UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73325031G>A | CA491478988 | HCN4 | c.1902C>T (p.Phe634=) c.684C>T (p.Phe228=) | dbSNP gnomAD v4 |
| 15 | g.73325031G>C | CA393090625 | HCN4 | c.1902C>G (p.Phe634Leu) c.684C>G (p.Phe228Leu) | |
| 15 | g.73325031G>T | CA393090626 | HCN4 | c.1902C>A (p.Phe634Leu) c.684C>A (p.Phe228Leu) | |
| 15 | g.73325032A>C | CA393090629 | HCN4 | c.1901T>G (p.Phe634Cys) c.683T>G (p.Phe228Cys) | |
| 15 | g.73325032A>G | CA393090627 | HCN4 | c.1901T>C (p.Phe634Ser) c.683T>C (p.Phe228Ser) | |
| 15 | g.73325032A>T | CA393090628 | HCN4 | c.1901T>A (p.Phe634Tyr) c.683T>A (p.Phe228Tyr) | |
| 15 | g.73325033A= | CA2187190414 | HCN4 | c.1900T= (p.Phe634=) c.682T= (p.Phe228=) | |
| 15 | g.73325033A>C | CA393090630 | HCN4 | c.1900T>G (p.Phe634Val) c.682T>G (p.Phe228Val) | |
| 15 | g.73325033A>G | CA393090631 | HCN4 | c.1900T>C (p.Phe634Leu) c.682T>C (p.Phe228Leu) | dbSNP gnomAD v4 |
| 15 | g.73325033A>T | CA393090632 | HCN4 | c.1900T>A (p.Phe634Ile) c.682T>A (p.Phe228Ile) | |
| 15 | g.73325034G>A | CA491478994 | HCN4 | c.1899C>T (p.Tyr633=) c.681C>T (p.Tyr227=) | gnomAD v4 |
| 15 | g.73325034G>C | CA393090633 | HCN4 | c.1899C>G (p.Tyr633Ter) c.681C>G (p.Tyr227Ter) | |
| 15 | g.73325034G>T | CA393090634 | HCN4 | c.1899C>A (p.Tyr633Ter) c.681C>A (p.Tyr227Ter) | |
| 15 | g.73325035T>A | CA393090635 | HCN4 | c.1898A>T (p.Tyr633Phe) c.680A>T (p.Tyr227Phe) | |
| 15 | g.73325035T>C | CA393090636 | HCN4 | c.1898A>G (p.Tyr633Cys) c.680A>G (p.Tyr227Cys) | |
| 15 | g.73325035T>G | CA393090637 | HCN4 | c.1898A>C (p.Tyr633Ser) c.680A>C (p.Tyr227Ser) | |
| 15 | g.73325036A>C | CA393090638 | HCN4 | c.1897T>G (p.Tyr633Asp) c.679T>G (p.Tyr227Asp) | |
| 15 | g.73325036A>G | CA393090639 | HCN4 | c.1897T>C (p.Tyr633His) c.679T>C (p.Tyr227His) | |
| 15 | g.73325036A>T | CA393090640 | HCN4 | c.1897T>A (p.Tyr633Asn) c.679T>A (p.Tyr227Asn) | |
| 15 | g.73325036_73325038del | CA2580090006 | HCN4 | c.1895_1897del (p.Met632_Tyr633delinsAsn) c.677_679del (p.Met226_Tyr227delinsAsn) | ClinVar |
| 15 | g.73325037C>A | CA393090641 | HCN4 | c.1896G>T (p.Met632Ile) c.678G>T (p.Met226Ile) | |
| 15 | g.73325037C= | CA2187190418 | HCN4 | c.1896G= (p.Met632=) c.678G= (p.Met226=) | |
| 15 | g.73325037C>G | CA393090642 | HCN4 | c.1896G>C (p.Met632Ile) c.678G>C (p.Met226Ile) | |
| 15 | g.73325037C>T | CA236703 | HCN4 | c.1896G>A (p.Met632Ile) c.678G>A (p.Met226Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73325038A= | CA2187190424 | HCN4 | c.1895T= (p.Met632=) c.677T= (p.Met226=) | |
| 15 | g.73325038A>C | CA272666320 | HCN4 | c.1895T>G (p.Met632Arg) c.677T>G (p.Met226Arg) | dbSNP |
| 15 | g.73325038A>G | CA393090643 | HCN4 | c.1895T>C (p.Met632Thr) c.677T>C (p.Met226Thr) | |
| 15 | g.73325038A>T | CA393090644 | HCN4 | c.1895T>A (p.Met632Lys) c.677T>A (p.Met226Lys) | |
| 15 | g.73325038_73325041delinsATCT | CA2187190426 | HCN4 | c.1892_1895delinsAGAT (p.Lys631=) c.674_677delinsAGAT (p.Lys225=) | |
| 15 | g.73325039T>A | CA393090645 | HCN4 | c.1894A>T (p.Met632Leu) c.676A>T (p.Met226Leu) | |
| 15 | g.73325039T>C | CA393090646 | HCN4 | c.1894A>G (p.Met632Val) c.676A>G (p.Met226Val) | gnomAD v4 |
| 15 | g.73325039T>G | CA393090647 | HCN4 | c.1894A>C (p.Met632Leu) c.676A>C (p.Met226Leu) | |
| 15 | g.73325043_73325045del | CA619410629 | HCN4 | c.1892_1894del (p.Lys631del) c.674_676del (p.Lys225del) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73325040C>A | CA393090648 | HCN4 | c.1893G>T (p.Lys631Asn) c.675G>T (p.Lys225Asn) | gnomAD v4 |
| 15 | g.73325040C>G | CA393090649 | HCN4 | c.1893G>C (p.Lys631Asn) c.675G>C (p.Lys225Asn) | |
| 15 | g.73325040C>T | CA491479000 | HCN4 | c.1893G>A (p.Lys631=) c.675G>A (p.Lys225=) | gnomAD v4 |
| 15 | g.73325041T>A | CA393090650 | HCN4 | c.1892A>T (p.Lys631Met) c.674A>T (p.Lys225Met) | |
| 15 | g.73325041T>C | CA393090651 | HCN4 | c.1892A>G (p.Lys631Arg) c.674A>G (p.Lys225Arg) | |
| 15 | g.73325041T>G | CA393090652 | HCN4 | c.1892A>C (p.Lys631Thr) c.674A>C (p.Lys225Thr) | |
| 15 | g.73325042T>A | CA393090653 | HCN4 | c.1891A>T (p.Lys631Ter) c.673A>T (p.Lys225Ter) | |
| 15 | g.73325042T>C | CA393090654 | HCN4 | c.1891A>G (p.Lys631Glu) c.673A>G (p.Lys225Glu) | |
