| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAS13g01770 | Scaffold13 | 14588968 | G | A | missense_variant | MODERATE | c.646C>T|p.Pro216Ser |
S209 |
| 2 | BAS13g01770 | Scaffold13 | 14589016 | C | T | missense_variant | MODERATE | c.598G>A|p.Glu200Lys |
S54 |
| 3 | BAS13g01770 | Scaffold13 | 14589217 | C | T | missense_variant&splice_region_variant | MODERATE | c.470G>A|p.Arg157Gln |
S206 |