Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.150974845T>C | CA005331 | KCNH2 | c.173A>G (p.Glu58Gly) c.-5A>G (n.-5A>G) n.396A>G | ClinVar dbSNP |
7 | g.150974845T>G | CA005322 | KCNH2 | c.173A>C (p.Glu58Ala) c.-5A>C (n.-5A>C) n.396A>C | ClinVar dbSNP |
7 | g.150974845T= | CA1752440965 | KCNH2 | c.173A= (p.Glu58=) c.-5A= (n.-5A=) n.396A= | dbSNP |