Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46540 | A02 | 37805818 | C | T | missense_variant | MODERATE | c.344C>T|p.Ala115Val |
S262 |