Across TCGA pan-cancer cohorts, THRAP3 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated THRAP3 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher THRAP3 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated THRAP3 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCEC, LUSC, and COAD are the cancer types where THRAP3 Mutation most reproducibly stratifies survival.