Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g42700 | A09 | 49002000 | A | G | missense_variant | MODERATE | c.505A>G|p.Ile169Val |
S152 |
2 | BAA09g42700 | A09 | 49002002 | C | T | synonymous_variant | LOW | c.507C>T|p.Ile169Ile |
S82 S92 |
3 | BAA09g42700 | A09 | 49002733 | G | A | missense_variant | MODERATE | c.1238G>A|p.Gly413Glu |
S71 |