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Variants search result for Homo sapiens
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35 records found for search term Sbk1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156205566CV2297892single nucleotide variantNM_001024401.3(SBK1):c.80C>T (p.Ala27Val)not specified [RCV004157828]uncertain significance162831747128317471Humanname
401736608CV2688833single nucleotide variantNM_001024401.3(SBK1):c.88C>A (p.Pro30Thr)not specified [RCV004303849]uncertain significance162831747928317479Humanname
401747138CV2698794single nucleotide variantNM_001024401.3(SBK1):c.71G>A (p.Gly24Glu)not specified [RCV004301242]uncertain significance162831746228317462Humanname
401888099CV2791249single nucleotide variantNM_001024401.3(SBK1):c.286C>T (p.Arg96Trp)not specified [RCV004356883]uncertain significance162831905428319054Humanname
598195213CV3900090single nucleotide variantNM_001024401.3(SBK1):c.234A>C (p.Lys78Asn)not specified [RCV005267711]uncertain significance162831900228319002Humanname
156104935CV2217456single nucleotide variantNM_001024401.3(SBK1):c.770C>G (p.Ser257Trp)not specified [RCV004090008]uncertain significance162832041628320416Humanname
156206045CV2311507single nucleotide variantNM_001024401.3(SBK1):c.449C>T (p.Thr150Met)not specified [RCV004168338]uncertain significance162832009528320095Humanname
155967408CV2312721single nucleotide variantNM_001024401.3(SBK1):c.503G>A (p.Arg168Gln)not specified [RCV004169445]uncertain significance162832014928320149Humanname
156095801CV2398996single nucleotide variantNM_001024401.3(SBK1):c.964C>G (p.Arg322Gly)not specified [RCV004245301]uncertain significance162832061028320610Humanname
156195432CV2400501single nucleotide variantNM_001024401.3(SBK1):c.499G>C (p.Gly167Arg)not specified [RCV004246700]uncertain significance162832014528320145Humanname
329371897CV2454976single nucleotide variantNM_001024401.3(SBK1):c.335A>G (p.Lys112Arg)not specified [RCV004272244]uncertain significance162831910328319103Humanname
401745770CV2693346single nucleotide variantNM_001024401.3(SBK1):c.997C>G (p.Pro333Ala)not specified [RCV004295309]uncertain significance162832064328320643Humanname
401748495CV2696481single nucleotide variantNM_001024401.3(SBK1):c.885A>C (p.Leu295Phe)not specified [RCV004312555]uncertain significance162832053128320531Humanname
401874218CV2773699single nucleotide variantNM_001024401.3(SBK1):c.941A>G (p.Lys314Arg)not specified [RCV004356381]uncertain significance162832058728320587Humanname
401888297CV2788275single nucleotide variantNM_001024401.3(SBK1):c.860C>G (p.Pro287Arg)not specified [RCV004352866]uncertain significance162832050628320506Humanname
401888102CV2791250single nucleotide variantNM_001024401.3(SBK1):c.362A>C (p.Glu121Ala)not specified [RCV004356884]uncertain significance162831913028319130Humanname
407460779CV3483734single nucleotide variantNM_001024401.3(SBK1):c.802C>T (p.Arg268Cys)not specified [RCV004658547]uncertain significance162832044828320448Humanname
407460782CV3483735single nucleotide variantNM_001024401.3(SBK1):c.626G>C (p.Ser209Thr)not specified [RCV004658548]uncertain significance162832027228320272Humanname
407460788CV3483736single nucleotide variantNM_001024401.3(SBK1):c.823C>A (p.Pro275Thr)not specified [RCV004658549]uncertain significance162832046928320469Humanname
407460792CV3483737single nucleotide variantNM_001024401.3(SBK1):c.391G>A (p.Ala131Thr)not specified [RCV004658550]uncertain significance162831915928319159Humanname
597669194CV3605265single nucleotide variantNM_001024401.3(SBK1):c.328A>G (p.Ile110Val)not specified [RCV004856041]uncertain significance162831909628319096Humanname
597669180CV3605267single nucleotide variantNM_001024401.3(SBK1):c.338T>C (p.Val113Ala)not specified [RCV004856043]uncertain significance162831910628319106Humanname
597669168CV3605268single nucleotide variantNM_001024401.3(SBK1):c.464T>C (p.Val155Ala)not specified [RCV004856044]uncertain significance162832011028320110Humanname
597669161CV3605269single nucleotide variantNM_001024401.3(SBK1):c.854C>G (p.Thr285Ser)not specified [RCV004856045]uncertain significance162832050028320500Humanname
598195194CV3900087single nucleotide variantNM_001024401.3(SBK1):c.989G>C (p.Arg330Pro)not specified [RCV005267708]uncertain significance162832063528320635Humanname
598195200CV3900088single nucleotide variantNM_001024401.3(SBK1):c.986C>A (p.Ala329Glu)not specified [RCV005267709]uncertain significance162832063228320632Humanname
156338277CV2370608single nucleotide variantNM_001024401.3(SBK1):c.1081A>G (p.Ser361Gly)not specified [RCV004215932]uncertain significance162832072728320727Humanname
156210692CV2378200single nucleotide variantNM_001024401.3(SBK1):c.1249G>C (p.Ala417Pro)not specified [RCV004226243]uncertain significance162832089528320895Humanname
155955625CV2387131single nucleotide variantNM_001024401.3(SBK1):c.1168C>T (p.Pro390Ser)not specified [RCV004238240]uncertain significance162832081428320814Humanname
401893981CV2770183single nucleotide variantNM_001024401.3(SBK1):c.1162C>G (p.Pro388Ala)not specified [RCV004356077]uncertain significance162832080828320808Humanname
405741247CV3320782single nucleotide variantNM_001024401.3(SBK1):c.1186C>A (p.Pro396Thr)not specified [RCV004452412]uncertain significance162832083228320832Humanname
405741254CV3320783single nucleotide variantNM_001024401.3(SBK1):c.1249G>A (p.Ala417Thr)not specified [RCV004452413]uncertain significance162832089528320895Humanname
407460770CV3483732single nucleotide variantNM_001024401.3(SBK1):c.1105G>A (p.Ala369Thr)not specified [RCV004658545]uncertain significance162832075128320751Humanname
597669187CV3605266single nucleotide variantNM_001024401.3(SBK1):c.1133C>T (p.Pro378Leu)not specified [RCV004856042]uncertain significance162832077928320779Humanname
598195208CV3900089single nucleotide variantNM_001024401.3(SBK1):c.1111G>C (p.Gly371Arg)not specified [RCV005267710]uncertain significance162832075728320757Humanname