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.73323651del | CA2629370653 | HCN4 | c.2444del (p.Gly815AlafsTer12) c.1226del (p.Gly409AlafsTer12) | gnomAD v4 |
| 15 | g.73323650C>A | CA393088884 | HCN4 | c.2443G>T (p.Gly815Cys) c.1225G>T (p.Gly409Cys) | gnomAD v4 |
| 15 | g.73323650C= | CA2187188586 | HCN4 | c.2443G= (p.Gly815=) c.1225G= (p.Gly409=) | |
| 15 | g.73323650C>G | CA393088886 | HCN4 | c.2443G>C (p.Gly815Arg) c.1225G>C (p.Gly409Arg) | |
| 15 | g.73323650C>T | CA393088885 | HCN4 | c.2443G>A (p.Gly815Ser) c.1225G>A (p.Gly409Ser) | dbSNP gnomAD v4 |
| 15 | g.73323651C>A | CA491478381 | HCN4 | c.2442G>T (p.Leu814=) c.1224G>T (p.Leu408=) | |
| 15 | g.73323651C= | CA2187188587 | HCN4 | c.2442G= (p.Leu814=) c.1224G= (p.Leu408=) | |
| 15 | g.73323651C>G | CA491478380 | HCN4 | c.2442G>C (p.Leu814=) c.1224G>C (p.Leu408=) | |
| 15 | g.73323651C>T | CA7649027 | HCN4 | c.2442G>A (p.Leu814=) c.1224G>A (p.Leu408=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323652A= | CA2187188588 | HCN4 | c.2441T= (p.Leu814=) c.1223T= (p.Leu408=) | |
| 15 | g.73323652A>C | CA393088887 | HCN4 | c.2441T>G (p.Leu814Arg) c.1223T>G (p.Leu408Arg) | |
| 15 | g.73323652A>G | CA393088888 | HCN4 | c.2441T>C (p.Leu814Pro) c.1223T>C (p.Leu408Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323652A>T | CA393088889 | HCN4 | c.2441T>A (p.Leu814Gln) c.1223T>A (p.Leu408Gln) | gnomAD v4 |
| 15 | g.73323653G>A | CA491478387 | HCN4 | c.2440C>T (p.Leu814=) c.1222C>T (p.Leu408=) | gnomAD v4 |
| 15 | g.73323653G>C | CA393088890 | HCN4 | c.2440C>G (p.Leu814Val) c.1222C>G (p.Leu408Val) | |
| 15 | g.73323653G>T | CA393088891 | HCN4 | c.2440C>A (p.Leu814Met) c.1222C>A (p.Leu408Met) | gnomAD v4 |
| 15 | g.73323654C>A | CA491478392 | HCN4 | c.2439G>T (p.Gly813=) c.1221G>T (p.Gly407=) | gnomAD v4 |
| 15 | g.73323654C>G | CA491478393 | HCN4 | c.2439G>C (p.Gly813=) c.1221G>C (p.Gly407=) | |
| 15 | g.73323654C>T | CA491478394 | HCN4 | c.2439G>A (p.Gly813=) c.1221G>A (p.Gly407=) | gnomAD v4 |
| 15 | g.73323655C>A | CA393088892 | HCN4 | c.2438G>T (p.Gly813Val) c.1220G>T (p.Gly407Val) | ClinVar gnomAD v4 |
| 15 | g.73323655C>G | CA393088893 | HCN4 | c.2438G>C (p.Gly813Ala) c.1220G>C (p.Gly407Ala) | |
| 15 | g.73323655C>T | CA393088894 | HCN4 | c.2438G>A (p.Gly813Glu) c.1220G>A (p.Gly407Glu) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73323656C>A | CA393088895 | HCN4 | c.2437G>T (p.Gly813Trp) c.1219G>T (p.Gly407Trp) | |
| 15 | g.73323656C= | CA2187188589 | HCN4 | c.2437G= (p.Gly813=) c.1219G= (p.Gly407=) | |
| 15 | g.73323656C>G | CA393088896 | HCN4 | c.2437G>C (p.Gly813Arg) c.1219G>C (p.Gly407Arg) | |
| 15 | g.73323656C>T | CA7649028 | HCN4 | c.2437G>A (p.Gly813Arg) c.1219G>A (p.Gly407Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323657A>C | CA491478396 | HCN4 | c.2436T>G (p.Ser812=) c.1218T>G (p.Ser406=) | |
| 15 | g.73323657A>G | CA491478395 | HCN4 | c.2436T>C (p.Ser812=) c.1218T>C (p.Ser406=) | |
| 15 | g.73323657A>T | CA491478398 | HCN4 | c.2436T>A (p.Ser812=) c.1218T>A (p.Ser406=) | ClinVar |
| 15 | g.73323658G>A | CA393088899 | HCN4 | c.2435C>T (p.Ser812Phe) c.1217C>T (p.Ser406Phe) | |
| 15 | g.73323658G>C | CA393088898 | HCN4 | c.2435C>G (p.Ser812Cys) c.1217C>G (p.Ser406Cys) | |
| 15 | g.73323658G>T | CA393088897 | HCN4 | c.2435C>A (p.Ser812Tyr) c.1217C>A (p.Ser406Tyr) | gnomAD v4 COSMIC |
| 15 | g.73323659A>C | CA393088900 | HCN4 | c.2434T>G (p.Ser812Ala) c.1216T>G (p.Ser406Ala) | |
| 15 | g.73323659A>G | CA393088902 | HCN4 | c.2434T>C (p.Ser812Pro) c.1216T>C (p.Ser406Pro) | |
| 15 | g.73323659A>T | CA393088901 | HCN4 | c.2434T>A (p.Ser812Thr) c.1216T>A (p.Ser406Thr) | gnomAD v4 |
| 15 | g.73323660T>A | CA491478405 | HCN4 | c.2433A>T (p.Gly811=) c.1215A>T (p.Gly405=) | |
| 15 | g.73323660T>C | CA491478406 | HCN4 | c.2433A>G (p.Gly811=) c.1215A>G (p.Gly405=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323660T>G | CA491478407 | HCN4 | c.2433A>C (p.Gly811=) c.1215A>C (p.Gly405=) | |
| 15 | g.73323660T= | CA2187188590 | HCN4 | c.2433A= (p.Gly811=) c.1215A= (p.Gly405=) | |
| 15 | g.73323661C>A | CA7649029 | HCN4 | c.2432G>T (p.Gly811Val) c.1214G>T (p.Gly405Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323661C= | CA2187188591 | HCN4 | c.2432G= (p.Gly811=) c.1214G= (p.Gly405=) | |
| 15 | g.73323661C>G | CA393088903 | HCN4 | c.2432G>C (p.Gly811Ala) c.1214G>C (p.Gly405Ala) | ClinVar dbSNP |
| 15 | g.73323661C>T | CA7649030 | HCN4 | c.2432G>A (p.Gly811Glu) c.1214G>A (p.Gly405Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323662C>A | CA393088904 | HCN4 | c.2431G>T (p.Gly811Ter) c.1213G>T (p.Gly405Ter) | gnomAD v4 |
