Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05790 | A02 | 2470027 | C | T | missense_variant | MODERATE | c.754C>T|p.Leu252Phe |
S275 |
2 | BAA02g05790 | A02 | 2470904 | C | T | missense_variant | MODERATE | c.1192C>T|p.Leu398Phe |
S104 |
3 | BAA02g05790 | A02 | 2471413 | C | T | downstream_gene_variant | MODIFIER | c.*221C>T| |
S229 |
4 | BAA02g05790 | A02 | 2472159 | G | A | downstream_gene_variant | MODIFIER | c.*967G>A| |
S244 S289 S290 |