Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323289G>T | CA7648952 | HCN4 | c.2804C>A (p.Ser935Tyr) c.1586C>A (p.Ser529Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323289G>A | CA301966 | HCN4 | c.2804C>T (p.Ser935Phe) c.1586C>T (p.Ser529Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323289G>C | CA393087921 | HCN4 | c.2804C>G (p.Ser935Cys) c.1586C>G (p.Ser529Cys) | ClinVar dbSNP |
15 | g.73323289G= | CA2187187930 | HCN4 | c.2804C= (p.Ser935=) c.1586C= (p.Ser529=) | dbSNP |