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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.73323059dup | CA7648896 | HCN4 | c.3040dup (p.Ala1014GlyfsTer?) c.1822dup (p.Ala608GlyfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323058_73323059dup | CA2804714151 | HCN4 | c.3039_3040dup (p.Ala1014GlyfsTer5) c.1821_1822dup (p.Ala608GlyfsTer5) | |
| 15 | g.73323059del | CA645586808 | HCN4 | c.3040del (p.Ala1014LeufsTer4) c.1822del (p.Ala608LeufsTer4) | gnomAD v4 COSMIC |
| 15 | g.73323057C>A | CA491478408 | HCN4 | c.3036G>T (p.Gly1012=) c.1818G>T (p.Gly606=) | gnomAD v4 |
| 15 | g.73323057C= | CA2187187356 | HCN4 | c.3036G= (p.Gly1012=) c.1818G= (p.Gly606=) | |
| 15 | g.73323057C>G | CA272663905 | HCN4 | c.3036G>C (p.Gly1012=) c.1818G>C (p.Gly606=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323057C>T | CA491478411 | HCN4 | c.3036G>A (p.Gly1012=) c.1818G>A (p.Gly606=) | gnomAD v4 |
| 15 | g.73323058C>A | CA393086378 | HCN4 | c.3035G>T (p.Gly1012Val) c.1817G>T (p.Gly606Val) | gnomAD v4 |
| 15 | g.73323058C= | CA2187187361 | HCN4 | c.3035G= (p.Gly1012=) c.1817G= (p.Gly606=) | |
| 15 | g.73323058C>G | CA7648897 | HCN4 | c.3035G>C (p.Gly1012Ala) c.1817G>C (p.Gly606Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323058C>T | CA393086380 | HCN4 | c.3035G>A (p.Gly1012Glu) c.1817G>A (p.Gly606Glu) | gnomAD v4 |
| 15 | g.73323059C>A | CA7648898 | HCN4 | c.3034G>T (p.Gly1012Trp) c.1816G>T (p.Gly606Trp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323059C= | CA2187187364 | HCN4 | c.3034G= (p.Gly1012=) c.1816G= (p.Gly606=) | |
| 15 | g.73323059C>G | CA393086382 | HCN4 | c.3034G>C (p.Gly1012Arg) c.1816G>C (p.Gly606Arg) | dbSNP gnomAD v4 |
| 15 | g.73323059C>T | CA7648899 | HCN4 | c.3034G>A (p.Gly1012Arg) c.1816G>A (p.Gly606Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323060A= | CA2187187372 | HCN4 | c.3033T= (p.Ser1011=) c.1815T= (p.Ser605=) | |
| 15 | g.73323060A>C | CA199745 | HCN4 | c.3033T>G (p.Ser1011=) c.1815T>G (p.Ser605=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323060A>G | CA491478417 | HCN4 | c.3033T>C (p.Ser1011=) c.1815T>C (p.Ser605=) | gnomAD v4 |
| 15 | g.73323060A>T | CA491478418 | HCN4 | c.3033T>A (p.Ser1011=) c.1815T>A (p.Ser605=) | |
| 15 | g.73323061G>A | CA393086385 | HCN4 | c.3032C>T (p.Ser1011Phe) c.1814C>T (p.Ser605Phe) | gnomAD v4 |
| 15 | g.73323061G>C | CA393086387 | HCN4 | c.3032C>G (p.Ser1011Cys) c.1814C>G (p.Ser605Cys) | |
| 15 | g.73323061G>T | CA393086389 | HCN4 | c.3032C>A (p.Ser1011Tyr) c.1814C>A (p.Ser605Tyr) | gnomAD v4 |
| 15 | g.73323062A= | CA2187187378 | HCN4 | c.3031T= (p.Ser1011=) c.1813T= (p.Ser605=) | |
| 15 | g.73323062A>C | CA393086391 | HCN4 | c.3031T>G (p.Ser1011Ala) c.1813T>G (p.Ser605Ala) | gnomAD v4 |
| 15 | g.73323062A>G | CA16607866 | HCN4 | c.3031T>C (p.Ser1011Pro) c.1813T>C (p.Ser605Pro) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323062A>T | CA393086393 | HCN4 | c.3031T>A (p.Ser1011Thr) c.1813T>A (p.Ser605Thr) | |
| 15 | g.73323063G>A | CA7648900 | HCN4 | c.3030C>T (p.Ala1010=) c.1812C>T (p.Ala604=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323063G>C | CA491478426 | HCN4 | c.3030C>G (p.Ala1010=) c.1812C>G (p.Ala604=) | |
| 15 | g.73323063G= | CA2187187381 | HCN4 | c.3030C= (p.Ala1010=) c.1812C= (p.Ala604=) | |
| 15 | g.73323063G>T | CA491478425 | HCN4 | c.3030C>A (p.Ala1010=) c.1812C>A (p.Ala604=) | gnomAD v4 |
| 15 | g.73323064G>A | CA393086397 | HCN4 | c.3029C>T (p.Ala1010Val) c.1811C>T (p.Ala604Val) | gnomAD v4 |
| 15 | g.73323064G>C | CA393086399 | HCN4 | c.3029C>G (p.Ala1010Gly) c.1811C>G (p.Ala604Gly) | gnomAD v4 |
| 15 | g.73323064G= | CA2187187384 | HCN4 | c.3029C= (p.Ala1010=) c.1811C= (p.Ala604=) | |
| 15 | g.73323064G>T | CA393086396 | HCN4 | c.3029C>A (p.Ala1010Asp) c.1811C>A (p.Ala604Asp) | gnomAD v4 |
| 15 | g.73323065C>A | CA393086402 | HCN4 | c.3028G>T (p.Ala1010Ser) c.1810G>T (p.Ala604Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323065C= | CA2187187391 | HCN4 | c.3028G= (p.Ala1010=) c.1810G= (p.Ala604=) | |
| 15 | g.73323065C>G | CA393086404 | HCN4 | c.3028G>C (p.Ala1010Pro) c.1810G>C (p.Ala604Pro) | |
| 15 | g.73323065C>T | CA7648901 | HCN4 | c.3028G>A (p.Ala1010Thr) c.1810G>A (p.Ala604Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323068dup | CA272663932 | HCN4 | c.3028dup (p.Ala1010GlyfsTer?) c.1810dup (p.Ala604GlyfsTer?) | dbSNP gnomAD v4 |
| 15 | g.73323068del | CA2629370545 | HCN4 | c.3028del (p.Ala1010ProfsTer8) c.1810del (p.Ala604ProfsTer8) | gnomAD v4 |
| 15 | g.73323066C>A | CA491478437 | HCN4 | c.3027G>T (p.Gly1009=) c.1809G>T (p.Gly603=) | gnomAD v4 |
| 15 | g.73323066C>G | CA491478438 | HCN4 | c.3027G>C (p.Gly1009=) c.1809G>C (p.Gly603=) | |
| 15 | g.73323066C>T | CA491478440 | HCN4 | c.3027G>A (p.Gly1009=) c.1809G>A (p.Gly603=) | |
| 15 | g.73323067C>A | CA393086406 | HCN4 | c.3026G>T (p.Gly1009Val) c.1808G>T (p.Gly603Val) | |
