| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g32590 | A05 | 34697242 | G | A | upstream_gene_variant | MODIFIER | c.-2691G>A| |
S116 S295 |
| 2 | BAA05g32590 | A05 | 34697556 | C | T | upstream_gene_variant | MODIFIER | c.-2377C>T| |
S125 S257 |
| 3 | BAA05g32590 | A05 | 34698117 | G | A | upstream_gene_variant | MODIFIER | c.-1816G>A| |
S190 |
| 4 | BAA05g32590 | A05 | 34700807 | A | T | synonymous_variant | LOW | c.327A>T|p.Leu109Leu |
S13 S154 S169 S173 S201 S206 S208 S219 S232 S239 S26 S279 S306 S63 S64 S72 |
| 5 | BAA05g32590 | A05 | 34700811 | T | C | synonymous_variant | LOW | c.331T>C|p.Leu111Leu |
S13 S154 S169 S173 S201 S206 S208 S219 S232 S239 S26 S279 S306 S63 S64 S72 |
| 6 | BAA05g32590 | A05 | 34700831 | T | G | synonymous_variant | LOW | c.351T>G|p.Ala117Ala |
S160 |
| 7 | BAA05g32590 | A05 | 34700922 | G | A | missense_variant | MODERATE | c.442G>A|p.Val148Ile |
S282 |