Across TCGA pan-cancer cohorts, IGHV3OR16-9 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated IGHV3OR16-9 data layer compared with 20 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in kidney chromophobe (KICH), where higher IGHV3OR16-9 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated IGHV3OR16-9 expression acts as an unfavorable survival marker.
KICH and LUSC are the cancer types where IGHV3OR16-9 Mutation most reproducibly stratifies survival.