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.73324121T>A | CA393089929 | HCN4 | c.2111A>T (p.Glu704Val) c.893A>T (p.Glu298Val) | |
| 15 | g.73324121T>C | CA393089931 | HCN4 | c.2111A>G (p.Glu704Gly) c.893A>G (p.Glu298Gly) | |
| 15 | g.73324121T>G | CA393089933 | HCN4 | c.2111A>C (p.Glu704Ala) c.893A>C (p.Glu298Ala) | |
| 15 | g.73324122C>A | CA393089935 | HCN4 | c.2110G>T (p.Glu704Ter) c.892G>T (p.Glu298Ter) | |
| 15 | g.73324122C>G | CA393089939 | HCN4 | c.2110G>C (p.Glu704Gln) c.892G>C (p.Glu298Gln) | |
| 15 | g.73324122C>T | CA393089937 | HCN4 | c.2110G>A (p.Glu704Lys) c.892G>A (p.Glu298Lys) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73324123G>A | CA7649127 | HCN4 | c.2109C>T (p.Phe703=) c.891C>T (p.Phe297=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324123G>C | CA393089943 | HCN4 | c.2109C>G (p.Phe703Leu) c.891C>G (p.Phe297Leu) | |
| 15 | g.73324123G= | CA2187189069 | HCN4 | c.2109C= (p.Phe703=) c.891C= (p.Phe297=) | |
| 15 | g.73324123G>T | CA393089945 | HCN4 | c.2109C>A (p.Phe703Leu) c.891C>A (p.Phe297Leu) | |
| 15 | g.73324124A>C | CA393089947 | HCN4 | c.2108T>G (p.Phe703Cys) c.890T>G (p.Phe297Cys) | |
| 15 | g.73324124A>G | CA393089949 | HCN4 | c.2108T>C (p.Phe703Ser) c.890T>C (p.Phe297Ser) | |
| 15 | g.73324124A>T | CA393089950 | HCN4 | c.2108T>A (p.Phe703Tyr) c.890T>A (p.Phe297Tyr) | |
| 15 | g.73324125A>C | CA393089953 | HCN4 | c.2107T>G (p.Phe703Val) c.889T>G (p.Phe297Val) | |
| 15 | g.73324125A>G | CA393089956 | HCN4 | c.2107T>C (p.Phe703Leu) c.889T>C (p.Phe297Leu) | ClinVar |
| 15 | g.73324125A>T | CA393089958 | HCN4 | c.2107T>A (p.Phe703Ile) c.889T>A (p.Phe297Ile) | |
| 15 | g.73324126G>A | CA272665439 | HCN4 | c.2106C>T (p.Ala702=) c.888C>T (p.Ala296=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324126G>C | CA491478840 | HCN4 | c.2106C>G (p.Ala702=) c.888C>G (p.Ala296=) | |
| 15 | g.73324126G= | CA2187189075 | HCN4 | c.2106C= (p.Ala702=) c.888C= (p.Ala296=) | |
| 15 | g.73324126G>T | CA491478838 | HCN4 | c.2106C>A (p.Ala702=) c.888C>A (p.Ala296=) | |
| 15 | g.73324127G>A | CA393089962 | HCN4 | c.2105C>T (p.Ala702Val) c.887C>T (p.Ala296Val) | |
| 15 | g.73324127G>C | CA393089963 | HCN4 | c.2105C>G (p.Ala702Gly) c.887C>G (p.Ala296Gly) | |
| 15 | g.73324127G>T | CA393089964 | HCN4 | c.2105C>A (p.Ala702Asp) c.887C>A (p.Ala296Asp) | |
| 15 | g.73324128C>A | CA393089970 | HCN4 | c.2104G>T (p.Ala702Ser) c.886G>T (p.Ala296Ser) | |
| 15 | g.73324128C= | CA2187189077 | HCN4 | c.2104G= (p.Ala702=) c.886G= (p.Ala296=) | |
| 15 | g.73324128C>G | CA393089965 | HCN4 | c.2104G>C (p.Ala702Pro) c.886G>C (p.Ala296Pro) | |
| 15 | g.73324128C>T | CA393089967 | HCN4 | c.2104G>A (p.Ala702Thr) c.886G>A (p.Ala296Thr) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73324129C>A | CA393089971 | HCN4 | c.2103G>T (p.Arg701Ser) c.885G>T (p.Arg295Ser) | |
| 15 | g.73324129C>G | CA393089973 | HCN4 | c.2103G>C (p.Arg701Ser) c.885G>C (p.Arg295Ser) | |
| 15 | g.73324129C>T | CA491478847 | HCN4 | c.2103G>A (p.Arg701=) c.885G>A (p.Arg295=) | |
| 15 | g.73324130C>A | CA393089975 | HCN4 | c.2102G>T (p.Arg701Met) c.884G>T (p.Arg295Met) | |
| 15 | g.73324130C>G | CA393089976 | HCN4 | c.2102G>C (p.Arg701Thr) c.884G>C (p.Arg295Thr) | |
| 15 | g.73324130C>T | CA393089978 | HCN4 | c.2102G>A (p.Arg701Lys) c.884G>A (p.Arg295Lys) | |
| 15 | g.73324131T>A | CA393089980 | HCN4 | c.2101A>T (p.Arg701Trp) c.883A>T (p.Arg295Trp) | |
| 15 | g.73324131T>C | CA393089981 | HCN4 | c.2101A>G (p.Arg701Gly) c.883A>G (p.Arg295Gly) | |
| 15 | g.73324131T>G | CA491478851 | HCN4 | c.2101A>C (p.Arg701=) c.883A>C (p.Arg295=) | |
| 15 | g.73324132T>A | CA491478852 | HCN4 | c.2100A>T (p.Arg700=) c.882A>T (p.Arg294=) | |
| 15 | g.73324132T>C | CA491478853 | HCN4 | c.2100A>G (p.Arg700=) c.882A>G (p.Arg294=) | |
| 15 | g.73324132T>G | CA491478854 | HCN4 | c.2100A>C (p.Arg700=) c.882A>C (p.Arg294=) | |
| 15 | g.73324133C>A | CA393089983 | HCN4 | c.2099G>T (p.Arg700Leu) c.881G>T (p.Arg294Leu) | |
| 15 | g.73324133C= | CA2187189079 | HCN4 | c.2099G= (p.Arg700=) c.881G= (p.Arg294=) | |
| 15 | g.73324133C>G | CA393089985 | HCN4 | c.2099G>C (p.Arg700Pro) c.881G>C (p.Arg294Pro) | |
