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.73322971del | CA2575783825 | HCN4 | c.3125del (p.Pro1042ArgfsTer?) c.1907del (p.Pro636ArgfsTer?) | gnomAD v4 |
| 15 | g.73322970_73322971del | CA2575783826 | HCN4 | c.3124_3125del (p.Pro1042AlafsTer?) c.1906_1907del (p.Pro636AlafsTer?) | |
| 15 | g.73322969G>A | CA393086167 | HCN4 | c.3124C>T (p.Pro1042Ser) c.1906C>T (p.Pro636Ser) | gnomAD v4 |
| 15 | g.73322969G>C | CA393086168 | HCN4 | c.3124C>G (p.Pro1042Ala) c.1906C>G (p.Pro636Ala) | dbSNP |
| 15 | g.73322969G= | CA2187187088 | HCN4 | c.3124C= (p.Pro1042=) c.1906C= (p.Pro636=) | |
| 15 | g.73322969G>T | CA393086166 | HCN4 | c.3124C>A (p.Pro1042Thr) c.1906C>A (p.Pro636Thr) | gnomAD v4 |
| 15 | g.73322970G>A | CA491478063 | HCN4 | c.3123C>T (p.Ala1041=) c.1905C>T (p.Ala635=) | gnomAD v4 |
| 15 | g.73322970G>C | CA491478064 | HCN4 | c.3123C>G (p.Ala1041=) c.1905C>G (p.Ala635=) | |
| 15 | g.73322970G>T | CA491478065 | HCN4 | c.3123C>A (p.Ala1041=) c.1905C>A (p.Ala635=) | gnomAD v4 |
| 15 | g.73322971G>A | CA393086169 | HCN4 | c.3122C>T (p.Ala1041Val) c.1904C>T (p.Ala635Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322971G>C | CA393086170 | HCN4 | c.3122C>G (p.Ala1041Gly) c.1904C>G (p.Ala635Gly) | |
| 15 | g.73322971G= | CA2187187092 | HCN4 | c.3122C= (p.Ala1041=) c.1904C= (p.Ala635=) | |
| 15 | g.73322971G>T | CA393086171 | HCN4 | c.3122C>A (p.Ala1041Asp) c.1904C>A (p.Ala635Asp) | gnomAD v4 |
| 15 | g.73322972C>A | CA393086172 | HCN4 | c.3121G>T (p.Ala1041Ser) c.1903G>T (p.Ala635Ser) | gnomAD v4 |
| 15 | g.73322972C= | CA2187187100 | HCN4 | c.3121G= (p.Ala1041=) c.1903G= (p.Ala635=) | |
| 15 | g.73322972C>G | CA393086173 | HCN4 | c.3121G>C (p.Ala1041Pro) c.1903G>C (p.Ala635Pro) | |
| 15 | g.73322972C>T | CA7648880 | HCN4 | c.3121G>A (p.Ala1041Thr) c.1903G>A (p.Ala635Thr) | dbSNP ExAC gnomAD v4 |
| 15 | g.73322973A>C | CA393086174 | HCN4 | c.3120T>G (p.Ser1040Arg) c.1902T>G (p.Ser634Arg) | |
| 15 | g.73322973A>G | CA491478069 | HCN4 | c.3120T>C (p.Ser1040=) c.1902T>C (p.Ser634=) | gnomAD v4 |
| 15 | g.73322973A>T | CA393086175 | HCN4 | c.3120T>A (p.Ser1040Arg) c.1902T>A (p.Ser634Arg) | COSMIC |
| 15 | g.73322974C>A | CA393086176 | HCN4 | c.3119G>T (p.Ser1040Ile) c.1901G>T (p.Ser634Ile) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322974C= | CA2187187103 | HCN4 | c.3119G= (p.Ser1040=) c.1901G= (p.Ser634=) | |
| 15 | g.73322974C>G | CA393086177 | HCN4 | c.3119G>C (p.Ser1040Thr) c.1901G>C (p.Ser634Thr) | |
| 15 | g.73322974C>T | CA393086178 | HCN4 | c.3119G>A (p.Ser1040Asn) c.1901G>A (p.Ser634Asn) | |
| 15 | g.73322975T>A | CA393086179 | HCN4 | c.3118A>T (p.Ser1040Cys) c.1900A>T (p.Ser634Cys) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322975T>C | CA393086180 | HCN4 | c.3118A>G (p.Ser1040Gly) c.1900A>G (p.Ser634Gly) | gnomAD v4 |
| 15 | g.73322975T>G | CA393086181 | HCN4 | c.3118A>C (p.Ser1040Arg) c.1900A>C (p.Ser634Arg) | |
| 15 | g.73322975T= | CA2187187106 | HCN4 | c.3118A= (p.Ser1040=) c.1900A= (p.Ser634=) | |
| 15 | g.73322976C>A | CA491478073 | HCN4 | c.3117G>T (p.Pro1039=) c.1899G>T (p.Pro633=) | gnomAD v4 |
| 15 | g.73322976C= | CA2187187110 | HCN4 | c.3117G= (p.Pro1039=) c.1899G= (p.Pro633=) | |
| 15 | g.73322976C>G | CA491478074 | HCN4 | c.3117G>C (p.Pro1039=) c.1899G>C (p.Pro633=) | gnomAD v4 |
| 15 | g.73322976C>T | CA7648881 | HCN4 | c.3117G>A (p.Pro1039=) c.1899G>A (p.Pro633=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322977G>A | CA7648882 | HCN4 | c.3116C>T (p.Pro1039Leu) c.1898C>T (p.Pro633Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322977G>C | CA393086182 | HCN4 | c.3116C>G (p.Pro1039Arg) c.1898C>G (p.Pro633Arg) | ClinVar dbSNP |
| 15 | g.73322977G= | CA2187187118 | HCN4 | c.3116C= (p.Pro1039=) c.1898C= (p.Pro633=) | |
| 15 | g.73322977G>T | CA393086183 | HCN4 | c.3116C>A (p.Pro1039Gln) c.1898C>A (p.Pro633Gln) | gnomAD v4 |
| 15 | g.73322978_73322979del | CA2575783827 | HCN4 | c.3115_3116del (p.Pro1039GlufsTer?) c.1897_1898del (p.Pro633GlufsTer?) | |
| 15 | g.73322978G>A | CA393086184 | HCN4 | c.3115C>T (p.Pro1039Ser) c.1897C>T (p.Pro633Ser) | gnomAD v4 COSMIC |
| 15 | g.73322978G>C | CA393086185 | HCN4 | c.3115C>G (p.Pro1039Ala) c.1897C>G (p.Pro633Ala) | |
| 15 | g.73322978G>T | CA393086186 | HCN4 | c.3115C>A (p.Pro1039Thr) c.1897C>A (p.Pro633Thr) | gnomAD v4 |
