Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34720 | A02 | 29861799 | G | A | missense_variant | MODERATE | c.170G>A|p.Arg57Gln |
S176 |
2 | BAA02g34720 | A02 | 29862603 | C | T | missense_variant | MODERATE | c.448C>T|p.Leu150Phe |
S168 S278 |
3 | BAA02g34720 | A02 | 29862849 | C | T | synonymous_variant | LOW | c.480C>T|p.Leu160Leu |
S178 |
4 | BAA02g34720 | A02 | 29863069 | C | T | missense_variant | MODERATE | c.622C>T|p.Leu208Phe |
S171 |
5 | BAA02g34720 | A02 | 29865718 | C | T | downstream_gene_variant | MODIFIER | c.*1531C>T| |
S259 |
6 | BAA02g34720 | A02 | 29865753 | C | T | downstream_gene_variant | MODIFIER | c.*1566C>T| |
S299 |
7 | BAA02g34720 | A02 | 29866410 | G | A | downstream_gene_variant | MODIFIER | c.*2223G>A| |
S35 |
8 | BAA02g34720 | A02 | 29866719 | G | A | downstream_gene_variant | MODIFIER | c.*2532G>A| |
S209 |
9 | BAA02g34720 | A02 | 29866777 | C | T | downstream_gene_variant | MODIFIER | c.*2590C>T| |
S235 |
10 | BAA02g34720 | A02 | 29866926 | C | T | downstream_gene_variant | MODIFIER | c.*2739C>T| |
S62 |