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46 records found for search term Gspt1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156093055CV2256720single nucleotide variantNM_002094.4(GSPT1):c.56G>C (p.Ser19Thr)not specified [RCV004118891]uncertain significance161191566511915665Humanname
156054010CV2361151single nucleotide variantNM_002094.4(GSPT1):c.52A>G (p.Ser18Gly)not specified [RCV004216339]uncertain significance161191566911915669Humanname
155930453CV2361152single nucleotide variantNM_002094.4(GSPT1):c.55A>G (p.Ser19Gly)not specified [RCV004216340]uncertain significance161191566611915666Humanname
155992481CV2381502single nucleotide variantNM_002094.4(GSPT1):c.83C>T (p.Pro28Leu)not specified [RCV004229980]uncertain significance161191563811915638Humanname
405773328CV3259177single nucleotide variantNM_002094.4(GSPT1):c.49A>G (p.Ser17Gly)not specified [RCV004396318]likely benign161191567211915672Humanname
405773340CV3259179single nucleotide variantNM_002094.4(GSPT1):c.61A>G (p.Ser21Gly)not specified [RCV004396320]uncertain significance161191566011915660Humanname
598189987CV3978456single nucleotide variantNM_002094.4(GSPT1):c.31G>A (p.Gly11Ser)not specified [RCV005354070]uncertain significance161191569011915690Humanname
156114456CV2268583single nucleotide variantNM_002094.4(GSPT1):c.105C>G (p.Asp35Glu)not specified [RCV004123999]uncertain significance161191561611915616Humanname
155966166CV2284237single nucleotide variantNM_002094.4(GSPT1):c.106A>G (p.Met36Val)not specified [RCV004146601]uncertain significance161191561511915615Humanname
401861235CV2769595single nucleotide variantNM_002094.4(GSPT1):c.284C>T (p.Ala95Val)not specified [RCV004351240]uncertain significance161191543711915437Humanname
405773302CV3259173single nucleotide variantNM_002094.4(GSPT1):c.176A>C (p.Glu59Ala)not specified [RCV004396314]uncertain significance161191554511915545Humanname
405773316CV3259175single nucleotide variantNM_002094.4(GSPT1):c.209A>G (p.Asn70Ser)not specified [RCV004396316]uncertain significance161191551211915512Humanname
597771351CV3688647single nucleotide variantNM_002094.4(GSPT1):c.152C>T (p.Ala51Val)not specified [RCV004928487]uncertain significance161191556911915569Humanname
597756531CV3688648single nucleotide variantNM_002094.4(GSPT1):c.287C>T (p.Pro96Leu)not specified [RCV004924888]uncertain significance161191543411915434Humanname
598189954CV3978452single nucleotide variantNM_002094.4(GSPT1):c.203A>G (p.Gln68Arg)not specified [RCV005354066]uncertain significance161191551811915518Humanname
156141836CV2260608single nucleotide variantNM_002094.4(GSPT1):c.602T>C (p.Val201Ala)not specified [RCV004123371]uncertain significance161189662011896620Humanname
155919874CV2279493single nucleotide variantNM_002094.4(GSPT1):c.545A>G (p.Glu182Gly)not specified [RCV004142015]uncertain significance161189667711896677Humanname
156292498CV2306234single nucleotide variantNM_002094.4(GSPT1):c.728C>T (p.Thr243Met)not specified [RCV004162968]uncertain significance161189111011891110Humanname
156106500CV2307650single nucleotide variantNM_002094.4(GSPT1):c.523T>A (p.Leu175Met)not specified [RCV004168067]uncertain significance161189669911896699Humanname
155922673CV2340660single nucleotide variantNM_002094.4(GSPT1):c.517G>C (p.Gly173Arg)not specified [RCV004190333]uncertain significance161189670511896705Humanname
156307460CV2369741single nucleotide variantNM_002094.4(GSPT1):c.546G>C (p.Glu182Asp)not specified [RCV004215133]uncertain significance161189667611896676Humanname
155904145CV2385430single nucleotide variantNM_002094.4(GSPT1):c.583A>G (p.Ile195Val)not specified [RCV004233084]uncertain significance161189663911896639Humanname
329368637CV2450389single nucleotide variantNM_002094.4(GSPT1):c.356C>G (p.Pro119Arg)not specified [RCV004265324]uncertain significance161189803211898032Humanname
