Across TCGA pan-cancer cohorts, MAGEA9B Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated MAGEA9B data layer compared with 19 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher MAGEA9B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MAGEA9B expression acts as an unfavorable survival marker.
UCEC are the cancer types where MAGEA9B Mutation most reproducibly stratifies survival.