| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73329692C>A | CA393093802 | HCN4 | c.1471G>T (p.Asp491Tyr) c.253G>T (p.Asp85Tyr) | |
| 15 | g.73329692C= | CA2187167535 | HCN4 | c.1471G= (p.Asp491=) c.253G= (p.Asp85=) | |
| 15 | g.73329692C>G | CA393093803 | HCN4 | c.1471G>C (p.Asp491His) c.253G>C (p.Asp85His) | ClinVar dbSNP |
| 15 | g.73329692C>T | CA16614921 | HCN4 | c.1471G>A (p.Asp491Asn) c.253G>A (p.Asp85Asn) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73329693G>A | CA7649289 | HCN4 | c.1470C>T (p.Ser490=) c.252C>T (p.Ser84=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329693G>C | CA491151649 | HCN4 | c.1470C>G (p.Ser490=) c.252C>G (p.Ser84=) | |
| 15 | g.73329693G= | CA2187167541 | HCN4 | c.1470C= (p.Ser490=) c.252C= (p.Ser84=) | |
| 15 | g.73329693G>T | CA491151651 | HCN4 | c.1470C>A (p.Ser490=) c.252C>A (p.Ser84=) | |
| 15 | g.73329694G>A | CA393093806 | HCN4 | c.1469C>T (p.Ser490Phe) c.251C>T (p.Ser84Phe) | |
| 15 | g.73329694G>C | CA393093804 | HCN4 | c.1469C>G (p.Ser490Cys) c.251C>G (p.Ser84Cys) | |
| 15 | g.73329694G>T | CA393093805 | HCN4 | c.1469C>A (p.Ser490Tyr) c.251C>A (p.Ser84Tyr) | |
| 15 | g.73329695A>C | CA393093807 | HCN4 | c.1468T>G (p.Ser490Ala) c.250T>G (p.Ser84Ala) | |
| 15 | g.73329695A>G | CA393093808 | HCN4 | c.1468T>C (p.Ser490Pro) c.250T>C (p.Ser84Pro) | |
| 15 | g.73329695A>T | CA393093810 | HCN4 | c.1468T>A (p.Ser490Thr) c.250T>A (p.Ser84Thr) | |
| 15 | g.73329696C>A | CA393093812 | HCN4 | c.1467G>T (p.Met489Ile) c.249G>T (p.Met83Ile) | |
| 15 | g.73329696C= | CA2187167544 | HCN4 | c.1467G= (p.Met489=) c.249G= (p.Met83=) | |
| 15 | g.73329696C>G | CA393093814 | HCN4 | c.1467G>C (p.Met489Ile) c.249G>C (p.Met83Ile) | |
| 15 | g.73329696C>T | CA7649290 | HCN4 | c.1467G>A (p.Met489Ile) c.249G>A (p.Met83Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329697A>C | CA393093817 | HCN4 | c.1466T>G (p.Met489Arg) c.248T>G (p.Met83Arg) | |
| 15 | g.73329697A>G | CA393093821 | HCN4 | c.1466T>C (p.Met489Thr) c.248T>C (p.Met83Thr) | gnomAD v4 |
| 15 | g.73329697A>T | CA393093819 | HCN4 | c.1466T>A (p.Met489Lys) c.248T>A (p.Met83Lys) | |
| 15 | g.73329698T>A | CA393093823 | HCN4 | c.1465A>T (p.Met489Leu) c.247A>T (p.Met83Leu) | |
| 15 | g.73329698T>C | CA393093825 | HCN4 | c.1465A>G (p.Met489Val) c.247A>G (p.Met83Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329698T>G | CA393093827 | HCN4 | c.1465A>C (p.Met489Leu) c.247A>C (p.Met83Leu) | |
| 15 | g.73329698T= | CA2187167548 | HCN4 | c.1465A= (p.Met489=) c.247A= (p.Met83=) | |
