| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g46100 | A02 | 37571047 | C | T | missense_variant | MODERATE | c.2483C>T|p.Ala828Val |
S34 |