| 15 | g.73325042T>G | CA393090655 | HCN4 | c.1891A>C (p.Lys631Gln) c.673A>C (p.Lys225Gln) | |
| 15 | g.73325043C>A | CA393090656 | HCN4 | c.1890G>T (p.Lys630Asn) c.672G>T (p.Lys224Asn) | |
| 15 | g.73325043C>G | CA393090657 | HCN4 | c.1890G>C (p.Lys630Asn) c.672G>C (p.Lys224Asn) | |
| 15 | g.73325043C>T | CA491479001 | HCN4 | c.1890G>A (p.Lys630=) c.672G>A (p.Lys224=) | gnomAD v4 |
| 15 | g.73325044T>A | CA393090658 | HCN4 | c.1889A>T (p.Lys630Met) c.671A>T (p.Lys224Met) | |
| 15 | g.73325044T>C | CA393090659 | HCN4 | c.1889A>G (p.Lys630Arg) c.671A>G (p.Lys224Arg) | gnomAD v4 |
| 15 | g.73325044T>G | CA7649169 | HCN4 | c.1889A>C (p.Lys630Thr) c.671A>C (p.Lys224Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73325044T= | CA2187190432 | HCN4 | c.1889A= (p.Lys630=) c.671A= (p.Lys224=) | |
| 15 | g.73325045T>A | CA393090660 | HCN4 | c.1888A>T (p.Lys630Ter) c.670A>T (p.Lys224Ter) | |
| 15 | g.73325045T>C | CA393090661 | HCN4 | c.1888A>G (p.Lys630Glu) c.670A>G (p.Lys224Glu) | |
| 15 | g.73325045T>G | CA393090662 | HCN4 | c.1888A>C (p.Lys630Gln) c.670A>C (p.Lys224Gln) | |
| 15 | g.73325046G>A | CA491479005 | HCN4 | c.1887C>T (p.Gly629=) c.669C>T (p.Gly223=) | |
| 15 | g.73325046G>C | CA491479006 | HCN4 | c.1887C>G (p.Gly629=) c.669C>G (p.Gly223=) | |
| 15 | g.73325046G>T | CA491479007 | HCN4 | c.1887C>A (p.Gly629=) c.669C>A (p.Gly223=) | |
| 15 | g.73325047C>A | CA393090663 | HCN4 | c.1886G>T (p.Gly629Val) c.668G>T (p.Gly223Val) | |
| 15 | g.73325047C>G | CA393090664 | HCN4 | c.1886G>C (p.Gly629Ala) c.668G>C (p.Gly223Ala) | |
| 15 | g.73325047C>T | CA393090665 | HCN4 | c.1886G>A (p.Gly629Asp) c.668G>A (p.Gly223Asp) | |
| 15 | g.73325048C>A | CA393090666 | HCN4 | c.1885G>T (p.Gly629Cys) c.667G>T (p.Gly223Cys) | |
| 15 | g.73325048C>G | CA393090667 | HCN4 | c.1885G>C (p.Gly629Arg) c.667G>C (p.Gly223Arg) | |
| 15 | g.73325048C>T | CA393090668 | HCN4 | c.1885G>A (p.Gly629Ser) c.667G>A (p.Gly223Ser) | |
| 15 | g.73325049A= | CA2187190437 | HCN4 | c.1884T= (p.Ile628=) c.666T= (p.Ile222=) | |
| 15 | g.73325049A>C | CA393090669 | HCN4 | c.1884T>G (p.Ile628Met) c.666T>G (p.Ile222Met) | |
| 15 | g.73325049A>G | CA491479010 | HCN4 | c.1884T>C (p.Ile628=) c.666T>C (p.Ile222=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73325049A>T | CA491479011 | HCN4 | c.1884T>A (p.Ile628=) c.666T>A (p.Ile222=) | |
| 15 | g.73325050A= | CA2187190440 | HCN4 | c.1883T= (p.Ile628=) c.665T= (p.Ile222=) | |
| 15 | g.73325050A>C | CA393090670 | HCN4 | c.1883T>G (p.Ile628Ser) c.665T>G (p.Ile222Ser) | |
| 15 | g.73325050A>G | CA393090672 | HCN4 | c.1883T>C (p.Ile628Thr) c.665T>C (p.Ile222Thr) | dbSNP gnomAD v4 |
| 15 | g.73325050A>T | CA393090671 | HCN4 | c.1883T>A (p.Ile628Asn) c.665T>A (p.Ile222Asn) | |
| 15 | g.73325051T>A | CA393090673 | HCN4 | c.1882A>T (p.Ile628Phe) c.664A>T (p.Ile222Phe) | |
| 15 | g.73325051T>C | CA393090675 | HCN4 | c.1882A>G (p.Ile628Val) c.664A>G (p.Ile222Val) | |
| 15 | g.73325051T>G | CA393090674 | HCN4 | c.1882A>C (p.Ile628Leu) c.664A>C (p.Ile222Leu) | |
| 15 | g.73325052G>A | CA491479018 | HCN4 | c.1881C>T (p.Thr627=) c.663C>T (p.Thr221=) | |
| 15 | g.73325052G>C | CA491479015 | HCN4 | c.1881C>G (p.Thr627=) c.663C>G (p.Thr221=) | |
| 15 | g.73325052G>T | CA491479016 | HCN4 | c.1881C>A (p.Thr627=) c.663C>A (p.Thr221=) | |
| 15 | g.73325053G>A | CA393090676 | HCN4 | c.1880C>T (p.Thr627Ile) c.662C>T (p.Thr221Ile) | |
| 15 | g.73325053G>C | CA393090678 | HCN4 | c.1880C>G (p.Thr627Ser) c.662C>G (p.Thr221Ser) | |
| 15 | g.73325053G>T | CA393090677 | HCN4 | c.1880C>A (p.Thr627Asn) c.662C>A (p.Thr221Asn) | gnomAD v4 |
| 15 | g.73325054T>A | CA393090679 | HCN4 | c.1879A>T (p.Thr627Ser) c.661A>T (p.Thr221Ser) | |
| 15 | g.73325054T>C | CA393090680 | HCN4 | c.1879A>G (p.Thr627Ala) c.661A>G (p.Thr221Ala) | COSMIC |
| 15 | g.73325054T>G | CA393090681 | HCN4 | c.1879A>C (p.Thr627Pro) c.661A>C (p.Thr221Pro) | |
| 15 | g.73325055G>A | CA491479022 | HCN4 | c.1878C>T (p.Gly626=) c.660C>T (p.Gly220=) | |
| 15 | g.73325055G>C | CA491479024 | HCN4 | c.1878C>G (p.Gly626=) c.660C>G (p.Gly220=) | |
| 15 | g.73325055G>T | CA491479026 | HCN4 | c.1878C>A (p.Gly626=) c.660C>A (p.Gly220=) | gnomAD v4 |
| 15 | g.73325056C>A | CA393090682 | HCN4 | c.1877G>T (p.Gly626Val) c.659G>T (p.Gly220Val) | |
