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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73323111T>A | CA491478567 | HCN4 | c.2982A>T (p.Pro994=) c.1764A>T (p.Pro588=) | |
| 15 | g.73323111T>C | CA491478570 | HCN4 | c.2982A>G (p.Pro994=) c.1764A>G (p.Pro588=) | dbSNP |
| 15 | g.73323111T>G | CA491478573 | HCN4 | c.2982A>C (p.Pro994=) c.1764A>C (p.Pro588=) | |
| 15 | g.73323111T= | CA2187187525 | HCN4 | c.2982A= (p.Pro994=) c.1764A= (p.Pro588=) | |
| 15 | g.73323112G>A | CA393086595 | HCN4 | c.2981C>T (p.Pro994Leu) c.1763C>T (p.Pro588Leu) | gnomAD v4 |
| 15 | g.73323112G>C | CA393086597 | HCN4 | c.2981C>G (p.Pro994Arg) c.1763C>G (p.Pro588Arg) | |
| 15 | g.73323112G>T | CA393086599 | HCN4 | c.2981C>A (p.Pro994Gln) c.1763C>A (p.Pro588Gln) | gnomAD v4 |
| 15 | g.73323113G>A | CA393086602 | HCN4 | c.2980C>T (p.Pro994Ser) c.1762C>T (p.Pro588Ser) | gnomAD v4 |
| 15 | g.73323113G>C | CA393086603 | HCN4 | c.2980C>G (p.Pro994Ala) c.1762C>G (p.Pro588Ala) | |
| 15 | g.73323113G>T | CA393086606 | HCN4 | c.2980C>A (p.Pro994Thr) c.1762C>A (p.Pro588Thr) | |
| 15 | g.73323114C>A | CA491478585 | HCN4 | c.2979G>T (p.Thr993=) c.1761G>T (p.Thr587=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323114C= | CA2187187528 | HCN4 | c.2979G= (p.Thr993=) c.1761G= (p.Thr587=) | |
| 15 | g.73323114C>G | CA491478584 | HCN4 | c.2979G>C (p.Thr993=) c.1761G>C (p.Thr587=) | ClinVar |
| 15 | g.73323114C>T | CA203637 | HCN4 | c.2979G>A (p.Thr993=) c.1761G>A (p.Thr587=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323115G>A | CA7648912 | HCN4 | c.2978C>T (p.Thr993Met) c.1760C>T (p.Thr587Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323115G>C | CA393086610 | HCN4 | c.2978C>G (p.Thr993Arg) c.1760C>G (p.Thr587Arg) | gnomAD v4 |
| 15 | g.73323115G= | CA2187187536 | HCN4 | c.2978C= (p.Thr993=) c.1760C= (p.Thr587=) | |
| 15 | g.73323115G>T | CA393086609 | HCN4 | c.2978C>A (p.Thr993Lys) c.1760C>A (p.Thr587Lys) | COSMIC |
| 15 | g.73323116T>A | CA393086614 | HCN4 | c.2977A>T (p.Thr993Ser) c.1759A>T (p.Thr587Ser) | dbSNP |
| 15 | g.73323116T>C | CA393086615 | HCN4 | c.2977A>G (p.Thr993Ala) c.1759A>G (p.Thr587Ala) | gnomAD v4 |
| 15 | g.73323116T>G | CA393086617 | HCN4 | c.2977A>C (p.Thr993Pro) c.1759A>C (p.Thr587Pro) | |
| 15 | g.73323116T= | CA2187187541 | HCN4 | c.2977A= (p.Thr993=) c.1759A= (p.Thr587=) | |
| 15 | g.73323117G>A | CA7648913 | HCN4 | c.2976C>T (p.Ser992=) c.1758C>T (p.Ser586=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323117G>C | CA393086619 | HCN4 | c.2976C>G (p.Ser992Arg) c.1758C>G (p.Ser586Arg) | |
| 15 | g.73323117G= | CA2187187543 | HCN4 | c.2976C= (p.Ser992=) c.1758C= (p.Ser586=) | |
| 15 | g.73323117G>T | CA393086620 | HCN4 | c.2976C>A (p.Ser992Arg) c.1758C>A (p.Ser586Arg) | gnomAD v4 |
| 15 | g.73323118C>A | CA7648914 | HCN4 | c.2975G>T (p.Ser992Ile) c.1757G>T (p.Ser586Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323118C= | CA2187187548 | HCN4 | c.2975G= (p.Ser992=) c.1757G= (p.Ser586=) | |
| 15 | g.73323118C>G | CA393086622 | HCN4 | c.2975G>C (p.Ser992Thr) c.1757G>C (p.Ser586Thr) | |
| 15 | g.73323118C>T | CA393086623 | HCN4 | c.2975G>A (p.Ser992Asn) c.1757G>A (p.Ser586Asn) | gnomAD v4 |
| 15 | g.73323119T>A | CA393086625 | HCN4 | c.2974A>T (p.Ser992Cys) c.1756A>T (p.Ser586Cys) | |
| 15 | g.73323119T>C | CA393086627 | HCN4 | c.2974A>G (p.Ser992Gly) c.1756A>G (p.Ser586Gly) | gnomAD v4 |
| 15 | g.73323119T>G | CA393086628 | HCN4 | c.2974A>C (p.Ser992Arg) c.1756A>C (p.Ser586Arg) | |
| 15 | g.73323120C>A | CA491478598 | HCN4 | c.2973G>T (p.Leu991=) c.1755G>T (p.Leu585=) | gnomAD v4 |
| 15 | g.73323120C= | CA2187187551 | HCN4 | c.2973G= (p.Leu991=) c.1755G= (p.Leu585=) | |
| 15 | g.73323120C>G | CA491478601 | HCN4 | c.2973G>C (p.Leu991=) c.1755G>C (p.Leu585=) | |
| 15 | g.73323120C>T | CA491478600 | HCN4 | c.2973G>A (p.Leu991=) c.1755G>A (p.Leu585=) | dbSNP |
| 15 | g.73323121A= | CA2187187553 | HCN4 | c.2972T= (p.Leu991=) c.1754T= (p.Leu585=) | |
| 15 | g.73323121A>C | CA393086631 | HCN4 | c.2972T>G (p.Leu991Arg) c.1754T>G (p.Leu585Arg) | |
| 15 | g.73323121A>G | CA272663993 | HCN4 | c.2972T>C (p.Leu991Pro) c.1754T>C (p.Leu585Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323121A>T | CA393086629 | HCN4 | c.2972T>A (p.Leu991Gln) c.1754T>A (p.Leu585Gln) | |
| 15 | g.73323122G>A | CA491478607 | HCN4 | c.2971C>T (p.Leu991=) c.1753C>T (p.Leu585=) | gnomAD v4 |
| 15 | g.73323122G>C | CA393086633 | HCN4 | c.2971C>G (p.Leu991Val) c.1753C>G (p.Leu585Val) | |
| 15 | g.73323122G>T | CA393086634 | HCN4 | c.2971C>A (p.Leu991Met) c.1753C>A (p.Leu585Met) | gnomAD v4 COSMIC |
| 15 | g.73323123T>A | CA491478609 | HCN4 | c.2970A>T (p.Pro990=) c.1752A>T (p.Pro584=) | gnomAD v4 |
| 15 | g.73323123T>C | CA491478611 | HCN4 | c.2970A>G (p.Pro990=) c.1752A>G (p.Pro584=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323123T>G | CA491478613 | HCN4 | c.2970A>C (p.Pro990=) c.1752A>C (p.Pro584=) | |
