Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46850 | A02 | 37961826 | G | A | synonymous_variant | LOW | c.1683C>T|p.Cys561Cys |
S10 |
2 | BAA02g46850 | A02 | 37962467 | G | A | missense_variant | MODERATE | c.1042C>T|p.Leu348Phe |
S14 |
3 | BAA02g46850 | A02 | 37962961 | G | A | missense_variant | MODERATE | c.548C>T|p.Ser183Phe |
S186 |
4 | BAA02g46850 | A02 | 37963120 | C | T | missense_variant | MODERATE | c.389G>A|p.Gly130Glu |
S128 |
5 | BAA02g46850 | A02 | 37963152 | G | A | synonymous_variant | LOW | c.357C>T|p.Ile119Ile |
S162 |
6 | BAA02g46850 | A02 | 37963179 | G | A | synonymous_variant | LOW | c.330C>T|p.Leu110Leu |
S176 |
7 | BAA02g46850 | A02 | 37963444 | G | A | missense_variant | MODERATE | c.65C>T|p.Pro22Leu |
S164 |
8 | BAA02g46850 | A02 | 37963462 | G | A | missense_variant | MODERATE | c.47C>T|p.Ser16Leu |
S10 |
9 | BAA02g46850 | A02 | 37964958 | C | T | upstream_gene_variant | MODIFIER | c.-1450G>A| |
S240 |
10 | BAA02g46850 | A02 | 37965912 | T | G | upstream_gene_variant | MODIFIER | c.-2404A>C| |
S138 |
11 | BAA02g46850 | A02 | 37966804 | G | A | upstream_gene_variant | MODIFIER | c.-3296C>T| |
S265 S39 |
12 | BAA02g46850 | A02 | 37967331 | C | T | upstream_gene_variant | MODIFIER | c.-3823G>A| |
S244 |
13 | BAA02g46850 | A02 | 37967637 | C | T | upstream_gene_variant | MODIFIER | c.-4129G>A| |
S306 S308 |
14 | BAA02g46850 | A02 | 37968190 | C | T | upstream_gene_variant | MODIFIER | c.-4682G>A| |
S178 |
15 | BAA02g46850 | A02 | 37968382 | C | T | upstream_gene_variant | MODIFIER | c.-4874G>A| |
S13 |
16 | BAA02g46850 | A02 | 37968488 | G | A | upstream_gene_variant | MODIFIER | c.-4980C>T| |
S229 |