Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66600 | A09 | 60782663 | G | A | missense_variant | MODERATE | c.560G>A|p.Arg187Lys |
S177 |
2 | BAA09g66600 | A09 | 60783321 | C | T | synonymous_variant | LOW | c.1218C>T|p.Tyr406Tyr |
S162 S261 |
3 | BAA09g66600 | A09 | 60783487 | C | T | missense_variant | MODERATE | c.1384C>T|p.Pro462Ser |
S172 |
4 | BAA09g66600 | A09 | 60783899 | C | T | missense_variant | MODERATE | c.1796C>T|p.Thr599Ile |
S56 |
5 | BAA09g66600 | A09 | 60788351 | C | T | downstream_gene_variant | MODIFIER | c.*4250C>T| |
S66 |