| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g15790 | A02 | 7655790 | C | T | missense_variant | MODERATE | c.40G>A|p.Gly14Ser |
S206 S26 |
| 2 | BAA02g15790 | A02 | 7660235 | C | T | upstream_gene_variant | MODIFIER | c.-4406G>A| |
S104 |
| 3 | BAA02g15790 | A02 | 7660784 | C | T | upstream_gene_variant | MODIFIER | c.-4955G>A| |
S174 S27 |
| 4 | BAA02g15790 | A02 | 7660787 | C | T | upstream_gene_variant | MODIFIER | c.-4958G>A| |
S233 |