| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g39050 | A01 | 25994407 | C | T | missense_variant | MODERATE | c.145C>T|p.Leu49Phe |
S272 |