Across TCGA pan-cancer cohorts, SEMA3B Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SEMA3B data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher SEMA3B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SEMA3B expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.
LIHC, LUSC, and UCEC are the cancer types where SEMA3B Mutation most reproducibly stratifies survival.