| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156251 | BAA02g04290 | A02 | 1877657 | G | A | missense_variant | MODERATE | c.220C>T|p.Pro74Ser |
S67 |
| 156252 | BAA02g04280 | A02 | 1877882 | G | A | upstream_gene_variant | MODIFIER | c.-4072C>T| |
S25 |
| 156253 | BAA02g04280 | A02 | 1877994 | C | T | upstream_gene_variant | MODIFIER | c.-4184G>A| |
S6 |
| 156254 | BAA02g04300 | A02 | 1878518 | G | A | missense_variant | MODERATE | c.2791C>T|p.Leu931Phe |
S105 S106 |
| 156255 | BAA02g04300 | A02 | 1878691 | G | A | splice_region_variant&intron_variant | LOW | c.2623-5C>T| |
S41 |
| 156256 | BAA02g04280 | A02 | 1878728 | C | T | upstream_gene_variant | MODIFIER | c.-4918G>A| |
S219 |
| 156257 | BAA02g04300 | A02 | 1878843 | G | A | synonymous_variant | LOW | c.2556C>T|p.Asn852Asn |
S125 |
| 156258 | BAA02g04290 | A02 | 1878887 | G | A | upstream_gene_variant | MODIFIER | c.-1011C>T| |
S10 |
| 156259 | BAA02g04300 | A02 | 1879134 | C | T | missense_variant | MODERATE | c.2356G>A|p.Val786Ile |
S76 |
| 156260 | BAA02g04300 | A02 | 1879419 | G | A | synonymous_variant | LOW | c.2268C>T|p.Gly756Gly |
S225 S73 |
| 156261 | BAA02g04300 | A02 | 1879729 | C | A | stop_gained | HIGH | c.2029G>T|p.Glu677* |
S203 |
| 156262 | BAA02g04300 | A02 | 1879903 | C | T | missense_variant | MODERATE | c.1855G>A|p.Glu619Lys |
S179 |
| 156263 | BAA02g04300 | A02 | 1880002 | C | T | missense_variant | MODERATE | c.1756G>A|p.Val586Met |
S89 |
| 156264 | BAA02g04300 | A02 | 1880066 | C | T | synonymous_variant | LOW | c.1692G>A|p.Val564Val |
S183 S198 |
| 156265 | BAA02g04300 | A02 | 1880551 | C | T | missense_variant | MODERATE | c.1207G>A|p.Gly403Arg |
S179 |
| 156266 | BAA02g04300 | A02 | 1880839 | C | T | missense_variant | MODERATE | c.919G>A|p.Glu307Lys |
S133 |
| 156267 | BAA02g04300 | A02 | 1881348 | C | T | synonymous_variant | LOW | c.498G>A|p.Glu166Glu |
S39 |
| 156268 | BAA02g04300 | A02 | 1881612 | G | A | stop_gained | HIGH | c.352C>T|p.Gln118* |
S209 |
| 156269 | BAA02g04300 | A02 | 1881632 | G | A | missense_variant | MODERATE | c.332C>T|p.Ala111Val |
S168 |
| 156270 | BAA02g04300 | A02 | 1882161 | C | T | synonymous_variant | LOW | c.165G>A|p.Lys55Lys |
S150 |
| 156271 | BAA02g04290 | A02 | 1882644 | G | A | upstream_gene_variant | MODIFIER | c.-4768C>T| |
S125 |
| 156272 | BAA02g04310 | A02 | 1884287 | C | T | missense_variant | MODERATE | c.337C>T|p.Leu113Phe |
S201 |
| 156273 | BAA02g04320 | A02 | 1884596 | C | T | missense_variant | MODERATE | c.208C>T|p.Pro70Ser |
S183 S198 |
| 156274 | BAA02g04320 | A02 | 1884875 | G | A | missense_variant | MODERATE | c.487G>A|p.Ala163Thr |
S62 |
| 156275 | BAA02g04320 | A02 | 1884933 | C | T | missense_variant | MODERATE | c.545C>T|p.Pro182Leu |
S249 |