| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAS13g00190 | Scaffold13 | 4439671 | G | A | upstream_gene_variant | MODIFIER | c.-1G>A| |
S292 |
| 2 | BAS13g00190 | Scaffold13 | 4439714 | G | A | missense_variant | MODERATE | c.43G>A|p.Gly15Arg |
S207 |
| 3 | BAS13g00190 | Scaffold13 | 4439816 | G | A | missense_variant | MODERATE | c.145G>A|p.Ala49Thr |
S199 |
| 4 | BAS13g00190 | Scaffold13 | 4439951 | C | T | splice_region_variant&intron_variant | LOW | c.203-8C>T| |
S245 |
| 5 | BAS13g00190 | Scaffold13 | 4439979 | C | T | synonymous_variant | LOW | c.223C>T|p.Leu75Leu |
S170 |