| 15 | g.73323067C= | CA2187187397 | HCN4 | c.3026G= (p.Gly1009=) c.1808G= (p.Gly603=) | |
| 15 | g.73323067C>G | CA393086407 | HCN4 | c.3026G>C (p.Gly1009Ala) c.1808G>C (p.Gly603Ala) | |
| 15 | g.73323067C>T | CA7648902 | HCN4 | c.3026G>A (p.Gly1009Glu) c.1808G>A (p.Gly603Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323068C>A | CA393086410 | HCN4 | c.3025G>T (p.Gly1009Trp) c.1807G>T (p.Gly603Trp) | |
| 15 | g.73323068C>G | CA393086411 | HCN4 | c.3025G>C (p.Gly1009Arg) c.1807G>C (p.Gly603Arg) | gnomAD v4 |
| 15 | g.73323068C>T | CA393086413 | HCN4 | c.3025G>A (p.Gly1009Arg) c.1807G>A (p.Gly603Arg) | gnomAD v4 |
| 15 | g.73323069T>A | CA491478447 | HCN4 | c.3024A>T (p.Ala1008=) c.1806A>T (p.Ala602=) | |
| 15 | g.73323069T>C | CA491478448 | HCN4 | c.3024A>G (p.Ala1008=) c.1806A>G (p.Ala602=) | gnomAD v4 |
| 15 | g.73323069T>G | CA491478449 | HCN4 | c.3024A>C (p.Ala1008=) c.1806A>C (p.Ala602=) | |
| 15 | g.73323070G>A | CA393086415 | HCN4 | c.3023C>T (p.Ala1008Val) c.1805C>T (p.Ala602Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323070G>C | CA393086417 | HCN4 | c.3023C>G (p.Ala1008Gly) c.1805C>G (p.Ala602Gly) | |
| 15 | g.73323070G= | CA2187187400 | HCN4 | c.3023C= (p.Ala1008=) c.1805C= (p.Ala602=) | |
| 15 | g.73323070G>T | CA393086419 | HCN4 | c.3023C>A (p.Ala1008Glu) c.1805C>A (p.Ala602Glu) | gnomAD v4 |
| 15 | g.73323071C>A | CA393086424 | HCN4 | c.3022G>T (p.Ala1008Ser) c.1804G>T (p.Ala602Ser) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323071C= | CA2187187403 | HCN4 | c.3022G= (p.Ala1008=) c.1804G= (p.Ala602=) | |
| 15 | g.73323071C>G | CA393086420 | HCN4 | c.3022G>C (p.Ala1008Pro) c.1804G>C (p.Ala602Pro) | |
| 15 | g.73323071C>T | CA393086422 | HCN4 | c.3022G>A (p.Ala1008Thr) c.1804G>A (p.Ala602Thr) | gnomAD v4 |
| 15 | g.73323072C>A | CA491478456 | HCN4 | c.3021G>T (p.Val1007=) c.1803G>T (p.Val601=) | gnomAD v4 |
| 15 | g.73323072C= | CA2187187406 | HCN4 | c.3021G= (p.Val1007=) c.1803G= (p.Val601=) | |
| 15 | g.73323072C>G | CA491478454 | HCN4 | c.3021G>C (p.Val1007=) c.1803G>C (p.Val601=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323072C>T | CA491478452 | HCN4 | c.3021G>A (p.Val1007=) c.1803G>A (p.Val601=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323072_73323079delinsCACAAGGG | CA2187187408 | HCN4 | c.3014_3021delinsCCCTTGTG (p.Ser1005=) c.1796_1803delinsCCCTTGTG (p.Ser599=) | |
| 15 | g.73323073A>C | CA393086426 | HCN4 | c.3020T>G (p.Val1007Gly) c.1802T>G (p.Val601Gly) | gnomAD v4 |
| 15 | g.73323073A>G | CA393086427 | HCN4 | c.3020T>C (p.Val1007Ala) c.1802T>C (p.Val601Ala) | ClinVar gnomAD v4 |
| 15 | g.73323073A>T | CA393086429 | HCN4 | c.3020T>A (p.Val1007Glu) c.1802T>A (p.Val601Glu) | |
| 15 | g.73323075_73323081del | CA971394547 | HCN4 | c.3014_3020del (p.Ser1005TrpfsTer11) c.1796_1802del (p.Ser599TrpfsTer11) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323074C>A | CA272663938 | HCN4 | c.3019G>T (p.Val1007Leu) c.1801G>T (p.Val601Leu) | dbSNP gnomAD v4 |
| 15 | g.73323074C= | CA2187187417 | HCN4 | c.3019G= (p.Val1007=) c.1801G= (p.Val601=) | |
| 15 | g.73323074C>G | CA393086431 | HCN4 | c.3019G>C (p.Val1007Leu) c.1801G>C (p.Val601Leu) | |
| 15 | g.73323074C>T | CA393086432 | HCN4 | c.3019G>A (p.Val1007Met) c.1801G>A (p.Val601Met) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323075A>C | CA491478462 | HCN4 | c.3018T>G (p.Leu1006=) c.1800T>G (p.Leu600=) | |
| 15 | g.73323075A>G | CA491478463 | HCN4 | c.3018T>C (p.Leu1006=) c.1800T>C (p.Leu600=) | gnomAD v4 |
| 15 | g.73323075A>T | CA491478465 | HCN4 | c.3018T>A (p.Leu1006=) c.1800T>A (p.Leu600=) | |
| 15 | g.73323076A= | CA2187187422 | HCN4 | c.3017T= (p.Leu1006=) c.1799T= (p.Leu600=) | |
| 15 | g.73323076A>C | CA393086434 | HCN4 | c.3017T>G (p.Leu1006Arg) c.1799T>G (p.Leu600Arg) | |
| 15 | g.73323076A>G | CA393086436 | HCN4 | c.3017T>C (p.Leu1006Pro) c.1799T>C (p.Leu600Pro) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323076A>T | CA393086438 | HCN4 | c.3017T>A (p.Leu1006His) c.1799T>A (p.Leu600His) | |
| 15 | g.73323077G>A | CA393086439 | HCN4 | c.3016C>T (p.Leu1006Phe) c.1798C>T (p.Leu600Phe) | gnomAD v4 |
| 15 | g.73323077G>C | CA393086440 | HCN4 | c.3016C>G (p.Leu1006Val) c.1798C>G (p.Leu600Val) | |
| 15 | g.73323077G>T | CA393086442 | HCN4 | c.3016C>A (p.Leu1006Ile) c.1798C>A (p.Leu600Ile) | gnomAD v4 |
| 15 | g.73323078G>A | CA491478469 | HCN4 | c.3015C>T (p.Ser1005=) c.1797C>T (p.Ser599=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323078G>C | CA491478472 | HCN4 | c.3015C>G (p.Ser1005=) c.1797C>G (p.Ser599=) | |
| 15 | g.73323078G= | CA2187187426 | HCN4 | c.3015C= (p.Ser1005=) c.1797C= (p.Ser599=) | |
| 15 | g.73323078G>T | CA491478473 | HCN4 | c.3015C>A (p.Ser1005=) c.1797C>A (p.Ser599=) | gnomAD v4 |
| 15 | g.73323079G>A | CA7648903 | HCN4 | c.3014C>T (p.Ser1005Phe) c.1796C>T (p.Ser599Phe) | ClinVar dbSNP ExAC gnomAD v4 |
