| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g00870 | A09 | 663848 | G | A | upstream_gene_variant | MODIFIER | c.-2519G>A| |
S153 S213 |
| 2 | BAA09g00870 | A09 | 663986 | G | A | upstream_gene_variant | MODIFIER | c.-2381G>A| |
S65 |
| 3 | BAA09g00870 | A09 | 664144 | G | A | upstream_gene_variant | MODIFIER | c.-2223G>A| |
S308 |
| 4 | BAA09g00870 | A09 | 666387 | C | T | synonymous_variant | LOW | c.21C>T|p.Leu7Leu |
S196 |
| 5 | BAA09g00870 | A09 | 666544 | C | T | missense_variant | MODERATE | c.178C>T|p.Pro60Ser |
S183 S198 |
| 6 | BAA09g00870 | A09 | 666571 | G | A | missense_variant | MODERATE | c.205G>A|p.Ala69Thr |
S204 |
| 7 | BAA09g00870 | A09 | 666633 | C | T | synonymous_variant | LOW | c.267C>T|p.Leu89Leu |
S247 |
| 8 | BAA09g00870 | A09 | 666772 | G | A | missense_variant | MODERATE | c.406G>A|p.Gly136Ser |
S60 |
| 9 | BAA09g00870 | A09 | 666993 | G | A | synonymous_variant | LOW | c.627G>A|p.Arg209Arg |
S110 |
| 10 | BAA09g00870 | A09 | 667518 | G | A | synonymous_variant | LOW | c.1152G>A|p.Glu384Glu |
S187 |
| 11 | BAA09g00870 | A09 | 667710 | C | T | synonymous_variant | LOW | c.1344C>T|p.Tyr448Tyr |
S244 |
| 12 | BAA09g00870 | A09 | 672287 | C | T | downstream_gene_variant | MODIFIER | c.*4382C>T| |
S158 |