Fig. 3From: Targeted exome sequencing identifies mutational landscape in a cohort of 1500 Chinese patients with non-small cell lung carcinoma (NSCLC)Recurrent SNV mutations in TP53, EGFR, KRAS, CDKN2A, PTCH1, and PIK3CA. Positional distribution of SNV mutations across blood and tissue NSCLC samples. SNV mutations detected by exome sequencing are depicted on lolliplot and mapped to the structure of the corresponding geneBack to article page