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12 records found for search term Sgtb
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156379707CV2217949single nucleotide variantNM_019072.3(SGTB):c.14A>T (p.Lys5Met)not specified [RCV004086402]uncertain significance56572079465720794Humanname
156045529CV2308091single nucleotide variantNM_019072.3(SGTB):c.17A>G (p.His6Arg)not specified [RCV004170511]uncertain significance56572079165720791Humanname
156056781CV2343495single nucleotide variantNM_019072.3(SGTB):c.62T>C (p.Met21Thr)not specified [RCV004197563]uncertain significance56572074665720746Humanname
598167203CV3921298single nucleotide variantNM_019072.3(SGTB):c.92G>A (p.Ser31Asn)not specified [RCV005283800]uncertain significance56572071665720716Humanname
405707577CV3317819single nucleotide variantNM_019072.3(SGTB):c.278A>G (p.Asn93Ser)not specified [RCV004447983]uncertain significance56570437565704375Humanname
407492858CV3484153single nucleotide variantNM_019072.3(SGTB):c.190A>G (p.Ser64Gly)not specified [RCV004667244]uncertain significance56571297565712975Humanname
597694661CV3605779single nucleotide variantNM_019072.3(SGTB):c.244G>A (p.Val82Met)not specified [RCV004859223]uncertain significance56570851965708519Humanname
598167199CV3921297single nucleotide variantNM_019072.3(SGTB):c.124G>A (p.Val42Ile)not specified [RCV005283799]uncertain significance56571304165713041Humanname
156305982CV2252677single nucleotide variantNM_019072.3(SGTB):c.683C>T (p.Ala228Val)not specified [RCV004118538]uncertain significance56567228065672280Humanname
405707583CV3317820single nucleotide variantNM_019072.3(SGTB):c.478G>A (p.Gly160Arg)not specified [RCV004447984]uncertain significance56568536965685369Humanname
407490328CV3484152single nucleotide variantNM_019072.3(SGTB):c.743C>G (p.Ala248Gly)not specified [RCV004666277]uncertain significance56567197565671975Humanname
598198661CV3921296single nucleotide variantNM_019072.3(SGTB):c.646G>A (p.Ala216Thr)not specified [RCV005268279]uncertain significance56568052965680529Humanname