Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26760 | A02 | 14974350 | G | A | upstream_gene_variant | MODIFIER | c.-4800G>A| |
S197 |
2 | BAA02g26760 | A02 | 14974482 | G | A | upstream_gene_variant | MODIFIER | c.-4668G>A| |
S126 |
3 | BAA02g26760 | A02 | 14974999 | C | T | upstream_gene_variant | MODIFIER | c.-4151C>T| |
S245 |
4 | BAA02g26760 | A02 | 14975083 | G | A | upstream_gene_variant | MODIFIER | c.-4067G>A| |
S202 S228 |
5 | BAA02g26760 | A02 | 14976082 | C | T | upstream_gene_variant | MODIFIER | c.-3068C>T| |
S283 |
6 | BAA02g26760 | A02 | 14977584 | C | T | upstream_gene_variant | MODIFIER | c.-1566C>T| |
S104 S52 |
7 | BAA02g26760 | A02 | 14978974 | G | A | upstream_gene_variant | MODIFIER | c.-176G>A| |
S148 S30 S31 |
8 | BAA02g26760 | A02 | 14979537 | C | T | intron_variant | MODIFIER | c.288+32C>T| |
S130 |
9 | BAA02g26760 | A02 | 14979728 | G | A | intron_variant | MODIFIER | c.349-63G>A| |
S251 S45 |
10 | BAA02g26760 | A02 | 14980146 | C | T | intron_variant | MODIFIER | c.609+13C>T| |
S157 S163 |
11 | BAA02g26760 | A02 | 14980887 | G | A | downstream_gene_variant | MODIFIER | c.*618G>A| |
S245 |
12 | BAA02g26760 | A02 | 14982042 | G | A | downstream_gene_variant | MODIFIER | c.*1773G>A| |
S34 |
13 | BAA02g26760 | A02 | 14982592 | G | A | downstream_gene_variant | MODIFIER | c.*2323G>A| |
S148 S30 S31 |