Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32420 | A02 | 27455081 | C | T | downstream_gene_variant | MODIFIER | c.*4076G>A| |
S162 |
2 | BAA02g32420 | A02 | 27455343 | C | T | downstream_gene_variant | MODIFIER | c.*3814G>A| |
S208 S219 |
3 | BAA02g32420 | A02 | 27455493 | G | A | downstream_gene_variant | MODIFIER | c.*3664C>T| |
S127 |
4 | BAA02g32420 | A02 | 27455731 | G | A | downstream_gene_variant | MODIFIER | c.*3426C>T| |
S228 |
5 | BAA02g32420 | A02 | 27456083 | C | T | downstream_gene_variant | MODIFIER | c.*3074G>A| |
S68 |
6 | BAA02g32420 | A02 | 27457110 | C | T | downstream_gene_variant | MODIFIER | c.*2047G>A| |
S164 |
7 | BAA02g32420 | A02 | 27457237 | C | T | downstream_gene_variant | MODIFIER | c.*1920G>A| |
S49 |
8 | BAA02g32420 | A02 | 27457328 | A | T | downstream_gene_variant | MODIFIER | c.*1829T>A| |
S259 |
9 | BAA02g32420 | A02 | 27457393 | G | A | downstream_gene_variant | MODIFIER | c.*1764C>T| |
S286 |
10 | BAA02g32420 | A02 | 27457490 | C | T | downstream_gene_variant | MODIFIER | c.*1667G>A| |
S203 |
11 | BAA02g32420 | A02 | 27458616 | C | T | downstream_gene_variant | MODIFIER | c.*541G>A| |
S180 |
12 | BAA02g32420 | A02 | 27459291 | C | T | missense_variant | MODERATE | c.1456G>A|p.Asp486Asn |
S140 |
13 | BAA02g32420 | A02 | 27459760 | C | T | synonymous_variant | LOW | c.987G>A|p.Thr329Thr |
S16 |
14 | BAA02g32420 | A02 | 27460579 | G | A | synonymous_variant | LOW | c.168C>T|p.Thr56Thr |
S155 S211 |
15 | BAA02g32420 | A02 | 27461533 | G | A | upstream_gene_variant | MODIFIER | c.-787C>T| |
S113 |
16 | BAA02g32420 | A02 | 27463553 | C | T | upstream_gene_variant | MODIFIER | c.-2807G>A| |
S105 S106 |
17 | BAA02g32420 | A02 | 27464707 | G | A | upstream_gene_variant | MODIFIER | c.-3961C>T| |
S143 S266 |
18 | BAA02g32420 | A02 | 27464806 | G | A | upstream_gene_variant | MODIFIER | c.-4060C>T| |
S5 |
19 | BAA02g32420 | A02 | 27465500 | T | C | upstream_gene_variant | MODIFIER | c.-4754A>G| |
S68 |