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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.73323547_73323548delinsAC | CA2187188513 | HCN4 | c.2545_2546delinsGT (p.Val849=) c.1327_1328delinsGT (p.Val443=) | |
| 15 | g.73323548C>A | CA236699 | HCN4 | c.2545G>T (p.Val849Leu) c.1327G>T (p.Val443Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323548C= | CA2187188516 | HCN4 | c.2545G= (p.Val849=) c.1327G= (p.Val443=) | |
| 15 | g.73323548C>G | CA393088686 | HCN4 | c.2545G>C (p.Val849Leu) c.1327G>C (p.Val443Leu) | |
| 15 | g.73323548C>T | CA393088687 | HCN4 | c.2545G>A (p.Val849Met) c.1327G>A (p.Val443Met) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323549del | CA7649002 | HCN4 | c.2545del (p.Val849TrpfsTer23) c.1327del (p.Val443TrpfsTer23) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323549C>A | CA393088688 | HCN4 | c.2544G>T (p.Gln848His) c.1326G>T (p.Gln442His) | |
| 15 | g.73323549C= | CA2187188527 | HCN4 | c.2544G= (p.Gln848=) c.1326G= (p.Gln442=) | |
| 15 | g.73323549C>G | CA393088689 | HCN4 | c.2544G>C (p.Gln848His) c.1326G>C (p.Gln442His) | |
| 15 | g.73323549C>T | CA491478205 | HCN4 | c.2544G>A (p.Gln848=) c.1326G>A (p.Gln442=) | dbSNP gnomAD v4 |
| 15 | g.73323550T>A | CA393088690 | HCN4 | c.2543A>T (p.Gln848Leu) c.1325A>T (p.Gln442Leu) | |
| 15 | g.73323550T>C | CA393088691 | HCN4 | c.2543A>G (p.Gln848Arg) c.1325A>G (p.Gln442Arg) | |
| 15 | g.73323550T>G | CA393088692 | HCN4 | c.2543A>C (p.Gln848Pro) c.1325A>C (p.Gln442Pro) | |
| 15 | g.73323551G>A | CA393088693 | HCN4 | c.2542C>T (p.Gln848Ter) c.1324C>T (p.Gln442Ter) | dbSNP gnomAD v2 |
| 15 | g.73323551G>C | CA393088694 | HCN4 | c.2542C>G (p.Gln848Glu) c.1324C>G (p.Gln442Glu) | |
| 15 | g.73323551G= | CA2187188530 | HCN4 | c.2542C= (p.Gln848=) c.1324C= (p.Gln442=) | |
| 15 | g.73323551G>T | CA393088695 | HCN4 | c.2542C>A (p.Gln848Lys) c.1324C>A (p.Gln442Lys) | |
| 15 | g.73323552G>A | CA7649003 | HCN4 | c.2541C>T (p.Ser847=) c.1323C>T (p.Ser441=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323552G>C | CA491478207 | HCN4 | c.2541C>G (p.Ser847=) c.1323C>G (p.Ser441=) | ClinVar dbSNP |
| 15 | g.73323552G= | CA2187188534 | HCN4 | c.2541C= (p.Ser847=) c.1323C= (p.Ser441=) | |
| 15 | g.73323552G>T | CA491478208 | HCN4 | c.2541C>A (p.Ser847=) c.1323C>A (p.Ser441=) | gnomAD v4 |
| 15 | g.73323553G>A | CA393088696 | HCN4 | c.2540C>T (p.Ser847Phe) c.1322C>T (p.Ser441Phe) | |
| 15 | g.73323553G>C | CA393088698 | HCN4 | c.2540C>G (p.Ser847Cys) c.1322C>G (p.Ser441Cys) | |
| 15 | g.73323553G>T | CA393088697 | HCN4 | c.2540C>A (p.Ser847Tyr) c.1322C>A (p.Ser441Tyr) | COSMIC |
| 15 | g.73323554A>C | CA393088699 | HCN4 | c.2539T>G (p.Ser847Ala) c.1321T>G (p.Ser441Ala) | |
| 15 | g.73323554A>G | CA393088700 | HCN4 | c.2539T>C (p.Ser847Pro) c.1321T>C (p.Ser441Pro) | |
| 15 | g.73323554A>T | CA393088701 | HCN4 | c.2539T>A (p.Ser847Thr) c.1321T>A (p.Ser441Thr) | |
| 15 | g.73323555C>A | CA491478209 | HCN4 | c.2538G>T (p.Pro846=) c.1320G>T (p.Pro440=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323555C= | CA2187188536 | HCN4 | c.2538G= (p.Pro846=) c.1320G= (p.Pro440=) | |
| 15 | g.73323555C>G | CA491478211 | HCN4 | c.2538G>C (p.Pro846=) c.1320G>C (p.Pro440=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323555C>T | CA7649004 | HCN4 | c.2538G>A (p.Pro846=) c.1320G>A (p.Pro440=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323556G>A | CA7649005 | HCN4 | c.2537C>T (p.Pro846Leu) c.1319C>T (p.Pro440Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323556G>C | CA393088702 | HCN4 | c.2537C>G (p.Pro846Arg) c.1319C>G (p.Pro440Arg) | gnomAD v4 |
| 15 | g.73323556G= | CA2187188537 | HCN4 | c.2537C= (p.Pro846=) c.1319C= (p.Pro440=) | |
| 15 | g.73323556G>T | CA393088703 | HCN4 | c.2537C>A (p.Pro846Gln) c.1319C>A (p.Pro440Gln) | |
| 15 | g.73323557G>A | CA393088704 | HCN4 | c.2536C>T (p.Pro846Ser) c.1318C>T (p.Pro440Ser) | COSMIC |
| 15 | g.73323557G>C | CA393088705 | HCN4 | c.2536C>G (p.Pro846Ala) c.1318C>G (p.Pro440Ala) | ClinVar |
| 15 | g.73323557G>T | CA393088706 | HCN4 | c.2536C>A (p.Pro846Thr) c.1318C>A (p.Pro440Thr) | gnomAD v4 |
| 15 | g.73323558G>A | CA491478214 | HCN4 | c.2535C>T (p.Ser845=) c.1317C>T (p.Ser439=) | |
| 15 | g.73323558G>C | CA393088708 | HCN4 | c.2535C>G (p.Ser845Arg) c.1317C>G (p.Ser439Arg) | |
| 15 | g.73323558G>T | CA393088707 | HCN4 | c.2535C>A (p.Ser845Arg) c.1317C>A (p.Ser439Arg) | gnomAD v4 |
| 15 | g.73323559C>A | CA393088709 | HCN4 | c.2534G>T (p.Ser845Ile) c.1316G>T (p.Ser439Ile) | gnomAD v4 |
| 15 | g.73323559C= | CA2187188538 | HCN4 | c.2534G= (p.Ser845=) c.1316G= (p.Ser439=) | |
| 15 | g.73323559C>G | CA393088710 | HCN4 | c.2534G>C (p.Ser845Thr) c.1316G>C (p.Ser439Thr) | ClinVar dbSNP |
