| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g42750 | A09 | 49035265 | C | T | stop_gained | HIGH | c.519G>A|p.Trp173* |
S60 |
| 2 | BAA09g42750 | A09 | 49035611 | C | T | missense_variant | MODERATE | c.340G>A|p.Ala114Thr |
S245 |
| 3 | BAA09g42750 | A09 | 49036868 | C | A | upstream_gene_variant | MODIFIER | c.-918G>T| |
S169 |
| 4 | BAA09g42750 | A09 | 49037559 | C | T | upstream_gene_variant | MODIFIER | c.-1609G>A| |
S272 |
| 5 | BAA09g42750 | A09 | 49037857 | G | A | upstream_gene_variant | MODIFIER | c.-1907C>T| |
S281 |
| 6 | BAA09g42750 | A09 | 49037945 | C | T | upstream_gene_variant | MODIFIER | c.-1995G>A| |
S269 |
| 7 | BAA09g42750 | A09 | 49038618 | G | A | upstream_gene_variant | MODIFIER | c.-2668C>T| |
S171 |
| 8 | BAA09g42750 | A09 | 49039802 | G | A | upstream_gene_variant | MODIFIER | c.-3852C>T| |
S247 |