Across TCGA pan-cancer cohorts, IGHV1-46 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated IGHV1-46 data layer compared with 22 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher IGHV1-46 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IGHV1-46 expression acts as an unfavorable survival marker.
KIRP, SKCM, and LUAD are the cancer types where IGHV1-46 Mutation most reproducibly stratifies survival.