Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10550 | A02 | 4682650 | G | A | missense_variant | MODERATE | c.482G>A|p.Cys161Tyr |
S232 |
2 | BAA02g10550 | A02 | 4682762 | C | T | synonymous_variant | LOW | c.594C>T|p.Leu198Leu |
S202 |
3 | BAA02g10550 | A02 | 4682838 | C | T | missense_variant | MODERATE | c.670C>T|p.Arg224Cys |
S181 |
4 | BAA02g10550 | A02 | 4683197 | C | T | synonymous_variant | LOW | c.1029C>T|p.Leu343Leu |
S136 |
5 | BAA02g10550 | A02 | 4683345 | G | A | missense_variant | MODERATE | c.1177G>A|p.Ala393Thr |
S52 |
6 | BAA02g10550 | A02 | 4683709 | G | A | downstream_gene_variant | MODIFIER | c.*242G>A| |
S161 |
7 | BAA02g10550 | A02 | 4685835 | G | A | downstream_gene_variant | MODIFIER | c.*2368G>A| |
S173 |
8 | BAA02g10550 | A02 | 4688309 | G | A | downstream_gene_variant | MODIFIER | c.*4842G>A| |
S296 |