Across TCGA pan-cancer cohorts, GARS1-DT Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated GARS1-DT data layer compared with 28 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher GARS1-DT Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated GARS1-DT expression acts as an unfavorable survival marker.
CESC are the cancer types where GARS1-DT Mutation most reproducibly stratifies survival.