Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26730 | A02 | 14953468 | G | A | intron_variant | MODIFIER | c.2509+174C>T| |
S249 |
2 | BAA02g26730 | A02 | 14953478 | G | A | intron_variant | MODIFIER | c.2509+164C>T| |
S155 S211 |
3 | BAA02g26730 | A02 | 14953993 | G | A | intron_variant | MODIFIER | c.2298+9C>T| |
S146 |
4 | BAA02g26730 | A02 | 14954775 | C | T | missense_variant | MODERATE | c.1783G>A|p.Glu595Lys |
S237 |
5 | BAA02g26730 | A02 | 14954946 | G | A | missense_variant | MODERATE | c.1697C>T|p.Ala566Val |
S28 |
6 | BAA02g26730 | A02 | 14955382 | G | A | intron_variant | MODIFIER | c.1576+41C>T| |
S34 |
7 | BAA02g26730 | A02 | 14955854 | G | A | intron_variant | MODIFIER | c.1323+13C>T| |
S148 S210 |
8 | BAA02g26730 | A02 | 14956129 | C | T | intron_variant | MODIFIER | c.1233-172G>A| |
S179 |
9 | BAA02g26730 | A02 | 14960912 | C | T | missense_variant | MODERATE | c.577G>A|p.Gly193Arg |
S278 |
10 | BAA02g26730 | A02 | 14961801 | C | T | missense_variant | MODERATE | c.55G>A|p.Glu19Lys |
S9 |
11 | BAA02g26730 | A02 | 14962388 | C | T | upstream_gene_variant | MODIFIER | c.-533G>A| |
S32 |
12 | BAA02g26730 | A02 | 14963856 | G | T | upstream_gene_variant | MODIFIER | c.-2001C>A| |
S294 |
13 | BAA02g26730 | A02 | 14964268 | T | G | upstream_gene_variant | MODIFIER | c.-2413A>C| |
S153 S213 |
14 | BAA02g26730 | A02 | 14964437 | G | A | upstream_gene_variant | MODIFIER | c.-2582C>T| |
S116 |
15 | BAA02g26730 | A02 | 14965305 | C | T | upstream_gene_variant | MODIFIER | c.-3450G>A| |
S299 |