Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19900 | A01 | 9800658 | C | T | missense_variant | MODERATE | c.803C>T|p.Ser268Phe |
S66 |