| 15 | g.73323559C>T | CA393088711 | HCN4 | c.2534G>A (p.Ser845Asn) c.1316G>A (p.Ser439Asn) | gnomAD v4 |
| 15 | g.73323560T>A | CA393088712 | HCN4 | c.2533A>T (p.Ser845Cys) c.1315A>T (p.Ser439Cys) | |
| 15 | g.73323560T>C | CA393088713 | HCN4 | c.2533A>G (p.Ser845Gly) c.1315A>G (p.Ser439Gly) | |
| 15 | g.73323560T>G | CA393088714 | HCN4 | c.2533A>C (p.Ser845Arg) c.1315A>C (p.Ser439Arg) | |
| 15 | g.73323561G>A | CA491478218 | HCN4 | c.2532C>T (p.Ser844=) c.1314C>T (p.Ser438=) | gnomAD v4 |
| 15 | g.73323561G>C | CA393088716 | HCN4 | c.2532C>G (p.Ser844Arg) c.1314C>G (p.Ser438Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323561G= | CA2187188539 | HCN4 | c.2532C= (p.Ser844=) c.1314C= (p.Ser438=) | |
| 15 | g.73323561G>T | CA393088715 | HCN4 | c.2532C>A (p.Ser844Arg) c.1314C>A (p.Ser438Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323562C>A | CA393088717 | HCN4 | c.2531G>T (p.Ser844Ile) c.1313G>T (p.Ser438Ile) | |
| 15 | g.73323562C>G | CA393088718 | HCN4 | c.2531G>C (p.Ser844Thr) c.1313G>C (p.Ser438Thr) | |
| 15 | g.73323562C>T | CA393088719 | HCN4 | c.2531G>A (p.Ser844Asn) c.1313G>A (p.Ser438Asn) | |
| 15 | g.73323563T>A | CA393088720 | HCN4 | c.2530A>T (p.Ser844Cys) c.1312A>T (p.Ser438Cys) | |
| 15 | g.73323563T>C | CA393088721 | HCN4 | c.2530A>G (p.Ser844Gly) c.1312A>G (p.Ser438Gly) | ClinVar |
| 15 | g.73323563T>G | CA393088722 | HCN4 | c.2530A>C (p.Ser844Arg) c.1312A>C (p.Ser438Arg) | |
| 15 | g.73323564G>A | CA491478219 | HCN4 | c.2529C>T (p.Ala843=) c.1311C>T (p.Ala437=) | |
| 15 | g.73323564G>C | CA491478220 | HCN4 | c.2529C>G (p.Ala843=) c.1311C>G (p.Ala437=) | |
| 15 | g.73323564G>T | CA491478221 | HCN4 | c.2529C>A (p.Ala843=) c.1311C>A (p.Ala437=) | |
| 15 | g.73323565del | CA2838290811 | HCN4 | c.2529del (p.Ser844AlafsTer28) c.1311del (p.Ser438AlafsTer28) | |
| 15 | g.73323565G>A | CA393088723 | HCN4 | c.2528C>T (p.Ala843Val) c.1310C>T (p.Ala437Val) | |
| 15 | g.73323565G>C | CA393088724 | HCN4 | c.2528C>G (p.Ala843Gly) c.1310C>G (p.Ala437Gly) | |
| 15 | g.73323565G= | CA2187188540 | HCN4 | c.2528C= (p.Ala843=) c.1310C= (p.Ala437=) | |
| 15 | g.73323565G>T | CA7649006 | HCN4 | c.2528C>A (p.Ala843Asp) c.1310C>A (p.Ala437Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323566C>A | CA393088725 | HCN4 | c.2527G>T (p.Ala843Ser) c.1309G>T (p.Ala437Ser) | gnomAD v4 |
| 15 | g.73323566C= | CA2187188541 | HCN4 | c.2527G= (p.Ala843=) c.1309G= (p.Ala437=) | |
| 15 | g.73323566C>G | CA393088726 | HCN4 | c.2527G>C (p.Ala843Pro) c.1309G>C (p.Ala437Pro) | |
| 15 | g.73323566C>T | CA301964 | HCN4 | c.2527G>A (p.Ala843Thr) c.1309G>A (p.Ala437Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323567G>A | CA7649007 | HCN4 | c.2526C>T (p.Pro842=) c.1308C>T (p.Pro436=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323567G>C | CA491478226 | HCN4 | c.2526C>G (p.Pro842=) c.1308C>G (p.Pro436=) | |
| 15 | g.73323567G= | CA2187188542 | HCN4 | c.2526C= (p.Pro842=) c.1308C= (p.Pro436=) | |
| 15 | g.73323567G>T | CA491478225 | HCN4 | c.2526C>A (p.Pro842=) c.1308C>A (p.Pro436=) | gnomAD v4 |
| 15 | g.73323568G>A | CA393088727 | HCN4 | c.2525C>T (p.Pro842Leu) c.1307C>T (p.Pro436Leu) | |
| 15 | g.73323568G>C | CA393088728 | HCN4 | c.2525C>G (p.Pro842Arg) c.1307C>G (p.Pro436Arg) | |
| 15 | g.73323568G>T | CA393088729 | HCN4 | c.2525C>A (p.Pro842His) c.1307C>A (p.Pro436His) | |
| 15 | g.73323569G>A | CA393088730 | HCN4 | c.2524C>T (p.Pro842Ser) c.1306C>T (p.Pro436Ser) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323569G>C | CA393088731 | HCN4 | c.2524C>G (p.Pro842Ala) c.1306C>G (p.Pro436Ala) | |
| 15 | g.73323569G>T | CA393088732 | HCN4 | c.2524C>A (p.Pro842Thr) c.1306C>A (p.Pro436Thr) | |
| 15 | g.73323570C>A | CA491478227 | HCN4 | c.2523G>T (p.Ser841=) c.1305G>T (p.Ser435=) | ClinVar dbSNP |
| 15 | g.73323570C= | CA2187188543 | HCN4 | c.2523G= (p.Ser841=) c.1305G= (p.Ser435=) | |
| 15 | g.73323570C>G | CA491478228 | HCN4 | c.2523G>C (p.Ser841=) c.1305G>C (p.Ser435=) | |
| 15 | g.73323570C>T | CA247657 | HCN4 | c.2523G>A (p.Ser841=) c.1305G>A (p.Ser435=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323571G>A | CA235703 | HCN4 | c.2522C>T (p.Ser841Leu) c.1304C>T (p.Ser435Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323571G>C | CA393088734 | HCN4 | c.2522C>G (p.Ser841Trp) c.1304C>G (p.Ser435Trp) | |
| 15 | g.73323571G= | CA2187188544 | HCN4 | c.2522C= (p.Ser841=) c.1304C= (p.Ser435=) | |
| 15 | g.73323571G>T | CA393088733 | HCN4 | c.2522C>A (p.Ser841Ter) c.1304C>A (p.Ser435Ter) | |
| 15 | g.73323572A>C | CA393088735 | HCN4 | c.2521T>G (p.Ser841Ala) c.1303T>G (p.Ser435Ala) | |
| 15 | g.73323572A>G | CA393088736 | HCN4 | c.2521T>C (p.Ser841Pro) c.1303T>C (p.Ser435Pro) | |
| 15 | g.73323572A>T | CA393088737 | HCN4 | c.2521T>A (p.Ser841Thr) c.1303T>A (p.Ser435Thr) | |
