Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g23080 | A02 | 12532211 | G | A | missense_variant | MODERATE | c.2521C>T|p.Pro841Ser |
S4 |
2 | BAA02g23080 | A02 | 12533235 | C | T | synonymous_variant | LOW | c.1656G>A|p.Glu552Glu |
S100 |
3 | BAA02g23080 | A02 | 12537012 | G | A | intron_variant | MODIFIER | c.492-2518C>T| |
S23 |
4 | BAA02g23080 | A02 | 12537168 | G | A | intron_variant | MODIFIER | c.492-2674C>T| |
S204 |
5 | BAA02g23080 | A02 | 12537789 | G | A | intron_variant | MODIFIER | c.491+2280C>T| |
S146 |
6 | BAA02g23080 | A02 | 12537855 | C | T | intron_variant | MODIFIER | c.491+2214G>A| |
S42 |
7 | BAA02g23080 | A02 | 12538350 | G | A | intron_variant | MODIFIER | c.491+1719C>T| |
S176 |
8 | BAA02g23080 | A02 | 12538540 | C | T | intron_variant | MODIFIER | c.491+1529G>A| |
S194 |
9 | BAA02g23080 | A02 | 12538611 | C | T | intron_variant | MODIFIER | c.491+1458G>A| |
S142 |
10 | BAA02g23080 | A02 | 12539493 | C | T | intron_variant | MODIFIER | c.491+576G>A| |
S152 |
11 | BAA02g23080 | A02 | 12540521 | C | T | synonymous_variant | LOW | c.39G>A|p.Pro13Pro |
S165 |
12 | BAA02g23080 | A02 | 12540736 | G | A | upstream_gene_variant | MODIFIER | c.-177C>T| |
S25 |
13 | BAA02g23080 | A02 | 12541414 | G | A | upstream_gene_variant | MODIFIER | c.-855C>T| |
S236 |
14 | BAA02g23080 | A02 | 12541519 | G | A | upstream_gene_variant | MODIFIER | c.-960C>T| |
S62 |
15 | BAA02g23080 | A02 | 12541932 | G | A | upstream_gene_variant | MODIFIER | c.-1373C>T| |
S146 |
16 | BAA02g23080 | A02 | 12543154 | G | A | upstream_gene_variant | MODIFIER | c.-2595C>T| |
S19 |
17 | BAA02g23080 | A02 | 12543207 | G | A | upstream_gene_variant | MODIFIER | c.-2648C>T| |
S89 |
18 | BAA02g23080 | A02 | 12543279 | G | A | upstream_gene_variant | MODIFIER | c.-2720C>T| |
S5 |
19 | BAA02g23080 | A02 | 12543577 | G | A | upstream_gene_variant | MODIFIER | c.-3018C>T| |
S34 |
20 | BAA02g23080 | A02 | 12544326 | G | A | upstream_gene_variant | MODIFIER | c.-3767C>T| |
S188 |
21 | BAA02g23080 | A02 | 12544751 | G | A | upstream_gene_variant | MODIFIER | c.-4192C>T| |
S136 |