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.73323694C>A | CA393088964 | HCN4 | c.2399G>T (p.Arg800Leu) c.1181G>T (p.Arg394Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323694C= | CA2187188609 | HCN4 | c.2399G= (p.Arg800=) c.1181G= (p.Arg394=) | |
| 15 | g.73323694C>G | CA393088965 | HCN4 | c.2399G>C (p.Arg800Pro) c.1181G>C (p.Arg394Pro) | gnomAD v4 |
| 15 | g.73323694C>T | CA7649035 | HCN4 | c.2399G>A (p.Arg800His) c.1181G>A (p.Arg394His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323695G>A | CA7649036 | HCN4 | c.2398C>T (p.Arg800Cys) c.1180C>T (p.Arg394Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323695G>C | CA393088967 | HCN4 | c.2398C>G (p.Arg800Gly) c.1180C>G (p.Arg394Gly) | |
| 15 | g.73323695G= | CA2187188610 | HCN4 | c.2398C= (p.Arg800=) c.1180C= (p.Arg394=) | |
| 15 | g.73323695G>T | CA393088966 | HCN4 | c.2398C>A (p.Arg800Ser) c.1180C>A (p.Arg394Ser) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323696A>C | CA491478493 | HCN4 | c.2397T>G (p.Pro799=) c.1179T>G (p.Pro393=) | |
| 15 | g.73323696A>G | CA491478496 | HCN4 | c.2397T>C (p.Pro799=) c.1179T>C (p.Pro393=) | |
| 15 | g.73323696A>T | CA491478497 | HCN4 | c.2397T>A (p.Pro799=) c.1179T>A (p.Pro393=) | |
| 15 | g.73323697G>A | CA393088968 | HCN4 | c.2396C>T (p.Pro799Leu) c.1178C>T (p.Pro393Leu) | |
| 15 | g.73323697G>C | CA393088969 | HCN4 | c.2396C>G (p.Pro799Arg) c.1178C>G (p.Pro393Arg) | gnomAD v4 |
| 15 | g.73323697G>T | CA393088970 | HCN4 | c.2396C>A (p.Pro799His) c.1178C>A (p.Pro393His) | |
| 15 | g.73323698G>A | CA393088971 | HCN4 | c.2395C>T (p.Pro799Ser) c.1177C>T (p.Pro393Ser) | gnomAD v4 |
| 15 | g.73323698G>C | CA393088972 | HCN4 | c.2395C>G (p.Pro799Ala) c.1177C>G (p.Pro393Ala) | |
| 15 | g.73323698G>T | CA393088973 | HCN4 | c.2395C>A (p.Pro799Thr) c.1177C>A (p.Pro393Thr) | gnomAD v4 |
| 15 | g.73323699G>A | CA491478502 | HCN4 | c.2394C>T (p.His798=) c.1176C>T (p.His392=) | gnomAD v4 |
| 15 | g.73323699G>C | CA393088974 | HCN4 | c.2394C>G (p.His798Gln) c.1176C>G (p.His392Gln) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323699G>T | CA393088975 | HCN4 | c.2394C>A (p.His798Gln) c.1176C>A (p.His392Gln) | gnomAD v4 |
| 15 | g.73323700T>A | CA393088976 | HCN4 | c.2393A>T (p.His798Leu) c.1175A>T (p.His392Leu) | gnomAD v4 |
| 15 | g.73323700T>C | CA393088977 | HCN4 | c.2393A>G (p.His798Arg) c.1175A>G (p.His392Arg) | dbSNP |
| 15 | g.73323700T>G | CA393088978 | HCN4 | c.2393A>C (p.His798Pro) c.1175A>C (p.His392Pro) | |
| 15 | g.73323700T= | CA2187188611 | HCN4 | c.2393A= (p.His798=) c.1175A= (p.His392=) | |
| 15 | g.73323701G>A | CA393088981 | HCN4 | c.2392C>T (p.His798Tyr) c.1174C>T (p.His392Tyr) | dbSNP gnomAD v4 |
| 15 | g.73323701G>C | CA393088980 | HCN4 | c.2392C>G (p.His798Asp) c.1174C>G (p.His392Asp) | |
| 15 | g.73323701G= | CA2187188612 | HCN4 | c.2392C= (p.His798=) c.1174C= (p.His392=) | |
| 15 | g.73323701G>T | CA393088979 | HCN4 | c.2392C>A (p.His798Asn) c.1174C>A (p.His392Asn) | gnomAD v4 |
| 15 | g.73323702G>A | CA491478507 | HCN4 | c.2391C>T (p.His797=) c.1173C>T (p.His391=) | dbSNP |
| 15 | g.73323702G>C | CA393088982 | HCN4 | c.2391C>G (p.His797Gln) c.1173C>G (p.His391Gln) | gnomAD v4 |
| 15 | g.73323702G= | CA2187188613 | HCN4 | c.2391C= (p.His797=) c.1173C= (p.His391=) | |
| 15 | g.73323702G>T | CA7649037 | HCN4 | c.2391C>A (p.His797Gln) c.1173C>A (p.His391Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323703T>A | CA393088983 | HCN4 | c.2390A>T (p.His797Leu) c.1172A>T (p.His391Leu) | |
| 15 | g.73323703T>C | CA393088984 | HCN4 | c.2390A>G (p.His797Arg) c.1172A>G (p.His391Arg) | |
| 15 | g.73323703T>G | CA393088985 | HCN4 | c.2390A>C (p.His797Pro) c.1172A>C (p.His391Pro) | |
| 15 | g.73323704G>A | CA393088986 | HCN4 | c.2389C>T (p.His797Tyr) c.1171C>T (p.His391Tyr) | |
| 15 | g.73323704G>C | CA393088987 | HCN4 | c.2389C>G (p.His797Asp) c.1171C>G (p.His391Asp) | |
| 15 | g.73323704G>T | CA393088988 | HCN4 | c.2389C>A (p.His797Asn) c.1171C>A (p.His391Asn) | gnomAD v4 |
| 15 | g.73323706dup | CA2575783835 | HCN4 | c.2389dup (p.His797ProfsTer?) c.1171dup (p.His391ProfsTer?) | |
| 15 | g.73323705G>A | CA491478512 | HCN4 | c.2388C>T (p.Thr796=) c.1170C>T (p.Thr390=) | |
| 15 | g.73323705G>C | CA491478513 | HCN4 | c.2388C>G (p.Thr796=) c.1170C>G (p.Thr390=) | |
| 15 | g.73323705G>T | CA491478514 | HCN4 | c.2388C>A (p.Thr796=) c.1170C>A (p.Thr390=) | gnomAD v4 |
| 15 | g.73323706G>A | CA393088989 | HCN4 | c.2387C>T (p.Thr796Ile) c.1169C>T (p.Thr390Ile) | |
| 15 | g.73323706G>C | CA393088990 | HCN4 | c.2387C>G (p.Thr796Ser) c.1169C>G (p.Thr390Ser) | |
