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27 records found for search term Bax
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329374090CV2443645single nucleotide variantNM_138761.4(BAX):c.474+76G>Anot specified [RCV004255951]uncertain significance194896099048960990Humanname
405704735CV3301488single nucleotide variantNM_138761.4(BAX):c.474+95G>Cnot specified [RCV004425915]uncertain significance194896100948961009Humanname
598244639CV3938344single nucleotide variantNM_138761.4(BAX):c.474+34C>Tnot specified [RCV005297468]uncertain significance194896094848960948Humanname
405704743CV3301489single nucleotide variantNM_138761.4(BAX):c.474+151G>Anot specified [RCV004425916]uncertain significance194896106548961065Humanname
155977792CV2342930single nucleotide variantNM_138761.4(BAX):c.7G>T (p.Gly3Trp)not specified [RCV004189962]uncertain significance194895493548954935Humanname
15141159CV716587single nucleotide variantNM_138761.4(BAX):c.69G>A (p.Gly23=)not provided [RCV000966260]likely benign194895558248955582Humanname
156178840CV2258272single nucleotide variantNM_138761.4(BAX):c.10T>C (p.Ser4Pro)not specified [RCV004121640]uncertain significance194895493848954938Humanname
156329438CV2342403single nucleotide variantNM_138761.4(BAX):c.43A>G (p.Ser15Gly)not specified [RCV004194015]uncertain significance194895555648955556Humanname
8598366CV24550duplicationNM_138761.4(BAX):c.121dup (p.Glu41fs)Carcinoma of colon [RCV000010119]|Inborn genetic diseases [RCV001267419]pathogenic|uncertain significance|other194895571348955714Human3name
8598367CV24551deletionNM_138761.4(BAX):c.121del (p.Glu41fs)Carcinoma of colon [RCV000010120]pathogenic|other194895571448955714Human2name
15116006CV742041single nucleotide variantNM_138761.4(BAX):c.306C>T (p.Asp102=)not provided [RCV000895127]benign194895627048956270Humanname
15123444CV757165single nucleotide variantNM_138761.4(BAX):c.501G>A (p.Thr167=)not provided [RCV000918822]likely benign194896155848961558Humanname
156187147CV2292446single nucleotide variantNM_138761.4(BAX):c.114G>T (p.Met38Ile)not specified [RCV004150239]uncertain significance194895571448955714Humanname
8598368CV24552single nucleotide variantNM_138761.4(BAX):c.199G>A (p.Gly67Arg)T-cell acute lymphoblastic leukemia [RCV000010121]pathogenic|other194895579948955799Human2name
401778993CV2701987single nucleotide variantNM_138761.4(BAX):c.167C>A (p.Thr56Asn)not specified [RCV004320582]uncertain significance194895576748955767Humanname
401759670CV2705668single nucleotide variantNM_138761.4(BAX):c.196A>G (p.Ile66Val)not specified [RCV004318522]uncertain significance194895579648955796Humanname
401767163CV2721671single nucleotide variantNM_138761.4(BAX):c.173A>G (p.Lys58Arg)not specified [RCV004316160]likely benign194895577348955773Humanname
405704706CV3301485single nucleotide variantNM_138761.4(BAX):c.114G>C (p.Met38Ile)not specified [RCV004425912]uncertain significance194895571448955714Humanname
405704713CV3301486single nucleotide variantNM_138761.4(BAX):c.241G>C (p.Ala81Pro)not specified [RCV004425913]uncertain significance194895620548956205Humanname
405704726CV3301487single nucleotide variantNM_138761.4(BAX):c.297G>C (p.Met99Ile)not specified [RCV004425914]uncertain significance194895626148956261Humanname
407494886CV3417502single nucleotide variantNM_138761.4(BAX):c.167C>T (p.Thr56Ile)not specified [RCV004605691]uncertain significance194895576748955767Humanname
407500347CV3417503single nucleotide variantNM_138761.4(BAX):c.278T>C (p.Phe93Ser)not specified [RCV004606983]uncertain significance194895624248956242Humanname
598171446CV3934466single nucleotide variantNM_138761.4(BAX):c.259T>A (p.Ser87Thr)not specified [RCV005309195]uncertain significance194895622348956223Humanname
597759525CV3642823single nucleotide variantNM_138761.4(BAX):c.322G>A (p.Gly108Ser)not specified [RCV004894542]uncertain significance194895628648956286Humanname
597759531CV3642824single nucleotide variantNM_138761.4(BAX):c.400A>G (p.Arg134Gly)not specified [RCV004894543]uncertain significance194896084048960840Humanname
598244660CV3938347single nucleotide variantNM_138761.4(BAX):c.404C>T (p.Thr135Ile)not specified [RCV005297471]uncertain significance194896084448960844Humanname
8598369CV24553deletionNM_138761.4(BAX):c.115_121del (p.Gly39fs)T-cell acute lymphoblastic leukemia [RCV000010122]pathogenic|other194895571448955720Human2name