Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04900 | A02 | 2138709 | C | T | synonymous_variant | LOW | c.747C>T|p.Tyr249Tyr |
S108 |
2 | BAA02g04900 | A02 | 2138796 | G | A | missense_variant | MODERATE | c.834G>A|p.Met278Ile |
S168 |
3 | BAA02g04900 | A02 | 2139592 | G | A | synonymous_variant | LOW | c.1212G>A|p.Glu404Glu |
S89 |
4 | BAA02g04900 | A02 | 2141939 | G | A | downstream_gene_variant | MODIFIER | c.*282G>A| |
S127 |
5 | BAA02g04900 | A02 | 2142345 | C | T | downstream_gene_variant | MODIFIER | c.*688C>T| |
S277 |
6 | BAA02g04900 | A02 | 2142514 | G | A | downstream_gene_variant | MODIFIER | c.*857G>A| |
S287 |