| 15 | g.73323662C>G | CA393088906 | HCN4 | c.2431G>C (p.Gly811Arg) c.1213G>C (p.Gly405Arg) | |
| 15 | g.73323662C>T | CA393088905 | HCN4 | c.2431G>A (p.Gly811Arg) c.1213G>A (p.Gly405Arg) | |
| 15 | g.73323663T>A | CA491478413 | HCN4 | c.2430A>T (p.Pro810=) c.1212A>T (p.Pro404=) | |
| 15 | g.73323663T>C | CA272664794 | HCN4 | c.2430A>G (p.Pro810=) c.1212A>G (p.Pro404=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323663T>G | CA491478416 | HCN4 | c.2430A>C (p.Pro810=) c.1212A>C (p.Pro404=) | gnomAD v4 |
| 15 | g.73323663T= | CA2187188592 | HCN4 | c.2430A= (p.Pro810=) c.1212A= (p.Pro404=) | |
| 15 | g.73323664G>A | CA393088907 | HCN4 | c.2429C>T (p.Pro810Leu) c.1211C>T (p.Pro404Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323664G>C | CA393088909 | HCN4 | c.2429C>G (p.Pro810Arg) c.1211C>G (p.Pro404Arg) | |
| 15 | g.73323664G= | CA2187188593 | HCN4 | c.2429C= (p.Pro810=) c.1211C= (p.Pro404=) | |
| 15 | g.73323664G>T | CA393088908 | HCN4 | c.2429C>A (p.Pro810Gln) c.1211C>A (p.Pro404Gln) | gnomAD v4 |
| 15 | g.73323668dup | CA2629370659 | HCN4 | c.2429dup (p.Gly811ArgfsTer?) c.1211dup (p.Gly405ArgfsTer?) | gnomAD v4 |
| 15 | g.73323668del | CA645586810 | HCN4 | c.2429del (p.Pro810GlnfsTer17) c.1211del (p.Pro404GlnfsTer17) | gnomAD v4 COSMIC |
| 15 | g.73323665G>A | CA393088910 | HCN4 | c.2428C>T (p.Pro810Ser) c.1210C>T (p.Pro404Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323665G>C | CA393088911 | HCN4 | c.2428C>G (p.Pro810Ala) c.1210C>G (p.Pro404Ala) | |
| 15 | g.73323665G= | CA2187188594 | HCN4 | c.2428C= (p.Pro810=) c.1210C= (p.Pro404=) | |
| 15 | g.73323665G>T | CA393088912 | HCN4 | c.2428C>A (p.Pro810Thr) c.1210C>A (p.Pro404Thr) | gnomAD v4 |
| 15 | g.73323666G>A | CA491478421 | HCN4 | c.2427C>T (p.Pro809=) c.1209C>T (p.Pro403=) | |
| 15 | g.73323666G>C | CA491478422 | HCN4 | c.2427C>G (p.Pro809=) c.1209C>G (p.Pro403=) | |
| 15 | g.73323666G>T | CA491478424 | HCN4 | c.2427C>A (p.Pro809=) c.1209C>A (p.Pro403=) | dbSNP gnomAD v4 |
| 15 | g.73323667G>A | CA393088913 | HCN4 | c.2426C>T (p.Pro809Leu) c.1208C>T (p.Pro403Leu) | gnomAD v4 |
| 15 | g.73323667G>C | CA393088914 | HCN4 | c.2426C>G (p.Pro809Arg) c.1208C>G (p.Pro403Arg) | |
| 15 | g.73323667G>T | CA393088915 | HCN4 | c.2426C>A (p.Pro809His) c.1208C>A (p.Pro403His) | ClinVar gnomAD v4 |
| 15 | g.73323668G>A | CA393088916 | HCN4 | c.2425C>T (p.Pro809Ser) c.1207C>T (p.Pro403Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323668G>C | CA393088917 | HCN4 | c.2425C>G (p.Pro809Ala) c.1207C>G (p.Pro403Ala) | COSMIC |
| 15 | g.73323668G= | CA2187188595 | HCN4 | c.2425C= (p.Pro809=) c.1207C= (p.Pro403=) | |
| 15 | g.73323668G>T | CA393088918 | HCN4 | c.2425C>A (p.Pro809Thr) c.1207C>A (p.Pro403Thr) | gnomAD v4 |
| 15 | g.73323669del | CA2629370660 | HCN4 | c.2424del (p.Pro810GlnfsTer17) c.1206del (p.Pro404GlnfsTer17) | gnomAD v4 |
| 15 | g.73323669A>C | CA491478427 | HCN4 | c.2424T>G (p.Pro808=) c.1206T>G (p.Pro402=) | |
| 15 | g.73323669A>G | CA491478429 | HCN4 | c.2424T>C (p.Pro808=) c.1206T>C (p.Pro402=) | gnomAD v4 |
| 15 | g.73323669A>T | CA491478430 | HCN4 | c.2424T>A (p.Pro808=) c.1206T>A (p.Pro402=) | |
| 15 | g.73323670G>A | CA7649031 | HCN4 | c.2423C>T (p.Pro808Leu) c.1205C>T (p.Pro402Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323670G>C | CA393088919 | HCN4 | c.2423C>G (p.Pro808Arg) c.1205C>G (p.Pro402Arg) | |
| 15 | g.73323670G= | CA2187188596 | HCN4 | c.2423C= (p.Pro808=) c.1205C= (p.Pro402=) | |
| 15 | g.73323670G>T | CA393088920 | HCN4 | c.2423C>A (p.Pro808His) c.1205C>A (p.Pro402His) | gnomAD v4 |
| 15 | g.73323672del | CA2629370661 | HCN4 | c.2423del (p.Pro808LeufsTer19) c.1205del (p.Pro402LeufsTer19) | gnomAD v4 |
| 15 | g.73323671G>A | CA393088923 | HCN4 | c.2422C>T (p.Pro808Ser) c.1204C>T (p.Pro402Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323671G>C | CA393088921 | HCN4 | c.2422C>G (p.Pro808Ala) c.1204C>G (p.Pro402Ala) | |
| 15 | g.73323671G= | CA2187188597 | HCN4 | c.2422C= (p.Pro808=) c.1204C= (p.Pro402=) | |
| 15 | g.73323671G>T | CA393088922 | HCN4 | c.2422C>A (p.Pro808Thr) c.1204C>A (p.Pro402Thr) | gnomAD v4 |
| 15 | g.73323672G>A | CA491478439 | HCN4 | c.2421C>T (p.Arg807=) c.1203C>T (p.Arg401=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323672G>C | CA491478436 | HCN4 | c.2421C>G (p.Arg807=) c.1203C>G (p.Arg401=) | |
| 15 | g.73323672G= | CA2187188598 | HCN4 | c.2421C= (p.Arg807=) c.1203C= (p.Arg401=) | |
| 15 | g.73323672G>T | CA491478435 | HCN4 | c.2421C>A (p.Arg807=) c.1203C>A (p.Arg401=) | gnomAD v4 |
| 15 | g.73323673C>A | CA393088924 | HCN4 | c.2420G>T (p.Arg807Leu) c.1202G>T (p.Arg401Leu) | gnomAD v4 |
