| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g09540 | A02 | 4202535 | G | A | missense_variant | MODERATE | c.697C>T|p.Pro233Ser |
S148 S30 S31 |
| 2 | BAA02g09540 | A02 | 4203356 | G | A | synonymous_variant | LOW | c.294C>T|p.Val98Val |
S148 S210 S30 S31 |
| 3 | BAA02g09540 | A02 | 4203367 | G | A | missense_variant | MODERATE | c.283C>T|p.Leu95Phe |
S187 |
| 4 | BAA02g09540 | A02 | 4205633 | C | T | upstream_gene_variant | MODIFIER | c.-1488G>A| |
S203 |
| 5 | BAA02g09540 | A02 | 4206847 | G | A | upstream_gene_variant | MODIFIER | c.-2702C>T| |
S13 S164 |
| 6 | BAA02g09540 | A02 | 4207177 | G | T | upstream_gene_variant | MODIFIER | c.-3032C>A| |
S107 S131 S255 S53 |
| 7 | BAA02g09540 | A02 | 4207936 | C | T | upstream_gene_variant | MODIFIER | c.-3791G>A| |
S262 |
| 8 | BAA02g09540 | A02 | 4208260 | G | A | upstream_gene_variant | MODIFIER | c.-4115C>T| |
S67 |
| 9 | BAA02g09540 | A02 | 4209025 | C | T | upstream_gene_variant | MODIFIER | c.-4880G>A| |
S28 |