| 15 | g.73324133C>T | CA393089987 | HCN4 | c.2099G>A (p.Arg700Gln) c.881G>A (p.Arg294Gln) | ClinVar dbSNP COSMIC |
| 15 | g.73324134G>A | CA393089989 | HCN4 | c.2098C>T (p.Arg700Ter) c.880C>T (p.Arg294Ter) | gnomAD v4 COSMIC |
| 15 | g.73324134G>C | CA393089990 | HCN4 | c.2098C>G (p.Arg700Gly) c.880C>G (p.Arg294Gly) | |
| 15 | g.73324134G>T | CA491478858 | HCN4 | c.2098C>A (p.Arg700=) c.880C>A (p.Arg294=) | |
| 15 | g.73324135C>A | CA393089996 | HCN4 | c.2097G>T (p.Met699Ile) c.879G>T (p.Met293Ile) | |
| 15 | g.73324135C>G | CA393089992 | HCN4 | c.2097G>C (p.Met699Ile) c.879G>C (p.Met293Ile) | |
| 15 | g.73324135C>T | CA393089994 | HCN4 | c.2097G>A (p.Met699Ile) c.879G>A (p.Met293Ile) | gnomAD v4 |
| 15 | g.73324136A>C | CA393089997 | HCN4 | c.2096T>G (p.Met699Arg) c.878T>G (p.Met293Arg) | |
| 15 | g.73324136A>G | CA393089998 | HCN4 | c.2096T>C (p.Met699Thr) c.878T>C (p.Met293Thr) | ClinVar |
| 15 | g.73324136A>T | CA393090000 | HCN4 | c.2096T>A (p.Met699Lys) c.878T>A (p.Met293Lys) | |
| 15 | g.73324137T>A | CA393090002 | HCN4 | c.2095A>T (p.Met699Leu) c.877A>T (p.Met293Leu) | |
| 15 | g.73324137T>C | CA393090003 | HCN4 | c.2095A>G (p.Met699Val) c.877A>G (p.Met293Val) | |
| 15 | g.73324137T>G | CA393090004 | HCN4 | c.2095A>C (p.Met699Leu) c.877A>C (p.Met293Leu) | |
| 15 | g.73324138C>A | CA393090010 | HCN4 | c.2094G>T (p.Met698Ile) c.876G>T (p.Met292Ile) | |
| 15 | g.73324138C>G | CA393090009 | HCN4 | c.2094G>C (p.Met698Ile) c.876G>C (p.Met292Ile) | |
| 15 | g.73324138C>T | CA393090007 | HCN4 | c.2094G>A (p.Met698Ile) c.876G>A (p.Met292Ile) | |
| 15 | g.73324139A>C | CA393090012 | HCN4 | c.2093T>G (p.Met698Arg) c.875T>G (p.Met292Arg) | |
| 15 | g.73324139A>G | CA393090014 | HCN4 | c.2093T>C (p.Met698Thr) c.875T>C (p.Met292Thr) | |
| 15 | g.73324139A>T | CA393090016 | HCN4 | c.2093T>A (p.Met698Lys) c.875T>A (p.Met292Lys) | |
| 15 | g.73324140T>A | CA393090017 | HCN4 | c.2092A>T (p.Met698Leu) c.874A>T (p.Met292Leu) | |
| 15 | g.73324140T>C | CA393090018 | HCN4 | c.2092A>G (p.Met698Val) c.874A>G (p.Met292Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324140T>G | CA393090019 | HCN4 | c.2092A>C (p.Met698Leu) c.874A>C (p.Met292Leu) | |
| 15 | g.73324140T= | CA2187189083 | HCN4 | c.2092A= (p.Met698=) c.874A= (p.Met292=) | |
| 15 | g.73324141G>A | CA491478867 | HCN4 | c.2091C>T (p.Pro697=) c.873C>T (p.Pro291=) | ClinVar |
| 15 | g.73324141G>C | CA491478868 | HCN4 | c.2091C>G (p.Pro697=) c.873C>G (p.Pro291=) | |
| 15 | g.73324141G>T | CA491478869 | HCN4 | c.2091C>A (p.Pro697=) c.873C>A (p.Pro291=) | |
| 15 | g.73324142G>A | CA393090023 | HCN4 | c.2090C>T (p.Pro697Leu) c.872C>T (p.Pro291Leu) | ClinVar dbSNP |
| 15 | g.73324142G>C | CA272665445 | HCN4 | c.2090C>G (p.Pro697Arg) c.872C>G (p.Pro291Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324142G= | CA2187189086 | HCN4 | c.2090C= (p.Pro697=) c.872C= (p.Pro291=) | |
| 15 | g.73324142G>T | CA393090022 | HCN4 | c.2090C>A (p.Pro697His) c.872C>A (p.Pro291His) | |
| 15 | g.73324143G>A | CA393090025 | HCN4 | c.2089C>T (p.Pro697Ser) c.871C>T (p.Pro291Ser) | |
| 15 | g.73324143G>C | CA393090027 | HCN4 | c.2089C>G (p.Pro697Ala) c.871C>G (p.Pro291Ala) | |
| 15 | g.73324143G>T | CA393090029 | HCN4 | c.2089C>A (p.Pro697Thr) c.871C>A (p.Pro291Thr) | |
| 15 | g.73324144G>A | CA491478876 | HCN4 | c.2088C>T (p.Tyr696=) c.870C>T (p.Tyr290=) | gnomAD v4 |
| 15 | g.73324144G>C | CA393090030 | HCN4 | c.2088C>G (p.Tyr696Ter) c.870C>G (p.Tyr290Ter) | |
| 15 | g.73324144G>T | CA393090032 | HCN4 | c.2088C>A (p.Tyr696Ter) c.870C>A (p.Tyr290Ter) | |
| 15 | g.73324145T>A | CA393090034 | HCN4 | c.2087A>T (p.Tyr696Phe) c.869A>T (p.Tyr290Phe) | |
| 15 | g.73324145T>C | CA393090036 | HCN4 | c.2087A>G (p.Tyr696Cys) c.869A>G (p.Tyr290Cys) | |
| 15 | g.73324145T>G | CA393090037 | HCN4 | c.2087A>C (p.Tyr696Ser) c.869A>C (p.Tyr290Ser) | |
| 15 | g.73324146A>C | CA393090039 | HCN4 | c.2086T>G (p.Tyr696Asp) c.868T>G (p.Tyr290Asp) | |
| 15 | g.73324146A>G | CA393090041 | HCN4 | c.2086T>C (p.Tyr696His) c.868T>C (p.Tyr290His) | |
| 15 | g.73324146A>T | CA393090042 | HCN4 | c.2086T>A (p.Tyr696Asn) c.868T>A (p.Tyr290Asn) | |
| 15 | g.73324147C>A | CA393090044 | HCN4 | c.2085G>T (p.Glu695Asp) c.867G>T (p.Glu289Asp) | |
