Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26660 | A10 | 21064826 | C | T | missense_variant | MODERATE | c.644C>T|p.Ser215Phe |
S203 |