| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10700 | A02 | 4777086 | C | T | missense_variant | MODERATE | c.1186G>A|p.Asp396Asn |
S54 |
| 2 | BAA02g10700 | A02 | 4777855 | C | T | synonymous_variant | LOW | c.585G>A|p.Arg195Arg |
S252 |
| 3 | BAA02g10700 | A02 | 4778805 | C | T | missense_variant | MODERATE | c.37G>A|p.Ala13Thr |
S292 |