| 15 | g.73325056C= | CA2187190444 | HCN4 | c.1877G= (p.Gly626=) c.659G= (p.Gly220=) | |
| 15 | g.73325056C>G | CA393090683 | HCN4 | c.1877G>C (p.Gly626Ala) c.659G>C (p.Gly220Ala) | |
| 15 | g.73325056C>T | CA393090684 | HCN4 | c.1877G>A (p.Gly626Asp) c.659G>A (p.Gly220Asp) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73325057C>A | CA393090685 | HCN4 | c.1876G>T (p.Gly626Cys) c.658G>T (p.Gly220Cys) | |
| 15 | g.73325057C>G | CA393090686 | HCN4 | c.1876G>C (p.Gly626Arg) c.658G>C (p.Gly220Arg) | |
| 15 | g.73325057C>T | CA393090687 | HCN4 | c.1876G>A (p.Gly626Ser) c.658G>A (p.Gly220Ser) | |
| 15 | g.73325058T>A | CA393090688 | HCN4 | c.1875A>T (p.Glu625Asp) c.657A>T (p.Glu219Asp) | |
| 15 | g.73325058T>C | CA491479028 | HCN4 | c.1875A>G (p.Glu625=) c.657A>G (p.Glu219=) | |
| 15 | g.73325058T>G | CA393090689 | HCN4 | c.1875A>C (p.Glu625Asp) c.657A>C (p.Glu219Asp) | |
| 15 | g.73325059T>A | CA393090692 | HCN4 | c.1874A>T (p.Glu625Val) c.656A>T (p.Glu219Val) | |
| 15 | g.73325059T>C | CA393090691 | HCN4 | c.1874A>G (p.Glu625Gly) c.656A>G (p.Glu219Gly) | |
| 15 | g.73325059T>G | CA393090690 | HCN4 | c.1874A>C (p.Glu625Ala) c.656A>C (p.Glu219Ala) | |
| 15 | g.73325060C>A | CA393090693 | HCN4 | c.1873G>T (p.Glu625Ter) c.655G>T (p.Glu219Ter) | |
| 15 | g.73325060C>G | CA393090694 | HCN4 | c.1873G>C (p.Glu625Gln) c.655G>C (p.Glu219Gln) | |
| 15 | g.73325060C>T | CA393090695 | HCN4 | c.1873G>A (p.Glu625Lys) c.655G>A (p.Glu219Lys) | |
| 15 | g.73325061C>A | CA491479032 | HCN4 | c.1872G>T (p.Arg624=) c.654G>T (p.Arg218=) | dbSNP |
| 15 | g.73325061C= | CA2187190447 | HCN4 | c.1872G= (p.Arg624=) c.654G= (p.Arg218=) | |
| 15 | g.73325061C>G | CA7649170 | HCN4 | c.1872G>C (p.Arg624=) c.654G>C (p.Arg218=) | dbSNP ExAC gnomAD v2 |
| 15 | g.73325061C>T | CA491479035 | HCN4 | c.1872G>A (p.Arg624=) c.654G>A (p.Arg218=) | |
| 15 | g.73325062C>A | CA393090696 | HCN4 | c.1871G>T (p.Arg624Leu) c.653G>T (p.Arg218Leu) | |
| 15 | g.73325062C= | CA2187190453 | HCN4 | c.1871G= (p.Arg624=) c.653G= (p.Arg218=) | |
| 15 | g.73325062C>G | CA393090697 | HCN4 | c.1871G>C (p.Arg624Pro) c.653G>C (p.Arg218Pro) | |
| 15 | g.73325062C>T | CA7649171 | HCN4 | c.1871G>A (p.Arg624Gln) c.653G>A (p.Arg218Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73325063G>A | CA393090698 | HCN4 | c.1870C>T (p.Arg624Trp) c.652C>T (p.Arg218Trp) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73325063G>C | CA393090699 | HCN4 | c.1870C>G (p.Arg624Gly) c.652C>G (p.Arg218Gly) | |
| 15 | g.73325063G= | CA2187190460 | HCN4 | c.1870C= (p.Arg624=) c.652C= (p.Arg218=) | |
| 15 | g.73325063G>T | CA7649172 | HCN4 | c.1870C>A (p.Arg624=) c.652C>A (p.Arg218=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73325064G>A | CA491479041 | HCN4 | c.1869C>T (p.Ile623=) c.651C>T (p.Ile217=) | |
| 15 | g.73325064G>C | CA393090700 | HCN4 | c.1869C>G (p.Ile623Met) c.651C>G (p.Ile217Met) | |
| 15 | g.73325064G>T | CA491479040 | HCN4 | c.1869C>A (p.Ile623=) c.651C>A (p.Ile217=) | |
| 15 | g.73325065A>C | CA393090703 | HCN4 | c.1868T>G (p.Ile623Ser) c.650T>G (p.Ile217Ser) | |
| 15 | g.73325065A>G | CA393090702 | HCN4 | c.1868T>C (p.Ile623Thr) c.650T>C (p.Ile217Thr) | |
| 15 | g.73325065A>T | CA393090701 | HCN4 | c.1868T>A (p.Ile623Asn) c.650T>A (p.Ile217Asn) | |
| 15 | g.73325066T>A | CA393090704 | HCN4 | c.1867A>T (p.Ile623Phe) c.649A>T (p.Ile217Phe) | |
| 15 | g.73325066T>C | CA393090705 | HCN4 | c.1867A>G (p.Ile623Val) c.649A>G (p.Ile217Val) | |
| 15 | g.73325066T>G | CA393090706 | HCN4 | c.1867A>C (p.Ile623Leu) c.649A>C (p.Ile217Leu) | |
| 15 | g.73325067G>A | CA7649173 | HCN4 | c.1866C>T (p.Ile622=) c.648C>T (p.Ile216=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73325067G>C | CA393090707 | HCN4 | c.1866C>G (p.Ile622Met) c.648C>G (p.Ile216Met) | |
| 15 | g.73325067G= | CA2187190464 | HCN4 | c.1866C= (p.Ile622=) c.648C= (p.Ile216=) | |
| 15 | g.73325067G>T | CA491479051 | HCN4 | c.1866C>A (p.Ile622=) c.648C>A (p.Ile216=) | |
| 15 | g.73325068A>C | CA393090708 | HCN4 | c.1865T>G (p.Ile622Ser) c.647T>G (p.Ile216Ser) | |
| 15 | g.73325068A>G | CA393090709 | HCN4 | c.1865T>C (p.Ile622Thr) c.647T>C (p.Ile216Thr) | |
| 15 | g.73325068A>T | CA393090710 | HCN4 | c.1865T>A (p.Ile622Asn) c.647T>A (p.Ile216Asn) | |
