| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156301 | BAA02g04320 | A02 | 1885357 | C | T | synonymous_variant | LOW | c.969C>T|p.Val323Val |
S79 S84 |
| 156302 | BAA02g04320 | A02 | 1885731 | C | T | missense_variant | MODERATE | c.1343C>T|p.Pro448Leu |
S216 |
| 156303 | BAA02g04300 | A02 | 1885932 | C | T | upstream_gene_variant | MODIFIER | c.-3342G>A| |
S250 |
| 156304 | BAA02g04300 | A02 | 1886329 | C | T | upstream_gene_variant | MODIFIER | c.-3739G>A| |
S284 |
| 156305 | BAA02g04300 | A02 | 1886565 | C | T | upstream_gene_variant | MODIFIER | c.-3975G>A| |
S257 |
| 156306 | BAA02g04330 | A02 | 1889559 | G | A | missense_variant | MODERATE | c.317C>T|p.Ala106Val |
S244 |
| 156307 | BAA02g04340 | A02 | 1890623 | G | A | missense_variant | MODERATE | c.971C>T|p.Thr324Ile |
S113 |
| 156308 | BAA02g04340 | A02 | 1890715 | C | T | stop_gained | HIGH | c.879G>A|p.Trp293* |
S80 |
| 156309 | BAA02g04340 | A02 | 1890951 | G | A | missense_variant | MODERATE | c.643C>T|p.Leu215Phe |
S110 |
| 156310 | BAA02g04340 | A02 | 1891123 | C | T | stop_gained | HIGH | c.471G>A|p.Trp157* |
S257 |
| 156311 | BAA02g04340 | A02 | 1891191 | G | A | missense_variant | MODERATE | c.403C>T|p.Pro135Ser |
S127 |
| 156312 | BAA02g04330 | A02 | 1891706 | C | T | upstream_gene_variant | MODIFIER | c.-1831G>A| |
S274 |
| 156313 | BAA02g04330 | A02 | 1891764 | G | A | upstream_gene_variant | MODIFIER | c.-1889C>T| |
S256 |
| 156314 | BAA02g04330 | A02 | 1893761 | C | T | upstream_gene_variant | MODIFIER | c.-3886G>A| |
S200 |
| 156315 | BAA02g04330 | A02 | 1894122 | G | A | upstream_gene_variant | MODIFIER | c.-4247C>T| |
S53 |
| 156316 | BAA02g04330 | A02 | 1894223 | C | T | upstream_gene_variant | MODIFIER | c.-4348G>A| |
S113 S115 S120 S122 S55 S65 S8 |
| 156317 | BAA02g04330 | A02 | 1894267 | C | T | upstream_gene_variant | MODIFIER | c.-4392G>A| |
S301 S304 |
| 156318 | BAA02g04330 | A02 | 1894366 | C | T | upstream_gene_variant | MODIFIER | c.-4491G>A| |
S108 |
| 156319 | BAA02g04330 | A02 | 1894530 | G | A | upstream_gene_variant | MODIFIER | c.-4655C>T| |
S162 |
| 156320 | BAA02g04340 | A02 | 1896348 | C | T | upstream_gene_variant | MODIFIER | c.-4755G>A| |
S71 |
| 156321 | BAA02g04350 | A02 | 1897623 | C | T | upstream_gene_variant | MODIFIER | c.-1040G>A| |
S115 |
| 156322 | BAA02g04350 | A02 | 1897723 | G | A | upstream_gene_variant | MODIFIER | c.-1140C>T| |
S67 |
| 156323 | BAA02g04350 | A02 | 1897798 | G | A | upstream_gene_variant | MODIFIER | c.-1215C>T| |
S279 |
| 156324 | BAA02g04350 | A02 | 1898688 | C | T | upstream_gene_variant | MODIFIER | c.-2105G>A| |
S13 |
| 156325 | BAA02g04350 | A02 | 1898764 | G | A | upstream_gene_variant | MODIFIER | c.-2181C>T| |
S192 |