| 15 | g.73323123T= | CA2187187556 | HCN4 | c.2970A= (p.Pro990=) c.1752A= (p.Pro584=) | |
| 15 | g.73323124G>A | CA7648915 | HCN4 | c.2969C>T (p.Pro990Leu) c.1751C>T (p.Pro584Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323124G>C | CA393086637 | HCN4 | c.2969C>G (p.Pro990Arg) c.1751C>G (p.Pro584Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323124G= | CA2187187559 | HCN4 | c.2969C= (p.Pro990=) c.1751C= (p.Pro584=) | |
| 15 | g.73323124G>T | CA393086639 | HCN4 | c.2969C>A (p.Pro990Gln) c.1751C>A (p.Pro584Gln) | gnomAD v4 |
| 15 | g.73323125G>A | CA393086643 | HCN4 | c.2968C>T (p.Pro990Ser) c.1750C>T (p.Pro584Ser) | gnomAD v4 |
| 15 | g.73323125G>C | CA393086642 | HCN4 | c.2968C>G (p.Pro990Ala) c.1750C>G (p.Pro584Ala) | ClinVar dbSNP |
| 15 | g.73323125G>T | CA393086640 | HCN4 | c.2968C>A (p.Pro990Thr) c.1750C>A (p.Pro584Thr) | gnomAD v4 |
| 15 | g.73323126G>A | CA491478615 | HCN4 | c.2967C>T (p.Gly989=) c.1749C>T (p.Gly583=) | gnomAD v4 |
| 15 | g.73323126G>C | CA491478617 | HCN4 | c.2967C>G (p.Gly989=) c.1749C>G (p.Gly583=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323126G= | CA2187187563 | HCN4 | c.2967C= (p.Gly989=) c.1749C= (p.Gly583=) | |
| 15 | g.73323126G>T | CA491478620 | HCN4 | c.2967C>A (p.Gly989=) c.1749C>A (p.Gly583=) | gnomAD v4 |
| 15 | g.73323127C>A | CA393086645 | HCN4 | c.2966G>T (p.Gly989Val) c.1748G>T (p.Gly583Val) | gnomAD v4 |
| 15 | g.73323127C>G | CA393086646 | HCN4 | c.2966G>C (p.Gly989Ala) c.1748G>C (p.Gly583Ala) | |
| 15 | g.73323127C>T | CA393086648 | HCN4 | c.2966G>A (p.Gly989Asp) c.1748G>A (p.Gly583Asp) | gnomAD v4 |
| 15 | g.73323128C>A | CA393086650 | HCN4 | c.2965G>T (p.Gly989Cys) c.1747G>T (p.Gly583Cys) | gnomAD v4 |
| 15 | g.73323128C>G | CA393086651 | HCN4 | c.2965G>C (p.Gly989Arg) c.1747G>C (p.Gly583Arg) | |
| 15 | g.73323128C>T | CA393086653 | HCN4 | c.2965G>A (p.Gly989Ser) c.1747G>A (p.Gly583Ser) | gnomAD v4 |
| 15 | g.73323129A= | CA2187187566 | HCN4 | c.2964T= (p.Thr988=) c.1746T= (p.Thr582=) | |
| 15 | g.73323129A>C | CA491478623 | HCN4 | c.2964T>G (p.Thr988=) c.1746T>G (p.Thr582=) | |
| 15 | g.73323129A>G | CA491478625 | HCN4 | c.2964T>C (p.Thr988=) c.1746T>C (p.Thr582=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323129A>T | CA491478629 | HCN4 | c.2964T>A (p.Thr988=) c.1746T>A (p.Thr582=) | gnomAD v4 |
| 15 | g.73323130G>A | CA393086654 | HCN4 | c.2963C>T (p.Thr988Ile) c.1745C>T (p.Thr582Ile) | gnomAD v4 |
| 15 | g.73323130G>C | CA393086656 | HCN4 | c.2963C>G (p.Thr988Ser) c.1745C>G (p.Thr582Ser) | |
| 15 | g.73323130G>T | CA393086655 | HCN4 | c.2963C>A (p.Thr988Asn) c.1745C>A (p.Thr582Asn) | gnomAD v4 |
| 15 | g.73323131T>A | CA393086658 | HCN4 | c.2962A>T (p.Thr988Ser) c.1744A>T (p.Thr582Ser) | gnomAD v4 |
| 15 | g.73323131T>C | CA393086660 | HCN4 | c.2962A>G (p.Thr988Ala) c.1744A>G (p.Thr582Ala) | |
| 15 | g.73323131T>G | CA393086661 | HCN4 | c.2962A>C (p.Thr988Pro) c.1744A>C (p.Thr582Pro) | |
| 15 | g.73323132G>A | CA491478635 | HCN4 | c.2961C>T (p.Ala987=) c.1743C>T (p.Ala581=) | gnomAD v4 |
| 15 | g.73323132G>C | CA491478636 | HCN4 | c.2961C>G (p.Ala987=) c.1743C>G (p.Ala581=) | |
| 15 | g.73323132G>T | CA491478638 | HCN4 | c.2961C>A (p.Ala987=) c.1743C>A (p.Ala581=) | gnomAD v4 |
| 15 | g.73323133G>A | CA393086663 | HCN4 | c.2960C>T (p.Ala987Val) c.1742C>T (p.Ala581Val) | gnomAD v4 |
| 15 | g.73323133G>C | CA393086665 | HCN4 | c.2960C>G (p.Ala987Gly) c.1742C>G (p.Ala581Gly) | |
| 15 | g.73323133G>T | CA393086666 | HCN4 | c.2960C>A (p.Ala987Asp) c.1742C>A (p.Ala581Asp) | gnomAD v4 |
| 15 | g.73323134C>A | CA393086669 | HCN4 | c.2959G>T (p.Ala987Ser) c.1741G>T (p.Ala581Ser) | gnomAD v4 |
| 15 | g.73323134C>G | CA393086672 | HCN4 | c.2959G>C (p.Ala987Pro) c.1741G>C (p.Ala581Pro) | |
| 15 | g.73323134C>T | CA393086674 | HCN4 | c.2959G>A (p.Ala987Thr) c.1741G>A (p.Ala581Thr) | gnomAD v4 |
| 15 | g.73323135C>A | CA491478644 | HCN4 | c.2958G>T (p.Leu986=) c.1740G>T (p.Leu580=) | gnomAD v4 |
| 15 | g.73323135C>G | CA491478645 | HCN4 | c.2958G>C (p.Leu986=) c.1740G>C (p.Leu580=) | |
| 15 | g.73323135C>T | CA491478647 | HCN4 | c.2958G>A (p.Leu986=) c.1740G>A (p.Leu580=) | gnomAD v4 |
| 15 | g.73323136A>C | CA393086677 | HCN4 | c.2957T>G (p.Leu986Arg) c.1739T>G (p.Leu580Arg) | |
| 15 | g.73323136A>G | CA393086680 | HCN4 | c.2957T>C (p.Leu986Pro) c.1739T>C (p.Leu580Pro) | gnomAD v4 |
| 15 | g.73323136A>T | CA393086682 | HCN4 | c.2957T>A (p.Leu986Gln) c.1739T>A (p.Leu580Gln) | gnomAD v4 |
| 15 | g.73323137G>A | CA491478651 | HCN4 | c.2956C>T (p.Leu986=) c.1738C>T (p.Leu580=) | gnomAD v4 |
| 15 | g.73323137G>C | CA393086685 | HCN4 | c.2956C>G (p.Leu986Val) c.1738C>G (p.Leu580Val) | |
| 15 | g.73323137G>T | CA393086687 | HCN4 | c.2956C>A (p.Leu986Met) c.1738C>A (p.Leu580Met) | gnomAD v4 |
