Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13840 | A02 | 6465005 | C | T | missense_variant | MODERATE | c.214C>T|p.His72Tyr |
S9 |