Across TCGA pan-cancer cohorts, SEMA5A Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated SEMA5A data layer compared with 23 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher SEMA5A Mutation is associated with better overall survival. In most high-consensus cancer types, elevated SEMA5A expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.
UCEC, LUSC, and SCLC are the cancer types where SEMA5A Mutation most reproducibly stratifies survival.