| 15 | g.73324147C>G | CA393090046 | HCN4 | c.2085G>C (p.Glu695Asp) c.867G>C (p.Glu289Asp) | |
| 15 | g.73324147C>T | CA491478881 | HCN4 | c.2085G>A (p.Glu695=) c.867G>A (p.Glu289=) | |
| 15 | g.73324148T>A | CA393090048 | HCN4 | c.2084A>T (p.Glu695Val) c.866A>T (p.Glu289Val) | gnomAD v4 |
| 15 | g.73324148T>C | CA393090052 | HCN4 | c.2084A>G (p.Glu695Gly) c.866A>G (p.Glu289Gly) | |
| 15 | g.73324148T>G | CA393090050 | HCN4 | c.2084A>C (p.Glu695Ala) c.866A>C (p.Glu289Ala) | |
| 15 | g.73324149C>A | CA393090053 | HCN4 | c.2083G>T (p.Glu695Ter) c.865G>T (p.Glu289Ter) | |
| 15 | g.73324149C>G | CA393090055 | HCN4 | c.2083G>C (p.Glu695Gln) c.865G>C (p.Glu289Gln) | |
| 15 | g.73324149C>T | CA393090057 | HCN4 | c.2083G>A (p.Glu695Lys) c.865G>A (p.Glu289Lys) | gnomAD v4 COSMIC |
| 15 | g.73324150C>A | CA393090059 | HCN4 | c.2082G>T (p.Glu694Asp) c.864G>T (p.Glu288Asp) | |
| 15 | g.73324150C>G | CA393090060 | HCN4 | c.2082G>C (p.Glu694Asp) c.864G>C (p.Glu288Asp) | |
| 15 | g.73324150C>T | CA491478886 | HCN4 | c.2082G>A (p.Glu694=) c.864G>A (p.Glu288=) | ClinVar |
| 15 | g.73324151T>A | CA393090062 | HCN4 | c.2081A>T (p.Glu694Val) c.863A>T (p.Glu288Val) | COSMIC |
| 15 | g.73324151T>C | CA393090064 | HCN4 | c.2081A>G (p.Glu694Gly) c.863A>G (p.Glu288Gly) | |
| 15 | g.73324151T>G | CA393090066 | HCN4 | c.2081A>C (p.Glu694Ala) c.863A>C (p.Glu288Ala) | |
| 15 | g.73324152C>A | CA393090068 | HCN4 | c.2080G>T (p.Glu694Ter) c.862G>T (p.Glu288Ter) | |
| 15 | g.73324152C>G | CA393090070 | HCN4 | c.2080G>C (p.Glu694Gln) c.862G>C (p.Glu288Gln) | |
| 15 | g.73324152C>T | CA393090071 | HCN4 | c.2080G>A (p.Glu694Lys) c.862G>A (p.Glu288Lys) | COSMIC |
| 15 | g.73324152_73324153delinsGA | CA2697549183 | HCN4 | c.2079_2080delinsTC (p.Glu694Gln) c.861_862delinsTC (p.Glu288Gln) | ClinVar |
| 15 | g.73324153C>A | CA491478894 | HCN4 | c.2079G>T (p.Leu693=) c.861G>T (p.Leu287=) | |
| 15 | g.73324153C>G | CA491478895 | HCN4 | c.2079G>C (p.Leu693=) c.861G>C (p.Leu287=) | ClinVar |
| 15 | g.73324153C>T | CA491478896 | HCN4 | c.2079G>A (p.Leu693=) c.861G>A (p.Leu287=) | gnomAD v4 |
| 15 | g.73324154A>C | CA393090073 | HCN4 | c.2078T>G (p.Leu693Arg) c.860T>G (p.Leu287Arg) | |
| 15 | g.73324154A>G | CA393090075 | HCN4 | c.2078T>C (p.Leu693Pro) c.860T>C (p.Leu287Pro) | |
| 15 | g.73324154A>T | CA393090077 | HCN4 | c.2078T>A (p.Leu693Gln) c.860T>A (p.Leu287Gln) | |
| 15 | g.73324155G>A | CA491478898 | HCN4 | c.2077C>T (p.Leu693=) c.859C>T (p.Leu287=) | |
| 15 | g.73324155G>C | CA393090078 | HCN4 | c.2077C>G (p.Leu693Val) c.859C>G (p.Leu287Val) | |
| 15 | g.73324155G>T | CA393090080 | HCN4 | c.2077C>A (p.Leu693Met) c.859C>A (p.Leu287Met) | |
| 15 | g.73324156C>A | CA491478903 | HCN4 | c.2076G>T (p.Val692=) c.858G>T (p.Val286=) | |
| 15 | g.73324156C>G | CA491478900 | HCN4 | c.2076G>C (p.Val692=) c.858G>C (p.Val286=) | |
| 15 | g.73324156C>T | CA491478899 | HCN4 | c.2076G>A (p.Val692=) c.858G>A (p.Val286=) | COSMIC |
| 15 | g.73324157A>C | CA393090082 | HCN4 | c.2075T>G (p.Val692Gly) c.857T>G (p.Val286Gly) | |
| 15 | g.73324157A>G | CA393090083 | HCN4 | c.2075T>C (p.Val692Ala) c.857T>C (p.Val286Ala) | |
| 15 | g.73324157A>T | CA393090084 | HCN4 | c.2075T>A (p.Val692Glu) c.857T>A (p.Val286Glu) | |
| 15 | g.73324158C>A | CA393090086 | HCN4 | c.2074G>T (p.Val692Leu) c.856G>T (p.Val286Leu) | gnomAD v4 |
| 15 | g.73324158C>G | CA393090088 | HCN4 | c.2074G>C (p.Val692Leu) c.856G>C (p.Val286Leu) | |
| 15 | g.73324158C>T | CA393090089 | HCN4 | c.2074G>A (p.Val692Met) c.856G>A (p.Val286Met) | |
| 15 | g.73324159C>A | CA393090091 | HCN4 | c.2073G>T (p.Glu691Asp) c.855G>T (p.Glu285Asp) | |
| 15 | g.73324159C>G | CA393090092 | HCN4 | c.2073G>C (p.Glu691Asp) c.855G>C (p.Glu285Asp) | |
| 15 | g.73324159C>T | CA491478909 | HCN4 | c.2073G>A (p.Glu691=) c.855G>A (p.Glu285=) | |
| 15 | g.73324160T>A | CA393090094 | HCN4 | c.2072A>T (p.Glu691Val) c.854A>T (p.Glu285Val) | |
| 15 | g.73324160T>C | CA393090096 | HCN4 | c.2072A>G (p.Glu691Gly) c.854A>G (p.Glu285Gly) | |
| 15 | g.73324160T>G | CA393090098 | HCN4 | c.2072A>C (p.Glu691Ala) c.854A>C (p.Glu285Ala) | |
| 15 | g.73324161C>A | CA393090099 | HCN4 | c.2071G>T (p.Glu691Ter) c.853G>T (p.Glu285Ter) | |
