Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27930 | A02 | 15733070 | G | A | missense_variant | MODERATE | c.664G>A|p.Gly222Ser |
S36 |