Besides the 3p deletion, TCGA analysis confirmed a frequent occurrence in chromosome 5 (67%) and chromosome 14q (45%) deletions, and the top ten mutated genes in ccRCC were VHL, PBRM1, BAP1, SETD2, KDM5C, TP53, mTOR, SMARCA, PTEN, and ARID1A (5, 6). This evidence concerns the gene BAP1 and nonpapillary renal cell carcinoma.