| 15 | g.73323673C= | CA2187188599 | HCN4 | c.2420G= (p.Arg807=) c.1202G= (p.Arg401=) | |
| 15 | g.73323673C>G | CA393088925 | HCN4 | c.2420G>C (p.Arg807Pro) c.1202G>C (p.Arg401Pro) | dbSNP |
| 15 | g.73323673C>T | CA090974 | HCN4 | c.2420G>A (p.Arg807His) c.1202G>A (p.Arg401His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323674G>A | CA7649032 | HCN4 | c.2419C>T (p.Arg807Cys) c.1201C>T (p.Arg401Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323674G>C | CA393088926 | HCN4 | c.2419C>G (p.Arg807Gly) c.1201C>G (p.Arg401Gly) | |
| 15 | g.73323674G= | CA2187188600 | HCN4 | c.2419C= (p.Arg807=) c.1201C= (p.Arg401=) | |
| 15 | g.73323674G>T | CA393088927 | HCN4 | c.2419C>A (p.Arg807Ser) c.1201C>A (p.Arg401Ser) | gnomAD v4 |
| 15 | g.73323675G>A | CA491478446 | HCN4 | c.2418C>T (p.Phe806=) c.1200C>T (p.Phe400=) | |
| 15 | g.73323675G>C | CA393088928 | HCN4 | c.2418C>G (p.Phe806Leu) c.1200C>G (p.Phe400Leu) | |
| 15 | g.73323675G>T | CA393088929 | HCN4 | c.2418C>A (p.Phe806Leu) c.1200C>A (p.Phe400Leu) | gnomAD v4 |
| 15 | g.73323676A>C | CA393088930 | HCN4 | c.2417T>G (p.Phe806Cys) c.1199T>G (p.Phe400Cys) | |
| 15 | g.73323676A>G | CA393088931 | HCN4 | c.2417T>C (p.Phe806Ser) c.1199T>C (p.Phe400Ser) | |
| 15 | g.73323676A>T | CA393088932 | HCN4 | c.2417T>A (p.Phe806Tyr) c.1199T>A (p.Phe400Tyr) | |
| 15 | g.73323677A>C | CA393088935 | HCN4 | c.2416T>G (p.Phe806Val) c.1198T>G (p.Phe400Val) | |
| 15 | g.73323677A>G | CA393088934 | HCN4 | c.2416T>C (p.Phe806Leu) c.1198T>C (p.Phe400Leu) | gnomAD v4 |
| 15 | g.73323677A>T | CA393088933 | HCN4 | c.2416T>A (p.Phe806Ile) c.1198T>A (p.Phe400Ile) | |
| 15 | g.73323678G>A | CA491478450 | HCN4 | c.2415C>T (p.Ile805=) c.1197C>T (p.Ile399=) | gnomAD v4 |
| 15 | g.73323678G>C | CA393088936 | HCN4 | c.2415C>G (p.Ile805Met) c.1197C>G (p.Ile399Met) | |
| 15 | g.73323678G>T | CA491478453 | HCN4 | c.2415C>A (p.Ile805=) c.1197C>A (p.Ile399=) | gnomAD v4 |
| 15 | g.73323679A>C | CA393088937 | HCN4 | c.2414T>G (p.Ile805Ser) c.1196T>G (p.Ile399Ser) | |
| 15 | g.73323679A>G | CA393088938 | HCN4 | c.2414T>C (p.Ile805Thr) c.1196T>C (p.Ile399Thr) | |
| 15 | g.73323679A>T | CA393088939 | HCN4 | c.2414T>A (p.Ile805Asn) c.1196T>A (p.Ile399Asn) | |
| 15 | g.73323680T>A | CA393088940 | HCN4 | c.2413A>T (p.Ile805Phe) c.1195A>T (p.Ile399Phe) | |
| 15 | g.73323680T>C | CA393088941 | HCN4 | c.2413A>G (p.Ile805Val) c.1195A>G (p.Ile399Val) | |
| 15 | g.73323680T>G | CA393088942 | HCN4 | c.2413A>C (p.Ile805Leu) c.1195A>C (p.Ile399Leu) | |
| 15 | g.73323681G>A | CA491478459 | HCN4 | c.2412C>T (p.Ala804=) c.1194C>T (p.Ala398=) | dbSNP gnomAD v2 |
| 15 | g.73323681G>C | CA491478460 | HCN4 | c.2412C>G (p.Ala804=) c.1194C>G (p.Ala398=) | |
| 15 | g.73323681G= | CA2187188601 | HCN4 | c.2412C= (p.Ala804=) c.1194C= (p.Ala398=) | |
| 15 | g.73323681G>T | CA491478461 | HCN4 | c.2412C>A (p.Ala804=) c.1194C>A (p.Ala398=) | gnomAD v4 |
| 15 | g.73323682G>A | CA393088943 | HCN4 | c.2411C>T (p.Ala804Val) c.1193C>T (p.Ala398Val) | gnomAD v4 |
| 15 | g.73323682G>C | CA393088944 | HCN4 | c.2411C>G (p.Ala804Gly) c.1193C>G (p.Ala398Gly) | |
| 15 | g.73323682G>T | CA393088945 | HCN4 | c.2411C>A (p.Ala804Asp) c.1193C>A (p.Ala398Asp) | gnomAD v4 |
| 15 | g.73323683C>A | CA393088946 | HCN4 | c.2410G>T (p.Ala804Ser) c.1192G>T (p.Ala398Ser) | gnomAD v4 |
| 15 | g.73323683C= | CA2187188602 | HCN4 | c.2410G= (p.Ala804=) c.1192G= (p.Ala398=) | |
| 15 | g.73323683C>G | CA393088947 | HCN4 | c.2410G>C (p.Ala804Pro) c.1192G>C (p.Ala398Pro) | |
| 15 | g.73323683C>T | CA393088948 | HCN4 | c.2410G>A (p.Ala804Thr) c.1192G>A (p.Ala398Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323684A= | CA2187188603 | HCN4 | c.2409T= (p.Ala803=) c.1191T= (p.Ala397=) | |
| 15 | g.73323684A>C | CA272664812 | HCN4 | c.2409T>G (p.Ala803=) c.1191T>G (p.Ala397=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323684A>G | CA491478470 | HCN4 | c.2409T>C (p.Ala803=) c.1191T>C (p.Ala397=) | |
| 15 | g.73323684A>T | CA491478471 | HCN4 | c.2409T>A (p.Ala803=) c.1191T>A (p.Ala397=) | |
| 15 | g.73323685G>A | CA7649033 | HCN4 | c.2408C>T (p.Ala803Val) c.1190C>T (p.Ala397Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323685G>C | CA393088950 | HCN4 | c.2408C>G (p.Ala803Gly) c.1190C>G (p.Ala397Gly) | |
| 15 | g.73323685G= | CA2187188604 | HCN4 | c.2408C= (p.Ala803=) c.1190C= (p.Ala397=) | |
| 15 | g.73323685G>T | CA393088949 | HCN4 | c.2408C>A (p.Ala803Asp) c.1190C>A (p.Ala397Asp) | gnomAD v4 |
| 15 | g.73323686C>A | CA393088951 | HCN4 | c.2407G>T (p.Ala803Ser) c.1189G>T (p.Ala397Ser) | gnomAD v4 |
