Across TCGA pan-cancer cohorts, H2AC16 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated H2AC16 data layer compared with 27 for mass-spec protein.
The strongest signal is observed in uterine carcinosarcoma (UCS), where higher H2AC16 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated H2AC16 expression acts as an unfavorable survival marker.
UCS are the cancer types where H2AC16 Mutation most reproducibly stratifies survival.