Across TCGA pan-cancer cohorts, MAGEA10 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated MAGEA10 data layer compared with 20 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher MAGEA10 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MAGEA10 expression acts as an unfavorable survival marker, although some lineages such as LUAD show a favorable association.
CESC, READ, and ACC are the cancer types where MAGEA10 Mutation most reproducibly stratifies survival.