Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45650 | A02 | 37316398 | C | T | synonymous_variant | LOW | c.30C>T|p.Ser10Ser |
S116 |
2 | BAA02g45650 | A02 | 37318890 | G | A | downstream_gene_variant | MODIFIER | c.*1178G>A| |
S226 |
3 | BAA02g45650 | A02 | 37322160 | G | A | downstream_gene_variant | MODIFIER | c.*4448G>A| |
S221 |
4 | BAA02g45650 | A02 | 37322230 | G | A | downstream_gene_variant | MODIFIER | c.*4518G>A| |
S244 S291 |
5 | BAA02g45650 | A02 | 37322583 | C | T | downstream_gene_variant | MODIFIER | c.*4871C>T| |
S249 |
6 | BAA02g45650 | A02 | 37322605 | G | A | downstream_gene_variant | MODIFIER | c.*4893G>A| |
S10 |