Across TCGA pan-cancer cohorts, RAP2C Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RAP2C data layer compared with 27 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher RAP2C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RAP2C expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
BLCA and UCEC are the cancer types where RAP2C Mutation most reproducibly stratifies survival.