Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13460 | A02 | 6190537 | C | T | downstream_gene_variant | MODIFIER | c.*128G>A| |
S174 |
2 | BAA02g13460 | A02 | 6190590 | G | A | downstream_gene_variant | MODIFIER | c.*75C>T| |
S92 |
3 | BAA02g13460 | A02 | 6190672 | C | T | missense_variant | MODERATE | c.1979G>A|p.Gly660Asp |
S245 |
4 | BAA02g13460 | A02 | 6191675 | C | T | missense_variant | MODERATE | c.1529G>A|p.Arg510Lys |
S261 |
5 | BAA02g13460 | A02 | 6191709 | C | T | missense_variant | MODERATE | c.1495G>A|p.Val499Met |
S199 |
6 | BAA02g13460 | A02 | 6191725 | C | T | synonymous_variant | LOW | c.1479G>A|p.Gln493Gln |
S63 |
7 | BAA02g13460 | A02 | 6193672 | G | A | synonymous_variant | LOW | c.549C>T|p.Ser183Ser |
S165 |
8 | BAA02g13460 | A02 | 6195823 | C | T | upstream_gene_variant | MODIFIER | c.-1415G>A| |
S249 |
9 | BAA02g13460 | A02 | 6197026 | C | T | upstream_gene_variant | MODIFIER | c.-2618G>A| |
S66 |
10 | BAA02g13460 | A02 | 6197348 | C | T | upstream_gene_variant | MODIFIER | c.-2940G>A| |
S208 S219 |
11 | BAA02g13460 | A02 | 6197487 | G | A | upstream_gene_variant | MODIFIER | c.-3079C>T| |
S225 S73 |