| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g11580 | A09 | 6493547 | C | T | upstream_gene_variant | MODIFIER | c.-2462C>T| |
S59 |
| 2 | BAA09g11580 | A09 | 6494326 | C | T | upstream_gene_variant | MODIFIER | c.-1683C>T| |
S132 S137 S215 |
| 3 | BAA09g11580 | A09 | 6494437 | G | A | upstream_gene_variant | MODIFIER | c.-1572G>A| |
S267 |
| 4 | BAA09g11580 | A09 | 6494520 | G | A | upstream_gene_variant | MODIFIER | c.-1489G>A| |
S159 S243 |
| 5 | BAA09g11580 | A09 | 6494711 | C | T | upstream_gene_variant | MODIFIER | c.-1298C>T| |
S94 |
| 6 | BAA09g11580 | A09 | 6495393 | G | A | upstream_gene_variant | MODIFIER | c.-616G>A| |
S12 |
| 7 | BAA09g11580 | A09 | 6496290 | C | T | synonymous_variant | LOW | c.282C>T|p.Phe94Phe |
S66 |
| 8 | BAA09g11580 | A09 | 6496360 | G | A | missense_variant | MODERATE | c.352G>A|p.Gly118Arg |
S259 |
| 9 | BAA09g11580 | A09 | 6496535 | C | T | missense_variant | MODERATE | c.527C>T|p.Thr176Ile |
S132 S137 S215 S89 |
| 10 | BAA09g11580 | A09 | 6498383 | C | T | stop_gained | HIGH | c.1132C>T|p.Arg378* |
S302 |