Across TCGA pan-cancer cohorts, MAP1LC3A Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated MAP1LC3A data layer compared with 26 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher MAP1LC3A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MAP1LC3A expression acts as an unfavorable survival marker.
COAD, LUAD, and UCEC are the cancer types where MAP1LC3A Mutation most reproducibly stratifies survival.