| 15 | g.73322979G>A | CA491478076 | HCN4 | c.3114C>T (p.Phe1038=) c.1896C>T (p.Phe632=) | |
| 15 | g.73322979G>C | CA393086187 | HCN4 | c.3114C>G (p.Phe1038Leu) c.1896C>G (p.Phe632Leu) | |
| 15 | g.73322979G= | CA2187187131 | HCN4 | c.3114C= (p.Phe1038=) c.1896C= (p.Phe632=) | |
| 15 | g.73322979G>T | CA393086188 | HCN4 | c.3114C>A (p.Phe1038Leu) c.1896C>A (p.Phe632Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322980A>C | CA393086189 | HCN4 | c.3113T>G (p.Phe1038Cys) c.1895T>G (p.Phe632Cys) | |
| 15 | g.73322980A>G | CA393086190 | HCN4 | c.3113T>C (p.Phe1038Ser) c.1895T>C (p.Phe632Ser) | |
| 15 | g.73322980A>T | CA393086191 | HCN4 | c.3113T>A (p.Phe1038Tyr) c.1895T>A (p.Phe632Tyr) | |
| 15 | g.73322981A= | CA2187187135 | HCN4 | c.3112T= (p.Phe1038=) c.1894T= (p.Phe632=) | |
| 15 | g.73322981A>C | CA393086192 | HCN4 | c.3112T>G (p.Phe1038Val) c.1894T>G (p.Phe632Val) | |
| 15 | g.73322981A>G | CA393086193 | HCN4 | c.3112T>C (p.Phe1038Leu) c.1894T>C (p.Phe632Leu) | dbSNP gnomAD v4 |
| 15 | g.73322981A>T | CA393086194 | HCN4 | c.3112T>A (p.Phe1038Ile) c.1894T>A (p.Phe632Ile) | |
| 15 | g.73322982G>A | CA491478079 | HCN4 | c.3111C>T (p.Thr1037=) c.1893C>T (p.Thr631=) | gnomAD v4 |
| 15 | g.73322982G>C | CA491478080 | HCN4 | c.3111C>G (p.Thr1037=) c.1893C>G (p.Thr631=) | |
| 15 | g.73322982G>T | CA491478081 | HCN4 | c.3111C>A (p.Thr1037=) c.1893C>A (p.Thr631=) | ClinVar gnomAD v4 |
| 15 | g.73322983G>A | CA393086196 | HCN4 | c.3110C>T (p.Thr1037Ile) c.1892C>T (p.Thr631Ile) | |
| 15 | g.73322983G>C | CA393086197 | HCN4 | c.3110C>G (p.Thr1037Ser) c.1892C>G (p.Thr631Ser) | |
| 15 | g.73322983G>T | CA393086195 | HCN4 | c.3110C>A (p.Thr1037Asn) c.1892C>A (p.Thr631Asn) | ClinVar gnomAD v4 |
| 15 | g.73322984T>A | CA393086198 | HCN4 | c.3109A>T (p.Thr1037Ser) c.1891A>T (p.Thr631Ser) | |
| 15 | g.73322984T>C | CA393086199 | HCN4 | c.3109A>G (p.Thr1037Ala) c.1891A>G (p.Thr631Ala) | gnomAD v4 |
| 15 | g.73322984T>G | CA393086200 | HCN4 | c.3109A>C (p.Thr1037Pro) c.1891A>C (p.Thr631Pro) | |
| 15 | g.73322985T>A | CA393086201 | HCN4 | c.3108A>T (p.Arg1036Ser) c.1890A>T (p.Arg630Ser) | ClinVar |
| 15 | g.73322985T>C | CA491478084 | HCN4 | c.3108A>G (p.Arg1036=) c.1890A>G (p.Arg630=) | |
| 15 | g.73322985T>G | CA393086202 | HCN4 | c.3108A>C (p.Arg1036Ser) c.1890A>C (p.Arg630Ser) | |
| 15 | g.73322986C>A | CA393086205 | HCN4 | c.3107G>T (p.Arg1036Ile) c.1889G>T (p.Arg630Ile) | gnomAD v4 |
| 15 | g.73322986C>G | CA393086203 | HCN4 | c.3107G>C (p.Arg1036Thr) c.1889G>C (p.Arg630Thr) | |
| 15 | g.73322986C>T | CA393086204 | HCN4 | c.3107G>A (p.Arg1036Lys) c.1889G>A (p.Arg630Lys) | |
| 15 | g.73322987T>A | CA393086206 | HCN4 | c.3106A>T (p.Arg1036Ter) c.1888A>T (p.Arg630Ter) | |
| 15 | g.73322987T>C | CA393086207 | HCN4 | c.3106A>G (p.Arg1036Gly) c.1888A>G (p.Arg630Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322987T>G | CA491478088 | HCN4 | c.3106A>C (p.Arg1036=) c.1888A>C (p.Arg630=) | |
| 15 | g.73322987T= | CA2187187138 | HCN4 | c.3106A= (p.Arg1036=) c.1888A= (p.Arg630=) | |
| 15 | g.73322988T>A | CA491478089 | HCN4 | c.3105A>T (p.Pro1035=) c.1887A>T (p.Pro629=) | |
| 15 | g.73322988T>C | CA491478090 | HCN4 | c.3105A>G (p.Pro1035=) c.1887A>G (p.Pro629=) | gnomAD v4 |
| 15 | g.73322988T>G | CA491478092 | HCN4 | c.3105A>C (p.Pro1035=) c.1887A>C (p.Pro629=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322988T= | CA2187187144 | HCN4 | c.3105A= (p.Pro1035=) c.1887A= (p.Pro629=) | |
| 15 | g.73322989G>A | CA393086208 | HCN4 | c.3104C>T (p.Pro1035Leu) c.1886C>T (p.Pro629Leu) | gnomAD v4 COSMIC |
| 15 | g.73322989G>C | CA393086209 | HCN4 | c.3104C>G (p.Pro1035Arg) c.1886C>G (p.Pro629Arg) | |
| 15 | g.73322989G>T | CA393086210 | HCN4 | c.3104C>A (p.Pro1035Gln) c.1886C>A (p.Pro629Gln) | gnomAD v4 |
| 15 | g.73322994dup | CA619410589 | HCN4 | c.3104dup (p.Arg1036LysfsTer?) c.1886dup (p.Arg630LysfsTer?) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322994del | CA2629370542 | HCN4 | c.3104del (p.Pro1035GlnfsTer?) c.1886del (p.Pro629GlnfsTer?) | gnomAD v4 |
| 15 | g.73322990G>A | CA393086212 | HCN4 | c.3103C>T (p.Pro1035Ser) c.1885C>T (p.Pro629Ser) | gnomAD v4 |
| 15 | g.73322990G>C | CA7648883 | HCN4 | c.3103C>G (p.Pro1035Ala) c.1885C>G (p.Pro629Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322990G= | CA2187187155 | HCN4 | c.3103C= (p.Pro1035=) c.1885C= (p.Pro629=) | |
