Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47180 | A02 | 38110585 | C | T | missense_variant | MODERATE | c.1381C>T|p.Pro461Ser |
S256 |