| 15 | g.73323706G>T | CA393088991 | HCN4 | c.2387C>A (p.Thr796Asn) c.1169C>A (p.Thr390Asn) | gnomAD v4 |
| 15 | g.73323707T>A | CA393088994 | HCN4 | c.2386A>T (p.Thr796Ser) c.1168A>T (p.Thr390Ser) | |
| 15 | g.73323707T>C | CA393088993 | HCN4 | c.2386A>G (p.Thr796Ala) c.1168A>G (p.Thr390Ala) | gnomAD v4 |
| 15 | g.73323707T>G | CA393088992 | HCN4 | c.2386A>C (p.Thr796Pro) c.1168A>C (p.Thr390Pro) | |
| 15 | g.73323708G>A | CA10583261 | HCN4 | c.2385C>T (p.Leu795=) c.1167C>T (p.Leu389=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323708G>C | CA491478522 | HCN4 | c.2385C>G (p.Leu795=) c.1167C>G (p.Leu389=) | dbSNP |
| 15 | g.73323708G= | CA2187188614 | HCN4 | c.2385C= (p.Leu795=) c.1167C= (p.Leu389=) | |
| 15 | g.73323708G>T | CA491478523 | HCN4 | c.2385C>A (p.Leu795=) c.1167C>A (p.Leu389=) | gnomAD v4 |
| 15 | g.73323709A>C | CA393088995 | HCN4 | c.2384T>G (p.Leu795Arg) c.1166T>G (p.Leu389Arg) | |
| 15 | g.73323709A>G | CA393088996 | HCN4 | c.2384T>C (p.Leu795Pro) c.1166T>C (p.Leu389Pro) | gnomAD v4 |
| 15 | g.73323709A>T | CA393088997 | HCN4 | c.2384T>A (p.Leu795His) c.1166T>A (p.Leu389His) | |
| 15 | g.73323710G>A | CA393088998 | HCN4 | c.2383C>T (p.Leu795Phe) c.1165C>T (p.Leu389Phe) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323710G>C | CA393088999 | HCN4 | c.2383C>G (p.Leu795Val) c.1165C>G (p.Leu389Val) | |
| 15 | g.73323710G= | CA2187188615 | HCN4 | c.2383C= (p.Leu795=) c.1165C= (p.Leu389=) | |
| 15 | g.73323710G>T | CA393089000 | HCN4 | c.2383C>A (p.Leu795Ile) c.1165C>A (p.Leu389Ile) | dbSNP gnomAD v4 |
| 15 | g.73323711G>A | CA491478529 | HCN4 | c.2382C>T (p.Ala794=) c.1164C>T (p.Ala388=) | gnomAD v4 |
| 15 | g.73323711G>C | CA491478532 | HCN4 | c.2382C>G (p.Ala794=) c.1164C>G (p.Ala388=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323711G= | CA2187188616 | HCN4 | c.2382C= (p.Ala794=) c.1164C= (p.Ala388=) | |
| 15 | g.73323711G>T | CA491478530 | HCN4 | c.2382C>A (p.Ala794=) c.1164C>A (p.Ala388=) | gnomAD v4 COSMIC |
| 15 | g.73323712G>A | CA393089001 | HCN4 | c.2381C>T (p.Ala794Val) c.1163C>T (p.Ala388Val) | gnomAD v4 |
| 15 | g.73323712G>C | CA393089003 | HCN4 | c.2381C>G (p.Ala794Gly) c.1163C>G (p.Ala388Gly) | |
| 15 | g.73323712G>T | CA393089002 | HCN4 | c.2381C>A (p.Ala794Asp) c.1163C>A (p.Ala388Asp) | ClinVar gnomAD v4 |
| 15 | g.73323713C>A | CA393089004 | HCN4 | c.2380G>T (p.Ala794Ser) c.1162G>T (p.Ala388Ser) | gnomAD v4 |
| 15 | g.73323713C= | CA2187188617 | HCN4 | c.2380G= (p.Ala794=) c.1162G= (p.Ala388=) | |
| 15 | g.73323713C>G | CA393089005 | HCN4 | c.2380G>C (p.Ala794Pro) c.1162G>C (p.Ala388Pro) | |
| 15 | g.73323713C>T | CA272664854 | HCN4 | c.2380G>A (p.Ala794Thr) c.1162G>A (p.Ala388Thr) | dbSNP |
| 15 | g.73323714T>A | CA491478536 | HCN4 | c.2379A>T (p.Ile793=) c.1161A>T (p.Ile387=) | gnomAD v4 |
| 15 | g.73323714T>C | CA393089006 | HCN4 | c.2379A>G (p.Ile793Met) c.1161A>G (p.Ile387Met) | gnomAD v4 |
| 15 | g.73323714T>G | CA491478538 | HCN4 | c.2379A>C (p.Ile793=) c.1161A>C (p.Ile387=) | |
| 15 | g.73323715A>C | CA393089007 | HCN4 | c.2378T>G (p.Ile793Arg) c.1160T>G (p.Ile387Arg) | |
| 15 | g.73323715A>G | CA393089009 | HCN4 | c.2378T>C (p.Ile793Thr) c.1160T>C (p.Ile387Thr) | COSMIC |
| 15 | g.73323715A>T | CA393089008 | HCN4 | c.2378T>A (p.Ile793Lys) c.1160T>A (p.Ile387Lys) | |
| 15 | g.73323716T>A | CA393089010 | HCN4 | c.2377A>T (p.Ile793Leu) c.1159A>T (p.Ile387Leu) | |
| 15 | g.73323716T>C | CA393089011 | HCN4 | c.2377A>G (p.Ile793Val) c.1159A>G (p.Ile387Val) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73323716T>G | CA393089012 | HCN4 | c.2377A>C (p.Ile793Leu) c.1159A>C (p.Ile387Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323716T= | CA2187188618 | HCN4 | c.2377A= (p.Ile793=) c.1159A= (p.Ile387=) | |
| 15 | g.73323717G>A | CA491478544 | HCN4 | c.2376C>T (p.Ala792=) c.1158C>T (p.Ala386=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323717G>C | CA491478545 | HCN4 | c.2376C>G (p.Ala792=) c.1158C>G (p.Ala386=) | ClinVar dbSNP |
| 15 | g.73323717G= | CA2187188619 | HCN4 | c.2376C= (p.Ala792=) c.1158C= (p.Ala386=) | |
| 15 | g.73323717G>T | CA491478546 | HCN4 | c.2376C>A (p.Ala792=) c.1158C>A (p.Ala386=) | gnomAD v4 |
| 15 | g.73323717_73323718delinsAC | CA645586811 | HCN4 | c.2375_2376delinsGT (p.Ala792Gly) c.1157_1158delinsGT (p.Ala386Gly) | COSMIC |
| 15 | g.73323718G>A | CA393089013 | HCN4 | c.2375C>T (p.Ala792Val) c.1157C>T (p.Ala386Val) | gnomAD v4 |
| 15 | g.73323718G>C | CA393089014 | HCN4 | c.2375C>G (p.Ala792Gly) c.1157C>G (p.Ala386Gly) | |
| 15 | g.73323718G>T | CA393089015 | HCN4 | c.2375C>A (p.Ala792Asp) c.1157C>A (p.Ala386Asp) | gnomAD v4 |
