| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g20660 | A09 | 12795550 | C | T | missense_variant | MODERATE | c.277G>A|p.Gly93Arg |
S283 |
| 2 | BAA09g20660 | A09 | 12796482 | G | A | upstream_gene_variant | MODIFIER | c.-406C>T| |
S40 S49 |
| 3 | BAA09g20660 | A09 | 12797156 | C | T | upstream_gene_variant | MODIFIER | c.-1080G>A| |
S134 |
| 4 | BAA09g20660 | A09 | 12797971 | G | A | upstream_gene_variant | MODIFIER | c.-1895C>T| |
S225 S40 S49 S73 |
| 5 | BAA09g20660 | A09 | 12798331 | C | T | upstream_gene_variant | MODIFIER | c.-2255G>A| |
S219 |
| 6 | BAA09g20660 | A09 | 12798955 | G | A | upstream_gene_variant | MODIFIER | c.-2879C>T| |
S20 |
| 7 | BAA09g20660 | A09 | 12801021 | G | A | upstream_gene_variant | MODIFIER | c.-4945C>T| |
S301 |
| 8 | BAA09g20660 | A09 | 12801058 | C | T | upstream_gene_variant | MODIFIER | c.-4982G>A| |
S107 |