| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g01060 | A02 | 487201 | G | A | missense_variant | MODERATE | c.496G>A|p.Gly166Ser |
S187 |
| 2 | BAA02g01060 | A02 | 487600 | C | T | missense_variant | MODERATE | c.631C>T|p.Pro211Ser |
S306 S308 |
| 3 | BAA02g01060 | A02 | 487646 | C | T | missense_variant | MODERATE | c.677C>T|p.Ser226Phe |
S301 S304 |
| 4 | BAA02g01060 | A02 | 492056 | C | T | downstream_gene_variant | MODIFIER | c.*3931C>T| |
S178 |