| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g17700 | A10 | 16902206 | C | T | missense_variant | MODERATE | c.8C>T|p.Pro3Leu |
S47 |