Across TCGA pan-cancer cohorts, C20orf27 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated C20orf27 data layer compared with 26 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher C20orf27 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated C20orf27 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CESC, ACC, and COAD are the cancer types where C20orf27 Mutation most reproducibly stratifies survival.