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.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.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 |
| 15 | g.73323649C>A | CA393088882 | HCN4 | c.2444G>T (p.Gly815Val) c.1226G>T (p.Gly409Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323649C= | CA2187188585 | HCN4 | c.2444G= (p.Gly815=) c.1226G= (p.Gly409=) | |
| 15 | g.73323649C>G | CA272664782 | HCN4 | c.2444G>C (p.Gly815Ala) c.1226G>C (p.Gly409Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323649C>T | CA393088883 | HCN4 | c.2444G>A (p.Gly815Asp) c.1226G>A (p.Gly409Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323651del | CA2629370653 | HCN4 | c.2444del (p.Gly815AlafsTer12) c.1226del (p.Gly409AlafsTer12) | gnomAD v4 |
| 15 | g.73323650C>A | CA393088884 | HCN4 | c.2443G>T (p.Gly815Cys) c.1225G>T (p.Gly409Cys) | gnomAD v4 |
| 15 | g.73323650C= | CA2187188586 | HCN4 | c.2443G= (p.Gly815=) c.1225G= (p.Gly409=) | |
| 15 | g.73323650C>G | CA393088886 | HCN4 | c.2443G>C (p.Gly815Arg) c.1225G>C (p.Gly409Arg) | |
| 15 | g.73323650C>T | CA393088885 | HCN4 | c.2443G>A (p.Gly815Ser) c.1225G>A (p.Gly409Ser) | dbSNP gnomAD v4 |
| 15 | g.73323651C>A | CA491478381 | HCN4 | c.2442G>T (p.Leu814=) c.1224G>T (p.Leu408=) | |
| 15 | g.73323651C= | CA2187188587 | HCN4 | c.2442G= (p.Leu814=) c.1224G= (p.Leu408=) | |
| 15 | g.73323651C>G | CA491478380 | HCN4 | c.2442G>C (p.Leu814=) c.1224G>C (p.Leu408=) | |
| 15 | g.73323651C>T | CA7649027 | HCN4 | c.2442G>A (p.Leu814=) c.1224G>A (p.Leu408=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323652A= | CA2187188588 | HCN4 | c.2441T= (p.Leu814=) c.1223T= (p.Leu408=) | |
| 15 | g.73323652A>C | CA393088887 | HCN4 | c.2441T>G (p.Leu814Arg) c.1223T>G (p.Leu408Arg) | |
| 15 | g.73323652A>G | CA393088888 | HCN4 | c.2441T>C (p.Leu814Pro) c.1223T>C (p.Leu408Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323652A>T | CA393088889 | HCN4 | c.2441T>A (p.Leu814Gln) c.1223T>A (p.Leu408Gln) | gnomAD v4 |
| 15 | g.73323653G>A | CA491478387 | HCN4 | c.2440C>T (p.Leu814=) c.1222C>T (p.Leu408=) | gnomAD v4 |
| 15 | g.73323653G>C | CA393088890 | HCN4 | c.2440C>G (p.Leu814Val) c.1222C>G (p.Leu408Val) | |
| 15 | g.73323653G>T | CA393088891 | HCN4 | c.2440C>A (p.Leu814Met) c.1222C>A (p.Leu408Met) | gnomAD v4 |
| 15 | g.73323654C>A | CA491478392 | HCN4 | c.2439G>T (p.Gly813=) c.1221G>T (p.Gly407=) | gnomAD v4 |
| 15 | g.73323654C>G | CA491478393 | HCN4 | c.2439G>C (p.Gly813=) c.1221G>C (p.Gly407=) | |
| 15 | g.73323654C>T | CA491478394 | HCN4 | c.2439G>A (p.Gly813=) c.1221G>A (p.Gly407=) | gnomAD v4 |
| 15 | g.73323655C>A | CA393088892 | HCN4 | c.2438G>T (p.Gly813Val) c.1220G>T (p.Gly407Val) | ClinVar gnomAD v4 |
| 15 | g.73323655C>G | CA393088893 | HCN4 | c.2438G>C (p.Gly813Ala) c.1220G>C (p.Gly407Ala) | |
