Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g61440 | A09 | 58486452 | C | T | missense_variant | MODERATE | c.1025G>A|p.Gly342Glu |
S20 |
2 | BAA09g61440 | A09 | 58488181 | G | A | synonymous_variant | LOW | c.309C>T|p.Ala103Ala |
S189 |
3 | BAA09g61440 | A09 | 58493804 | C | T | upstream_gene_variant | MODIFIER | c.-4824G>A| |
S26 |