| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g47230 | A09 | 51613898 | G | A | upstream_gene_variant | MODIFIER | c.-4482G>A| |
S110 |
| 2 | BAA09g47230 | A09 | 51613966 | G | A | upstream_gene_variant | MODIFIER | c.-4414G>A| |
S234 |
| 3 | BAA09g47230 | A09 | 51614462 | G | A | upstream_gene_variant | MODIFIER | c.-3918G>A| |
S12 |
| 4 | BAA09g47230 | A09 | 51615611 | C | T | upstream_gene_variant | MODIFIER | c.-2769C>T| |
S235 S236 S260 |
| 5 | BAA09g47230 | A09 | 51615774 | G | A | upstream_gene_variant | MODIFIER | c.-2606G>A| |
S189 |
| 6 | BAA09g47230 | A09 | 51616206 | C | T | upstream_gene_variant | MODIFIER | c.-2174C>T| |
S295 |
| 7 | BAA09g47230 | A09 | 51617198 | C | T | upstream_gene_variant | MODIFIER | c.-1182C>T| |
S122 |
| 8 | BAA09g47230 | A09 | 51617478 | G | A | upstream_gene_variant | MODIFIER | c.-902G>A| |
S1 |
| 9 | BAA09g47230 | A09 | 51617685 | C | T | upstream_gene_variant | MODIFIER | c.-695C>T| |
S297 |
| 10 | BAA09g47230 | A09 | 51618127 | C | T | upstream_gene_variant | MODIFIER | c.-253C>T| |
S213 |
| 11 | BAA09g47230 | A09 | 51619177 | G | A | synonymous_variant | LOW | c.453G>A|p.Thr151Thr |
S105 S106 |
| 12 | BAA09g47230 | A09 | 51619246 | C | T | synonymous_variant | LOW | c.522C>T|p.Leu174Leu |
S303 |
| 13 | BAA09g47230 | A09 | 51619619 | G | A | missense_variant | MODERATE | c.895G>A|p.Glu299Lys |
S13 |
| 14 | BAA09g47230 | A09 | 51620127 | C | T | missense_variant | MODERATE | c.1403C>T|p.Ala468Val |
S33 |
| 15 | BAA09g47230 | A09 | 51620720 | C | T | missense_variant | MODERATE | c.1996C>T|p.Pro666Ser |
S13 |
| 16 | BAA09g47230 | A09 | 51620848 | G | A | synonymous_variant | LOW | c.2124G>A|p.Leu708Leu |
S149 |
| 17 | BAA09g47230 | A09 | 51621380 | C | T | downstream_gene_variant | MODIFIER | c.*484C>T| |
S115 |