| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g01860 | A05 | 1024186 | C | T | missense_variant | MODERATE | c.1243G>A|p.Asp415Asn |
S84 |
| 2 | BAA05g01860 | A05 | 1024574 | C | T | synonymous_variant | LOW | c.855G>A|p.Glu285Glu |
S121 |
| 3 | BAA05g01860 | A05 | 1024591 | C | T | missense_variant | MODERATE | c.838G>A|p.Ala280Thr |
S17 |
| 4 | BAA05g01860 | A05 | 1024889 | C | T | synonymous_variant | LOW | c.540G>A|p.Arg180Arg |
S247 |
| 5 | BAA05g01860 | A05 | 1025291 | G | A | synonymous_variant | LOW | c.138C>T|p.Leu46Leu |
S233 |
| 6 | BAA05g01860 | A05 | 1027866 | G | A | upstream_gene_variant | MODIFIER | c.-2438C>T| |
S122 |
| 7 | BAA05g01860 | A05 | 1028671 | G | T | upstream_gene_variant | MODIFIER | c.-3243C>A| |
S208 S225 S247 S308 S37 S56 |
| 8 | BAA05g01860 | A05 | 1028959 | G | A | upstream_gene_variant | MODIFIER | c.-3531C>T| |
S276 |