Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34020 | A02 | 29130661 | C | T | synonymous_variant | LOW | c.2424G>A|p.Lys808Lys |
S308 |
2 | BAA02g34020 | A02 | 29130691 | C | T | missense_variant | MODERATE | c.2394G>A|p.Met798Ile |
S179 |
3 | BAA02g34020 | A02 | 29130744 | G | A | missense_variant | MODERATE | c.2341C>T|p.Leu781Phe |
S13 |
4 | BAA02g34020 | A02 | 29131142 | G | A | missense_variant | MODERATE | c.1943C>T|p.Ser648Phe |
S113 |
5 | BAA02g34020 | A02 | 29131345 | C | T | synonymous_variant | LOW | c.1824G>A|p.Leu608Leu |
S293 |
6 | BAA02g34020 | A02 | 29131920 | G | A | synonymous_variant | LOW | c.1398C>T|p.Phe466Phe |
S153 S213 |
7 | BAA02g34020 | A02 | 29135157 | C | T | intron_variant | MODIFIER | c.533+417G>A| |
S165 |
8 | BAA02g34020 | A02 | 29136844 | G | A | upstream_gene_variant | MODIFIER | c.-738C>T| |
S187 |
9 | BAA02g34020 | A02 | 29137065 | C | T | upstream_gene_variant | MODIFIER | c.-959G>A| |
S9 |
10 | BAA02g34020 | A02 | 29137595 | G | A | upstream_gene_variant | MODIFIER | c.-1489C>T| |
S293 |
11 | BAA02g34020 | A02 | 29137636 | C | T | upstream_gene_variant | MODIFIER | c.-1530G>A| |
S299 |
12 | BAA02g34020 | A02 | 29138797 | C | T | upstream_gene_variant | MODIFIER | c.-2691G>A| |
S203 |
13 | BAA02g34020 | A02 | 29139397 | G | A | upstream_gene_variant | MODIFIER | c.-3291C>T| |
S42 |