| 15 | g.73324161C>G | CA393090102 | HCN4 | c.2071G>C (p.Glu691Gln) c.853G>C (p.Glu285Gln) | |
| 15 | g.73324161C>T | CA393090100 | HCN4 | c.2071G>A (p.Glu691Lys) c.853G>A (p.Glu285Lys) | COSMIC |
| 15 | g.73324162A= | CA2187189089 | HCN4 | c.2070T= (p.Asn690=) c.852T= (p.Asn284=) | |
| 15 | g.73324162A>C | CA393090103 | HCN4 | c.2070T>G (p.Asn690Lys) c.852T>G (p.Asn284Lys) | |
| 15 | g.73324162A>G | CA491478915 | HCN4 | c.2070T>C (p.Asn690=) c.852T>C (p.Asn284=) | dbSNP |
| 15 | g.73324162A>T | CA393090105 | HCN4 | c.2070T>A (p.Asn690Lys) c.852T>A (p.Asn284Lys) | |
| 15 | g.73324163T>A | CA393090106 | HCN4 | c.2069A>T (p.Asn690Ile) c.851A>T (p.Asn284Ile) | ClinVar gnomAD v4 |
| 15 | g.73324163T>C | CA7649128 | HCN4 | c.2069A>G (p.Asn690Ser) c.851A>G (p.Asn284Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324163T>G | CA393090109 | HCN4 | c.2069A>C (p.Asn690Thr) c.851A>C (p.Asn284Thr) | |
| 15 | g.73324163T= | CA2187189092 | HCN4 | c.2069A= (p.Asn690=) c.851A= (p.Asn284=) | |
| 15 | g.73324164T>A | CA393090111 | HCN4 | c.2068A>T (p.Asn690Tyr) c.850A>T (p.Asn284Tyr) | |
| 15 | g.73324164T>C | CA393090112 | HCN4 | c.2068A>G (p.Asn690Asp) c.850A>G (p.Asn284Asp) | |
| 15 | g.73324164T>G | CA393090114 | HCN4 | c.2068A>C (p.Asn690His) c.850A>C (p.Asn284His) | |
| 15 | g.73324165G>A | CA7649129 | HCN4 | c.2067C>T (p.Phe689=) c.849C>T (p.Phe283=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324165G>C | CA393090118 | HCN4 | c.2067C>G (p.Phe689Leu) c.849C>G (p.Phe283Leu) | |
| 15 | g.73324165G= | CA2187189094 | HCN4 | c.2067C= (p.Phe689=) c.849C= (p.Phe283=) | |
| 15 | g.73324165G>T | CA393090117 | HCN4 | c.2067C>A (p.Phe689Leu) c.849C>A (p.Phe283Leu) | |
| 15 | g.73324166A>C | CA393090121 | HCN4 | c.2066T>G (p.Phe689Cys) c.848T>G (p.Phe283Cys) | |
| 15 | g.73324166A>G | CA393090122 | HCN4 | c.2066T>C (p.Phe689Ser) c.848T>C (p.Phe283Ser) | |
| 15 | g.73324166A>T | CA393090123 | HCN4 | c.2066T>A (p.Phe689Tyr) c.848T>A (p.Phe283Tyr) | |
| 15 | g.73324167A>C | CA393090125 | HCN4 | c.2065T>G (p.Phe689Val) c.847T>G (p.Phe283Val) | |
| 15 | g.73324167A>G | CA393090127 | HCN4 | c.2065T>C (p.Phe689Leu) c.847T>C (p.Phe283Leu) | |
| 15 | g.73324167A>T | CA393090129 | HCN4 | c.2065T>A (p.Phe689Ile) c.847T>A (p.Phe283Ile) | |
| 15 | g.73324168G>A | CA7649130 | HCN4 | c.2064C>T (p.Asn688=) c.846C>T (p.Asn282=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324168G>C | CA393090133 | HCN4 | c.2064C>G (p.Asn688Lys) c.846C>G (p.Asn282Lys) | |
| 15 | g.73324168G= | CA2187189097 | HCN4 | c.2064C= (p.Asn688=) c.846C= (p.Asn282=) | |
| 15 | g.73324168G>T | CA393090130 | HCN4 | c.2064C>A (p.Asn688Lys) c.846C>A (p.Asn282Lys) | |
| 15 | g.73324169T>A | CA393090135 | HCN4 | c.2063A>T (p.Asn688Ile) c.845A>T (p.Asn282Ile) | |
| 15 | g.73324169T>C | CA7649131 | HCN4 | c.2063A>G (p.Asn688Ser) c.845A>G (p.Asn282Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324169T>G | CA393090137 | HCN4 | c.2063A>C (p.Asn688Thr) c.845A>C (p.Asn282Thr) | |
| 15 | g.73324169T= | CA2187189100 | HCN4 | c.2063A= (p.Asn688=) c.845A= (p.Asn282=) | |
| 15 | g.73324170T>A | CA393090139 | HCN4 | c.2062A>T (p.Asn688Tyr) c.844A>T (p.Asn282Tyr) | |
| 15 | g.73324170T>C | CA393090141 | HCN4 | c.2062A>G (p.Asn688Asp) c.844A>G (p.Asn282Asp) | ClinVar dbSNP |
| 15 | g.73324170T>G | CA393090142 | HCN4 | c.2062A>C (p.Asn688His) c.844A>C (p.Asn282His) | |
| 15 | g.73324171G>A | CA491478927 | HCN4 | c.2061C>T (p.Asp687=) c.843C>T (p.Asp281=) | |
| 15 | g.73324171G>C | CA393090144 | HCN4 | c.2061C>G (p.Asp687Glu) c.843C>G (p.Asp281Glu) | dbSNP gnomAD v4 |
| 15 | g.73324171G= | CA2187189103 | HCN4 | c.2061C= (p.Asp687=) c.843C= (p.Asp281=) | |
| 15 | g.73324171G>T | CA393090146 | HCN4 | c.2061C>A (p.Asp687Glu) c.843C>A (p.Asp281Glu) | |
| 15 | g.73324172T>A | CA393090148 | HCN4 | c.2060A>T (p.Asp687Val) c.842A>T (p.Asp281Val) | |
| 15 | g.73324172T>C | CA393090149 | HCN4 | c.2060A>G (p.Asp687Gly) c.842A>G (p.Asp281Gly) | |
| 15 | g.73324172T>G | CA393090151 | HCN4 | c.2060A>C (p.Asp687Ala) c.842A>C (p.Asp281Ala) | |
| 15 | g.73324173C>A | CA393090153 | HCN4 | c.2059G>T (p.Asp687Tyr) c.841G>T (p.Asp281Tyr) | gnomAD v4 |
| 15 | g.73324173C>G | CA393090156 | HCN4 | c.2059G>C (p.Asp687His) c.841G>C (p.Asp281His) | |