| 15 | g.73323655C>T | CA393088894 | HCN4 | c.2438G>A (p.Gly813Glu) c.1220G>A (p.Gly407Glu) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73323656C>A | CA393088895 | HCN4 | c.2437G>T (p.Gly813Trp) c.1219G>T (p.Gly407Trp) | |
| 15 | g.73323656C= | CA2187188589 | HCN4 | c.2437G= (p.Gly813=) c.1219G= (p.Gly407=) | |
| 15 | g.73323656C>G | CA393088896 | HCN4 | c.2437G>C (p.Gly813Arg) c.1219G>C (p.Gly407Arg) | |
| 15 | g.73323656C>T | CA7649028 | HCN4 | c.2437G>A (p.Gly813Arg) c.1219G>A (p.Gly407Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323657A>C | CA491478396 | HCN4 | c.2436T>G (p.Ser812=) c.1218T>G (p.Ser406=) | |
| 15 | g.73323657A>G | CA491478395 | HCN4 | c.2436T>C (p.Ser812=) c.1218T>C (p.Ser406=) | |
| 15 | g.73323657A>T | CA491478398 | HCN4 | c.2436T>A (p.Ser812=) c.1218T>A (p.Ser406=) | ClinVar |
| 15 | g.73323658G>A | CA393088899 | HCN4 | c.2435C>T (p.Ser812Phe) c.1217C>T (p.Ser406Phe) | |
| 15 | g.73323658G>C | CA393088898 | HCN4 | c.2435C>G (p.Ser812Cys) c.1217C>G (p.Ser406Cys) | |
| 15 | g.73323658G>T | CA393088897 | HCN4 | c.2435C>A (p.Ser812Tyr) c.1217C>A (p.Ser406Tyr) | gnomAD v4 COSMIC |
| 15 | g.73323659A>C | CA393088900 | HCN4 | c.2434T>G (p.Ser812Ala) c.1216T>G (p.Ser406Ala) | |
| 15 | g.73323659A>G | CA393088902 | HCN4 | c.2434T>C (p.Ser812Pro) c.1216T>C (p.Ser406Pro) | |
| 15 | g.73323659A>T | CA393088901 | HCN4 | c.2434T>A (p.Ser812Thr) c.1216T>A (p.Ser406Thr) | gnomAD v4 |
| 15 | g.73323660T>A | CA491478405 | HCN4 | c.2433A>T (p.Gly811=) c.1215A>T (p.Gly405=) | |
| 15 | g.73323660T>C | CA491478406 | HCN4 | c.2433A>G (p.Gly811=) c.1215A>G (p.Gly405=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323660T>G | CA491478407 | HCN4 | c.2433A>C (p.Gly811=) c.1215A>C (p.Gly405=) | |
| 15 | g.73323660T= | CA2187188590 | HCN4 | c.2433A= (p.Gly811=) c.1215A= (p.Gly405=) | |
| 15 | g.73323661C>A | CA7649029 | HCN4 | c.2432G>T (p.Gly811Val) c.1214G>T (p.Gly405Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323661C= | CA2187188591 | HCN4 | c.2432G= (p.Gly811=) c.1214G= (p.Gly405=) | |
| 15 | g.73323661C>G | CA393088903 | HCN4 | c.2432G>C (p.Gly811Ala) c.1214G>C (p.Gly405Ala) | ClinVar dbSNP |
| 15 | g.73323661C>T | CA7649030 | HCN4 | c.2432G>A (p.Gly811Glu) c.1214G>A (p.Gly405Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323662C>A | CA393088904 | HCN4 | c.2431G>T (p.Gly811Ter) c.1213G>T (p.Gly405Ter) | gnomAD v4 |
| 15 | g.73323662C>G | CA393088906 | HCN4 | c.2431G>C (p.Gly811Arg) c.1213G>C (p.Gly405Arg) | |
| 15 | g.73323662C>T | CA393088905 | HCN4 | c.2431G>A (p.Gly811Arg) c.1213G>A (p.Gly405Arg) | |
| 15 | g.73323663T>A | CA491478413 | HCN4 | c.2430A>T (p.Pro810=) c.1212A>T (p.Pro404=) | |
| 15 | g.73323663T>C | CA272664794 | HCN4 | c.2430A>G (p.Pro810=) c.1212A>G (p.Pro404=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323663T>G | CA491478416 | HCN4 | c.2430A>C (p.Pro810=) c.1212A>C (p.Pro404=) | gnomAD v4 |
