Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18880 | A10 | 17512863 | C | T | missense_variant | MODERATE | c.223C>T|p.Arg75Trp |
S231 |