Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g24180 | A02 | 13176326 | G | A | missense_variant | MODERATE | c.470C>T|p.Thr157Ile |
S156 |
2 | BAA02g24180 | A02 | 13177617 | C | T | upstream_gene_variant | MODIFIER | c.-658G>A| |
S234 |
3 | BAA02g24180 | A02 | 13177829 | G | A | upstream_gene_variant | MODIFIER | c.-870C>T| |
S58 |
4 | BAA02g24180 | A02 | 13178380 | C | T | upstream_gene_variant | MODIFIER | c.-1421G>A| |
S270 |
5 | BAA02g24180 | A02 | 13180370 | G | A | upstream_gene_variant | MODIFIER | c.-3411C>T| |
S203 |
6 | BAA02g24180 | A02 | 13180507 | G | A | upstream_gene_variant | MODIFIER | c.-3548C>T| |
S188 |
7 | BAA02g24180 | A02 | 13180956 | C | T | upstream_gene_variant | MODIFIER | c.-3997G>A| |
S182 |
8 | BAA02g24180 | A02 | 13181673 | G | A | upstream_gene_variant | MODIFIER | c.-4714C>T| |
S55 |
9 | BAA02g24180 | A02 | 13181883 | C | T | upstream_gene_variant | MODIFIER | c.-4924G>A| |
S33 |