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


1 records found for search term Ccdc130
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8636621CV91846single nucleotide variantNM_030818.2(CCDC130):c.257+1G>CMalignant melanoma [RCV000071944]not provided191375784713757847Humanname