| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g30210 | A02 | 17557447 | G | A | upstream_gene_variant | MODIFIER | c.-4351G>A| |
S173 |
| 2 | BAA02g30210 | A02 | 17557614 | C | T | upstream_gene_variant | MODIFIER | c.-4184C>T| |
S130 S246 |
| 3 | BAA02g30210 | A02 | 17557960 | C | T | upstream_gene_variant | MODIFIER | c.-3838C>T| |
S167 |
| 4 | BAA02g30210 | A02 | 17558303 | C | T | upstream_gene_variant | MODIFIER | c.-3495C>T| |
S162 |
| 5 | BAA02g30210 | A02 | 17558319 | G | A | upstream_gene_variant | MODIFIER | c.-3479G>A| |
S265 |
| 6 | BAA02g30210 | A02 | 17558698 | C | T | upstream_gene_variant | MODIFIER | c.-3100C>T| |
S231 |
| 7 | BAA02g30210 | A02 | 17559560 | G | A | upstream_gene_variant | MODIFIER | c.-2238G>A| |
S153 S213 |
| 8 | BAA02g30210 | A02 | 17559873 | C | T | upstream_gene_variant | MODIFIER | c.-1925C>T| |
S203 |
| 9 | BAA02g30210 | A02 | 17560021 | C | T | upstream_gene_variant | MODIFIER | c.-1777C>T| |
S267 |
| 10 | BAA02g30210 | A02 | 17560485 | G | A | upstream_gene_variant | MODIFIER | c.-1313G>A| |
S241 |
| 11 | BAA02g30210 | A02 | 17561151 | G | A | upstream_gene_variant | MODIFIER | c.-647G>A| |
S251 |
| 12 | BAA02g30210 | A02 | 17562169 | C | T | intron_variant | MODIFIER | c.132+240C>T| |
S239 |
| 13 | BAA02g30210 | A02 | 17562554 | C | T | intron_variant | MODIFIER | c.133-85C>T| |
S218 |
| 14 | BAA02g30210 | A02 | 17562743 | C | T | synonymous_variant | LOW | c.237C>T|p.Leu79Leu |
S108 |
| 15 | BAA02g30210 | A02 | 17562788 | G | A | intron_variant | MODIFIER | c.242+40G>A| |
S107 |
| 16 | BAA02g30210 | A02 | 17564138 | G | A | missense_variant | MODERATE | c.1301G>A|p.Arg434His |
S247 |
| 17 | BAA02g30210 | A02 | 17564141 | G | A | missense_variant | MODERATE | c.1304G>A|p.Gly435Asp |
S133 |
| 18 | BAA02g30210 | A02 | 17564285 | G | A | intron_variant | MODIFIER | c.1386-17G>A| |
S79 S91 |
| 19 | BAA02g30210 | A02 | 17569462 | C | T | downstream_gene_variant | MODIFIER | c.*4700C>T| |
S224 |