Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05390 | A08 | 4015740 | C | T | upstream_gene_variant | MODIFIER | c.-4688C>T| |
S243 S299 |
2 | BAA08g05390 | A08 | 4015777 | C | T | upstream_gene_variant | MODIFIER | c.-4651C>T| |
S69 |
3 | BAA08g05390 | A08 | 4017078 | C | T | upstream_gene_variant | MODIFIER | c.-3350C>T| |
S67 |
4 | BAA08g05390 | A08 | 4017134 | C | T | upstream_gene_variant | MODIFIER | c.-3294C>T| |
S235 |
5 | BAA08g05390 | A08 | 4018157 | C | T | upstream_gene_variant | MODIFIER | c.-2271C>T| |
S172 S217 |
6 | BAA08g05390 | A08 | 4018686 | C | T | upstream_gene_variant | MODIFIER | c.-1742C>T| |
S189 |
7 | BAA08g05390 | A08 | 4018836 | G | A | upstream_gene_variant | MODIFIER | c.-1592G>A| |
S238 |
8 | BAA08g05390 | A08 | 4018881 | G | T | upstream_gene_variant | MODIFIER | c.-1547G>T| |
|
9 | BAA08g05390 | A08 | 4018947 | C | T | upstream_gene_variant | MODIFIER | c.-1481C>T| |
S162 |
10 | BAA08g05390 | A08 | 4019056 | C | T | upstream_gene_variant | MODIFIER | c.-1372C>T| |
S149 |
11 | BAA08g05390 | A08 | 4019378 | G | A | upstream_gene_variant | MODIFIER | c.-1050G>A| |
S37 |
12 | BAA08g05390 | A08 | 4019642 | G | A | upstream_gene_variant | MODIFIER | c.-786G>A| |
S193 |
13 | BAA08g05390 | A08 | 4019708 | C | T | upstream_gene_variant | MODIFIER | c.-720C>T| |
S216 |
14 | BAA08g05390 | A08 | 4019903 | G | A | upstream_gene_variant | MODIFIER | c.-525G>A| |
S221 |
15 | BAA08g05390 | A08 | 4021648 | C | T | downstream_gene_variant | MODIFIER | c.*753C>T| |
S226 |
16 | BAA08g05390 | A08 | 4021724 | C | T | downstream_gene_variant | MODIFIER | c.*829C>T| |
S126 |
17 | BAA08g05390 | A08 | 4022352 | C | T | downstream_gene_variant | MODIFIER | c.*1457C>T| |
S305 |
18 | BAA08g05390 | A08 | 4022532 | G | A | downstream_gene_variant | MODIFIER | c.*1637G>A| |
S278 |