Gene | Exon | Type of mutation | Nucleotide change | Amino acid change | No. with mutation (%) |
---|---|---|---|---|---|
EGFR | 19 | Missense | c.2239TT>CC | p.L747P | 1 (0.20) |
 | 19 | Deletion | c.2235_2249del15 | p.E746_A750 | 53 (10.73) |
 |  |  | c.2236_2250del15 | p.E746_A750 | 18 (3.64) |
 |  |  | c.2237_2251del15 | p.E746_T751 | 2 (0.40) |
 |  |  | c.2237_2253del17 | p.E746_T751 | 1 (0.20) |
 |  |  | c.2237_2255del19 | p.E746_S752 | 1 (0.20) |
 |  |  | c.2237_2257del21 | p.E746_P753 | 1 (0.20) |
 |  |  | c.2239_2248del10 | p.L747_E749 | 2 (0.40) |
 |  |  | c.2239_2253del15 | p.L747_T751 | 1 (0.20) |
 |  |  | c.2239_2256del18 | p.L747_S752 | 2 (0.40) |
 |  |  | c.2240_2254del15 | p.L747_T751 | 2 (0.40) |
 |  |  | c.2240_2257del18 | p.L747_P753 | 5 (1.01) |
 |  |  | c.2253_2276del24 | p.S752_I759 | 3 (0.61) |
 |  |  | c.2254_2277del24 | p.S752_I759 | 1 (0.20) |
 | 21 | Missense | c.2573T>G | p.L858R | 81 (16.40) |
 |  |  | c.2582T>A | p.L861Q | 2 (0.40) |
Total | Â | Â | Â | Â | 176 (35.63) |
KRAS | 2 | Missense | c.34G>T | p.G12C | 24 (2.18) |
 |  |  | c.34G>A | p.G12S | 26 (2.37) |
 |  |  | c.34G>C | p.G12R | 1 (0.09) |
 |  |  | c.35G>A | p.G12D | 168 (15.29) |
 |  |  | c.35G>C | p.G12A | 23 (2.09) |
 |  |  | c.35G>T | p.G12V | 85 (7.73) |
 |  |  | c.34G>A + c.35G>A | p.G12S + p.G12D | 6 (0.55) |
 |  |  | c.37G>T | p.G13C | 4 (0.36) |
 |  |  | c.38G>A | p.G13D | 100 (9.10) |
Total | Â | Â | Â | Â | 437 (39.76) |