Across TCGA pan-cancer cohorts, NT5C3B Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated NT5C3B data layer compared with 27 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in adrenocortical carcinoma (ACC), where higher NT5C3B Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated NT5C3B expression acts as an unfavorable survival marker.
ACC and LUSC are the cancer types where NT5C3B Mutation most reproducibly stratifies survival.