Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73324216G>T | CA117310 | HCN4 | c.2016C>A (p.Ser672Arg) c.798C>A (p.Ser266Arg) | ClinVar dbSNP |
15 | g.73324216G>A | CA7649139 | HCN4 | c.2016C>T (p.Ser672=) c.798C>T (p.Ser266=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73324216G= | CA2187189422 | HCN4 | c.2016C= (p.Ser672=) c.798C= (p.Ser266=) | dbSNP |