Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17090 | A09 | 10142366 | G | A | missense_variant | MODERATE | c.730C>T|p.Arg244Cys |
S20 |
2 | BAA09g17090 | A09 | 10142565 | G | A | synonymous_variant | LOW | c.531C>T|p.Ser177Ser |
S243 |
3 | BAA09g17090 | A09 | 10142688 | C | T | synonymous_variant | LOW | c.408G>A|p.Glu136Glu |
S186 |
4 | BAA09g17090 | A09 | 10145623 | C | T | upstream_gene_variant | MODIFIER | c.-2528G>A| |
S85 |
5 | BAA09g17090 | A09 | 10146441 | C | T | upstream_gene_variant | MODIFIER | c.-3346G>A| |
S179 |