| 15 | g.73325069T>A | CA393090711 | HCN4 | c.1864A>T (p.Ile622Phe) c.646A>T (p.Ile216Phe) | |
| 15 | g.73325069T>C | CA7649174 | HCN4 | c.1864A>G (p.Ile622Val) c.646A>G (p.Ile216Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73325069T>G | CA393090712 | HCN4 | c.1864A>C (p.Ile622Leu) c.646A>C (p.Ile216Leu) | |
| 15 | g.73325069T= | CA2187190471 | HCN4 | c.1864A= (p.Ile622=) c.646A= (p.Ile216=) | |
| 15 | g.73325070G>A | CA491479052 | HCN4 | c.1863C>T (p.Tyr621=) c.645C>T (p.Tyr215=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73325070G>C | CA393090713 | HCN4 | c.1863C>G (p.Tyr621Ter) c.645C>G (p.Tyr215Ter) | |
| 15 | g.73325070G= | CA2187190476 | HCN4 | c.1863C= (p.Tyr621=) c.645C= (p.Tyr215=) | |
| 15 | g.73325070G>T | CA393090714 | HCN4 | c.1863C>A (p.Tyr621Ter) c.645C>A (p.Tyr215Ter) | |
| 15 | g.73325071T>A | CA393090717 | HCN4 | c.1862A>T (p.Tyr621Phe) c.644A>T (p.Tyr215Phe) | |
| 15 | g.73325071T>C | CA393090715 | HCN4 | c.1862A>G (p.Tyr621Cys) c.644A>G (p.Tyr215Cys) | gnomAD v4 |
| 15 | g.73325071T>G | CA393090716 | HCN4 | c.1862A>C (p.Tyr621Ser) c.644A>C (p.Tyr215Ser) | |
| 15 | g.73325072A= | CA2187190479 | HCN4 | c.1861T= (p.Tyr621=) c.643T= (p.Tyr215=) | |
| 15 | g.73325072A>C | CA393090718 | HCN4 | c.1861T>G (p.Tyr621Asp) c.643T>G (p.Tyr215Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73325072A>G | CA393090719 | HCN4 | c.1861T>C (p.Tyr621His) c.643T>C (p.Tyr215His) | |
| 15 | g.73325072A>T | CA393090720 | HCN4 | c.1861T>A (p.Tyr621Asn) c.643T>A (p.Tyr215Asn) | |
| 15 | g.73325073G>A | CA491479053 | HCN4 | c.1860C>T (p.Asp620=) c.642C>T (p.Asp214=) | |
| 15 | g.73325073G>C | CA393090721 | HCN4 | c.1860C>G (p.Asp620Glu) c.642C>G (p.Asp214Glu) | |
| 15 | g.73325073G>T | CA393090722 | HCN4 | c.1860C>A (p.Asp620Glu) c.642C>A (p.Asp214Glu) | |
| 15 | g.73325074T>A | CA393090723 | HCN4 | c.1859A>T (p.Asp620Val) c.641A>T (p.Asp214Val) | |
| 15 | g.73325074T>C | CA393090724 | HCN4 | c.1859A>G (p.Asp620Gly) c.641A>G (p.Asp214Gly) | gnomAD v4 |
| 15 | g.73325074T>G | CA393090725 | HCN4 | c.1859A>C (p.Asp620Ala) c.641A>C (p.Asp214Ala) | |
| 15 | g.73325075C>A | CA393090726 | HCN4 | c.1858G>T (p.Asp620Tyr) c.640G>T (p.Asp214Tyr) | |
| 15 | g.73325075C>G | CA393090727 | HCN4 | c.1858G>C (p.Asp620His) c.640G>C (p.Asp214His) | |
| 15 | g.73325075C>T | CA393090728 | HCN4 | c.1858G>A (p.Asp620Asn) c.640G>A (p.Asp214Asn) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73325078dup | CA645586812 | HCN4 | c.1858dup (p.Asp620GlyfsTer?) c.640dup (p.Asp214GlyfsTer?) | COSMIC |
| 15 | g.73325078del | CA645586813 | HCN4 | c.1858del (p.Asp620ThrfsTer?) c.640del (p.Asp214ThrfsTer?) | COSMIC |
| 15 | g.73325076C>A | CA491479054 | HCN4 | c.1857G>T (p.Gly619=) c.639G>T (p.Gly213=) | |
| 15 | g.73325076C>G | CA491479055 | HCN4 | c.1857G>C (p.Gly619=) c.639G>C (p.Gly213=) | |
| 15 | g.73325076C>T | CA491479056 | HCN4 | c.1857G>A (p.Gly619=) c.639G>A (p.Gly213=) | gnomAD v4 |
| 15 | g.73325077C>A | CA393090731 | HCN4 | c.1856G>T (p.Gly619Val) c.638G>T (p.Gly213Val) | |
| 15 | g.73325077C>G | CA393090730 | HCN4 | c.1856G>C (p.Gly619Ala) c.638G>C (p.Gly213Ala) | |
| 15 | g.73325077C>T | CA393090729 | HCN4 | c.1856G>A (p.Gly619Glu) c.638G>A (p.Gly213Glu) | |
| 15 | g.73325078C>A | CA393090732 | HCN4 | c.1855G>T (p.Gly619Trp) c.637G>T (p.Gly213Trp) | |
| 15 | g.73325078C>G | CA393090734 | HCN4 | c.1855G>C (p.Gly619Arg) c.637G>C (p.Gly213Arg) | |
| 15 | g.73325078C>T | CA393090733 | HCN4 | c.1855G>A (p.Gly619Arg) c.637G>A (p.Gly213Arg) | |
| 15 | g.73325079A= | CA2187190484 | HCN4 | c.1854T= (p.Pro618=) c.636T= (p.Pro212=) | |
| 15 | g.73325079A>C | CA491479057 | HCN4 | c.1854T>G (p.Pro618=) c.636T>G (p.Pro212=) | |
| 15 | g.73325079A>G | CA272666341 | HCN4 | c.1854T>C (p.Pro618=) c.636T>C (p.Pro212=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73325079A>T | CA491479058 | HCN4 | c.1854T>A (p.Pro618=) c.636T>A (p.Pro212=) | |
| 15 | g.73325080G>A | CA7649175 | HCN4 | c.1853C>T (p.Pro618Leu) c.635C>T (p.Pro212Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73325080G>C | CA393090735 | HCN4 | c.1853C>G (p.Pro618Arg) c.635C>G (p.Pro212Arg) | |
