Across TCGA pan-cancer cohorts, RBM4B Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RBM4B data layer compared with 24 for mass-spec protein and 3 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher RBM4B Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RBM4B expression acts as an unfavorable survival marker.
PRAD, UCEC, and THCA are the cancer types where RBM4B Mutation most reproducibly stratifies survival.