| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 175151 | BAA02g17740 | A02 | 8833876 | G | A | upstream_gene_variant | MODIFIER | c.-2933C>T| |
S143 |
| 175152 | BAA02g17740 | A02 | 8835052 | C | T | upstream_gene_variant | MODIFIER | c.-4109G>A| |
S202 |
| 175153 | BAA02g17760 | A02 | 8836155 | G | A | upstream_gene_variant | MODIFIER | c.-1890G>A| |
S132 S137 S215 |
| 175154 | BAA02g17760 | A02 | 8837509 | G | A | upstream_gene_variant | MODIFIER | c.-536G>A| |
S48 |
| 175155 | BAA02g17760 | A02 | 8837646 | G | A | upstream_gene_variant | MODIFIER | c.-399G>A| |
S288 |
| 175156 | BAA02g17760 | A02 | 8837911 | C | T | upstream_gene_variant | MODIFIER | c.-134C>T| |
S275 |
| 175157 | BAA02g17760 | A02 | 8837937 | C | T | upstream_gene_variant | MODIFIER | c.-108C>T| |
S255 |
| 175158 | BAA02g17760 | A02 | 8838322 | C | T | missense_variant | MODERATE | c.278C>T|p.Thr93Ile |
S263 |
| 175159 | BAA02g17760 | A02 | 8838743 | C | T | synonymous_variant | LOW | c.699C>T|p.Asp233Asp |
S244 |
| 175160 | BAA02g17760 | A02 | 8839111 | C | T | missense_variant | MODERATE | c.1067C>T|p.Thr356Ile |
S260 |
| 175161 | BAA02g17760 | A02 | 8839635 | G | A | missense_variant | MODERATE | c.1591G>A|p.Asp531Asn |
S51 |
| 175162 | BAA02g17760 | A02 | 8839739 | G | A | synonymous_variant | LOW | c.1695G>A|p.Leu565Leu |
S197 |
| 175163 | BAA02g17760 | A02 | 8839993 | G | A | missense_variant | MODERATE | c.1949G>A|p.Gly650Glu |
S166 |
| 175164 | BAA02g17770 | A02 | 8840886 | G | A | upstream_gene_variant | MODIFIER | c.-1415G>A| |
S166 |
| 175165 | BAA02g17770 | A02 | 8841273 | C | T | upstream_gene_variant | MODIFIER | c.-1028C>T| |
S121 |
| 175166 | BAA02g17770 | A02 | 8841863 | C | T | upstream_gene_variant | MODIFIER | c.-438C>T| |
S228 |
| 175167 | BAA02g17770 | A02 | 8842315 | C | T | synonymous_variant | LOW | c.15C>T|p.Ala5Ala |
S208 S219 |
| 175168 | BAA02g17770 | A02 | 8842991 | G | A | missense_variant | MODERATE | c.380G>A|p.Arg127Gln |
S263 |
| 175169 | BAA02g17770 | A02 | 8843357 | C | T | splice_region_variant&intron_variant | LOW | c.579+6C>T| |
S292 |
| 175170 | BAA02g17760 | A02 | 8843430 | C | T | downstream_gene_variant | MODIFIER | c.*3172C>T| |
S208 S219 |
| 175171 | BAA02g17760 | A02 | 8843584 | C | T | downstream_gene_variant | MODIFIER | c.*3326C>T| |
S267 |
| 175172 | BAA02g17760 | A02 | 8844313 | G | A | downstream_gene_variant | MODIFIER | c.*4055G>A| |
S298 |
| 175173 | BAA02g17780 | A02 | 8845739 | C | T | upstream_gene_variant | MODIFIER | c.-385G>A| |
S46 |
| 175174 | BAA02g17790 | A02 | 8847816 | G | A | synonymous_variant | LOW | c.1536C>T|p.Asn512Asn |
S35 |
| 175175 | BAA02g17780 | A02 | 8848368 | G | A | upstream_gene_variant | MODIFIER | c.-3014C>T| |
S183 S198 |