| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAS60g00160 | Scaffold60 | 2957181 | C | T | upstream_gene_variant | MODIFIER | c.-629C>T| |
S192 |
| 2 | BAS60g00160 | Scaffold60 | 2957284 | C | T | upstream_gene_variant | MODIFIER | c.-526C>T| |
S111 |
| 3 | BAS60g00160 | Scaffold60 | 2958960 | C | T | missense_variant&splice_region_variant | MODERATE | c.409C>T|p.Leu137Phe |
S133 |
| 4 | BAS60g00160 | Scaffold60 | 2959256 | C | T | synonymous_variant | LOW | c.609C>T|p.Tyr203Tyr |
S92 |
| 5 | BAS60g00160 | Scaffold60 | 2961491 | G | A | downstream_gene_variant | MODIFIER | c.*399G>A| |
S10 |