Across TCGA pan-cancer cohorts, CORO1C Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated CORO1C data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher CORO1C Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated CORO1C expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCEC, STAD, and SKCM are the cancer types where CORO1C Mutation most reproducibly stratifies survival.