Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18820 | A02 | 9677714 | C | T | missense_variant | MODERATE | c.1217G>A|p.Gly406Asp |
S18 |
2 | BAA02g18820 | A02 | 9678364 | C | T | synonymous_variant | LOW | c.807G>A|p.Glu269Glu |
S155 S211 |
3 | BAA02g18820 | A02 | 9682758 | G | A | upstream_gene_variant | MODIFIER | c.-2932C>T| |
S11 |
4 | BAA02g18820 | A02 | 9682816 | C | T | upstream_gene_variant | MODIFIER | c.-2990G>A| |
S163 |
5 | BAA02g18820 | A02 | 9683077 | G | A | upstream_gene_variant | MODIFIER | c.-3251C>T| |
S56 |
6 | BAA02g18820 | A02 | 9684129 | G | A | upstream_gene_variant | MODIFIER | c.-4303C>T| |
S269 |