| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g69860 | A09 | 62176111 | G | A | upstream_gene_variant | MODIFIER | c.-4017G>A| |
S68 |
| 2 | BAA09g69860 | A09 | 62176601 | G | A | upstream_gene_variant | MODIFIER | c.-3527G>A| |
S159 S187 S243 S276 S298 S299 |
| 3 | BAA09g69860 | A09 | 62181587 | G | A | missense_variant | MODERATE | c.664G>A|p.Val222Ile |
S244 |
| 4 | BAA09g69860 | A09 | 62181627 | C | T | missense_variant | MODERATE | c.704C>T|p.Ser235Phe |
S117 |
| 5 | BAA09g69860 | A09 | 62182587 | G | A | missense_variant | MODERATE | c.1219G>A|p.Ala407Thr |
S151 |
| 6 | BAA09g69860 | A09 | 62182751 | G | A | synonymous_variant | LOW | c.1317G>A|p.Glu439Glu |
S295 |
| 7 | BAA09g69860 | A09 | 62182779 | C | T | synonymous_variant | LOW | c.1345C>T|p.Leu449Leu |
S87 |
| 8 | BAA09g69860 | A09 | 62183621 | C | T | missense_variant | MODERATE | c.1778C>T|p.Ser593Leu |
S257 |