| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g27050 | A10 | 21198519 | C | T | missense_variant | MODERATE | c.503C>T|p.Ser168Leu |
S42 |