Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11600 | A02 | 5245042 | C | T | missense_variant | MODERATE | c.1018G>A|p.Asp340Asn |
S3 |
2 | BAA02g11600 | A02 | 5245448 | C | T | stop_gained | HIGH | c.929G>A|p.Trp310* |
S200 |
3 | BAA02g11600 | A02 | 5246163 | C | T | missense_variant | MODERATE | c.502G>A|p.Asp168Asn |
S115 |
4 | BAA02g11600 | A02 | 5246792 | G | A | missense_variant | MODERATE | c.35C>T|p.Pro12Leu |
S177 |
5 | BAA02g11600 | A02 | 5246878 | C | T | upstream_gene_variant | MODIFIER | c.-52G>A| |
S124 |
6 | BAA02g11600 | A02 | 5248953 | C | T | upstream_gene_variant | MODIFIER | c.-2127G>A| |
S195 |
7 | BAA02g11600 | A02 | 5250263 | C | T | upstream_gene_variant | MODIFIER | c.-3437G>A| |
S138 |
8 | BAA02g11600 | A02 | 5250594 | G | A | upstream_gene_variant | MODIFIER | c.-3768C>T| |
S236 |