| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g22760 | A02 | 12331283 | C | T | upstream_gene_variant | MODIFIER | c.-2907C>T| |
S246 |
| 2 | BAA02g22760 | A02 | 12332062 | C | T | upstream_gene_variant | MODIFIER | c.-2128C>T| |
S240 |
| 3 | BAA02g22760 | A02 | 12338815 | G | A | missense_variant | MODERATE | c.79G>A|p.Ala27Thr |
S157 S166 S167 S257 |
| 4 | BAA02g22760 | A02 | 12339020 | G | A | missense_variant | MODERATE | c.224G>A|p.Ser75Asn |
S61 |
| 5 | BAA02g22760 | A02 | 12339241 | C | T | missense_variant | MODERATE | c.445C>T|p.Leu149Phe |
S286 |
| 6 | BAA02g22760 | A02 | 12339353 | C | T | missense_variant | MODERATE | c.557C>T|p.Ser186Leu |
S117 |
| 7 | BAA02g22760 | A02 | 12339384 | C | T | downstream_gene_variant | MODIFIER | c.*18C>T| |
S75 S81 |
| 8 | BAA02g22760 | A02 | 12339413 | C | T | downstream_gene_variant | MODIFIER | c.*47C>T| |
S40 S49 |
| 9 | BAA02g22760 | A02 | 12339586 | G | A | downstream_gene_variant | MODIFIER | c.*220G>A| |
S64 |
| 10 | BAA02g22760 | A02 | 12339746 | G | A | downstream_gene_variant | MODIFIER | c.*380G>A| |
S146 |
| 11 | BAA02g22760 | A02 | 12339748 | G | A | downstream_gene_variant | MODIFIER | c.*382G>A| |
S12 |
| 12 | BAA02g22760 | A02 | 12339906 | C | T | downstream_gene_variant | MODIFIER | c.*540C>T| |
S164 |