Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45470 | A01 | 30316012 | C | T | stop_gained | HIGH | c.1325G>A|p.Trp442* |
S65 |
2 | BAA01g45470 | A01 | 30316120 | C | T | missense_variant | MODERATE | c.1217G>A|p.Gly406Glu |
S27 |
3 | BAA01g45470 | A01 | 30316130 | G | A | synonymous_variant | LOW | c.1207C>T|p.Leu403Leu |
S185 |
4 | BAA01g45470 | A01 | 30316773 | G | A | synonymous_variant | LOW | c.648C>T|p.Pro216Pro |
S71 |
5 | BAA01g45470 | A01 | 30319267 | C | T | upstream_gene_variant | MODIFIER | c.-1847G>A| |
S120 |
6 | BAA01g45470 | A01 | 30320600 | G | A | upstream_gene_variant | MODIFIER | c.-3180C>T| |
S20 |
7 | BAA01g45470 | A01 | 30320796 | G | A | upstream_gene_variant | MODIFIER | c.-3376C>T| |
S180 |