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


1 records found for search term Fam65b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8581806CV116251single nucleotide variantNM_001286445.1(FAM65B):c.651+1969A>CLung cancer [RCV000096774]uncertain significance62486333224863332Humanname