| 15 | g.73323719C>A | CA7649038 | HCN4 | c.2374G>T (p.Ala792Ser) c.1156G>T (p.Ala386Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323719C= | CA2187188620 | HCN4 | c.2374G= (p.Ala792=) c.1156G= (p.Ala386=) | |
| 15 | g.73323719C>G | CA393089016 | HCN4 | c.2374G>C (p.Ala792Pro) c.1156G>C (p.Ala386Pro) | |
| 15 | g.73323719C>T | CA393089017 | HCN4 | c.2374G>A (p.Ala792Thr) c.1156G>A (p.Ala386Thr) | gnomAD v4 |
| 15 | g.73323720C>A | CA7649039 | HCN4 | c.2373G>T (p.Val791=) c.1155G>T (p.Val385=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323720C= | CA2187188621 | HCN4 | c.2373G= (p.Val791=) c.1155G= (p.Val385=) | |
| 15 | g.73323720C>G | CA491478554 | HCN4 | c.2373G>C (p.Val791=) c.1155G>C (p.Val385=) | |
| 15 | g.73323720C>T | CA491478555 | HCN4 | c.2373G>A (p.Val791=) c.1155G>A (p.Val385=) | |
| 15 | g.73323721A>C | CA393089018 | HCN4 | c.2372T>G (p.Val791Gly) c.1154T>G (p.Val385Gly) | |
| 15 | g.73323721A>G | CA393089020 | HCN4 | c.2372T>C (p.Val791Ala) c.1154T>C (p.Val385Ala) | |
| 15 | g.73323721A>T | CA393089019 | HCN4 | c.2372T>A (p.Val791Glu) c.1154T>A (p.Val385Glu) | gnomAD v4 |
| 15 | g.73323722C>A | CA393089021 | HCN4 | c.2371G>T (p.Val791Leu) c.1153G>T (p.Val385Leu) | |
| 15 | g.73323722C= | CA2187188622 | HCN4 | c.2371G= (p.Val791=) c.1153G= (p.Val385=) | |
| 15 | g.73323722C>G | CA393089022 | HCN4 | c.2371G>C (p.Val791Leu) c.1153G>C (p.Val385Leu) | |
| 15 | g.73323722C>T | CA272664876 | HCN4 | c.2371G>A (p.Val791Met) c.1153G>A (p.Val385Met) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323723A= | CA2187188623 | HCN4 | c.2370T= (p.Ser790=) c.1152T= (p.Ser384=) | |
| 15 | g.73323723A>C | CA491478558 | HCN4 | c.2370T>G (p.Ser790=) c.1152T>G (p.Ser384=) | |
| 15 | g.73323723A>G | CA7649040 | HCN4 | c.2370T>C (p.Ser790=) c.1152T>C (p.Ser384=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323723A>T | CA491478561 | HCN4 | c.2370T>A (p.Ser790=) c.1152T>A (p.Ser384=) | |
| 15 | g.73323724G>A | CA393089023 | HCN4 | c.2369C>T (p.Ser790Phe) c.1151C>T (p.Ser384Phe) | |
| 15 | g.73323724G>C | CA393089024 | HCN4 | c.2369C>G (p.Ser790Cys) c.1151C>G (p.Ser384Cys) | |
| 15 | g.73323724G>T | CA393089025 | HCN4 | c.2369C>A (p.Ser790Tyr) c.1151C>A (p.Ser384Tyr) | gnomAD v4 COSMIC |
| 15 | g.73323725A= | CA2187188624 | HCN4 | c.2368T= (p.Ser790=) c.1150T= (p.Ser384=) | |
| 15 | g.73323725A>C | CA393089026 | HCN4 | c.2368T>G (p.Ser790Ala) c.1150T>G (p.Ser384Ala) | |
| 15 | g.73323725A>G | CA393089027 | HCN4 | c.2368T>C (p.Ser790Pro) c.1150T>C (p.Ser384Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323725A>T | CA393089028 | HCN4 | c.2368T>A (p.Ser790Thr) c.1150T>A (p.Ser384Thr) | |
| 15 | g.73323726A>C | CA491478564 | HCN4 | c.2367T>G (p.Thr789=) c.1149T>G (p.Thr383=) | |
| 15 | g.73323726A>G | CA491478565 | HCN4 | c.2367T>C (p.Thr789=) c.1149T>C (p.Thr383=) | |
| 15 | g.73323726A>T | CA491478566 | HCN4 | c.2367T>A (p.Thr789=) c.1149T>A (p.Thr383=) | |
| 15 | g.73323727G>A | CA393089029 | HCN4 | c.2366C>T (p.Thr789Ile) c.1148C>T (p.Thr383Ile) | |
| 15 | g.73323727G>C | CA393089030 | HCN4 | c.2366C>G (p.Thr789Ser) c.1148C>G (p.Thr383Ser) | |
| 15 | g.73323727G>T | CA393089031 | HCN4 | c.2366C>A (p.Thr789Asn) c.1148C>A (p.Thr383Asn) | gnomAD v4 |
| 15 | g.73323728T>A | CA393089032 | HCN4 | c.2365A>T (p.Thr789Ser) c.1147A>T (p.Thr383Ser) | |
| 15 | g.73323728T>C | CA393089033 | HCN4 | c.2365A>G (p.Thr789Ala) c.1147A>G (p.Thr383Ala) | gnomAD v4 |
| 15 | g.73323728T>G | CA393089034 | HCN4 | c.2365A>C (p.Thr789Pro) c.1147A>C (p.Thr383Pro) | |
| 15 | g.73323729G>A | CA491478575 | HCN4 | c.2364C>T (p.Thr788=) c.1146C>T (p.Thr382=) | gnomAD v4 |
| 15 | g.73323729G>C | CA491478576 | HCN4 | c.2364C>G (p.Thr788=) c.1146C>G (p.Thr382=) | |
| 15 | g.73323729G>T | CA491478577 | HCN4 | c.2364C>A (p.Thr788=) c.1146C>A (p.Thr382=) | gnomAD v4 |
| 15 | g.73323730G>A | CA393089037 | HCN4 | c.2363C>T (p.Thr788Ile) c.1145C>T (p.Thr382Ile) | gnomAD v4 |
| 15 | g.73323730G>C | CA393089035 | HCN4 | c.2363C>G (p.Thr788Ser) c.1145C>G (p.Thr382Ser) | |
| 15 | g.73323730G>T | CA393089036 | HCN4 | c.2363C>A (p.Thr788Asn) c.1145C>A (p.Thr382Asn) | gnomAD v4 |
| 15 | g.73323731T>A | CA393089038 | HCN4 | c.2362A>T (p.Thr788Ser) c.1144A>T (p.Thr382Ser) | |
| 15 | g.73323731T>C | CA393089039 | HCN4 | c.2362A>G (p.Thr788Ala) c.1144A>G (p.Thr382Ala) | gnomAD v4 |
| 15 | g.73323731T>G | CA393089040 | HCN4 | c.2362A>C (p.Thr788Pro) c.1144A>C (p.Thr382Pro) | |
