Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20780 | A02 | 11043177 | C | T | upstream_gene_variant | MODIFIER | c.-1047C>T| |
S94 |
2 | BAA02g20780 | A02 | 11043228 | G | A | upstream_gene_variant | MODIFIER | c.-996G>A| |
S19 |
3 | BAA02g20780 | A02 | 11044417 | G | A | missense_variant | MODERATE | c.118G>A|p.Ala40Thr |
S116 |