| 15 | g.73323079G>C | CA393086446 | HCN4 | c.3014C>G (p.Ser1005Cys) c.1796C>G (p.Ser599Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323079G= | CA2187187433 | HCN4 | c.3014C= (p.Ser1005=) c.1796C= (p.Ser599=) | |
| 15 | g.73323079G>T | CA393086445 | HCN4 | c.3014C>A (p.Ser1005Tyr) c.1796C>A (p.Ser599Tyr) | gnomAD v4 |
| 15 | g.73323080A>C | CA393086448 | HCN4 | c.3013T>G (p.Ser1005Ala) c.1795T>G (p.Ser599Ala) | |
| 15 | g.73323080A>G | CA393086451 | HCN4 | c.3013T>C (p.Ser1005Pro) c.1795T>C (p.Ser599Pro) | gnomAD v4 |
| 15 | g.73323080A>T | CA393086450 | HCN4 | c.3013T>A (p.Ser1005Thr) c.1795T>A (p.Ser599Thr) | |
| 15 | g.73323081C>A | CA491478480 | HCN4 | c.3012G>T (p.Pro1004=) c.1794G>T (p.Pro598=) | gnomAD v4 |
| 15 | g.73323081C= | CA2187187439 | HCN4 | c.3012G= (p.Pro1004=) c.1794G= (p.Pro598=) | |
| 15 | g.73323081C>G | CA272663947 | HCN4 | c.3012G>C (p.Pro1004=) c.1794G>C (p.Pro598=) | dbSNP |
| 15 | g.73323081C>T | CA7648904 | HCN4 | c.3012G>A (p.Pro1004=) c.1794G>A (p.Pro598=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323082G>A | CA393086455 | HCN4 | c.3011C>T (p.Pro1004Leu) c.1793C>T (p.Pro598Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323082G>C | CA393086454 | HCN4 | c.3011C>G (p.Pro1004Arg) c.1793C>G (p.Pro598Arg) | gnomAD v4 |
| 15 | g.73323082G= | CA2187187444 | HCN4 | c.3011C= (p.Pro1004=) c.1793C= (p.Pro598=) | |
| 15 | g.73323082G>T | CA393086457 | HCN4 | c.3011C>A (p.Pro1004Gln) c.1793C>A (p.Pro598Gln) | gnomAD v4 |
| 15 | g.73323083del | CA2499223089 | HCN4 | c.3011del (p.Pro1004ArgfsTer14) c.1793del (p.Pro598ArgfsTer14) | ClinVar dbSNP |
| 15 | g.73323083G>A | CA7648905 | HCN4 | c.3010C>T (p.Pro1004Ser) c.1792C>T (p.Pro598Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323083G>C | CA393086458 | HCN4 | c.3010C>G (p.Pro1004Ala) c.1792C>G (p.Pro598Ala) | |
| 15 | g.73323083G= | CA2187187448 | HCN4 | c.3010C= (p.Pro1004=) c.1792C= (p.Pro598=) | |
| 15 | g.73323083G>T | CA393086460 | HCN4 | c.3010C>A (p.Pro1004Thr) c.1792C>A (p.Pro598Thr) | |
| 15 | g.73323084C>A | CA491478491 | HCN4 | c.3009G>T (p.Pro1003=) c.1791G>T (p.Pro597=) | gnomAD v4 |
| 15 | g.73323084C= | CA2187187456 | HCN4 | c.3009G= (p.Pro1003=) c.1791G= (p.Pro597=) | |
| 15 | g.73323084C>G | CA491478492 | HCN4 | c.3009G>C (p.Pro1003=) c.1791G>C (p.Pro597=) | |
| 15 | g.73323084C>T | CA7648906 | HCN4 | c.3009G>A (p.Pro1003=) c.1791G>A (p.Pro597=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323085G>A | CA393086462 | HCN4 | c.3008C>T (p.Pro1003Leu) c.1790C>T (p.Pro597Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323085G>C | CA393086464 | HCN4 | c.3008C>G (p.Pro1003Arg) c.1790C>G (p.Pro597Arg) | |
| 15 | g.73323085G= | CA2187187458 | HCN4 | c.3008C= (p.Pro1003=) c.1790C= (p.Pro597=) | |
| 15 | g.73323085G>T | CA393086466 | HCN4 | c.3008C>A (p.Pro1003Gln) c.1790C>A (p.Pro597Gln) | gnomAD v4 |
| 15 | g.73323086G>A | CA393086467 | HCN4 | c.3007C>T (p.Pro1003Ser) c.1789C>T (p.Pro597Ser) | gnomAD v4 |
| 15 | g.73323086G>C | CA393086469 | HCN4 | c.3007C>G (p.Pro1003Ala) c.1789C>G (p.Pro597Ala) | |
| 15 | g.73323086G>T | CA393086471 | HCN4 | c.3007C>A (p.Pro1003Thr) c.1789C>A (p.Pro597Thr) | gnomAD v4 |
| 15 | g.73323087C>A | CA393086473 | HCN4 | c.3006G>T (p.Glu1002Asp) c.1788G>T (p.Glu596Asp) | gnomAD v4 |
| 15 | g.73323087C>G | CA393086474 | HCN4 | c.3006G>C (p.Glu1002Asp) c.1788G>C (p.Glu596Asp) | |
| 15 | g.73323087C>T | CA491478498 | HCN4 | c.3006G>A (p.Glu1002=) c.1788G>A (p.Glu596=) | |
| 15 | g.73323088T>A | CA393086479 | HCN4 | c.3005A>T (p.Glu1002Val) c.1787A>T (p.Glu596Val) | |
| 15 | g.73323088T>C | CA393086477 | HCN4 | c.3005A>G (p.Glu1002Gly) c.1787A>G (p.Glu596Gly) | gnomAD v4 |
| 15 | g.73323088T>G | CA393086478 | HCN4 | c.3005A>C (p.Glu1002Ala) c.1787A>C (p.Glu596Ala) | |
| 15 | g.73323089C>A | CA393086481 | HCN4 | c.3004G>T (p.Glu1002Ter) c.1786G>T (p.Glu596Ter) | gnomAD v4 |
| 15 | g.73323089C= | CA2187187464 | HCN4 | c.3004G= (p.Glu1002=) c.1786G= (p.Glu596=) | |
| 15 | g.73323089C>G | CA16614917 | HCN4 | c.3004G>C (p.Glu1002Gln) c.1786G>C (p.Glu596Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323089C>T | CA393086483 | HCN4 | c.3004G>A (p.Glu1002Lys) c.1786G>A (p.Glu596Lys) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323090A>C | CA491478503 | HCN4 | c.3003T>G (p.Pro1001=) c.1785T>G (p.Pro595=) | |
| 15 | g.73323090A>G | CA491478504 | HCN4 | c.3003T>C (p.Pro1001=) c.1785T>C (p.Pro595=) | gnomAD v4 |
| 15 | g.73323090A>T | CA491478505 | HCN4 | c.3003T>A (p.Pro1001=) c.1785T>A (p.Pro595=) | gnomAD v4 |
| 15 | g.73323091G>A | CA393086485 | HCN4 | c.3002C>T (p.Pro1001Leu) c.1784C>T (p.Pro595Leu) | |
| 15 | g.73323091G>C | CA393086486 | HCN4 | c.3002C>G (p.Pro1001Arg) c.1784C>G (p.Pro595Arg) | |
| 15 | g.73323091G= | CA2187187469 | HCN4 | c.3002C= (p.Pro1001=) c.1784C= (p.Pro595=) | |
| 15 | g.73323091G>T | CA272663955 | HCN4 | c.3002C>A (p.Pro1001His) c.1784C>A (p.Pro595His) | dbSNP gnomAD v4 |
