| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g33060 | A01 | 21960643 | C | T | upstream_gene_variant | MODIFIER | c.-4680C>T| |
S194 |
| 2 | BAA01g33060 | A01 | 21960719 | C | T | upstream_gene_variant | MODIFIER | c.-4604C>T| |
S167 |
| 3 | BAA01g33060 | A01 | 21961346 | G | A | upstream_gene_variant | MODIFIER | c.-3977G>A| |
S209 |
| 4 | BAA01g33060 | A01 | 21962581 | C | T | upstream_gene_variant | MODIFIER | c.-2742C>T| |
S56 |
| 5 | BAA01g33060 | A01 | 21963206 | G | A | upstream_gene_variant | MODIFIER | c.-2117G>A| |
S238 |
| 6 | BAA01g33060 | A01 | 21963279 | G | T | upstream_gene_variant | MODIFIER | c.-2044G>T| |
S193 |
| 7 | BAA01g33060 | A01 | 21963460 | C | T | upstream_gene_variant | MODIFIER | c.-1863C>T| |
S168 |
| 8 | BAA01g33060 | A01 | 21963671 | C | T | upstream_gene_variant | MODIFIER | c.-1652C>T| |
S81 S85 |
| 9 | BAA01g33060 | A01 | 21965353 | C | T | synonymous_variant | LOW | c.31C>T|p.Leu11Leu |
S28 |
| 10 | BAA01g33060 | A01 | 21966687 | G | A | intron_variant | MODIFIER | c.334-32G>A| |
S297 |
| 11 | BAA01g33060 | A01 | 21967137 | C | T | downstream_gene_variant | MODIFIER | c.*281C>T| |
S179 |
| 12 | BAA01g33060 | A01 | 21967139 | C | T | downstream_gene_variant | MODIFIER | c.*283C>T| |
S8 |
| 13 | BAA01g33060 | A01 | 21967251 | C | T | downstream_gene_variant | MODIFIER | c.*395C>T| |
S42 |
| 14 | BAA01g33060 | A01 | 21967827 | G | A | downstream_gene_variant | MODIFIER | c.*971G>A| |
S97 |
| 15 | BAA01g33060 | A01 | 21968559 | C | T | downstream_gene_variant | MODIFIER | c.*1703C>T| |
S153 |
| 16 | BAA01g33060 | A01 | 21968830 | C | T | downstream_gene_variant | MODIFIER | c.*1974C>T| |
S247 |
| 17 | BAA01g33060 | A01 | 21970521 | C | T | downstream_gene_variant | MODIFIER | c.*3665C>T| |
S178 |
| 18 | BAA01g33060 | A01 | 21970939 | G | A | downstream_gene_variant | MODIFIER | c.*4083G>A| |
S292 |
| 19 | BAA01g33060 | A01 | 21971653 | G | A | downstream_gene_variant | MODIFIER | c.*4797G>A| |
S278 |