| 15 | g.73323732G>A | CA491478578 | HCN4 | c.2361C>T (p.Ala787=) c.1143C>T (p.Ala381=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323732G>C | CA491478581 | HCN4 | c.2361C>G (p.Ala787=) c.1143C>G (p.Ala381=) | |
| 15 | g.73323732G= | CA2187188625 | HCN4 | c.2361C= (p.Ala787=) c.1143C= (p.Ala381=) | |
| 15 | g.73323732G>T | CA491478582 | HCN4 | c.2361C>A (p.Ala787=) c.1143C>A (p.Ala381=) | gnomAD v4 |
| 15 | g.73323733G>A | CA393089041 | HCN4 | c.2360C>T (p.Ala787Val) c.1142C>T (p.Ala381Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323733G>C | CA393089042 | HCN4 | c.2360C>G (p.Ala787Gly) c.1142C>G (p.Ala381Gly) | |
| 15 | g.73323733G= | CA2187188626 | HCN4 | c.2360C= (p.Ala787=) c.1142C= (p.Ala381=) | |
| 15 | g.73323733G>T | CA393089043 | HCN4 | c.2360C>A (p.Ala787Asp) c.1142C>A (p.Ala381Asp) | gnomAD v4 |
| 15 | g.73323734C>A | CA393089044 | HCN4 | c.2359G>T (p.Ala787Ser) c.1141G>T (p.Ala381Ser) | ClinVar gnomAD v4 |
| 15 | g.73323734C>G | CA393089045 | HCN4 | c.2359G>C (p.Ala787Pro) c.1141G>C (p.Ala381Pro) | |
| 15 | g.73323734C>T | CA393089046 | HCN4 | c.2359G>A (p.Ala787Thr) c.1141G>A (p.Ala381Thr) | gnomAD v4 COSMIC |
| 15 | g.73323735A>C | CA491478589 | HCN4 | c.2358T>G (p.Ala786=) c.1140T>G (p.Ala380=) | |
| 15 | g.73323735A>G | CA491478592 | HCN4 | c.2358T>C (p.Ala786=) c.1140T>C (p.Ala380=) | |
| 15 | g.73323735A>T | CA491478593 | HCN4 | c.2358T>A (p.Ala786=) c.1140T>A (p.Ala380=) | |
| 15 | g.73323736G>A | CA393089047 | HCN4 | c.2357C>T (p.Ala786Val) c.1139C>T (p.Ala380Val) | |
| 15 | g.73323736G>C | CA393089048 | HCN4 | c.2357C>G (p.Ala786Gly) c.1139C>G (p.Ala380Gly) | |
| 15 | g.73323736G>T | CA393089049 | HCN4 | c.2357C>A (p.Ala786Asp) c.1139C>A (p.Ala380Asp) | gnomAD v4 |
| 15 | g.73323737C>A | CA393089050 | HCN4 | c.2356G>T (p.Ala786Ser) c.1138G>T (p.Ala380Ser) | gnomAD v4 |
| 15 | g.73323737C= | CA2187188627 | HCN4 | c.2356G= (p.Ala786=) c.1138G= (p.Ala380=) | |
| 15 | g.73323737C>G | CA393089051 | HCN4 | c.2356G>C (p.Ala786Pro) c.1138G>C (p.Ala380Pro) | |
| 15 | g.73323737C>T | CA7649041 | HCN4 | c.2356G>A (p.Ala786Thr) c.1138G>A (p.Ala380Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323738G>A | CA7649042 | HCN4 | c.2355C>T (p.Ala785=) c.1137C>T (p.Ala379=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323738G>C | CA491478596 | HCN4 | c.2355C>G (p.Ala785=) c.1137C>G (p.Ala379=) | gnomAD v4 |
| 15 | g.73323738G= | CA2187188628 | HCN4 | c.2355C= (p.Ala785=) c.1137C= (p.Ala379=) | |
| 15 | g.73323738G>T | CA491478599 | HCN4 | c.2355C>A (p.Ala785=) c.1137C>A (p.Ala379=) | |
| 15 | g.73323739G>A | CA393089052 | HCN4 | c.2354C>T (p.Ala785Val) c.1136C>T (p.Ala379Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323739G>C | CA393089053 | HCN4 | c.2354C>G (p.Ala785Gly) c.1136C>G (p.Ala379Gly) | |
| 15 | g.73323739G= | CA2187188629 | HCN4 | c.2354C= (p.Ala785=) c.1136C= (p.Ala379=) | |
| 15 | g.73323739G>T | CA393089054 | HCN4 | c.2354C>A (p.Ala785Asp) c.1136C>A (p.Ala379Asp) | gnomAD v4 |
| 15 | g.73323740C>A | CA393089055 | HCN4 | c.2353G>T (p.Ala785Ser) c.1135G>T (p.Ala379Ser) | gnomAD v4 |
| 15 | g.73323740C>G | CA393089056 | HCN4 | c.2353G>C (p.Ala785Pro) c.1135G>C (p.Ala379Pro) | |
| 15 | g.73323740C>T | CA393089057 | HCN4 | c.2353G>A (p.Ala785Thr) c.1135G>A (p.Ala379Thr) | gnomAD v4 |
| 15 | g.73323741A>C | CA491478604 | HCN4 | c.2352T>G (p.Ala784=) c.1134T>G (p.Ala378=) | |
| 15 | g.73323741A>G | CA491478606 | HCN4 | c.2352T>C (p.Ala784=) c.1134T>C (p.Ala378=) | |
| 15 | g.73323741A>T | CA491478602 | HCN4 | c.2352T>A (p.Ala784=) c.1134T>A (p.Ala378=) | |
| 15 | g.73323742G>A | CA393089058 | HCN4 | c.2351C>T (p.Ala784Val) c.1133C>T (p.Ala378Val) | gnomAD v4 |
| 15 | g.73323742G>C | CA393089059 | HCN4 | c.2351C>G (p.Ala784Gly) c.1133C>G (p.Ala378Gly) | |
| 15 | g.73323742G>T | CA393089060 | HCN4 | c.2351C>A (p.Ala784Asp) c.1133C>A (p.Ala378Asp) | gnomAD v4 |
| 15 | g.73323743C>A | CA393089063 | HCN4 | c.2350G>T (p.Ala784Ser) c.1132G>T (p.Ala378Ser) | gnomAD v4 |
| 15 | g.73323743C= | CA2187188630 | HCN4 | c.2350G= (p.Ala784=) c.1132G= (p.Ala378=) | |
| 15 | g.73323743C>G | CA393089062 | HCN4 | c.2350G>C (p.Ala784Pro) c.1132G>C (p.Ala378Pro) | |
| 15 | g.73323743C>T | CA393089061 | HCN4 | c.2350G>A (p.Ala784Thr) c.1132G>A (p.Ala378Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323744C>A | CA393089064 | HCN4 | c.2349G>T (p.Gln783His) c.1131G>T (p.Gln377His) | |
| 15 | g.73323744C= | CA2187188631 | HCN4 | c.2349G= (p.Gln783=) c.1131G= (p.Gln377=) | |
| 15 | g.73323744C>G | CA393089065 | HCN4 | c.2349G>C (p.Gln783His) c.1131G>C (p.Gln377His) | |
