Across TCGA pan-cancer cohorts, IGHV3-38 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated IGHV3-38 data layer compared with 26 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in head and neck squamous cell carcinoma (HNSC), where higher IGHV3-38 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated IGHV3-38 expression acts as an unfavorable survival marker.
HNSC, LUAD, and UCEC are the cancer types where IGHV3-38 Mutation most reproducibly stratifies survival.