Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49200 | A09 | 52669722 | C | T | missense_variant | MODERATE | c.440C>T|p.Ser147Phe |
S35 |