| 15 | g.73323092G>A | CA393086489 | HCN4 | c.3001C>T (p.Pro1001Ser) c.1783C>T (p.Pro595Ser) | gnomAD v4 |
| 15 | g.73323092G>C | CA393086491 | HCN4 | c.3001C>G (p.Pro1001Ala) c.1783C>G (p.Pro595Ala) | |
| 15 | g.73323092G>T | CA393086492 | HCN4 | c.3001C>A (p.Pro1001Thr) c.1783C>A (p.Pro595Thr) | ClinVar gnomAD v4 |
| 15 | g.73323093C>A | CA393086494 | HCN4 | c.3000G>T (p.Gln1000His) c.1782G>T (p.Gln594His) | gnomAD v4 |
| 15 | g.73323093C>G | CA393086495 | HCN4 | c.3000G>C (p.Gln1000His) c.1782G>C (p.Gln594His) | |
| 15 | g.73323093C>T | CA491478508 | HCN4 | c.3000G>A (p.Gln1000=) c.1782G>A (p.Gln594=) | gnomAD v4 |
| 15 | g.73323094T>A | CA393086500 | HCN4 | c.2999A>T (p.Gln1000Leu) c.1781A>T (p.Gln594Leu) | |
| 15 | g.73323094T>C | CA393086499 | HCN4 | c.2999A>G (p.Gln1000Arg) c.1781A>G (p.Gln594Arg) | |
| 15 | g.73323094T>G | CA393086497 | HCN4 | c.2999A>C (p.Gln1000Pro) c.1781A>C (p.Gln594Pro) | |
| 15 | g.73323095G>A | CA393086502 | HCN4 | c.2998C>T (p.Gln1000Ter) c.1780C>T (p.Gln594Ter) | gnomAD v4 |
| 15 | g.73323095G>C | CA393086504 | HCN4 | c.2998C>G (p.Gln1000Glu) c.1780C>G (p.Gln594Glu) | |
| 15 | g.73323095G= | CA2187187474 | HCN4 | c.2998C= (p.Gln1000=) c.1780C= (p.Gln594=) | |
| 15 | g.73323095G>T | CA393086506 | HCN4 | c.2998C>A (p.Gln1000Lys) c.1780C>A (p.Gln594Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323096C>A | CA491478517 | HCN4 | c.2997G>T (p.Arg999=) c.1779G>T (p.Arg593=) | gnomAD v4 |
| 15 | g.73323096C= | CA2187187481 | HCN4 | c.2997G= (p.Arg999=) c.1779G= (p.Arg593=) | |
| 15 | g.73323096C>G | CA7648907 | HCN4 | c.2997G>C (p.Arg999=) c.1779G>C (p.Arg593=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323096C>T | CA7648908 | HCN4 | c.2997G>A (p.Arg999=) c.1779G>A (p.Arg593=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323097C>A | CA393086514 | HCN4 | c.2996G>T (p.Arg999Leu) c.1778G>T (p.Arg593Leu) | gnomAD v4 |
| 15 | g.73323097C= | CA2187187487 | HCN4 | c.2996G= (p.Arg999=) c.1778G= (p.Arg593=) | |
| 15 | g.73323097C>G | CA393086516 | HCN4 | c.2996G>C (p.Arg999Pro) c.1778G>C (p.Arg593Pro) | |
| 15 | g.73323097C>T | CA393086517 | HCN4 | c.2996G>A (p.Arg999Gln) c.1778G>A (p.Arg593Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323098G>A | CA272663979 | HCN4 | c.2995C>T (p.Arg999Trp) c.1777C>T (p.Arg593Trp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323098G>C | CA393086522 | HCN4 | c.2995C>G (p.Arg999Gly) c.1777C>G (p.Arg593Gly) | |
| 15 | g.73323098G= | CA2187187494 | HCN4 | c.2995C= (p.Arg999=) c.1777C= (p.Arg593=) | |
| 15 | g.73323098G>T | CA491478524 | HCN4 | c.2995C>A (p.Arg999=) c.1777C>A (p.Arg593=) | gnomAD v4 |
| 15 | g.73323099T>A | CA491478526 | HCN4 | c.2994A>T (p.Pro998=) c.1776A>T (p.Pro592=) | |
| 15 | g.73323099T>C | CA491478527 | HCN4 | c.2994A>G (p.Pro998=) c.1776A>G (p.Pro592=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323099T>G | CA491478528 | HCN4 | c.2994A>C (p.Pro998=) c.1776A>C (p.Pro592=) | |
| 15 | g.73323099T= | CA2187187499 | HCN4 | c.2994A= (p.Pro998=) c.1776A= (p.Pro592=) | |
| 15 | g.73323100G>A | CA7648909 | HCN4 | c.2993C>T (p.Pro998Leu) c.1775C>T (p.Pro592Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323100G>C | CA393086525 | HCN4 | c.2993C>G (p.Pro998Arg) c.1775C>G (p.Pro592Arg) | |
| 15 | g.73323100G= | CA2187187502 | HCN4 | c.2993C= (p.Pro998=) c.1775C= (p.Pro592=) | |
| 15 | g.73323100G>T | CA393086528 | HCN4 | c.2993C>A (p.Pro998Gln) c.1775C>A (p.Pro592Gln) | gnomAD v4 |
| 15 | g.73323104del | CA491478535 | HCN4 | c.2993del (p.Pro998HisfsTer20) c.1775del (p.Pro592HisfsTer20) | gnomAD v4 COSMIC |
| 15 | g.73323101G>A | CA393086536 | HCN4 | c.2992C>T (p.Pro998Ser) c.1774C>T (p.Pro592Ser) | gnomAD v4 |
| 15 | g.73323101G>C | CA7648910 | HCN4 | c.2992C>G (p.Pro998Ala) c.1774C>G (p.Pro592Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323101G= | CA2187187504 | HCN4 | c.2992C= (p.Pro998=) c.1774C= (p.Pro592=) | |
| 15 | g.73323101G>T | CA393086534 | HCN4 | c.2992C>A (p.Pro998Thr) c.1774C>A (p.Pro592Thr) | gnomAD v4 |
| 15 | g.73323102G>A | CA491478537 | HCN4 | c.2991C>T (p.Pro997=) c.1773C>T (p.Pro591=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323102G>C | CA491478539 | HCN4 | c.2991C>G (p.Pro997=) c.1773C>G (p.Pro591=) | gnomAD v4 |
| 15 | g.73323102G= | CA2187187506 | HCN4 | c.2991C= (p.Pro997=) c.1773C= (p.Pro591=) | |
| 15 | g.73323102G>T | CA491478540 | HCN4 | c.2991C>A (p.Pro997=) c.1773C>A (p.Pro591=) | |
| 15 | g.73323103G>A | CA393086539 | HCN4 | c.2990C>T (p.Pro997Leu) c.1772C>T (p.Pro591Leu) | gnomAD v4 |
| 15 | g.73323103G>C | CA393086541 | HCN4 | c.2990C>G (p.Pro997Arg) c.1772C>G (p.Pro591Arg) | |
| 15 | g.73323103G= | CA2187187511 | HCN4 | c.2990C= (p.Pro997=) c.1772C= (p.Pro591=) | |
| 15 | g.73323103G>T | CA272663982 | HCN4 | c.2990C>A (p.Pro997His) c.1772C>A (p.Pro591His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323104G>A | CA393086551 | HCN4 | c.2989C>T (p.Pro997Ser) c.1771C>T (p.Pro591Ser) | gnomAD v4 |
