Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47880 | A02 | 38551598 | C | T | missense_variant | MODERATE | c.1135G>A|p.Val379Ile |
S289 S290 |
2 | BAA02g47880 | A02 | 38551671 | C | T | synonymous_variant | LOW | c.1062G>A|p.Gly354Gly |
S33 |
3 | BAA02g47880 | A02 | 38551732 | C | T | missense_variant | MODERATE | c.1001G>A|p.Gly334Asp |
S18 |
4 | BAA02g47880 | A02 | 38551742 | C | T | missense_variant | MODERATE | c.991G>A|p.Asp331Asn |
S121 |
5 | BAA02g47880 | A02 | 38552342 | G | A | missense_variant | MODERATE | c.391C>T|p.Pro131Ser |
S68 |
6 | BAA02g47880 | A02 | 38553721 | C | T | upstream_gene_variant | MODIFIER | c.-989G>A| |
S178 |
7 | BAA02g47880 | A02 | 38556096 | G | A | upstream_gene_variant | MODIFIER | c.-3364C>T| |
S5 |
8 | BAA02g47880 | A02 | 38557525 | C | T | upstream_gene_variant | MODIFIER | c.-4793G>A| |
S149 |