Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30960 | A02 | 18274915 | C | T | upstream_gene_variant | MODIFIER | c.-4988C>T| |
S283 |
2 | BAA02g30960 | A02 | 18275327 | G | A | upstream_gene_variant | MODIFIER | c.-4576G>A| |
S260 |
3 | BAA02g30960 | A02 | 18275475 | C | T | upstream_gene_variant | MODIFIER | c.-4428C>T| |
S206 |
4 | BAA02g30960 | A02 | 18276885 | G | A | upstream_gene_variant | MODIFIER | c.-3018G>A| |
S19 |
5 | BAA02g30960 | A02 | 18277209 | C | T | upstream_gene_variant | MODIFIER | c.-2694C>T| |
S286 |
6 | BAA02g30960 | A02 | 18278069 | G | A | upstream_gene_variant | MODIFIER | c.-1834G>A| |
S86 |
7 | BAA02g30960 | A02 | 18279939 | G | A | missense_variant | MODERATE | c.37G>A|p.Val13Ile |
S187 |
8 | BAA02g30960 | A02 | 18280456 | C | T | downstream_gene_variant | MODIFIER | c.*200C>T| |
S52 |
9 | BAA02g30960 | A02 | 18280834 | C | T | downstream_gene_variant | MODIFIER | c.*578C>T| |
S157 S163 |
10 | BAA02g30960 | A02 | 18281247 | C | T | downstream_gene_variant | MODIFIER | c.*991C>T| |
S212 |
11 | BAA02g30960 | A02 | 18281540 | G | A | downstream_gene_variant | MODIFIER | c.*1284G>A| |
S263 |
12 | BAA02g30960 | A02 | 18281957 | C | T | downstream_gene_variant | MODIFIER | c.*1701C>T| |
S299 |
13 | BAA02g30960 | A02 | 18282040 | G | A | downstream_gene_variant | MODIFIER | c.*1784G>A| |
S217 S248 |
14 | BAA02g30960 | A02 | 18282201 | C | T | downstream_gene_variant | MODIFIER | c.*1945C>T| |
S139 |
15 | BAA02g30960 | A02 | 18282644 | C | T | downstream_gene_variant | MODIFIER | c.*2388C>T| |
S250 |
16 | BAA02g30960 | A02 | 18283637 | C | T | downstream_gene_variant | MODIFIER | c.*3381C>T| |
S178 |
17 | BAA02g30960 | A02 | 18284864 | G | A | downstream_gene_variant | MODIFIER | c.*4608G>A| |
S110 |
18 | BAA02g30960 | A02 | 18284916 | C | T | downstream_gene_variant | MODIFIER | c.*4660C>T| |
S277 |