Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g38530 | A01 | 25709188 | C | T | missense_variant | MODERATE | c.626C>T|p.Thr209Met |
S7 |