| 15 | g.73323663T= | CA2187188592 | HCN4 | c.2430A= (p.Pro810=) c.1212A= (p.Pro404=) | |
| 15 | g.73323664G>A | CA393088907 | HCN4 | c.2429C>T (p.Pro810Leu) c.1211C>T (p.Pro404Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323664G>C | CA393088909 | HCN4 | c.2429C>G (p.Pro810Arg) c.1211C>G (p.Pro404Arg) | |
| 15 | g.73323664G= | CA2187188593 | HCN4 | c.2429C= (p.Pro810=) c.1211C= (p.Pro404=) | |
| 15 | g.73323664G>T | CA393088908 | HCN4 | c.2429C>A (p.Pro810Gln) c.1211C>A (p.Pro404Gln) | gnomAD v4 |
| 15 | g.73323668dup | CA2629370659 | HCN4 | c.2429dup (p.Gly811ArgfsTer?) c.1211dup (p.Gly405ArgfsTer?) | gnomAD v4 |
| 15 | g.73323668del | CA645586810 | HCN4 | c.2429del (p.Pro810GlnfsTer17) c.1211del (p.Pro404GlnfsTer17) | gnomAD v4 COSMIC |
| 15 | g.73323665G>A | CA393088910 | HCN4 | c.2428C>T (p.Pro810Ser) c.1210C>T (p.Pro404Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323665G>C | CA393088911 | HCN4 | c.2428C>G (p.Pro810Ala) c.1210C>G (p.Pro404Ala) | |
| 15 | g.73323665G= | CA2187188594 | HCN4 | c.2428C= (p.Pro810=) c.1210C= (p.Pro404=) | |
| 15 | g.73323665G>T | CA393088912 | HCN4 | c.2428C>A (p.Pro810Thr) c.1210C>A (p.Pro404Thr) | gnomAD v4 |
| 15 | g.73323666G>A | CA491478421 | HCN4 | c.2427C>T (p.Pro809=) c.1209C>T (p.Pro403=) | |
| 15 | g.73323666G>C | CA491478422 | HCN4 | c.2427C>G (p.Pro809=) c.1209C>G (p.Pro403=) | |
| 15 | g.73323666G>T | CA491478424 | HCN4 | c.2427C>A (p.Pro809=) c.1209C>A (p.Pro403=) | dbSNP gnomAD v4 |
| 15 | g.73323667G>A | CA393088913 | HCN4 | c.2426C>T (p.Pro809Leu) c.1208C>T (p.Pro403Leu) | gnomAD v4 |
| 15 | g.73323667G>C | CA393088914 | HCN4 | c.2426C>G (p.Pro809Arg) c.1208C>G (p.Pro403Arg) | |
| 15 | g.73323667G>T | CA393088915 | HCN4 | c.2426C>A (p.Pro809His) c.1208C>A (p.Pro403His) | ClinVar gnomAD v4 |
| 15 | g.73323668G>A | CA393088916 | HCN4 | c.2425C>T (p.Pro809Ser) c.1207C>T (p.Pro403Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323668G>C | CA393088917 | HCN4 | c.2425C>G (p.Pro809Ala) c.1207C>G (p.Pro403Ala) | COSMIC |
| 15 | g.73323668G= | CA2187188595 | HCN4 | c.2425C= (p.Pro809=) c.1207C= (p.Pro403=) | |
| 15 | g.73323668G>T | CA393088918 | HCN4 | c.2425C>A (p.Pro809Thr) c.1207C>A (p.Pro403Thr) | gnomAD v4 |
| 15 | g.73323669del | CA2629370660 | HCN4 | c.2424del (p.Pro810GlnfsTer17) c.1206del (p.Pro404GlnfsTer17) | gnomAD v4 |
| 15 | g.73323669A>C | CA491478427 | HCN4 | c.2424T>G (p.Pro808=) c.1206T>G (p.Pro402=) | |
| 15 | g.73323669A>G | CA491478429 | HCN4 | c.2424T>C (p.Pro808=) c.1206T>C (p.Pro402=) | gnomAD v4 |
| 15 | g.73323669A>T | CA491478430 | HCN4 | c.2424T>A (p.Pro808=) c.1206T>A (p.Pro402=) | |
| 15 | g.73323670G>A | CA7649031 | HCN4 | c.2423C>T (p.Pro808Leu) c.1205C>T (p.Pro402Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323670G>C | CA393088919 | HCN4 | c.2423C>G (p.Pro808Arg) c.1205C>G (p.Pro402Arg) | |
