Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45210 | A02 | 37081043 | C | T | missense_variant | MODERATE | c.170C>T|p.Ser57Phe |
S182 |