Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16790 | A02 | 8285444 | C | T | missense_variant | MODERATE | c.337G>A|p.Glu113Lys |
S83 S88 |
2 | BAA02g16790 | A02 | 8285464 | G | A | missense_variant | MODERATE | c.317C>T|p.Ser106Phe |
S288 |
3 | BAA02g16790 | A02 | 8285573 | C | T | missense_variant | MODERATE | c.208G>A|p.Glu70Lys |
S208 S219 |
4 | BAA02g16790 | A02 | 8285702 | C | T | missense_variant | MODERATE | c.79G>A|p.Glu27Lys |
S128 |
5 | BAA02g16790 | A02 | 8286854 | C | T | upstream_gene_variant | MODIFIER | c.-1074G>A| |
S255 |
6 | BAA02g16790 | A02 | 8287402 | C | T | upstream_gene_variant | MODIFIER | c.-1622G>A| |
S73 S91 |
7 | BAA02g16790 | A02 | 8289762 | C | T | upstream_gene_variant | MODIFIER | c.-3982G>A| |
S276 |
8 | BAA02g16790 | A02 | 8290090 | G | A | upstream_gene_variant | MODIFIER | c.-4310C>T| |
S247 |
9 | BAA02g16790 | A02 | 8290688 | C | T | upstream_gene_variant | MODIFIER | c.-4908G>A| |
S171 |