Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323818C>A | CA272664960 | HCN4 | c.2275G>T (p.Val759Phe) c.1057G>T (p.Val353Phe) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323818C>T | CA235701 | HCN4 | c.2275G>A (p.Val759Ile) c.1057G>A (p.Val353Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323818C= | CA2187188669 | HCN4 | c.2275G= (p.Val759=) c.1057G= (p.Val353=) | dbSNP |