| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g03690 | A02 | 1622814 | C | T | missense_variant | MODERATE | c.1319G>A|p.Gly440Asp |
S172 |
| 2 | BAA02g03690 | A02 | 1627276 | C | T | upstream_gene_variant | MODIFIER | c.-2610G>A| |
S252 |
| 3 | BAA02g03690 | A02 | 1628653 | G | A | upstream_gene_variant | MODIFIER | c.-3987C>T| |
S168 |