Across TCGA pan-cancer cohorts, AP3B2 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated AP3B2 data layer compared with 22 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in adrenocortical carcinoma (ACC), where higher AP3B2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated AP3B2 expression acts as an unfavorable survival marker, although some lineages such as COAD show a favorable association.
ACC, ESCA, and COAD are the cancer types where AP3B2 Mutation most reproducibly stratifies survival.