| 15 | g.73323104G>C | CA393086554 | HCN4 | c.2989C>G (p.Pro997Ala) c.1771C>G (p.Pro591Ala) | |
| 15 | g.73323104G= | CA2187187516 | HCN4 | c.2989C= (p.Pro997=) c.1771C= (p.Pro591=) | |
| 15 | g.73323104G>T | CA7648911 | HCN4 | c.2989C>A (p.Pro997Thr) c.1771C>A (p.Pro591Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323105T>A | CA491478550 | HCN4 | c.2988A>T (p.Thr996=) c.1770A>T (p.Thr590=) | dbSNP |
| 15 | g.73323105T>C | CA491478551 | HCN4 | c.2988A>G (p.Thr996=) c.1770A>G (p.Thr590=) | gnomAD v4 |
| 15 | g.73323105T>G | CA491478553 | HCN4 | c.2988A>C (p.Thr996=) c.1770A>C (p.Thr590=) | ClinVar |
| 15 | g.73323105T= | CA2187187520 | HCN4 | c.2988A= (p.Thr996=) c.1770A= (p.Thr590=) | |
| 15 | g.73323106G>A | CA393086559 | HCN4 | c.2987C>T (p.Thr996Ile) c.1769C>T (p.Thr590Ile) | gnomAD v4 |
| 15 | g.73323106G>C | CA393086561 | HCN4 | c.2987C>G (p.Thr996Arg) c.1769C>G (p.Thr590Arg) | |
| 15 | g.73323106G>T | CA393086563 | HCN4 | c.2987C>A (p.Thr996Lys) c.1769C>A (p.Thr590Lys) | gnomAD v4 |
| 15 | g.73323107T>A | CA393086567 | HCN4 | c.2986A>T (p.Thr996Ser) c.1768A>T (p.Thr590Ser) | dbSNP |
| 15 | g.73323107T>C | CA393086568 | HCN4 | c.2986A>G (p.Thr996Ala) c.1768A>G (p.Thr590Ala) | gnomAD v4 |
| 15 | g.73323107T>G | CA393086570 | HCN4 | c.2986A>C (p.Thr996Pro) c.1768A>C (p.Thr590Pro) | |
| 15 | g.73323107T= | CA2187187523 | HCN4 | c.2986A= (p.Thr996=) c.1768A= (p.Thr590=) | |
| 15 | g.73323108C>A | CA393086573 | HCN4 | c.2985G>T (p.Glu995Asp) c.1767G>T (p.Glu589Asp) | gnomAD v4 |
| 15 | g.73323108C>G | CA393086575 | HCN4 | c.2985G>C (p.Glu995Asp) c.1767G>C (p.Glu589Asp) | ClinVar gnomAD v4 |
| 15 | g.73323108C>T | CA491478563 | HCN4 | c.2985G>A (p.Glu995=) c.1767G>A (p.Glu589=) | gnomAD v4 |
| 15 | g.73323109T>A | CA393086579 | HCN4 | c.2984A>T (p.Glu995Val) c.1766A>T (p.Glu589Val) | |
| 15 | g.73323109T>C | CA393086583 | HCN4 | c.2984A>G (p.Glu995Gly) c.1766A>G (p.Glu589Gly) | gnomAD v4 |
| 15 | g.73323109T>G | CA393086581 | HCN4 | c.2984A>C (p.Glu995Ala) c.1766A>C (p.Glu589Ala) | |
| 15 | g.73323110C>A | CA393086587 | HCN4 | c.2983G>T (p.Glu995Ter) c.1765G>T (p.Glu589Ter) | gnomAD v4 |
| 15 | g.73323110C>G | CA393086590 | HCN4 | c.2983G>C (p.Glu995Gln) c.1765G>C (p.Glu589Gln) | |
| 15 | g.73323110C>T | CA393086591 | HCN4 | c.2983G>A (p.Glu995Lys) c.1765G>A (p.Glu589Lys) | |
| 15 | g.73323111T>A | CA491478567 | HCN4 | c.2982A>T (p.Pro994=) c.1764A>T (p.Pro588=) | |
| 15 | g.73323111T>C | CA491478570 | HCN4 | c.2982A>G (p.Pro994=) c.1764A>G (p.Pro588=) | dbSNP |
| 15 | g.73323111T>G | CA491478573 | HCN4 | c.2982A>C (p.Pro994=) c.1764A>C (p.Pro588=) | |
| 15 | g.73323111T= | CA2187187525 | HCN4 | c.2982A= (p.Pro994=) c.1764A= (p.Pro588=) | |
| 15 | g.73323112G>A | CA393086595 | HCN4 | c.2981C>T (p.Pro994Leu) c.1763C>T (p.Pro588Leu) | gnomAD v4 |
| 15 | g.73323112G>C | CA393086597 | HCN4 | c.2981C>G (p.Pro994Arg) c.1763C>G (p.Pro588Arg) | |
| 15 | g.73323112G>T | CA393086599 | HCN4 | c.2981C>A (p.Pro994Gln) c.1763C>A (p.Pro588Gln) | gnomAD v4 |
| 15 | g.73323113G>A | CA393086602 | HCN4 | c.2980C>T (p.Pro994Ser) c.1762C>T (p.Pro588Ser) | gnomAD v4 |
| 15 | g.73323113G>C | CA393086603 | HCN4 | c.2980C>G (p.Pro994Ala) c.1762C>G (p.Pro588Ala) | |
| 15 | g.73323113G>T | CA393086606 | HCN4 | c.2980C>A (p.Pro994Thr) c.1762C>A (p.Pro588Thr) | |
| 15 | g.73323114C>A | CA491478585 | HCN4 | c.2979G>T (p.Thr993=) c.1761G>T (p.Thr587=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323114C= | CA2187187528 | HCN4 | c.2979G= (p.Thr993=) c.1761G= (p.Thr587=) | |
| 15 | g.73323114C>G | CA491478584 | HCN4 | c.2979G>C (p.Thr993=) c.1761G>C (p.Thr587=) | ClinVar |
| 15 | g.73323114C>T | CA203637 | HCN4 | c.2979G>A (p.Thr993=) c.1761G>A (p.Thr587=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323115G>A | CA7648912 | HCN4 | c.2978C>T (p.Thr993Met) c.1760C>T (p.Thr587Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323115G>C | CA393086610 | HCN4 | c.2978C>G (p.Thr993Arg) c.1760C>G (p.Thr587Arg) | gnomAD v4 |
| 15 | g.73323115G= | CA2187187536 | HCN4 | c.2978C= (p.Thr993=) c.1760C= (p.Thr587=) | |
| 15 | g.73323115G>T | CA393086609 | HCN4 | c.2978C>A (p.Thr993Lys) c.1760C>A (p.Thr587Lys) | COSMIC |
| 15 | g.73323116T>A | CA393086614 | HCN4 | c.2977A>T (p.Thr993Ser) c.1759A>T (p.Thr587Ser) | dbSNP |
| 15 | g.73323116T>C | CA393086615 | HCN4 | c.2977A>G (p.Thr993Ala) c.1759A>G (p.Thr587Ala) | gnomAD v4 |
| 15 | g.73323116T>G | CA393086617 | HCN4 | c.2977A>C (p.Thr993Pro) c.1759A>C (p.Thr587Pro) | |
| 15 | g.73323116T= | CA2187187541 | HCN4 | c.2977A= (p.Thr993=) c.1759A= (p.Thr587=) | |
| 15 | g.73323117G>A | CA7648913 | HCN4 | c.2976C>T (p.Ser992=) c.1758C>T (p.Ser586=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323117G>C | CA393086619 | HCN4 | c.2976C>G (p.Ser992Arg) c.1758C>G (p.Ser586Arg) | |
| 15 | g.73323117G= | CA2187187543 | HCN4 | c.2976C= (p.Ser992=) c.1758C= (p.Ser586=) | |