| 15 | g.73322990G>T | CA393086211 | HCN4 | c.3103C>A (p.Pro1035Thr) c.1885C>A (p.Pro629Thr) | gnomAD v4 |
| 15 | g.73322991G>A | CA491478095 | HCN4 | c.3102C>T (p.Pro1034=) c.1884C>T (p.Pro628=) | gnomAD v4 COSMIC |
| 15 | g.73322991G>C | CA491478096 | HCN4 | c.3102C>G (p.Pro1034=) c.1884C>G (p.Pro628=) | |
| 15 | g.73322991G>T | CA491478097 | HCN4 | c.3102C>A (p.Pro1034=) c.1884C>A (p.Pro628=) | gnomAD v4 |
| 15 | g.73322992G>A | CA393086213 | HCN4 | c.3101C>T (p.Pro1034Leu) c.1883C>T (p.Pro628Leu) | ClinVar gnomAD v4 |
| 15 | g.73322992G>C | CA272663736 | HCN4 | c.3101C>G (p.Pro1034Arg) c.1883C>G (p.Pro628Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322992G= | CA2187187164 | HCN4 | c.3101C= (p.Pro1034=) c.1883C= (p.Pro628=) | |
| 15 | g.73322992G>T | CA393086214 | HCN4 | c.3101C>A (p.Pro1034His) c.1883C>A (p.Pro628His) | gnomAD v4 |
| 15 | g.73322993G>A | CA393086215 | HCN4 | c.3100C>T (p.Pro1034Ser) c.1882C>T (p.Pro628Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322993G>C | CA393086216 | HCN4 | c.3100C>G (p.Pro1034Ala) c.1882C>G (p.Pro628Ala) | |
| 15 | g.73322993G= | CA2187187173 | HCN4 | c.3100C= (p.Pro1034=) c.1882C= (p.Pro628=) | |
| 15 | g.73322993G>T | CA393086217 | HCN4 | c.3100C>A (p.Pro1034Thr) c.1882C>A (p.Pro628Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322994G>A | CA7648884 | HCN4 | c.3099C>T (p.Gly1033=) c.1881C>T (p.Gly627=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322994G>C | CA491478100 | HCN4 | c.3099C>G (p.Gly1033=) c.1881C>G (p.Gly627=) | dbSNP gnomAD v4 |
| 15 | g.73322994G= | CA2187187181 | HCN4 | c.3099C= (p.Gly1033=) c.1881C= (p.Gly627=) | |
| 15 | g.73322994G>T | CA491478101 | HCN4 | c.3099C>A (p.Gly1033=) c.1881C>A (p.Gly627=) | dbSNP gnomAD v4 |
| 15 | g.73322995C>A | CA393086218 | HCN4 | c.3098G>T (p.Gly1033Val) c.1880G>T (p.Gly627Val) | gnomAD v4 |
| 15 | g.73322995C= | CA2187187186 | HCN4 | c.3098G= (p.Gly1033=) c.1880G= (p.Gly627=) | |
| 15 | g.73322995C>G | CA393086219 | HCN4 | c.3098G>C (p.Gly1033Ala) c.1880G>C (p.Gly627Ala) | gnomAD v4 |
| 15 | g.73322995C>T | CA393086220 | HCN4 | c.3098G>A (p.Gly1033Asp) c.1880G>A (p.Gly627Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322996C>A | CA393086221 | HCN4 | c.3097G>T (p.Gly1033Cys) c.1879G>T (p.Gly627Cys) | gnomAD v4 |
| 15 | g.73322996C>G | CA393086222 | HCN4 | c.3097G>C (p.Gly1033Arg) c.1879G>C (p.Gly627Arg) | |
| 15 | g.73322996C>T | CA393086223 | HCN4 | c.3097G>A (p.Gly1033Ser) c.1879G>A (p.Gly627Ser) | |
| 15 | g.73322997T>A | CA491478106 | HCN4 | c.3096A>T (p.Pro1032=) c.1878A>T (p.Pro626=) | |
| 15 | g.73322997T>C | CA491478107 | HCN4 | c.3096A>G (p.Pro1032=) c.1878A>G (p.Pro626=) | ClinVar gnomAD v4 |
| 15 | g.73322997T>G | CA491478105 | HCN4 | c.3096A>C (p.Pro1032=) c.1878A>C (p.Pro626=) | dbSNP gnomAD v4 |
| 15 | g.73322997T= | CA2187187189 | HCN4 | c.3096A= (p.Pro1032=) c.1878A= (p.Pro626=) | |
| 15 | g.73322998G>A | CA393086224 | HCN4 | c.3095C>T (p.Pro1032Leu) c.1877C>T (p.Pro626Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322998G>C | CA393086225 | HCN4 | c.3095C>G (p.Pro1032Arg) c.1877C>G (p.Pro626Arg) | |
| 15 | g.73322998G= | CA2187187192 | HCN4 | c.3095C= (p.Pro1032=) c.1877C= (p.Pro626=) | |
| 15 | g.73322998G>T | CA393086226 | HCN4 | c.3095C>A (p.Pro1032Gln) c.1877C>A (p.Pro626Gln) | |
| 15 | g.73322999G>A | CA393086227 | HCN4 | c.3094C>T (p.Pro1032Ser) c.1876C>T (p.Pro626Ser) | gnomAD v3 gnomAD v4 |
| 15 | g.73322999G>C | CA393086228 | HCN4 | c.3094C>G (p.Pro1032Ala) c.1876C>G (p.Pro626Ala) | |
| 15 | g.73322999G= | CA2187187195 | HCN4 | c.3094C= (p.Pro1032=) c.1876C= (p.Pro626=) | |
| 15 | g.73322999G>T | CA7648885 | HCN4 | c.3094C>A (p.Pro1032Thr) c.1876C>A (p.Pro626Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323000G>A | CA491478110 | HCN4 | c.3093C>T (p.Ser1031=) c.1875C>T (p.Ser625=) | ClinVar gnomAD v4 |
| 15 | g.73323000G>C | CA393086229 | HCN4 | c.3093C>G (p.Ser1031Arg) c.1875C>G (p.Ser625Arg) | |
| 15 | g.73323000G= | CA2187187199 | HCN4 | c.3093C= (p.Ser1031=) c.1875C= (p.Ser625=) | |
| 15 | g.73323000G>T | CA393086230 | HCN4 | c.3093C>A (p.Ser1031Arg) c.1875C>A (p.Ser625Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323001C>A | CA393086231 | HCN4 | c.3092G>T (p.Ser1031Ile) c.1874G>T (p.Ser625Ile) | gnomAD v4 |
