Across TCGA pan-cancer cohorts, H3-3A Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated H3-3A data layer compared with 23 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher H3-3A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated H3-3A expression acts as an unfavorable survival marker.
CESC, LUSC, and DLBC are the cancer types where H3-3A Mutation most reproducibly stratifies survival.