Across TCGA pan-cancer cohorts, RFC1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RFC1 data layer compared with 22 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher RFC1 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated RFC1 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCEC, PRAD, and SKCM are the cancer types where RFC1 Mutation most reproducibly stratifies survival.