| 15 | g.73323744C>T | CA7649043 | HCN4 | c.2349G>A (p.Gln783=) c.1131G>A (p.Gln377=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323745T>A | CA393089066 | HCN4 | c.2348A>T (p.Gln783Leu) c.1130A>T (p.Gln377Leu) | |
| 15 | g.73323745T>C | CA393089067 | HCN4 | c.2348A>G (p.Gln783Arg) c.1130A>G (p.Gln377Arg) | |
| 15 | g.73323745T>G | CA393089068 | HCN4 | c.2348A>C (p.Gln783Pro) c.1130A>C (p.Gln377Pro) | |
| 15 | g.73323746G>A | CA393089069 | HCN4 | c.2347C>T (p.Gln783Ter) c.1129C>T (p.Gln377Ter) | gnomAD v4 |
| 15 | g.73323746G>C | CA393089070 | HCN4 | c.2347C>G (p.Gln783Glu) c.1129C>G (p.Gln377Glu) | |
| 15 | g.73323746G>T | CA393089071 | HCN4 | c.2347C>A (p.Gln783Lys) c.1129C>A (p.Gln377Lys) | gnomAD v4 |
| 15 | g.73323747C>A | CA272664904 | HCN4 | c.2346G>T (p.Leu782=) c.1128G>T (p.Leu376=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323747C= | CA2187188632 | HCN4 | c.2346G= (p.Leu782=) c.1128G= (p.Leu376=) | |
| 15 | g.73323747C>G | CA491478618 | HCN4 | c.2346G>C (p.Leu782=) c.1128G>C (p.Leu376=) | |
| 15 | g.73323747C>T | CA491478616 | HCN4 | c.2346G>A (p.Leu782=) c.1128G>A (p.Leu376=) | |
| 15 | g.73323748A= | CA2187188633 | HCN4 | c.2345T= (p.Leu782=) c.1127T= (p.Leu376=) | |
| 15 | g.73323748A>C | CA393089072 | HCN4 | c.2345T>G (p.Leu782Arg) c.1127T>G (p.Leu376Arg) | ClinVar dbSNP |
| 15 | g.73323748A>G | CA393089073 | HCN4 | c.2345T>C (p.Leu782Pro) c.1127T>C (p.Leu376Pro) | |
| 15 | g.73323748A>T | CA393089074 | HCN4 | c.2345T>A (p.Leu782Gln) c.1127T>A (p.Leu376Gln) | |
| 15 | g.73323749G>A | CA491478622 | HCN4 | c.2344C>T (p.Leu782=) c.1126C>T (p.Leu376=) | |
| 15 | g.73323749G>C | CA393089076 | HCN4 | c.2344C>G (p.Leu782Val) c.1126C>G (p.Leu376Val) | |
| 15 | g.73323749G>T | CA393089075 | HCN4 | c.2344C>A (p.Leu782Met) c.1126C>A (p.Leu376Met) | gnomAD v4 |
| 15 | g.73323750T>A | CA491478624 | HCN4 | c.2343A>T (p.Pro781=) c.1125A>T (p.Pro375=) | |
| 15 | g.73323750T>C | CA491478626 | HCN4 | c.2343A>G (p.Pro781=) c.1125A>G (p.Pro375=) | dbSNP |
| 15 | g.73323750T>G | CA491478628 | HCN4 | c.2343A>C (p.Pro781=) c.1125A>C (p.Pro375=) | |
| 15 | g.73323750T= | CA2187188634 | HCN4 | c.2343A= (p.Pro781=) c.1125A= (p.Pro375=) | |
| 15 | g.73323751G>A | CA393089077 | HCN4 | c.2342C>T (p.Pro781Leu) c.1124C>T (p.Pro375Leu) | |
| 15 | g.73323751G>C | CA393089079 | HCN4 | c.2342C>G (p.Pro781Arg) c.1124C>G (p.Pro375Arg) | |
| 15 | g.73323751G>T | CA393089078 | HCN4 | c.2342C>A (p.Pro781Gln) c.1124C>A (p.Pro375Gln) | gnomAD v4 |
| 15 | g.73323752G>A | CA393089080 | HCN4 | c.2341C>T (p.Pro781Ser) c.1123C>T (p.Pro375Ser) | |
| 15 | g.73323752G>C | CA393089081 | HCN4 | c.2341C>G (p.Pro781Ala) c.1123C>G (p.Pro375Ala) | COSMIC |
| 15 | g.73323752G>T | CA393089082 | HCN4 | c.2341C>A (p.Pro781Thr) c.1123C>A (p.Pro375Thr) | |
| 15 | g.73323753T>A | CA491478632 | HCN4 | c.2340A>T (p.Ala780=) c.1122A>T (p.Ala374=) | |
| 15 | g.73323753T>C | CA491478633 | HCN4 | c.2340A>G (p.Ala780=) c.1122A>G (p.Ala374=) | |
| 15 | g.73323753T>G | CA491478634 | HCN4 | c.2340A>C (p.Ala780=) c.1122A>C (p.Ala374=) | |
| 15 | g.73323754G>A | CA393089083 | HCN4 | c.2339C>T (p.Ala780Val) c.1121C>T (p.Ala374Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323754G>C | CA393089084 | HCN4 | c.2339C>G (p.Ala780Gly) c.1121C>G (p.Ala374Gly) | |
| 15 | g.73323754G= | CA2187188635 | HCN4 | c.2339C= (p.Ala780=) c.1121C= (p.Ala374=) | |
| 15 | g.73323754G>T | CA393089085 | HCN4 | c.2339C>A (p.Ala780Glu) c.1121C>A (p.Ala374Glu) | gnomAD v4 |
| 15 | g.73323755C>A | CA393089086 | HCN4 | c.2338G>T (p.Ala780Ser) c.1120G>T (p.Ala374Ser) | gnomAD v4 COSMIC |
| 15 | g.73323755C>G | CA393089087 | HCN4 | c.2338G>C (p.Ala780Pro) c.1120G>C (p.Ala374Pro) | |
| 15 | g.73323755C>T | CA393089088 | HCN4 | c.2338G>A (p.Ala780Thr) c.1120G>A (p.Ala374Thr) | |
| 15 | g.73323756C>A | CA393089089 | HCN4 | c.2337G>T (p.Gln779His) c.1119G>T (p.Gln373His) | gnomAD v4 |
| 15 | g.73323756C= | CA2187188636 | HCN4 | c.2337G= (p.Gln779=) c.1119G= (p.Gln373=) | |
| 15 | g.73323756C>G | CA393089090 | HCN4 | c.2337G>C (p.Gln779His) c.1119G>C (p.Gln373His) | |
| 15 | g.73323756C>T | CA491478637 | HCN4 | c.2337G>A (p.Gln779=) c.1119G>A (p.Gln373=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323757T>A | CA393089093 | HCN4 | c.2336A>T (p.Gln779Leu) c.1118A>T (p.Gln373Leu) | |
| 15 | g.73323757T>C | CA393089092 | HCN4 | c.2336A>G (p.Gln779Arg) c.1118A>G (p.Gln373Arg) | gnomAD v4 |
| 15 | g.73323757T>G | CA393089091 | HCN4 | c.2336A>C (p.Gln779Pro) c.1118A>C (p.Gln373Pro) | |
| 15 | g.73323758G>A | CA393089094 | HCN4 | c.2335C>T (p.Gln779Ter) c.1117C>T (p.Gln373Ter) | |
| 15 | g.73323758G>C | CA393089095 | HCN4 | c.2335C>G (p.Gln779Glu) c.1117C>G (p.Gln373Glu) | |
