T (p.Asp111Val)not specified [RCV004473684]uncertain significance2105881433105881433Humanname
405789743CV3336809single nucleotide variantNM_003581.5(NCK2):c.460A>T (p.Asn154Tyr)not specified [RCV004473688]uncertain significance2105881561105881561Humanname
405789803CV3336825single nucleotide variantNM_003581.5(NCK2):c.686A>C (p.Glu229Ala)not specified [RCV004473704]uncertain significance2105881787105881787Humanname
597649173CV3562421single nucleotide variantNM_003581.5(NCK2):c.577G>A (p.Gly193Ser)not specified [RCV004826596]uncertain significance2105881678105881678Humanname
598217056CV3983775single nucleotide variantNM_003581.5(NCK2):c.983G>A (p.Gly328Glu)not specified [RCV005379002]uncertain significance2105893016105893016Humanname
598253142CV3983773single nucleotide variantNM_003581.5(NCK2):c.1084G>A (p.Ala362Thr)not specified [RCV005385289]uncertain significance2105893117105893117Humanname
598217049CV3983774single nucleotide variantNM_003581.5(NCK2):c.1121A>G (p.Tyr374Cys)not specified [RCV005379001]uncertain significance2105893154105893154Humanname