| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g09840 | A02 | 4339446 | C | T | missense_variant | MODERATE | c.466C>T|p.Pro156Ser |
S200 |