Across TCGA pan-cancer cohorts, SULT1C2 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SULT1C2 data layer compared with 25 for mass-spec protein and 3 for mass-spec protein.
The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher SULT1C2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SULT1C2 expression acts as an unfavorable survival marker.
DLBC, PAAD, and UCEC are the cancer types where SULT1C2 Mutation most reproducibly stratifies survival.