Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45990 | A02 | 37509574 | C | T | synonymous_variant | LOW | c.165G>A|p.Ser55Ser |
S9 |
2 | BAA02g45990 | A02 | 37509630 | C | T | missense_variant | MODERATE | c.109G>A|p.Asp37Asn |
S270 |
3 | BAA02g45990 | A02 | 37509653 | C | T | missense_variant | MODERATE | c.86G>A|p.Arg29Lys |
S303 |
4 | BAA02g45990 | A02 | 37511468 | C | T | upstream_gene_variant | MODIFIER | c.-1730G>A| |
S87 |
5 | BAA02g45990 | A02 | 37513583 | C | T | upstream_gene_variant | MODIFIER | c.-3845G>A| |
S295 |
6 | BAA02g45990 | A02 | 37513704 | C | T | upstream_gene_variant | MODIFIER | c.-3966G>A| |
S42 |
7 | BAA02g45990 | A02 | 37514544 | C | T | upstream_gene_variant | MODIFIER | c.-4806G>A| |
S123 |