Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g40760 | A05 | 39258067 | C | T | missense_variant | MODERATE | c.710C>T|p.Ala237Val |
S236 |