| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g20100 | A10 | 18229653 | C | T | missense_variant | MODERATE | c.401C>T|p.Thr134Ile |
S123 |
| 2 | BAA10g20100 | A10 | 18229954 | C | T | downstream_gene_variant | MODIFIER | c.*66C>T| |
S26 |
| 3 | BAA10g20100 | A10 | 18230634 | G | A | downstream_gene_variant | MODIFIER | c.*746G>A| |
S184 |