Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.70175500G>A | CA400860648 | KCNJ2 | c.461G>A (p.Cys154Tyr) | ClinVar dbSNP |
17 | g.70175500G>T | CA329684 | KCNJ2 | c.461G>T (p.Cys154Phe) | ClinVar dbSNP |
17 | g.70175500G= | CA2272996584 | KCNJ2 | c.461G= (p.Cys154=) | dbSNP |