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


1 records found for search term Sepp1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8631648CV86852single nucleotide variantNM_001085486.1(SEPP1):c.455C>T (p.Ser152Phe)Malignant melanoma [RCV000066943]not provided54280473542804735Humanname