| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g11390 | A02 | 5159168 | G | A | upstream_gene_variant | MODIFIER | c.-2202G>A| |
S298 |
| 2 | BAA02g11390 | A02 | 5159792 | C | T | upstream_gene_variant | MODIFIER | c.-1578C>T| |
S157 S163 |
| 3 | BAA02g11390 | A02 | 5160168 | C | T | upstream_gene_variant | MODIFIER | c.-1202C>T| |
S189 |
| 4 | BAA02g11390 | A02 | 5160293 | C | T | upstream_gene_variant | MODIFIER | c.-1077C>T| |
S171 |
| 5 | BAA02g11390 | A02 | 5161392 | C | T | missense_variant | MODERATE | c.23C>T|p.Ser8Phe |
S157 S163 |
| 6 | BAA02g11390 | A02 | 5161703 | G | A | missense_variant | MODERATE | c.334G>A|p.Asp112Asn |
S131 |
| 7 | BAA02g11390 | A02 | 5163545 | G | A | downstream_gene_variant | MODIFIER | c.*255G>A| |
S140 S219 S64 S72 |
| 8 | BAA02g11390 | A02 | 5164216 | C | T | downstream_gene_variant | MODIFIER | c.*926C>T| |
S243 |