Across TCGA pan-cancer cohorts, SYNM Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated SYNM data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in kidney chromophobe (KICH), where higher SYNM Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SYNM expression acts as an unfavorable survival marker, although some lineages such as UCEC and GBM show a favorable association.
KICH, UCEC, and HNSC are the cancer types where SYNM Mutation most reproducibly stratifies survival.