| 15 | g.73324173C>T | CA393090154 | HCN4 | c.2059G>A (p.Asp687Asn) c.841G>A (p.Asp281Asn) | |
| 15 | g.73324174C>A | CA491478935 | HCN4 | c.2058G>T (p.Val686=) c.840G>T (p.Val280=) | |
| 15 | g.73324174C>G | CA491478937 | HCN4 | c.2058G>C (p.Val686=) c.840G>C (p.Val280=) | |
| 15 | g.73324174C>T | CA491478936 | HCN4 | c.2058G>A (p.Val686=) c.840G>A (p.Val280=) | gnomAD v4 |
| 15 | g.73324175A>C | CA393090157 | HCN4 | c.2057T>G (p.Val686Gly) c.839T>G (p.Val280Gly) | |
| 15 | g.73324175A>G | CA393090158 | HCN4 | c.2057T>C (p.Val686Ala) c.839T>C (p.Val280Ala) | |
| 15 | g.73324175A>T | CA393090159 | HCN4 | c.2057T>A (p.Val686Glu) c.839T>A (p.Val280Glu) | |
| 15 | g.73324176C>A | CA393090161 | HCN4 | c.2056G>T (p.Val686Leu) c.838G>T (p.Val280Leu) | |
| 15 | g.73324176C= | CA2187189108 | HCN4 | c.2056G= (p.Val686=) c.838G= (p.Val280=) | |
| 15 | g.73324176C>G | CA393090163 | HCN4 | c.2056G>C (p.Val686Leu) c.838G>C (p.Val280Leu) | |
| 15 | g.73324176C>T | CA7649132 | HCN4 | c.2056G>A (p.Val686Met) c.838G>A (p.Val280Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73324177G>A | CA10604720 | HCN4 | c.2055C>T (p.Ser685=) c.837C>T (p.Ser279=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324177G>C | CA393090166 | HCN4 | c.2055C>G (p.Ser685Arg) c.837C>G (p.Ser279Arg) | |
| 15 | g.73324177G= | CA2187189112 | HCN4 | c.2055C= (p.Ser685=) c.837C= (p.Ser279=) | |
| 15 | g.73324177G>T | CA393090168 | HCN4 | c.2055C>A (p.Ser685Arg) c.837C>A (p.Ser279Arg) | |
| 15 | g.73324178C>A | CA393090169 | HCN4 | c.2054G>T (p.Ser685Ile) c.836G>T (p.Ser279Ile) | |
| 15 | g.73324178C>G | CA393090170 | HCN4 | c.2054G>C (p.Ser685Thr) c.836G>C (p.Ser279Thr) | gnomAD v4 |
| 15 | g.73324178C>T | CA393090172 | HCN4 | c.2054G>A (p.Ser685Asn) c.836G>A (p.Ser279Asn) | |
| 15 | g.73324182_73324214del | CA2697549184 | HCN4 | c.2022_2054del (p.Arg674_Leu684del) c.804_836del (p.Arg268_Leu278del) | ClinVar |
| 15 | g.73324179T>A | CA393090176 | HCN4 | c.2053A>T (p.Ser685Cys) c.835A>T (p.Ser279Cys) | |
| 15 | g.73324179T>C | CA393090173 | HCN4 | c.2053A>G (p.Ser685Gly) c.835A>G (p.Ser279Gly) | |
| 15 | g.73324179T>G | CA393090175 | HCN4 | c.2053A>C (p.Ser685Arg) c.835A>C (p.Ser279Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324179T= | CA2187189117 | HCN4 | c.2053A= (p.Ser685=) c.835A= (p.Ser279=) | |
| 15 | g.73324180C>A | CA491478944 | HCN4 | c.2052G>T (p.Leu684=) c.834G>T (p.Leu278=) | |
| 15 | g.73324180C= | CA2187189121 | HCN4 | c.2052G= (p.Leu684=) c.834G= (p.Leu278=) | |
| 15 | g.73324180C>G | CA491478947 | HCN4 | c.2052G>C (p.Leu684=) c.834G>C (p.Leu278=) | |
| 15 | g.73324180C>T | CA7649133 | HCN4 | c.2052G>A (p.Leu684=) c.834G>A (p.Leu278=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324181A= | CA2187189125 | HCN4 | c.2051T= (p.Leu684=) c.833T= (p.Leu278=) | |
| 15 | g.73324181A>C | CA393090178 | HCN4 | c.2051T>G (p.Leu684Arg) c.833T>G (p.Leu278Arg) | |
| 15 | g.73324181A>G | CA393090179 | HCN4 | c.2051T>C (p.Leu684Pro) c.833T>C (p.Leu278Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324181A>T | CA393090180 | HCN4 | c.2051T>A (p.Leu684Gln) c.833T>A (p.Leu278Gln) | |
| 15 | g.73324182G>A | CA491478948 | HCN4 | c.2050C>T (p.Leu684=) c.832C>T (p.Leu278=) | |
| 15 | g.73324182G>C | CA393090182 | HCN4 | c.2050C>G (p.Leu684Val) c.832C>G (p.Leu278Val) | |
| 15 | g.73324182G>T | CA393090183 | HCN4 | c.2050C>A (p.Leu684Met) c.832C>A (p.Leu278Met) | |
| 15 | g.73324183C>A | CA491478951 | HCN4 | c.2049G>T (p.Ser683=) c.831G>T (p.Ser277=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73324183C= | CA2187189129 | HCN4 | c.2049G= (p.Ser683=) c.831G= (p.Ser277=) | |
| 15 | g.73324183C>G | CA491478952 | HCN4 | c.2049G>C (p.Ser683=) c.831G>C (p.Ser277=) | |
| 15 | g.73324183C>T | CA491478953 | HCN4 | c.2049G>A (p.Ser683=) c.831G>A (p.Ser277=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324184G>A | CA393090184 | HCN4 | c.2048C>T (p.Ser683Leu) c.830C>T (p.Ser277Leu) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73324184G>C | CA393090185 | HCN4 | c.2048C>G (p.Ser683Trp) c.830C>G (p.Ser277Trp) | |
| 15 | g.73324184G= | CA2187189131 | HCN4 | c.2048C= (p.Ser683=) c.830C= (p.Ser277=) | |
