Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00690 | A05 | 389371 | C | T | downstream_gene_variant | MODIFIER | c.*1018G>A| |
S292 |
2 | BAA05g00690 | A05 | 389958 | C | T | downstream_gene_variant | MODIFIER | c.*431G>A| |
S68 |
3 | BAA05g00690 | A05 | 390158 | C | T | downstream_gene_variant | MODIFIER | c.*231G>A| |
S182 |
4 | BAA05g00690 | A05 | 391474 | G | A | intron_variant | MODIFIER | c.876+21C>T| |
S167 |
5 | BAA05g00690 | A05 | 391480 | G | A | intron_variant | MODIFIER | c.876+15C>T| |
S157 S163 |
6 | BAA05g00690 | A05 | 391635 | C | T | missense_variant | MODERATE | c.736G>A|p.Ala246Thr |
S18 |
7 | BAA05g00690 | A05 | 392085 | C | T | intron_variant | MODIFIER | c.591+69G>A| |
S69 |
8 | BAA05g00690 | A05 | 392623 | G | A | intron_variant | MODIFIER | c.337-44C>T| |
S295 S98 |
9 | BAA05g00690 | A05 | 392921 | G | A | intron_variant | MODIFIER | c.211-15C>T| |
S125 |
10 | BAA05g00690 | A05 | 393417 | C | T | upstream_gene_variant | MODIFIER | c.-141G>A| |
S262 |
11 | BAA05g00690 | A05 | 394203 | G | A | upstream_gene_variant | MODIFIER | c.-927C>T| |
S35 |
12 | BAA05g00690 | A05 | 396094 | C | T | upstream_gene_variant | MODIFIER | c.-2818G>A| |
S183 S198 |
13 | BAA05g00690 | A05 | 396748 | C | T | upstream_gene_variant | MODIFIER | c.-3472G>A| |
|
14 | BAA05g00690 | A05 | 397447 | T | C | upstream_gene_variant | MODIFIER | c.-4171A>G| |
S180 S38 S67 S74 |
15 | BAA05g00690 | A05 | 397558 | G | A | upstream_gene_variant | MODIFIER | c.-4282C>T| |
S142 S15 S153 S208 S243 S297 S38 S98 |
16 | BAA05g00690 | A05 | 397629 | C | G | upstream_gene_variant | MODIFIER | c.-4353G>C| |
S38 |
17 | BAA05g00690 | A05 | 397700 | G | A | upstream_gene_variant | MODIFIER | c.-4424C>T| |
S95 |
18 | BAA05g00690 | A05 | 397778 | C | T | upstream_gene_variant | MODIFIER | c.-4502G>A| |
S164 |