| 15 | g.73323758G>T | CA393089096 | HCN4 | c.2335C>A (p.Gln779Lys) c.1117C>A (p.Gln373Lys) | |
| 15 | g.73323759G>A | CA491478643 | HCN4 | c.2334C>T (p.Ile778=) c.1116C>T (p.Ile372=) | COSMIC |
| 15 | g.73323759G>C | CA393089097 | HCN4 | c.2334C>G (p.Ile778Met) c.1116C>G (p.Ile372Met) | |
| 15 | g.73323759G>T | CA491478646 | HCN4 | c.2334C>A (p.Ile778=) c.1116C>A (p.Ile372=) | ClinVar gnomAD v4 |
| 15 | g.73323760A>C | CA393089098 | HCN4 | c.2333T>G (p.Ile778Ser) c.1115T>G (p.Ile372Ser) | |
| 15 | g.73323760A>G | CA393089099 | HCN4 | c.2333T>C (p.Ile778Thr) c.1115T>C (p.Ile372Thr) | |
| 15 | g.73323760A>T | CA393089100 | HCN4 | c.2333T>A (p.Ile778Asn) c.1115T>A (p.Ile372Asn) | |
| 15 | g.73323761T>A | CA393089101 | HCN4 | c.2332A>T (p.Ile778Phe) c.1114A>T (p.Ile372Phe) | |
| 15 | g.73323761T>C | CA393089102 | HCN4 | c.2332A>G (p.Ile778Val) c.1114A>G (p.Ile372Val) | |
| 15 | g.73323761T>G | CA393089103 | HCN4 | c.2332A>C (p.Ile778Leu) c.1114A>C (p.Ile372Leu) | |
| 15 | g.73323762C>A | CA491478654 | HCN4 | c.2331G>T (p.Leu777=) c.1113G>T (p.Leu371=) | |
| 15 | g.73323762C= | CA2187188637 | HCN4 | c.2331G= (p.Leu777=) c.1113G= (p.Leu371=) | |
| 15 | g.73323762C>G | CA491478653 | HCN4 | c.2331G>C (p.Leu777=) c.1113G>C (p.Leu371=) | ClinVar dbSNP |
| 15 | g.73323762C>T | CA491478652 | HCN4 | c.2331G>A (p.Leu777=) c.1113G>A (p.Leu371=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323763A>C | CA393089104 | HCN4 | c.2330T>G (p.Leu777Arg) c.1112T>G (p.Leu371Arg) | ClinVar |
| 15 | g.73323763A>G | CA393089105 | HCN4 | c.2330T>C (p.Leu777Pro) c.1112T>C (p.Leu371Pro) | |
| 15 | g.73323763A>T | CA393089106 | HCN4 | c.2330T>A (p.Leu777Gln) c.1112T>A (p.Leu371Gln) | |
| 15 | g.73323764G>A | CA491478658 | HCN4 | c.2329C>T (p.Leu777=) c.1111C>T (p.Leu371=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323764G>C | CA393089107 | HCN4 | c.2329C>G (p.Leu777Val) c.1111C>G (p.Leu371Val) | |
| 15 | g.73323764G= | CA2187188638 | HCN4 | c.2329C= (p.Leu777=) c.1111C= (p.Leu371=) | |
| 15 | g.73323764G>T | CA393089108 | HCN4 | c.2329C>A (p.Leu777Met) c.1111C>A (p.Leu371Met) | gnomAD v4 COSMIC |
| 15 | g.73323765del | CA2629370750 | HCN4 | c.2328del (p.Leu777Ter) c.1110del (p.Leu371Ter) | gnomAD v4 |
| 15 | g.73323765C>A | CA491478665 | HCN4 | c.2328G>T (p.Pro776=) c.1110G>T (p.Pro370=) | gnomAD v4 |
| 15 | g.73323765C= | CA2187188639 | HCN4 | c.2328G= (p.Pro776=) c.1110G= (p.Pro370=) | |
| 15 | g.73323765C>G | CA491478664 | HCN4 | c.2328G>C (p.Pro776=) c.1110G>C (p.Pro370=) | |
| 15 | g.73323765C>T | CA491478663 | HCN4 | c.2328G>A (p.Pro776=) c.1110G>A (p.Pro370=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323766G>A | CA272664908 | HCN4 | c.2327C>T (p.Pro776Leu) c.1109C>T (p.Pro370Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323766G>C | CA393089109 | HCN4 | c.2327C>G (p.Pro776Arg) c.1109C>G (p.Pro370Arg) | |
| 15 | g.73323766G= | CA2187188640 | HCN4 | c.2327C= (p.Pro776=) c.1109C= (p.Pro370=) | |
| 15 | g.73323766G>T | CA393089110 | HCN4 | c.2327C>A (p.Pro776Gln) c.1109C>A (p.Pro370Gln) | gnomAD v4 |
| 15 | g.73323767G>A | CA393089111 | HCN4 | c.2326C>T (p.Pro776Ser) c.1108C>T (p.Pro370Ser) | COSMIC |
| 15 | g.73323767G>C | CA393089112 | HCN4 | c.2326C>G (p.Pro776Ala) c.1108C>G (p.Pro370Ala) | |
| 15 | g.73323767G= | CA2187188641 | HCN4 | c.2326C= (p.Pro776=) c.1108C= (p.Pro370=) | |
| 15 | g.73323767G>T | CA7649044 | HCN4 | c.2326C>A (p.Pro776Thr) c.1108C>A (p.Pro370Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323768G>A | CA491478670 | HCN4 | c.2325C>T (p.Thr775=) c.1107C>T (p.Thr369=) | |
| 15 | g.73323768G>C | CA491478672 | HCN4 | c.2325C>G (p.Thr775=) c.1107C>G (p.Thr369=) | |
| 15 | g.73323768G>T | CA491478671 | HCN4 | c.2325C>A (p.Thr775=) c.1107C>A (p.Thr369=) | gnomAD v4 |
| 15 | g.73323769G>A | CA393089113 | HCN4 | c.2324C>T (p.Thr775Ile) c.1106C>T (p.Thr369Ile) | |
| 15 | g.73323769G>C | CA393089114 | HCN4 | c.2324C>G (p.Thr775Ser) c.1106C>G (p.Thr369Ser) | |
| 15 | g.73323769G>T | CA393089115 | HCN4 | c.2324C>A (p.Thr775Asn) c.1106C>A (p.Thr369Asn) | gnomAD v4 |
| 15 | g.73323770T>A | CA393089116 | HCN4 | c.2323A>T (p.Thr775Ser) c.1105A>T (p.Thr369Ser) | |
| 15 | g.73323770T>C | CA393089117 | HCN4 | c.2323A>G (p.Thr775Ala) c.1105A>G (p.Thr369Ala) | |
| 15 | g.73323770T>G | CA393089118 | HCN4 | c.2323A>C (p.Thr775Pro) c.1105A>C (p.Thr369Pro) | |
| 15 | g.73323771C>A | CA393089121 | HCN4 | c.2322G>T (p.Trp774Cys) c.1104G>T (p.Trp368Cys) | gnomAD v4 |
| 15 | g.73323771C>G | CA393089120 | HCN4 | c.2322G>C (p.Trp774Cys) c.1104G>C (p.Trp368Cys) | |
