Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.70175470G>C | CA329672 | KCNJ2 | c.431G>C (p.Gly144Ala) | ClinVar dbSNP |
17 | g.70175470G>A | CA329669 | KCNJ2 | c.431G>A (p.Gly144Asp) | ClinVar dbSNP |
17 | g.70175470G>T | CA400860583 | KCNJ2 | c.431G>T (p.Gly144Val) | ClinVar dbSNP |
17 | g.70175470G= | CA2272996572 | KCNJ2 | c.431G= (p.Gly144=) | dbSNP |