Across TCGA pan-cancer cohorts, C7orf65 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated C7orf65 data layer compared with 22 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher C7orf65 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated C7orf65 expression acts as an unfavorable survival marker.
READ and LUAD are the cancer types where C7orf65 Mutation most reproducibly stratifies survival.