| 15 | g.73323686C= | CA2187188605 | HCN4 | c.2407G= (p.Ala803=) c.1189G= (p.Ala397=) | |
| 15 | g.73323686C>G | CA393088952 | HCN4 | c.2407G>C (p.Ala803Pro) c.1189G>C (p.Ala397Pro) | |
| 15 | g.73323686C>T | CA7649034 | HCN4 | c.2407G>A (p.Ala803Thr) c.1189G>A (p.Ala397Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323687A>C | CA491478474 | HCN4 | c.2406T>G (p.Pro802=) c.1188T>G (p.Pro396=) | |
| 15 | g.73323687A>G | CA491478475 | HCN4 | c.2406T>C (p.Pro802=) c.1188T>C (p.Pro396=) | |
| 15 | g.73323687A>T | CA491478476 | HCN4 | c.2406T>A (p.Pro802=) c.1188T>A (p.Pro396=) | |
| 15 | g.73323688G>A | CA393088953 | HCN4 | c.2405C>T (p.Pro802Leu) c.1187C>T (p.Pro396Leu) | dbSNP gnomAD v2 |
| 15 | g.73323688G>C | CA393088954 | HCN4 | c.2405C>G (p.Pro802Arg) c.1187C>G (p.Pro396Arg) | |
| 15 | g.73323688G= | CA2187188606 | HCN4 | c.2405C= (p.Pro802=) c.1187C= (p.Pro396=) | |
| 15 | g.73323688G>T | CA393088955 | HCN4 | c.2405C>A (p.Pro802His) c.1187C>A (p.Pro396His) | gnomAD v4 |
| 15 | g.73323689G>A | CA393088956 | HCN4 | c.2404C>T (p.Pro802Ser) c.1186C>T (p.Pro396Ser) | gnomAD v4 |
| 15 | g.73323689G>C | CA393088958 | HCN4 | c.2404C>G (p.Pro802Ala) c.1186C>G (p.Pro396Ala) | |
| 15 | g.73323689G>T | CA393088957 | HCN4 | c.2404C>A (p.Pro802Thr) c.1186C>A (p.Pro396Thr) | gnomAD v4 |
| 15 | g.73323690C>A | CA491478478 | HCN4 | c.2403G>T (p.Leu801=) c.1185G>T (p.Leu395=) | gnomAD v4 |
| 15 | g.73323690C>G | CA491478479 | HCN4 | c.2403G>C (p.Leu801=) c.1185G>C (p.Leu395=) | |
| 15 | g.73323690C>T | CA491478481 | HCN4 | c.2403G>A (p.Leu801=) c.1185G>A (p.Leu395=) | gnomAD v4 |
| 15 | g.73323691A>C | CA393088959 | HCN4 | c.2402T>G (p.Leu801Arg) c.1184T>G (p.Leu395Arg) | |
| 15 | g.73323691A>G | CA393088960 | HCN4 | c.2402T>C (p.Leu801Pro) c.1184T>C (p.Leu395Pro) | |
| 15 | g.73323691A>T | CA393088961 | HCN4 | c.2402T>A (p.Leu801Gln) c.1184T>A (p.Leu395Gln) | |
| 15 | g.73323692G>A | CA272664827 | HCN4 | c.2401C>T (p.Leu801=) c.1183C>T (p.Leu395=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323692G>C | CA393088962 | HCN4 | c.2401C>G (p.Leu801Val) c.1183C>G (p.Leu395Val) | |
| 15 | g.73323692G= | CA2187188607 | HCN4 | c.2401C= (p.Leu801=) c.1183C= (p.Leu395=) | |
| 15 | g.73323692G>T | CA393088963 | HCN4 | c.2401C>A (p.Leu801Met) c.1183C>A (p.Leu395Met) | gnomAD v4 |
| 15 | g.73323693G>A | CA491478490 | HCN4 | c.2400C>T (p.Arg800=) c.1182C>T (p.Arg394=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323693G>C | CA491478488 | HCN4 | c.2400C>G (p.Arg800=) c.1182C>G (p.Arg394=) | |
| 15 | g.73323693G= | CA2187188608 | HCN4 | c.2400C= (p.Arg800=) c.1182C= (p.Arg394=) | |
| 15 | g.73323693G>T | CA491478487 | HCN4 | c.2400C>A (p.Arg800=) c.1182C>A (p.Arg394=) | gnomAD v4 |
| 15 | g.73323694C>A | CA393088964 | HCN4 | c.2399G>T (p.Arg800Leu) c.1181G>T (p.Arg394Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323694C= | CA2187188609 | HCN4 | c.2399G= (p.Arg800=) c.1181G= (p.Arg394=) | |
| 15 | g.73323694C>G | CA393088965 | HCN4 | c.2399G>C (p.Arg800Pro) c.1181G>C (p.Arg394Pro) | gnomAD v4 |
| 15 | g.73323694C>T | CA7649035 | HCN4 | c.2399G>A (p.Arg800His) c.1181G>A (p.Arg394His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323695G>A | CA7649036 | HCN4 | c.2398C>T (p.Arg800Cys) c.1180C>T (p.Arg394Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323695G>C | CA393088967 | HCN4 | c.2398C>G (p.Arg800Gly) c.1180C>G (p.Arg394Gly) | |
| 15 | g.73323695G= | CA2187188610 | HCN4 | c.2398C= (p.Arg800=) c.1180C= (p.Arg394=) | |
| 15 | g.73323695G>T | CA393088966 | HCN4 | c.2398C>A (p.Arg800Ser) c.1180C>A (p.Arg394Ser) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323696A>C | CA491478493 | HCN4 | c.2397T>G (p.Pro799=) c.1179T>G (p.Pro393=) | |
| 15 | g.73323696A>G | CA491478496 | HCN4 | c.2397T>C (p.Pro799=) c.1179T>C (p.Pro393=) | |
| 15 | g.73323696A>T | CA491478497 | HCN4 | c.2397T>A (p.Pro799=) c.1179T>A (p.Pro393=) | |
| 15 | g.73323697G>A | CA393088968 | HCN4 | c.2396C>T (p.Pro799Leu) c.1178C>T (p.Pro393Leu) | |
| 15 | g.73323697G>C | CA393088969 | HCN4 | c.2396C>G (p.Pro799Arg) c.1178C>G (p.Pro393Arg) | gnomAD v4 |
| 15 | g.73323697G>T | CA393088970 | HCN4 | c.2396C>A (p.Pro799His) c.1178C>A (p.Pro393His) | |
| 15 | g.73323698G>A | CA393088971 | HCN4 | c.2395C>T (p.Pro799Ser) c.1177C>T (p.Pro393Ser) | gnomAD v4 |
| 15 | g.73323698G>C | CA393088972 | HCN4 | c.2395C>G (p.Pro799Ala) c.1177C>G (p.Pro393Ala) | |
| 15 | g.73323698G>T | CA393088973 | HCN4 | c.2395C>A (p.Pro799Thr) c.1177C>A (p.Pro393Thr) | gnomAD v4 |
| 15 | g.73323699G>A | CA491478502 | HCN4 | c.2394C>T (p.His798=) c.1176C>T (p.His392=) | gnomAD v4 |
