| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g18580 | A05 | 10695627 | C | T | missense_variant | MODERATE | c.461G>A|p.Arg154Gln |
S149 |
| 2 | BAA05g18580 | A05 | 10697680 | T | C | upstream_gene_variant | MODIFIER | c.-846A>G| |
S294 |
| 3 | BAA05g18580 | A05 | 10697818 | C | T | upstream_gene_variant | MODIFIER | c.-984G>A| |
S117 |
| 4 | BAA05g18580 | A05 | 10697823 | G | A | upstream_gene_variant | MODIFIER | c.-989C>T| |
S308 |
| 5 | BAA05g18580 | A05 | 10697828 | C | T | upstream_gene_variant | MODIFIER | c.-994G>A| |
S61 |
| 6 | BAA05g18580 | A05 | 10699020 | G | A | upstream_gene_variant | MODIFIER | c.-2186C>T| |
S11 |
| 7 | BAA05g18580 | A05 | 10699058 | C | T | upstream_gene_variant | MODIFIER | c.-2224G>A| |
S227 S258 |
| 8 | BAA05g18580 | A05 | 10700068 | C | T | upstream_gene_variant | MODIFIER | c.-3234G>A| |
S99 |
| 9 | BAA05g18580 | A05 | 10700808 | C | T | upstream_gene_variant | MODIFIER | c.-3974G>A| |
S2 |