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


1 records found for search term Fam102b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8628770CV83914single nucleotide variantNM_001010883.2(FAM102B):c.396C>T (p.Ser132=)Malignant melanoma [RCV000063995]not provided1108612285108612285Humanname