Evidence that the BRCA1/BCLAF1 splicing complex may carry out an essential tumor suppressor function arises from the identification of cancer driver mutations within members of the complex, such as BRCA1, SF3B1, U2AF1/2, etc. We therefore set out to assess the impact of the two most common cancer associated mutations within THRAP3, C301>T (R101*) and C2509>T (R837*) (identified through the catalog of somatic mutations in cancer (cancer.sanger.ac.uk)) on THRAP3 function (30). Here, THRAP3 is linked to neoplasm.