Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g36280 | A09 | 44672027 | G | A | downstream_gene_variant | MODIFIER | c.*4641C>T| |
S127 |
2 | BAA09g36280 | A09 | 44672126 | C | T | downstream_gene_variant | MODIFIER | c.*4542G>A| |
S256 |
3 | BAA09g36280 | A09 | 44672181 | G | A | downstream_gene_variant | MODIFIER | c.*4487C>T| |
S298 |
4 | BAA09g36280 | A09 | 44672251 | G | A | downstream_gene_variant | MODIFIER | c.*4417C>T| |
S28 |
5 | BAA09g36280 | A09 | 44673353 | C | T | downstream_gene_variant | MODIFIER | c.*3315G>A| |
S201 |
6 | BAA09g36280 | A09 | 44674722 | C | T | downstream_gene_variant | MODIFIER | c.*1946G>A| |
S240 |
7 | BAA09g36280 | A09 | 44674775 | C | T | downstream_gene_variant | MODIFIER | c.*1893G>A| |
S241 |
8 | BAA09g36280 | A09 | 44674839 | C | T | downstream_gene_variant | MODIFIER | c.*1829G>A| |
S173 S225 |
9 | BAA09g36280 | A09 | 44674898 | G | A | downstream_gene_variant | MODIFIER | c.*1770C>T| |
S202 |
10 | BAA09g36280 | A09 | 44676711 | C | T | missense_variant | MODERATE | c.2090G>A|p.Arg697Lys |
S138 |
11 | BAA09g36280 | A09 | 44676749 | C | T | synonymous_variant | LOW | c.2052G>A|p.Lys684Lys |
S306 S308 |
12 | BAA09g36280 | A09 | 44678383 | C | T | missense_variant | MODERATE | c.418G>A|p.Val140Met |
S297 |
13 | BAA09g36280 | A09 | 44678826 | C | T | upstream_gene_variant | MODIFIER | c.-26G>A| |
S32 |
14 | BAA09g36280 | A09 | 44679198 | G | A | upstream_gene_variant | MODIFIER | c.-398C>T| |
S59 |
15 | BAA09g36280 | A09 | 44679766 | C | T | upstream_gene_variant | MODIFIER | c.-966G>A| |
S250 |