| 15 | g.73323670G= | CA2187188596 | HCN4 | c.2423C= (p.Pro808=) c.1205C= (p.Pro402=) | |
| 15 | g.73323670G>T | CA393088920 | HCN4 | c.2423C>A (p.Pro808His) c.1205C>A (p.Pro402His) | gnomAD v4 |
| 15 | g.73323672del | CA2629370661 | HCN4 | c.2423del (p.Pro808LeufsTer19) c.1205del (p.Pro402LeufsTer19) | gnomAD v4 |
| 15 | g.73323671G>A | CA393088923 | HCN4 | c.2422C>T (p.Pro808Ser) c.1204C>T (p.Pro402Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323671G>C | CA393088921 | HCN4 | c.2422C>G (p.Pro808Ala) c.1204C>G (p.Pro402Ala) | |
| 15 | g.73323671G= | CA2187188597 | HCN4 | c.2422C= (p.Pro808=) c.1204C= (p.Pro402=) | |
| 15 | g.73323671G>T | CA393088922 | HCN4 | c.2422C>A (p.Pro808Thr) c.1204C>A (p.Pro402Thr) | gnomAD v4 |
| 15 | g.73323672G>A | CA491478439 | HCN4 | c.2421C>T (p.Arg807=) c.1203C>T (p.Arg401=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323672G>C | CA491478436 | HCN4 | c.2421C>G (p.Arg807=) c.1203C>G (p.Arg401=) | |
| 15 | g.73323672G= | CA2187188598 | HCN4 | c.2421C= (p.Arg807=) c.1203C= (p.Arg401=) | |
| 15 | g.73323672G>T | CA491478435 | HCN4 | c.2421C>A (p.Arg807=) c.1203C>A (p.Arg401=) | gnomAD v4 |
| 15 | g.73323673C>A | CA393088924 | HCN4 | c.2420G>T (p.Arg807Leu) c.1202G>T (p.Arg401Leu) | gnomAD v4 |
| 15 | g.73323673C= | CA2187188599 | HCN4 | c.2420G= (p.Arg807=) c.1202G= (p.Arg401=) | |
| 15 | g.73323673C>G | CA393088925 | HCN4 | c.2420G>C (p.Arg807Pro) c.1202G>C (p.Arg401Pro) | dbSNP |
| 15 | g.73323673C>T | CA090974 | HCN4 | c.2420G>A (p.Arg807His) c.1202G>A (p.Arg401His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323674G>A | CA7649032 | HCN4 | c.2419C>T (p.Arg807Cys) c.1201C>T (p.Arg401Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323674G>C | CA393088926 | HCN4 | c.2419C>G (p.Arg807Gly) c.1201C>G (p.Arg401Gly) | |
| 15 | g.73323674G= | CA2187188600 | HCN4 | c.2419C= (p.Arg807=) c.1201C= (p.Arg401=) | |
| 15 | g.73323674G>T | CA393088927 | HCN4 | c.2419C>A (p.Arg807Ser) c.1201C>A (p.Arg401Ser) | gnomAD v4 |
| 15 | g.73323675G>A | CA491478446 | HCN4 | c.2418C>T (p.Phe806=) c.1200C>T (p.Phe400=) | |
| 15 | g.73323675G>C | CA393088928 | HCN4 | c.2418C>G (p.Phe806Leu) c.1200C>G (p.Phe400Leu) | |
| 15 | g.73323675G>T | CA393088929 | HCN4 | c.2418C>A (p.Phe806Leu) c.1200C>A (p.Phe400Leu) | gnomAD v4 |
| 15 | g.73323676A>C | CA393088930 | HCN4 | c.2417T>G (p.Phe806Cys) c.1199T>G (p.Phe400Cys) | |
| 15 | g.73323676A>G | CA393088931 | HCN4 | c.2417T>C (p.Phe806Ser) c.1199T>C (p.Phe400Ser) | |
| 15 | g.73323676A>T | CA393088932 | HCN4 | c.2417T>A (p.Phe806Tyr) c.1199T>A (p.Phe400Tyr) | |
| 15 | g.73323677A>C | CA393088935 | HCN4 | c.2416T>G (p.Phe806Val) c.1198T>G (p.Phe400Val) | |
| 15 | g.73323677A>G | CA393088934 | HCN4 | c.2416T>C (p.Phe806Leu) c.1198T>C (p.Phe400Leu) | gnomAD v4 |
| 15 | g.73323677A>T | CA393088933 | HCN4 | c.2416T>A (p.Phe806Ile) c.1198T>A (p.Phe400Ile) | |
