| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.70175596C>A | CA400860997 | KCNJ2 | c.557C>A (p.Pro186Gln) | ClinVar dbSNP |
| 17 | g.70175596C>T | CA254596 | KCNJ2 | c.557C>T (p.Pro186Leu) | ClinVar dbSNP |
| 17 | g.70175596C= | CA2272996615 | KCNJ2 | c.557C= (p.Pro186=) | dbSNP |