Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00170 | Scaffold13 | 4418249 | G | A | downstream_gene_variant | MODIFIER | c.*4746C>T| |
S281 |
2 | BAS13g00170 | Scaffold13 | 4418567 | C | T | downstream_gene_variant | MODIFIER | c.*4428G>A| |
S148 S210 |
3 | BAS13g00170 | Scaffold13 | 4418831 | G | A | downstream_gene_variant | MODIFIER | c.*4164C>T| |
S210 S225 |
4 | BAS13g00170 | Scaffold13 | 4419394 | G | A | downstream_gene_variant | MODIFIER | c.*3601C>T| |
S120 |
5 | BAS13g00170 | Scaffold13 | 4419894 | G | A | downstream_gene_variant | MODIFIER | c.*3101C>T| |
S97 |
6 | BAS13g00170 | Scaffold13 | 4420385 | G | A | downstream_gene_variant | MODIFIER | c.*2610C>T| |
S5 |
7 | BAS13g00170 | Scaffold13 | 4421540 | C | T | downstream_gene_variant | MODIFIER | c.*1455G>A| |
S15 S153 S156 S213 S3 S34 |
8 | BAS13g00170 | Scaffold13 | 4422128 | C | T | downstream_gene_variant | MODIFIER | c.*867G>A| |
S217 S248 |
9 | BAS13g00170 | Scaffold13 | 4422335 | C | T | downstream_gene_variant | MODIFIER | c.*660G>A| |
S130 |
10 | BAS13g00170 | Scaffold13 | 4422413 | C | T | downstream_gene_variant | MODIFIER | c.*582G>A| |
S168 |
11 | BAS13g00170 | Scaffold13 | 4422988 | C | T | downstream_gene_variant | MODIFIER | c.*7G>A| |
S88 |
12 | BAS13g00170 | Scaffold13 | 4423511 | G | A | upstream_gene_variant | MODIFIER | c.-274C>T| |
S140 |
13 | BAS13g00170 | Scaffold13 | 4423609 | C | T | upstream_gene_variant | MODIFIER | c.-372G>A| |
S83 S88 |
14 | BAS13g00170 | Scaffold13 | 4424098 | T | G | upstream_gene_variant | MODIFIER | c.-861A>C| |
S28 |
15 | BAS13g00170 | Scaffold13 | 4424235 | G | A | upstream_gene_variant | MODIFIER | c.-998C>T| |
S281 |
16 | BAS13g00170 | Scaffold13 | 4424726 | C | T | upstream_gene_variant | MODIFIER | c.-1489G>A| |
S109 |
17 | BAS13g00170 | Scaffold13 | 4425593 | C | T | upstream_gene_variant | MODIFIER | c.-2356G>A| |
S43 |
18 | BAS13g00170 | Scaffold13 | 4427197 | G | A | upstream_gene_variant | MODIFIER | c.-3960C>T| |
S218 |
19 | BAS13g00170 | Scaffold13 | 4427502 | G | A | upstream_gene_variant | MODIFIER | c.-4265C>T| |
S164 |
20 | BAS13g00170 | Scaffold13 | 4427683 | G | A | upstream_gene_variant | MODIFIER | c.-4446C>T| |
S231 |
21 | BAS13g00170 | Scaffold13 | 4427950 | G | A | upstream_gene_variant | MODIFIER | c.-4713C>T| |
S209 |