Across TCGA pan-cancer cohorts, RABL3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RABL3 data layer compared with 18 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in lung adenocarcinoma (LUAD), where higher RABL3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RABL3 expression acts as an unfavorable survival marker.
LUAD and READ are the cancer types where RABL3 Mutation most reproducibly stratifies survival.