| 15 | g.73324184G>T | CA393090186 | HCN4 | c.2048C>A (p.Ser683Ter) c.830C>A (p.Ser277Ter) | |
| 15 | g.73324185A>C | CA393090188 | HCN4 | c.2047T>G (p.Ser683Ala) c.829T>G (p.Ser277Ala) | |
| 15 | g.73324185A>G | CA393090190 | HCN4 | c.2047T>C (p.Ser683Pro) c.829T>C (p.Ser277Pro) | |
| 15 | g.73324185A>T | CA393090191 | HCN4 | c.2047T>A (p.Ser683Thr) c.829T>A (p.Ser277Thr) | |
| 15 | g.73324186G>A | CA491478954 | HCN4 | c.2046C>T (p.Tyr682=) c.828C>T (p.Tyr276=) | |
| 15 | g.73324186G>C | CA393090195 | HCN4 | c.2046C>G (p.Tyr682Ter) c.828C>G (p.Tyr276Ter) | |
| 15 | g.73324186G>T | CA393090193 | HCN4 | c.2046C>A (p.Tyr682Ter) c.828C>A (p.Tyr276Ter) | |
| 15 | g.73324187T>A | CA393090197 | HCN4 | c.2045A>T (p.Tyr682Phe) c.827A>T (p.Tyr276Phe) | |
| 15 | g.73324187T>C | CA393090200 | HCN4 | c.2045A>G (p.Tyr682Cys) c.827A>G (p.Tyr276Cys) | |
| 15 | g.73324187T>G | CA393090198 | HCN4 | c.2045A>C (p.Tyr682Ser) c.827A>C (p.Tyr276Ser) | |
| 15 | g.73324188A>C | CA393090202 | HCN4 | c.2044T>G (p.Tyr682Asp) c.826T>G (p.Tyr276Asp) | |
| 15 | g.73324188A>G | CA393090204 | HCN4 | c.2044T>C (p.Tyr682His) c.826T>C (p.Tyr276His) | |
| 15 | g.73324188A>T | CA393090205 | HCN4 | c.2044T>A (p.Tyr682Asn) c.826T>A (p.Tyr276Asn) | |
| 15 | g.73324189G>A | CA491478961 | HCN4 | c.2043C>T (p.Leu681=) c.825C>T (p.Leu275=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73324189G>C | CA491478962 | HCN4 | c.2043C>G (p.Leu681=) c.825C>G (p.Leu275=) | |
| 15 | g.73324189G>T | CA491478963 | HCN4 | c.2043C>A (p.Leu681=) c.825C>A (p.Leu275=) | COSMIC |
| 15 | g.73324190A>C | CA393090209 | HCN4 | c.2042T>G (p.Leu681Arg) c.824T>G (p.Leu275Arg) | |
| 15 | g.73324190A>G | CA393090210 | HCN4 | c.2042T>C (p.Leu681Pro) c.824T>C (p.Leu275Pro) | |
| 15 | g.73324190A>T | CA393090211 | HCN4 | c.2042T>A (p.Leu681His) c.824T>A (p.Leu275His) | |
| 15 | g.73324191G>A | CA393090214 | HCN4 | c.2041C>T (p.Leu681Phe) c.823C>T (p.Leu275Phe) | |
| 15 | g.73324191G>C | CA393090216 | HCN4 | c.2041C>G (p.Leu681Val) c.823C>G (p.Leu275Val) | |
| 15 | g.73324191G>T | CA393090217 | HCN4 | c.2041C>A (p.Leu681Ile) c.823C>A (p.Leu275Ile) | |
| 15 | g.73324192dup | CA2629370962 | HCN4 | c.2041dup (p.Leu681ProfsTer11) c.823dup (p.Leu275ProfsTer11) | gnomAD v4 |
| 15 | g.73324192G>A | CA491478968 | HCN4 | c.2040C>T (p.Arg680=) c.822C>T (p.Arg274=) | |
| 15 | g.73324192G>C | CA491478969 | HCN4 | c.2040C>G (p.Arg680=) c.822C>G (p.Arg274=) | |
| 15 | g.73324192G>T | CA491478970 | HCN4 | c.2040C>A (p.Arg680=) c.822C>A (p.Arg274=) | |
| 15 | g.73324193C>A | CA393090219 | HCN4 | c.2039G>T (p.Arg680Leu) c.821G>T (p.Arg274Leu) | |
| 15 | g.73324193C= | CA2187189134 | HCN4 | c.2039G= (p.Arg680=) c.821G= (p.Arg274=) | |
| 15 | g.73324193C>G | CA393090220 | HCN4 | c.2039G>C (p.Arg680Pro) c.821G>C (p.Arg274Pro) | |
| 15 | g.73324193C>T | CA7649134 | HCN4 | c.2039G>A (p.Arg680His) c.821G>A (p.Arg274His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324194G>A | CA393090226 | HCN4 | c.2038C>T (p.Arg680Cys) c.820C>T (p.Arg274Cys) | gnomAD v4 COSMIC |
| 15 | g.73324194G>C | CA393090223 | HCN4 | c.2038C>G (p.Arg680Gly) c.820C>G (p.Arg274Gly) | |
| 15 | g.73324194G>T | CA393090224 | HCN4 | c.2038C>A (p.Arg680Ser) c.820C>A (p.Arg274Ser) | |
| 15 | g.73324195G>A | CA491478974 | HCN4 | c.2037C>T (p.Cys679=) c.819C>T (p.Cys273=) | |
| 15 | g.73324195G>C | CA393090228 | HCN4 | c.2037C>G (p.Cys679Trp) c.819C>G (p.Cys273Trp) | |
| 15 | g.73324195G>T | CA393090229 | HCN4 | c.2037C>A (p.Cys679Ter) c.819C>A (p.Cys273Ter) | |
| 15 | g.73324196C>A | CA393090231 | HCN4 | c.2036G>T (p.Cys679Phe) c.818G>T (p.Cys273Phe) | |
| 15 | g.73324196C= | CA2187189138 | HCN4 | c.2036G= (p.Cys679=) c.818G= (p.Cys273=) | |
| 15 | g.73324196C>G | CA393090233 | HCN4 | c.2036G>C (p.Cys679Ser) c.818G>C (p.Cys273Ser) | |
| 15 | g.73324196C>T | CA393090234 | HCN4 | c.2036G>A (p.Cys679Tyr) c.818G>A (p.Cys273Tyr) | ClinVar dbSNP |
| 15 | g.73324196_73324199delinsCAGT | CA2187189140 | HCN4 | c.2033_2036delinsACTG (p.Tyr678=) c.815_818delinsACTG (p.Tyr272=) | |
| 15 | g.73324197A>C | CA393090237 | HCN4 | c.2035T>G (p.Cys679Gly) c.817T>G (p.Cys273Gly) | |
| 15 | g.73324197A>G | CA393090239 | HCN4 | c.2035T>C (p.Cys679Arg) c.817T>C (p.Cys273Arg) | |
