Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.70175605G>T | CA302038 | KCNJ2 | c.566G>T (p.Arg189Ile) | ClinVar dbSNP |
17 | g.70175605G>A | CA302035 | KCNJ2 | c.566G>A (p.Arg189Lys) | ClinVar dbSNP |
17 | g.70175605G>C | CA400861034 | KCNJ2 | c.566G>C (p.Arg189Thr) | ClinVar dbSNP |
17 | g.70175605G= | CA2272996619 | KCNJ2 | c.566G= (p.Arg189=) | dbSNP |