Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09970 | A02 | 4402023 | C | T | upstream_gene_variant | MODIFIER | c.-714C>T| |
S65 |
2 | BAA02g09970 | A02 | 4402784 | G | A | synonymous_variant | LOW | c.48G>A|p.Ala16Ala |
S296 |
3 | BAA02g09970 | A02 | 4404000 | C | T | missense_variant | MODERATE | c.499C>T|p.Leu167Phe |
S182 |
4 | BAA02g09970 | A02 | 4405982 | G | A | missense_variant | MODERATE | c.1559G>A|p.Gly520Glu |
S265 |
5 | BAA02g09970 | A02 | 4406282 | G | A | downstream_gene_variant | MODIFIER | c.*146G>A| |
S206 S26 |