| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g44130 | A02 | 36407531 | G | A | synonymous_variant | LOW | c.393C>T|p.Phe131Phe |
S10 |
| 2 | BAA02g44130 | A02 | 36407712 | G | A | missense_variant | MODERATE | c.212C>T|p.Thr71Ile |
S13 |
| 3 | BAA02g44130 | A02 | 36412252 | G | A | upstream_gene_variant | MODIFIER | c.-4329C>T| |
S45 |
| 4 | BAA02g44130 | A02 | 36412381 | C | T | upstream_gene_variant | MODIFIER | c.-4458G>A| |
S260 |
| 5 | BAA02g44130 | A02 | 36412570 | C | T | upstream_gene_variant | MODIFIER | c.-4647G>A| |
S157 |
| 6 | BAA02g44130 | A02 | 36412689 | C | T | upstream_gene_variant | MODIFIER | c.-4766G>A| |
S262 |