| 15 | g.73323138A= | CA2187187569 | HCN4 | c.2955T= (p.Gly985=) c.1737T= (p.Gly579=) | |
| 15 | g.73323138A>C | CA491478655 | HCN4 | c.2955T>G (p.Gly985=) c.1737T>G (p.Gly579=) | |
| 15 | g.73323138A>G | CA491478656 | HCN4 | c.2955T>C (p.Gly985=) c.1737T>C (p.Gly579=) | dbSNP gnomAD v4 |
| 15 | g.73323138A>T | CA491478657 | HCN4 | c.2955T>A (p.Gly985=) c.1737T>A (p.Gly579=) | |
| 15 | g.73323139C>A | CA393086690 | HCN4 | c.2954G>T (p.Gly985Val) c.1736G>T (p.Gly579Val) | gnomAD v4 |
| 15 | g.73323139C>G | CA393086693 | HCN4 | c.2954G>C (p.Gly985Ala) c.1736G>C (p.Gly579Ala) | |
| 15 | g.73323139C>T | CA393086696 | HCN4 | c.2954G>A (p.Gly985Asp) c.1736G>A (p.Gly579Asp) | |
| 15 | g.73323140C>A | CA393086698 | HCN4 | c.2953G>T (p.Gly985Cys) c.1735G>T (p.Gly579Cys) | gnomAD v4 |
| 15 | g.73323140C>G | CA393086706 | HCN4 | c.2953G>C (p.Gly985Arg) c.1735G>C (p.Gly579Arg) | |
| 15 | g.73323140C>T | CA393086709 | HCN4 | c.2953G>A (p.Gly985Ser) c.1735G>A (p.Gly579Ser) | gnomAD v4 |
| 15 | g.73323141T>A | CA491478667 | HCN4 | c.2952A>T (p.Leu984=) c.1734A>T (p.Leu578=) | gnomAD v4 |
| 15 | g.73323141T>C | CA7648916 | HCN4 | c.2952A>G (p.Leu984=) c.1734A>G (p.Leu578=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323141T>G | CA491478666 | HCN4 | c.2952A>C (p.Leu984=) c.1734A>C (p.Leu578=) | |
| 15 | g.73323141T= | CA2187187571 | HCN4 | c.2952A= (p.Leu984=) c.1734A= (p.Leu578=) | |
| 15 | g.73323142A>C | CA393086718 | HCN4 | c.2951T>G (p.Leu984Arg) c.1733T>G (p.Leu578Arg) | |
| 15 | g.73323142A>G | CA393086713 | HCN4 | c.2951T>C (p.Leu984Pro) c.1733T>C (p.Leu578Pro) | gnomAD v4 |
| 15 | g.73323142A>T | CA393086714 | HCN4 | c.2951T>A (p.Leu984Gln) c.1733T>A (p.Leu578Gln) | |
| 15 | g.73323143G>A | CA491478668 | HCN4 | c.2950C>T (p.Leu984=) c.1732C>T (p.Leu578=) | gnomAD v4 |
| 15 | g.73323143G>C | CA393086721 | HCN4 | c.2950C>G (p.Leu984Val) c.1732C>G (p.Leu578Val) | ClinVar dbSNP |
| 15 | g.73323143G>T | CA393086724 | HCN4 | c.2950C>A (p.Leu984Ile) c.1732C>A (p.Leu578Ile) | gnomAD v4 |
| 15 | g.73323143_73323144insT | CA2804714152 | HCN4 | c.2949_2950insA (p.Leu984ThrfsTer19) c.1731_1732insA (p.Leu578ThrfsTer19) | |
| 15 | g.73323144G>A | CA272664002 | HCN4 | c.2949C>T (p.Ser983=) c.1731C>T (p.Ser577=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323144G>C | CA491478673 | HCN4 | c.2949C>G (p.Ser983=) c.1731C>G (p.Ser577=) | |
| 15 | g.73323144G= | CA2187187574 | HCN4 | c.2949C= (p.Ser983=) c.1731C= (p.Ser577=) | |
| 15 | g.73323144G>T | CA491478675 | HCN4 | c.2949C>A (p.Ser983=) c.1731C>A (p.Ser577=) | gnomAD v4 |
| 15 | g.73323145G>A | CA7648917 | HCN4 | c.2948C>T (p.Ser983Phe) c.1730C>T (p.Ser577Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323145G>C | CA393086731 | HCN4 | c.2948C>G (p.Ser983Cys) c.1730C>G (p.Ser577Cys) | |
| 15 | g.73323145G= | CA2187187576 | HCN4 | c.2948C= (p.Ser983=) c.1730C= (p.Ser577=) | |
| 15 | g.73323145G>T | CA393086734 | HCN4 | c.2948C>A (p.Ser983Tyr) c.1730C>A (p.Ser577Tyr) | gnomAD v4 |
| 15 | g.73323146A>C | CA393086736 | HCN4 | c.2947T>G (p.Ser983Ala) c.1729T>G (p.Ser577Ala) | |
| 15 | g.73323146A>G | CA393086741 | HCN4 | c.2947T>C (p.Ser983Pro) c.1729T>C (p.Ser577Pro) | |
| 15 | g.73323146A>T | CA393086739 | HCN4 | c.2947T>A (p.Ser983Thr) c.1729T>A (p.Ser577Thr) | gnomAD v4 |
| 15 | g.73323147C>A | CA393086744 | HCN4 | c.2946G>T (p.Leu982Phe) c.1728G>T (p.Leu576Phe) | gnomAD v4 |
| 15 | g.73323147C= | CA2187187581 | HCN4 | c.2946G= (p.Leu982=) c.1728G= (p.Leu576=) | |
| 15 | g.73323147C>G | CA393086747 | HCN4 | c.2946G>C (p.Leu982Phe) c.1728G>C (p.Leu576Phe) | |
| 15 | g.73323147C>T | CA16607136 | HCN4 | c.2946G>A (p.Leu982=) c.1728G>A (p.Leu576=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323148A>C | CA393086749 | HCN4 | c.2945T>G (p.Leu982Trp) c.1727T>G (p.Leu576Trp) | |
| 15 | g.73323148A>G | CA393086751 | HCN4 | c.2945T>C (p.Leu982Ser) c.1727T>C (p.Leu576Ser) | gnomAD v4 |
| 15 | g.73323148A>T | CA393086753 | HCN4 | c.2945T>A (p.Leu982Ter) c.1727T>A (p.Leu576Ter) | |
| 15 | g.73323149A>C | CA393086755 | HCN4 | c.2944T>G (p.Leu982Val) c.1726T>G (p.Leu576Val) | |
| 15 | g.73323149A>G | CA491478682 | HCN4 | c.2944T>C (p.Leu982=) c.1726T>C (p.Leu576=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323149A>T | CA393086758 | HCN4 | c.2944T>A (p.Leu982Met) c.1726T>A (p.Leu576Met) | |
| 15 | g.73323150C>A | CA393086760 | HCN4 | c.2943G>T (p.Glu981Asp) c.1725G>T (p.Glu575Asp) | gnomAD v4 |
| 15 | g.73323150C>G | CA393086762 | HCN4 | c.2943G>C (p.Glu981Asp) c.1725G>C (p.Glu575Asp) | gnomAD v4 COSMIC |
| 15 | g.73323150C>T | CA491478684 | HCN4 | c.2943G>A (p.Glu981=) c.1725G>A (p.Glu575=) | gnomAD v4 |
| 15 | g.73323159_73323250del | CA619410578 | HCN4 | c.2852_2943del (p.Gly951ValfsTer21) c.1634_1725del (p.Gly545ValfsTer21) | gnomAD v2 |
| 15 | g.73323151T>A | CA393086766 | HCN4 | c.2942A>T (p.Glu981Val) c.1724A>T (p.Glu575Val) | |
