Fig. 2

a The somatic mutation spectrum in different renal carcinoma. The hybrid capture-based NGS was used to sequence a panel of 295 well-established oncogene or oncosuppressors. In each analyzed MA patient, 85 somatic mutational events were detected. b The ratio of different mutant species in MA. The vast majority of mutation types were missense and synonymous variants (56.8 and 26.3%, respectively), while a smaller percentage was represented by copy number gain, indel, stop-gained, splice-region variants, or fusion (8.1, 2.1, 2.3, 1.2 and 3.2%, respectively)