Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02110 | A02 | 945152 | C | T | downstream_gene_variant | MODIFIER | c.*1112G>A| |
S40 S49 |
2 | BAA02g02110 | A02 | 946733 | G | A | intron_variant | MODIFIER | c.409-152C>T| |
S162 |
3 | BAA02g02110 | A02 | 948079 | G | A | intron_variant | MODIFIER | c.238-780C>T| |
S204 |
4 | BAA02g02110 | A02 | 948394 | T | A | intron_variant | MODIFIER | c.238-1095A>T| |
S119 |
5 | BAA02g02110 | A02 | 952753 | C | T | intron_variant | MODIFIER | c.237+782G>A| |
S111 |
6 | BAA02g02110 | A02 | 952779 | C | A | intron_variant | MODIFIER | c.237+756G>T| |
S287 |
7 | BAA02g02110 | A02 | 952885 | G | A | intron_variant | MODIFIER | c.237+650C>T| |
S265 |
8 | BAA02g02110 | A02 | 952933 | G | A | intron_variant | MODIFIER | c.237+602C>T| |
S59 |
9 | BAA02g02110 | A02 | 957094 | G | A | upstream_gene_variant | MODIFIER | c.-947C>T| |
S48 |
10 | BAA02g02110 | A02 | 957512 | G | A | upstream_gene_variant | MODIFIER | c.-1365C>T| |
S168 |
11 | BAA02g02110 | A02 | 957691 | G | A | upstream_gene_variant | MODIFIER | c.-1544C>T| |
S174 |
12 | BAA02g02110 | A02 | 958976 | G | A | upstream_gene_variant | MODIFIER | c.-2829C>T| |
S286 |
13 | BAA02g02110 | A02 | 959581 | C | T | upstream_gene_variant | MODIFIER | c.-3434G>A| |
S71 |
14 | BAA02g02110 | A02 | 959938 | C | T | upstream_gene_variant | MODIFIER | c.-3791G>A| |
S170 |