| 15 | g.73323117G>T | CA393086620 | HCN4 | c.2976C>A (p.Ser992Arg) c.1758C>A (p.Ser586Arg) | gnomAD v4 |
| 15 | g.73323118C>A | CA7648914 | HCN4 | c.2975G>T (p.Ser992Ile) c.1757G>T (p.Ser586Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323118C= | CA2187187548 | HCN4 | c.2975G= (p.Ser992=) c.1757G= (p.Ser586=) | |
| 15 | g.73323118C>G | CA393086622 | HCN4 | c.2975G>C (p.Ser992Thr) c.1757G>C (p.Ser586Thr) | |
| 15 | g.73323118C>T | CA393086623 | HCN4 | c.2975G>A (p.Ser992Asn) c.1757G>A (p.Ser586Asn) | gnomAD v4 |
| 15 | g.73323119T>A | CA393086625 | HCN4 | c.2974A>T (p.Ser992Cys) c.1756A>T (p.Ser586Cys) | |
| 15 | g.73323119T>C | CA393086627 | HCN4 | c.2974A>G (p.Ser992Gly) c.1756A>G (p.Ser586Gly) | gnomAD v4 |
| 15 | g.73323119T>G | CA393086628 | HCN4 | c.2974A>C (p.Ser992Arg) c.1756A>C (p.Ser586Arg) | |
| 15 | g.73323120C>A | CA491478598 | HCN4 | c.2973G>T (p.Leu991=) c.1755G>T (p.Leu585=) | gnomAD v4 |
| 15 | g.73323120C= | CA2187187551 | HCN4 | c.2973G= (p.Leu991=) c.1755G= (p.Leu585=) | |
| 15 | g.73323120C>G | CA491478601 | HCN4 | c.2973G>C (p.Leu991=) c.1755G>C (p.Leu585=) | |
| 15 | g.73323120C>T | CA491478600 | HCN4 | c.2973G>A (p.Leu991=) c.1755G>A (p.Leu585=) | dbSNP |
| 15 | g.73323121A= | CA2187187553 | HCN4 | c.2972T= (p.Leu991=) c.1754T= (p.Leu585=) | |
| 15 | g.73323121A>C | CA393086631 | HCN4 | c.2972T>G (p.Leu991Arg) c.1754T>G (p.Leu585Arg) | |
| 15 | g.73323121A>G | CA272663993 | HCN4 | c.2972T>C (p.Leu991Pro) c.1754T>C (p.Leu585Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323121A>T | CA393086629 | HCN4 | c.2972T>A (p.Leu991Gln) c.1754T>A (p.Leu585Gln) | |
| 15 | g.73323122G>A | CA491478607 | HCN4 | c.2971C>T (p.Leu991=) c.1753C>T (p.Leu585=) | gnomAD v4 |
| 15 | g.73323122G>C | CA393086633 | HCN4 | c.2971C>G (p.Leu991Val) c.1753C>G (p.Leu585Val) | |
| 15 | g.73323122G>T | CA393086634 | HCN4 | c.2971C>A (p.Leu991Met) c.1753C>A (p.Leu585Met) | gnomAD v4 COSMIC |
| 15 | g.73323123T>A | CA491478609 | HCN4 | c.2970A>T (p.Pro990=) c.1752A>T (p.Pro584=) | gnomAD v4 |
| 15 | g.73323123T>C | CA491478611 | HCN4 | c.2970A>G (p.Pro990=) c.1752A>G (p.Pro584=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323123T>G | CA491478613 | HCN4 | c.2970A>C (p.Pro990=) c.1752A>C (p.Pro584=) | |
| 15 | g.73323123T= | CA2187187556 | HCN4 | c.2970A= (p.Pro990=) c.1752A= (p.Pro584=) | |
| 15 | g.73323124G>A | CA7648915 | HCN4 | c.2969C>T (p.Pro990Leu) c.1751C>T (p.Pro584Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323124G>C | CA393086637 | HCN4 | c.2969C>G (p.Pro990Arg) c.1751C>G (p.Pro584Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323124G= | CA2187187559 | HCN4 | c.2969C= (p.Pro990=) c.1751C= (p.Pro584=) | |
| 15 | g.73323124G>T | CA393086639 | HCN4 | c.2969C>A (p.Pro990Gln) c.1751C>A (p.Pro584Gln) | gnomAD v4 |
| 15 | g.73323125G>A | CA393086643 | HCN4 | c.2968C>T (p.Pro990Ser) c.1750C>T (p.Pro584Ser) | gnomAD v4 |
| 15 | g.73323125G>C | CA393086642 | HCN4 | c.2968C>G (p.Pro990Ala) c.1750C>G (p.Pro584Ala) | ClinVar dbSNP |
| 15 | g.73323125G>T | CA393086640 | HCN4 | c.2968C>A (p.Pro990Thr) c.1750C>A (p.Pro584Thr) | gnomAD v4 |
| 15 | g.73323126G>A | CA491478615 | HCN4 | c.2967C>T (p.Gly989=) c.1749C>T (p.Gly583=) | gnomAD v4 |
| 15 | g.73323126G>C | CA491478617 | HCN4 | c.2967C>G (p.Gly989=) c.1749C>G (p.Gly583=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323126G= | CA2187187563 | HCN4 | c.2967C= (p.Gly989=) c.1749C= (p.Gly583=) | |
| 15 | g.73323126G>T | CA491478620 | HCN4 | c.2967C>A (p.Gly989=) c.1749C>A (p.Gly583=) | gnomAD v4 |
| 15 | g.73323127C>A | CA393086645 | HCN4 | c.2966G>T (p.Gly989Val) c.1748G>T (p.Gly583Val) | gnomAD v4 |
| 15 | g.73323127C>G | CA393086646 | HCN4 | c.2966G>C (p.Gly989Ala) c.1748G>C (p.Gly583Ala) | |
| 15 | g.73323127C>T | CA393086648 | HCN4 | c.2966G>A (p.Gly989Asp) c.1748G>A (p.Gly583Asp) | gnomAD v4 |
| 15 | g.73323128C>A | CA393086650 | HCN4 | c.2965G>T (p.Gly989Cys) c.1747G>T (p.Gly583Cys) | gnomAD v4 |
| 15 | g.73323128C>G | CA393086651 | HCN4 | c.2965G>C (p.Gly989Arg) c.1747G>C (p.Gly583Arg) | |
| 15 | g.73323128C>T | CA393086653 | HCN4 | c.2965G>A (p.Gly989Ser) c.1747G>A (p.Gly583Ser) | gnomAD v4 |
| 15 | g.73323129A= | CA2187187566 | HCN4 | c.2964T= (p.Thr988=) c.1746T= (p.Thr582=) | |
| 15 | g.73323129A>C | CA491478623 | HCN4 | c.2964T>G (p.Thr988=) c.1746T>G (p.Thr582=) | |
| 15 | g.73323129A>G | CA491478625 | HCN4 | c.2964T>C (p.Thr988=) c.1746T>C (p.Thr582=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323129A>T | CA491478629 | HCN4 | c.2964T>A (p.Thr988=) c.1746T>A (p.Thr582=) | gnomAD v4 |
| 15 | g.73323130G>A | CA393086654 | HCN4 | c.2963C>T (p.Thr988Ile) c.1745C>T (p.Thr582Ile) | gnomAD v4 |
| 15 | g.73323130G>C | CA393086656 | HCN4 | c.2963C>G (p.Thr988Ser) c.1745C>G (p.Thr582Ser) | |
| 15 | g.73323130G>T | CA393086655 | HCN4 | c.2963C>A (p.Thr988Asn) c.1745C>A (p.Thr582Asn) | gnomAD v4 |
