SOAT1 and nonpapillary renal cell carcinoma: In ICGC cohort, oxidative phosphorylation and ribosome were significantly enriched in ccRCC samples of high-risk group, while hallmarks such as apoptosis, basal transcription factors, JAK/STAT signaling pathway, RIG I like receptor signaling pathway, and T cell receptor signaling pathway were markedly enriched in ccRCC samples of low-risk group (Figure 7G).