Across TCGA pan-cancer cohorts, NT5C1A Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated NT5C1A data layer compared with 15 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in kidney chromophobe (KICH), where higher NT5C1A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated NT5C1A expression acts as an unfavorable survival marker, although some lineages such as STAD show a favorable association.
KICH, UCEC, and READ are the cancer types where NT5C1A Mutation most reproducibly stratifies survival.