Across TCGA pan-cancer cohorts, CNTNAP3P2 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CNTNAP3P2 data layer compared with 19 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher CNTNAP3P2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated CNTNAP3P2 expression acts as an unfavorable survival marker.
COAD, PRAD, and BLCA are the cancer types where CNTNAP3P2 Mutation most reproducibly stratifies survival.