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Variants search result for Homo sapiens
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31 records found for search term St13
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405719993CV3327236single nucleotide variantNM_003932.5(ST13):c.10C>T (p.Arg4Cys)not specified [RCV004462999]uncertain significance224085653140856531Humanname
156076241CV2248315single nucleotide variantNM_003932.5(ST13):c.64G>T (p.Val22Phe)not specified [RCV004119474]uncertain significance224085647740856477Humanname
405720002CV3327237single nucleotide variantNM_003932.5(ST13):c.74C>T (p.Thr25Ile)not specified [RCV004463000]uncertain significance224085646740856467Humanname
155914521CV2242747single nucleotide variantNM_003932.5(ST13):c.280G>A (p.Asp94Asn)not specified [RCV004113777]uncertain significance224084487440844874Humanname
156277765CV2284868single nucleotide variantNM_003932.5(ST13):c.109A>C (p.Ser37Arg)not specified [RCV004143324]uncertain significance224085643240856432Humanname
155993021CV2381668single nucleotide variantNM_003932.5(ST13):c.171A>T (p.Glu57Asp)not specified [RCV004232134]uncertain significance224084836740848367Humanname
329390767CV2437242single nucleotide variantNM_003932.5(ST13):c.277A>G (p.Thr93Ala)not specified [RCV004256130]uncertain significance224084487740844877Humanname
407517172CV3475046single nucleotide variantNM_003932.5(ST13):c.140A>G (p.Gln47Arg)not specified [RCV004675554]uncertain significance224085085140850851Humanname
597745802CV3608541single nucleotide variantNM_003932.5(ST13):c.214G>A (p.Asp72Asn)not specified [RCV004865738]uncertain significance224084832440848324Humanname
598175319CV3923043single nucleotide variantNM_003932.5(ST13):c.118G>A (p.Gly40Ser)not specified [RCV005285470]uncertain significance224085087340850873Humanname
598175326CV3923044single nucleotide variantNM_003932.5(ST13):c.282T>A (p.Asp94Glu)not specified [RCV005285471]uncertain significance224084487240844872Humanname
156035886CV2208262single nucleotide variantNM_003932.5(ST13):c.883G>A (p.Gly295Arg)not specified [RCV004088709]uncertain significance224082719440827194Humanname
155976926CV2266356single nucleotide variantNM_003932.5(ST13):c.303T>G (p.Asp101Glu)not specified [RCV004129170]uncertain significance224084485140844851Humanname
156173860CV2284159single nucleotide variantNM_003932.5(ST13):c.932C>G (p.Pro311Arg)not specified [RCV004144748]uncertain significance224082714540827145Humanname
156284641CV2288996single nucleotide variantNM_003932.5(ST13):c.907G>A (p.Gly303Ser)not specified [RCV004149949]uncertain significance224082717040827170Humanname
156071967CV2295928single nucleotide variantNM_003932.5(ST13):c.877T>C (p.Phe293Leu)not specified [RCV004151829]uncertain significance224082720040827200Humanname
156073935CV2299302single nucleotide variantNM_003932.5(ST13):c.655G>A (p.Ala219Thr)not specified [RCV004152623]uncertain significance224083259540832595Humanname
156008655CV2361892single nucleotide variantNM_003932.5(ST13):c.736G>A (p.Glu246Lys)not specified [RCV004207665]uncertain significance224083090240830902Humanname
155963947CV2395782single nucleotide variantNM_003932.5(ST13):c.752T>C (p.Ile251Thr)not specified [RCV004235310]uncertain significance224083088640830886Humanname
401747693CV2691660single nucleotide variantNM_003932.5(ST13):c.623C>G (p.Ala208Gly)not specified [RCV004305472]uncertain significance224083262740832627Humanname
401894274CV2780570single nucleotide variantNM_003932.5(ST13):c.436C>G (p.Arg146Gly)not specified [RCV004351943]uncertain significance224083583440835834Humanname
405720028CV3323402single nucleotide variantNM_003932.5(ST13):c.980A>T (p.Gln327Leu)not specified [RCV004463003]uncertain significance224082709740827097Humanname
405720008CV3327238single nucleotide variantNM_003932.5(ST13):c.758G>A (p.Arg253Gln)not specified [RCV004463001]uncertain significance224083088040830880Humanname
407517168CV3475045single nucleotide variantNM_003932.5(ST13):c.734G>A (p.Arg245Gln)not specified [RCV004675553]uncertain significance224083090440830904Humanname
597681700CV3608545single nucleotide variantNM_003932.5(ST13):c.616G>T (p.Ala206Ser)not specified [RCV004857593]uncertain significance224083263440832634Humanname
15187602CV729206single nucleotide variantNM_003932.5(ST13):c.875A>G (p.Asn292Ser)not provided [RCV000887299]benign224082720240827202Humanname
155919074CV2279351single nucleotide variantNM_003932.5(ST13):c.1106C>A (p.Ala369Glu)not specified [RCV004139865]uncertain significance224082654240826542Humanname
405719977CV3327234single nucleotide variantNM_003932.5(ST13):c.1021A>G (p.Asn341Asp)not specified [RCV004462997]uncertain significance224082662740826627Humanname
405719985CV3327235single nucleotide variantNM_003932.5(ST13):c.1066A>C (p.Asn356His)not specified [RCV004462998]uncertain significance224082658240826582Humanname
597745807CV3608543single nucleotide variantNM_003932.5(ST13):c.1001C>A (p.Ala334Asp)not specified [RCV004865739]uncertain significance224082664740826647Humanname
597745813CV3608544single nucleotide variantNM_003932.5(ST13):c.1031A>G (p.Asn344Ser)not specified [RCV004865740]uncertain significance224082661740826617Humanname