Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03580 | A02 | 1577290 | C | T | missense_variant | MODERATE | c.173C>T|p.Ser58Leu |
S94 |