| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.150951707G>A | CA458645580 | KCNH2 | n.984C>T n.2519C>T c.1686C>T (p.His562=) c.666C>T (p.His222=) c.1338C>T (p.His446=) n.973C>T n.991C>T n.1909C>T c.1386C>T (p.His462=) c.1536C>T (p.His512=) c.1509C>T (p.His503=) | ClinVar dbSNP |
| 7 | g.150951707G>C | CA16605170 | KCNH2 | n.984C>G n.2519C>G c.1686C>G (p.His562Gln) c.666C>G (p.His222Gln) c.1338C>G (p.His446Gln) n.973C>G n.991C>G n.1909C>G c.1386C>G (p.His462Gln) c.1536C>G (p.His512Gln) c.1509C>G (p.His503Gln) | ClinVar dbSNP |