| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g26630 | A09 | 17341961 | G | A | upstream_gene_variant | MODIFIER | c.-4567G>A| |
S175 |
| 2 | BAA09g26630 | A09 | 17343045 | G | A | upstream_gene_variant | MODIFIER | c.-3483G>A| |
S280 |
| 3 | BAA09g26630 | A09 | 17344076 | C | T | upstream_gene_variant | MODIFIER | c.-2452C>T| |
S292 |
| 4 | BAA09g26630 | A09 | 17344336 | C | T | upstream_gene_variant | MODIFIER | c.-2192C>T| |
S283 |
| 5 | BAA09g26630 | A09 | 17344643 | G | A | upstream_gene_variant | MODIFIER | c.-1885G>A| |
S196 |
| 6 | BAA09g26630 | A09 | 17344675 | C | T | upstream_gene_variant | MODIFIER | c.-1853C>T| |
S261 |
| 7 | BAA09g26630 | A09 | 17347684 | G | A | missense_variant | MODERATE | c.896G>A|p.Arg299Gln |
S185 |
| 8 | BAA09g26630 | A09 | 17348015 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1045-1G>A| |
S79 S84 |
| 9 | BAA09g26630 | A09 | 17349270 | G | A | missense_variant | MODERATE | c.1198G>A|p.Ala400Thr |
S185 |
| 10 | BAA09g26630 | A09 | 17349753 | C | T | downstream_gene_variant | MODIFIER | c.*289C>T| |
S159 S243 S299 |