| 15 | g.73323573G>A | CA491478232 | HCN4 | c.2520C>T (p.Ala840=) c.1302C>T (p.Ala434=) | |
| 15 | g.73323573G>C | CA491478234 | HCN4 | c.2520C>G (p.Ala840=) c.1302C>G (p.Ala434=) | |
| 15 | g.73323573G>T | CA491478233 | HCN4 | c.2520C>A (p.Ala840=) c.1302C>A (p.Ala434=) | |
| 15 | g.73323574G>A | CA393088738 | HCN4 | c.2519C>T (p.Ala840Val) c.1301C>T (p.Ala434Val) | |
| 15 | g.73323574G>C | CA393088739 | HCN4 | c.2519C>G (p.Ala840Gly) c.1301C>G (p.Ala434Gly) | |
| 15 | g.73323574G>T | CA393088740 | HCN4 | c.2519C>A (p.Ala840Asp) c.1301C>A (p.Ala434Asp) | |
| 15 | g.73323575del | CA2840286486 | HCN4 | c.2518del (p.Ala840ProfsTer?) c.1300del (p.Ala434ProfsTer?) | |
| 15 | g.73323575C>A | CA393088741 | HCN4 | c.2518G>T (p.Ala840Ser) c.1300G>T (p.Ala434Ser) | dbSNP gnomAD v4 |
| 15 | g.73323575C= | CA2187188545 | HCN4 | c.2518G= (p.Ala840=) c.1300G= (p.Ala434=) | |
| 15 | g.73323575C>G | CA7649008 | HCN4 | c.2518G>C (p.Ala840Pro) c.1300G>C (p.Ala434Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323575C>T | CA7649009 | HCN4 | c.2518G>A (p.Ala840Thr) c.1300G>A (p.Ala434Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323575_73323578dup | CA2580089986 | HCN4 | c.2515_2518dup (p.Ala840ValfsTer?) c.1297_1300dup (p.Ala434ValfsTer?) | ClinVar |
| 15 | g.73323576G>A | CA7649010 | HCN4 | c.2517C>T (p.Ser839=) c.1299C>T (p.Ser433=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323576G>C | CA491478238 | HCN4 | c.2517C>G (p.Ser839=) c.1299C>G (p.Ser433=) | |
| 15 | g.73323576G= | CA2187188546 | HCN4 | c.2517C= (p.Ser839=) c.1299C= (p.Ser433=) | |
| 15 | g.73323576G>T | CA491478239 | HCN4 | c.2517C>A (p.Ser839=) c.1299C>A (p.Ser433=) | |
| 15 | g.73323577G>A | CA393088742 | HCN4 | c.2516C>T (p.Ser839Phe) c.1298C>T (p.Ser433Phe) | |
| 15 | g.73323577G>C | CA393088743 | HCN4 | c.2516C>G (p.Ser839Cys) c.1298C>G (p.Ser433Cys) | |
| 15 | g.73323577G>T | CA393088744 | HCN4 | c.2516C>A (p.Ser839Tyr) c.1298C>A (p.Ser433Tyr) | |
| 15 | g.73323578A>C | CA393088747 | HCN4 | c.2515T>G (p.Ser839Ala) c.1297T>G (p.Ser433Ala) | gnomAD v4 |
| 15 | g.73323578A>G | CA393088746 | HCN4 | c.2515T>C (p.Ser839Pro) c.1297T>C (p.Ser433Pro) | |
| 15 | g.73323578A>T | CA393088745 | HCN4 | c.2515T>A (p.Ser839Thr) c.1297T>A (p.Ser433Thr) | |
| 15 | g.73323579G>A | CA491478241 | HCN4 | c.2514C>T (p.Gly838=) c.1296C>T (p.Gly432=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323579G>C | CA7649011 | HCN4 | c.2514C>G (p.Gly838=) c.1296C>G (p.Gly432=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323579G= | CA2187188547 | HCN4 | c.2514C= (p.Gly838=) c.1296C= (p.Gly432=) | |
| 15 | g.73323579G>T | CA491478243 | HCN4 | c.2514C>A (p.Gly838=) c.1296C>A (p.Gly432=) | |
| 15 | g.73323580C>A | CA393088748 | HCN4 | c.2513G>T (p.Gly838Val) c.1295G>T (p.Gly432Val) | |
| 15 | g.73323580C>G | CA393088749 | HCN4 | c.2513G>C (p.Gly838Ala) c.1295G>C (p.Gly432Ala) | |
| 15 | g.73323580C>T | CA393088750 | HCN4 | c.2513G>A (p.Gly838Asp) c.1295G>A (p.Gly432Asp) | gnomAD v4 |
| 15 | g.73323581C>A | CA393088751 | HCN4 | c.2512G>T (p.Gly838Cys) c.1294G>T (p.Gly432Cys) | |
| 15 | g.73323581C>G | CA393088752 | HCN4 | c.2512G>C (p.Gly838Arg) c.1294G>C (p.Gly432Arg) | ClinVar gnomAD v4 |
| 15 | g.73323581C>T | CA393088753 | HCN4 | c.2512G>A (p.Gly838Ser) c.1294G>A (p.Gly432Ser) | gnomAD v4 |
| 15 | g.73323582C>A | CA491478246 | HCN4 | c.2511G>T (p.Leu837=) c.1293G>T (p.Leu431=) | |
| 15 | g.73323582C>G | CA491478247 | HCN4 | c.2511G>C (p.Leu837=) c.1293G>C (p.Leu431=) | |
| 15 | g.73323582C>T | CA491478248 | HCN4 | c.2511G>A (p.Leu837=) c.1293G>A (p.Leu431=) | gnomAD v4 |
| 15 | g.73323583A>C | CA393088754 | HCN4 | c.2510T>G (p.Leu837Arg) c.1292T>G (p.Leu431Arg) | |
| 15 | g.73323583A>G | CA393088755 | HCN4 | c.2510T>C (p.Leu837Pro) c.1292T>C (p.Leu431Pro) | gnomAD v4 |
| 15 | g.73323583A>T | CA393088756 | HCN4 | c.2510T>A (p.Leu837Gln) c.1292T>A (p.Leu431Gln) | |
| 15 | g.73323584G>A | CA491478251 | HCN4 | c.2509C>T (p.Leu837=) c.1291C>T (p.Leu431=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323584G>C | CA393088757 | HCN4 | c.2509C>G (p.Leu837Val) c.1291C>G (p.Leu431Val) | |
| 15 | g.73323584G= | CA2187188548 | HCN4 | c.2509C= (p.Leu837=) c.1291C= (p.Leu431=) | |
| 15 | g.73323584G>T | CA393088758 | HCN4 | c.2509C>A (p.Leu837Met) c.1291C>A (p.Leu431Met) | dbSNP gnomAD v2 |
| 15 | g.73323585C>A | CA7649013 | HCN4 | c.2508G>T (p.Ala836=) c.1290G>T (p.Ala430=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323585C= | CA2187188549 | HCN4 | c.2508G= (p.Ala836=) c.1290G= (p.Ala430=) | |
| 15 | g.73323585C>G | CA491478253 | HCN4 | c.2508G>C (p.Ala836=) c.1290G>C (p.Ala430=) | |
