Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47600 | A02 | 38345660 | C | T | upstream_gene_variant | MODIFIER | c.-644C>T| |
S38 |
2 | BAA02g47600 | A02 | 38345765 | C | T | upstream_gene_variant | MODIFIER | c.-539C>T| |
S252 |
3 | BAA02g47600 | A02 | 38347141 | C | T | intron_variant | MODIFIER | c.639+199C>T| |
S260 |
4 | BAA02g47600 | A02 | 38347298 | C | T | intron_variant | MODIFIER | c.639+356C>T| |
S249 |
5 | BAA02g47600 | A02 | 38348272 | G | A | missense_variant | MODERATE | c.694G>A|p.Asp232Asn |
S5 |
6 | BAA02g47600 | A02 | 38352872 | C | T | downstream_gene_variant | MODIFIER | c.*3960C>T| |
S117 S189 |
7 | BAA02g47600 | A02 | 38353323 | G | A | downstream_gene_variant | MODIFIER | c.*4411G>A| |
S67 |