Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS60g00040 | Scaffold60 | 1875821 | G | A | splice_region_variant&synonymous_variant | LOW | c.105G>A|p.Arg35Arg |
S288 |
2 | BAS60g00040 | Scaffold60 | 1876807 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.179-1G>A| |
S13 |
3 | BAS60g00040 | Scaffold60 | 1876864 | C | T | missense_variant | MODERATE | c.235C>T|p.Pro79Ser |
S3 |
4 | BAS60g00040 | Scaffold60 | 1881382 | C | T | intron_variant | MODIFIER | c.1154-368C>T| |
S64 |
5 | BAS60g00040 | Scaffold60 | 1881709 | C | T | intron_variant | MODIFIER | c.1154-41C>T| |
S180 |
6 | BAS60g00040 | Scaffold60 | 1883530 | G | A | downstream_gene_variant | MODIFIER | c.*1481G>A| |
S25 |