| 15 | g.73323678G>A | CA491478450 | HCN4 | c.2415C>T (p.Ile805=) c.1197C>T (p.Ile399=) | gnomAD v4 |
| 15 | g.73323678G>C | CA393088936 | HCN4 | c.2415C>G (p.Ile805Met) c.1197C>G (p.Ile399Met) | |
| 15 | g.73323678G>T | CA491478453 | HCN4 | c.2415C>A (p.Ile805=) c.1197C>A (p.Ile399=) | gnomAD v4 |
| 15 | g.73323679A>C | CA393088937 | HCN4 | c.2414T>G (p.Ile805Ser) c.1196T>G (p.Ile399Ser) | |
| 15 | g.73323679A>G | CA393088938 | HCN4 | c.2414T>C (p.Ile805Thr) c.1196T>C (p.Ile399Thr) | |
| 15 | g.73323679A>T | CA393088939 | HCN4 | c.2414T>A (p.Ile805Asn) c.1196T>A (p.Ile399Asn) | |
| 15 | g.73323680T>A | CA393088940 | HCN4 | c.2413A>T (p.Ile805Phe) c.1195A>T (p.Ile399Phe) | |
| 15 | g.73323680T>C | CA393088941 | HCN4 | c.2413A>G (p.Ile805Val) c.1195A>G (p.Ile399Val) | |
| 15 | g.73323680T>G | CA393088942 | HCN4 | c.2413A>C (p.Ile805Leu) c.1195A>C (p.Ile399Leu) | |
| 15 | g.73323681G>A | CA491478459 | HCN4 | c.2412C>T (p.Ala804=) c.1194C>T (p.Ala398=) | dbSNP gnomAD v2 |
| 15 | g.73323681G>C | CA491478460 | HCN4 | c.2412C>G (p.Ala804=) c.1194C>G (p.Ala398=) | |
| 15 | g.73323681G= | CA2187188601 | HCN4 | c.2412C= (p.Ala804=) c.1194C= (p.Ala398=) | |
| 15 | g.73323681G>T | CA491478461 | HCN4 | c.2412C>A (p.Ala804=) c.1194C>A (p.Ala398=) | gnomAD v4 |
| 15 | g.73323682G>A | CA393088943 | HCN4 | c.2411C>T (p.Ala804Val) c.1193C>T (p.Ala398Val) | gnomAD v4 |
| 15 | g.73323682G>C | CA393088944 | HCN4 | c.2411C>G (p.Ala804Gly) c.1193C>G (p.Ala398Gly) | |
| 15 | g.73323682G>T | CA393088945 | HCN4 | c.2411C>A (p.Ala804Asp) c.1193C>A (p.Ala398Asp) | gnomAD v4 |
| 15 | g.73323683C>A | CA393088946 | HCN4 | c.2410G>T (p.Ala804Ser) c.1192G>T (p.Ala398Ser) | gnomAD v4 |
| 15 | g.73323683C= | CA2187188602 | HCN4 | c.2410G= (p.Ala804=) c.1192G= (p.Ala398=) | |
| 15 | g.73323683C>G | CA393088947 | HCN4 | c.2410G>C (p.Ala804Pro) c.1192G>C (p.Ala398Pro) | |
| 15 | g.73323683C>T | CA393088948 | HCN4 | c.2410G>A (p.Ala804Thr) c.1192G>A (p.Ala398Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323684A= | CA2187188603 | HCN4 | c.2409T= (p.Ala803=) c.1191T= (p.Ala397=) | |
| 15 | g.73323684A>C | CA272664812 | HCN4 | c.2409T>G (p.Ala803=) c.1191T>G (p.Ala397=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323684A>G | CA491478470 | HCN4 | c.2409T>C (p.Ala803=) c.1191T>C (p.Ala397=) | |
| 15 | g.73323684A>T | CA491478471 | HCN4 | c.2409T>A (p.Ala803=) c.1191T>A (p.Ala397=) | |
| 15 | g.73323685G>A | CA7649033 | HCN4 | c.2408C>T (p.Ala803Val) c.1190C>T (p.Ala397Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323685G>C | CA393088950 | HCN4 | c.2408C>G (p.Ala803Gly) c.1190C>G (p.Ala397Gly) | |
| 15 | g.73323685G= | CA2187188604 | HCN4 | c.2408C= (p.Ala803=) c.1190C= (p.Ala397=) | |
| 15 | g.73323685G>T | CA393088949 | HCN4 | c.2408C>A (p.Ala803Asp) c.1190C>A (p.Ala397Asp) | gnomAD v4 |
