| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10960 | A02 | 4926392 | C | T | missense_variant | MODERATE | c.244G>A|p.Val82Met |
S293 |
| 2 | BAA02g10960 | A02 | 4928158 | G | A | upstream_gene_variant | MODIFIER | c.-1523C>T| |
S282 |
| 3 | BAA02g10960 | A02 | 4928988 | C | T | upstream_gene_variant | MODIFIER | c.-2353G>A| |
S250 |
| 4 | BAA02g10960 | A02 | 4931240 | G | A | upstream_gene_variant | MODIFIER | c.-4605C>T| |
S239 |
| 5 | BAA02g10960 | A02 | 4931521 | G | A | upstream_gene_variant | MODIFIER | c.-4886C>T| |
S67 |