Across TCGA pan-cancer cohorts, IGHV3OR15-7 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated IGHV3OR15-7 data layer compared with 24 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher IGHV3OR15-7 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated IGHV3OR15-7 expression acts as an unfavorable survival marker.
OV, LUSC, and GBM are the cancer types where IGHV3OR15-7 Mutation most reproducibly stratifies survival.