Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g02150 | Scaffold13 | 18193907 | C | T | missense_variant | MODERATE | c.110C>T|p.Ala37Val |
S115 |