Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34180 | A02 | 29298190 | C | T | missense_variant | MODERATE | c.191C>T|p.Ala64Val |
S282 |