| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAS13g00160 | Scaffold13 | 4403267 | C | T | missense_variant | MODERATE | c.1822G>A|p.Ala608Thr |
S206 S26 |
| 2 | BAS13g00160 | Scaffold13 | 4403975 | G | A | missense_variant | MODERATE | c.1259C>T|p.Ser420Phe |
S59 |
| 3 | BAS13g00160 | Scaffold13 | 4405092 | C | T | missense_variant | MODERATE | c.502G>A|p.Asp168Asn |
S8 |
| 4 | BAS13g00160 | Scaffold13 | 4405819 | G | A | missense_variant | MODERATE | c.11C>T|p.Ser4Phe |
S75 |
| 5 | BAS13g00160 | Scaffold13 | 4406480 | A | G | upstream_gene_variant | MODIFIER | c.-651T>C| |
S18 |