Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09400 | A01 | 4187177 | G | A | synonymous_variant | LOW | c.912C>T|p.Tyr304Tyr |
S292 |
2 | BAA01g09400 | A01 | 4187941 | C | T | missense_variant | MODERATE | c.266G>A|p.Gly89Glu |
S70 |
3 | BAA01g09400 | A01 | 4188556 | C | T | missense_variant | MODERATE | c.92G>A|p.Gly31Glu |
S286 |
4 | BAA01g09400 | A01 | 4191610 | G | A | upstream_gene_variant | MODIFIER | c.-2963C>T| |
S67 |
5 | BAA01g09400 | A01 | 4193109 | G | A | upstream_gene_variant | MODIFIER | c.-4462C>T| |
S236 |
6 | BAA01g09400 | A01 | 4193568 | G | A | upstream_gene_variant | MODIFIER | c.-4921C>T| |
S115 |