Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01790 | A02 | 784928 | C | T | upstream_gene_variant | MODIFIER | c.-4352C>T| |
S182 |
2 | BAA02g01790 | A02 | 785056 | C | T | upstream_gene_variant | MODIFIER | c.-4224C>T| |
S298 |
3 | BAA02g01790 | A02 | 789299 | C | T | missense_variant | MODERATE | c.20C>T|p.Ala7Val |
S255 |
4 | BAA02g01790 | A02 | 789785 | C | T | synonymous_variant | LOW | c.306C>T|p.Ile102Ile |
S37 |