Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20950 | A02 | 11172308 | C | T | missense_variant | MODERATE | c.53G>A|p.Cys18Tyr |
S2 |
2 | BAA02g20950 | A02 | 11172578 | C | T | upstream_gene_variant | MODIFIER | c.-218G>A| |
S250 |
3 | BAA02g20950 | A02 | 11172716 | G | A | upstream_gene_variant | MODIFIER | c.-356C>T| |
S200 |
4 | BAA02g20950 | A02 | 11172742 | G | A | upstream_gene_variant | MODIFIER | c.-382C>T| |
S291 |
5 | BAA02g20950 | A02 | 11172826 | G | A | upstream_gene_variant | MODIFIER | c.-466C>T| |
S150 |
6 | BAA02g20950 | A02 | 11175428 | C | T | upstream_gene_variant | MODIFIER | c.-3068G>A| |
S178 |
7 | BAA02g20950 | A02 | 11176546 | C | T | upstream_gene_variant | MODIFIER | c.-4186G>A| |
S183 S198 |
8 | BAA02g20950 | A02 | 11176834 | G | A | upstream_gene_variant | MODIFIER | c.-4474C>T| |
S156 |