Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42030 | A02 | 35065063 | C | T | missense_variant | MODERATE | c.182C>T|p.Pro61Leu |
S112 |