| 15 | g.73329699G>A | CA491151671 | HCN4 | c.1464C>T (p.Gly488=) c.246C>T (p.Gly82=) | |
| 15 | g.73329699G>C | CA491151669 | HCN4 | c.1464C>G (p.Gly488=) c.246C>G (p.Gly82=) | |
| 15 | g.73329699G>T | CA491151668 | HCN4 | c.1464C>A (p.Gly488=) c.246C>A (p.Gly82=) | |
| 15 | g.73329700C>A | CA393093829 | HCN4 | c.1463G>T (p.Gly488Val) c.245G>T (p.Gly82Val) | |
| 15 | g.73329700C>G | CA393093831 | HCN4 | c.1463G>C (p.Gly488Ala) c.245G>C (p.Gly82Ala) | |
| 15 | g.73329700C>T | CA393093833 | HCN4 | c.1463G>A (p.Gly488Asp) c.245G>A (p.Gly82Asp) | gnomAD v4 |
| 15 | g.73329701C>A | CA393093835 | HCN4 | c.1462G>T (p.Gly488Cys) c.244G>T (p.Gly82Cys) | |
| 15 | g.73329701C= | CA2187167554 | HCN4 | c.1462G= (p.Gly488=) c.244G= (p.Gly82=) | |
| 15 | g.73329701C>G | CA393093836 | HCN4 | c.1462G>C (p.Gly488Arg) c.244G>C (p.Gly82Arg) | |
| 15 | g.73329701C>T | CA10604722 | HCN4 | c.1462G>A (p.Gly488Ser) c.244G>A (p.Gly82Ser) | ClinVar dbSNP |
| 15 | g.73329702C>A | CA491151679 | HCN4 | c.1461G>T (p.Val487=) c.243G>T (p.Val81=) | |
| 15 | g.73329702C>G | CA491151681 | HCN4 | c.1461G>C (p.Val487=) c.243G>C (p.Val81=) | |
| 15 | g.73329702C>T | CA491151683 | HCN4 | c.1461G>A (p.Val487=) c.243G>A (p.Val81=) | gnomAD v4 |
| 15 | g.73329703A>C | CA393093840 | HCN4 | c.1460T>G (p.Val487Gly) c.242T>G (p.Val81Gly) | |
| 15 | g.73329703A>G | CA393093842 | HCN4 | c.1460T>C (p.Val487Ala) c.242T>C (p.Val81Ala) | |
| 15 | g.73329703A>T | CA393093843 | HCN4 | c.1460T>A (p.Val487Glu) c.242T>A (p.Val81Glu) | |
| 15 | g.73329704C>A | CA393093845 | HCN4 | c.1459G>T (p.Val487Leu) c.241G>T (p.Val81Leu) | |
| 15 | g.73329704C= | CA2187167560 | HCN4 | c.1459G= (p.Val487=) c.241G= (p.Val81=) | |
| 15 | g.73329704C>G | CA393093848 | HCN4 | c.1459G>C (p.Val487Leu) c.241G>C (p.Val81Leu) | |
| 15 | g.73329704C>T | CA234114 | HCN4 | c.1459G>A (p.Val487Met) c.241G>A (p.Val81Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329705G>A | CA7649291 | HCN4 | c.1458C>T (p.Pro486=) c.240C>T (p.Pro80=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329705G>C | CA491151694 | HCN4 | c.1458C>G (p.Pro486=) c.240C>G (p.Pro80=) | gnomAD v4 |
| 15 | g.73329705G= | CA2187167569 | HCN4 | c.1458C= (p.Pro486=) c.240C= (p.Pro80=) | |
| 15 | g.73329705G>T | CA491151695 | HCN4 | c.1458C>A (p.Pro486=) c.240C>A (p.Pro80=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329706G>A | CA393093852 | HCN4 | c.1457C>T (p.Pro486Leu) c.239C>T (p.Pro80Leu) | gnomAD v4 |