| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.70175692G>C | CA400861474 | KCNJ2 | c.653G>C (p.Arg218Pro) | ClinVar dbSNP |
| 17 | g.70175692G>T | CA302043 | KCNJ2 | c.653G>T (p.Arg218Leu) | ClinVar dbSNP |
| 17 | g.70175692G>A | CA329699 | KCNJ2 | c.653G>A (p.Arg218Gln) | ClinVar dbSNP COSMIC |
| 17 | g.70175692G= | CA2272996652 | KCNJ2 | c.653G= (p.Arg218=) | dbSNP |