Across TCGA pan-cancer cohorts, PPP2R3C Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated PPP2R3C data layer compared with 23 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher PPP2R3C Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PPP2R3C expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
KIRP, UCEC, and SKCM are the cancer types where PPP2R3C Mutation most reproducibly stratifies survival.