Across TCGA pan-cancer cohorts, SCGB3A2 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SCGB3A2 data layer compared with 27 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher SCGB3A2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SCGB3A2 expression acts as an unfavorable survival marker.
READ, ESCA, and SKCM are the cancer types where SCGB3A2 Mutation most reproducibly stratifies survival.