| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10680 | A02 | 4772424 | C | T | missense_variant | MODERATE | c.491C>T|p.Ser164Phe |
S186 S268 |
| 2 | BAA02g10680 | A02 | 4772756 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.637-1G>A| |
S166 |
| 3 | BAA02g10680 | A02 | 4773248 | G | A | synonymous_variant | LOW | c.1038G>A|p.Lys346Lys |
S191 |