| 15 | g.73323131T>A | CA393086658 | HCN4 | c.2962A>T (p.Thr988Ser) c.1744A>T (p.Thr582Ser) | gnomAD v4 |
| 15 | g.73323131T>C | CA393086660 | HCN4 | c.2962A>G (p.Thr988Ala) c.1744A>G (p.Thr582Ala) | |
| 15 | g.73323131T>G | CA393086661 | HCN4 | c.2962A>C (p.Thr988Pro) c.1744A>C (p.Thr582Pro) | |
| 15 | g.73323132G>A | CA491478635 | HCN4 | c.2961C>T (p.Ala987=) c.1743C>T (p.Ala581=) | gnomAD v4 |
| 15 | g.73323132G>C | CA491478636 | HCN4 | c.2961C>G (p.Ala987=) c.1743C>G (p.Ala581=) | |
| 15 | g.73323132G>T | CA491478638 | HCN4 | c.2961C>A (p.Ala987=) c.1743C>A (p.Ala581=) | gnomAD v4 |
| 15 | g.73323133G>A | CA393086663 | HCN4 | c.2960C>T (p.Ala987Val) c.1742C>T (p.Ala581Val) | gnomAD v4 |
| 15 | g.73323133G>C | CA393086665 | HCN4 | c.2960C>G (p.Ala987Gly) c.1742C>G (p.Ala581Gly) | |
| 15 | g.73323133G>T | CA393086666 | HCN4 | c.2960C>A (p.Ala987Asp) c.1742C>A (p.Ala581Asp) | gnomAD v4 |
| 15 | g.73323134C>A | CA393086669 | HCN4 | c.2959G>T (p.Ala987Ser) c.1741G>T (p.Ala581Ser) | gnomAD v4 |
| 15 | g.73323134C>G | CA393086672 | HCN4 | c.2959G>C (p.Ala987Pro) c.1741G>C (p.Ala581Pro) | |
| 15 | g.73323134C>T | CA393086674 | HCN4 | c.2959G>A (p.Ala987Thr) c.1741G>A (p.Ala581Thr) | gnomAD v4 |
| 15 | g.73323135C>A | CA491478644 | HCN4 | c.2958G>T (p.Leu986=) c.1740G>T (p.Leu580=) | gnomAD v4 |
| 15 | g.73323135C>G | CA491478645 | HCN4 | c.2958G>C (p.Leu986=) c.1740G>C (p.Leu580=) | |
| 15 | g.73323135C>T | CA491478647 | HCN4 | c.2958G>A (p.Leu986=) c.1740G>A (p.Leu580=) | gnomAD v4 |
| 15 | g.73323136A>C | CA393086677 | HCN4 | c.2957T>G (p.Leu986Arg) c.1739T>G (p.Leu580Arg) | |
| 15 | g.73323136A>G | CA393086680 | HCN4 | c.2957T>C (p.Leu986Pro) c.1739T>C (p.Leu580Pro) | gnomAD v4 |
| 15 | g.73323136A>T | CA393086682 | HCN4 | c.2957T>A (p.Leu986Gln) c.1739T>A (p.Leu580Gln) | gnomAD v4 |
| 15 | g.73323137G>A | CA491478651 | HCN4 | c.2956C>T (p.Leu986=) c.1738C>T (p.Leu580=) | gnomAD v4 |
| 15 | g.73323137G>C | CA393086685 | HCN4 | c.2956C>G (p.Leu986Val) c.1738C>G (p.Leu580Val) | |
| 15 | g.73323137G>T | CA393086687 | HCN4 | c.2956C>A (p.Leu986Met) c.1738C>A (p.Leu580Met) | gnomAD v4 |
| 15 | g.73323138A= | CA2187187569 | HCN4 | c.2955T= (p.Gly985=) c.1737T= (p.Gly579=) | |
| 15 | g.73323138A>C | CA491478655 | HCN4 | c.2955T>G (p.Gly985=) c.1737T>G (p.Gly579=) | |
| 15 | g.73323138A>G | CA491478656 | HCN4 | c.2955T>C (p.Gly985=) c.1737T>C (p.Gly579=) | dbSNP gnomAD v4 |
| 15 | g.73323138A>T | CA491478657 | HCN4 | c.2955T>A (p.Gly985=) c.1737T>A (p.Gly579=) | |
| 15 | g.73323139C>A | CA393086690 | HCN4 | c.2954G>T (p.Gly985Val) c.1736G>T (p.Gly579Val) | gnomAD v4 |
| 15 | g.73323139C>G | CA393086693 | HCN4 | c.2954G>C (p.Gly985Ala) c.1736G>C (p.Gly579Ala) | |
| 15 | g.73323139C>T | CA393086696 | HCN4 | c.2954G>A (p.Gly985Asp) c.1736G>A (p.Gly579Asp) | |
| 15 | g.73323140C>A | CA393086698 | HCN4 | c.2953G>T (p.Gly985Cys) c.1735G>T (p.Gly579Cys) | gnomAD v4 |
| 15 | g.73323140C>G | CA393086706 | HCN4 | c.2953G>C (p.Gly985Arg) c.1735G>C (p.Gly579Arg) | |
| 15 | g.73323140C>T | CA393086709 | HCN4 | c.2953G>A (p.Gly985Ser) c.1735G>A (p.Gly579Ser) | gnomAD v4 |
| 15 | g.73323141T>A | CA491478667 | HCN4 | c.2952A>T (p.Leu984=) c.1734A>T (p.Leu578=) | gnomAD v4 |
| 15 | g.73323141T>C | CA7648916 | HCN4 | c.2952A>G (p.Leu984=) c.1734A>G (p.Leu578=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323141T>G | CA491478666 | HCN4 | c.2952A>C (p.Leu984=) c.1734A>C (p.Leu578=) | |
| 15 | g.73323141T= | CA2187187571 | HCN4 | c.2952A= (p.Leu984=) c.1734A= (p.Leu578=) | |
| 15 | g.73323142A>C | CA393086718 | HCN4 | c.2951T>G (p.Leu984Arg) c.1733T>G (p.Leu578Arg) | |
| 15 | g.73323142A>G | CA393086713 | HCN4 | c.2951T>C (p.Leu984Pro) c.1733T>C (p.Leu578Pro) | gnomAD v4 |
| 15 | g.73323142A>T | CA393086714 | HCN4 | c.2951T>A (p.Leu984Gln) c.1733T>A (p.Leu578Gln) | |
| 15 | g.73323143G>A | CA491478668 | HCN4 | c.2950C>T (p.Leu984=) c.1732C>T (p.Leu578=) | gnomAD v4 |
| 15 | g.73323143G>C | CA393086721 | HCN4 | c.2950C>G (p.Leu984Val) c.1732C>G (p.Leu578Val) | ClinVar dbSNP |
| 15 | g.73323143G>T | CA393086724 | HCN4 | c.2950C>A (p.Leu984Ile) c.1732C>A (p.Leu578Ile) | gnomAD v4 |
| 15 | g.73323143_73323144insT | CA2804714152 | HCN4 | c.2949_2950insA (p.Leu984ThrfsTer19) c.1731_1732insA (p.Leu578ThrfsTer19) | |
| 15 | g.73323144G>A | CA272664002 | HCN4 | c.2949C>T (p.Ser983=) c.1731C>T (p.Ser577=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323144G>C | CA491478673 | HCN4 | c.2949C>G (p.Ser983=) c.1731C>G (p.Ser577=) | |
| 15 | g.73323144G= | CA2187187574 | HCN4 | c.2949C= (p.Ser983=) c.1731C= (p.Ser577=) | |
| 15 | g.73323144G>T | CA491478675 | HCN4 | c.2949C>A (p.Ser983=) c.1731C>A (p.Ser577=) | gnomAD v4 |
| 15 | g.73323145G>A | CA7648917 | HCN4 | c.2948C>T (p.Ser983Phe) c.1730C>T (p.Ser577Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323145G>C | CA393086731 | HCN4 | c.2948C>G (p.Ser983Cys) c.1730C>G (p.Ser577Cys) | |
| 15 | g.73323145G= | CA2187187576 | HCN4 | c.2948C= (p.Ser983=) c.1730C= (p.Ser577=) | |