| 15 | g.73323585C>T | CA7649012 | HCN4 | c.2508G>A (p.Ala836=) c.1290G>A (p.Ala430=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323586G>A | CA7649014 | HCN4 | c.2507C>T (p.Ala836Val) c.1289C>T (p.Ala430Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323586G>C | CA393088760 | HCN4 | c.2507C>G (p.Ala836Gly) c.1289C>G (p.Ala430Gly) | ClinVar |
| 15 | g.73323586G= | CA2187188550 | HCN4 | c.2507C= (p.Ala836=) c.1289C= (p.Ala430=) | |
| 15 | g.73323586G>T | CA393088759 | HCN4 | c.2507C>A (p.Ala836Glu) c.1289C>A (p.Ala430Glu) | gnomAD v4 |
| 15 | g.73323587C>A | CA393088761 | HCN4 | c.2506G>T (p.Ala836Ser) c.1288G>T (p.Ala430Ser) | |
| 15 | g.73323587C>G | CA393088762 | HCN4 | c.2506G>C (p.Ala836Pro) c.1288G>C (p.Ala430Pro) | |
| 15 | g.73323587C>T | CA393088763 | HCN4 | c.2506G>A (p.Ala836Thr) c.1288G>A (p.Ala430Thr) | |
| 15 | g.73323587_73323590delinsCAGA | CA2187188551 | HCN4 | c.2503_2506delinsTCTG (p.Ser835=) c.1285_1288delinsTCTG (p.Ser429=) | |
| 15 | g.73323588A>C | CA491478257 | HCN4 | c.2505T>G (p.Ser835=) c.1287T>G (p.Ser429=) | |
| 15 | g.73323588A>G | CA491478255 | HCN4 | c.2505T>C (p.Ser835=) c.1287T>C (p.Ser429=) | gnomAD v4 |
| 15 | g.73323588A>T | CA491478256 | HCN4 | c.2505T>A (p.Ser835=) c.1287T>A (p.Ser429=) | |
| 15 | g.73323590_73323592del | CA715545777 | HCN4 | c.2503_2505del (p.Ser835del) c.1285_1287del (p.Ser429del) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323589G>A | CA393088764 | HCN4 | c.2504C>T (p.Ser835Phe) c.1286C>T (p.Ser429Phe) | ClinVar gnomAD v4 |
| 15 | g.73323589G>C | CA393088765 | HCN4 | c.2504C>G (p.Ser835Cys) c.1286C>G (p.Ser429Cys) | |
| 15 | g.73323589G>T | CA393088766 | HCN4 | c.2504C>A (p.Ser835Tyr) c.1286C>A (p.Ser429Tyr) | gnomAD v4 |
| 15 | g.73323590A>C | CA393088767 | HCN4 | c.2503T>G (p.Ser835Ala) c.1285T>G (p.Ser429Ala) | |
| 15 | g.73323590A>G | CA393088768 | HCN4 | c.2503T>C (p.Ser835Pro) c.1285T>C (p.Ser429Pro) | |
| 15 | g.73323590A>T | CA393088769 | HCN4 | c.2503T>A (p.Ser835Thr) c.1285T>A (p.Ser429Thr) | |
| 15 | g.73323591A= | CA2187188552 | HCN4 | c.2502T= (p.Pro834=) c.1284T= (p.Pro428=) | |
| 15 | g.73323591A>C | CA491478258 | HCN4 | c.2502T>G (p.Pro834=) c.1284T>G (p.Pro428=) | |
| 15 | g.73323591A>G | CA491478259 | HCN4 | c.2502T>C (p.Pro834=) c.1284T>C (p.Pro428=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323591A>T | CA491478260 | HCN4 | c.2502T>A (p.Pro834=) c.1284T>A (p.Pro428=) | |
| 15 | g.73323592G>A | CA393088770 | HCN4 | c.2501C>T (p.Pro834Leu) c.1283C>T (p.Pro428Leu) | gnomAD v4 |
| 15 | g.73323592G>C | CA393088771 | HCN4 | c.2501C>G (p.Pro834Arg) c.1283C>G (p.Pro428Arg) | |
| 15 | g.73323592G= | CA2187188553 | HCN4 | c.2501C= (p.Pro834=) c.1283C= (p.Pro428=) | |
| 15 | g.73323592G>T | CA393088772 | HCN4 | c.2501C>A (p.Pro834His) c.1283C>A (p.Pro428His) | dbSNP gnomAD v4 |
| 15 | g.73323592_73323593delinsAA | CA645586809 | HCN4 | c.2500_2501delinsTT (p.Pro834Phe) c.1282_1283delinsTT (p.Pro428Phe) | COSMIC |
| 15 | g.73323592_73323593insC | CA658798404 | HCN4 | c.2500_2501insG (p.Pro834ArgfsTer?) c.1282_1283insG (p.Pro428ArgfsTer?) | ClinVar dbSNP |
| 15 | g.73323593G>A | CA7649015 | HCN4 | c.2500C>T (p.Pro834Ser) c.1282C>T (p.Pro428Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323593G>C | CA393088773 | HCN4 | c.2500C>G (p.Pro834Ala) c.1282C>G (p.Pro428Ala) | |
| 15 | g.73323593G= | CA2187188554 | HCN4 | c.2500C= (p.Pro834=) c.1282C= (p.Pro428=) | |
| 15 | g.73323593G>T | CA393088774 | HCN4 | c.2500C>A (p.Pro834Thr) c.1282C>A (p.Pro428Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323594G>A | CA491478263 | HCN4 | c.2499C>T (p.Ile833=) c.1281C>T (p.Ile427=) | |
| 15 | g.73323594G>C | CA393088775 | HCN4 | c.2499C>G (p.Ile833Met) c.1281C>G (p.Ile427Met) | |
| 15 | g.73323594G>T | CA491478264 | HCN4 | c.2499C>A (p.Ile833=) c.1281C>A (p.Ile427=) | gnomAD v4 |
| 15 | g.73323595A= | CA2187188555 | HCN4 | c.2498T= (p.Ile833=) c.1280T= (p.Ile427=) | |
| 15 | g.73323595A>C | CA393088776 | HCN4 | c.2498T>G (p.Ile833Ser) c.1280T>G (p.Ile427Ser) | |
| 15 | g.73323595A>G | CA393088777 | HCN4 | c.2498T>C (p.Ile833Thr) c.1280T>C (p.Ile427Thr) | ClinVar dbSNP |
| 15 | g.73323595A>T | CA393088778 | HCN4 | c.2498T>A (p.Ile833Asn) c.1280T>A (p.Ile427Asn) | |
| 15 | g.73323596T>A | CA393088779 | HCN4 | c.2497A>T (p.Ile833Phe) c.1279A>T (p.Ile427Phe) | |
| 15 | g.73323596T>C | CA393088780 | HCN4 | c.2497A>G (p.Ile833Val) c.1279A>G (p.Ile427Val) | |
| 15 | g.73323596T>G | CA393088781 | HCN4 | c.2497A>C (p.Ile833Leu) c.1279A>C (p.Ile427Leu) | |
| 15 | g.73323597C>A | CA7649016 | HCN4 | c.2496G>T (p.Leu832=) c.1278G>T (p.Leu426=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323597C= | CA2187188556 | HCN4 | c.2496G= (p.Leu832=) c.1278G= (p.Leu426=) | |
| 15 | g.73323597C>G | CA491478266 | HCN4 | c.2496G>C (p.Leu832=) c.1278G>C (p.Leu426=) | |
| 15 | g.73323597C>T | CA491478268 | HCN4 | c.2496G>A (p.Leu832=) c.1278G>A (p.Leu426=) | |
