Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00180 | Scaffold13 | 4437633 | G | A | upstream_gene_variant | MODIFIER | c.-1365G>A| |
S192 |
2 | BAS13g00180 | Scaffold13 | 4437732 | G | A | upstream_gene_variant | MODIFIER | c.-1266G>A| |
S176 |
3 | BAS13g00180 | Scaffold13 | 4437937 | G | A | upstream_gene_variant | MODIFIER | c.-1061G>A| |
S289 S290 |
4 | BAS13g00180 | Scaffold13 | 4438857 | C | T | upstream_gene_variant | MODIFIER | c.-141C>T| |
S270 |
5 | BAS13g00180 | Scaffold13 | 4439115 | G | A | missense_variant | MODERATE | c.118G>A|p.Glu40Lys |
S58 |
6 | BAS13g00180 | Scaffold13 | 4440757 | G | A | downstream_gene_variant | MODIFIER | c.*1106G>A| |
S20 |
7 | BAS13g00180 | Scaffold13 | 4440776 | G | A | downstream_gene_variant | MODIFIER | c.*1125G>A| |
S246 |
8 | BAS13g00180 | Scaffold13 | 4441570 | G | A | downstream_gene_variant | MODIFIER | c.*1919G>A| |
S179 |
9 | BAS13g00180 | Scaffold13 | 4441669 | C | T | downstream_gene_variant | MODIFIER | c.*2018C>T| |
S303 |
10 | BAS13g00180 | Scaffold13 | 4441948 | C | T | downstream_gene_variant | MODIFIER | c.*2297C>T| |
S286 |
11 | BAS13g00180 | Scaffold13 | 4441970 | G | A | downstream_gene_variant | MODIFIER | c.*2319G>A| |
S202 |
12 | BAS13g00180 | Scaffold13 | 4442645 | G | A | downstream_gene_variant | MODIFIER | c.*2994G>A| |
S32 |
13 | BAS13g00180 | Scaffold13 | 4442905 | G | A | downstream_gene_variant | MODIFIER | c.*3254G>A| |
S35 |
14 | BAS13g00180 | Scaffold13 | 4442988 | G | A | downstream_gene_variant | MODIFIER | c.*3337G>A| |
S229 |
15 | BAS13g00180 | Scaffold13 | 4443279 | G | A | downstream_gene_variant | MODIFIER | c.*3628G>A| |
S176 |
16 | BAS13g00180 | Scaffold13 | 4443462 | C | T | downstream_gene_variant | MODIFIER | c.*3811C>T| |
S209 |
17 | BAS13g00180 | Scaffold13 | 4443889 | G | A | downstream_gene_variant | MODIFIER | c.*4238G>A| |
S263 |
18 | BAS13g00180 | Scaffold13 | 4444075 | C | T | downstream_gene_variant | MODIFIER | c.*4424C>T| |
S138 |
19 | BAS13g00180 | Scaffold13 | 4444579 | G | A | downstream_gene_variant | MODIFIER | c.*4928G>A| |
S194 |