| 15 | g.73325080G= | CA2187190487 | HCN4 | c.1853C= (p.Pro618=) c.635C= (p.Pro212=) | |
| 15 | g.73325080G>T | CA393090736 | HCN4 | c.1853C>A (p.Pro618His) c.635C>A (p.Pro212His) | |
| 15 | g.73325081G>A | CA393090737 | HCN4 | c.1852C>T (p.Pro618Ser) c.634C>T (p.Pro212Ser) | |
| 15 | g.73325081G>C | CA393090738 | HCN4 | c.1852C>G (p.Pro618Ala) c.634C>G (p.Pro212Ala) | |
| 15 | g.73325081G>T | CA393090739 | HCN4 | c.1852C>A (p.Pro618Thr) c.634C>A (p.Pro212Thr) | COSMIC |
| 15 | g.73325082C>A | CA393090740 | HCN4 | c.1851G>T (p.Gln617His) c.633G>T (p.Gln211His) | |
| 15 | g.73325082C>G | CA393090741 | HCN4 | c.1851G>C (p.Gln617His) c.633G>C (p.Gln211His) | |
| 15 | g.73325082C>T | CA491479059 | HCN4 | c.1851G>A (p.Gln617=) c.633G>A (p.Gln211=) | gnomAD v4 |
| 15 | g.73325083T>A | CA393090742 | HCN4 | c.1850A>T (p.Gln617Leu) c.632A>T (p.Gln211Leu) | |
| 15 | g.73325083T>C | CA393090743 | HCN4 | c.1850A>G (p.Gln617Arg) c.632A>G (p.Gln211Arg) | |
| 15 | g.73325083T>G | CA393090744 | HCN4 | c.1850A>C (p.Gln617Pro) c.632A>C (p.Gln211Pro) | |
| 15 | g.73325084G>A | CA393090747 | HCN4 | c.1849C>T (p.Gln617Ter) c.631C>T (p.Gln211Ter) | |
| 15 | g.73325084G>C | CA393090745 | HCN4 | c.1849C>G (p.Gln617Glu) c.631C>G (p.Gln211Glu) | |
| 15 | g.73325084G>T | CA393090746 | HCN4 | c.1849C>A (p.Gln617Lys) c.631C>A (p.Gln211Lys) | |
| 15 | g.73325085G>A | CA491479060 | HCN4 | c.1848C>T (p.Phe616=) c.630C>T (p.Phe210=) | |
| 15 | g.73325085G>C | CA393090748 | HCN4 | c.1848C>G (p.Phe616Leu) c.630C>G (p.Phe210Leu) | |
| 15 | g.73325085G>T | CA393090749 | HCN4 | c.1848C>A (p.Phe616Leu) c.630C>A (p.Phe210Leu) | |
| 15 | g.73325086A>C | CA393090750 | HCN4 | c.1847T>G (p.Phe616Cys) c.629T>G (p.Phe210Cys) | |
| 15 | g.73325086A>G | CA393090751 | HCN4 | c.1847T>C (p.Phe616Ser) c.629T>C (p.Phe210Ser) | |
| 15 | g.73325086A>T | CA393090752 | HCN4 | c.1847T>A (p.Phe616Tyr) c.629T>A (p.Phe210Tyr) | |
| 15 | g.73325087A>C | CA393090753 | HCN4 | c.1846T>G (p.Phe616Val) c.628T>G (p.Phe210Val) | |
| 15 | g.73325087A>G | CA393090754 | HCN4 | c.1846T>C (p.Phe616Leu) c.628T>C (p.Phe210Leu) | |
| 15 | g.73325087A>T | CA393090755 | HCN4 | c.1846T>A (p.Phe616Ile) c.628T>A (p.Phe210Ile) | |
| 15 | g.73325088G>A | CA491479061 | HCN4 | c.1845C>T (p.Val615=) c.627C>T (p.Val209=) | |
| 15 | g.73325088G>C | CA491479062 | HCN4 | c.1845C>G (p.Val615=) c.627C>G (p.Val209=) | |
| 15 | g.73325088G>T | CA491479063 | HCN4 | c.1845C>A (p.Val615=) c.627C>A (p.Val209=) | |
| 15 | g.73325089A= | CA2187190494 | HCN4 | c.1844T= (p.Val615=) c.626T= (p.Val209=) | |
| 15 | g.73325089A>C | CA393090756 | HCN4 | c.1844T>G (p.Val615Gly) c.626T>G (p.Val209Gly) | ClinVar dbSNP |
| 15 | g.73325089A>G | CA393090757 | HCN4 | c.1844T>C (p.Val615Ala) c.626T>C (p.Val209Ala) | |
| 15 | g.73325089A>T | CA393090758 | HCN4 | c.1844T>A (p.Val615Asp) c.626T>A (p.Val209Asp) | |
| 15 | g.73325090C>A | CA393090760 | HCN4 | c.1843G>T (p.Val615Phe) c.625G>T (p.Val209Phe) | |
| 15 | g.73325090C>G | CA393090761 | HCN4 | c.1843G>C (p.Val615Leu) c.625G>C (p.Val209Leu) | |
| 15 | g.73325090C>T | CA393090759 | HCN4 | c.1843G>A (p.Val615Ile) c.625G>A (p.Val209Ile) | |
| 15 | g.73325091C>A | CA393090762 | HCN4 | c.1842G>T (p.Glu614Asp) c.624G>T (p.Glu208Asp) | |
| 15 | g.73325091C= | CA2187190499 | HCN4 | c.1842G= (p.Glu614=) c.624G= (p.Glu208=) | |
| 15 | g.73325091C>G | CA393090763 | HCN4 | c.1842G>C (p.Glu614Asp) c.624G>C (p.Glu208Asp) | |
| 15 | g.73325091C>T | CA7649176 | HCN4 | c.1842G>A (p.Glu614=) c.624G>A (p.Glu208=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73325092T>A | CA393090764 | HCN4 | c.1841A>T (p.Glu614Val) c.623A>T (p.Glu208Val) | |
| 15 | g.73325092T>C | CA393090765 | HCN4 | c.1841A>G (p.Glu614Gly) c.623A>G (p.Glu208Gly) | gnomAD v4 |
| 15 | g.73325092T>G | CA393090766 | HCN4 | c.1841A>C (p.Glu614Ala) c.623A>C (p.Glu208Ala) | |
| 15 | g.73325093C>A | CA393090767 | HCN4 | c.1840G>T (p.Glu614Ter) c.622G>T (p.Glu208Ter) | |
| 15 | g.73325093C= | CA2187190503 | HCN4 | c.1840G= (p.Glu614=) c.622G= (p.Glu208=) | |
| 15 | g.73325093C>G | CA393090768 | HCN4 | c.1840G>C (p.Glu614Gln) c.622G>C (p.Glu208Gln) | dbSNP COSMIC |
