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Variants search result for Homo sapiens
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18 records found for search term Timm8b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405768574CV3345921single nucleotide variantNM_012459.4(TIMM8B):c.-8G>Cnot specified [RCV004469883]likely benign11112086731112086731Humanname
156001949CV2284537single nucleotide variantNM_012459.4(TIMM8B):c.-32G>Anot specified [RCV004140711]uncertain significance11112086755112086755Humanname
405768568CV3345920single nucleotide variantNM_012459.4(TIMM8B):c.-15A>Gnot specified [RCV004469882]uncertain significance11112086738112086738Humanname
597774129CV3613499single nucleotide variantNM_012459.4(TIMM8B):c.-11T>Cnot specified [RCV004872219]uncertain significance11112086734112086734Humanname
405768580CV3345922single nucleotide variantNM_012459.4(TIMM8B):c.2T>C (p.Met1Thr)not specified [RCV004469884]uncertain significance11112086722112086722Humanname
405768551CV3345917single nucleotide variantNM_012459.2(TIMM8B):c.10C>T (p.His4Tyr)not specified [RCV004469879]uncertain significance11112086759112086759Humanname
155997655CV2393333single nucleotide variantNM_012459.4(TIMM8B):c.65A>G (p.Lys22Arg)not specified [RCV004228839]uncertain significance11112086659112086659Humanname
405768546CV3345916single nucleotide variantNM_012459.4(TIMM8B):c.56A>T (p.Glu19Val)not specified [RCV004469878]uncertain significance11112086668112086668Humanname
405768586CV3345923single nucleotide variantNM_012459.4(TIMM8B):c.31G>A (p.Glu11Lys)not specified [RCV004469885]uncertain significance11112086693112086693Humanname
401772652CV2719712single nucleotide variantNM_012459.4(TIMM8B):c.199A>G (p.Thr67Ala)not specified [RCV004329152]uncertain significance11112085348112085348Humanname
401782742CV2719968single nucleotide variantNM_012459.4(TIMM8B):c.217C>T (p.Arg73Trp)not specified [RCV004329352]uncertain significance11112085330112085330Humanname
401877115CV2769341single nucleotide variantNM_012459.4(TIMM8B):c.140G>A (p.Arg47His)not specified [RCV004357336]uncertain significance11112085407112085407Humanname
405768556CV3345918single nucleotide variantNM_012459.4(TIMM8B):c.124G>A (p.Glu42Lys)not specified [RCV004469880]uncertain significance11112085423112085423Humanname
405768562CV3345919single nucleotide variantNM_012459.4(TIMM8B):c.152G>A (p.Arg51His)not specified [RCV004469881]uncertain significance11112085395112085395Humanname
407520498CV3475709single nucleotide variantNM_012459.4(TIMM8B):c.173G>A (p.Ser58Asn)not specified [RCV004676977]uncertain significance11112085374112085374Humanname
597774134CV3613500single nucleotide variantNM_012459.4(TIMM8B):c.139C>T (p.Arg47Cys)not specified [RCV004872220]uncertain significance11112085408112085408Humanname
598197781CV3924258single nucleotide variantNM_012459.4(TIMM8B):c.218G>A (p.Arg73Gln)not specified [RCV005289624]uncertain significance11112085329112085329Humanname
598176666CV3924259single nucleotide variantNM_012459.4(TIMM8B):c.230T>C (p.Ile77Thr)not specified [RCV005285678]uncertain significance11112085317112085317Humanname