Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00830 | Scaffold13 | 8117720 | T | G | missense_variant | MODERATE | c.1552A>C|p.Ile518Leu |
S203 |
2 | BAS13g00830 | Scaffold13 | 8117723 | G | A | stop_gained | HIGH | c.1549C>T|p.Gln517* |
S273 |
3 | BAS13g00830 | Scaffold13 | 8117724 | T | C | synonymous_variant | LOW | c.1548A>G|p.Ser516Ser |
S273 |