Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00320-BAA09g00330 | A09 | 396965 | G | A | intergenic_region | MODIFIER | n.396965G>A| |
S19 |
2 | BAA09g00320-BAA09g00330 | A09 | 398035 | C | T | intergenic_region | MODIFIER | n.398035C>T| |
S297 |
3 | BAA09g00320-BAA09g00330 | A09 | 398423 | C | T | intergenic_region | MODIFIER | n.398423C>T| |
S247 |
4 | BAA09g00320-BAA09g00330 | A09 | 401451 | G | A | intergenic_region | MODIFIER | n.401451G>A| |
S153 S213 |
5 | BAA09g00320-BAA09g00330 | A09 | 401944 | C | T | intergenic_region | MODIFIER | n.401944C>T| |
S206 S26 |
6 | BAA09g00320-BAA09g00330 | A09 | 402143 | G | A | intergenic_region | MODIFIER | n.402143G>A| |
S30 S31 |
7 | BAA09g00320-BAA09g00330 | A09 | 404045 | C | T | intergenic_region | MODIFIER | n.404045C>T| |
S286 |
8 | BAA09g00320-BAA09g00330 | A09 | 404466 | T | C | intergenic_region | MODIFIER | n.404466T>C| |
S18 |
9 | BAA09g00320-BAA09g00330 | A09 | 404681 | G | A | intergenic_region | MODIFIER | n.404681G>A| |
S34 |
10 | BAA09g00320-BAA09g00330 | A09 | 405136 | C | T | intergenic_region | MODIFIER | n.405136C>T| |
S166 S263 |
11 | BAA09g00320-BAA09g00330 | A09 | 406102 | C | T | intergenic_region | MODIFIER | n.406102C>T| |
S148 |
12 | BAA09g00320-BAA09g00330 | A09 | 408005 | T | A | intergenic_region | MODIFIER | n.408005T>A| |
S152 |
13 | BAA09g00320-BAA09g00330 | A09 | 408491 | G | A | intergenic_region | MODIFIER | n.408491G>A| |
S4 |
14 | BAA09g00320-BAA09g00330 | A09 | 409873 | C | T | intergenic_region | MODIFIER | n.409873C>T| |
S188 S276 |
15 | BAA09g00320-BAA09g00330 | A09 | 411632 | G | A | intergenic_region | MODIFIER | n.411632G>A| |
S238 |
16 | BAA09g00320-BAA09g00330 | A09 | 415211 | G | A | intergenic_region | MODIFIER | n.415211G>A| |
S186 |
17 | BAA09g00320-BAA09g00330 | A09 | 417942 | C | T | intergenic_region | MODIFIER | n.417942C>T| |
S249 |
18 | BAA09g00320-BAA09g00330 | A09 | 418292 | C | T | intergenic_region | MODIFIER | n.418292C>T| |
S161 |