| 15 | g.73323001C>G | CA393086232 | HCN4 | c.3092G>C (p.Ser1031Thr) c.1874G>C (p.Ser625Thr) | |
| 15 | g.73323001C>T | CA393086233 | HCN4 | c.3092G>A (p.Ser1031Asn) c.1874G>A (p.Ser625Asn) | gnomAD v4 |
| 15 | g.73323002T>A | CA393086234 | HCN4 | c.3091A>T (p.Ser1031Cys) c.1873A>T (p.Ser625Cys) | |
| 15 | g.73323002T>C | CA393086235 | HCN4 | c.3091A>G (p.Ser1031Gly) c.1873A>G (p.Ser625Gly) | gnomAD v4 |
| 15 | g.73323002T>G | CA393086236 | HCN4 | c.3091A>C (p.Ser1031Arg) c.1873A>C (p.Ser625Arg) | |
| 15 | g.73323003G>A | CA491478112 | HCN4 | c.3090C>T (p.His1030=) c.1872C>T (p.His624=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323003G>C | CA393086237 | HCN4 | c.3090C>G (p.His1030Gln) c.1872C>G (p.His624Gln) | |
| 15 | g.73323003G= | CA2187187202 | HCN4 | c.3090C= (p.His1030=) c.1872C= (p.His624=) | |
| 15 | g.73323003G>T | CA393086238 | HCN4 | c.3090C>A (p.His1030Gln) c.1872C>A (p.His624Gln) | gnomAD v4 |
| 15 | g.73323004T>A | CA393086241 | HCN4 | c.3089A>T (p.His1030Leu) c.1871A>T (p.His624Leu) | |
| 15 | g.73323004T>C | CA393086240 | HCN4 | c.3089A>G (p.His1030Arg) c.1871A>G (p.His624Arg) | |
| 15 | g.73323004T>G | CA393086239 | HCN4 | c.3089A>C (p.His1030Pro) c.1871A>C (p.His624Pro) | |
| 15 | g.73323005G>A | CA393086244 | HCN4 | c.3088C>T (p.His1030Tyr) c.1870C>T (p.His624Tyr) | |
| 15 | g.73323005G>C | CA393086242 | HCN4 | c.3088C>G (p.His1030Asp) c.1870C>G (p.His624Asp) | |
| 15 | g.73323005G>T | CA393086243 | HCN4 | c.3088C>A (p.His1030Asn) c.1870C>A (p.His624Asn) | gnomAD v4 |
| 15 | g.73323006G>A | CA491478116 | HCN4 | c.3087C>T (p.Gly1029=) c.1869C>T (p.Gly623=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323006G>C | CA491478118 | HCN4 | c.3087C>G (p.Gly1029=) c.1869C>G (p.Gly623=) | ClinVar dbSNP |
| 15 | g.73323006G= | CA2187187204 | HCN4 | c.3087C= (p.Gly1029=) c.1869C= (p.Gly623=) | |
| 15 | g.73323006G>T | CA491478120 | HCN4 | c.3087C>A (p.Gly1029=) c.1869C>A (p.Gly623=) | gnomAD v4 |
| 15 | g.73323007C>A | CA393086245 | HCN4 | c.3086G>T (p.Gly1029Val) c.1868G>T (p.Gly623Val) | gnomAD v4 |
| 15 | g.73323007C>G | CA393086246 | HCN4 | c.3086G>C (p.Gly1029Ala) c.1868G>C (p.Gly623Ala) | |
| 15 | g.73323007C>T | CA393086247 | HCN4 | c.3086G>A (p.Gly1029Asp) c.1868G>A (p.Gly623Asp) | gnomAD v4 |
| 15 | g.73323008C>A | CA393086250 | HCN4 | c.3085G>T (p.Gly1029Cys) c.1867G>T (p.Gly623Cys) | gnomAD v4 |
| 15 | g.73323008C>G | CA393086249 | HCN4 | c.3085G>C (p.Gly1029Arg) c.1867G>C (p.Gly623Arg) | |
| 15 | g.73323008C>T | CA393086248 | HCN4 | c.3085G>A (p.Gly1029Ser) c.1867G>A (p.Gly623Ser) | gnomAD v4 |
| 15 | g.73323009A>C | CA491478121 | HCN4 | c.3084T>G (p.Pro1028=) c.1866T>G (p.Pro622=) | |
| 15 | g.73323009A>G | CA491478122 | HCN4 | c.3084T>C (p.Pro1028=) c.1866T>C (p.Pro622=) | |
| 15 | g.73323009A>T | CA491478123 | HCN4 | c.3084T>A (p.Pro1028=) c.1866T>A (p.Pro622=) | |
| 15 | g.73323010G>A | CA393086251 | HCN4 | c.3083C>T (p.Pro1028Leu) c.1865C>T (p.Pro622Leu) | gnomAD v4 |
| 15 | g.73323010G>C | CA393086252 | HCN4 | c.3083C>G (p.Pro1028Arg) c.1865C>G (p.Pro622Arg) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323010G= | CA2187187206 | HCN4 | c.3083C= (p.Pro1028=) c.1865C= (p.Pro622=) | |
| 15 | g.73323010G>T | CA393086253 | HCN4 | c.3083C>A (p.Pro1028His) c.1865C>A (p.Pro622His) | gnomAD v4 |
| 15 | g.73323015dup | CA2575783828 | HCN4 | c.3083dup (p.Gly1029TrpfsTer?) c.1865dup (p.Gly623TrpfsTer?) | gnomAD v4 |
| 15 | g.73323015del | CA645586807 | HCN4 | c.3083del (p.Pro1028LeufsTer?) c.1865del (p.Pro622LeufsTer?) | gnomAD v4 COSMIC |
| 15 | g.73323011G>A | CA393086254 | HCN4 | c.3082C>T (p.Pro1028Ser) c.1864C>T (p.Pro622Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323011G>C | CA393086255 | HCN4 | c.3082C>G (p.Pro1028Ala) c.1864C>G (p.Pro622Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323011G= | CA2187187210 | HCN4 | c.3082C= (p.Pro1028=) c.1864C= (p.Pro622=) | |
| 15 | g.73323011G>T | CA393086256 | HCN4 | c.3082C>A (p.Pro1028Thr) c.1864C>A (p.Pro622Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323012G>A | CA491478124 | HCN4 | c.3081C>T (p.Pro1027=) c.1863C>T (p.Pro621=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323012G>C | CA491478125 | HCN4 | c.3081C>G (p.Pro1027=) c.1863C>G (p.Pro621=) | |
