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


6 records found for search term Scgb1c1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15159575CV701695single nucleotide variantNM_145651.3(SCGB1C1):c.66A>G (p.Thr22=)not provided [RCV000947303]benign11193722193722Humanname
15159569CV701694single nucleotide variantNM_145651.3(SCGB1C1):c.13C>T (p.Arg5Cys)not provided [RCV000947302]benign11193112193112Human3name
15159569CV701694single nucleotide variantNM_145651.3(SCGB1C1):c.13C>T (p.Arg5Cys)not provided [RCV000947302]benign11193112193113Human3name
15159580CV701696single nucleotide variantNM_145651.3(SCGB1C1):c.207T>C (p.Cys69=)not provided [RCV000947304]likely benign11193863193863Human4name
15159580CV701696single nucleotide variantNM_145651.3(SCGB1C1):c.207T>C (p.Cys69=)not provided [RCV000947304]likely benign11193863193864Human4name
8626959CV82103single nucleotide variantNM_145651.2(SCGB1C1):c.218T>C (p.Leu73Pro)Malignant melanoma [RCV000062182]not provided11193874193874Humanname