Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20350 | A02 | 10789231 | G | A | upstream_gene_variant | MODIFIER | c.-4704G>A| |
S72 S78 |
2 | BAA02g20350 | A02 | 10789538 | G | A | upstream_gene_variant | MODIFIER | c.-4397G>A| |
S47 |
3 | BAA02g20350 | A02 | 10789634 | C | T | upstream_gene_variant | MODIFIER | c.-4301C>T| |
S166 |
4 | BAA02g20350 | A02 | 10789916 | G | A | upstream_gene_variant | MODIFIER | c.-4019G>A| |
S293 |
5 | BAA02g20350 | A02 | 10790272 | G | A | upstream_gene_variant | MODIFIER | c.-3663G>A| |
S134 |
6 | BAA02g20350 | A02 | 10790420 | C | T | upstream_gene_variant | MODIFIER | c.-3515C>T| |
S181 |
7 | BAA02g20350 | A02 | 10790725 | G | A | upstream_gene_variant | MODIFIER | c.-3210G>A| |
S60 |
8 | BAA02g20350 | A02 | 10790841 | C | T | upstream_gene_variant | MODIFIER | c.-3094C>T| |
S292 |
9 | BAA02g20350 | A02 | 10791197 | G | A | upstream_gene_variant | MODIFIER | c.-2738G>A| |
S157 S40 S49 |
10 | BAA02g20350 | A02 | 10791393 | G | A | upstream_gene_variant | MODIFIER | c.-2542G>A| |
S190 |
11 | BAA02g20350 | A02 | 10791399 | C | T | upstream_gene_variant | MODIFIER | c.-2536C>T| |
S73 S91 |
12 | BAA02g20350 | A02 | 10791497 | G | A | upstream_gene_variant | MODIFIER | c.-2438G>A| |
S149 |
13 | BAA02g20350 | A02 | 10791773 | C | T | upstream_gene_variant | MODIFIER | c.-2162C>T| |
S208 S219 S255 |
14 | BAA02g20350 | A02 | 10792044 | G | A | upstream_gene_variant | MODIFIER | c.-1891G>A| |
S265 |
15 | BAA02g20350 | A02 | 10794404 | C | T | splice_region_variant&intron_variant | LOW | c.408-8C>T| |
S16 |
16 | BAA02g20350 | A02 | 10794765 | G | A | missense_variant | MODERATE | c.679G>A|p.Ala227Thr |
S240 |
17 | BAA02g20350 | A02 | 10796075 | C | T | downstream_gene_variant | MODIFIER | c.*1011C>T| |
S25 |
18 | BAA02g20350 | A02 | 10796254 | G | A | downstream_gene_variant | MODIFIER | c.*1190G>A| |
S257 |
19 | BAA02g20350 | A02 | 10797176 | G | A | downstream_gene_variant | MODIFIER | c.*2112G>A| |
S28 |
20 | BAA02g20350 | A02 | 10797856 | C | T | downstream_gene_variant | MODIFIER | c.*2792C>T| |
S186 |