| 15 | g.73323686C>A | CA393088951 | HCN4 | c.2407G>T (p.Ala803Ser) c.1189G>T (p.Ala397Ser) | gnomAD v4 |
| 15 | g.73323686C= | CA2187188605 | HCN4 | c.2407G= (p.Ala803=) c.1189G= (p.Ala397=) | |
| 15 | g.73323686C>G | CA393088952 | HCN4 | c.2407G>C (p.Ala803Pro) c.1189G>C (p.Ala397Pro) | |
| 15 | g.73323686C>T | CA7649034 | HCN4 | c.2407G>A (p.Ala803Thr) c.1189G>A (p.Ala397Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323687A>C | CA491478474 | HCN4 | c.2406T>G (p.Pro802=) c.1188T>G (p.Pro396=) | |
| 15 | g.73323687A>G | CA491478475 | HCN4 | c.2406T>C (p.Pro802=) c.1188T>C (p.Pro396=) | |
| 15 | g.73323687A>T | CA491478476 | HCN4 | c.2406T>A (p.Pro802=) c.1188T>A (p.Pro396=) | |
| 15 | g.73323688G>A | CA393088953 | HCN4 | c.2405C>T (p.Pro802Leu) c.1187C>T (p.Pro396Leu) | dbSNP gnomAD v2 |
| 15 | g.73323688G>C | CA393088954 | HCN4 | c.2405C>G (p.Pro802Arg) c.1187C>G (p.Pro396Arg) | |
| 15 | g.73323688G= | CA2187188606 | HCN4 | c.2405C= (p.Pro802=) c.1187C= (p.Pro396=) | |
| 15 | g.73323688G>T | CA393088955 | HCN4 | c.2405C>A (p.Pro802His) c.1187C>A (p.Pro396His) | gnomAD v4 |
| 15 | g.73323689G>A | CA393088956 | HCN4 | c.2404C>T (p.Pro802Ser) c.1186C>T (p.Pro396Ser) | gnomAD v4 |
| 15 | g.73323689G>C | CA393088958 | HCN4 | c.2404C>G (p.Pro802Ala) c.1186C>G (p.Pro396Ala) | |
| 15 | g.73323689G>T | CA393088957 | HCN4 | c.2404C>A (p.Pro802Thr) c.1186C>A (p.Pro396Thr) | gnomAD v4 |
| 15 | g.73323690C>A | CA491478478 | HCN4 | c.2403G>T (p.Leu801=) c.1185G>T (p.Leu395=) | gnomAD v4 |
| 15 | g.73323690C>G | CA491478479 | HCN4 | c.2403G>C (p.Leu801=) c.1185G>C (p.Leu395=) | |
| 15 | g.73323690C>T | CA491478481 | HCN4 | c.2403G>A (p.Leu801=) c.1185G>A (p.Leu395=) | gnomAD v4 |
| 15 | g.73323691A>C | CA393088959 | HCN4 | c.2402T>G (p.Leu801Arg) c.1184T>G (p.Leu395Arg) | |
| 15 | g.73323691A>G | CA393088960 | HCN4 | c.2402T>C (p.Leu801Pro) c.1184T>C (p.Leu395Pro) | |
| 15 | g.73323691A>T | CA393088961 | HCN4 | c.2402T>A (p.Leu801Gln) c.1184T>A (p.Leu395Gln) | |
| 15 | g.73323692G>A | CA272664827 | HCN4 | c.2401C>T (p.Leu801=) c.1183C>T (p.Leu395=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323692G>C | CA393088962 | HCN4 | c.2401C>G (p.Leu801Val) c.1183C>G (p.Leu395Val) | |
| 15 | g.73323692G= | CA2187188607 | HCN4 | c.2401C= (p.Leu801=) c.1183C= (p.Leu395=) | |
| 15 | g.73323692G>T | CA393088963 | HCN4 | c.2401C>A (p.Leu801Met) c.1183C>A (p.Leu395Met) | gnomAD v4 |
| 15 | g.73323693G>A | CA491478490 | HCN4 | c.2400C>T (p.Arg800=) c.1182C>T (p.Arg394=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323693G>C | CA491478488 | HCN4 | c.2400C>G (p.Arg800=) c.1182C>G (p.Arg394=) | |
| 15 | g.73323693G= | CA2187188608 | HCN4 | c.2400C= (p.Arg800=) c.1182C= (p.Arg394=) | |
| 15 | g.73323693G>T | CA491478487 | HCN4 | c.2400C>A (p.Arg800=) c.1182C>A (p.Arg394=) | gnomAD v4 |
| 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 |