| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g66380 | A09 | 60706922 | G | A | missense_variant | MODERATE | c.3322C>T|p.Pro1108Ser |
S167 S69 |
| 2 | BAA09g66380 | A09 | 60708087 | C | T | missense_variant | MODERATE | c.2650G>A|p.Glu884Lys |
S169 |
| 3 | BAA09g66380 | A09 | 60710712 | G | A | synonymous_variant | LOW | c.1275C>T|p.Phe425Phe |
S79 S84 |
| 4 | BAA09g66380 | A09 | 60712009 | C | T | missense_variant | MODERATE | c.679G>A|p.Val227Ile |
S139 |
| 5 | BAA09g66380 | A09 | 60714281 | C | T | upstream_gene_variant | MODIFIER | c.-800G>A| |
S271 |
| 6 | BAA09g66380 | A09 | 60714387 | A | G | upstream_gene_variant | MODIFIER | c.-906T>C| |
S293 |
| 7 | BAA09g66380 | A09 | 60717453 | G | A | upstream_gene_variant | MODIFIER | c.-3972C>T| |
S263 |
| 8 | BAA09g66380 | A09 | 60718013 | G | A | upstream_gene_variant | MODIFIER | c.-4532C>T| |
S4 |