Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94762760A>C | CA5616289 | CYP2C19 | c.55A>C (p.Ile19Leu) c.932-12298A>C (n.932-12298A>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94762760A= | CA1929213733 | CYP2C19 | c.55A= (p.Ile19=) c.932-12298A= (n.932-12298A=) | dbSNP |
10 | g.94762760A>G | CA377667918 | CYP2C19 | c.55A>G (p.Ile19Val) c.932-12298A>G (n.932-12298A>G) | dbSNP gnomAD v4 |