Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46690 | A02 | 37874926 | G | A | upstream_gene_variant | MODIFIER | c.-4571G>A| |
S11 |
2 | BAA02g46690 | A02 | 37877118 | C | T | upstream_gene_variant | MODIFIER | c.-2379C>T| |
S68 |
3 | BAA02g46690 | A02 | 37881435 | G | A | missense_variant | MODERATE | c.766G>A|p.Glu256Lys |
S94 |