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


3 records found for search term Ccdc67
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8653379CV129954single nucleotide variantNM_181645.3(CCDC67):c.298-2287C>TLung cancer [RCV000110441]uncertain significance119336187393361873Humanname
8634435CV89655single nucleotide variantNM_181645.3(CCDC67):c.1201G>A (p.Glu401Lys)Malignant melanoma [RCV000069752]not provided119339461893394618Humanname
8634436CV89656single nucleotide variantNM_181645.3(CCDC67):c.1585C>T (p.Gln529Ter)Malignant melanoma [RCV000069753]not provided119341506193415061Humanname