| 15 | g.73325093C>T | CA236705 | HCN4 | c.1840G>A (p.Glu614Lys) c.622G>A (p.Glu208Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73325094G>A | CA163176 | HCN4 | c.1839C>T (p.Phe613=) c.621C>T (p.Phe207=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73325094G>C | CA7649177 | HCN4 | c.1839C>G (p.Phe613Leu) c.621C>G (p.Phe207Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73325094G= | CA2187190510 | HCN4 | c.1839C= (p.Phe613=) c.621C= (p.Phe207=) | |
| 15 | g.73325094G>T | CA393090769 | HCN4 | c.1839C>A (p.Phe613Leu) c.621C>A (p.Phe207Leu) | |
| 15 | g.73325095A>C | CA393090771 | HCN4 | c.1838T>G (p.Phe613Cys) c.620T>G (p.Phe207Cys) | |
| 15 | g.73325095A>G | CA393090772 | HCN4 | c.1838T>C (p.Phe613Ser) c.620T>C (p.Phe207Ser) | |
| 15 | g.73325095A>T | CA393090770 | HCN4 | c.1838T>A (p.Phe613Tyr) c.620T>A (p.Phe207Tyr) | |
| 15 | g.73325096A>C | CA393090773 | HCN4 | c.1837T>G (p.Phe613Val) c.619T>G (p.Phe207Val) | |
| 15 | g.73325096A>G | CA393090774 | HCN4 | c.1837T>C (p.Phe613Leu) c.619T>C (p.Phe207Leu) | |
| 15 | g.73325096A>T | CA393090775 | HCN4 | c.1837T>A (p.Phe613Ile) c.619T>A (p.Phe207Ile) | |
| 15 | g.73325097A>C | CA491479064 | HCN4 | c.1836T>G (p.Arg612=) c.618T>G (p.Arg206=) | |
| 15 | g.73325097A>G | CA491479065 | HCN4 | c.1836T>C (p.Arg612=) c.618T>C (p.Arg206=) | |
| 15 | g.73325097A>T | CA491479066 | HCN4 | c.1836T>A (p.Arg612=) c.618T>A (p.Arg206=) | |
| 15 | g.73325098C>A | CA393090776 | HCN4 | c.1835G>T (p.Arg612Leu) c.617G>T (p.Arg206Leu) | |
| 15 | g.73325098C= | CA2187190516 | HCN4 | c.1835G= (p.Arg612=) c.617G= (p.Arg206=) | |
| 15 | g.73325098C>G | CA393090777 | HCN4 | c.1835G>C (p.Arg612Pro) c.617G>C (p.Arg206Pro) | gnomAD v4 |
| 15 | g.73325098C>T | CA7649178 | HCN4 | c.1835G>A (p.Arg612His) c.617G>A (p.Arg206His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73325099G>A | CA7649179 | HCN4 | c.1834C>T (p.Arg612Cys) c.616C>T (p.Arg206Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73325099G>C | CA393090779 | HCN4 | c.1834C>G (p.Arg612Gly) c.616C>G (p.Arg206Gly) | |
| 15 | g.73325099G= | CA2187190520 | HCN4 | c.1834C= (p.Arg612=) c.616C= (p.Arg206=) | |
| 15 | g.73325099G>T | CA393090778 | HCN4 | c.1834C>A (p.Arg612Ser) c.616C>A (p.Arg206Ser) | |
| 15 | g.73325100C>A | CA491479067 | HCN4 | c.1833G>T (p.Leu611=) c.615G>T (p.Leu205=) | |
| 15 | g.73325100C>G | CA491479068 | HCN4 | c.1833G>C (p.Leu611=) c.615G>C (p.Leu205=) | |
| 15 | g.73325100C>T | CA491479069 | HCN4 | c.1833G>A (p.Leu611=) c.615G>A (p.Leu205=) | |
| 15 | g.73325101A>C | CA393090781 | HCN4 | c.1832T>G (p.Leu611Arg) c.614T>G (p.Leu205Arg) | |
| 15 | g.73325101A>G | CA393090782 | HCN4 | c.1832T>C (p.Leu611Pro) c.614T>C (p.Leu205Pro) | gnomAD v4 |
| 15 | g.73325101A>T | CA393090783 | HCN4 | c.1832T>A (p.Leu611Gln) c.614T>A (p.Leu205Gln) | |
| 15 | g.73325102G>A | CA491479070 | HCN4 | c.1831C>T (p.Leu611=) c.613C>T (p.Leu205=) | gnomAD v4 |
| 15 | g.73325102G>C | CA393090784 | HCN4 | c.1831C>G (p.Leu611Val) c.613C>G (p.Leu205Val) | |
| 15 | g.73325102G>T | CA393090785 | HCN4 | c.1831C>A (p.Leu611Met) c.613C>A (p.Leu205Met) | |
| 15 | g.73325103C>A | CA393090786 | HCN4 | c.1830G>T (p.Lys610Asn) c.612G>T (p.Lys204Asn) | |
| 15 | g.73325103C>G | CA393090787 | HCN4 | c.1830G>C (p.Lys610Asn) c.612G>C (p.Lys204Asn) | |
| 15 | g.73325103C>T | CA491479071 | HCN4 | c.1830G>A (p.Lys610=) c.612G>A (p.Lys204=) | gnomAD v4 |
| 15 | g.73325104T>A | CA393090788 | HCN4 | c.1829A>T (p.Lys610Met) c.611A>T (p.Lys204Met) | |
| 15 | g.73325104T>C | CA393090790 | HCN4 | c.1829A>G (p.Lys610Arg) c.611A>G (p.Lys204Arg) | |
| 15 | g.73325104T>G | CA393090789 | HCN4 | c.1829A>C (p.Lys610Thr) c.611A>C (p.Lys204Thr) | |
| 15 | g.73325105T>A | CA393090791 | HCN4 | c.1828A>T (p.Lys610Ter) c.610A>T (p.Lys204Ter) | |
| 15 | g.73325105T>C | CA393090792 | HCN4 | c.1828A>G (p.Lys610Glu) c.610A>G (p.Lys204Glu) | |
| 15 | g.73325105T>G | CA393090793 | HCN4 | c.1828A>C (p.Lys610Gln) c.610A>C (p.Lys204Gln) | |
| 15 | g.73325106G>A | CA491479074 | HCN4 | c.1827C>T (p.Thr609=) c.609C>T (p.Thr203=) | dbSNP |
| 15 | g.73325106G>C | CA491479073 | HCN4 | c.1827C>G (p.Thr609=) c.609C>G (p.Thr203=) | |
| 15 | g.73325106G= | CA2187190522 | HCN4 | c.1827C= (p.Thr609=) c.609C= (p.Thr203=) | |
| 15 | g.73325106G>T | CA491479072 | HCN4 | c.1827C>A (p.Thr609=) c.609C>A (p.Thr203=) | gnomAD v4 |
