Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22110 | A02 | 11905545 | G | A | missense_variant | MODERATE | c.244C>T|p.Leu82Phe |
S228 |
2 | BAA02g22110 | A02 | 11906444 | C | T | upstream_gene_variant | MODIFIER | c.-656G>A| |
S179 |
3 | BAA02g22110 | A02 | 11907718 | G | A | upstream_gene_variant | MODIFIER | c.-1930C>T| |
S129 |
4 | BAA02g22110 | A02 | 11908265 | G | A | upstream_gene_variant | MODIFIER | c.-2477C>T| |
S228 |
5 | BAA02g22110 | A02 | 11908332 | C | T | upstream_gene_variant | MODIFIER | c.-2544G>A| |
S87 |
6 | BAA02g22110 | A02 | 11909055 | C | T | upstream_gene_variant | MODIFIER | c.-3267G>A| |
S138 |
7 | BAA02g22110 | A02 | 11909116 | G | A | upstream_gene_variant | MODIFIER | c.-3328C>T| |
S150 |
8 | BAA02g22110 | A02 | 11909135 | G | A | upstream_gene_variant | MODIFIER | c.-3347C>T| |
S269 |
9 | BAA02g22110 | A02 | 11909185 | C | T | upstream_gene_variant | MODIFIER | c.-3397G>A| |
S100 |
10 | BAA02g22110 | A02 | 11909489 | G | A | upstream_gene_variant | MODIFIER | c.-3701C>T| |
S17 |
11 | BAA02g22110 | A02 | 11909833 | G | A | upstream_gene_variant | MODIFIER | c.-4045C>T| |
S48 |
12 | BAA02g22110 | A02 | 11910714 | C | T | upstream_gene_variant | MODIFIER | c.-4926G>A| |
S64 |