Five patients with either MET amplification or METex14 mutation are identified. MET amplification was detected by FISH in 2/3 (67%) of the patients. Next-generation sequencing detected a concurrent KRAS G12C mutation in both. Amplification in case 3 was detected by next-generation sequencing. One out of three patients that were MET amplified were also MET IHC positive by H-score. METex14 was seen in two patients and both were MET IHC positive. These results were unchanged when using IHC status by MetMab scoring criteria.