| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10390 | A02 | 4597781 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.221-1G>A| |
S129 |
| 2 | BAA02g10390 | A02 | 4598013 | G | A | missense_variant | MODERATE | c.188C>T|p.Thr63Ile |
S280 |
| 3 | BAA02g10390 | A02 | 4601361 | G | A | upstream_gene_variant | MODIFIER | c.-3161C>T| |
S62 |