Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g29600 | A05 | 33040575 | C | T | synonymous_variant | LOW | c.2748G>A|p.Gln916Gln |
S33 |
2 | BAA05g29600 | A05 | 33040712 | C | T | splice_region_variant&intron_variant | LOW | c.2700+5G>A| |
S202 |
3 | BAA05g29600 | A05 | 33041841 | C | T | missense_variant | MODERATE | c.1663G>A|p.Glu555Lys |
S289 |
4 | BAA05g29600 | A05 | 33042538 | G | A | missense_variant | MODERATE | c.1361C>T|p.Thr454Ile |
S18 |
5 | BAA05g29600 | A05 | 33043549 | T | C | synonymous_variant | LOW | c.576A>G|p.Arg192Arg |
S290 |
6 | BAA05g29600 | A05 | 33043583 | G | A | missense_variant | MODERATE | c.542C>T|p.Thr181Ile |
S163 |
7 | BAA05g29600 | A05 | 33043636 | C | T | synonymous_variant | LOW | c.489G>A|p.Gln163Gln |
S170 |
8 | BAA05g29600 | A05 | 33044044 | G | A | synonymous_variant | LOW | c.363C>T|p.Thr121Thr |
S291 |
9 | BAA05g29600 | A05 | 33045348 | C | T | upstream_gene_variant | MODIFIER | c.-942G>A| |
S297 |
10 | BAA05g29600 | A05 | 33049030 | G | A | upstream_gene_variant | MODIFIER | c.-4624C>T| |
S282 |
11 | BAA05g29600 | A05 | 33049046 | G | A | upstream_gene_variant | MODIFIER | c.-4640C>T| |
S291 |