Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46670 | A02 | 37874015 | G | A | missense_variant | MODERATE | c.295G>A|p.Ala99Thr |
S200 |