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Variants search result for Homo sapiens
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33 records found for search term Nt5m
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597708409CV3573304single nucleotide variantNM_020201.4(NT5M):c.8G>T (p.Arg3Leu)not specified [RCV004840557]uncertain significance171730355817303558Humanname
598221580CV3994881single nucleotide variantNM_020201.4(NT5M):c.5T>G (p.Ile2Ser)not specified [RCV005379668]uncertain significance171730355517303555Humanname
598265199CV3994882single nucleotide variantNM_020201.4(NT5M):c.11T>C (p.Leu4Pro)not specified [RCV005387903]uncertain significance171730356117303561Humanname
405727210CV3359601single nucleotide variantNM_020201.4(NT5M):c.76G>A (p.Gly26Ser)not specified [RCV004495933]uncertain significance171730362617303626Humanname
156267338CV2243968single nucleotide variantNM_020201.4(NT5M):c.193C>G (p.Pro65Ala)not specified [RCV004108466]uncertain significance171730374317303743Humanname
156358343CV2251032single nucleotide variantNM_020201.4(NT5M):c.103G>A (p.Ala35Thr)not specified [RCV004123592]uncertain significance171730365317303653Humanname
156103546CV2291621single nucleotide variantNM_020201.4(NT5M):c.253C>T (p.Arg85Trp)not specified [RCV004155912]uncertain significance171730380317303803Humanname
329359156CV2450896single nucleotide variantNM_020201.4(NT5M):c.229G>T (p.Val77Leu)not specified [RCV004267799]uncertain significance171730377917303779Humanname
401889808CV2755010single nucleotide variantNM_020201.4(NT5M):c.124A>G (p.Met42Val)not specified [RCV004335167]uncertain significance171730367417303674Humanname
597643396CV3573303single nucleotide variantNM_020201.4(NT5M):c.187G>A (p.Asp63Asn)not specified [RCV004832601]uncertain significance171730373717303737Humanname
597708417CV3573305single nucleotide variantNM_020201.4(NT5M):c.173G>A (p.Arg58His)not specified [RCV004840558]uncertain significance171730372317303723Humanname
598221559CV3994878single nucleotide variantNM_020201.4(NT5M):c.126G>A (p.Met42Ile)not specified [RCV005379665]uncertain significance171730367617303676Humanname
598221566CV3994879single nucleotide variantNM_020201.4(NT5M):c.241T>C (p.Tyr81His)not specified [RCV005379666]uncertain significance171730379117303791Humanname
598221587CV3994883single nucleotide variantNM_020201.4(NT5M):c.101G>T (p.Arg34Leu)not specified [RCV005379669]uncertain significance171730365117303651Humanname
156115923CV2221590single nucleotide variantNM_020201.4(NT5M):c.567G>C (p.Trp189Cys)not specified [RCV004096849]uncertain significance171734682717346827Humanname
156121270CV2240800single nucleotide variantNM_020201.4(NT5M):c.679C>T (p.Pro227Ser)not specified [RCV004102097]uncertain significance171734693917346939Humanname
156084022CV2244516single nucleotide variantNM_020201.4(NT5M):c.625C>T (p.Arg209Cys)not specified [RCV004100470]uncertain significance171734688517346885Humanname
156298938CV2310672single nucleotide variantNM_020201.4(NT5M):c.359G>A (p.Ser120Asn)not specified [RCV004157331]likely benign171730663417306634Humanname
156286073CV2334901single nucleotide variantNM_020201.4(NT5M):c.550G>A (p.Glu184Lys)not specified [RCV004182007]uncertain significance171734681017346810Humanname
155914536CV2342022single nucleotide variantNM_020201.4(NT5M):c.626G>A (p.Arg209His)not specified [RCV004184959]uncertain significance171734688617346886Humanname
156004468CV2400988single nucleotide variantNM_020201.4(NT5M):c.617C>A (p.Pro206His)not specified [RCV004244270]uncertain significance171734687717346877Humanname
156004481CV2400989single nucleotide variantNM_020201.4(NT5M):c.640T>A (p.Trp214Arg)not specified [RCV004244271]uncertain significance171734690017346900Humanname
329376068CV2431718single nucleotide variantNM_020201.4(NT5M):c.586G>A (p.Ala196Thr)not specified [RCV004248880]uncertain significance171734684617346846Humanname
401730689CV2711450single nucleotide variantNM_020201.4(NT5M):c.479T>A (p.Val160Glu)not specified [RCV004306775]uncertain significance171734484317344843Humanname
405727190CV3359599single nucleotide variantNM_020201.4(NT5M):c.407T>G (p.Phe136Cys)not specified [RCV004495931]uncertain significance171732322317323223Humanname
405727198CV3359600single nucleotide variantNM_020201.4(NT5M):c.529C>T (p.Arg177Trp)not specified [RCV004495932]uncertain significance171734489317344893Humanname
597643389CV3573298single nucleotide variantNM_020201.4(NT5M):c.644C>T (p.Ala215Val)not specified [RCV004832600]uncertain significance171734690417346904Humanname
597708385CV3573299single nucleotide variantNM_020201.4(NT5M):c.334G>A (p.Val112Met)not specified [RCV004840554]uncertain significance171730660917306609Humanname
597708393CV3573301single nucleotide variantNM_020201.4(NT5M):c.538A>C (p.Ile180Leu)not specified [RCV004840555]uncertain significance171734490217344902Humanname
597708402CV3573302single nucleotide variantNM_020201.4(NT5M):c.676C>T (p.Arg226Trp)not specified [RCV004840556]uncertain significance171734693617346936Humanname
597708426CV3573306single nucleotide variantNM_020201.4(NT5M):c.298A>G (p.Asn100Asp)not specified [RCV004840559]uncertain significance171730657317306573Humanname
597708365CV3577190single nucleotide variantNM_020201.4(NT5M):c.648C>A (p.Asp216Glu)not specified [RCV004840552]uncertain significance171734690817346908Humanname
597708376CV3577191single nucleotide variantNM_020201.4(NT5M):c.622C>T (p.Arg208Cys)not specified [RCV004840553]uncertain significance171734688217346882Humanname