Table 1. Patient genomic variations information.
| Gene name | Amino acid variation | Variation site | Variation type |
|---|---|---|---|
| EGFR | L858R | Exon 21 | SNV |
| KRAS | G12D | Exon 2 | SNV |
| NOTCH1 | M771I, T772A | Exon 14 | SNV |
| K814* | Exon 15 | SNV | |
| CTNNA2 | K873N | Exon 18 | SNV |
| DNMT3A | A572S | Exon 15 | SNV |
| FAM1358 | E515A | Exon 13 | SNV |
| GRIN2A | P1053S | Exon 14 | SNV |
| LRP1B | H42Q | Exon 2 | SNV |
| G3378V | Exon 64 | SNV | |
| MTAP | – | – | Deletion |
| PIK3CG | E415Q | Exon 2 | SNV |
| RBM10 | L454Sfs*31 | Exon 13 | InDel |
| TNFRSF19 | E82* | Exon 4 | SNV |
| TRIO | S1948F | Exon 38 | SNV |
*, Stop codon. SNV, single nucleotide variant; InDel, short insertion/deletion.