| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g31950 | A02 | 25986156 | C | T | downstream_gene_variant | MODIFIER | c.*374G>A| |
S35 |
| 2 | BAA02g31950 | A02 | 25986588 | G | A | intron_variant | MODIFIER | c.374-33C>T| |
S239 |
| 3 | BAA02g31950 | A02 | 25986716 | G | A | missense_variant | MODERATE | c.316C>T|p.His106Tyr |
S303 |
| 4 | BAA02g31950 | A02 | 25987534 | C | T | upstream_gene_variant | MODIFIER | c.-220G>A| |
S107 |
| 5 | BAA02g31950 | A02 | 25987675 | G | A | upstream_gene_variant | MODIFIER | c.-361C>T| |
S130 |
| 6 | BAA02g31950 | A02 | 25987716 | C | T | upstream_gene_variant | MODIFIER | c.-402G>A| |
S155 S211 |
| 7 | BAA02g31950 | A02 | 25988068 | G | A | upstream_gene_variant | MODIFIER | c.-754C>T| |
S23 |
| 8 | BAA02g31950 | A02 | 25988629 | C | T | upstream_gene_variant | MODIFIER | c.-1315G>A| |
S35 |
| 9 | BAA02g31950 | A02 | 25988900 | C | T | upstream_gene_variant | MODIFIER | c.-1586G>A| |
S228 |
| 10 | BAA02g31950 | A02 | 25989030 | G | A | upstream_gene_variant | MODIFIER | c.-1716C>T| |
S116 |
| 11 | BAA02g31950 | A02 | 25990345 | C | T | upstream_gene_variant | MODIFIER | c.-3031G>A| |
S103 |
| 12 | BAA02g31950 | A02 | 25990402 | G | A | upstream_gene_variant | MODIFIER | c.-3088C>T| |
S246 |
| 13 | BAA02g31950 | A02 | 25990632 | C | T | upstream_gene_variant | MODIFIER | c.-3318G>A| |
S155 |
| 14 | BAA02g31950 | A02 | 25990705 | C | T | upstream_gene_variant | MODIFIER | c.-3391G>A| |
S306 S308 |
| 15 | BAA02g31950 | A02 | 25990726 | G | A | upstream_gene_variant | MODIFIER | c.-3412C>T| |
S260 |
| 16 | BAA02g31950 | A02 | 25990823 | G | A | upstream_gene_variant | MODIFIER | c.-3509C>T| |
S293 |
| 17 | BAA02g31950 | A02 | 25990883 | C | T | upstream_gene_variant | MODIFIER | c.-3569G>A| |
S122 |
| 18 | BAA02g31950 | A02 | 25990983 | C | T | upstream_gene_variant | MODIFIER | c.-3669G>A| |
S278 |
| 19 | BAA02g31950 | A02 | 25992080 | G | A | upstream_gene_variant | MODIFIER | c.-4766C>T| |
S140 |