| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g40110 | A02 | 33885905 | G | A | upstream_gene_variant | MODIFIER | c.-3196G>A| |
S62 |
| 2 | BAA02g40110 | A02 | 33885932 | C | T | upstream_gene_variant | MODIFIER | c.-3169C>T| |
S116 |
| 3 | BAA02g40110 | A02 | 33887015 | G | A | upstream_gene_variant | MODIFIER | c.-2086G>A| |
S237 |
| 4 | BAA02g40110 | A02 | 33887572 | G | A | upstream_gene_variant | MODIFIER | c.-1529G>A| |
S224 |
| 5 | BAA02g40110 | A02 | 33889703 | G | A | synonymous_variant | LOW | c.603G>A|p.Glu201Glu |
S19 |
| 6 | BAA02g40110 | A02 | 33889707 | G | A | missense_variant | MODERATE | c.607G>A|p.Val203Ile |
S69 |
| 7 | BAA02g40110 | A02 | 33889845 | C | T | synonymous_variant | LOW | c.745C>T|p.Leu249Leu |
S266 |
| 8 | BAA02g40110 | A02 | 33890714 | C | T | synonymous_variant | LOW | c.1614C>T|p.Tyr538Tyr |
S266 |
| 9 | BAA02g40110 | A02 | 33893472 | C | T | downstream_gene_variant | MODIFIER | c.*311C>T| |
S261 |
| 10 | BAA02g40110 | A02 | 33894148 | C | T | downstream_gene_variant | MODIFIER | c.*987C>T| |
S19 |
| 11 | BAA02g40110 | A02 | 33894256 | C | T | downstream_gene_variant | MODIFIER | c.*1095C>T| |
S63 |
| 12 | BAA02g40110 | A02 | 33894704 | C | T | downstream_gene_variant | MODIFIER | c.*1543C>T| |
S212 S267 |
| 13 | BAA02g40110 | A02 | 33894747 | G | A | downstream_gene_variant | MODIFIER | c.*1586G>A| |
S267 |
| 14 | BAA02g40110 | A02 | 33894785 | C | T | downstream_gene_variant | MODIFIER | c.*1624C>T| |
S211 |
| 15 | BAA02g40110 | A02 | 33895187 | C | T | downstream_gene_variant | MODIFIER | c.*2026C>T| |
S138 |
| 16 | BAA02g40110 | A02 | 33896943 | C | T | downstream_gene_variant | MODIFIER | c.*3782C>T| |
S193 |
| 17 | BAA02g40110 | A02 | 33897119 | C | T | downstream_gene_variant | MODIFIER | c.*3958C>T| |
S266 |
| 18 | BAA02g40110 | A02 | 33897844 | G | A | downstream_gene_variant | MODIFIER | c.*4683G>A| |
S129 |