Across TCGA pan-cancer cohorts, RAP2B Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated RAP2B data layer compared with 25 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher RAP2B Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RAP2B expression acts as an unfavorable survival marker.
LIHC, CESC, and UCEC are the cancer types where RAP2B Mutation most reproducibly stratifies survival.
Mutation survival associations by lineage
Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.