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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


6 records found for search term Muc20
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401923045CV2825151single nucleotide variantNM_001282506.2(MUC20):c.615C>T (p.Val205=)not provided [RCV003434838]likely benign3195725218195725218Humanname
407426283CV3409817single nucleotide variantNM_001282506.2(MUC20):c.603C>T (p.Gly201=)not provided [RCV004585749]likely benign3195725206195725206Humanname
401927658CV2825152single nucleotide variantNM_001282506.2(MUC20):c.1128C>T (p.Val376=)not provided [RCV003439099]likely benign3195725731195725731Humanname
401927660CV2825153single nucleotide variantNM_001282506.2(MUC20):c.1137G>A (p.Pro379=)not provided [RCV003439100]likely benign3195725740195725740Humanname
401923081CV2825154single nucleotide variantNM_001282506.2(MUC20):c.1158C>T (p.Ser386=)not provided [RCV003434839]likely benign3195725761195725761Humanname
596945791CV3548067single nucleotide variantNM_001282506.2(MUC20):c.1170C>T (p.Asp390=)not provided [RCV004809398]likely benign3195725773195725773Humanname