Across TCGA pan-cancer cohorts, VAMP5 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated VAMP5 data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher VAMP5 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated VAMP5 expression acts as an unfavorable survival marker.
PRAD and CHOL are the cancer types where VAMP5 Mutation most reproducibly stratifies survival.