Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26790 | A02 | 15003569 | C | T | upstream_gene_variant | MODIFIER | c.-1282G>A| |
S185 |
2 | BAA02g26790 | A02 | 15003687 | C | T | upstream_gene_variant | MODIFIER | c.-1400G>A| |
S296 |
3 | BAA02g26790 | A02 | 15003710 | C | T | upstream_gene_variant | MODIFIER | c.-1423G>A| |
S219 S72 |
4 | BAA02g26790 | A02 | 15003725 | G | A | upstream_gene_variant | MODIFIER | c.-1438C>T| |
S61 |
5 | BAA02g26790 | A02 | 15004056 | C | T | upstream_gene_variant | MODIFIER | c.-1769G>A| |
S167 |
6 | BAA02g26790 | A02 | 15004341 | G | A | upstream_gene_variant | MODIFIER | c.-2054C>T| |
S4 |
7 | BAA02g26790 | A02 | 15004930 | G | A | upstream_gene_variant | MODIFIER | c.-2643C>T| |
S174 S27 |
8 | BAA02g26790 | A02 | 15005920 | G | A | upstream_gene_variant | MODIFIER | c.-3633C>T| |
S47 |
9 | BAA02g26790 | A02 | 15006294 | C | T | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S270 |
10 | BAA02g26790 | A02 | 15006498 | C | T | upstream_gene_variant | MODIFIER | c.-4211G>A| |
S218 |
11 | BAA02g26790 | A02 | 15007065 | G | A | upstream_gene_variant | MODIFIER | c.-4778C>T| |
S56 |