Across TCGA pan-cancer cohorts, IGHG3 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated IGHG3 data layer compared with 21 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher IGHG3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IGHG3 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.
READ, LGG, and UCEC are the cancer types where IGHG3 Mutation most reproducibly stratifies survival.