| 15 | g.73323151T>C | CA393086769 | HCN4 | c.2942A>G (p.Glu981Gly) c.1724A>G (p.Glu575Gly) | gnomAD v4 |
| 15 | g.73323151T>G | CA393086771 | HCN4 | c.2942A>C (p.Glu981Ala) c.1724A>C (p.Glu575Ala) | |
| 15 | g.73323152C>A | CA393086774 | HCN4 | c.2941G>T (p.Glu981Ter) c.1723G>T (p.Glu575Ter) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323152C= | CA2187187584 | HCN4 | c.2941G= (p.Glu981=) c.1723G= (p.Glu575=) | |
| 15 | g.73323152C>G | CA393086778 | HCN4 | c.2941G>C (p.Glu981Gln) c.1723G>C (p.Glu575Gln) | |
| 15 | g.73323152C>T | CA393086776 | HCN4 | c.2941G>A (p.Glu981Lys) c.1723G>A (p.Glu575Lys) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323155del | CA2629370546 | HCN4 | c.2941del (p.Glu981SerfsTer4) c.1723del (p.Glu575SerfsTer4) | gnomAD v4 |
| 15 | g.73323153C>A | CA491478692 | HCN4 | c.2940G>T (p.Gly980=) c.1722G>T (p.Gly574=) | gnomAD v4 |
| 15 | g.73323153C>G | CA491478694 | HCN4 | c.2940G>C (p.Gly980=) c.1722G>C (p.Gly574=) | ClinVar |
| 15 | g.73323153C>T | CA491478693 | HCN4 | c.2940G>A (p.Gly980=) c.1722G>A (p.Gly574=) | gnomAD v4 COSMIC |
| 15 | g.73323154C>A | CA393086782 | HCN4 | c.2939G>T (p.Gly980Val) c.1721G>T (p.Gly574Val) | |
| 15 | g.73323154C= | CA2187187591 | HCN4 | c.2939G= (p.Gly980=) c.1721G= (p.Gly574=) | |
| 15 | g.73323154C>G | CA7648918 | HCN4 | c.2939G>C (p.Gly980Ala) c.1721G>C (p.Gly574Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323154C>T | CA393086786 | HCN4 | c.2939G>A (p.Gly980Glu) c.1721G>A (p.Gly574Glu) | ClinVar gnomAD v4 |
| 15 | g.73323155C>A | CA393086790 | HCN4 | c.2938G>T (p.Gly980Trp) c.1720G>T (p.Gly574Trp) | gnomAD v4 COSMIC |
| 15 | g.73323155C= | CA2187187599 | HCN4 | c.2938G= (p.Gly980=) c.1720G= (p.Gly574=) | |
| 15 | g.73323155C>G | CA393086791 | HCN4 | c.2938G>C (p.Gly980Arg) c.1720G>C (p.Gly574Arg) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323155C>T | CA7648919 | HCN4 | c.2938G>A (p.Gly980Arg) c.1720G>A (p.Gly574Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323156G>A | CA7648920 | HCN4 | c.2937C>T (p.Pro979=) c.1719C>T (p.Pro573=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323156G>C | CA491478702 | HCN4 | c.2937C>G (p.Pro979=) c.1719C>G (p.Pro573=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323156G= | CA2187187605 | HCN4 | c.2937C= (p.Pro979=) c.1719C= (p.Pro573=) | |
| 15 | g.73323156G>T | CA7648921 | HCN4 | c.2937C>A (p.Pro979=) c.1719C>A (p.Pro573=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323158del | CA2629370547 | HCN4 | c.2937del (p.Glu981SerfsTer4) c.1719del (p.Glu575SerfsTer4) | gnomAD v4 |
| 15 | g.73323157G>A | CA393086799 | HCN4 | c.2936C>T (p.Pro979Leu) c.1718C>T (p.Pro573Leu) | gnomAD v4 |
| 15 | g.73323157G>C | CA393086801 | HCN4 | c.2936C>G (p.Pro979Arg) c.1718C>G (p.Pro573Arg) | |
| 15 | g.73323157G>T | CA393086804 | HCN4 | c.2936C>A (p.Pro979His) c.1718C>A (p.Pro573His) | |
| 15 | g.73323158G>A | CA393086808 | HCN4 | c.2935C>T (p.Pro979Ser) c.1717C>T (p.Pro573Ser) | gnomAD v4 |
| 15 | g.73323158G>C | CA393086811 | HCN4 | c.2935C>G (p.Pro979Ala) c.1717C>G (p.Pro573Ala) | |
| 15 | g.73323158G>T | CA393086813 | HCN4 | c.2935C>A (p.Pro979Thr) c.1717C>A (p.Pro573Thr) | gnomAD v4 |
| 15 | g.73323159A>C | CA491478709 | HCN4 | c.2934T>G (p.Pro978=) c.1716T>G (p.Pro572=) | |
| 15 | g.73323159A>G | CA491478710 | HCN4 | c.2934T>C (p.Pro978=) c.1716T>C (p.Pro572=) | gnomAD v4 |
| 15 | g.73323159A>T | CA491478711 | HCN4 | c.2934T>A (p.Pro978=) c.1716T>A (p.Pro572=) | |
| 15 | g.73323160G>A | CA393086817 | HCN4 | c.2933C>T (p.Pro978Leu) c.1715C>T (p.Pro572Leu) | |
| 15 | g.73323160G>C | CA393086823 | HCN4 | c.2933C>G (p.Pro978Arg) c.1715C>G (p.Pro572Arg) | |
| 15 | g.73323160G>T | CA393086819 | HCN4 | c.2933C>A (p.Pro978His) c.1715C>A (p.Pro572His) | gnomAD v4 |
| 15 | g.73323161G>A | CA393086826 | HCN4 | c.2932C>T (p.Pro978Ser) c.1714C>T (p.Pro572Ser) | gnomAD v4 |
| 15 | g.73323161G>C | CA393086829 | HCN4 | c.2932C>G (p.Pro978Ala) c.1714C>G (p.Pro572Ala) | |
| 15 | g.73323161G= | CA2187187614 | HCN4 | c.2932C= (p.Pro978=) c.1714C= (p.Pro572=) | |
| 15 | g.73323161G>T | CA393086830 | HCN4 | c.2932C>A (p.Pro978Thr) c.1714C>A (p.Pro572Thr) | dbSNP gnomAD v4 |
| 15 | g.73323162C>A | CA393086832 | HCN4 | c.2931G>T (p.Gln977His) c.1713G>T (p.Gln571His) | dbSNP gnomAD v4 |
| 15 | g.73323162C= | CA2187187618 | HCN4 | c.2931G= (p.Gln977=) c.1713G= (p.Gln571=) | |
| 15 | g.73323162C>G | CA393086836 | HCN4 | c.2931G>C (p.Gln977His) c.1713G>C (p.Gln571His) | |
| 15 | g.73323162C>T | CA491478717 | HCN4 | c.2931G>A (p.Gln977=) c.1713G>A (p.Gln571=) | gnomAD v4 |
| 15 | g.73323162dup | CA2840286482 | HCN4 | c.2931dup (p.Pro978AlafsTer25) c.1713dup (p.Pro572AlafsTer25) | |
| 15 | g.73323163T>A | CA393086839 | HCN4 | c.2930A>T (p.Gln977Leu) c.1712A>T (p.Gln571Leu) | |
