Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17650 | A02 | 8796635 | G | A | missense_variant | MODERATE | c.862G>A|p.Ala288Thr |
S296 |