| 15 | g.73323771C>T | CA393089119 | HCN4 | c.2322G>A (p.Trp774Ter) c.1104G>A (p.Trp368Ter) | |
| 15 | g.73323772C>A | CA393089122 | HCN4 | c.2321G>T (p.Trp774Leu) c.1103G>T (p.Trp368Leu) | |
| 15 | g.73323772C= | CA2187188642 | HCN4 | c.2321G= (p.Trp774=) c.1103G= (p.Trp368=) | |
| 15 | g.73323772C>G | CA393089123 | HCN4 | c.2321G>C (p.Trp774Ser) c.1103G>C (p.Trp368Ser) | |
| 15 | g.73323772C>T | CA393089124 | HCN4 | c.2321G>A (p.Trp774Ter) c.1103G>A (p.Trp368Ter) | dbSNP gnomAD v2 |
| 15 | g.73323773A= | CA2187188643 | HCN4 | c.2320T= (p.Trp774=) c.1102T= (p.Trp368=) | |
| 15 | g.73323773A>C | CA393089125 | HCN4 | c.2320T>G (p.Trp774Gly) c.1102T>G (p.Trp368Gly) | |
| 15 | g.73323773A>G | CA393089126 | HCN4 | c.2320T>C (p.Trp774Arg) c.1102T>C (p.Trp368Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323773A>T | CA393089127 | HCN4 | c.2320T>A (p.Trp774Arg) c.1102T>A (p.Trp368Arg) | gnomAD v4 |
| 15 | g.73323774G>A | CA491478681 | HCN4 | c.2319C>T (p.Ile773=) c.1101C>T (p.Ile367=) | |
| 15 | g.73323774G>C | CA393089128 | HCN4 | c.2319C>G (p.Ile773Met) c.1101C>G (p.Ile367Met) | |
| 15 | g.73323774G>T | CA491478683 | HCN4 | c.2319C>A (p.Ile773=) c.1101C>A (p.Ile367=) | gnomAD v4 |
| 15 | g.73323775A= | CA2187188644 | HCN4 | c.2318T= (p.Ile773=) c.1100T= (p.Ile367=) | |
| 15 | g.73323775A>C | CA393089129 | HCN4 | c.2318T>G (p.Ile773Ser) c.1100T>G (p.Ile367Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323775A>G | CA393089130 | HCN4 | c.2318T>C (p.Ile773Thr) c.1100T>C (p.Ile367Thr) | |
| 15 | g.73323775A>T | CA393089131 | HCN4 | c.2318T>A (p.Ile773Asn) c.1100T>A (p.Ile367Asn) | |
| 15 | g.73323776T>A | CA393089132 | HCN4 | c.2317A>T (p.Ile773Phe) c.1099A>T (p.Ile367Phe) | |
| 15 | g.73323776T>C | CA393089133 | HCN4 | c.2317A>G (p.Ile773Val) c.1099A>G (p.Ile367Val) | ClinVar dbSNP gnomAD v2 |
| 15 | g.73323776T>G | CA393089134 | HCN4 | c.2317A>C (p.Ile773Leu) c.1099A>C (p.Ile367Leu) | |
| 15 | g.73323776T= | CA2187188645 | HCN4 | c.2317A= (p.Ile773=) c.1099A= (p.Ile367=) | |
| 15 | g.73323777G>A | CA491478685 | HCN4 | c.2316C>T (p.Val772=) c.1098C>T (p.Val366=) | |
| 15 | g.73323777G>C | CA491478686 | HCN4 | c.2316C>G (p.Val772=) c.1098C>G (p.Val366=) | |
| 15 | g.73323777G>T | CA491478687 | HCN4 | c.2316C>A (p.Val772=) c.1098C>A (p.Val366=) | gnomAD v4 |
| 15 | g.73323778A>C | CA393089136 | HCN4 | c.2315T>G (p.Val772Gly) c.1097T>G (p.Val366Gly) | |
| 15 | g.73323778A>G | CA393089137 | HCN4 | c.2315T>C (p.Val772Ala) c.1097T>C (p.Val366Ala) | gnomAD v4 |
| 15 | g.73323778A>T | CA393089135 | HCN4 | c.2315T>A (p.Val772Asp) c.1097T>A (p.Val366Asp) | |
| 15 | g.73323779C>A | CA393089138 | HCN4 | c.2314G>T (p.Val772Phe) c.1096G>T (p.Val366Phe) | gnomAD v4 |
| 15 | g.73323779C= | CA2187188646 | HCN4 | c.2314G= (p.Val772=) c.1096G= (p.Val366=) | |
| 15 | g.73323779C>G | CA7649045 | HCN4 | c.2314G>C (p.Val772Leu) c.1096G>C (p.Val366Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323779C>T | CA7649046 | HCN4 | c.2314G>A (p.Val772Ile) c.1096G>A (p.Val366Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323780G>A | CA7649047 | HCN4 | c.2313C>T (p.Pro771=) c.1095C>T (p.Pro365=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323780G>C | CA491478695 | HCN4 | c.2313C>G (p.Pro771=) c.1095C>G (p.Pro365=) | ClinVar |
| 15 | g.73323780G= | CA2187188647 | HCN4 | c.2313C= (p.Pro771=) c.1095C= (p.Pro365=) | |
| 15 | g.73323780G>T | CA491478696 | HCN4 | c.2313C>A (p.Pro771=) c.1095C>A (p.Pro365=) | gnomAD v4 |
| 15 | g.73323781G>A | CA393089141 | HCN4 | c.2312C>T (p.Pro771Leu) c.1094C>T (p.Pro365Leu) | |
| 15 | g.73323781G>C | CA393089139 | HCN4 | c.2312C>G (p.Pro771Arg) c.1094C>G (p.Pro365Arg) | |
| 15 | g.73323781G>T | CA393089140 | HCN4 | c.2312C>A (p.Pro771His) c.1094C>A (p.Pro365His) | gnomAD v4 |
| 15 | g.73323782G>A | CA7649048 | HCN4 | c.2311C>T (p.Pro771Ser) c.1093C>T (p.Pro365Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323782G>C | CA393089142 | HCN4 | c.2311C>G (p.Pro771Ala) c.1093C>G (p.Pro365Ala) | |
| 15 | g.73323782G= | CA2187188648 | HCN4 | c.2311C= (p.Pro771=) c.1093C= (p.Pro365=) | |
| 15 | g.73323782G>T | CA393089143 | HCN4 | c.2311C>A (p.Pro771Thr) c.1093C>A (p.Pro365Thr) | gnomAD v4 |
| 15 | g.73323783C>A | CA491478704 | HCN4 | c.2310G>T (p.Thr770=) c.1092G>T (p.Thr364=) | |
| 15 | g.73323783C= | CA2187188649 | HCN4 | c.2310G= (p.Thr770=) c.1092G= (p.Thr364=) | |
| 15 | g.73323783C>G | CA491478705 | HCN4 | c.2310G>C (p.Thr770=) c.1092G>C (p.Thr364=) | |