| 15 | g.73323163T>C | CA393086841 | HCN4 | c.2930A>G (p.Gln977Arg) c.1712A>G (p.Gln571Arg) | gnomAD v4 |
| 15 | g.73323163T>G | CA393086844 | HCN4 | c.2930A>C (p.Gln977Pro) c.1712A>C (p.Gln571Pro) | |
| 15 | g.73323164G>A | CA393086848 | HCN4 | c.2929C>T (p.Gln977Ter) c.1711C>T (p.Gln571Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323164G>C | CA393086850 | HCN4 | c.2929C>G (p.Gln977Glu) c.1711C>G (p.Gln571Glu) | |
| 15 | g.73323164G= | CA2187187620 | HCN4 | c.2929C= (p.Gln977=) c.1711C= (p.Gln571=) | |
| 15 | g.73323164G>T | CA393086853 | HCN4 | c.2929C>A (p.Gln977Lys) c.1711C>A (p.Gln571Lys) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323165G>A | CA491478722 | HCN4 | c.2928C>T (p.Gly976=) c.1710C>T (p.Gly570=) | gnomAD v4 |
| 15 | g.73323165G>C | CA491478723 | HCN4 | c.2928C>G (p.Gly976=) c.1710C>G (p.Gly570=) | |
| 15 | g.73323165G>T | CA491478724 | HCN4 | c.2928C>A (p.Gly976=) c.1710C>A (p.Gly570=) | gnomAD v4 |
| 15 | g.73323166C>A | CA393086857 | HCN4 | c.2927G>T (p.Gly976Val) c.1709G>T (p.Gly570Val) | gnomAD v4 |
| 15 | g.73323166C>G | CA393086863 | HCN4 | c.2927G>C (p.Gly976Ala) c.1709G>C (p.Gly570Ala) | |
| 15 | g.73323166C>T | CA393086859 | HCN4 | c.2927G>A (p.Gly976Asp) c.1709G>A (p.Gly570Asp) | gnomAD v4 |
| 15 | g.73323168del | CA2629370548 | HCN4 | c.2927del (p.Gly976AlafsTer9) c.1709del (p.Gly570AlafsTer9) | gnomAD v4 |
| 15 | g.73323167C>A | CA393086868 | HCN4 | c.2926G>T (p.Gly976Cys) c.1708G>T (p.Gly570Cys) | gnomAD v4 |
| 15 | g.73323167C>G | CA393086873 | HCN4 | c.2926G>C (p.Gly976Arg) c.1708G>C (p.Gly570Arg) | |
| 15 | g.73323167C>T | CA393086870 | HCN4 | c.2926G>A (p.Gly976Ser) c.1708G>A (p.Gly570Ser) | |
| 15 | g.73323168C>A | CA491478726 | HCN4 | c.2925G>T (p.Leu975=) c.1707G>T (p.Leu569=) | gnomAD v4 |
| 15 | g.73323168C>G | CA491478727 | HCN4 | c.2925G>C (p.Leu975=) c.1707G>C (p.Leu569=) | |
| 15 | g.73323168C>T | CA491478728 | HCN4 | c.2925G>A (p.Leu975=) c.1707G>A (p.Leu569=) | |
| 15 | g.73323169A>C | CA393086875 | HCN4 | c.2924T>G (p.Leu975Arg) c.1706T>G (p.Leu569Arg) | gnomAD v4 |
| 15 | g.73323169A>G | CA393086877 | HCN4 | c.2924T>C (p.Leu975Pro) c.1706T>C (p.Leu569Pro) | gnomAD v4 |
| 15 | g.73323169A>T | CA393086878 | HCN4 | c.2924T>A (p.Leu975Gln) c.1706T>A (p.Leu569Gln) | |
| 15 | g.73323170G>A | CA7648922 | HCN4 | c.2923C>T (p.Leu975=) c.1705C>T (p.Leu569=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323170G>C | CA393086882 | HCN4 | c.2923C>G (p.Leu975Val) c.1705C>G (p.Leu569Val) | |
| 15 | g.73323170G= | CA2187187624 | HCN4 | c.2923C= (p.Leu975=) c.1705C= (p.Leu569=) | |
| 15 | g.73323170G>T | CA393086885 | HCN4 | c.2923C>A (p.Leu975Met) c.1705C>A (p.Leu569Met) | gnomAD v4 |
| 15 | g.73323171C>A | CA393086889 | HCN4 | c.2922G>T (p.Gln974His) c.1704G>T (p.Gln568His) | gnomAD v4 |
| 15 | g.73323171C>G | CA393086892 | HCN4 | c.2922G>C (p.Gln974His) c.1704G>C (p.Gln568His) | |
| 15 | g.73323171C>T | CA491478731 | HCN4 | c.2922G>A (p.Gln974=) c.1704G>A (p.Gln568=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323172T>A | CA393086896 | HCN4 | c.2921A>T (p.Gln974Leu) c.1703A>T (p.Gln568Leu) | |
| 15 | g.73323172T>C | CA393086901 | HCN4 | c.2921A>G (p.Gln974Arg) c.1703A>G (p.Gln568Arg) | dbSNP |
| 15 | g.73323172T>G | CA393086904 | HCN4 | c.2921A>C (p.Gln974Pro) c.1703A>C (p.Gln568Pro) | |
| 15 | g.73323172T= | CA2187187627 | HCN4 | c.2921A= (p.Gln974=) c.1703A= (p.Gln568=) | |
| 15 | g.73323173G>A | CA393086910 | HCN4 | c.2920C>T (p.Gln974Ter) c.1702C>T (p.Gln568Ter) | gnomAD v4 |
| 15 | g.73323173G>C | CA393086906 | HCN4 | c.2920C>G (p.Gln974Glu) c.1702C>G (p.Gln568Glu) | |
| 15 | g.73323173G>T | CA393086907 | HCN4 | c.2920C>A (p.Gln974Lys) c.1702C>A (p.Gln568Lys) | gnomAD v4 |
| 15 | g.73323174C>A | CA491478736 | HCN4 | c.2919G>T (p.Gly973=) c.1701G>T (p.Gly567=) | gnomAD v4 |
| 15 | g.73323174C>G | CA491478738 | HCN4 | c.2919G>C (p.Gly973=) c.1701G>C (p.Gly567=) | |
| 15 | g.73323174C>T | CA491478740 | HCN4 | c.2919G>A (p.Gly973=) c.1701G>A (p.Gly567=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323175C>A | CA393086911 | HCN4 | c.2918G>T (p.Gly973Val) c.1700G>T (p.Gly567Val) | gnomAD v4 |
| 15 | g.73323175C= | CA2187187632 | HCN4 | c.2918G= (p.Gly973=) c.1700G= (p.Gly567=) | |
| 15 | g.73323175C>G | CA393086914 | HCN4 | c.2918G>C (p.Gly973Ala) c.1700G>C (p.Gly567Ala) | |
| 15 | g.73323175C>T | CA7648923 | HCN4 | c.2918G>A (p.Gly973Glu) c.1700G>A (p.Gly567Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323176C>A | CA7648925 | HCN4 | c.2917G>T (p.Gly973Trp) c.1699G>T (p.Gly567Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323176C= | CA2187187636 | HCN4 | c.2917G= (p.Gly973=) c.1699G= (p.Gly567=) | |
| 15 | g.73323176C>G | CA393086921 | HCN4 | c.2917G>C (p.Gly973Arg) c.1699G>C (p.Gly567Arg) | gnomAD v4 |
