Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40500 | A02 | 34134348 | C | T | missense_variant | MODERATE | c.136C>T|p.Leu46Phe |
S165 |