Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18780 | A02 | 9659418 | C | T | missense_variant | MODERATE | c.2023G>A|p.Glu675Lys |
S186 |
2 | BAA02g18780 | A02 | 9659781 | C | T | missense_variant | MODERATE | c.1660G>A|p.Ala554Thr |
S167 |
3 | BAA02g18780 | A02 | 9660040 | C | T | synonymous_variant | LOW | c.1401G>A|p.Glu467Glu |
S308 |
4 | BAA02g18780 | A02 | 9660171 | C | T | missense_variant | MODERATE | c.1270G>A|p.Glu424Lys |
S71 |
5 | BAA02g18780 | A02 | 9661255 | C | T | synonymous_variant | LOW | c.543G>A|p.Glu181Glu |
S200 |
6 | BAA02g18780 | A02 | 9662326 | C | T | upstream_gene_variant | MODIFIER | c.-98G>A| |
S208 S219 |
7 | BAA02g18780 | A02 | 9663317 | C | A | upstream_gene_variant | MODIFIER | c.-1089G>T| |
S255 |
8 | BAA02g18780 | A02 | 9663751 | G | A | upstream_gene_variant | MODIFIER | c.-1523C>T| |
S134 |
9 | BAA02g18780 | A02 | 9664982 | G | A | upstream_gene_variant | MODIFIER | c.-2754C>T| |
S263 |
10 | BAA02g18780 | A02 | 9665382 | C | T | upstream_gene_variant | MODIFIER | c.-3154G>A| |
S46 |
11 | BAA02g18780 | A02 | 9665747 | G | A | upstream_gene_variant | MODIFIER | c.-3519C>T| |
S7 |
12 | BAA02g18780 | A02 | 9665836 | G | A | upstream_gene_variant | MODIFIER | c.-3608C>T| |
S204 S32 |
13 | BAA02g18780 | A02 | 9666173 | G | A | upstream_gene_variant | MODIFIER | c.-3945C>T| |
S236 |
14 | BAA02g18780 | A02 | 9666505 | G | A | upstream_gene_variant | MODIFIER | c.-4277C>T| |
S202 |
15 | BAA02g18780 | A02 | 9666512 | G | A | upstream_gene_variant | MODIFIER | c.-4284C>T| |
S19 |