Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39890 | A02 | 33762224 | G | A | missense_variant | MODERATE | c.148G>A|p.Asp50Asn |
S176 |