Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46250 | A02 | 37656225 | C | T | missense_variant | MODERATE | c.992G>A|p.Arg331Lys |
S270 |
2 | BAA02g46250 | A02 | 37658090 | C | T | synonymous_variant | LOW | c.177G>A|p.Arg59Arg |
S128 |
3 | BAA02g46250 | A02 | 37660107 | G | T | upstream_gene_variant | MODIFIER | c.-1757C>A| |
S288 |
4 | BAA02g46250 | A02 | 37660379 | C | T | upstream_gene_variant | MODIFIER | c.-2029G>A| |
S162 |
5 | BAA02g46250 | A02 | 37661055 | G | A | upstream_gene_variant | MODIFIER | c.-2705C>T| |
S298 |
6 | BAA02g46250 | A02 | 37663311 | C | T | upstream_gene_variant | MODIFIER | c.-4961G>A| |
S18 |