| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.70175938G>C | CA329705 | KCNJ2 | c.899G>C (p.Gly300Ala) | ClinVar dbSNP gnomAD v4 |
| 17 | g.70175938G>A | CA329702 | KCNJ2 | c.899G>A (p.Gly300Asp) | ClinVar dbSNP |
| 17 | g.70175938G>T | CA254594 | KCNJ2 | c.899G>T (p.Gly300Val) | ClinVar dbSNP |
| 17 | g.70175938G= | CA2272996732 | KCNJ2 | c.899G= (p.Gly300=) | dbSNP |