| 15 | g.73323598A= | CA2187188557 | HCN4 | c.2495T= (p.Leu832=) c.1277T= (p.Leu426=) | |
| 15 | g.73323598A>C | CA393088782 | HCN4 | c.2495T>G (p.Leu832Arg) c.1277T>G (p.Leu426Arg) | |
| 15 | g.73323598A>G | CA393088783 | HCN4 | c.2495T>C (p.Leu832Pro) c.1277T>C (p.Leu426Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323598A>T | CA393088784 | HCN4 | c.2495T>A (p.Leu832Gln) c.1277T>A (p.Leu426Gln) | |
| 15 | g.73323599G>A | CA7649017 | HCN4 | c.2494C>T (p.Leu832=) c.1276C>T (p.Leu426=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323599G>C | CA393088786 | HCN4 | c.2494C>G (p.Leu832Val) c.1276C>G (p.Leu426Val) | gnomAD v4 |
| 15 | g.73323599G= | CA2187188558 | HCN4 | c.2494C= (p.Leu832=) c.1276C= (p.Leu426=) | |
| 15 | g.73323599G>T | CA393088785 | HCN4 | c.2494C>A (p.Leu832Met) c.1276C>A (p.Leu426Met) | gnomAD v4 |
| 15 | g.73323600G>A | CA491478270 | HCN4 | c.2493C>T (p.Ser831=) c.1275C>T (p.Ser425=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323600G>C | CA491478271 | HCN4 | c.2493C>G (p.Ser831=) c.1275C>G (p.Ser425=) | gnomAD v4 |
| 15 | g.73323600G= | CA2187188559 | HCN4 | c.2493C= (p.Ser831=) c.1275C= (p.Ser425=) | |
| 15 | g.73323600G>T | CA491478272 | HCN4 | c.2493C>A (p.Ser831=) c.1275C>A (p.Ser425=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323601G>A | CA393088787 | HCN4 | c.2492C>T (p.Ser831Phe) c.1274C>T (p.Ser425Phe) | ClinVar |
| 15 | g.73323601G>C | CA393088789 | HCN4 | c.2492C>G (p.Ser831Cys) c.1274C>G (p.Ser425Cys) | |
| 15 | g.73323601G>T | CA393088788 | HCN4 | c.2492C>A (p.Ser831Tyr) c.1274C>A (p.Ser425Tyr) | gnomAD v4 COSMIC |
| 15 | g.73323602A>C | CA393088790 | HCN4 | c.2491T>G (p.Ser831Ala) c.1273T>G (p.Ser425Ala) | |
| 15 | g.73323602A>G | CA393088792 | HCN4 | c.2491T>C (p.Ser831Pro) c.1273T>C (p.Ser425Pro) | |
| 15 | g.73323602A>T | CA393088791 | HCN4 | c.2491T>A (p.Ser831Thr) c.1273T>A (p.Ser425Thr) | |
| 15 | g.73323603C>A | CA393088793 | HCN4 | c.2490G>T (p.Gln830His) c.1272G>T (p.Gln424His) | |
| 15 | g.73323603C>G | CA393088794 | HCN4 | c.2490G>C (p.Gln830His) c.1272G>C (p.Gln424His) | |
| 15 | g.73323603C>T | CA491478278 | HCN4 | c.2490G>A (p.Gln830=) c.1272G>A (p.Gln424=) | |
| 15 | g.73323604T>A | CA393088795 | HCN4 | c.2489A>T (p.Gln830Leu) c.1271A>T (p.Gln424Leu) | |
| 15 | g.73323604T>C | CA393088796 | HCN4 | c.2489A>G (p.Gln830Arg) c.1271A>G (p.Gln424Arg) | gnomAD v4 |
| 15 | g.73323604T>G | CA393088797 | HCN4 | c.2489A>C (p.Gln830Pro) c.1271A>C (p.Gln424Pro) | |
| 15 | g.73323605G>A | CA393088798 | HCN4 | c.2488C>T (p.Gln830Ter) c.1270C>T (p.Gln424Ter) | gnomAD v4 |
| 15 | g.73323605G>C | CA393088799 | HCN4 | c.2488C>G (p.Gln830Glu) c.1270C>G (p.Gln424Glu) | |
| 15 | g.73323605G>T | CA393088800 | HCN4 | c.2488C>A (p.Gln830Lys) c.1270C>A (p.Gln424Lys) | gnomAD v4 |
| 15 | g.73323606C>A | CA491478280 | HCN4 | c.2487G>T (p.Leu829=) c.1269G>T (p.Leu423=) | |
| 15 | g.73323606C= | CA2187188560 | HCN4 | c.2487G= (p.Leu829=) c.1269G= (p.Leu423=) | |
| 15 | g.73323606C>G | CA491478281 | HCN4 | c.2487G>C (p.Leu829=) c.1269G>C (p.Leu423=) | |
| 15 | g.73323606C>T | CA491478283 | HCN4 | c.2487G>A (p.Leu829=) c.1269G>A (p.Leu423=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323607A>C | CA393088801 | HCN4 | c.2486T>G (p.Leu829Arg) c.1268T>G (p.Leu423Arg) | |
| 15 | g.73323607A>G | CA393088802 | HCN4 | c.2486T>C (p.Leu829Pro) c.1268T>C (p.Leu423Pro) | gnomAD v4 |
| 15 | g.73323607A>T | CA393088803 | HCN4 | c.2486T>A (p.Leu829Gln) c.1268T>A (p.Leu423Gln) | |
| 15 | g.73323608G>A | CA491478288 | HCN4 | c.2485C>T (p.Leu829=) c.1267C>T (p.Leu423=) | dbSNP gnomAD v2 |
| 15 | g.73323608G>C | CA393088805 | HCN4 | c.2485C>G (p.Leu829Val) c.1267C>G (p.Leu423Val) | |
| 15 | g.73323608G= | CA2187188561 | HCN4 | c.2485C= (p.Leu829=) c.1267C= (p.Leu423=) | |
| 15 | g.73323608G>T | CA393088804 | HCN4 | c.2485C>A (p.Leu829Met) c.1267C>A (p.Leu423Met) | gnomAD v4 |
| 15 | g.73323609C>A | CA7649018 | HCN4 | c.2484G>T (p.Arg828=) c.1266G>T (p.Arg422=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323609C= | CA2187188562 | HCN4 | c.2484G= (p.Arg828=) c.1266G= (p.Arg422=) | |
| 15 | g.73323609C>G | CA491478290 | HCN4 | c.2484G>C (p.Arg828=) c.1266G>C (p.Arg422=) | |
| 15 | g.73323609C>T | CA491478289 | HCN4 | c.2484G>A (p.Arg828=) c.1266G>A (p.Arg422=) | |
| 15 | g.73323610dup | CA2840286487 | HCN4 | c.2484dup (p.Leu829AlafsTer?) c.1266dup (p.Leu423AlafsTer?) | |
| 15 | g.73323610C>A | CA393088806 | HCN4 | c.2483G>T (p.Arg828Leu) c.1265G>T (p.Arg422Leu) | |
| 15 | g.73323610C= | CA2187188563 | HCN4 | c.2483G= (p.Arg828=) c.1265G= (p.Arg422=) | |
| 15 | g.73323610C>G | CA393088807 | HCN4 | c.2483G>C (p.Arg828Pro) c.1265G>C (p.Arg422Pro) | |
