Across TCGA pan-cancer cohorts, C22orf34 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated C22orf34 data layer compared with 24 for mass-spec protein.
The strongest signal is observed in kidney chromophobe (KICH), where higher C22orf34 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated C22orf34 expression acts as an unfavorable survival marker.
KICH, COAD, and UCEC are the cancer types where C22orf34 Mutation most reproducibly stratifies survival.