Across TCGA pan-cancer cohorts, DRAP1 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated DRAP1 data layer compared with 28 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher DRAP1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated DRAP1 expression acts as an unfavorable survival marker.
LIHC and COAD are the cancer types where DRAP1 Mutation most reproducibly stratifies survival.