Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26600 | A02 | 14884022 | C | T | upstream_gene_variant | MODIFIER | c.-2826C>T| |
S271 |
2 | BAA02g26600 | A02 | 14884213 | C | T | upstream_gene_variant | MODIFIER | c.-2635C>T| |
S6 |
3 | BAA02g26600 | A02 | 14884343 | C | T | upstream_gene_variant | MODIFIER | c.-2505C>T| |
S97 |
4 | BAA02g26600 | A02 | 14884723 | G | A | upstream_gene_variant | MODIFIER | c.-2125G>A| |
S144 |
5 | BAA02g26600 | A02 | 14884991 | C | T | upstream_gene_variant | MODIFIER | c.-1857C>T| |
S283 |
6 | BAA02g26600 | A02 | 14885558 | G | A | upstream_gene_variant | MODIFIER | c.-1290G>A| |
S229 |
7 | BAA02g26600 | A02 | 14885727 | C | T | upstream_gene_variant | MODIFIER | c.-1121C>T| |
S164 |
8 | BAA02g26600 | A02 | 14889624 | G | A | downstream_gene_variant | MODIFIER | c.*2462G>A| |
S25 |
9 | BAA02g26600 | A02 | 14892159 | G | A | downstream_gene_variant | MODIFIER | c.*4997G>A| |
S5 |