| 15 | g.73325107G>A | CA393090794 | HCN4 | c.1826C>T (p.Thr609Ile) c.608C>T (p.Thr203Ile) | dbSNP |
| 15 | g.73325107G>C | CA393090795 | HCN4 | c.1826C>G (p.Thr609Ser) c.608C>G (p.Thr203Ser) | |
| 15 | g.73325107G>T | CA393090796 | HCN4 | c.1826C>A (p.Thr609Asn) c.608C>A (p.Thr203Asn) | |
| 15 | g.73325108T>A | CA393090799 | HCN4 | c.1825A>T (p.Thr609Ser) c.607A>T (p.Thr203Ser) | |
| 15 | g.73325108T>C | CA393090797 | HCN4 | c.1825A>G (p.Thr609Ala) c.607A>G (p.Thr203Ala) | |
| 15 | g.73325108T>G | CA393090798 | HCN4 | c.1825A>C (p.Thr609Pro) c.607A>C (p.Thr203Pro) | |
| 15 | g.73325109C>A | CA491479077 | HCN4 | c.1824G>T (p.Leu608=) c.606G>T (p.Leu202=) | |
| 15 | g.73325109C>G | CA491479076 | HCN4 | c.1824G>C (p.Leu608=) c.606G>C (p.Leu202=) | |
| 15 | g.73325109C>T | CA491479075 | HCN4 | c.1824G>A (p.Leu608=) c.606G>A (p.Leu202=) | |
| 15 | g.73325110A>C | CA393090800 | HCN4 | c.1823T>G (p.Leu608Arg) c.605T>G (p.Leu202Arg) | |
| 15 | g.73325110A>G | CA393090801 | HCN4 | c.1823T>C (p.Leu608Pro) c.605T>C (p.Leu202Pro) | ClinVar |
| 15 | g.73325110A>T | CA393090802 | HCN4 | c.1823T>A (p.Leu608Gln) c.605T>A (p.Leu202Gln) | |
| 15 | g.73325111G>A | CA491479078 | HCN4 | c.1822C>T (p.Leu608=) c.604C>T (p.Leu202=) | |
| 15 | g.73325111G>C | CA393090803 | HCN4 | c.1822C>G (p.Leu608Val) c.604C>G (p.Leu202Val) | |
| 15 | g.73325111G>T | CA393090804 | HCN4 | c.1822C>A (p.Leu608Met) c.604C>A (p.Leu202Met) | |
| 15 | g.73325112C>A | CA393090807 | HCN4 | c.1821G>T (p.Met607Ile) c.603G>T (p.Met201Ile) | |
| 15 | g.73325112C>G | CA393090805 | HCN4 | c.1821G>C (p.Met607Ile) c.603G>C (p.Met201Ile) | |
| 15 | g.73325112C>T | CA393090806 | HCN4 | c.1821G>A (p.Met607Ile) c.603G>A (p.Met201Ile) | |
| 15 | g.73325113A= | CA2187190527 | HCN4 | c.1820T= (p.Met607=) c.602T= (p.Met201=) | |
| 15 | g.73325113A>C | CA393090808 | HCN4 | c.1820T>G (p.Met607Arg) c.602T>G (p.Met201Arg) | |
| 15 | g.73325113A>G | CA393090809 | HCN4 | c.1820T>C (p.Met607Thr) c.602T>C (p.Met201Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73325113A>T | CA393090810 | HCN4 | c.1820T>A (p.Met607Lys) c.602T>A (p.Met201Lys) | |
| 15 | g.73325114T>A | CA393090811 | HCN4 | c.1819A>T (p.Met607Leu) c.601A>T (p.Met201Leu) | gnomAD v4 |
| 15 | g.73325114T>C | CA7649180 | HCN4 | c.1819A>G (p.Met607Val) c.601A>G (p.Met201Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73325114T>G | CA393090812 | HCN4 | c.1819A>C (p.Met607Leu) c.601A>C (p.Met201Leu) | |
| 15 | g.73325114T= | CA2187190530 | HCN4 | c.1819A= (p.Met607=) c.601A= (p.Met201=) | |
| 15 | g.73325115G>A | CA491479079 | HCN4 | c.1818C>T (p.Ser606=) c.600C>T (p.Ser200=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73325115G>C | CA491479080 | HCN4 | c.1818C>G (p.Ser606=) c.600C>G (p.Ser200=) | |
| 15 | g.73325115G= | CA2187190533 | HCN4 | c.1818C= (p.Ser606=) c.600C= (p.Ser200=) | |
| 15 | g.73325115G>T | CA491479081 | HCN4 | c.1818C>A (p.Ser606=) c.600C>A (p.Ser200=) | |
| 15 | g.73325116G>A | CA393090813 | HCN4 | c.1817C>T (p.Ser606Phe) c.599C>T (p.Ser200Phe) | |
| 15 | g.73325116G>C | CA393090814 | HCN4 | c.1817C>G (p.Ser606Cys) c.599C>G (p.Ser200Cys) | |
| 15 | g.73325116G>T | CA393090815 | HCN4 | c.1817C>A (p.Ser606Tyr) c.599C>A (p.Ser200Tyr) | gnomAD v4 |
| 15 | g.73325117A>C | CA393090816 | HCN4 | c.1816T>G (p.Ser606Ala) c.598T>G (p.Ser200Ala) | |
| 15 | g.73325117A>G | CA393090817 | HCN4 | c.1816T>C (p.Ser606Pro) c.598T>C (p.Ser200Pro) | |
| 15 | g.73325117A>T | CA393090818 | HCN4 | c.1816T>A (p.Ser606Thr) c.598T>A (p.Ser200Thr) | |
| 15 | g.73325118C>A | CA491479082 | HCN4 | c.1815G>T (p.Thr605=) c.597G>T (p.Thr199=) | |
| 15 | g.73325118C= | CA2187190541 | HCN4 | c.1815G= (p.Thr605=) c.597G= (p.Thr199=) | |
| 15 | g.73325118C>G | CA491479083 | HCN4 | c.1815G>C (p.Thr605=) c.597G>C (p.Thr199=) | |
| 15 | g.73325118C>T | CA7649181 | HCN4 | c.1815G>A (p.Thr605=) c.597G>A (p.Thr199=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73325119G>A | CA272666402 | HCN4 | c.1814C>T (p.Thr605Met) c.596C>T (p.Thr199Met) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73325119G>C | CA393090819 | HCN4 | c.1814C>G (p.Thr605Arg) c.596C>G (p.Thr199Arg) | |
