Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09960 | A02 | 4393743 | G | A | upstream_gene_variant | MODIFIER | c.-4532G>A| |
S161 |
2 | BAA02g09960 | A02 | 4393791 | C | T | upstream_gene_variant | MODIFIER | c.-4484C>T| |
S189 |
3 | BAA02g09960 | A02 | 4395070 | C | T | upstream_gene_variant | MODIFIER | c.-3205C>T| |
S135 |
4 | BAA02g09960 | A02 | 4395858 | C | T | upstream_gene_variant | MODIFIER | c.-2417C>T| |
S156 S34 |
5 | BAA02g09960 | A02 | 4396467 | G | A | upstream_gene_variant | MODIFIER | c.-1808G>A| |
S53 |
6 | BAA02g09960 | A02 | 4396573 | G | A | upstream_gene_variant | MODIFIER | c.-1702G>A| |
S282 |
7 | BAA02g09960 | A02 | 4396852 | G | A | upstream_gene_variant | MODIFIER | c.-1423G>A| |
S260 |
8 | BAA02g09960 | A02 | 4396935 | G | A | upstream_gene_variant | MODIFIER | c.-1340G>A| |
S150 |
9 | BAA02g09960 | A02 | 4397980 | C | T | upstream_gene_variant | MODIFIER | c.-295C>T| |
S168 |
10 | BAA02g09960 | A02 | 4398379 | G | A | stop_gained | HIGH | c.105G>A|p.Trp35* |
S187 |
11 | BAA02g09960 | A02 | 4404705 | G | A | downstream_gene_variant | MODIFIER | c.*4143G>A| |
S149 |