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Variants search result for Homo sapiens
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33 records found for search term Zbtb34
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156379662CV2211504single nucleotide variantNM_001099270.4(ZBTB34):c.526C>T (p.Arg176Trp)not specified [RCV004084414]uncertain significance9126879925126879925Humanname
156211603CV2259892single nucleotide variantNM_001099270.4(ZBTB34):c.416A>C (p.Asp139Ala)not specified [RCV004118927]uncertain significance9126879815126879815Humanname
156168447CV2315385single nucleotide variantNM_001099270.4(ZBTB34):c.593T>C (p.Leu198Ser)not specified [RCV004167353]uncertain significance9126879992126879992Humanname
156056512CV2320624single nucleotide variantNM_001099270.4(ZBTB34):c.967C>T (p.Arg323Cys)not specified [RCV004172239]uncertain significance9126880366126880366Humanname
156059457CV2323011single nucleotide variantNM_001099270.4(ZBTB34):c.821T>C (p.Val274Ala)not specified [RCV004185440]uncertain significance9126880220126880220Humanname
156213755CV2385869single nucleotide variantNM_001099270.4(ZBTB34):c.886C>T (p.Pro296Ser)not specified [RCV004226911]uncertain significance9126880285126880285Humanname
401856720CV2764903single nucleotide variantNM_001099270.4(ZBTB34):c.479T>C (p.Phe160Ser)not specified [RCV004334995]uncertain significance9126879878126879878Humanname
405807930CV3356883single nucleotide variantNM_001099270.4(ZBTB34):c.563C>T (p.Thr188Met)not specified [RCV004480953]uncertain significance9126879962126879962Humanname
405807932CV3356884single nucleotide variantNM_001099270.4(ZBTB34):c.968G>A (p.Arg323His)not specified [RCV004480954]uncertain significance9126880367126880367Humanname
405807982CV3356885single nucleotide variantNM_001099270.4(ZBTB34):c.970G>T (p.Ala324Ser)not specified [RCV004480955]uncertain significance9126880369126880369Humanname
405807984CV3356886single nucleotide variantNM_001099270.4(ZBTB34):c.974G>A (p.Arg325His)not specified [RCV004480956]uncertain significance9126880373126880373Humanname
597693579CV3624307single nucleotide variantNM_001099270.4(ZBTB34):c.803G>T (p.Gly268Val)not specified [RCV004884835]uncertain significance9126880202126880202Humanname
597692977CV3627762single nucleotide variantNM_001099270.4(ZBTB34):c.961G>A (p.Gly321Arg)not specified [RCV004884833]uncertain significance9126880360126880360Humanname
597693590CV3627763single nucleotide variantNM_001099270.4(ZBTB34):c.895G>C (p.Val299Leu)not specified [RCV004884834]uncertain significance9126880294126880294Humanname
598243285CV3930377single nucleotide variantNM_001099270.4(ZBTB34):c.983G>A (p.Arg328Gln)not specified [RCV005297264]uncertain significance9126880382126880382Humanname
598196643CV3930380single nucleotide variantNM_001099270.4(ZBTB34):c.758G>A (p.Ser253Asn)not specified [RCV005313549]uncertain significance9126880157126880157Humanname
155918460CV2205879single nucleotide variantNM_001099270.4(ZBTB34):c.1094C>G (p.Ala365Gly)not specified [RCV004078316]uncertain significance9126880493126880493Humanname
156200874CV2237754single nucleotide variantNM_001099270.4(ZBTB34):c.1208C>A (p.Pro403His)not specified [RCV004100533]uncertain significance9126880607126880607Humanname
156088605CV2295524single nucleotide variantNM_001099270.4(ZBTB34):c.1211T>A (p.Phe404Tyr)not specified [RCV004160626]uncertain significance9126880610126880610Humanname
329371495CV2458146single nucleotide variantNM_001099270.4(ZBTB34):c.1090A>C (p.Ser364Arg)not specified [RCV004271956]uncertain significance9126880489126880489Humanname
401750301CV2696010single nucleotide variantNM_001099270.4(ZBTB34):c.1087A>G (p.Arg363Gly)not specified [RCV004308268]uncertain significance9126880486126880486Humanname
401892699CV2791683single nucleotide variantNM_001099270.4(ZBTB34):c.1180C>T (p.His394Tyr)not specified [RCV004353023]uncertain significance9126880579126880579Humanname
405807917CV3356876single nucleotide variantNM_001099270.4(ZBTB34):c.1042G>A (p.Glu348Lys)not specified [RCV004480946]uncertain significance9126880441126880441Humanname
405807919CV3356877single nucleotide variantNM_001099270.4(ZBTB34):c.1060C>T (p.Pro354Ser)not specified [RCV004480947]uncertain significance9126880459126880459Humanname
405807920CV3356878single nucleotide variantNM_001099270.4(ZBTB34):c.1088G>A (p.Arg363Lys)not specified [RCV004480948]uncertain significance9126880487126880487Humanname
405807925CV3356880single nucleotide variantNM_001099270.4(ZBTB34):c.1112C>A (p.Pro371Gln)not specified [RCV004480950]uncertain significance9126880511126880511Humanname
405807926CV3356881single nucleotide variantNM_001099270.4(ZBTB34):c.1423G>A (p.Val475Met)not specified [RCV004480951]uncertain significance9126880822126880822Humanname
405807928CV3356882single nucleotide variantNM_001099270.4(ZBTB34):c.1484A>G (p.Glu495Gly)not specified [RCV004480952]uncertain significance9126880883126880883Humanname
407465970CV3494052single nucleotide variantNM_001099270.4(ZBTB34):c.1250A>T (p.Asp417Val)not specified [RCV004688910]uncertain significance9126880649126880649Humanname
407465974CV3494053single nucleotide variantNM_001099270.4(ZBTB34):c.1393A>G (p.Ile465Val)not specified [RCV004688911]uncertain significance9126880792126880792Humanname
598196631CV3930378single nucleotide variantNM_001099270.4(ZBTB34):c.1004A>G (p.His335Arg)not specified [RCV005313547]uncertain significance9126880403126880403Humanname
598196637CV3930379single nucleotide variantNM_001099270.4(ZBTB34):c.1367C>T (p.Pro456Leu)not specified [RCV005313548]uncertain significance9126880766126880766Humanname
407424913CV3410857deletionNM_001099270.4(ZBTB34):c.490_491del (p.Pro164fs)Neurodevelopmental disorder [RCV004586501]uncertain significance9126879888126879889Human1name