Across TCGA pan-cancer cohorts, SYNGR3 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated SYNGR3 data layer compared with 28 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher SYNGR3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SYNGR3 expression acts as an unfavorable survival marker.
PRAD are the cancer types where SYNGR3 Mutation most reproducibly stratifies survival.