| 15 | g.73324197A>T | CA393090240 | HCN4 | c.2035T>A (p.Cys679Ser) c.817T>A (p.Cys273Ser) | |
| 15 | g.73324199_73324201del | CA1139664083 | HCN4 | c.2033_2035del (p.Tyr678del) c.815_817del (p.Tyr272del) | ClinVar dbSNP |
| 15 | g.73324198G>A | CA7649135 | HCN4 | c.2034C>T (p.Tyr678=) c.816C>T (p.Tyr272=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324198G>C | CA393090242 | HCN4 | c.2034C>G (p.Tyr678Ter) c.816C>G (p.Tyr272Ter) | |
| 15 | g.73324198G= | CA2187189145 | HCN4 | c.2034C= (p.Tyr678=) c.816C= (p.Tyr272=) | |
| 15 | g.73324198G>T | CA393090244 | HCN4 | c.2034C>A (p.Tyr678Ter) c.816C>A (p.Tyr272Ter) | |
| 15 | g.73324199T>A | CA393090249 | HCN4 | c.2033A>T (p.Tyr678Phe) c.815A>T (p.Tyr272Phe) | |
| 15 | g.73324199T>C | CA393090247 | HCN4 | c.2033A>G (p.Tyr678Cys) c.815A>G (p.Tyr272Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324199T>G | CA393090245 | HCN4 | c.2033A>C (p.Tyr678Ser) c.815A>C (p.Tyr272Ser) | |
| 15 | g.73324199T= | CA2187189149 | HCN4 | c.2033A= (p.Tyr678=) c.815A= (p.Tyr272=) | |
| 15 | g.73324200A>C | CA393090251 | HCN4 | c.2032T>G (p.Tyr678Asp) c.814T>G (p.Tyr272Asp) | dbSNP |
| 15 | g.73324200A>G | CA393090252 | HCN4 | c.2032T>C (p.Tyr678His) c.814T>C (p.Tyr272His) | gnomAD v4 |
| 15 | g.73324200A>T | CA393090254 | HCN4 | c.2032T>A (p.Tyr678Asn) c.814T>A (p.Tyr272Asn) | |
| 15 | g.73324201G>A | CA491478979 | HCN4 | c.2031C>T (p.Thr677=) c.813C>T (p.Thr271=) | |
| 15 | g.73324201G>C | CA491478980 | HCN4 | c.2031C>G (p.Thr677=) c.813C>G (p.Thr271=) | gnomAD v4 |
| 15 | g.73324201G>T | CA491478982 | HCN4 | c.2031C>A (p.Thr677=) c.813C>A (p.Thr271=) | |
| 15 | g.73324202G>A | CA393090257 | HCN4 | c.2030C>T (p.Thr677Ile) c.812C>T (p.Thr271Ile) | ClinVar |
| 15 | g.73324202G>C | CA393090258 | HCN4 | c.2030C>G (p.Thr677Ser) c.812C>G (p.Thr271Ser) | |
| 15 | g.73324202G>T | CA393090260 | HCN4 | c.2030C>A (p.Thr677Asn) c.812C>A (p.Thr271Asn) | |
| 15 | g.73324203T>A | CA393090265 | HCN4 | c.2029A>T (p.Thr677Ser) c.811A>T (p.Thr271Ser) | |
| 15 | g.73324203T>C | CA393090262 | HCN4 | c.2029A>G (p.Thr677Ala) c.811A>G (p.Thr271Ala) | |
| 15 | g.73324203T>G | CA393090264 | HCN4 | c.2029A>C (p.Thr677Pro) c.811A>C (p.Thr271Pro) | dbSNP |
| 15 | g.73324203T= | CA2187189153 | HCN4 | c.2029A= (p.Thr677=) c.811A= (p.Thr271=) | |
| 15 | g.73324204G>A | CA491478987 | HCN4 | c.2028C>T (p.Asp676=) c.810C>T (p.Asp270=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73324204G>C | CA393090267 | HCN4 | c.2028C>G (p.Asp676Glu) c.810C>G (p.Asp270Glu) | |
| 15 | g.73324204G= | CA2187189158 | HCN4 | c.2028C= (p.Asp676=) c.810C= (p.Asp270=) | |
| 15 | g.73324204G>T | CA16614560 | HCN4 | c.2028C>A (p.Asp676Glu) c.810C>A (p.Asp270Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324205T>A | CA393090269 | HCN4 | c.2027A>T (p.Asp676Val) c.809A>T (p.Asp270Val) | |
| 15 | g.73324205T>C | CA393090271 | HCN4 | c.2027A>G (p.Asp676Gly) c.809A>G (p.Asp270Gly) | |
| 15 | g.73324205T>G | CA393090273 | HCN4 | c.2027A>C (p.Asp676Ala) c.809A>C (p.Asp270Ala) | |
| 15 | g.73324206C>A | CA393090275 | HCN4 | c.2026G>T (p.Asp676Tyr) c.808G>T (p.Asp270Tyr) | |
| 15 | g.73324206C= | CA2187189164 | HCN4 | c.2026G= (p.Asp676=) c.808G= (p.Asp270=) | |
| 15 | g.73324206C>G | CA393090277 | HCN4 | c.2026G>C (p.Asp676His) c.808G>C (p.Asp270His) | |
| 15 | g.73324206C>T | CA7649136 | HCN4 | c.2026G>A (p.Asp676Asn) c.808G>A (p.Asp270Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324207G>A | CA7649137 | HCN4 | c.2025C>T (p.Ala675=) c.807C>T (p.Ala269=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324207G>C | CA491478992 | HCN4 | c.2025C>G (p.Ala675=) c.807C>G (p.Ala269=) | dbSNP |
| 15 | g.73324207G= | CA2187189172 | HCN4 | c.2025C= (p.Ala675=) c.807C= (p.Ala269=) | |
| 15 | g.73324207G>T | CA491478993 | HCN4 | c.2025C>A (p.Ala675=) c.807C>A (p.Ala269=) | gnomAD v4 |
| 15 | g.73324208G>A | CA393090280 | HCN4 | c.2024C>T (p.Ala675Val) c.806C>T (p.Ala269Val) | |
| 15 | g.73324208G>C | CA393090281 | HCN4 | c.2024C>G (p.Ala675Gly) c.806C>G (p.Ala269Gly) | |
| 15 | g.73324208G>T | CA393090283 | HCN4 | c.2024C>A (p.Ala675Asp) c.806C>A (p.Ala269Asp) | |
