Across TCGA pan-cancer cohorts, MAP1S Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated MAP1S data layer compared with 26 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher MAP1S Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MAP1S expression acts as an unfavorable survival marker.
DLBC, ACC, and GBM are the cancer types where MAP1S Mutation most reproducibly stratifies survival.