Across TCGA pan-cancer cohorts, SMAP1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SMAP1 data layer compared with 29 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in uterine carcinosarcoma (UCS), where higher SMAP1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SMAP1 expression acts as an unfavorable survival marker.
UCS, PRAD, and HNSC are the cancer types where SMAP1 Mutation most reproducibly stratifies survival.