Across TCGA pan-cancer cohorts, AP3M2 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated AP3M2 data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in head and neck squamous cell carcinoma (HNSC), where higher AP3M2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated AP3M2 expression acts as an unfavorable survival marker.
HNSC, KICH, and BLCA are the cancer types where AP3M2 Mutation most reproducibly stratifies survival.