| 15 | g.73323012G= | CA2187187214 | HCN4 | c.3081C= (p.Pro1027=) c.1863C= (p.Pro621=) | |
| 15 | g.73323012G>T | CA491478126 | HCN4 | c.3081C>A (p.Pro1027=) c.1863C>A (p.Pro621=) | gnomAD v4 |
| 15 | g.73323013G>A | CA7648886 | HCN4 | c.3080C>T (p.Pro1027Leu) c.1862C>T (p.Pro621Leu) | dbSNP ExAC gnomAD v2 |
| 15 | g.73323013G>C | CA393086257 | HCN4 | c.3080C>G (p.Pro1027Arg) c.1862C>G (p.Pro621Arg) | |
| 15 | g.73323013G= | CA2187187223 | HCN4 | c.3080C= (p.Pro1027=) c.1862C= (p.Pro621=) | |
| 15 | g.73323013G>T | CA272663752 | HCN4 | c.3080C>A (p.Pro1027His) c.1862C>A (p.Pro621His) | dbSNP gnomAD v4 |
| 15 | g.73323014G>A | CA393086258 | HCN4 | c.3079C>T (p.Pro1027Ser) c.1861C>T (p.Pro621Ser) | ClinVar |
| 15 | g.73323014G>C | CA393086259 | HCN4 | c.3079C>G (p.Pro1027Ala) c.1861C>G (p.Pro621Ala) | gnomAD v4 |
| 15 | g.73323014G= | CA2187187225 | HCN4 | c.3079C= (p.Pro1027=) c.1861C= (p.Pro621=) | |
| 15 | g.73323014G>T | CA393086260 | HCN4 | c.3079C>A (p.Pro1027Thr) c.1861C>A (p.Pro621Thr) | dbSNP gnomAD v4 |
| 15 | g.73323015G>A | CA7648887 | HCN4 | c.3078C>T (p.Ser1026=) c.1860C>T (p.Ser620=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323015G>C | CA393086261 | HCN4 | c.3078C>G (p.Ser1026Arg) c.1860C>G (p.Ser620Arg) | gnomAD v4 |
| 15 | g.73323015G= | CA2187187229 | HCN4 | c.3078C= (p.Ser1026=) c.1860C= (p.Ser620=) | |
| 15 | g.73323015G>T | CA393086262 | HCN4 | c.3078C>A (p.Ser1026Arg) c.1860C>A (p.Ser620Arg) | gnomAD v4 |
| 15 | g.73323016C>A | CA393086263 | HCN4 | c.3077G>T (p.Ser1026Ile) c.1859G>T (p.Ser620Ile) | gnomAD v4 |
| 15 | g.73323016C= | CA2187187234 | HCN4 | c.3077G= (p.Ser1026=) c.1859G= (p.Ser620=) | |
| 15 | g.73323016C>G | CA393086264 | HCN4 | c.3077G>C (p.Ser1026Thr) c.1859G>C (p.Ser620Thr) | |
| 15 | g.73323016C>T | CA10587881 | HCN4 | c.3077G>A (p.Ser1026Asn) c.1859G>A (p.Ser620Asn) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323017T>A | CA393086265 | HCN4 | c.3076A>T (p.Ser1026Cys) c.1858A>T (p.Ser620Cys) | |
| 15 | g.73323017T>C | CA393086266 | HCN4 | c.3076A>G (p.Ser1026Gly) c.1858A>G (p.Ser620Gly) | gnomAD v4 |
| 15 | g.73323017T>G | CA393086267 | HCN4 | c.3076A>C (p.Ser1026Arg) c.1858A>C (p.Ser620Arg) | gnomAD v4 |
| 15 | g.73323018G>A | CA272663782 | HCN4 | c.3075C>T (p.Leu1025=) c.1857C>T (p.Leu619=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323018G>C | CA491478276 | HCN4 | c.3075C>G (p.Leu1025=) c.1857C>G (p.Leu619=) | |
| 15 | g.73323018G= | CA2187187239 | HCN4 | c.3075C= (p.Leu1025=) c.1857C= (p.Leu619=) | |
| 15 | g.73323018G>T | CA491478274 | HCN4 | c.3075C>A (p.Leu1025=) c.1857C>A (p.Leu619=) | gnomAD v4 |
| 15 | g.73323019A>C | CA393086269 | HCN4 | c.3074T>G (p.Leu1025Arg) c.1856T>G (p.Leu619Arg) | |
| 15 | g.73323019A>G | CA393086270 | HCN4 | c.3074T>C (p.Leu1025Pro) c.1856T>C (p.Leu619Pro) | |
| 15 | g.73323019A>T | CA393086268 | HCN4 | c.3074T>A (p.Leu1025His) c.1856T>A (p.Leu619His) | |
| 15 | g.73323020G>A | CA393086271 | HCN4 | c.3073C>T (p.Leu1025Phe) c.1855C>T (p.Leu619Phe) | |
| 15 | g.73323020G>C | CA393086272 | HCN4 | c.3073C>G (p.Leu1025Val) c.1855C>G (p.Leu619Val) | |
| 15 | g.73323020G= | CA2187187243 | HCN4 | c.3073C= (p.Leu1025=) c.1855C= (p.Leu619=) | |
| 15 | g.73323020G>T | CA7648888 | HCN4 | c.3073C>A (p.Leu1025Ile) c.1855C>A (p.Leu619Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323021A>C | CA491478284 | HCN4 | c.3072T>G (p.Gly1024=) c.1854T>G (p.Gly618=) | |
| 15 | g.73323021A>G | CA491478286 | HCN4 | c.3072T>C (p.Gly1024=) c.1854T>C (p.Gly618=) | |
| 15 | g.73323021A>T | CA491478287 | HCN4 | c.3072T>A (p.Gly1024=) c.1854T>A (p.Gly618=) | gnomAD v4 |
| 15 | g.73323022C>A | CA7648889 | HCN4 | c.3071G>T (p.Gly1024Val) c.1853G>T (p.Gly618Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323022C= | CA2187187247 | HCN4 | c.3071G= (p.Gly1024=) c.1853G= (p.Gly618=) | |
| 15 | g.73323022C>G | CA393086274 | HCN4 | c.3071G>C (p.Gly1024Ala) c.1853G>C (p.Gly618Ala) | |
| 15 | g.73323022C>T | CA393086273 | HCN4 | c.3071G>A (p.Gly1024Asp) c.1853G>A (p.Gly618Asp) | |
| 15 | g.73323026_73323028del | CA2804714150 | HCN4 | c.3069_3071del (p.Gly1024del) c.1851_1853del (p.Gly618del) | |
| 15 | g.73323023C>A | CA393086275 | HCN4 | c.3070G>T (p.Gly1024Cys) c.1852G>T (p.Gly618Cys) | gnomAD v4 |
