Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45110 | A02 | 37031507 | G | A | missense_variant | MODERATE | c.1382C>T|p.Ala461Val |
S67 |
2 | BAA02g45110 | A02 | 37031938 | C | T | missense_variant | MODERATE | c.1120G>A|p.Ala374Thr |
S202 |
3 | BAA02g45110 | A02 | 37033031 | G | A | synonymous_variant | LOW | c.508C>T|p.Leu170Leu |
S50 |
4 | BAA02g45110 | A02 | 37033385 | C | T | missense_variant | MODERATE | c.308G>A|p.Gly103Glu |
S68 |
5 | BAA02g45110 | A02 | 37036838 | C | T | upstream_gene_variant | MODIFIER | c.-3047G>A| |
S65 |
6 | BAA02g45110 | A02 | 37037264 | G | A | upstream_gene_variant | MODIFIER | c.-3473C>T| |
S168 |
7 | BAA02g45110 | A02 | 37037989 | C | T | upstream_gene_variant | MODIFIER | c.-4198G>A| |
S46 |
8 | BAA02g45110 | A02 | 37038055 | G | A | upstream_gene_variant | MODIFIER | c.-4264C>T| |
S134 |
9 | BAA02g45110 | A02 | 37038714 | G | A | upstream_gene_variant | MODIFIER | c.-4923C>T| |
S8 |