| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g48170 | A02 | 38716599 | C | T | synonymous_variant | LOW | c.354C>T|p.Leu118Leu |
S176 |
| 2 | BAA02g48170 | A02 | 38716813 | G | A | missense_variant | MODERATE | c.568G>A|p.Gly190Ser |
S186 |
| 3 | BAA02g48170 | A02 | 38717007 | C | T | synonymous_variant | LOW | c.762C>T|p.Thr254Thr |
S221 |
| 4 | BAA02g48170 | A02 | 38717327 | G | A | missense_variant | MODERATE | c.1082G>A|p.Gly361Asp |
S223 |
| 5 | BAA02g48170 | A02 | 38720971 | G | A | downstream_gene_variant | MODIFIER | c.*2809G>A| |
S132 S137 S215 |
| 6 | BAA02g48170 | A02 | 38722308 | G | A | downstream_gene_variant | MODIFIER | c.*4146G>A| |
S268 |