| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g10250 | A09 | 5639593 | C | T | missense_variant | MODERATE | c.413C>T|p.Ala138Val |
S2 |