Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.128911725G>C | CA383248212 | KCNJ5 | c.452G>C (p.Gly151Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.128911725G>A | CA163131 | KCNJ5 | c.452G>A (p.Gly151Glu) | ClinVar dbSNP |
11 | g.128911725G= | CA2008292584 | KCNJ5 | c.452G= (p.Gly151=) | dbSNP |