Across TCGA pan-cancer cohorts, C20orf96 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated C20orf96 data layer compared with 22 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher C20orf96 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated C20orf96 expression acts as an unfavorable survival marker.
CESC, BLCA, and SKCM are the cancer types where C20orf96 Mutation most reproducibly stratifies survival.