Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09200 | A02 | 4066504 | C | T | missense_variant | MODERATE | c.232C>T|p.Arg78Cys |
S138 |