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Pathways
Variants search result for All species
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34 records found for search term Stk25
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407530124CV3485502single nucleotide variantNM_001271977.2(STK25):c.9C>G (p.His3Gln)not specified [RCV004681666]uncertain significance2241508027241508027Humanname
329370115CV2461618single nucleotide variantNM_001271977.2(STK25):c.23C>T (p.Ala8Val)not specified [RCV004269794]uncertain significance2241508013241508013Humanname
401892285CV2777390single nucleotide variantNM_001271977.2(STK25):c.154G>A (p.Asp52Asn)not specified [RCV004354393]uncertain significance2241501585241501585Humanname
598207506CV3919683single nucleotide variantNM_001271977.2(STK25):c.295G>T (p.Gly99Cys)not specified [RCV005291295]uncertain significance2241500763241500763Humanname
156230624CV2264187single nucleotide variantNM_001271977.2(STK25):c.301G>A (p.Gly101Ser)not specified [RCV004136335]uncertain significance2241500757241500757Humanname
156003738CV2290061single nucleotide variantNM_001271977.2(STK25):c.764C>T (p.Pro255Leu)not specified [RCV004152744]uncertain significance2241498996241498996Humanname
329395849CV2454649single nucleotide variantNM_001271977.2(STK25):c.976C>T (p.Arg326Trp)not specified [RCV004268108]uncertain significance2241498291241498291Humanname
329367751CV2457039single nucleotide variantNM_001271977.2(STK25):c.953T>G (p.Ile318Ser)not specified [RCV004264830]uncertain significance2241498314241498314Humanname
329401648CV2457268single nucleotide variantNM_001271977.2(STK25):c.386A>G (p.Asp129Gly)not specified [RCV004267121]uncertain significance2241500214241500214Humanname
405740949CV3334491single nucleotide variantNM_001271977.2(STK25):c.577G>A (p.Asp193Asn)not specified [RCV004465704]uncertain significance2241499265241499265Humanname
405740957CV3334492single nucleotide variantNM_001271977.2(STK25):c.767G>A (p.Arg256Gln)not specified [RCV004465705]uncertain significance2241498993241498993Humanname
405740964CV3334493single nucleotide variantNM_001271977.2(STK25):c.856C>T (p.Arg286Cys)not specified [RCV004465706]uncertain significance2241498700241498700Humanname
405740972CV3334494single nucleotide variantNM_001271977.2(STK25):c.865C>T (p.Arg289Cys)not specified [RCV004465707]uncertain significance2241498691241498691Humanname
405740979CV3334495single nucleotide variantNM_001271977.2(STK25):c.875C>T (p.Ser292Leu)not specified [RCV004465708]uncertain significance2241498681241498681Humanname
405740986CV3334496single nucleotide variantNM_001271977.2(STK25):c.929C>T (p.Ala310Val)not specified [RCV004465709]uncertain significance2241498338241498338Humanname
405740993CV3334497single nucleotide variantNM_001271977.2(STK25):c.932A>C (p.Glu311Ala)not specified [RCV004465710]uncertain significance2241498335241498335Humanname
405741002CV3334498single nucleotide variantNM_001271977.2(STK25):c.967C>G (p.Pro323Ala)not specified [RCV004465711]uncertain significance2241498300241498300Humanname
597747636CV3614844single nucleotide variantNM_001271977.2(STK25):c.413A>G (p.His138Arg)not specified [RCV004866106]uncertain significance2241500187241500187Humanname
597747643CV3614845single nucleotide variantNM_001271977.2(STK25):c.962T>C (p.Phe321Ser)not specified [RCV004866107]uncertain significance2241498305241498305Humanname
597747648CV3614846single nucleotide variantNM_001271977.2(STK25):c.985C>T (p.Pro329Ser)not specified [RCV004866108]uncertain significance2241498282241498282Humanname
597747653CV3614847single nucleotide variantNM_001271977.2(STK25):c.305C>T (p.Ser102Leu)not specified [RCV004866109]uncertain significance2241500753241500753Humanname
598251489CV3919684single nucleotide variantNM_001271977.2(STK25):c.857G>A (p.Arg286His)not specified [RCV005277898]uncertain significance2241498699241498699Humanname
598207511CV3919686single nucleotide variantNM_001271977.2(STK25):c.652C>T (p.Leu218Phe)not specified [RCV005291296]uncertain significance2241499108241499108Humanname
155917490CV2236568single nucleotide variantNM_001271977.2(STK25):c.1021A>G (p.Ser341Gly)not specified [RCV004110561]likely benign2241498246241498246Humanname
156336931CV2270980single nucleotide variantNM_001271977.2(STK25):c.1034C>T (p.Pro345Leu)not specified [RCV004132007]uncertain significance2241497686241497686Humanname
156248029CV2276945single nucleotide variantNM_001271977.2(STK25):c.1093G>A (p.Val365Ile)not specified [RCV004140279]uncertain significance2241497627241497627Humanname
155997454CV2373184single nucleotide variantNM_001271977.2(STK25):c.1276C>T (p.Arg426Cys)not specified [RCV004217865]uncertain significance2241495667241495667Humanname
156388963CV2376261single nucleotide variantNM_001271977.2(STK25):c.1277G>A (p.Arg426His)not specified [RCV004220480]uncertain significance2241495666241495666Humanname
329361825CV2448059single nucleotide variantNM_001271977.2(STK25):c.1087C>T (p.Arg363Trp)not specified [RCV004263285]uncertain significance2241497633241497633Humanname
329353515CV2466813single nucleotide variantNM_001271977.2(STK25):c.1230G>T (p.Glu410Asp)not specified [RCV004280757]uncertain significance2241496409241496409Humanname
405740942CV3334490single nucleotide variantNM_001271977.2(STK25):c.1045G>A (p.Val349Ile)not specified [RCV004465703]uncertain significance2241497675241497675Humanname
597747625CV3614842single nucleotide variantNM_001271977.2(STK25):c.1276C>A (p.Arg426Ser)not specified [RCV004866104]uncertain significance2241495667241495667Humanname
597747631CV3614843single nucleotide variantNM_001271977.2(STK25):c.1009A>G (p.Thr337Ala)not specified [RCV004866105]uncertain significance2241498258241498258Humanname
598251494CV3919685single nucleotide variantNM_001271977.2(STK25):c.1138G>A (p.Val380Met)not specified [RCV005277899]uncertain significance2241496501241496501Humanname