| 15 | g.73323699G>C | CA393088974 | HCN4 | c.2394C>G (p.His798Gln) c.1176C>G (p.His392Gln) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323699G>T | CA393088975 | HCN4 | c.2394C>A (p.His798Gln) c.1176C>A (p.His392Gln) | gnomAD v4 |
| 15 | g.73323700T>A | CA393088976 | HCN4 | c.2393A>T (p.His798Leu) c.1175A>T (p.His392Leu) | gnomAD v4 |
| 15 | g.73323700T>C | CA393088977 | HCN4 | c.2393A>G (p.His798Arg) c.1175A>G (p.His392Arg) | dbSNP |
| 15 | g.73323700T>G | CA393088978 | HCN4 | c.2393A>C (p.His798Pro) c.1175A>C (p.His392Pro) | |
| 15 | g.73323700T= | CA2187188611 | HCN4 | c.2393A= (p.His798=) c.1175A= (p.His392=) | |
| 15 | g.73323701G>A | CA393088981 | HCN4 | c.2392C>T (p.His798Tyr) c.1174C>T (p.His392Tyr) | dbSNP gnomAD v4 |
| 15 | g.73323701G>C | CA393088980 | HCN4 | c.2392C>G (p.His798Asp) c.1174C>G (p.His392Asp) | |
| 15 | g.73323701G= | CA2187188612 | HCN4 | c.2392C= (p.His798=) c.1174C= (p.His392=) | |
| 15 | g.73323701G>T | CA393088979 | HCN4 | c.2392C>A (p.His798Asn) c.1174C>A (p.His392Asn) | gnomAD v4 |
| 15 | g.73323702G>A | CA491478507 | HCN4 | c.2391C>T (p.His797=) c.1173C>T (p.His391=) | dbSNP |
| 15 | g.73323702G>C | CA393088982 | HCN4 | c.2391C>G (p.His797Gln) c.1173C>G (p.His391Gln) | gnomAD v4 |
| 15 | g.73323702G= | CA2187188613 | HCN4 | c.2391C= (p.His797=) c.1173C= (p.His391=) | |
| 15 | g.73323702G>T | CA7649037 | HCN4 | c.2391C>A (p.His797Gln) c.1173C>A (p.His391Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323703T>A | CA393088983 | HCN4 | c.2390A>T (p.His797Leu) c.1172A>T (p.His391Leu) | |
| 15 | g.73323703T>C | CA393088984 | HCN4 | c.2390A>G (p.His797Arg) c.1172A>G (p.His391Arg) | |
| 15 | g.73323703T>G | CA393088985 | HCN4 | c.2390A>C (p.His797Pro) c.1172A>C (p.His391Pro) | |
| 15 | g.73323704G>A | CA393088986 | HCN4 | c.2389C>T (p.His797Tyr) c.1171C>T (p.His391Tyr) | |
| 15 | g.73323704G>C | CA393088987 | HCN4 | c.2389C>G (p.His797Asp) c.1171C>G (p.His391Asp) | |
| 15 | g.73323704G>T | CA393088988 | HCN4 | c.2389C>A (p.His797Asn) c.1171C>A (p.His391Asn) | gnomAD v4 |
| 15 | g.73323706dup | CA2575783835 | HCN4 | c.2389dup (p.His797ProfsTer?) c.1171dup (p.His391ProfsTer?) | |
| 15 | g.73323705G>A | CA491478512 | HCN4 | c.2388C>T (p.Thr796=) c.1170C>T (p.Thr390=) | |
| 15 | g.73323705G>C | CA491478513 | HCN4 | c.2388C>G (p.Thr796=) c.1170C>G (p.Thr390=) | |
| 15 | g.73323705G>T | CA491478514 | HCN4 | c.2388C>A (p.Thr796=) c.1170C>A (p.Thr390=) | gnomAD v4 |
| 15 | g.73323706G>A | CA393088989 | HCN4 | c.2387C>T (p.Thr796Ile) c.1169C>T (p.Thr390Ile) | |
| 15 | g.73323706G>C | CA393088990 | HCN4 | c.2387C>G (p.Thr796Ser) c.1169C>G (p.Thr390Ser) | |
| 15 | g.73323706G>T | CA393088991 | HCN4 | c.2387C>A (p.Thr796Asn) c.1169C>A (p.Thr390Asn) | gnomAD v4 |
| 15 | g.73323707T>A | CA393088994 | HCN4 | c.2386A>T (p.Thr796Ser) c.1168A>T (p.Thr390Ser) | |
| 15 | g.73323707T>C | CA393088993 | HCN4 | c.2386A>G (p.Thr796Ala) c.1168A>G (p.Thr390Ala) | gnomAD v4 |
| 15 | g.73323707T>G | CA393088992 | HCN4 | c.2386A>C (p.Thr796Pro) c.1168A>C (p.Thr390Pro) | |
| 15 | g.73323708G>A | CA10583261 | HCN4 | c.2385C>T (p.Leu795=) c.1167C>T (p.Leu389=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323708G>C | CA491478522 | HCN4 | c.2385C>G (p.Leu795=) c.1167C>G (p.Leu389=) | dbSNP |
| 15 | g.73323708G= | CA2187188614 | HCN4 | c.2385C= (p.Leu795=) c.1167C= (p.Leu389=) | |
| 15 | g.73323708G>T | CA491478523 | HCN4 | c.2385C>A (p.Leu795=) c.1167C>A (p.Leu389=) | gnomAD v4 |
| 15 | g.73323709A>C | CA393088995 | HCN4 | c.2384T>G (p.Leu795Arg) c.1166T>G (p.Leu389Arg) | |
| 15 | g.73323709A>G | CA393088996 | HCN4 | c.2384T>C (p.Leu795Pro) c.1166T>C (p.Leu389Pro) | gnomAD v4 |
| 15 | g.73323709A>T | CA393088997 | HCN4 | c.2384T>A (p.Leu795His) c.1166T>A (p.Leu389His) | |
| 15 | g.73323710G>A | CA393088998 | HCN4 | c.2383C>T (p.Leu795Phe) c.1165C>T (p.Leu389Phe) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323710G>C | CA393088999 | HCN4 | c.2383C>G (p.Leu795Val) c.1165C>G (p.Leu389Val) | |
| 15 | g.73323710G= | CA2187188615 | HCN4 | c.2383C= (p.Leu795=) c.1165C= (p.Leu389=) | |
| 15 | g.73323710G>T | CA393089000 | HCN4 | c.2383C>A (p.Leu795Ile) c.1165C>A (p.Leu389Ile) | dbSNP gnomAD v4 |
| 15 | g.73323711G>A | CA491478529 | HCN4 | c.2382C>T (p.Ala794=) c.1164C>T (p.Ala388=) | gnomAD v4 |
| 15 | g.73323711G>C | CA491478532 | HCN4 | c.2382C>G (p.Ala794=) c.1164C>G (p.Ala388=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323711G= | CA2187188616 | HCN4 | c.2382C= (p.Ala794=) c.1164C= (p.Ala388=) | |
| 15 | g.73323711G>T | CA491478530 | HCN4 | c.2382C>A (p.Ala794=) c.1164C>A (p.Ala388=) | gnomAD v4 COSMIC |