| 15 | g.73323023C= | CA2187187253 | HCN4 | c.3070G= (p.Gly1024=) c.1852G= (p.Gly618=) | |
| 15 | g.73323023C>G | CA272663833 | HCN4 | c.3070G>C (p.Gly1024Arg) c.1852G>C (p.Gly618Arg) | dbSNP gnomAD v4 |
| 15 | g.73323023C>T | CA393086276 | HCN4 | c.3070G>A (p.Gly1024Ser) c.1852G>A (p.Gly618Ser) | dbSNP gnomAD v4 |
| 15 | g.73323024T>A | CA491478298 | HCN4 | c.3069A>T (p.Gly1023=) c.1851A>T (p.Gly617=) | |
| 15 | g.73323024T>C | CA491478295 | HCN4 | c.3069A>G (p.Gly1023=) c.1851A>G (p.Gly617=) | gnomAD v4 |
| 15 | g.73323024T>G | CA491478297 | HCN4 | c.3069A>C (p.Gly1023=) c.1851A>C (p.Gly617=) | |
| 15 | g.73323025C>A | CA393086277 | HCN4 | c.3068G>T (p.Gly1023Val) c.1850G>T (p.Gly617Val) | gnomAD v4 |
| 15 | g.73323025C>G | CA393086278 | HCN4 | c.3068G>C (p.Gly1023Ala) c.1850G>C (p.Gly617Ala) | |
| 15 | g.73323025C>T | CA393086279 | HCN4 | c.3068G>A (p.Gly1023Glu) c.1850G>A (p.Gly617Glu) | |
| 15 | g.73323026C>A | CA393086280 | HCN4 | c.3067G>T (p.Gly1023Ter) c.1849G>T (p.Gly617Ter) | |
| 15 | g.73323026C>G | CA393086281 | HCN4 | c.3067G>C (p.Gly1023Arg) c.1849G>C (p.Gly617Arg) | |
| 15 | g.73323026C>T | CA393086282 | HCN4 | c.3067G>A (p.Gly1023Arg) c.1849G>A (p.Gly617Arg) | gnomAD v4 |
| 15 | g.73323027T>A | CA491478306 | HCN4 | c.3066A>T (p.Arg1022=) c.1848A>T (p.Arg616=) | |
| 15 | g.73323027T>C | CA491478307 | HCN4 | c.3066A>G (p.Arg1022=) c.1848A>G (p.Arg616=) | gnomAD v4 |
| 15 | g.73323027T>G | CA491478308 | HCN4 | c.3066A>C (p.Arg1022=) c.1848A>C (p.Arg616=) | |
| 15 | g.73323028C>A | CA393086285 | HCN4 | c.3065G>T (p.Arg1022Leu) c.1847G>T (p.Arg616Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323028C= | CA2187187258 | HCN4 | c.3065G= (p.Arg1022=) c.1847G= (p.Arg616=) | |
| 15 | g.73323028C>G | CA393086284 | HCN4 | c.3065G>C (p.Arg1022Pro) c.1847G>C (p.Arg616Pro) | |
| 15 | g.73323028C>T | CA393086283 | HCN4 | c.3065G>A (p.Arg1022Gln) c.1847G>A (p.Arg616Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323029G>A | CA7648890 | HCN4 | c.3064C>T (p.Arg1022Ter) c.1846C>T (p.Arg616Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323029G>C | CA393086286 | HCN4 | c.3064C>G (p.Arg1022Gly) c.1846C>G (p.Arg616Gly) | |
| 15 | g.73323029G= | CA2187187265 | HCN4 | c.3064C= (p.Arg1022=) c.1846C= (p.Arg616=) | |
| 15 | g.73323029G>T | CA491478310 | HCN4 | c.3064C>A (p.Arg1022=) c.1846C>A (p.Arg616=) | gnomAD v4 |
| 15 | g.73323032del | CA2629370543 | HCN4 | c.3064del (p.Arg1022GlufsTer?) c.1846del (p.Arg616GlufsTer?) | gnomAD v4 |
| 15 | g.73323030G>A | CA491478317 | HCN4 | c.3063C>T (p.Pro1021=) c.1845C>T (p.Pro615=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323030G>C | CA491478315 | HCN4 | c.3063C>G (p.Pro1021=) c.1845C>G (p.Pro615=) | |
| 15 | g.73323030G= | CA2187187275 | HCN4 | c.3063C= (p.Pro1021=) c.1845C= (p.Pro615=) | |
| 15 | g.73323030G>T | CA491478316 | HCN4 | c.3063C>A (p.Pro1021=) c.1845C>A (p.Pro615=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323031G>A | CA393086288 | HCN4 | c.3062C>T (p.Pro1021Leu) c.1844C>T (p.Pro615Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323031G>C | CA393086289 | HCN4 | c.3062C>G (p.Pro1021Arg) c.1844C>G (p.Pro615Arg) | |
| 15 | g.73323031G= | CA2187187279 | HCN4 | c.3062C= (p.Pro1021=) c.1844C= (p.Pro615=) | |
| 15 | g.73323031G>T | CA393086291 | HCN4 | c.3062C>A (p.Pro1021His) c.1844C>A (p.Pro615His) | gnomAD v4 |
| 15 | g.73323032G>A | CA393086293 | HCN4 | c.3061C>T (p.Pro1021Ser) c.1843C>T (p.Pro615Ser) | gnomAD v4 |
| 15 | g.73323032G>C | CA393086294 | HCN4 | c.3061C>G (p.Pro1021Ala) c.1843C>G (p.Pro615Ala) | |
| 15 | g.73323032G= | CA2187187282 | HCN4 | c.3061C= (p.Pro1021=) c.1843C= (p.Pro615=) | |
| 15 | g.73323032G>T | CA272663837 | HCN4 | c.3061C>A (p.Pro1021Thr) c.1843C>A (p.Pro615Thr) | dbSNP gnomAD v4 |
| 15 | g.73323033A= | CA2187187289 | HCN4 | c.3060T= (p.Thr1020=) c.1842T= (p.Thr614=) | |
| 15 | g.73323033A>C | CA491478326 | HCN4 | c.3060T>G (p.Thr1020=) c.1842T>G (p.Thr614=) | |
| 15 | g.73323033A>G | CA491478329 | HCN4 | c.3060T>C (p.Thr1020=) c.1842T>C (p.Thr614=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323033A>T | CA491478331 | HCN4 | c.3060T>A (p.Thr1020=) c.1842T>A (p.Thr614=) | gnomAD v4 |
| 15 | g.73323034G>A | CA7648891 | HCN4 | c.3059C>T (p.Thr1020Ile) c.1841C>T (p.Thr614Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323034G>C | CA393086298 | HCN4 | c.3059C>G (p.Thr1020Ser) c.1841C>G (p.Thr614Ser) | |
