Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41760 | A02 | 34936190 | C | T | missense_variant | MODERATE | c.244C>T|p.Leu82Phe |
S18 |