| 15 | g.73323145G>T | CA393086734 | HCN4 | c.2948C>A (p.Ser983Tyr) c.1730C>A (p.Ser577Tyr) | gnomAD v4 |
| 15 | g.73323146A>C | CA393086736 | HCN4 | c.2947T>G (p.Ser983Ala) c.1729T>G (p.Ser577Ala) | |
| 15 | g.73323146A>G | CA393086741 | HCN4 | c.2947T>C (p.Ser983Pro) c.1729T>C (p.Ser577Pro) | |
| 15 | g.73323146A>T | CA393086739 | HCN4 | c.2947T>A (p.Ser983Thr) c.1729T>A (p.Ser577Thr) | gnomAD v4 |
| 15 | g.73323147C>A | CA393086744 | HCN4 | c.2946G>T (p.Leu982Phe) c.1728G>T (p.Leu576Phe) | gnomAD v4 |
| 15 | g.73323147C= | CA2187187581 | HCN4 | c.2946G= (p.Leu982=) c.1728G= (p.Leu576=) | |
| 15 | g.73323147C>G | CA393086747 | HCN4 | c.2946G>C (p.Leu982Phe) c.1728G>C (p.Leu576Phe) | |
| 15 | g.73323147C>T | CA16607136 | HCN4 | c.2946G>A (p.Leu982=) c.1728G>A (p.Leu576=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323148A>C | CA393086749 | HCN4 | c.2945T>G (p.Leu982Trp) c.1727T>G (p.Leu576Trp) | |
| 15 | g.73323148A>G | CA393086751 | HCN4 | c.2945T>C (p.Leu982Ser) c.1727T>C (p.Leu576Ser) | gnomAD v4 |
| 15 | g.73323148A>T | CA393086753 | HCN4 | c.2945T>A (p.Leu982Ter) c.1727T>A (p.Leu576Ter) | |
| 15 | g.73323149A>C | CA393086755 | HCN4 | c.2944T>G (p.Leu982Val) c.1726T>G (p.Leu576Val) | |
| 15 | g.73323149A>G | CA491478682 | HCN4 | c.2944T>C (p.Leu982=) c.1726T>C (p.Leu576=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323149A>T | CA393086758 | HCN4 | c.2944T>A (p.Leu982Met) c.1726T>A (p.Leu576Met) | |
| 15 | g.73323150C>A | CA393086760 | HCN4 | c.2943G>T (p.Glu981Asp) c.1725G>T (p.Glu575Asp) | gnomAD v4 |
| 15 | g.73323150C>G | CA393086762 | HCN4 | c.2943G>C (p.Glu981Asp) c.1725G>C (p.Glu575Asp) | gnomAD v4 COSMIC |
| 15 | g.73323150C>T | CA491478684 | HCN4 | c.2943G>A (p.Glu981=) c.1725G>A (p.Glu575=) | gnomAD v4 |
| 15 | g.73323159_73323250del | CA619410578 | HCN4 | c.2852_2943del (p.Gly951ValfsTer21) c.1634_1725del (p.Gly545ValfsTer21) | gnomAD v2 |
| 15 | g.73323151T>A | CA393086766 | HCN4 | c.2942A>T (p.Glu981Val) c.1724A>T (p.Glu575Val) | |
| 15 | g.73323151T>C | CA393086769 | HCN4 | c.2942A>G (p.Glu981Gly) c.1724A>G (p.Glu575Gly) | gnomAD v4 |
| 15 | g.73323151T>G | CA393086771 | HCN4 | c.2942A>C (p.Glu981Ala) c.1724A>C (p.Glu575Ala) | |
| 15 | g.73323152C>A | CA393086774 | HCN4 | c.2941G>T (p.Glu981Ter) c.1723G>T (p.Glu575Ter) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323152C= | CA2187187584 | HCN4 | c.2941G= (p.Glu981=) c.1723G= (p.Glu575=) | |
| 15 | g.73323152C>G | CA393086778 | HCN4 | c.2941G>C (p.Glu981Gln) c.1723G>C (p.Glu575Gln) | |
| 15 | g.73323152C>T | CA393086776 | HCN4 | c.2941G>A (p.Glu981Lys) c.1723G>A (p.Glu575Lys) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323155del | CA2629370546 | HCN4 | c.2941del (p.Glu981SerfsTer4) c.1723del (p.Glu575SerfsTer4) | gnomAD v4 |
| 15 | g.73323153C>A | CA491478692 | HCN4 | c.2940G>T (p.Gly980=) c.1722G>T (p.Gly574=) | gnomAD v4 |
| 15 | g.73323153C>G | CA491478694 | HCN4 | c.2940G>C (p.Gly980=) c.1722G>C (p.Gly574=) | ClinVar |
| 15 | g.73323153C>T | CA491478693 | HCN4 | c.2940G>A (p.Gly980=) c.1722G>A (p.Gly574=) | gnomAD v4 COSMIC |
| 15 | g.73323154C>A | CA393086782 | HCN4 | c.2939G>T (p.Gly980Val) c.1721G>T (p.Gly574Val) | |
| 15 | g.73323154C= | CA2187187591 | HCN4 | c.2939G= (p.Gly980=) c.1721G= (p.Gly574=) | |
| 15 | g.73323154C>G | CA7648918 | HCN4 | c.2939G>C (p.Gly980Ala) c.1721G>C (p.Gly574Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323154C>T | CA393086786 | HCN4 | c.2939G>A (p.Gly980Glu) c.1721G>A (p.Gly574Glu) | ClinVar gnomAD v4 |
| 15 | g.73323155C>A | CA393086790 | HCN4 | c.2938G>T (p.Gly980Trp) c.1720G>T (p.Gly574Trp) | gnomAD v4 COSMIC |
| 15 | g.73323155C= | CA2187187599 | HCN4 | c.2938G= (p.Gly980=) c.1720G= (p.Gly574=) | |
| 15 | g.73323155C>G | CA393086791 | HCN4 | c.2938G>C (p.Gly980Arg) c.1720G>C (p.Gly574Arg) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323155C>T | CA7648919 | HCN4 | c.2938G>A (p.Gly980Arg) c.1720G>A (p.Gly574Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323156G>A | CA7648920 | HCN4 | c.2937C>T (p.Pro979=) c.1719C>T (p.Pro573=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323156G>C | CA491478702 | HCN4 | c.2937C>G (p.Pro979=) c.1719C>G (p.Pro573=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323156G= | CA2187187605 | HCN4 | c.2937C= (p.Pro979=) c.1719C= (p.Pro573=) | |
| 15 | g.73323156G>T | CA7648921 | HCN4 | c.2937C>A (p.Pro979=) c.1719C>A (p.Pro573=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323158del | CA2629370547 | HCN4 | c.2937del (p.Glu981SerfsTer4) c.1719del (p.Glu575SerfsTer4) | gnomAD v4 |
| 15 | g.73323157G>A | CA393086799 | HCN4 | c.2936C>T (p.Pro979Leu) c.1718C>T (p.Pro573Leu) | gnomAD v4 |
| 15 | g.73323157G>C | CA393086801 | HCN4 | c.2936C>G (p.Pro979Arg) c.1718C>G (p.Pro573Arg) | |
| 15 | g.73323157G>T | CA393086804 | HCN4 | c.2936C>A (p.Pro979His) c.1718C>A (p.Pro573His) |