Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10590 | A02 | 4707743 | C | T | upstream_gene_variant | MODIFIER | c.-2166C>T| |
S178 |
2 | BAA02g10590 | A02 | 4710179 | G | A | missense_variant | MODERATE | c.46G>A|p.Val16Ile |
S134 |
3 | BAA02g10590 | A02 | 4716449 | G | A | downstream_gene_variant | MODIFIER | c.*3175G>A| |
S191 |