Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44270 | A09 | 50036859 | C | T | missense_variant | MODERATE | c.712G>A|p.Gly238Arg |
S286 |
2 | BAA09g44270 | A09 | 50036938 | C | T | synonymous_variant | LOW | c.633G>A|p.Glu211Glu |
S159 S243 S299 |
3 | BAA09g44270 | A09 | 50038571 | C | T | upstream_gene_variant | MODIFIER | c.-423G>A| |
S146 |
4 | BAA09g44270 | A09 | 50042034 | G | A | upstream_gene_variant | MODIFIER | c.-3886C>T| |
S112 |
5 | BAA09g44270 | A09 | 50043044 | G | A | upstream_gene_variant | MODIFIER | c.-4896C>T| |
S298 |