Across TCGA pan-cancer cohorts, RUNX1 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RUNX1 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in acute myeloid leukemia (LAML), where higher RUNX1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RUNX1 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
LAML and UCEC are the cancer types where RUNX1 Mutation most reproducibly stratifies survival.