| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 192151 | BAA02g26780 | A02 | 14997975 | G | A | upstream_gene_variant | MODIFIER | c.-2178G>A| |
S11 |
| 192152 | BAA02g26770 | A02 | 14998370 | G | A | missense_variant | MODERATE | c.532G>A|p.Ala178Thr |
S125 |
| 192153 | BAA02g26770 | A02 | 14998793 | C | T | missense_variant | MODERATE | c.695C>T|p.Pro232Leu |
S78 S83 |
| 192154 | BAA02g26770 | A02 | 14998807 | G | A | missense_variant | MODERATE | c.709G>A|p.Asp237Asn |
S153 S213 |
| 192155 | BAA02g26780 | A02 | 14999348 | C | T | upstream_gene_variant | MODIFIER | c.-805C>T| |
S172 S217 |
| 192156 | BAA02g26800 | A02 | 15001134 | G | A | upstream_gene_variant | MODIFIER | c.-3850G>A| |
S159 S243 |
| 192157 | BAA02g26780 | A02 | 15001225 | G | A | missense_variant | MODERATE | c.674G>A|p.Gly225Glu |
S153 S213 |
| 192158 | BAA02g26780 | A02 | 15001297 | C | T | missense_variant | MODERATE | c.746C>T|p.Ala249Val |
S18 |
| 192159 | BAA02g26800 | A02 | 15001547 | G | A | upstream_gene_variant | MODIFIER | c.-3437G>A| |
S111 |
| 192160 | BAA02g26800 | A02 | 15002003 | C | T | upstream_gene_variant | MODIFIER | c.-2981C>T| |
S108 |
| 192161 | BAA02g26790 | A02 | 15003569 | C | T | upstream_gene_variant | MODIFIER | c.-1282G>A| |
S185 |
| 192162 | BAA02g26790 | A02 | 15003687 | C | T | upstream_gene_variant | MODIFIER | c.-1400G>A| |
S296 |
| 192163 | BAA02g26790 | A02 | 15003710 | C | T | upstream_gene_variant | MODIFIER | c.-1423G>A| |
S219 S72 |
| 192164 | BAA02g26790 | A02 | 15003725 | G | A | upstream_gene_variant | MODIFIER | c.-1438C>T| |
S61 |
| 192165 | BAA02g26790 | A02 | 15004056 | C | T | upstream_gene_variant | MODIFIER | c.-1769G>A| |
S167 |
| 192166 | BAA02g26790 | A02 | 15004341 | G | A | upstream_gene_variant | MODIFIER | c.-2054C>T| |
S4 |
| 192167 | BAA02g26790 | A02 | 15004930 | G | A | upstream_gene_variant | MODIFIER | c.-2643C>T| |
S174 S27 |
| 192168 | BAA02g26800 | A02 | 15005070 | C | T | synonymous_variant | LOW | c.87C>T|p.Phe29Phe |
S122 |
| 192169 | BAA02g26790 | A02 | 15005920 | G | A | upstream_gene_variant | MODIFIER | c.-3633C>T| |
S47 |
| 192170 | BAA02g26790 | A02 | 15006294 | C | T | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S270 |
| 192171 | BAA02g26790 | A02 | 15006498 | C | T | upstream_gene_variant | MODIFIER | c.-4211G>A| |
S218 |
| 192172 | BAA02g26790 | A02 | 15007065 | G | A | upstream_gene_variant | MODIFIER | c.-4778C>T| |
S56 |
| 192173 | BAA02g26800 | A02 | 15008206 | G | A | downstream_gene_variant | MODIFIER | c.*2298G>A| |
S41 |
| 192174 | BAA02g26800 | A02 | 15008839 | C | T | downstream_gene_variant | MODIFIER | c.*2931C>T| |
S262 |
| 192175 | BAA02g26800 | A02 | 15009805 | G | A | downstream_gene_variant | MODIFIER | c.*3897G>A| |
S94 |