Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g15080 | A05 | 8042962 | C | T | downstream_gene_variant | MODIFIER | c.*1785G>A| |
S295 |
2 | BAA05g15080 | A05 | 8045009 | T | A | missense_variant | MODERATE | c.1958A>T|p.Gln653Leu |
S153 S213 |
3 | BAA05g15080 | A05 | 8045058 | C | T | missense_variant | MODERATE | c.1909G>A|p.Glu637Lys |
S277 |
4 | BAA05g15080 | A05 | 8045129 | C | T | missense_variant | MODERATE | c.1838G>A|p.Gly613Glu |
S100 |
5 | BAA05g15080 | A05 | 8045810 | C | T | missense_variant | MODERATE | c.1157G>A|p.Arg386Lys |
S148 S210 S31 |
6 | BAA05g15080 | A05 | 8046014 | G | A | missense_variant | MODERATE | c.953C>T|p.Ala318Val |
S284 |
7 | BAA05g15080 | A05 | 8046708 | C | T | missense_variant | MODERATE | c.259G>A|p.Val87Met |
S267 |
8 | BAA05g15080 | A05 | 8048323 | C | T | upstream_gene_variant | MODIFIER | c.-1357G>A| |
S246 |
9 | BAA05g15080 | A05 | 8050637 | G | A | upstream_gene_variant | MODIFIER | c.-3671C>T| |
S282 |
10 | BAA05g15080 | A05 | 8051734 | G | A | upstream_gene_variant | MODIFIER | c.-4768C>T| |
S219 |