| 15 | g.73323610C>T | CA7649019 | HCN4 | c.2483G>A (p.Arg828Gln) c.1265G>A (p.Arg422Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323611G>A | CA393088808 | HCN4 | c.2482C>T (p.Arg828Trp) c.1264C>T (p.Arg422Trp) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323611G>C | CA393088809 | HCN4 | c.2482C>G (p.Arg828Gly) c.1264C>G (p.Arg422Gly) | gnomAD v4 |
| 15 | g.73323611G= | CA2187188564 | HCN4 | c.2482C= (p.Arg828=) c.1264C= (p.Arg422=) | |
| 15 | g.73323611G>T | CA491478296 | HCN4 | c.2482C>A (p.Arg828=) c.1264C>A (p.Arg422=) | gnomAD v4 |
| 15 | g.73323612T>A | CA393088810 | HCN4 | c.2481A>T (p.Lys827Asn) c.1263A>T (p.Lys421Asn) | |
| 15 | g.73323612T>C | CA491478299 | HCN4 | c.2481A>G (p.Lys827=) c.1263A>G (p.Lys421=) | gnomAD v4 |
| 15 | g.73323612T>G | CA393088811 | HCN4 | c.2481A>C (p.Lys827Asn) c.1263A>C (p.Lys421Asn) | |
| 15 | g.73323613T>A | CA393088812 | HCN4 | c.2480A>T (p.Lys827Ile) c.1262A>T (p.Lys421Ile) | |
| 15 | g.73323613T>C | CA393088813 | HCN4 | c.2480A>G (p.Lys827Arg) c.1262A>G (p.Lys421Arg) | |
| 15 | g.73323613T>G | CA393088814 | HCN4 | c.2480A>C (p.Lys827Thr) c.1262A>C (p.Lys421Thr) | |
| 15 | g.73323614T>A | CA393088817 | HCN4 | c.2479A>T (p.Lys827Ter) c.1261A>T (p.Lys421Ter) | gnomAD v4 |
| 15 | g.73323614T>C | CA393088816 | HCN4 | c.2479A>G (p.Lys827Glu) c.1261A>G (p.Lys421Glu) | dbSNP |
| 15 | g.73323614T>G | CA393088815 | HCN4 | c.2479A>C (p.Lys827Gln) c.1261A>C (p.Lys421Gln) | |
| 15 | g.73323614T= | CA2187188565 | HCN4 | c.2479A= (p.Lys827=) c.1261A= (p.Lys421=) | |
| 15 | g.73323615C>A | CA491478301 | HCN4 | c.2478G>T (p.Leu826=) c.1260G>T (p.Leu420=) | gnomAD v4 |
| 15 | g.73323615C>G | CA491478305 | HCN4 | c.2478G>C (p.Leu826=) c.1260G>C (p.Leu420=) | |
| 15 | g.73323615C>T | CA491478303 | HCN4 | c.2478G>A (p.Leu826=) c.1260G>A (p.Leu420=) | |
| 15 | g.73323616A= | CA2187188566 | HCN4 | c.2477T= (p.Leu826=) c.1259T= (p.Leu420=) | |
| 15 | g.73323616A>C | CA393088818 | HCN4 | c.2477T>G (p.Leu826Arg) c.1259T>G (p.Leu420Arg) | |
| 15 | g.73323616A>G | CA272664726 | HCN4 | c.2477T>C (p.Leu826Pro) c.1259T>C (p.Leu420Pro) | dbSNP gnomAD v4 |
| 15 | g.73323616A>T | CA393088819 | HCN4 | c.2477T>A (p.Leu826Gln) c.1259T>A (p.Leu420Gln) | |
| 15 | g.73323617G>A | CA491478309 | HCN4 | c.2476C>T (p.Leu826=) c.1258C>T (p.Leu420=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323617G>C | CA393088820 | HCN4 | c.2476C>G (p.Leu826Val) c.1258C>G (p.Leu420Val) | |
| 15 | g.73323617G= | CA2187188567 | HCN4 | c.2476C= (p.Leu826=) c.1258C= (p.Leu420=) | |
| 15 | g.73323617G>T | CA393088821 | HCN4 | c.2476C>A (p.Leu826Met) c.1258C>A (p.Leu420Met) | gnomAD v4 |
| 15 | g.73323618G>A | CA491478312 | HCN4 | c.2475C>T (p.His825=) c.1257C>T (p.His419=) | gnomAD v4 |
| 15 | g.73323618G>C | CA393088822 | HCN4 | c.2475C>G (p.His825Gln) c.1257C>G (p.His419Gln) | |
| 15 | g.73323618G>T | CA393088823 | HCN4 | c.2475C>A (p.His825Gln) c.1257C>A (p.His419Gln) | gnomAD v4 |
| 15 | g.73323619T>A | CA393088824 | HCN4 | c.2474A>T (p.His825Leu) c.1256A>T (p.His419Leu) | ClinVar gnomAD v4 |
| 15 | g.73323619T>C | CA393088825 | HCN4 | c.2474A>G (p.His825Arg) c.1256A>G (p.His419Arg) | |
| 15 | g.73323619T>G | CA393088826 | HCN4 | c.2474A>C (p.His825Pro) c.1256A>C (p.His419Pro) | |
| 15 | g.73323620G>A | CA7649020 | HCN4 | c.2473C>T (p.His825Tyr) c.1255C>T (p.His419Tyr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323620G>C | CA393088827 | HCN4 | c.2473C>G (p.His825Asp) c.1255C>G (p.His419Asp) | |
| 15 | g.73323620G= | CA2187188568 | HCN4 | c.2473C= (p.His825=) c.1255C= (p.His419=) | |
| 15 | g.73323620G>T | CA393088828 | HCN4 | c.2473C>A (p.His825Asn) c.1255C>A (p.His419Asn) | |
| 15 | g.73323621C>A | CA393088829 | HCN4 | c.2472G>T (p.Arg824Ser) c.1254G>T (p.Arg418Ser) | |
| 15 | g.73323621C>G | CA393088830 | HCN4 | c.2472G>C (p.Arg824Ser) c.1254G>C (p.Arg418Ser) | |
| 15 | g.73323621C>T | CA491478318 | HCN4 | c.2472G>A (p.Arg824=) c.1254G>A (p.Arg418=) | ClinVar gnomAD v4 |
| 15 | g.73323622C>A | CA393088831 | HCN4 | c.2471G>T (p.Arg824Met) c.1253G>T (p.Arg418Met) | COSMIC |
| 15 | g.73323622C>G | CA393088832 | HCN4 | c.2471G>C (p.Arg824Thr) c.1253G>C (p.Arg418Thr) | |
| 15 | g.73323622C>T | CA393088833 | HCN4 | c.2471G>A (p.Arg824Lys) c.1253G>A (p.Arg418Lys) | ClinVar dbSNP |
| 15 | g.73323623T>A | CA393088834 | HCN4 | c.2470A>T (p.Arg824Trp) c.1252A>T (p.Arg418Trp) | gnomAD v4 |
| 15 | g.73323623T>C | CA393088835 | HCN4 | c.2470A>G (p.Arg824Gly) c.1252A>G (p.Arg418Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323623T>G | CA491478323 | HCN4 | c.2470A>C (p.Arg824=) c.1252A>C (p.Arg418=) | gnomAD v4 |
| 15 | g.73323623T= | CA2187188569 | HCN4 | c.2470A= (p.Arg824=) c.1252A= (p.Arg418=) | |
| 15 | g.73323624T>A | CA491478325 | HCN4 | c.2469A>T (p.Pro823=) c.1251A>T (p.Pro417=) | |
