Across TCGA pan-cancer cohorts, INKA1 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated INKA1 data layer compared with 25 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher INKA1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated INKA1 expression acts as an unfavorable survival marker.
UCEC and PRAD are the cancer types where INKA1 Mutation most reproducibly stratifies survival.