Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13500 | A02 | 6217722 | G | A | intron_variant | MODIFIER | c.16-5681G>A| |
S136 |
2 | BAA02g13500 | A02 | 6217754 | C | T | intron_variant | MODIFIER | c.16-5649C>T| |
S44 |
3 | BAA02g13500 | A02 | 6218477 | G | A | intron_variant | MODIFIER | c.16-4926G>A| |
S246 |
4 | BAA02g13500 | A02 | 6220167 | G | A | intron_variant | MODIFIER | c.16-3236G>A| |
S265 |
5 | BAA02g13500 | A02 | 6220318 | G | A | intron_variant | MODIFIER | c.16-3085G>A| |
S76 |
6 | BAA02g13500 | A02 | 6220872 | G | A | intron_variant | MODIFIER | c.16-2531G>A| |
S223 |
7 | BAA02g13500 | A02 | 6220947 | G | A | intron_variant | MODIFIER | c.16-2456G>A| |
S295 |
8 | BAA02g13500 | A02 | 6221227 | G | A | intron_variant | MODIFIER | c.16-2176G>A| |
S235 |
9 | BAA02g13500 | A02 | 6221471 | G | A | intron_variant | MODIFIER | c.16-1932G>A| |
S245 |
10 | BAA02g13500 | A02 | 6221513 | G | A | intron_variant | MODIFIER | c.16-1890G>A| |
S223 |
11 | BAA02g13500 | A02 | 6223312 | G | A | intron_variant | MODIFIER | c.16-91G>A| |
S308 |
12 | BAA02g13500 | A02 | 6224207 | G | A | intron_variant | MODIFIER | c.306+98G>A| |
S176 |
13 | BAA02g13500 | A02 | 6224664 | G | A | intron_variant | MODIFIER | c.306+555G>A| |
S166 |
14 | BAA02g13500 | A02 | 6224948 | C | T | intron_variant | MODIFIER | c.306+839C>T| |
S219 S72 |