Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41130 | A02 | 34514781 | C | T | downstream_gene_variant | MODIFIER | c.*4012G>A| |
S296 |
2 | BAA02g41130 | A02 | 34518842 | C | T | missense_variant | MODERATE | c.416G>A|p.Cys139Tyr |
S172 S217 |
3 | BAA02g41130 | A02 | 34518878 | G | A | missense_variant | MODERATE | c.380C>T|p.Ser127Phe |
S103 |
4 | BAA02g41130 | A02 | 34519475 | G | A | upstream_gene_variant | MODIFIER | c.-218C>T| |
S255 |
5 | BAA02g41130 | A02 | 34523884 | C | T | upstream_gene_variant | MODIFIER | c.-4627G>A| |
S165 |
6 | BAA02g41130 | A02 | 34524152 | C | T | upstream_gene_variant | MODIFIER | c.-4895G>A| |
S88 |