| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.70175475G>C | CA400860592 | KCNJ2 | c.436G>C (p.Gly146Arg) | ClinVar dbSNP |
| 17 | g.70175475G>A | CA329675 | KCNJ2 | c.436G>A (p.Gly146Ser) | ClinVar dbSNP |
| 17 | g.70175475G= | CA2272996576 | KCNJ2 | c.436G= (p.Gly146=) | dbSNP |