| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g05990 | A10 | 3071826 | C | T | missense_variant | MODERATE | c.323C>T|p.Ser108Phe |
S139 |