Across TCGA pan-cancer cohorts, RBM28 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RBM28 data layer compared with 30 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher RBM28 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RBM28 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
COAD, UCEC, and PRAD are the cancer types where RBM28 Mutation most reproducibly stratifies survival.