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


3 records found for search term Sept14
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8590931CV125641single nucleotide variantNM_207366.2(SEPT14):c.818-1618T>CLung cancer [RCV000106160]uncertain significance75580887655808876Humanname
8590930CV125640single nucleotide variantNM_207366.2(SEPT14):c.1120-3959A>GLung cancer [RCV000106159]uncertain significance75580005155800051Humanname
8632607CV87822single nucleotide variantNM_207366.2(SEPT14):c.442C>T (p.Arg148Cys)Malignant melanoma [RCV000067914]not provided75584305855843058Humanname