| 15 | g.73323624T>C | CA491478328 | HCN4 | c.2469A>G (p.Pro823=) c.1251A>G (p.Pro417=) | dbSNP |
| 15 | g.73323624T>G | CA491478330 | HCN4 | c.2469A>C (p.Pro823=) c.1251A>C (p.Pro417=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323624T= | CA2187188570 | HCN4 | c.2469A= (p.Pro823=) c.1251A= (p.Pro417=) | |
| 15 | g.73323625G>A | CA393088836 | HCN4 | c.2468C>T (p.Pro823Leu) c.1250C>T (p.Pro417Leu) | gnomAD v4 |
| 15 | g.73323625G>C | CA393088837 | HCN4 | c.2468C>G (p.Pro823Arg) c.1250C>G (p.Pro417Arg) | |
| 15 | g.73323625G>T | CA393088838 | HCN4 | c.2468C>A (p.Pro823Gln) c.1250C>A (p.Pro417Gln) | gnomAD v4 COSMIC |
| 15 | g.73323626G>A | CA7649021 | HCN4 | c.2467C>T (p.Pro823Ser) c.1249C>T (p.Pro417Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323626G>C | CA393088839 | HCN4 | c.2467C>G (p.Pro823Ala) c.1249C>G (p.Pro417Ala) | |
| 15 | g.73323626G= | CA2187188571 | HCN4 | c.2467C= (p.Pro823=) c.1249C= (p.Pro417=) | |
| 15 | g.73323626G>T | CA393088840 | HCN4 | c.2467C>A (p.Pro823Thr) c.1249C>A (p.Pro417Thr) | gnomAD v4 |
| 15 | g.73323627C>A | CA491478334 | HCN4 | c.2466G>T (p.Thr822=) c.1248G>T (p.Thr416=) | gnomAD v4 |
| 15 | g.73323627C= | CA2187188572 | HCN4 | c.2466G= (p.Thr822=) c.1248G= (p.Thr416=) | |
| 15 | g.73323627C>G | CA491478335 | HCN4 | c.2466G>C (p.Thr822=) c.1248G>C (p.Thr416=) | gnomAD v4 |
| 15 | g.73323627C>T | CA7649022 | HCN4 | c.2466G>A (p.Thr822=) c.1248G>A (p.Thr416=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323628G>A | CA7649023 | HCN4 | c.2465C>T (p.Thr822Met) c.1247C>T (p.Thr416Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323628G>C | CA393088842 | HCN4 | c.2465C>G (p.Thr822Arg) c.1247C>G (p.Thr416Arg) | |
| 15 | g.73323628G= | CA2187188573 | HCN4 | c.2465C= (p.Thr822=) c.1247C= (p.Thr416=) | |
| 15 | g.73323628G>T | CA393088841 | HCN4 | c.2465C>A (p.Thr822Lys) c.1247C>A (p.Thr416Lys) | gnomAD v4 |
| 15 | g.73323629T>A | CA393088843 | HCN4 | c.2464A>T (p.Thr822Ser) c.1246A>T (p.Thr416Ser) | |
| 15 | g.73323629T>C | CA393088844 | HCN4 | c.2464A>G (p.Thr822Ala) c.1246A>G (p.Thr416Ala) | |
| 15 | g.73323629T>G | CA393088845 | HCN4 | c.2464A>C (p.Thr822Pro) c.1246A>C (p.Thr416Pro) | |
| 15 | g.73323630C>A | CA393088846 | HCN4 | c.2463G>T (p.Gln821His) c.1245G>T (p.Gln415His) | |
| 15 | g.73323630C>G | CA393088847 | HCN4 | c.2463G>C (p.Gln821His) c.1245G>C (p.Gln415His) | |
| 15 | g.73323630C>T | CA491478337 | HCN4 | c.2463G>A (p.Gln821=) c.1245G>A (p.Gln415=) | gnomAD v4 |
| 15 | g.73323631T>A | CA393088849 | HCN4 | c.2462A>T (p.Gln821Leu) c.1244A>T (p.Gln415Leu) | |
| 15 | g.73323631T>C | CA7649024 | HCN4 | c.2462A>G (p.Gln821Arg) c.1244A>G (p.Gln415Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323631T>G | CA393088848 | HCN4 | c.2462A>C (p.Gln821Pro) c.1244A>C (p.Gln415Pro) | gnomAD v4 |
| 15 | g.73323631T= | CA2187188574 | HCN4 | c.2462A= (p.Gln821=) c.1244A= (p.Gln415=) | |
| 15 | g.73323632G>A | CA393088850 | HCN4 | c.2461C>T (p.Gln821Ter) c.1243C>T (p.Gln415Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323632G>C | CA393088851 | HCN4 | c.2461C>G (p.Gln821Glu) c.1243C>G (p.Gln415Glu) | |
| 15 | g.73323632G= | CA2187188575 | HCN4 | c.2461C= (p.Gln821=) c.1243C= (p.Gln415=) | |
| 15 | g.73323632G>T | CA393088852 | HCN4 | c.2461C>A (p.Gln821Lys) c.1243C>A (p.Gln415Lys) | gnomAD v4 |
| 15 | g.73323633C>A | CA491478340 | HCN4 | c.2460G>T (p.Gly820=) c.1242G>T (p.Gly414=) | |
| 15 | g.73323633C= | CA2187188576 | HCN4 | c.2460G= (p.Gly820=) c.1242G= (p.Gly414=) | |
| 15 | g.73323633C>G | CA491478341 | HCN4 | c.2460G>C (p.Gly820=) c.1242G>C (p.Gly414=) | |
| 15 | g.73323633C>T | CA491478342 | HCN4 | c.2460G>A (p.Gly820=) c.1242G>A (p.Gly414=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323635del | CA2840286488 | HCN4 | c.2460del (p.Gln821ArgfsTer6) c.1242del (p.Gln415ArgfsTer6) | |
| 15 | g.73323634_73323635del | CA2512555845 | HCN4 | c.2459_2460del (p.Gly820AlafsTer?) c.1241_1242del (p.Gly414AlafsTer?) | |
| 15 | g.73323634C>A | CA393088853 | HCN4 | c.2459G>T (p.Gly820Val) c.1241G>T (p.Gly414Val) | gnomAD v4 |
| 15 | g.73323634C>G | CA393088854 | HCN4 | c.2459G>C (p.Gly820Ala) c.1241G>C (p.Gly414Ala) | ClinVar |
| 15 | g.73323634C>T | CA393088855 | HCN4 | c.2459G>A (p.Gly820Glu) c.1241G>A (p.Gly414Glu) | gnomAD v4 |
| 15 | g.73323634_73323635insAAA | CA2548620346 | HCN4 | c.2458_2459insTTT (p.Gly820delinsValTrp) c.1240_1241insTTT (p.Gly414delinsValTrp) | |
| 15 | g.73323635C>A | CA393088857 | HCN4 | c.2458G>T (p.Gly820Trp) c.1240G>T (p.Gly414Trp) | gnomAD v4 |
| 15 | g.73323635C= | CA2187188577 | HCN4 | c.2458G= (p.Gly820=) c.1240G= (p.Gly414=) | |
| 15 | g.73323635C>G | CA393088856 | HCN4 | c.2458G>C (p.Gly820Arg) c.1240G>C (p.Gly414Arg) | |
