Across TCGA pan-cancer cohorts, THOC3 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated THOC3 data layer compared with 22 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher THOC3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated THOC3 expression acts as an unfavorable survival marker.
READ are the cancer types where THOC3 Mutation most reproducibly stratifies survival.