Across TCGA pan-cancer cohorts, H2AC17 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated H2AC17 data layer compared with 20 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher H2AC17 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated H2AC17 expression acts as an unfavorable survival marker.
OV, HNSC, and DLBC are the cancer types where H2AC17 Mutation most reproducibly stratifies survival.