Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19980 | A02 | 10509234 | G | T | downstream_gene_variant | MODIFIER | c.*3807C>A| |
S294 |
2 | BAA02g19980 | A02 | 10510291 | C | T | downstream_gene_variant | MODIFIER | c.*2750G>A| |
S233 |
3 | BAA02g19980 | A02 | 10513038 | C | T | downstream_gene_variant | MODIFIER | c.*3G>A| |
S174 |
4 | BAA02g19980 | A02 | 10513582 | A | G | upstream_gene_variant | MODIFIER | c.-359T>C| |
S133 |
5 | BAA02g19980 | A02 | 10516322 | G | A | upstream_gene_variant | MODIFIER | c.-3099C>T| |
S116 |
6 | BAA02g19980 | A02 | 10516361 | C | T | upstream_gene_variant | MODIFIER | c.-3138G>A| |
S138 |
7 | BAA02g19980 | A02 | 10516836 | G | A | upstream_gene_variant | MODIFIER | c.-3613C>T| |
S133 S172 S217 |
8 | BAA02g19980 | A02 | 10517367 | G | A | upstream_gene_variant | MODIFIER | c.-4144C>T| |
S238 |
9 | BAA02g19980 | A02 | 10517727 | C | T | upstream_gene_variant | MODIFIER | c.-4504G>A| |
S268 |