Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13440 | A02 | 6160212 | G | A | upstream_gene_variant | MODIFIER | c.-4160G>A| |
S146 |
2 | BAA02g13440 | A02 | 6163210 | G | A | upstream_gene_variant | MODIFIER | c.-1162G>A| |
S156 |
3 | BAA02g13440 | A02 | 6163851 | C | T | upstream_gene_variant | MODIFIER | c.-521C>T| |
S158 |
4 | BAA02g13440 | A02 | 6164587 | C | T | synonymous_variant | LOW | c.216C>T|p.Leu72Leu |
S34 |
5 | BAA02g13440 | A02 | 6164737 | G | A | missense_variant | MODERATE | c.271G>A|p.Glu91Lys |
S156 |
6 | BAA02g13440 | A02 | 6165169 | G | A | missense_variant | MODERATE | c.625G>A|p.Ala209Thr |
S10 |
7 | BAA02g13440 | A02 | 6165252 | G | A | synonymous_variant | LOW | c.708G>A|p.Arg236Arg |
S144 |
8 | BAA02g13440 | A02 | 6165285 | G | A | synonymous_variant | LOW | c.741G>A|p.Lys247Lys |
S198 |
9 | BAA02g13440 | A02 | 6165882 | G | A | missense_variant | MODERATE | c.1076G>A|p.Gly359Glu |
S11 |
10 | BAA02g13440 | A02 | 6166060 | C | T | downstream_gene_variant | MODIFIER | c.*120C>T| |
S277 |
11 | BAA02g13440 | A02 | 6167145 | C | T | downstream_gene_variant | MODIFIER | c.*1205C>T| |
S281 |
12 | BAA02g13440 | A02 | 6170091 | G | A | downstream_gene_variant | MODIFIER | c.*4151G>A| |
S10 |
13 | BAA02g13440 | A02 | 6170693 | G | A | downstream_gene_variant | MODIFIER | c.*4753G>A| |
S269 |