| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g43950 | A09 | 49876847 | C | T | missense_variant | MODERATE | c.4022C>T|p.Pro1341Leu |
S303 |