| 15 | g.73323635C>T | CA301973 | HCN4 | c.2458G>A (p.Gly820Arg) c.1240G>A (p.Gly414Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323636G>A | CA7649025 | HCN4 | c.2457C>T (p.Ala819=) c.1239C>T (p.Ala413=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323636G>C | CA491478344 | HCN4 | c.2457C>G (p.Ala819=) c.1239C>G (p.Ala413=) | |
| 15 | g.73323636G= | CA2187188578 | HCN4 | c.2457C= (p.Ala819=) c.1239C= (p.Ala413=) | |
| 15 | g.73323636G>T | CA491478343 | HCN4 | c.2457C>A (p.Ala819=) c.1239C>A (p.Ala413=) | gnomAD v4 |
| 15 | g.73323637G>A | CA272664775 | HCN4 | c.2456C>T (p.Ala819Val) c.1238C>T (p.Ala413Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323637G>C | CA393088858 | HCN4 | c.2456C>G (p.Ala819Gly) c.1238C>G (p.Ala413Gly) | |
| 15 | g.73323637G= | CA2187188579 | HCN4 | c.2456C= (p.Ala819=) c.1238C= (p.Ala413=) | |
| 15 | g.73323637G>T | CA393088859 | HCN4 | c.2456C>A (p.Ala819Asp) c.1238C>A (p.Ala413Asp) | gnomAD v4 |
| 15 | g.73323638C>A | CA393088860 | HCN4 | c.2455G>T (p.Ala819Ser) c.1237G>T (p.Ala413Ser) | gnomAD v4 |
| 15 | g.73323638C>G | CA393088861 | HCN4 | c.2455G>C (p.Ala819Pro) c.1237G>C (p.Ala413Pro) | |
| 15 | g.73323638C>T | CA393088862 | HCN4 | c.2455G>A (p.Ala819Thr) c.1237G>A (p.Ala413Thr) | gnomAD v4 |
| 15 | g.73323639A>C | CA491478351 | HCN4 | c.2454T>G (p.Gly818=) c.1236T>G (p.Gly412=) | |
| 15 | g.73323639A>G | CA491478352 | HCN4 | c.2454T>C (p.Gly818=) c.1236T>C (p.Gly412=) | |
| 15 | g.73323639A>T | CA491478353 | HCN4 | c.2454T>A (p.Gly818=) c.1236T>A (p.Gly412=) | gnomAD v4 |
| 15 | g.73323640C>A | CA393088863 | HCN4 | c.2453G>T (p.Gly818Val) c.1235G>T (p.Gly412Val) | |
| 15 | g.73323640C= | CA2187188580 | HCN4 | c.2453G= (p.Gly818=) c.1235G= (p.Gly412=) | |
| 15 | g.73323640C>G | CA393088864 | HCN4 | c.2453G>C (p.Gly818Ala) c.1235G>C (p.Gly412Ala) | |
| 15 | g.73323640C>T | CA393088865 | HCN4 | c.2453G>A (p.Gly818Asp) c.1235G>A (p.Gly412Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323641C>A | CA393088866 | HCN4 | c.2452G>T (p.Gly818Cys) c.1234G>T (p.Gly412Cys) | gnomAD v4 |
| 15 | g.73323641C= | CA2187188581 | HCN4 | c.2452G= (p.Gly818=) c.1234G= (p.Gly412=) | |
| 15 | g.73323641C>G | CA393088867 | HCN4 | c.2452G>C (p.Gly818Arg) c.1234G>C (p.Gly412Arg) | |
| 15 | g.73323641C>T | CA393088868 | HCN4 | c.2452G>A (p.Gly818Ser) c.1234G>A (p.Gly412Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323642G>A | CA491478356 | HCN4 | c.2451C>T (p.Leu817=) c.1233C>T (p.Leu411=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323642G>C | CA491478360 | HCN4 | c.2451C>G (p.Leu817=) c.1233C>G (p.Leu411=) | |
| 15 | g.73323642G= | CA2187188582 | HCN4 | c.2451C= (p.Leu817=) c.1233C= (p.Leu411=) | |
| 15 | g.73323642G>T | CA491478358 | HCN4 | c.2451C>A (p.Leu817=) c.1233C>A (p.Leu411=) | gnomAD v4 |
| 15 | g.73323643A>C | CA393088869 | HCN4 | c.2450T>G (p.Leu817Arg) c.1232T>G (p.Leu411Arg) | |
| 15 | g.73323643A>G | CA393088871 | HCN4 | c.2450T>C (p.Leu817Pro) c.1232T>C (p.Leu411Pro) | |
| 15 | g.73323643A>T | CA393088870 | HCN4 | c.2450T>A (p.Leu817His) c.1232T>A (p.Leu411His) | |
| 15 | g.73323644G>A | CA393088872 | HCN4 | c.2449C>T (p.Leu817Phe) c.1231C>T (p.Leu411Phe) | |
| 15 | g.73323644G>C | CA393088873 | HCN4 | c.2449C>G (p.Leu817Val) c.1231C>G (p.Leu411Val) | |
| 15 | g.73323644G>T | CA393088874 | HCN4 | c.2449C>A (p.Leu817Ile) c.1231C>A (p.Leu411Ile) | gnomAD v4 COSMIC |
| 15 | g.73323645G>A | CA491478363 | HCN4 | c.2448C>T (p.Asn816=) c.1230C>T (p.Asn410=) | gnomAD v4 |
| 15 | g.73323645G>C | CA393088875 | HCN4 | c.2448C>G (p.Asn816Lys) c.1230C>G (p.Asn410Lys) | COSMIC |
| 15 | g.73323645G>T | CA393088876 | HCN4 | c.2448C>A (p.Asn816Lys) c.1230C>A (p.Asn410Lys) | gnomAD v4 |
| 15 | g.73323646T>A | CA393088878 | HCN4 | c.2447A>T (p.Asn816Ile) c.1229A>T (p.Asn410Ile) | |
| 15 | g.73323646T>C | CA7649026 | HCN4 | c.2447A>G (p.Asn816Ser) c.1229A>G (p.Asn410Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323646T>G | CA393088877 | HCN4 | c.2447A>C (p.Asn816Thr) c.1229A>C (p.Asn410Thr) | |
| 15 | g.73323646T= | CA2187188583 | HCN4 | c.2447A= (p.Asn816=) c.1229A= (p.Asn410=) | |
| 15 | g.73323647T>A | CA393088879 | HCN4 | c.2446A>T (p.Asn816Tyr) c.1228A>T (p.Asn410Tyr) | |
| 15 | g.73323647T>C | CA393088880 | HCN4 | c.2446A>G (p.Asn816Asp) c.1228A>G (p.Asn410Asp) | |
| 15 | g.73323647T>G | CA393088881 | HCN4 | c.2446A>C (p.Asn816His) c.1228A>C (p.Asn410His) | |
| 15 | g.73323648G>A | CA491478371 | HCN4 | c.2445C>T (p.Gly815=) c.1227C>T (p.Gly409=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323648G>C | CA491478372 | HCN4 | c.2445C>G (p.Gly815=) c.1227C>G (p.Gly409=) | |
| 15 | g.73323648G= | CA2187188584 | HCN4 | c.2445C= (p.Gly815=) c.1227C= (p.Gly409=) | |
| 15 | g.73323648G>T | CA491478373 | HCN4 | c.2445C>A (p.Gly815=) c.1227C>A (p.Gly409=) | gnomAD v4 |