| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g41440 | A02 | 34767180 | A | G | downstream_gene_variant | MODIFIER | c.*3436T>C| |
S260 |
| 2 | BAA02g41440 | A02 | 34768943 | C | T | downstream_gene_variant | MODIFIER | c.*1673G>A| |
S42 |
| 3 | BAA02g41440 | A02 | 34770876 | C | T | missense_variant | MODERATE | c.871G>A|p.Ala291Thr |
S79 S84 |