Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g34200 | A10 | 24113766 | C | T | missense_variant | MODERATE | c.422C>T|p.Ser141Leu |
S48 |