Across TCGA pan-cancer cohorts, SCP2 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SCP2 data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher SCP2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SCP2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
BLCA, UCEC, and SKCM are the cancer types where SCP2 Mutation most reproducibly stratifies survival.