| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g52100 | A09 | 54063741 | C | T | missense_variant | MODERATE | c.292C>T|p.Pro98Ser |
S7 |