| 15 | g.73323712G>A | CA393089001 | HCN4 | c.2381C>T (p.Ala794Val) c.1163C>T (p.Ala388Val) | gnomAD v4 |
| 15 | g.73323712G>C | CA393089003 | HCN4 | c.2381C>G (p.Ala794Gly) c.1163C>G (p.Ala388Gly) | |
| 15 | g.73323712G>T | CA393089002 | HCN4 | c.2381C>A (p.Ala794Asp) c.1163C>A (p.Ala388Asp) | ClinVar gnomAD v4 |
| 15 | g.73323713C>A | CA393089004 | HCN4 | c.2380G>T (p.Ala794Ser) c.1162G>T (p.Ala388Ser) | gnomAD v4 |
| 15 | g.73323713C= | CA2187188617 | HCN4 | c.2380G= (p.Ala794=) c.1162G= (p.Ala388=) | |
| 15 | g.73323713C>G | CA393089005 | HCN4 | c.2380G>C (p.Ala794Pro) c.1162G>C (p.Ala388Pro) | |
| 15 | g.73323713C>T | CA272664854 | HCN4 | c.2380G>A (p.Ala794Thr) c.1162G>A (p.Ala388Thr) | dbSNP |
| 15 | g.73323714T>A | CA491478536 | HCN4 | c.2379A>T (p.Ile793=) c.1161A>T (p.Ile387=) | gnomAD v4 |
| 15 | g.73323714T>C | CA393089006 | HCN4 | c.2379A>G (p.Ile793Met) c.1161A>G (p.Ile387Met) | gnomAD v4 |
| 15 | g.73323714T>G | CA491478538 | HCN4 | c.2379A>C (p.Ile793=) c.1161A>C (p.Ile387=) | |
| 15 | g.73323715A>C | CA393089007 | HCN4 | c.2378T>G (p.Ile793Arg) c.1160T>G (p.Ile387Arg) | |
| 15 | g.73323715A>G | CA393089009 | HCN4 | c.2378T>C (p.Ile793Thr) c.1160T>C (p.Ile387Thr) | COSMIC |
| 15 | g.73323715A>T | CA393089008 | HCN4 | c.2378T>A (p.Ile793Lys) c.1160T>A (p.Ile387Lys) | |
| 15 | g.73323716T>A | CA393089010 | HCN4 | c.2377A>T (p.Ile793Leu) c.1159A>T (p.Ile387Leu) | |
| 15 | g.73323716T>C | CA393089011 | HCN4 | c.2377A>G (p.Ile793Val) c.1159A>G (p.Ile387Val) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73323716T>G | CA393089012 | HCN4 | c.2377A>C (p.Ile793Leu) c.1159A>C (p.Ile387Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323716T= | CA2187188618 | HCN4 | c.2377A= (p.Ile793=) c.1159A= (p.Ile387=) | |
| 15 | g.73323717G>A | CA491478544 | HCN4 | c.2376C>T (p.Ala792=) c.1158C>T (p.Ala386=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323717G>C | CA491478545 | HCN4 | c.2376C>G (p.Ala792=) c.1158C>G (p.Ala386=) | ClinVar dbSNP |
| 15 | g.73323717G= | CA2187188619 | HCN4 | c.2376C= (p.Ala792=) c.1158C= (p.Ala386=) | |
| 15 | g.73323717G>T | CA491478546 | HCN4 | c.2376C>A (p.Ala792=) c.1158C>A (p.Ala386=) | gnomAD v4 |
| 15 | g.73323717_73323718delinsAC | CA645586811 | HCN4 | c.2375_2376delinsGT (p.Ala792Gly) c.1157_1158delinsGT (p.Ala386Gly) | COSMIC |
| 15 | g.73323718G>A | CA393089013 | HCN4 | c.2375C>T (p.Ala792Val) c.1157C>T (p.Ala386Val) | gnomAD v4 |
| 15 | g.73323718G>C | CA393089014 | HCN4 | c.2375C>G (p.Ala792Gly) c.1157C>G (p.Ala386Gly) | |
| 15 | g.73323718G>T | CA393089015 | HCN4 | c.2375C>A (p.Ala792Asp) c.1157C>A (p.Ala386Asp) | gnomAD v4 |
| 15 | g.73323719C>A | CA7649038 | HCN4 | c.2374G>T (p.Ala792Ser) c.1156G>T (p.Ala386Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323719C= | CA2187188620 | HCN4 | c.2374G= (p.Ala792=) c.1156G= (p.Ala386=) | |
| 15 | g.73323719C>G | CA393089016 | HCN4 | c.2374G>C (p.Ala792Pro) c.1156G>C (p.Ala386Pro) | |
| 15 | g.73323719C>T | CA393089017 | HCN4 | c.2374G>A (p.Ala792Thr) c.1156G>A (p.Ala386Thr) | gnomAD v4 |
| 15 | g.73323720C>A | CA7649039 | HCN4 | c.2373G>T (p.Val791=) c.1155G>T (p.Val385=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323720C= | CA2187188621 | HCN4 | c.2373G= (p.Val791=) c.1155G= (p.Val385=) | |
| 15 | g.73323720C>G | CA491478554 | HCN4 | c.2373G>C (p.Val791=) c.1155G>C (p.Val385=) | |
| 15 | g.73323720C>T | CA491478555 | HCN4 | c.2373G>A (p.Val791=) c.1155G>A (p.Val385=) | |
| 15 | g.73323721A>C | CA393089018 | HCN4 | c.2372T>G (p.Val791Gly) c.1154T>G (p.Val385Gly) | |
| 15 | g.73323721A>G | CA393089020 | HCN4 | c.2372T>C (p.Val791Ala) c.1154T>C (p.Val385Ala) | |
| 15 | g.73323721A>T | CA393089019 | HCN4 | c.2372T>A (p.Val791Glu) c.1154T>A (p.Val385Glu) | gnomAD v4 |
| 15 | g.73323722C>A | CA393089021 | HCN4 | c.2371G>T (p.Val791Leu) c.1153G>T (p.Val385Leu) | |
| 15 | g.73323722C= | CA2187188622 | HCN4 | c.2371G= (p.Val791=) c.1153G= (p.Val385=) | |
| 15 | g.73323722C>G | CA393089022 | HCN4 | c.2371G>C (p.Val791Leu) c.1153G>C (p.Val385Leu) | |
| 15 | g.73323722C>T | CA272664876 | HCN4 | c.2371G>A (p.Val791Met) c.1153G>A (p.Val385Met) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323723A= | CA2187188623 | HCN4 | c.2370T= (p.Ser790=) c.1152T= (p.Ser384=) | |
| 15 | g.73323723A>C | CA491478558 | HCN4 | c.2370T>G (p.Ser790=) c.1152T>G (p.Ser384=) | |
| 15 | g.73323723A>G | CA7649040 | HCN4 | c.2370T>C (p.Ser790=) c.1152T>C (p.Ser384=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323723A>T | CA491478561 | HCN4 | c.2370T>A (p.Ser790=) c.1152T>A (p.Ser384=) | |
| 15 | g.73323724G>A | CA393089023 | HCN4 | c.2369C>T (p.Ser790Phe) c.1151C>T (p.Ser384Phe) | |
