Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05730 | A08 | 4409320 | C | T | missense_variant | MODERATE | c.226G>A|p.Gly76Arg |
S245 |