Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06960 | A02 | 2974751 | G | A | missense_variant | MODERATE | c.197C>T|p.Thr66Ile |
S292 |