Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


1 records found for search term Fam188b
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8590758CV125467single nucleotide variantNM_032222.2(FAM188B):c.1445+4131T>ALung cancer [RCV000105986]uncertain significance73084497930844979Humanname