| 15 | g.73323176C>T | CA7648924 | HCN4 | c.2917G>A (p.Gly973Arg) c.1699G>A (p.Gly567Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323176_73323177insA | CA2629370550 | HCN4 | c.2916_2917insT (p.Gly973TrpfsTer30) c.1698_1699insT (p.Gly567TrpfsTer30) | gnomAD v4 |
| 15 | g.73323177G>A | CA7648926 | HCN4 | c.2916C>T (p.Pro972=) c.1698C>T (p.Pro566=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323177G>C | CA491478743 | HCN4 | c.2916C>G (p.Pro972=) c.1698C>G (p.Pro566=) | gnomAD v4 |
| 15 | g.73323177G= | CA2187187641 | HCN4 | c.2916C= (p.Pro972=) c.1698C= (p.Pro566=) | |
| 15 | g.73323177G>T | CA491478744 | HCN4 | c.2916C>A (p.Pro972=) c.1698C>A (p.Pro566=) | dbSNP gnomAD v4 |
| 15 | g.73323180del | CA2629370549 | HCN4 | c.2916del (p.Gln974SerfsTer11) c.1698del (p.Gln568SerfsTer11) | gnomAD v4 |
| 15 | g.73323178G>A | CA393086926 | HCN4 | c.2915C>T (p.Pro972Leu) c.1697C>T (p.Pro566Leu) | gnomAD v4 |
| 15 | g.73323178G>C | CA393086928 | HCN4 | c.2915C>G (p.Pro972Arg) c.1697C>G (p.Pro566Arg) | |
| 15 | g.73323178G>T | CA393086930 | HCN4 | c.2915C>A (p.Pro972His) c.1697C>A (p.Pro566His) | gnomAD v4 |
| 15 | g.73323179G>A | CA7648927 | HCN4 | c.2914C>T (p.Pro972Ser) c.1696C>T (p.Pro566Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323179G>C | CA393086937 | HCN4 | c.2914C>G (p.Pro972Ala) c.1696C>G (p.Pro566Ala) | |
| 15 | g.73323179G= | CA2187187647 | HCN4 | c.2914C= (p.Pro972=) c.1696C= (p.Pro566=) | |
| 15 | g.73323179G>T | CA393086932 | HCN4 | c.2914C>A (p.Pro972Thr) c.1696C>A (p.Pro566Thr) | gnomAD v4 |
| 15 | g.73323180G>A | CA491478751 | HCN4 | c.2913C>T (p.Ser971=) c.1695C>T (p.Ser565=) | gnomAD v4 |
| 15 | g.73323180G>C | CA393086940 | HCN4 | c.2913C>G (p.Ser971Arg) c.1695C>G (p.Ser565Arg) | |
| 15 | g.73323180G>T | CA393086941 | HCN4 | c.2913C>A (p.Ser971Arg) c.1695C>A (p.Ser565Arg) | gnomAD v4 |
| 15 | g.73323181C>A | CA393086944 | HCN4 | c.2912G>T (p.Ser971Ile) c.1694G>T (p.Ser565Ile) | gnomAD v4 |
| 15 | g.73323181C= | CA2187187650 | HCN4 | c.2912G= (p.Ser971=) c.1694G= (p.Ser565=) | |
| 15 | g.73323181C>G | CA393086948 | HCN4 | c.2912G>C (p.Ser971Thr) c.1694G>C (p.Ser565Thr) | gnomAD v4 |
| 15 | g.73323181C>T | CA393086951 | HCN4 | c.2912G>A (p.Ser971Asn) c.1694G>A (p.Ser565Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323182T>A | CA393086953 | HCN4 | c.2911A>T (p.Ser971Cys) c.1693A>T (p.Ser565Cys) | |
| 15 | g.73323182T>C | CA393086955 | HCN4 | c.2911A>G (p.Ser971Gly) c.1693A>G (p.Ser565Gly) | |
| 15 | g.73323182T>G | CA393086957 | HCN4 | c.2911A>C (p.Ser971Arg) c.1693A>C (p.Ser565Arg) | |
| 15 | g.73323183_73323186dup | CA2575783830 | HCN4 | c.2908_2911dup (p.Ser971IlefsTer2) c.1690_1693dup (p.Ser565IlefsTer2) | |
| 15 | g.73323183A>C | CA491478764 | HCN4 | c.2910T>G (p.Ser970=) c.1692T>G (p.Ser564=) | gnomAD v4 |
| 15 | g.73323183A>G | CA491478760 | HCN4 | c.2910T>C (p.Ser970=) c.1692T>C (p.Ser564=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323183A>T | CA491478762 | HCN4 | c.2910T>A (p.Ser970=) c.1692T>A (p.Ser564=) | gnomAD v4 |
| 15 | g.73323183_73323186delinsAGAT | CA2187187652 | HCN4 | c.2907_2910delinsATCT (p.Ser969=) c.1689_1692delinsATCT (p.Ser563=) | |
| 15 | g.73323184G>A | CA393086960 | HCN4 | c.2909C>T (p.Ser970Phe) c.1691C>T (p.Ser564Phe) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323184G>C | CA393086963 | HCN4 | c.2909C>G (p.Ser970Cys) c.1691C>G (p.Ser564Cys) | |
| 15 | g.73323184G= | CA2187187656 | HCN4 | c.2909C= (p.Ser970=) c.1691C= (p.Ser564=) | |
| 15 | g.73323184G>T | CA393086965 | HCN4 | c.2909C>A (p.Ser970Tyr) c.1691C>A (p.Ser564Tyr) | gnomAD v4 |
| 15 | g.73323186_73323188del | CA2187187654 | HCN4 | c.2907_2909del (p.Ser970del) c.1689_1691del (p.Ser564del) | dbSNP |
| 15 | g.73323185A>C | CA393086967 | HCN4 | c.2908T>G (p.Ser970Ala) c.1690T>G (p.Ser564Ala) | |
| 15 | g.73323185A>G | CA393086969 | HCN4 | c.2908T>C (p.Ser970Pro) c.1690T>C (p.Ser564Pro) | ClinVar gnomAD v4 |
| 15 | g.73323185A>T | CA393086972 | HCN4 | c.2908T>A (p.Ser970Thr) c.1690T>A (p.Ser564Thr) | |
| 15 | g.73323186T>A | CA491478769 | HCN4 | c.2907A>T (p.Ser969=) c.1689A>T (p.Ser563=) | |
| 15 | g.73323186T>C | CA7648928 | HCN4 | c.2907A>G (p.Ser969=) c.1689A>G (p.Ser563=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323186T>G | CA491478772 | HCN4 | c.2907A>C (p.Ser969=) c.1689A>C (p.Ser563=) | |
| 15 | g.73323186T= | CA2187187658 | HCN4 | c.2907A= (p.Ser969=) c.1689A= (p.Ser563=) | |
| 15 | g.73323187G>A | CA393086978 | HCN4 | c.2906C>T (p.Ser969Leu) c.1688C>T (p.Ser563Leu) | gnomAD v4 |
| 15 | g.73323187G>C | CA393086980 | HCN4 | c.2906C>G (p.Ser969Ter) c.1688C>G (p.Ser563Ter) | |
| 15 | g.73323187G>T | CA393086983 | HCN4 | c.2906C>A (p.Ser969Ter) c.1688C>A (p.Ser563Ter) | gnomAD v4 |
| 15 | g.73323188A>C | CA393086987 | HCN4 | c.2905T>G (p.Ser969Ala) c.1687T>G (p.Ser563Ala) | |
| 15 | g.73323188A>G | CA393086990 | HCN4 | c.2905T>C (p.Ser969Pro) c.1687T>C (p.Ser563Pro) | gnomAD v4 |