| 15 | g.73323034G= | CA2187187298 | HCN4 | c.3059C= (p.Thr1020=) c.1841C= (p.Thr614=) | |
| 15 | g.73323034G>T | CA393086299 | HCN4 | c.3059C>A (p.Thr1020Asn) c.1841C>A (p.Thr614Asn) | gnomAD v4 |
| 15 | g.73323035T>A | CA393086303 | HCN4 | c.3058A>T (p.Thr1020Ser) c.1840A>T (p.Thr614Ser) | |
| 15 | g.73323035T>C | CA393086304 | HCN4 | c.3058A>G (p.Thr1020Ala) c.1840A>G (p.Thr614Ala) | gnomAD v4 |
| 15 | g.73323035T>G | CA393086302 | HCN4 | c.3058A>C (p.Thr1020Pro) c.1840A>C (p.Thr614Pro) | ClinVar dbSNP |
| 15 | g.73323036A= | CA2187187307 | HCN4 | c.3057T= (p.Phe1019=) c.1839T= (p.Phe613=) | |
| 15 | g.73323036A>C | CA393086305 | HCN4 | c.3057T>G (p.Phe1019Leu) c.1839T>G (p.Phe613Leu) | gnomAD v4 |
| 15 | g.73323036A>G | CA7648892 | HCN4 | c.3057T>C (p.Phe1019=) c.1839T>C (p.Phe613=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323036A>T | CA393086307 | HCN4 | c.3057T>A (p.Phe1019Leu) c.1839T>A (p.Phe613Leu) | |
| 15 | g.73323037A>C | CA393086309 | HCN4 | c.3056T>G (p.Phe1019Cys) c.1838T>G (p.Phe613Cys) | |
| 15 | g.73323037A>G | CA393086310 | HCN4 | c.3056T>C (p.Phe1019Ser) c.1838T>C (p.Phe613Ser) | |
| 15 | g.73323037A>T | CA393086311 | HCN4 | c.3056T>A (p.Phe1019Tyr) c.1838T>A (p.Phe613Tyr) | |
| 15 | g.73323038A>C | CA393086314 | HCN4 | c.3055T>G (p.Phe1019Val) c.1837T>G (p.Phe613Val) | |
| 15 | g.73323038A>G | CA393086315 | HCN4 | c.3055T>C (p.Phe1019Leu) c.1837T>C (p.Phe613Leu) | gnomAD v4 |
| 15 | g.73323038A>T | CA393086317 | HCN4 | c.3055T>A (p.Phe1019Ile) c.1837T>A (p.Phe613Ile) | |
| 15 | g.73323039G>A | CA272663846 | HCN4 | c.3054C>T (p.Gly1018=) c.1836C>T (p.Gly612=) | dbSNP gnomAD v2 |
| 15 | g.73323039G>C | CA491478349 | HCN4 | c.3054C>G (p.Gly1018=) c.1836C>G (p.Gly612=) | |
| 15 | g.73323039G= | CA2187187310 | HCN4 | c.3054C= (p.Gly1018=) c.1836C= (p.Gly612=) | |
| 15 | g.73323039G>T | CA491478350 | HCN4 | c.3054C>A (p.Gly1018=) c.1836C>A (p.Gly612=) | gnomAD v4 |
| 15 | g.73323040C>A | CA393086319 | HCN4 | c.3053G>T (p.Gly1018Val) c.1835G>T (p.Gly612Val) | gnomAD v4 |
| 15 | g.73323040C>G | CA393086321 | HCN4 | c.3053G>C (p.Gly1018Ala) c.1835G>C (p.Gly612Ala) | |
| 15 | g.73323040C>T | CA393086322 | HCN4 | c.3053G>A (p.Gly1018Asp) c.1835G>A (p.Gly612Asp) | |
| 15 | g.73323041C>A | CA393086328 | HCN4 | c.3052G>T (p.Gly1018Cys) c.1834G>T (p.Gly612Cys) | |
| 15 | g.73323041C>G | CA393086325 | HCN4 | c.3052G>C (p.Gly1018Arg) c.1834G>C (p.Gly612Arg) | |
| 15 | g.73323041C>T | CA393086326 | HCN4 | c.3052G>A (p.Gly1018Ser) c.1834G>A (p.Gly612Ser) | |
| 15 | g.73323042T>A | CA491478359 | HCN4 | c.3051A>T (p.Val1017=) c.1833A>T (p.Val611=) | |
| 15 | g.73323042T>C | CA491478361 | HCN4 | c.3051A>G (p.Val1017=) c.1833A>G (p.Val611=) | |
| 15 | g.73323042T>G | CA491478362 | HCN4 | c.3051A>C (p.Val1017=) c.1833A>C (p.Val611=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323042T= | CA2187187313 | HCN4 | c.3051A= (p.Val1017=) c.1833A= (p.Val611=) | |
| 15 | g.73323043A= | CA2187187316 | HCN4 | c.3050T= (p.Val1017=) c.1832T= (p.Val611=) | |
| 15 | g.73323043A>C | CA393086329 | HCN4 | c.3050T>G (p.Val1017Gly) c.1832T>G (p.Val611Gly) | |
| 15 | g.73323043A>G | CA393086331 | HCN4 | c.3050T>C (p.Val1017Ala) c.1832T>C (p.Val611Ala) | |
| 15 | g.73323043A>T | CA272663851 | HCN4 | c.3050T>A (p.Val1017Glu) c.1832T>A (p.Val611Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323044C>A | CA393086334 | HCN4 | c.3049G>T (p.Val1017Leu) c.1831G>T (p.Val611Leu) | gnomAD v4 |
| 15 | g.73323044C= | CA2187187318 | HCN4 | c.3049G= (p.Val1017=) c.1831G= (p.Val611=) | |
| 15 | g.73323044C>G | CA393086336 | HCN4 | c.3049G>C (p.Val1017Leu) c.1831G>C (p.Val611Leu) | |
| 15 | g.73323044C>T | CA393086337 | HCN4 | c.3049G>A (p.Val1017Ile) c.1831G>A (p.Val611Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323045A>C | CA491478368 | HCN4 | c.3048T>G (p.Pro1016=) c.1830T>G (p.Pro610=) | |
| 15 | g.73323045A>G | CA491478369 | HCN4 | c.3048T>C (p.Pro1016=) c.1830T>C (p.Pro610=) | gnomAD v4 COSMIC |
| 15 | g.73323045A>T | CA491478370 | HCN4 | c.3048T>A (p.Pro1016=) c.1830T>A (p.Pro610=) | |
| 15 | g.73323046G>A | CA7648893 | HCN4 | c.3047C>T (p.Pro1016Leu) c.1829C>T (p.Pro610Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323046G>C | CA393086339 | HCN4 | c.3047C>G (p.Pro1016Arg) c.1829C>G (p.Pro610Arg) | |
