Across TCGA pan-cancer cohorts, C16orf96 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated C16orf96 data layer compared with 26 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher C16orf96 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated C16orf96 expression acts as an unfavorable survival marker, although some lineages such as LIHC show a favorable association.
STAD, UCEC, and ESCA are the cancer types where C16orf96 Mutation most reproducibly stratifies survival.