| 15 | g.73323188A>T | CA393086992 | HCN4 | c.2905T>A (p.Ser969Thr) c.1687T>A (p.Ser563Thr) | gnomAD v4 |
| 15 | g.73323189C>A | CA491478777 | HCN4 | c.2904G>T (p.Pro968=) c.1686G>T (p.Pro562=) | gnomAD v4 |
| 15 | g.73323189C= | CA2187187662 | HCN4 | c.2904G= (p.Pro968=) c.1686G= (p.Pro562=) | |
| 15 | g.73323189C>G | CA491478781 | HCN4 | c.2904G>C (p.Pro968=) c.1686G>C (p.Pro562=) | |
| 15 | g.73323189C>T | CA7648929 | HCN4 | c.2904G>A (p.Pro968=) c.1686G>A (p.Pro562=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323190G>A | CA7648930 | HCN4 | c.2903C>T (p.Pro968Leu) c.1685C>T (p.Pro562Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323190G>C | CA7648931 | HCN4 | c.2903C>G (p.Pro968Arg) c.1685C>G (p.Pro562Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323190G= | CA2187187670 | HCN4 | c.2903C= (p.Pro968=) c.1685C= (p.Pro562=) | |
| 15 | g.73323190G>T | CA393087002 | HCN4 | c.2903C>A (p.Pro968Gln) c.1685C>A (p.Pro562Gln) | gnomAD v4 |
| 15 | g.73323193del | CA2629370551 | HCN4 | c.2903del (p.Pro968ArgfsTer17) c.1685del (p.Pro562ArgfsTer17) | gnomAD v4 |
| 15 | g.73323191G>A | CA7648932 | HCN4 | c.2902C>T (p.Pro968Ser) c.1684C>T (p.Pro562Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323191G>C | CA393087008 | HCN4 | c.2902C>G (p.Pro968Ala) c.1684C>G (p.Pro562Ala) | |
| 15 | g.73323191G= | CA2187187673 | HCN4 | c.2902C= (p.Pro968=) c.1684C= (p.Pro562=) | |
| 15 | g.73323191G>T | CA393087010 | HCN4 | c.2902C>A (p.Pro968Thr) c.1684C>A (p.Pro562Thr) | gnomAD v4 |
| 15 | g.73323192G>A | CA7648933 | HCN4 | c.2901C>T (p.Ser967=) c.1683C>T (p.Ser561=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323192G>C | CA491478789 | HCN4 | c.2901C>G (p.Ser967=) c.1683C>G (p.Ser561=) | |
| 15 | g.73323192G= | CA2187187675 | HCN4 | c.2901C= (p.Ser967=) c.1683C= (p.Ser561=) | |
| 15 | g.73323192G>T | CA491478787 | HCN4 | c.2901C>A (p.Ser967=) c.1683C>A (p.Ser561=) | |
| 15 | g.73323193G>A | CA393087019 | HCN4 | c.2900C>T (p.Ser967Phe) c.1682C>T (p.Ser561Phe) | gnomAD v4 |
| 15 | g.73323193G>C | CA393087016 | HCN4 | c.2900C>G (p.Ser967Cys) c.1682C>G (p.Ser561Cys) | gnomAD v4 |
| 15 | g.73323193G>T | CA393087014 | HCN4 | c.2900C>A (p.Ser967Tyr) c.1682C>A (p.Ser561Tyr) | gnomAD v4 |
| 15 | g.73323194A= | CA2187187681 | HCN4 | c.2899T= (p.Ser967=) c.1681T= (p.Ser561=) | |
| 15 | g.73323194A>C | CA393087025 | HCN4 | c.2899T>G (p.Ser967Ala) c.1681T>G (p.Ser561Ala) | |
| 15 | g.73323194A>G | CA393087023 | HCN4 | c.2899T>C (p.Ser967Pro) c.1681T>C (p.Ser561Pro) | dbSNP |
| 15 | g.73323194A>T | CA393087027 | HCN4 | c.2899T>A (p.Ser967Thr) c.1681T>A (p.Ser561Thr) | |
| 15 | g.73323195T>A | CA393087030 | HCN4 | c.2898A>T (p.Arg966Ser) c.1680A>T (p.Arg560Ser) | |
| 15 | g.73323195T>C | CA491478790 | HCN4 | c.2898A>G (p.Arg966=) c.1680A>G (p.Arg560=) | |
| 15 | g.73323195T>G | CA393087031 | HCN4 | c.2898A>C (p.Arg966Ser) c.1680A>C (p.Arg560Ser) | gnomAD v4 |
| 15 | g.73323196C>A | CA393087035 | HCN4 | c.2897G>T (p.Arg966Ile) c.1679G>T (p.Arg560Ile) | gnomAD v4 |
| 15 | g.73323196C>G | CA393087039 | HCN4 | c.2897G>C (p.Arg966Thr) c.1679G>C (p.Arg560Thr) | |
| 15 | g.73323196C>T | CA393087038 | HCN4 | c.2897G>A (p.Arg966Lys) c.1679G>A (p.Arg560Lys) | |
| 15 | g.73323196_73323197delinsCT | CA2187187685 | HCN4 | c.2896_2897delinsAG (p.Arg966=) c.1678_1679delinsAG (p.Arg560=) | |
| 15 | g.73323197del | CA7648934 | HCN4 | c.2896del (p.Arg966AspfsTer19) c.1678del (p.Arg560AspfsTer19) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323197T>A | CA393087041 | HCN4 | c.2896A>T (p.Arg966Ter) c.1678A>T (p.Arg560Ter) | gnomAD v4 |
| 15 | g.73323197T>C | CA393087046 | HCN4 | c.2896A>G (p.Arg966Gly) c.1678A>G (p.Arg560Gly) | gnomAD v4 |
| 15 | g.73323197T>G | CA491478792 | HCN4 | c.2896A>C (p.Arg966=) c.1678A>C (p.Arg560=) | ClinVar |
| 15 | g.73323198G>A | CA491478795 | HCN4 | c.2895C>T (p.Ser965=) c.1677C>T (p.Ser559=) | dbSNP gnomAD v4 |
| 15 | g.73323198G>C | CA491478797 | HCN4 | c.2895C>G (p.Ser965=) c.1677C>G (p.Ser559=) | |
| 15 | g.73323198G= | CA2187187690 | HCN4 | c.2895C= (p.Ser965=) c.1677C= (p.Ser559=) | |
| 15 | g.73323198G>T | CA491478798 | HCN4 | c.2895C>A (p.Ser965=) c.1677C>A (p.Ser559=) | ClinVar gnomAD v4 |
| 15 | g.73323199G>A | CA393087050 | HCN4 | c.2894C>T (p.Ser965Phe) c.1676C>T (p.Ser559Phe) | gnomAD v4 |
| 15 | g.73323199G>C | CA393087052 | HCN4 | c.2894C>G (p.Ser965Cys) c.1676C>G (p.Ser559Cys) | |
| 15 | g.73323199G>T | CA393087054 | HCN4 | c.2894C>A (p.Ser965Tyr) c.1676C>A (p.Ser559Tyr) | gnomAD v4 |
| 15 | g.73323200A>C | CA393087055 | HCN4 | c.2893T>G (p.Ser965Ala) c.1675T>G (p.Ser559Ala) | |
| 15 | g.73323200A>G | CA393087057 | HCN4 | c.2893T>C (p.Ser965Pro) c.1675T>C (p.Ser559Pro) | gnomAD v4 |
| 15 | g.73323200A>T | CA393087060 | HCN4 | c.2893T>A (p.Ser965Thr) c.1675T>A (p.Ser559Thr) | |
