| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g09190 | A02 | 4062163 | C | T | synonymous_variant | LOW | c.1746G>A|p.Gly582Gly |
S6 |
| 2 | BAA02g09190 | A02 | 4063346 | C | T | synonymous_variant | LOW | c.957G>A|p.Gln319Gln |
S268 |
| 3 | BAA02g09190 | A02 | 4063782 | G | A | missense_variant | MODERATE | c.802C>T|p.His268Tyr |
S18 S221 S252 |
| 4 | BAA02g09190 | A02 | 4064869 | C | A | missense_variant | MODERATE | c.11G>T|p.Arg4Leu |
S241 |
| 5 | BAA02g09190 | A02 | 4067126 | G | A | upstream_gene_variant | MODIFIER | c.-2247C>T| |
S69 |
| 6 | BAA02g09190 | A02 | 4068370 | C | T | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S286 |
| 7 | BAA02g09190 | A02 | 4068437 | G | A | upstream_gene_variant | MODIFIER | c.-3558C>T| |
S231 |