| 15 | g.73323724G>C | CA393089024 | HCN4 | c.2369C>G (p.Ser790Cys) c.1151C>G (p.Ser384Cys) | |
| 15 | g.73323724G>T | CA393089025 | HCN4 | c.2369C>A (p.Ser790Tyr) c.1151C>A (p.Ser384Tyr) | gnomAD v4 COSMIC |
| 15 | g.73323725A= | CA2187188624 | HCN4 | c.2368T= (p.Ser790=) c.1150T= (p.Ser384=) | |
| 15 | g.73323725A>C | CA393089026 | HCN4 | c.2368T>G (p.Ser790Ala) c.1150T>G (p.Ser384Ala) | |
| 15 | g.73323725A>G | CA393089027 | HCN4 | c.2368T>C (p.Ser790Pro) c.1150T>C (p.Ser384Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323725A>T | CA393089028 | HCN4 | c.2368T>A (p.Ser790Thr) c.1150T>A (p.Ser384Thr) | |
| 15 | g.73323726A>C | CA491478564 | HCN4 | c.2367T>G (p.Thr789=) c.1149T>G (p.Thr383=) | |
| 15 | g.73323726A>G | CA491478565 | HCN4 | c.2367T>C (p.Thr789=) c.1149T>C (p.Thr383=) | |
| 15 | g.73323726A>T | CA491478566 | HCN4 | c.2367T>A (p.Thr789=) c.1149T>A (p.Thr383=) | |
| 15 | g.73323727G>A | CA393089029 | HCN4 | c.2366C>T (p.Thr789Ile) c.1148C>T (p.Thr383Ile) | |
| 15 | g.73323727G>C | CA393089030 | HCN4 | c.2366C>G (p.Thr789Ser) c.1148C>G (p.Thr383Ser) | |
| 15 | g.73323727G>T | CA393089031 | HCN4 | c.2366C>A (p.Thr789Asn) c.1148C>A (p.Thr383Asn) | gnomAD v4 |
| 15 | g.73323728T>A | CA393089032 | HCN4 | c.2365A>T (p.Thr789Ser) c.1147A>T (p.Thr383Ser) | |
| 15 | g.73323728T>C | CA393089033 | HCN4 | c.2365A>G (p.Thr789Ala) c.1147A>G (p.Thr383Ala) | gnomAD v4 |
| 15 | g.73323728T>G | CA393089034 | HCN4 | c.2365A>C (p.Thr789Pro) c.1147A>C (p.Thr383Pro) | |
| 15 | g.73323729G>A | CA491478575 | HCN4 | c.2364C>T (p.Thr788=) c.1146C>T (p.Thr382=) | gnomAD v4 |
| 15 | g.73323729G>C | CA491478576 | HCN4 | c.2364C>G (p.Thr788=) c.1146C>G (p.Thr382=) | |
| 15 | g.73323729G>T | CA491478577 | HCN4 | c.2364C>A (p.Thr788=) c.1146C>A (p.Thr382=) | gnomAD v4 |
| 15 | g.73323730G>A | CA393089037 | HCN4 | c.2363C>T (p.Thr788Ile) c.1145C>T (p.Thr382Ile) | gnomAD v4 |
| 15 | g.73323730G>C | CA393089035 | HCN4 | c.2363C>G (p.Thr788Ser) c.1145C>G (p.Thr382Ser) | |
| 15 | g.73323730G>T | CA393089036 | HCN4 | c.2363C>A (p.Thr788Asn) c.1145C>A (p.Thr382Asn) | gnomAD v4 |
| 15 | g.73323731T>A | CA393089038 | HCN4 | c.2362A>T (p.Thr788Ser) c.1144A>T (p.Thr382Ser) | |
| 15 | g.73323731T>C | CA393089039 | HCN4 | c.2362A>G (p.Thr788Ala) c.1144A>G (p.Thr382Ala) | gnomAD v4 |
| 15 | g.73323731T>G | CA393089040 | HCN4 | c.2362A>C (p.Thr788Pro) c.1144A>C (p.Thr382Pro) | |
| 15 | g.73323732G>A | CA491478578 | HCN4 | c.2361C>T (p.Ala787=) c.1143C>T (p.Ala381=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323732G>C | CA491478581 | HCN4 | c.2361C>G (p.Ala787=) c.1143C>G (p.Ala381=) | |
| 15 | g.73323732G= | CA2187188625 | HCN4 | c.2361C= (p.Ala787=) c.1143C= (p.Ala381=) | |
| 15 | g.73323732G>T | CA491478582 | HCN4 | c.2361C>A (p.Ala787=) c.1143C>A (p.Ala381=) | gnomAD v4 |
| 15 | g.73323733G>A | CA393089041 | HCN4 | c.2360C>T (p.Ala787Val) c.1142C>T (p.Ala381Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323733G>C | CA393089042 | HCN4 | c.2360C>G (p.Ala787Gly) c.1142C>G (p.Ala381Gly) | |
| 15 | g.73323733G= | CA2187188626 | HCN4 | c.2360C= (p.Ala787=) c.1142C= (p.Ala381=) | |
| 15 | g.73323733G>T | CA393089043 | HCN4 | c.2360C>A (p.Ala787Asp) c.1142C>A (p.Ala381Asp) | gnomAD v4 |
| 15 | g.73323734C>A | CA393089044 | HCN4 | c.2359G>T (p.Ala787Ser) c.1141G>T (p.Ala381Ser) | ClinVar gnomAD v4 |
| 15 | g.73323734C>G | CA393089045 | HCN4 | c.2359G>C (p.Ala787Pro) c.1141G>C (p.Ala381Pro) | |
| 15 | g.73323734C>T | CA393089046 | HCN4 | c.2359G>A (p.Ala787Thr) c.1141G>A (p.Ala381Thr) | gnomAD v4 COSMIC |
| 15 | g.73323735A>C | CA491478589 | HCN4 | c.2358T>G (p.Ala786=) c.1140T>G (p.Ala380=) | |
| 15 | g.73323735A>G | CA491478592 | HCN4 | c.2358T>C (p.Ala786=) c.1140T>C (p.Ala380=) | |
| 15 | g.73323735A>T | CA491478593 | HCN4 | c.2358T>A (p.Ala786=) c.1140T>A (p.Ala380=) | |
| 15 | g.73323736G>A | CA393089047 | HCN4 | c.2357C>T (p.Ala786Val) c.1139C>T (p.Ala380Val) | |
| 15 | g.73323736G>C | CA393089048 | HCN4 | c.2357C>G (p.Ala786Gly) c.1139C>G (p.Ala380Gly) | |
| 15 | g.73323736G>T | CA393089049 | HCN4 | c.2357C>A (p.Ala786Asp) c.1139C>A (p.Ala380Asp) | gnomAD v4 |
| 15 | g.73323737C>A | CA393089050 | HCN4 | c.2356G>T (p.Ala786Ser) c.1138G>T (p.Ala380Ser) | gnomAD v4 |
| 15 | g.73323737C= | CA2187188627 | HCN4 | c.2356G= (p.Ala786=) c.1138G= (p.Ala380=) | |
| 15 | g.73323737C>G | CA393089051 | HCN4 | c.2356G>C (p.Ala786Pro) c.1138G>C (p.Ala380Pro) | |