| 15 | g.73325119G= | CA2187190550 | HCN4 | c.1814C= (p.Thr605=) c.596C= (p.Thr199=) | |
| 15 | g.73325119G>T | CA393090820 | HCN4 | c.1814C>A (p.Thr605Lys) c.596C>A (p.Thr199Lys) | COSMIC |
| 15 | g.73325120T>A | CA393090821 | HCN4 | c.1813A>T (p.Thr605Ser) c.595A>T (p.Thr199Ser) | |
| 15 | g.73325120T>C | CA393090822 | HCN4 | c.1813A>G (p.Thr605Ala) c.595A>G (p.Thr199Ala) | gnomAD v4 |
| 15 | g.73325120T>G | CA393090823 | HCN4 | c.1813A>C (p.Thr605Pro) c.595A>C (p.Thr199Pro) | |
| 15 | g.73325121C>A | CA491479084 | HCN4 | c.1812G>T (p.Val604=) c.594G>T (p.Val198=) | |
| 15 | g.73325121C= | CA2187190555 | HCN4 | c.1812G= (p.Val604=) c.594G= (p.Val198=) | |
| 15 | g.73325121C>G | CA491479085 | HCN4 | c.1812G>C (p.Val604=) c.594G>C (p.Val198=) | |
| 15 | g.73325121C>T | CA16607873 | HCN4 | c.1812G>A (p.Val604=) c.594G>A (p.Val198=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73325122A>C | CA393090825 | HCN4 | c.1811T>G (p.Val604Gly) c.593T>G (p.Val198Gly) | |
| 15 | g.73325122A>G | CA393090827 | HCN4 | c.1811T>C (p.Val604Ala) c.593T>C (p.Val198Ala) | |
| 15 | g.73325122A>T | CA393090829 | HCN4 | c.1811T>A (p.Val604Glu) c.593T>A (p.Val198Glu) | |
| 15 | g.73325123C>A | CA393090835 | HCN4 | c.1810G>T (p.Val604Leu) c.592G>T (p.Val198Leu) | |
| 15 | g.73325123C= | CA2187190558 | HCN4 | c.1810G= (p.Val604=) c.592G= (p.Val198=) | |
| 15 | g.73325123C>G | CA393090834 | HCN4 | c.1810G>C (p.Val604Leu) c.592G>C (p.Val198Leu) | |
| 15 | g.73325123C>T | CA393090831 | HCN4 | c.1810G>A (p.Val604Met) c.592G>A (p.Val198Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73325124G>A | CA7649182 | HCN4 | c.1809C>T (p.Phe603=) c.591C>T (p.Phe197=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73325124G>C | CA393090838 | HCN4 | c.1809C>G (p.Phe603Leu) c.591C>G (p.Phe197Leu) | gnomAD v4 |
| 15 | g.73325124G= | CA2187190565 | HCN4 | c.1809C= (p.Phe603=) c.591C= (p.Phe197=) | |
| 15 | g.73325124G>T | CA393090839 | HCN4 | c.1809C>A (p.Phe603Leu) c.591C>A (p.Phe197Leu) | ClinVar dbSNP |
| 15 | g.73325125A>C | CA393090842 | HCN4 | c.1808T>G (p.Phe603Cys) c.590T>G (p.Phe197Cys) | |
| 15 | g.73325125A>G | CA393090844 | HCN4 | c.1808T>C (p.Phe603Ser) c.590T>C (p.Phe197Ser) | |
| 15 | g.73325125A>T | CA393090846 | HCN4 | c.1808T>A (p.Phe603Tyr) c.590T>A (p.Phe197Tyr) | |
| 15 | g.73325126A= | CA2187190573 | HCN4 | c.1807T= (p.Phe603=) c.589T= (p.Phe197=) | |
| 15 | g.73325126A>C | CA393090848 | HCN4 | c.1807T>G (p.Phe603Val) c.589T>G (p.Phe197Val) | |
| 15 | g.73325126A>G | CA393090851 | HCN4 | c.1807T>C (p.Phe603Leu) c.589T>C (p.Phe197Leu) | dbSNP gnomAD v4 |
| 15 | g.73325126A>T | CA393090850 | HCN4 | c.1807T>A (p.Phe603Ile) c.589T>A (p.Phe197Ile) | gnomAD v4 |
| 15 | g.73325127G>A | CA491479086 | HCN4 | c.1806C>T (p.Asn602=) c.588C>T (p.Asn196=) | |
| 15 | g.73325127G>C | CA393090854 | HCN4 | c.1806C>G (p.Asn602Lys) c.588C>G (p.Asn196Lys) | |
| 15 | g.73325127G>T | CA393090855 | HCN4 | c.1806C>A (p.Asn602Lys) c.588C>A (p.Asn196Lys) | |
| 15 | g.73325128T>A | CA393090858 | HCN4 | c.1805A>T (p.Asn602Ile) c.587A>T (p.Asn196Ile) | |
| 15 | g.73325128T>C | CA393090860 | HCN4 | c.1805A>G (p.Asn602Ser) c.587A>G (p.Asn196Ser) | ClinVar gnomAD v4 |
| 15 | g.73325128T>G | CA393090861 | HCN4 | c.1805A>C (p.Asn602Thr) c.587A>C (p.Asn196Thr) | |
| 15 | g.73325129T>A | CA393090862 | HCN4 | c.1804A>T (p.Asn602Tyr) c.586A>T (p.Asn196Tyr) | |
| 15 | g.73325129T>C | CA393090865 | HCN4 | c.1804A>G (p.Asn602Asp) c.586A>G (p.Asn196Asp) | |
| 15 | g.73325129T>G | CA393090867 | HCN4 | c.1804A>C (p.Asn602His) c.586A>C (p.Asn196His) | |
| 15 | g.73325130G>A | CA491479087 | HCN4 | c.1803C>T (p.Pro601=) c.585C>T (p.Pro195=) | |
| 15 | g.73325130G>C | CA491479088 | HCN4 | c.1803C>G (p.Pro601=) c.585C>G (p.Pro195=) | |
| 15 | g.73325130G>T | CA491479089 | HCN4 | c.1803C>A (p.Pro601=) c.585C>A (p.Pro195=) | |
| 15 | g.73325131G>A | CA393090869 | HCN4 | c.1802C>T (p.Pro601Leu) c.584C>T (p.Pro195Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73325131G>C | CA393090871 | HCN4 | c.1802C>G (p.Pro601Arg) c.584C>G (p.Pro195Arg) | |
| 15 | g.73325131G= | CA2187190576 | HCN4 | c.1802C= (p.Pro601=) c.584C= (p.Pro195=) | |
| 15 | g.73325131G>T | CA393090873 | HCN4 | c.1802C>A (p.Pro601His) c.584C>A (p.Pro195His) |