Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09670 | A02 | 4253589 | C | T | missense_variant | MODERATE | c.388G>A|p.Gly130Arg |
S18 |
2 | BAA02g09670 | A02 | 4255628 | G | A | upstream_gene_variant | MODIFIER | c.-1652C>T| |
S294 |
3 | BAA02g09670 | A02 | 4255718 | G | A | upstream_gene_variant | MODIFIER | c.-1742C>T| |
S10 |
4 | BAA02g09670 | A02 | 4257741 | C | T | upstream_gene_variant | MODIFIER | c.-3765G>A| |
S156 S34 |
5 | BAA02g09670 | A02 | 4258623 | C | T | upstream_gene_variant | MODIFIER | c.-4647G>A| |
S202 |