Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18470 | A10 | 17258682 | C | T | missense_variant | MODERATE | c.169G>A|p.Gly57Arg |
S186 |