Across TCGA pan-cancer cohorts, H2AP Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated H2AP data layer compared with 11 for mass-spec protein.
The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher H2AP Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated H2AP expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
KIRP, UCEC, and LUAD are the cancer types where H2AP Mutation most reproducibly stratifies survival.