| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAS13g00650 | Scaffold13 | 7702774 | C | T | missense_variant | MODERATE | c.121G>A|p.Asp41Asn |
S161 |