| 15 | g.73323737C>T | CA7649041 | HCN4 | c.2356G>A (p.Ala786Thr) c.1138G>A (p.Ala380Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323738G>A | CA7649042 | HCN4 | c.2355C>T (p.Ala785=) c.1137C>T (p.Ala379=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323738G>C | CA491478596 | HCN4 | c.2355C>G (p.Ala785=) c.1137C>G (p.Ala379=) | gnomAD v4 |
| 15 | g.73323738G= | CA2187188628 | HCN4 | c.2355C= (p.Ala785=) c.1137C= (p.Ala379=) | |
| 15 | g.73323738G>T | CA491478599 | HCN4 | c.2355C>A (p.Ala785=) c.1137C>A (p.Ala379=) | |
| 15 | g.73323739G>A | CA393089052 | HCN4 | c.2354C>T (p.Ala785Val) c.1136C>T (p.Ala379Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323739G>C | CA393089053 | HCN4 | c.2354C>G (p.Ala785Gly) c.1136C>G (p.Ala379Gly) | |
| 15 | g.73323739G= | CA2187188629 | HCN4 | c.2354C= (p.Ala785=) c.1136C= (p.Ala379=) | |
| 15 | g.73323739G>T | CA393089054 | HCN4 | c.2354C>A (p.Ala785Asp) c.1136C>A (p.Ala379Asp) | gnomAD v4 |
| 15 | g.73323740C>A | CA393089055 | HCN4 | c.2353G>T (p.Ala785Ser) c.1135G>T (p.Ala379Ser) | gnomAD v4 |
| 15 | g.73323740C>G | CA393089056 | HCN4 | c.2353G>C (p.Ala785Pro) c.1135G>C (p.Ala379Pro) | |
| 15 | g.73323740C>T | CA393089057 | HCN4 | c.2353G>A (p.Ala785Thr) c.1135G>A (p.Ala379Thr) | gnomAD v4 |
| 15 | g.73323741A>C | CA491478604 | HCN4 | c.2352T>G (p.Ala784=) c.1134T>G (p.Ala378=) | |
| 15 | g.73323741A>G | CA491478606 | HCN4 | c.2352T>C (p.Ala784=) c.1134T>C (p.Ala378=) | |
| 15 | g.73323741A>T | CA491478602 | HCN4 | c.2352T>A (p.Ala784=) c.1134T>A (p.Ala378=) | |
| 15 | g.73323742G>A | CA393089058 | HCN4 | c.2351C>T (p.Ala784Val) c.1133C>T (p.Ala378Val) | gnomAD v4 |
| 15 | g.73323742G>C | CA393089059 | HCN4 | c.2351C>G (p.Ala784Gly) c.1133C>G (p.Ala378Gly) | |
| 15 | g.73323742G>T | CA393089060 | HCN4 | c.2351C>A (p.Ala784Asp) c.1133C>A (p.Ala378Asp) | gnomAD v4 |
| 15 | g.73323743C>A | CA393089063 | HCN4 | c.2350G>T (p.Ala784Ser) c.1132G>T (p.Ala378Ser) | gnomAD v4 |
| 15 | g.73323743C= | CA2187188630 | HCN4 | c.2350G= (p.Ala784=) c.1132G= (p.Ala378=) | |
| 15 | g.73323743C>G | CA393089062 | HCN4 | c.2350G>C (p.Ala784Pro) c.1132G>C (p.Ala378Pro) | |
| 15 | g.73323743C>T | CA393089061 | HCN4 | c.2350G>A (p.Ala784Thr) c.1132G>A (p.Ala378Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323744C>A | CA393089064 | HCN4 | c.2349G>T (p.Gln783His) c.1131G>T (p.Gln377His) | |
| 15 | g.73323744C= | CA2187188631 | HCN4 | c.2349G= (p.Gln783=) c.1131G= (p.Gln377=) | |
| 15 | g.73323744C>G | CA393089065 | HCN4 | c.2349G>C (p.Gln783His) c.1131G>C (p.Gln377His) | |
| 15 | g.73323744C>T | CA7649043 | HCN4 | c.2349G>A (p.Gln783=) c.1131G>A (p.Gln377=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323745T>A | CA393089066 | HCN4 | c.2348A>T (p.Gln783Leu) c.1130A>T (p.Gln377Leu) | |
| 15 | g.73323745T>C | CA393089067 | HCN4 | c.2348A>G (p.Gln783Arg) c.1130A>G (p.Gln377Arg) | |
| 15 | g.73323745T>G | CA393089068 | HCN4 | c.2348A>C (p.Gln783Pro) c.1130A>C (p.Gln377Pro) | |
| 15 | g.73323746G>A | CA393089069 | HCN4 | c.2347C>T (p.Gln783Ter) c.1129C>T (p.Gln377Ter) | gnomAD v4 |
| 15 | g.73323746G>C | CA393089070 | HCN4 | c.2347C>G (p.Gln783Glu) c.1129C>G (p.Gln377Glu) | |
| 15 | g.73323746G>T | CA393089071 | HCN4 | c.2347C>A (p.Gln783Lys) c.1129C>A (p.Gln377Lys) | gnomAD v4 |
| 15 | g.73323747C>A | CA272664904 | HCN4 | c.2346G>T (p.Leu782=) c.1128G>T (p.Leu376=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323747C= | CA2187188632 | HCN4 | c.2346G= (p.Leu782=) c.1128G= (p.Leu376=) | |
| 15 | g.73323747C>G | CA491478618 | HCN4 | c.2346G>C (p.Leu782=) c.1128G>C (p.Leu376=) | |
| 15 | g.73323747C>T | CA491478616 | HCN4 | c.2346G>A (p.Leu782=) c.1128G>A (p.Leu376=) | |
| 15 | g.73323748A= | CA2187188633 | HCN4 | c.2345T= (p.Leu782=) c.1127T= (p.Leu376=) | |
| 15 | g.73323748A>C | CA393089072 | HCN4 | c.2345T>G (p.Leu782Arg) c.1127T>G (p.Leu376Arg) | ClinVar dbSNP |
| 15 | g.73323748A>G | CA393089073 | HCN4 | c.2345T>C (p.Leu782Pro) c.1127T>C (p.Leu376Pro) | |
| 15 | g.73323748A>T | CA393089074 | HCN4 | c.2345T>A (p.Leu782Gln) c.1127T>A (p.Leu376Gln) | |
| 15 | g.73323749G>A | CA491478622 | HCN4 | c.2344C>T (p.Leu782=) c.1126C>T (p.Leu376=) | |
| 15 | g.73323749G>C | CA393089076 | HCN4 | c.2344C>G (p.Leu782Val) c.1126C>G (p.Leu376Val) | |
| 15 | g.73323749G>T | CA393089075 | HCN4 | c.2344C>A (p.Leu782Met) c.1126C>A (p.Leu376Met) | gnomAD v4 |
| 15 | g.73323750T>A | CA491478624 | HCN4 | c.2343A>T (p.Pro781=) c.1125A>T (p.Pro375=) | |
| 15 | g.73323750T>C | CA491478626 | HCN4 | c.2343A>G (p.Pro781=) c.1125A>G (p.Pro375=) | dbSNP |
| 15 | g.73323750T>G | CA491478628 | HCN4 | c.2343A>C (p.Pro781=) c.1125A>C (p.Pro375=) | |
| 15 | g.73323750T= | CA2187188634 | HCN4 | c.2343A= (p.Pro781=) c.1125A= (p.Pro375=) |