| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g44650 | A09 | 50212305 | C | T | missense_variant | MODERATE | c.535G>A|p.Asp179Asn |
S121 |
| 2 | BAA09g44650 | A09 | 50216832 | C | T | upstream_gene_variant | MODIFIER | c.-3993G>A| |
S139 |
| 3 | BAA09g44650 | A09 | 50217053 | C | T | upstream_gene_variant | MODIFIER | c.-4214G>A| |
S30 S31 |