| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10780 | A02 | 4822326 | C | T | missense_variant | MODERATE | c.333G>A|p.Met111Ile |
S19 |
| 2 | BAA02g10780 | A02 | 4823257 | G | A | upstream_gene_variant | MODIFIER | c.-599C>T| |
S17 |
| 3 | BAA02g10780 | A02 | 4824111 | T | A | upstream_gene_variant | MODIFIER | c.-1453A>T| |
S28 |
| 4 | BAA02g10780 | A02 | 4824729 | G | A | upstream_gene_variant | MODIFIER | c.-2071C>T| |
S125 |
| 5 | BAA02g10780 | A02 | 4827421 | C | T | upstream_gene_variant | MODIFIER | c.-4763G>A| |
S277 |