| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g24830 | A03 | 11369183 | C | T | upstream_gene_variant | MODIFIER | c.-1672C>T| |
S272 |
| 2 | BAA03g24830 | A03 | 11369622 | G | A | upstream_gene_variant | MODIFIER | c.-1233G>A| |
S262 |
| 3 | BAA03g24830 | A03 | 11369809 | C | T | upstream_gene_variant | MODIFIER | c.-1046C>T| |
S173 |
| 4 | BAA03g24830 | A03 | 11369921 | G | A | upstream_gene_variant | MODIFIER | c.-934G>A| |
S206 S26 |
| 5 | BAA03g24830 | A03 | 11370339 | C | T | upstream_gene_variant | MODIFIER | c.-516C>T| |
S205 |
| 6 | BAA03g24830 | A03 | 11370655 | G | A | upstream_gene_variant | MODIFIER | c.-200G>A| |
S94 |
| 7 | BAA03g24830 | A03 | 11371122 | C | T | missense_variant | MODERATE | c.268C>T|p.Pro90Ser |
S263 |
| 8 | BAA03g24830 | A03 | 11371136 | A | T | synonymous_variant | LOW | c.282A>T|p.Pro94Pro |
S108 S201 S238 S239 S267 |
| 9 | BAA03g24830 | A03 | 11371143 | G | A | missense_variant | MODERATE | c.289G>A|p.Ala97Thr |
S108 S201 S238 S239 S267 |
| 10 | BAA03g24830 | A03 | 11371152 | A | C | missense_variant | MODERATE | c.298A>C|p.Asn100His |
S108 S201 S238 S239 S267 |
| 11 | BAA03g24830 | A03 | 11371154 | T | A | missense_variant | MODERATE | c.300T>A|p.Asn100Lys |
S108 S201 S238 S239 S267 |
| 12 | BAA03g24830 | A03 | 11371167 | G | C | missense_variant | MODERATE | c.313G>C|p.Val105Leu |
S108 S201 S238 S239 S267 |
| 13 | BAA03g24830 | A03 | 11371187 | T | C | synonymous_variant | LOW | c.333T>C|p.Leu111Leu |
S201 S238 S239 S267 |
| 14 | BAA03g24830 | A03 | 11375661 | C | T | downstream_gene_variant | MODIFIER | c.*4360C>T| |
S159 S243 |
| 15 | BAA03g24830 | A03 | 11375784 | C | T | downstream_gene_variant | MODIFIER | c.*4483C>T| |
S81 S85 |