Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11550 | A02 | 5211902 | G | A | missense_variant | MODERATE | c.1118C>T|p.Ser373Phe |
S298 |
2 | BAA02g11550 | A02 | 5212055 | C | T | missense_variant | MODERATE | c.965G>A|p.Gly322Glu |
S146 |
3 | BAA02g11550 | A02 | 5212324 | G | A | synonymous_variant | LOW | c.696C>T|p.Phe232Phe |
S56 |
4 | BAA02g11550 | A02 | 5212371 | G | A | missense_variant | MODERATE | c.649C>T|p.Arg217Trp |
S176 |
5 | BAA02g11550 | A02 | 5212415 | C | T | missense_variant | MODERATE | c.605G>A|p.Arg202Lys |
S238 |
6 | BAA02g11550 | A02 | 5212458 | C | T | missense_variant | MODERATE | c.562G>A|p.Val188Ile |
S138 |
7 | BAA02g11550 | A02 | 5214005 | C | T | upstream_gene_variant | MODIFIER | c.-664G>A| |
S25 S264 |
8 | BAA02g11550 | A02 | 5214021 | G | A | upstream_gene_variant | MODIFIER | c.-680C>T| |
S191 |
9 | BAA02g11550 | A02 | 5217000 | C | T | upstream_gene_variant | MODIFIER | c.-3659G>A| |
S63 |