| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAS13g00140 | Scaffold13 | 4365518 | G | A | missense_variant | MODERATE | c.20G>A|p.Arg7Gln |
S59 |
| 2 | BAS13g00140 | Scaffold13 | 4366106 | G | A | synonymous_variant | LOW | c.222G>A|p.Gln74Gln |
S297 |
| 3 | BAS13g00140 | Scaffold13 | 4367237 | C | T | downstream_gene_variant | MODIFIER | c.*1089C>T| |
S6 |
| 4 | BAS13g00140 | Scaffold13 | 4370588 | C | T | downstream_gene_variant | MODIFIER | c.*4440C>T| |
S155 |
| 5 | BAS13g00140 | Scaffold13 | 4370930 | G | A | downstream_gene_variant | MODIFIER | c.*4782G>A| |
S271 |