| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g16280 | A02 | 7938863 | G | A | missense_variant | MODERATE | c.169G>A|p.Ala57Thr |
S297 |