| 15 | g.73323783C>T | CA7649049 | HCN4 | c.2310G>A (p.Thr770=) c.1092G>A (p.Thr364=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323783_73323786delinsCGTG | CA2187188650 | HCN4 | c.2307_2310delinsCACG (p.Pro769=) c.1089_1092delinsCACG (p.Pro363=) | |
| 15 | g.73323784G>A | CA7649051 | HCN4 | c.2309C>T (p.Thr770Met) c.1091C>T (p.Thr364Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323784G>C | CA393089144 | HCN4 | c.2309C>G (p.Thr770Arg) c.1091C>G (p.Thr364Arg) | |
| 15 | g.73323784G= | CA2187188651 | HCN4 | c.2309C= (p.Thr770=) c.1091C= (p.Thr364=) | |
| 15 | g.73323784G>T | CA393089145 | HCN4 | c.2309C>A (p.Thr770Lys) c.1091C>A (p.Thr364Lys) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323785_73323787del | CA7649050 | HCN4 | c.2307_2309del (p.Thr770del) c.1089_1091del (p.Thr364del) | dbSNP ExAC gnomAD v2 |
| 15 | g.73323785T>A | CA393089146 | HCN4 | c.2308A>T (p.Thr770Ser) c.1090A>T (p.Thr364Ser) | |
| 15 | g.73323785T>C | CA393089147 | HCN4 | c.2308A>G (p.Thr770Ala) c.1090A>G (p.Thr364Ala) | |
| 15 | g.73323785T>G | CA393089148 | HCN4 | c.2308A>C (p.Thr770Pro) c.1090A>C (p.Thr364Pro) | dbSNP |
| 15 | g.73323786G>A | CA491478322 | HCN4 | c.2307C>T (p.Pro769=) c.1089C>T (p.Pro363=) | |
| 15 | g.73323786G>C | CA491478324 | HCN4 | c.2307C>G (p.Pro769=) c.1089C>G (p.Pro363=) | |
| 15 | g.73323786G>T | CA491478327 | HCN4 | c.2307C>A (p.Pro769=) c.1089C>A (p.Pro363=) | gnomAD v4 |
| 15 | g.73323790del | CA2575783836 | HCN4 | c.2307del (p.Thr770ArgfsTer8) c.1089del (p.Thr364ArgfsTer8) | |
| 15 | g.73323787G>A | CA393089149 | HCN4 | c.2306C>T (p.Pro769Leu) c.1088C>T (p.Pro363Leu) | dbSNP gnomAD v4 |
| 15 | g.73323787G>C | CA393089150 | HCN4 | c.2306C>G (p.Pro769Arg) c.1088C>G (p.Pro363Arg) | |
| 15 | g.73323787G= | CA2187188652 | HCN4 | c.2306C= (p.Pro769=) c.1088C= (p.Pro363=) | |
| 15 | g.73323787G>T | CA7649052 | HCN4 | c.2306C>A (p.Pro769His) c.1088C>A (p.Pro363His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323788G>A | CA7649053 | HCN4 | c.2305C>T (p.Pro769Ser) c.1087C>T (p.Pro363Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323788G>C | CA393089151 | HCN4 | c.2305C>G (p.Pro769Ala) c.1087C>G (p.Pro363Ala) | |
| 15 | g.73323788G= | CA2187188653 | HCN4 | c.2305C= (p.Pro769=) c.1087C= (p.Pro363=) | |
| 15 | g.73323788G>T | CA393089152 | HCN4 | c.2305C>A (p.Pro769Thr) c.1087C>A (p.Pro363Thr) | gnomAD v4 |
| 15 | g.73323789G>A | CA491478338 | HCN4 | c.2304C>T (p.Thr768=) c.1086C>T (p.Thr362=) | gnomAD v4 |
| 15 | g.73323789G>C | CA491478339 | HCN4 | c.2304C>G (p.Thr768=) c.1086C>G (p.Thr362=) | |
| 15 | g.73323789G= | CA2187188654 | HCN4 | c.2304C= (p.Thr768=) c.1086C= (p.Thr362=) | |
| 15 | g.73323789G>T | CA7649054 | HCN4 | c.2304C>A (p.Thr768=) c.1086C>A (p.Thr362=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323790G>A | CA393089153 | HCN4 | c.2303C>T (p.Thr768Ile) c.1085C>T (p.Thr362Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323790G>C | CA393089154 | HCN4 | c.2303C>G (p.Thr768Ser) c.1085C>G (p.Thr362Ser) | |
| 15 | g.73323790G= | CA2187188655 | HCN4 | c.2303C= (p.Thr768=) c.1085C= (p.Thr362=) | |
| 15 | g.73323790G>T | CA393089155 | HCN4 | c.2303C>A (p.Thr768Asn) c.1085C>A (p.Thr362Asn) | gnomAD v4 |
| 15 | g.73323791T>A | CA393089156 | HCN4 | c.2302A>T (p.Thr768Ser) c.1084A>T (p.Thr362Ser) | |
| 15 | g.73323791T>C | CA393089157 | HCN4 | c.2302A>G (p.Thr768Ala) c.1084A>G (p.Thr362Ala) | gnomAD v4 |
| 15 | g.73323791T>G | CA393089158 | HCN4 | c.2302A>C (p.Thr768Pro) c.1084A>C (p.Thr362Pro) | |
| 15 | g.73323792T>A | CA491478345 | HCN4 | c.2301A>T (p.Pro767=) c.1083A>T (p.Pro361=) | |
| 15 | g.73323792T>C | CA491478347 | HCN4 | c.2301A>G (p.Pro767=) c.1083A>G (p.Pro361=) | |
| 15 | g.73323792T>G | CA491478348 | HCN4 | c.2301A>C (p.Pro767=) c.1083A>C (p.Pro361=) | |
| 15 | g.73323792_73323793del | CA2629370794 | HCN4 | c.2300_2301del (p.Pro767HisfsTer?) c.1082_1083del (p.Pro361HisfsTer?) | gnomAD v4 |
| 15 | g.73323793G>A | CA393089160 | HCN4 | c.2300C>T (p.Pro767Leu) c.1082C>T (p.Pro361Leu) | |
| 15 | g.73323793G>C | CA393089161 | HCN4 | c.2300C>G (p.Pro767Arg) c.1082C>G (p.Pro361Arg) | |
| 15 | g.73323793G>T | CA393089159 | HCN4 | c.2300C>A (p.Pro767Gln) c.1082C>A (p.Pro361Gln) | gnomAD v4 |
| 15 | g.73323796del | CA2629370796 | HCN4 | c.2300del (p.Pro767GlnfsTer11) c.1082del (p.Pro361GlnfsTer11) | gnomAD v4 |
| 15 | g.73323794G>A | CA393089162 | HCN4 | c.2299C>T (p.Pro767Ser) c.1081C>T (p.Pro361Ser) | |
| 15 | g.73323794G>C | CA393089163 | HCN4 | c.2299C>G (p.Pro767Ala) c.1081C>G (p.Pro361Ala) | |
| 15 | g.73323794G>T | CA393089164 | HCN4 | c.2299C>A (p.Pro767Thr) c.1081C>A (p.Pro361Thr) | gnomAD v4 |