Across TCGA pan-cancer cohorts, IGHV3-30 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated IGHV3-30 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher IGHV3-30 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IGHV3-30 expression acts as an unfavorable survival marker.
DLBC, LUAD, and LUSC are the cancer types where IGHV3-30 Mutation most reproducibly stratifies survival.