In the present study, we detected EGFR mutations in 14.39 % (19/132) of NSCLC patients, and the mutations were in codons 861, 719 and 858 with the following rates: 10.52 % (2/19), 10.52 % (2/19) and 31.58 % (6/19), respectively, and deletion of exon 19 was seen in a ratio of 47.37 % (9/19). Here, EGFR is linked to non-small cell lung carcinoma.