Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08120 | A10 | 5544090 | C | T | upstream_gene_variant | MODIFIER | c.-4287C>T| |
S40 S49 |
2 | BAA10g08120 | A10 | 5544181 | C | T | upstream_gene_variant | MODIFIER | c.-4196C>T| |
S10 |
3 | BAA10g08120 | A10 | 5544311 | C | T | upstream_gene_variant | MODIFIER | c.-4066C>T| |
S286 |
4 | BAA10g08120 | A10 | 5544447 | G | A | upstream_gene_variant | MODIFIER | c.-3930G>A| |
S290 |
5 | BAA10g08120 | A10 | 5544522 | G | A | upstream_gene_variant | MODIFIER | c.-3855G>A| |
S69 |
6 | BAA10g08120 | A10 | 5544787 | C | T | upstream_gene_variant | MODIFIER | c.-3590C>T| |
S208 S93 |
7 | BAA10g08120 | A10 | 5545094 | C | T | upstream_gene_variant | MODIFIER | c.-3283C>T| |
S63 |
8 | BAA10g08120 | A10 | 5545292 | G | A | upstream_gene_variant | MODIFIER | c.-3085G>A| |
S45 |
9 | BAA10g08120 | A10 | 5545566 | C | T | upstream_gene_variant | MODIFIER | c.-2811C>T| |
S177 |
10 | BAA10g08120 | A10 | 5545752 | C | T | upstream_gene_variant | MODIFIER | c.-2625C>T| |
S146 |
11 | BAA10g08120 | A10 | 5545786 | G | A | upstream_gene_variant | MODIFIER | c.-2591G>A| |
S230 |
12 | BAA10g08120 | A10 | 5546955 | C | T | upstream_gene_variant | MODIFIER | c.-1422C>T| |
S88 |
13 | BAA10g08120 | A10 | 5546959 | C | T | upstream_gene_variant | MODIFIER | c.-1418C>T| |
S191 |
14 | BAA10g08120 | A10 | 5547141 | C | T | upstream_gene_variant | MODIFIER | c.-1236C>T| |
S199 |
15 | BAA10g08120 | A10 | 5547239 | C | T | upstream_gene_variant | MODIFIER | c.-1138C>T| |
S275 |
16 | BAA10g08120 | A10 | 5547443 | T | A | upstream_gene_variant | MODIFIER | c.-934T>A| |
S235 |
17 | BAA10g08120 | A10 | 5547778 | C | T | upstream_gene_variant | MODIFIER | c.-599C>T| |
S272 |