Across TCGA pan-cancer cohorts, SEC22C Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SEC22C data layer compared with 25 for mass-spec protein.
The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher SEC22C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SEC22C expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
KIRP, COAD, and UCEC are the cancer types where SEC22C Mutation most reproducibly stratifies survival.