329390787CV2455469single nucleotide variantNM_002094.4(GSPT1):c.514G>T (p.Gly172Cys)not specified [RCV004276739]uncertain significance161189670811896708Humanname
401737411CV2699810single nucleotide variantNM_002094.4(GSPT1):c.463C>A (p.Pro155Thr)not specified [RCV004308460]uncertain significance161189675911896759Humanname
401731856CV2712186single nucleotide variantNM_002094.4(GSPT1):c.845G>A (p.Arg282His)not specified [RCV004311905]uncertain significance161188768211887682Humanname
401872614CV2754407single nucleotide variantNM_002094.4(GSPT1):c.400A>G (p.Asn134Asp)not specified [RCV004336623]uncertain significance161189787611897876Humanname
405773321CV3259176single nucleotide variantNM_002094.4(GSPT1):c.315T>A (p.Asn105Lys)not specified [RCV004396317]uncertain significance161191540611915406Humanname
405773333CV3259178single nucleotide variantNM_002094.4(GSPT1):c.611C>T (p.Pro204Leu)not specified [RCV004396319]uncertain significance161189661111896611Humanname
405773346CV3259180single nucleotide variantNM_002094.4(GSPT1):c.631G>C (p.Glu211Gln)not specified [RCV004396321]uncertain significance161189659111896591Humanname
405773352CV3259181single nucleotide variantNM_002094.4(GSPT1):c.712A>G (p.Met238Val)not specified [RCV004396322]uncertain significance161189112611891126Humanname
597771750CV3688642single nucleotide variantNM_002094.4(GSPT1):c.310G>T (p.Ala104Ser)not specified [RCV004928484]uncertain significance161191541111915411Humanname
598189962CV3978453single nucleotide variantNM_002094.4(GSPT1):c.490G>A (p.Glu164Lys)not specified [RCV005354067]uncertain significance161189673211896732Humanname
598189971CV3978454single nucleotide variantNM_002094.4(GSPT1):c.331A>C (p.Ser111Arg)not specified [RCV005354068]uncertain significance161191539011915390Humanname
155919866CV2279492single nucleotide variantNM_002094.4(GSPT1):c.1107T>A (p.Asn369Lys)not specified [RCV004142014]uncertain significance161188678211886782Humanname
156282642CV2291755single nucleotide variantNM_002094.4(GSPT1):c.1646A>G (p.Asn549Ser)not specified [RCV004158299]uncertain significance161187613211876132Humanname
156353027CV2324091single nucleotide variantNM_002094.4(GSPT1):c.1595A>G (p.Asp532Gly)not specified [RCV004178382]uncertain significance161187741411877414Humanname
156061632CV2351345single nucleotide variantNM_002094.4(GSPT1):c.1363G>A (p.Val455Ile)not specified [RCV004193046]uncertain significance161188308011883080Humanname
401875411CV2789046single nucleotide variantNM_002094.4(GSPT1):c.1765C>G (p.Gln589Glu)not specified [RCV004363349]uncertain significance161187585711875857Humanname
405773309CV3259174single nucleotide variantNM_002094.4(GSPT1):c.1900C>T (p.Pro634Ser)not specified [RCV004396315]uncertain significance161187313311873133Humanname
407464127CV3433454single nucleotide variantNM_002094.4(GSPT1):c.1166A>G (p.Asn389Ser)not specified [RCV004635002]uncertain significance161188655811886558Humanname
597756521CV3688643single nucleotide variantNM_002094.4(GSPT1):c.1604T>C (p.Ile535Thr)not specified [RCV004924886]uncertain significance161187617411876174Humanname
597756526CV3688644single nucleotide variantNM_002094.4(GSPT1):c.1909G>A (p.Asp637Asn)not specified [RCV004924887]uncertain significance161187312411873124Humanname
597771755CV3688645single nucleotide variantNM_002094.4(GSPT1):c.1742G>A (p.Arg581Gln)not specified [RCV004928485]uncertain significance161187588011875880Humanname
597771762CV3688646single nucleotide variantNM_002094.4(GSPT1):c.1057C>A (p.Leu353Ile)not specified [RCV004928486]uncertain significance161188683211886832Humanname
598189979CV3978455single nucleotide variantNM_002094.4(GSPT1):c.1204C>G (p.Leu402Val)not specified [RCV005354069]uncertain significance161188652011886520Humanname