Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46530 | A02 | 37801268 | C | T | missense_variant | MODERATE | c.73C>T|p.Leu25Phe |
S122 |