Across TCGA pan-cancer cohorts, SEMA3A Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated SEMA3A data layer compared with 20 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher SEMA3A Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated SEMA3A expression acts as an unfavorable survival marker, although some lineages such as UCEC and HNSC show a favorable association.
UCEC, KIRC, and HNSC are the cancer types where SEMA3A Mutation most reproducibly stratifies survival.