These results are in line with the number of unique starting sites (SS) detected by the NGS panel—the fusion involving NTRK1 was identified by 72 unique SS reads, whereas the two less expressed fusions of NTRK3 by 23 (ETV6→NTRK3 in the LAC) and 33 (ETV6→NTRK3 in the CRC) unique reads (Table 2). The gene discussed is NTRK1; the disease is colorectal carcinoma.