Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15660 | A02 | 7578647 | C | T | missense_variant | MODERATE | c.439C>T|p.His147Tyr |
S210 |
2 | BAA02g15660 | A02 | 7578756 | G | A | missense_variant | MODERATE | c.548G>A|p.Gly183Glu |
S246 |
3 | BAA02g15660 | A02 | 7579742 | G | A | missense_variant | MODERATE | c.1169G>A|p.Ser390Asn |
S67 |