| 15 | g.73323046G= | CA2187187323 | HCN4 | c.3047C= (p.Pro1016=) c.1829C= (p.Pro610=) | |
| 15 | g.73323046G>T | CA393086341 | HCN4 | c.3047C>A (p.Pro1016His) c.1829C>A (p.Pro610His) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323049del | CA2575783829 | HCN4 | c.3047del (p.Pro1016LeufsTer2) c.1829del (p.Pro610LeufsTer2) | gnomAD v4 |
| 15 | g.73323047G>A | CA393086343 | HCN4 | c.3046C>T (p.Pro1016Ser) c.1828C>T (p.Pro610Ser) | |
| 15 | g.73323047G>C | CA393086345 | HCN4 | c.3046C>G (p.Pro1016Ala) c.1828C>G (p.Pro610Ala) | |
| 15 | g.73323047G>T | CA393086346 | HCN4 | c.3046C>A (p.Pro1016Thr) c.1828C>A (p.Pro610Thr) | gnomAD v4 |
| 15 | g.73323048G>A | CA7648894 | HCN4 | c.3045C>T (p.Ser1015=) c.1827C>T (p.Ser609=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323048G>C | CA491478374 | HCN4 | c.3045C>G (p.Ser1015=) c.1827C>G (p.Ser609=) | |
| 15 | g.73323048G= | CA2187187333 | HCN4 | c.3045C= (p.Ser1015=) c.1827C= (p.Ser609=) | |
| 15 | g.73323048G>T | CA491478376 | HCN4 | c.3045C>A (p.Ser1015=) c.1827C>A (p.Ser609=) | gnomAD v4 |
| 15 | g.73323049G>A | CA393086350 | HCN4 | c.3044C>T (p.Ser1015Phe) c.1826C>T (p.Ser609Phe) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323049G>C | CA7648895 | HCN4 | c.3044C>G (p.Ser1015Cys) c.1826C>G (p.Ser609Cys) | ClinVar dbSNP ExAC gnomAD v4 |
| 15 | g.73323049G= | CA2187187337 | HCN4 | c.3044C= (p.Ser1015=) c.1826C= (p.Ser609=) | |
| 15 | g.73323049G>T | CA393086348 | HCN4 | c.3044C>A (p.Ser1015Tyr) c.1826C>A (p.Ser609Tyr) | gnomAD v4 |
| 15 | g.73323050A>C | CA393086353 | HCN4 | c.3043T>G (p.Ser1015Ala) c.1825T>G (p.Ser609Ala) | |
| 15 | g.73323050A>G | CA393086354 | HCN4 | c.3043T>C (p.Ser1015Pro) c.1825T>C (p.Ser609Pro) | gnomAD v4 |
| 15 | g.73323050A>T | CA393086355 | HCN4 | c.3043T>A (p.Ser1015Thr) c.1825T>A (p.Ser609Thr) | |
| 15 | g.73323051del | CA2629370544 | HCN4 | c.3043del (p.Ser1015ProfsTer3) c.1825del (p.Ser609ProfsTer3) | gnomAD v4 |
| 15 | g.73323051A= | CA2187187341 | HCN4 | c.3042T= (p.Ala1014=) c.1824T= (p.Ala608=) | |
| 15 | g.73323051A>C | CA491478386 | HCN4 | c.3042T>G (p.Ala1014=) c.1824T>G (p.Ala608=) | |
| 15 | g.73323051A>G | CA491478382 | HCN4 | c.3042T>C (p.Ala1014=) c.1824T>C (p.Ala608=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323051A>T | CA491478383 | HCN4 | c.3042T>A (p.Ala1014=) c.1824T>A (p.Ala608=) | |
| 15 | g.73323052G>A | CA393086357 | HCN4 | c.3041C>T (p.Ala1014Val) c.1823C>T (p.Ala608Val) | gnomAD v4 |
| 15 | g.73323052G>C | CA393086359 | HCN4 | c.3041C>G (p.Ala1014Gly) c.1823C>G (p.Ala608Gly) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323052G= | CA2187187343 | HCN4 | c.3041C= (p.Ala1014=) c.1823C= (p.Ala608=) | |
| 15 | g.73323052G>T | CA393086361 | HCN4 | c.3041C>A (p.Ala1014Asp) c.1823C>A (p.Ala608Asp) | gnomAD v4 |
| 15 | g.73323053C>A | CA393086364 | HCN4 | c.3040G>T (p.Ala1014Ser) c.1822G>T (p.Ala608Ser) | gnomAD v4 |
| 15 | g.73323053C>G | CA393086365 | HCN4 | c.3040G>C (p.Ala1014Pro) c.1822G>C (p.Ala608Pro) | |
| 15 | g.73323053C>T | CA393086366 | HCN4 | c.3040G>A (p.Ala1014Thr) c.1822G>A (p.Ala608Thr) | gnomAD v4 |
| 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.73323054C>A | CA491478397 | HCN4 | c.3039G>T (p.Gly1013=) c.1821G>T (p.Gly607=) | gnomAD v4 |
| 15 | g.73323054C= | CA2187187352 | HCN4 | c.3039G= (p.Gly1013=) c.1821G= (p.Gly607=) | |
| 15 | g.73323054C>G | CA491478399 | HCN4 | c.3039G>C (p.Gly1013=) c.1821G>C (p.Gly607=) | |
| 15 | g.73323054C>T | CA491478402 | HCN4 | c.3039G>A (p.Gly1013=) c.1821G>A (p.Gly607=) | dbSNP gnomAD v2 |
| 15 | g.73323055C>A | CA393086368 | HCN4 | c.3038G>T (p.Gly1013Val) c.1820G>T (p.Gly607Val) | |
| 15 | g.73323055C>G | CA393086370 | HCN4 | c.3038G>C (p.Gly1013Ala) c.1820G>C (p.Gly607Ala) | dbSNP |
| 15 | g.73323055C>T | CA393086371 | HCN4 | c.3038G>A (p.Gly1013Glu) c.1820G>A (p.Gly607Glu) | gnomAD v4 COSMIC |
| 15 | g.73323056C>A | CA393086377 | HCN4 | c.3037G>T (p.Gly1013Trp) c.1819G>T (p.Gly607Trp) | |
| 15 | g.73323056C>G | CA393086375 | HCN4 | c.3037G>C (p.Gly1013Arg) c.1819G>C (p.Gly607Arg) | |
| 15 | g.73323056C>T | CA393086373 | HCN4 | c.3037G>A (p.Gly1013Arg) c.1819G>A (p.Gly607Arg) | |
| 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=) |