Across TCGA pan-cancer cohorts, RASL11A Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RASL11A data layer compared with 25 for mass-spec protein.
The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher RASL11A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RASL11A expression acts as an unfavorable survival marker.
LIHC and UCEC are the cancer types where RASL11A Mutation most reproducibly stratifies survival.