| 15 | g.73324209C>A | CA393090285 | HCN4 | c.2023G>T (p.Ala675Ser) c.805G>T (p.Ala269Ser) | |
| 15 | g.73324209C= | CA2187189177 | HCN4 | c.2023G= (p.Ala675=) c.805G= (p.Ala269=) | |
| 15 | g.73324209C>G | CA393090286 | HCN4 | c.2023G>C (p.Ala675Pro) c.805G>C (p.Ala269Pro) | |
| 15 | g.73324209C>T | CA7649138 | HCN4 | c.2023G>A (p.Ala675Thr) c.805G>A (p.Ala269Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73324210C>A | CA393090288 | HCN4 | c.2022G>T (p.Arg674Ser) c.804G>T (p.Arg268Ser) | |
| 15 | g.73324210C= | CA2187189180 | HCN4 | c.2022G= (p.Arg674=) c.804G= (p.Arg268=) | |
| 15 | g.73324210C>G | CA393090289 | HCN4 | c.2022G>C (p.Arg674Ser) c.804G>C (p.Arg268Ser) | |
| 15 | g.73324210C>T | CA491478995 | HCN4 | c.2022G>A (p.Arg674=) c.804G>A (p.Arg268=) | ClinVar dbSNP |
| 15 | g.73324211C>A | CA393090291 | HCN4 | c.2021G>T (p.Arg674Met) c.803G>T (p.Arg268Met) | |
| 15 | g.73324211C>G | CA393090293 | HCN4 | c.2021G>C (p.Arg674Thr) c.803G>C (p.Arg268Thr) | |
| 15 | g.73324211C>T | CA393090294 | HCN4 | c.2021G>A (p.Arg674Lys) c.803G>A (p.Arg268Lys) | gnomAD v4 |
| 15 | g.73324212T>A | CA393090299 | HCN4 | c.2020A>T (p.Arg674Trp) c.802A>T (p.Arg268Trp) | |
| 15 | g.73324212T>C | CA393090296 | HCN4 | c.2020A>G (p.Arg674Gly) c.802A>G (p.Arg268Gly) | |
| 15 | g.73324212T>G | CA491478996 | HCN4 | c.2020A>C (p.Arg674=) c.802A>C (p.Arg268=) | gnomAD v4 |
| 15 | g.73324213C>A | CA491478997 | HCN4 | c.2019G>T (p.Val673=) c.801G>T (p.Val267=) | gnomAD v4 |
| 15 | g.73324213C>G | CA491478998 | HCN4 | c.2019G>C (p.Val673=) c.801G>C (p.Val267=) | |
| 15 | g.73324213C>T | CA491478999 | HCN4 | c.2019G>A (p.Val673=) c.801G>A (p.Val267=) | |
| 15 | g.73324214A>C | CA393090300 | HCN4 | c.2018T>G (p.Val673Gly) c.800T>G (p.Val267Gly) | |
| 15 | g.73324214A>G | CA393090303 | HCN4 | c.2018T>C (p.Val673Ala) c.800T>C (p.Val267Ala) | |
| 15 | g.73324214A>T | CA393090302 | HCN4 | c.2018T>A (p.Val673Glu) c.800T>A (p.Val267Glu) | |
| 15 | g.73324215C>A | CA393090304 | HCN4 | c.2017G>T (p.Val673Leu) c.799G>T (p.Val267Leu) | gnomAD v4 |
| 15 | g.73324215C= | CA2187189183 | HCN4 | c.2017G= (p.Val673=) c.799G= (p.Val267=) | |
| 15 | g.73324215C>G | CA393090307 | HCN4 | c.2017G>C (p.Val673Leu) c.799G>C (p.Val267Leu) | |
| 15 | g.73324215C>T | CA393090306 | HCN4 | c.2017G>A (p.Val673Met) c.799G>A (p.Val267Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73324216G>A | CA7649139 | HCN4 | c.2016C>T (p.Ser672=) c.798C>T (p.Ser266=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73324216G>C | CA393090311 | HCN4 | c.2016C>G (p.Ser672Arg) c.798C>G (p.Ser266Arg) | |
| 15 | g.73324216G= | CA2187189422 | HCN4 | c.2016C= (p.Ser672=) c.798C= (p.Ser266=) | |
| 15 | g.73324216G>T | CA117310 | HCN4 | c.2016C>A (p.Ser672Arg) c.798C>A (p.Ser266Arg) | ClinVar dbSNP |
| 15 | g.73324217C>A | CA393090312 | HCN4 | c.2015G>T (p.Ser672Ile) c.797G>T (p.Ser266Ile) | |
| 15 | g.73324217C>G | CA393090316 | HCN4 | c.2015G>C (p.Ser672Thr) c.797G>C (p.Ser266Thr) | |
| 15 | g.73324217C>T | CA393090314 | HCN4 | c.2015G>A (p.Ser672Asn) c.797G>A (p.Ser266Asn) | dbSNP |
| 15 | g.73324218T>A | CA393090318 | HCN4 | c.2014A>T (p.Ser672Cys) c.796A>T (p.Ser266Cys) | |
| 15 | g.73324218T>C | CA393090320 | HCN4 | c.2014A>G (p.Ser672Gly) c.796A>G (p.Ser266Gly) | |
| 15 | g.73324218T>G | CA393090319 | HCN4 | c.2014A>C (p.Ser672Arg) c.796A>C (p.Ser266Arg) | |
| 15 | g.73324219G>A | CA491479002 | HCN4 | c.2013C>T (p.Ala671=) c.795C>T (p.Ala265=) | gnomAD v4 |
| 15 | g.73324219G>C | CA491479003 | HCN4 | c.2013C>G (p.Ala671=) c.795C>G (p.Ala265=) | ClinVar |
| 15 | g.73324219G>T | CA491479004 | HCN4 | c.2013C>A (p.Ala671=) c.795C>A (p.Ala265=) | |
| 15 | g.73324220G>A | CA393090322 | HCN4 | c.2012C>T (p.Ala671Val) c.794C>T (p.Ala265Val) | |
| 15 | g.73324220G>C | CA393090323 | HCN4 | c.2012C>G (p.Ala671Gly) c.794C>G (p.Ala265Gly) | |
| 15 | g.73324220G>T | CA393090324 | HCN4 | c.2012C>A (p.Ala671Asp) c.794C>A (p.Ala265Asp) | |
| 15 | g.73324221C>A | CA393090326 | HCN4 | c.2011G>T (p.Ala671Ser) c.793G>T (p.Ala265Ser) | |
| 15 | g.73324221C>G | CA393090327 | HCN4 | c.2011G>C (p.Ala671Pro) c.793G>C (p.Ala265Pro) | |
| 15 | g.73324221C>T | CA393090328 | HCN4 | c.2011G>A (p.Ala671Thr) c.793G>A (p.Ala265Thr) |