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Variants search result for Homo sapiens
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24 records found for search term Nlk
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8585295CV119878single nucleotide variantNM_016231.4(NLK):c.645-3154T>GLung cancer [RCV000100398]uncertain significance172815800628158006Humanname
405707479CV3358820single nucleotide variantNM_016231.5(NLK):c.7C>G (p.Leu3Val)not specified [RCV004493341]uncertain significance172804288028042880Humanname
405707459CV3358817single nucleotide variantNM_016231.5(NLK):c.23C>T (p.Ala8Val)not specified [RCV004493338]uncertain significance172804289628042896Humanname
407508970CV3458690single nucleotide variantNM_016231.5(NLK):c.20G>C (p.Arg7Thr)not specified [RCV004647287]uncertain significance172804289328042893Humanname
156094444CV2252951single nucleotide variantNM_016231.5(NLK):c.84C>G (p.His28Gln)not specified [RCV004120768]uncertain significance172804295728042957Humanname
156094461CV2252952single nucleotide variantNM_016231.5(NLK):c.85C>A (p.His29Asn)not specified [RCV004120769]uncertain significance172804295828042958Humanname
156057498CV2322854single nucleotide variantNM_016231.5(NLK):c.208T>A (p.Ser70Thr)not specified [RCV004185313]uncertain significance172804308128043081Humanname
155929992CV2361013single nucleotide variantNM_016231.5(NLK):c.197A>G (p.Gln66Arg)not specified [RCV004216209]uncertain significance172804307028043070Humanname
156141746CV2383720single nucleotide variantNM_016231.5(NLK):c.186C>G (p.His62Gln)not specified [RCV004231604]uncertain significance172804305928043059Humanname
156141760CV2383721single nucleotide variantNM_016231.5(NLK):c.187C>G (p.Pro63Ala)not specified [RCV004231605]uncertain significance172804306028043060Humanname
156141791CV2383723single nucleotide variantNM_016231.5(NLK):c.188C>G (p.Pro63Arg)not specified [RCV004231607]uncertain significance172804306128043061Humanname
405707453CV3358816single nucleotide variantNM_016231.5(NLK):c.106C>T (p.Pro36Ser)not specified [RCV004493337]uncertain significance172804297928042979Humanname
407497587CV3458691single nucleotide variantNM_016231.5(NLK):c.226G>A (p.Ala76Thr)not specified [RCV004643786]uncertain significance172804309928043099Humanname
597651619CV3556425single nucleotide variantNM_016231.5(NLK):c.119C>G (p.Pro40Arg)not specified [RCV004826907]uncertain significance172804299228042992Humanname
156217548CV2253877single nucleotide variantNM_016231.5(NLK):c.356C>G (p.Ala119Gly)not specified [RCV004127562]uncertain significance172804322928043229Humanname
155912959CV2341681single nucleotide variantNM_016231.5(NLK):c.793A>G (p.Ile265Val)not specified [RCV004182603]uncertain significance172816358428163584Humanname
155956323CV2387265single nucleotide variantNM_016231.5(NLK):c.947G>A (p.Arg316His)not specified [RCV004238357]uncertain significance172816855728168557Humanname
405707464CV3358818single nucleotide variantNM_016231.5(NLK):c.412A>G (p.Ile138Val)not specified [RCV004493339]uncertain significance172804328528043285Humanname
405707472CV3358819single nucleotide variantNM_016231.5(NLK):c.647A>G (p.Tyr216Cys)not specified [RCV004493340]uncertain significance172816116228161162Humanname
405707487CV3358821single nucleotide variantNM_016231.5(NLK):c.887A>C (p.His296Pro)not specified [RCV004493342]uncertain significance172816849728168497Humanname
401763652CV2714631single nucleotide variantNM_016231.5(NLK):c.1138C>G (p.Pro380Ala)not specified [RCV004319913]uncertain significance172817260728172607Humanname
597651609CV3556424single nucleotide variantNM_016231.5(NLK):c.1424G>A (p.Arg475Gln)not specified [RCV004826906]uncertain significance172819120828191208Humanname
597651629CV3556426single nucleotide variantNM_016231.5(NLK):c.1217G>T (p.Arg406Met)not specified [RCV004826908]uncertain significance172818524628185246Humanname
598193983CV3994697single nucleotide variantNM_016231.5(NLK):c.1027G>T (p.Ala343Ser)not specified [RCV005374651]uncertain significance172816863728168637Humanname