| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10690 | A02 | 4773694 | C | T | missense_variant | MODERATE | c.1576G>A|p.Gly526Arg |
S116 |
| 2 | BAA02g10690 | A02 | 4775962 | C | T | missense_variant | MODERATE | c.200G>A|p.Gly67Glu |
S255 |
| 3 | BAA02g10690 | A02 | 4776683 | C | T | upstream_gene_variant | MODIFIER | c.-381G>A| |
S97 |
| 4 | BAA02g10690 | A02 | 4780890 | C | T | upstream_gene_variant | MODIFIER | c.-4588G>A| |
S305 |