Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94852914A>C | CA5616874 | CYP2C19 | c.1473A>C (p.Ter491Cys) n.2384A>C c.2236A>C (n.2236A>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94852914A>T | CA211697020 | CYP2C19 | c.1473A>T (p.Ter491Cys) n.2384A>T c.2236A>T (n.2236A>T) | dbSNP |
10 | g.94852914A>G | CA377676111 | CYP2C19 | c.1473A>G (p.Ter491Trp) n.2384A>G c.2236A>G (n.2236A>G) | dbSNP gnomAD v4 |
10 | g.94852914A= | CA1929279956 | CYP2C19 | c.1473A= (p.Ter491=) n.2384A= c.2236A= (n.2236A=) | dbSNP |