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Variants search result for Homo sapiens
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31 records found for search term Dnajb8
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15172369CV708542single nucleotide variantNM_153330.6(DNAJB8):c.18A>G (p.Glu6=)not provided [RCV000972390]benign3128463228128463228Humanname
597643742CV3662918single nucleotide variantNM_153330.6(DNAJB8):c.47C>T (p.Pro16Leu)not specified [RCV004909537]uncertain significance3128463199128463199Humanname
598163230CV3953457single nucleotide variantNM_153330.6(DNAJB8):c.86G>A (p.Arg29His)not specified [RCV005329324]uncertain significance3128463160128463160Humanname
156312547CV2256885single nucleotide variantNM_153330.6(DNAJB8):c.202G>A (p.Ala68Thr)not specified [RCV004121091]uncertain significance3128463044128463044Humanname
156290243CV2342558single nucleotide variantNM_153330.6(DNAJB8):c.280C>T (p.Arg94Cys)not specified [RCV004196653]uncertain significance3128462966128462966Humanname
156077806CV2351068single nucleotide variantNM_153330.6(DNAJB8):c.262G>A (p.Asp88Asn)not specified [RCV004213936]uncertain significance3128462984128462984Humanname
155923907CV2351940single nucleotide variantNM_153330.6(DNAJB8):c.221G>A (p.Arg74Gln)not specified [RCV004198076]uncertain significance3128463025128463025Humanname
329396885CV2468297single nucleotide variantNM_153330.6(DNAJB8):c.172G>A (p.Asp58Asn)not specified [RCV004275854]uncertain significance3128463074128463074Humanname
405731792CV3244569single nucleotide variantNM_153330.6(DNAJB8):c.112A>C (p.Asn38His)not specified [RCV004379298]uncertain significance3128463134128463134Humanname
405731807CV3244571single nucleotide variantNM_153330.6(DNAJB8):c.143T>C (p.Leu48Pro)not specified [RCV004379300]uncertain significance3128463103128463103Humanname
405731815CV3244572single nucleotide variantNM_153330.6(DNAJB8):c.176C>A (p.Ser59Tyr)not specified [RCV004379301]uncertain significance3128463070128463070Humanname
407497269CV3437497single nucleotide variantNM_153330.6(DNAJB8):c.242C>T (p.Thr81Met)not specified [RCV004622160]uncertain significance3128463004128463004Humanname
156398615CV2194682single nucleotide variantNM_153330.6(DNAJB8):c.617G>A (p.Arg206His)not specified [RCV004075242]uncertain significance3128462629128462629Humanname
156061317CV2239980single nucleotide variantNM_153330.6(DNAJB8):c.508G>A (p.Gly170Arg)not specified [RCV004110773]uncertain significance3128462738128462738Humanname
155981763CV2244113single nucleotide variantNM_153330.6(DNAJB8):c.586A>G (p.Thr196Ala)not specified [RCV004108577]uncertain significance3128462660128462660Humanname
156260507CV2277924single nucleotide variantNM_153330.6(DNAJB8):c.343T>C (p.Trp115Arg)not specified [RCV004140905]uncertain significance3128462903128462903Humanname
156303743CV2308460single nucleotide variantNM_153330.6(DNAJB8):c.358A>C (p.Asn120His)not specified [RCV004166752]uncertain significance3128462888128462888Humanname
405731821CV3244573single nucleotide variantNM_153330.6(DNAJB8):c.428C>G (p.Ala143Gly)not specified [RCV004379302]uncertain significance3128462818128462818Humanname
405731827CV3244574single nucleotide variantNM_153330.6(DNAJB8):c.491T>G (p.Phe164Cys)not specified [RCV004379303]uncertain significance3128462755128462755Humanname
405731834CV3244575single nucleotide variantNM_153330.6(DNAJB8):c.658G>A (p.Val220Met)not specified [RCV004379304]uncertain significance3128462588128462588Humanname
405731840CV3244576single nucleotide variantNM_153330.6(DNAJB8):c.682T>C (p.Trp228Arg)not specified [RCV004379305]likely benign3128462564128462564Humanname
407497265CV3437496single nucleotide variantNM_153330.6(DNAJB8):c.367C>T (p.Arg123Cys)not specified [RCV004622159]likely benign3128462879128462879Humanname
597643723CV3662915single nucleotide variantNM_153330.6(DNAJB8):c.440C>T (p.Ala147Val)not specified [RCV004909534]uncertain significance3128462806128462806Humanname
597643729CV3662916single nucleotide variantNM_153330.6(DNAJB8):c.485C>A (p.Thr162Asn)not specified [RCV004909535]uncertain significance3128462761128462761Humanname
597643736CV3662917single nucleotide variantNM_153330.6(DNAJB8):c.393G>T (p.Arg131Ser)not specified [RCV004909536]uncertain significance3128462853128462853Humanname
597643749CV3662919single nucleotide variantNM_153330.6(DNAJB8):c.634G>A (p.Asp212Asn)not specified [RCV004909538]uncertain significance3128462612128462612Humanname
598163235CV3953458single nucleotide variantNM_153330.6(DNAJB8):c.379G>A (p.Gly127Ser)not specified [RCV005329325]uncertain significance3128462867128462867Humanname
598163241CV3953459single nucleotide variantNM_153330.6(DNAJB8):c.322G>A (p.Asp108Asn)not specified [RCV005329326]uncertain significance3128462924128462924Humanname
598163246CV3953460single nucleotide variantNM_153330.6(DNAJB8):c.637G>A (p.Gly213Arg)not specified [RCV005329327]uncertain significance3128462609128462609Humanname
15156773CV697817single nucleotide variantNM_153330.6(DNAJB8):c.302G>A (p.Arg101Gln)not provided [RCV000946762]benign3128462944128462944Humanname
15184015CV708541single nucleotide variantNM_153330.6(DNAJB8):c.457A>C (p.Met153Leu)not provided [RCV000975011]benign3128462789128462789Humanname