Across TCGA pan-cancer cohorts, ATG16L1 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated ATG16L1 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher ATG16L1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ATG16L1 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.
COAD, LIHC, and PRAD are the cancer types where ATG16L1 Mutation most reproducibly stratifies survival.