Across TCGA pan-cancer cohorts, AMT Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated AMT data layer compared with 23 for mass-spec protein and 8 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher AMT Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated AMT expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
SKCM, TGCT, and BRCA are the cancer types where AMT Mutation most reproducibly stratifies survival.