| 15 | g.73323201T>A | CA491478802 | HCN4 | c.2892A>T (p.Ser964=) c.1674A>T (p.Ser558=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323201T>C | CA491478804 | HCN4 | c.2892A>G (p.Ser964=) c.1674A>G (p.Ser558=) | |
| 15 | g.73323201T>G | CA491478805 | HCN4 | c.2892A>C (p.Ser964=) c.1674A>C (p.Ser558=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323201T= | CA2187187692 | HCN4 | c.2892A= (p.Ser964=) c.1674A= (p.Ser558=) | |
| 15 | g.73323202G>A | CA393087064 | HCN4 | c.2891C>T (p.Ser964Leu) c.1673C>T (p.Ser558Leu) | dbSNP gnomAD v4 |
| 15 | g.73323202G>C | CA393087065 | HCN4 | c.2891C>G (p.Ser964Ter) c.1673C>G (p.Ser558Ter) | |
| 15 | g.73323202G= | CA2187187695 | HCN4 | c.2891C= (p.Ser964=) c.1673C= (p.Ser558=) | |
| 15 | g.73323202G>T | CA393087068 | HCN4 | c.2891C>A (p.Ser964Ter) c.1673C>A (p.Ser558Ter) | |
| 15 | g.73323203A>C | CA393087070 | HCN4 | c.2890T>G (p.Ser964Ala) c.1672T>G (p.Ser558Ala) | dbSNP |
| 15 | g.73323203A>G | CA393087074 | HCN4 | c.2890T>C (p.Ser964Pro) c.1672T>C (p.Ser558Pro) | gnomAD v4 |
| 15 | g.73323203A>T | CA393087075 | HCN4 | c.2890T>A (p.Ser964Thr) c.1672T>A (p.Ser558Thr) | gnomAD v4 |
| 15 | g.73323203_73323209delinsAGGGTGG | CA2187187699 | HCN4 | c.2884_2890delinsCCACCCT (p.Pro962=) c.1666_1672delinsCCACCCT (p.Pro556=) | |
| 15 | g.73323204G>A | CA491478818 | HCN4 | c.2889C>T (p.Pro963=) c.1671C>T (p.Pro557=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323204G>C | CA491478815 | HCN4 | c.2889C>G (p.Pro963=) c.1671C>G (p.Pro557=) | |
| 15 | g.73323204G= | CA2187187704 | HCN4 | c.2889C= (p.Pro963=) c.1671C= (p.Pro557=) | |
| 15 | g.73323204G>T | CA491478812 | HCN4 | c.2889C>A (p.Pro963=) c.1671C>A (p.Pro557=) | gnomAD v4 |
| 15 | g.73323206del | CA2629370552 | HCN4 | c.2889del (p.Ser964HisfsTer21) c.1671del (p.Ser558HisfsTer21) | gnomAD v4 |
| 15 | g.73323210_73323215dup | CA2575783831 | HCN4 | c.2884_2889dup (p.Pro963_Ser964insProPro) c.1666_1671dup (p.Pro557_Ser558insProPro) | |
| 15 | g.73323210_73323215del | CA7648935 | HCN4 | c.2884_2889del (p.Pro962_Pro963del) c.1666_1671del (p.Pro556_Pro557del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323205G>A | CA393087078 | HCN4 | c.2888C>T (p.Pro963Leu) c.1670C>T (p.Pro557Leu) | ClinVar gnomAD v4 |
| 15 | g.73323205G>C | CA393087082 | HCN4 | c.2888C>G (p.Pro963Arg) c.1670C>G (p.Pro557Arg) | |
| 15 | g.73323205G>T | CA393087079 | HCN4 | c.2888C>A (p.Pro963His) c.1670C>A (p.Pro557His) | gnomAD v4 |
| 15 | g.73323206G>A | CA393087086 | HCN4 | c.2887C>T (p.Pro963Ser) c.1669C>T (p.Pro557Ser) | dbSNP gnomAD v4 |
| 15 | g.73323206G>C | CA393087088 | HCN4 | c.2887C>G (p.Pro963Ala) c.1669C>G (p.Pro557Ala) | |
| 15 | g.73323206G= | CA2187187709 | HCN4 | c.2887C= (p.Pro963=) c.1669C= (p.Pro557=) | |
| 15 | g.73323206G>T | CA393087091 | HCN4 | c.2887C>A (p.Pro963Thr) c.1669C>A (p.Pro557Thr) | gnomAD v4 |
| 15 | g.73323207T>A | CA491478823 | HCN4 | c.2886A>T (p.Pro962=) c.1668A>T (p.Pro556=) | gnomAD v4 |
| 15 | g.73323207T>C | CA491478825 | HCN4 | c.2886A>G (p.Pro962=) c.1668A>G (p.Pro556=) | |
| 15 | g.73323207T>G | CA491478826 | HCN4 | c.2886A>C (p.Pro962=) c.1668A>C (p.Pro556=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323208G>A | CA393087094 | HCN4 | c.2885C>T (p.Pro962Leu) c.1667C>T (p.Pro556Leu) | ClinVar |
| 15 | g.73323208G>C | CA393087097 | HCN4 | c.2885C>G (p.Pro962Arg) c.1667C>G (p.Pro556Arg) | |
| 15 | g.73323208G>T | CA393087099 | HCN4 | c.2885C>A (p.Pro962Gln) c.1667C>A (p.Pro556Gln) | gnomAD v4 |
| 15 | g.73323212dup | CA2629370554 | HCN4 | c.2885dup (p.Pro963ThrfsTer9) c.1667dup (p.Pro557ThrfsTer9) | gnomAD v4 |
| 15 | g.73323212del | CA2629370553 | HCN4 | c.2885del (p.Pro962HisfsTer23) c.1667del (p.Pro556HisfsTer23) | gnomAD v4 |
| 15 | g.73323209G>A | CA393087101 | HCN4 | c.2884C>T (p.Pro962Ser) c.1666C>T (p.Pro556Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323209G>C | CA393087105 | HCN4 | c.2884C>G (p.Pro962Ala) c.1666C>G (p.Pro556Ala) | |
| 15 | g.73323209G= | CA2187187712 | HCN4 | c.2884C= (p.Pro962=) c.1666C= (p.Pro556=) | |
| 15 | g.73323209G>T | CA393087110 | HCN4 | c.2884C>A (p.Pro962Thr) c.1666C>A (p.Pro556Thr) | gnomAD v4 |
| 15 | g.73323210G>A | CA491478831 | HCN4 | c.2883C>T (p.Pro961=) c.1665C>T (p.Pro555=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323210G>C | CA491478832 | HCN4 | c.2883C>G (p.Pro961=) c.1665C>G (p.Pro555=) | gnomAD v4 |
| 15 | g.73323210G= | CA2187187716 | HCN4 | c.2883C= (p.Pro961=) c.1665C= (p.Pro555=) | |
| 15 | g.73323210G>T | CA491478833 | HCN4 | c.2883C>A (p.Pro961=) c.1665C>A (p.Pro555=) | gnomAD v4 |
| 15 | g.73323211G>A | CA393087117 | HCN4 | c.2882C>T (p.Pro961Leu) c.1664C>T (p.Pro555Leu) | gnomAD v4 |
| 15 | g.73323211G>C | CA393087115 | HCN4 | c.2882C>G (p.Pro961Arg) c.1664C>G (p.Pro555Arg) | |
| 15 | g.73323211G>T | CA393087112 | HCN4 | c.2882C>A (p.Pro961His) c.1664C>A (p.Pro555His) | gnomAD v4 |