Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38630 | A02 | 32894954 | G | A | missense_variant | MODERATE | c.149C>T|p.Thr50Met |
S11 |