| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g22130 | A02 | 11925183 | C | T | missense_variant | MODERATE | c.377C>T|p.Ala126Val |
S289 S290 |
| 2 | BAA02g22130 | A02 | 11925898 | C | T | intron_variant | MODIFIER | c.853-50C>T| |
S212 |
| 3 | BAA02g22130 | A02 | 11926309 | C | T | missense_variant | MODERATE | c.1138C>T|p.Leu380Phe |
S267 |
| 4 | BAA02g22130 | A02 | 11926588 | G | A | missense_variant | MODERATE | c.1417G>A|p.Gly473Arg |
S177 |