Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10760 | A10 | 12501934 | G | A | upstream_gene_variant | MODIFIER | c.-3705G>A| |
S71 |
2 | BAA10g10760 | A10 | 12502388 | C | T | upstream_gene_variant | MODIFIER | c.-3251C>T| |
S149 |
3 | BAA10g10760 | A10 | 12502523 | C | T | upstream_gene_variant | MODIFIER | c.-3116C>T| |
S8 |
4 | BAA10g10760 | A10 | 12504323 | A | G | upstream_gene_variant | MODIFIER | c.-1316A>G| |
S284 |
5 | BAA10g10760 | A10 | 12504386 | C | T | upstream_gene_variant | MODIFIER | c.-1253C>T| |
S123 |
6 | BAA10g10760 | A10 | 12504783 | G | A | upstream_gene_variant | MODIFIER | c.-856G>A| |
S289 |
7 | BAA10g10760 | A10 | 12505374 | G | A | upstream_gene_variant | MODIFIER | c.-265G>A| |
S255 |
8 | BAA10g10760 | A10 | 12507137 | C | T | downstream_gene_variant | MODIFIER | c.*928C>T| |
S123 |
9 | BAA10g10760 | A10 | 12507608 | C | T | downstream_gene_variant | MODIFIER | c.*1399C>T| |
S294 |
10 | BAA10g10760 | A10 | 12508453 | G | A | downstream_gene_variant | MODIFIER | c.*2244G>A| |
S245 |
11 | BAA10g10760 | A10 | 12508603 | C | T | downstream_gene_variant | MODIFIER | c.*2394C>T| |
S133 |
12 | BAA10g10760 | A10 | 12508891 | C | T | downstream_gene_variant | MODIFIER | c.*2682C>T| |
S68 |
13 | BAA10g10760 | A10 | 12508930 | G | A | downstream_gene_variant | MODIFIER | c.*2721G>A| |
S241 |
14 | BAA10g10760 | A10 | 12509314 | G | A | downstream_gene_variant | MODIFIER | c.*3105G>A| |
S35 |
15 | BAA10g10760 | A10 | 12510114 | C | T | downstream_gene_variant | MODIFIER | c.*3905C>T| |
S173 S34 |
16 | BAA10g10760 | A10 | 12510197 | C | T | downstream_gene_variant | MODIFIER | c.*3988C>T| |
S287 |
17 | BAA10g10760 | A10 | 12510745 | G | A | downstream_gene_variant | MODIFIER | c.*4536G>A| |
S130 |