Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44170 | A02 | 36458667 | G | A | downstream_gene_variant | MODIFIER | c.*2262C>T| |
S146 |
2 | BAA02g44170 | A02 | 36462545 | G | A | upstream_gene_variant | MODIFIER | c.-373C>T| |
S6 |
3 | BAA02g44170 | A02 | 36462696 | C | T | upstream_gene_variant | MODIFIER | c.-524G>A| |
S15 |
4 | BAA02g44170 | A02 | 36463080 | C | T | upstream_gene_variant | MODIFIER | c.-908G>A| |
S237 |
5 | BAA02g44170 | A02 | 36463606 | C | T | upstream_gene_variant | MODIFIER | c.-1434G>A| |
S301 S304 |
6 | BAA02g44170 | A02 | 36463880 | T | A | upstream_gene_variant | MODIFIER | c.-1708A>T| |
S156 |
7 | BAA02g44170 | A02 | 36464344 | C | T | upstream_gene_variant | MODIFIER | c.-2172G>A| |
S162 |
8 | BAA02g44170 | A02 | 36465387 | C | T | upstream_gene_variant | MODIFIER | c.-3215G>A| |
S270 S67 |
9 | BAA02g44170 | A02 | 36466225 | C | T | upstream_gene_variant | MODIFIER | c.-4053G>A| |
S121 |
10 | BAA02g44170 | A02 | 36466758 | G | A | upstream_gene_variant | MODIFIER | c.-4586C>T| |
S297 |