Across TCGA pan-cancer cohorts, PRR3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated PRR3 data layer compared with 28 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in cholangiocarcinoma (CHOL), where higher PRR3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PRR3 expression acts as an unfavorable survival marker.
CHOL and SKCM are the cancer types where PRR3 Mutation most reproducibly stratifies survival.