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.73323299C>A | CA393087966 | HCN4 | c.2794G>T (p.Gly932Cys) c.1576G>T (p.Gly526Cys) | gnomAD v4 |
| 15 | g.73323299C>G | CA393087968 | HCN4 | c.2794G>C (p.Gly932Arg) c.1576G>C (p.Gly526Arg) | |
| 15 | g.73323299C>T | CA393087965 | HCN4 | c.2794G>A (p.Gly932Ser) c.1576G>A (p.Gly526Ser) | gnomAD v4 |
| 15 | g.73323300T>A | CA491478202 | HCN4 | c.2793A>T (p.Pro931=) c.1575A>T (p.Pro525=) | |
| 15 | g.73323300T>C | CA491478203 | HCN4 | c.2793A>G (p.Pro931=) c.1575A>G (p.Pro525=) | gnomAD v4 |
| 15 | g.73323300T>G | CA491478204 | HCN4 | c.2793A>C (p.Pro931=) c.1575A>C (p.Pro525=) | |
| 15 | g.73323301G>A | CA393087970 | HCN4 | c.2792C>T (p.Pro931Leu) c.1574C>T (p.Pro525Leu) | gnomAD v4 |
| 15 | g.73323301G>C | CA393087972 | HCN4 | c.2792C>G (p.Pro931Arg) c.1574C>G (p.Pro525Arg) | |
| 15 | g.73323301G>T | CA393087974 | HCN4 | c.2792C>A (p.Pro931Gln) c.1574C>A (p.Pro525Gln) | gnomAD v4 |
| 15 | g.73323302G>A | CA393087977 | HCN4 | c.2791C>T (p.Pro931Ser) c.1573C>T (p.Pro525Ser) | gnomAD v4 |
| 15 | g.73323302G>C | CA393087978 | HCN4 | c.2791C>G (p.Pro931Ala) c.1573C>G (p.Pro525Ala) | |
| 15 | g.73323302G>T | CA393087981 | HCN4 | c.2791C>A (p.Pro931Thr) c.1573C>A (p.Pro525Thr) | gnomAD v4 |
| 15 | g.73323303C>A | CA393087983 | HCN4 | c.2790G>T (p.Gln930His) c.1572G>T (p.Gln524His) | gnomAD v4 |
| 15 | g.73323303C>G | CA393087986 | HCN4 | c.2790G>C (p.Gln930His) c.1572G>C (p.Gln524His) | |
| 15 | g.73323303C>T | CA491478206 | HCN4 | c.2790G>A (p.Gln930=) c.1572G>A (p.Gln524=) | gnomAD v4 |
| 15 | g.73323304T>A | CA393087990 | HCN4 | c.2789A>T (p.Gln930Leu) c.1571A>T (p.Gln524Leu) | |
| 15 | g.73323304T>C | CA393087991 | HCN4 | c.2789A>G (p.Gln930Arg) c.1571A>G (p.Gln524Arg) | gnomAD v4 |
| 15 | g.73323304T>G | CA393087993 | HCN4 | c.2789A>C (p.Gln930Pro) c.1571A>C (p.Gln524Pro) | |
| 15 | g.73323305G>A | CA393088001 | HCN4 | c.2788C>T (p.Gln930Ter) c.1570C>T (p.Gln524Ter) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323305G>C | CA393087999 | HCN4 | c.2788C>G (p.Gln930Glu) c.1570C>G (p.Gln524Glu) | |
| 15 | g.73323305G= | CA2187187978 | HCN4 | c.2788C= (p.Gln930=) c.1570C= (p.Gln524=) | |
| 15 | g.73323305G>T | CA393087997 | HCN4 | c.2788C>A (p.Gln930Lys) c.1570C>A (p.Gln524Lys) | gnomAD v4 COSMIC |
| 15 | g.73323306C>A | CA491478210 | HCN4 | c.2787G>T (p.Leu929=) c.1569G>T (p.Leu523=) | gnomAD v4 |
| 15 | g.73323306C>G | CA491478212 | HCN4 | c.2787G>C (p.Leu929=) c.1569G>C (p.Leu523=) | |
| 15 | g.73323306C>T | CA491478213 | HCN4 | c.2787G>A (p.Leu929=) c.1569G>A (p.Leu523=) | gnomAD v4 |
| 15 | g.73323307A= | CA2187187989 | HCN4 | c.2786T= (p.Leu929=) c.1568T= (p.Leu523=) | |
| 15 | g.73323307A>C | CA393088004 | HCN4 | c.2786T>G (p.Leu929Arg) c.1568T>G (p.Leu523Arg) | |
| 15 | g.73323307A>G | CA7648955 | HCN4 | c.2786T>C (p.Leu929Pro) c.1568T>C (p.Leu523Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323307A>T | CA393088008 | HCN4 | c.2786T>A (p.Leu929Gln) c.1568T>A (p.Leu523Gln) | |
| 15 | g.73323308G>A | CA491478215 | HCN4 | c.2785C>T (p.Leu929=) c.1567C>T (p.Leu523=) | gnomAD v4 |
| 15 | g.73323308G>C | CA393088010 | HCN4 | c.2785C>G (p.Leu929Val) c.1567C>G (p.Leu523Val) | |
| 15 | g.73323308G>T | CA393088011 | HCN4 | c.2785C>A (p.Leu929Met) c.1567C>A (p.Leu523Met) | gnomAD v4 |
| 15 | g.73323309C>A | CA491478216 | HCN4 | c.2784G>T (p.Pro928=) c.1566G>T (p.Pro522=) | gnomAD v4 |
| 15 | g.73323309C= | CA2187187992 | HCN4 | c.2784G= (p.Pro928=) c.1566G= (p.Pro522=) | |
| 15 | g.73323309C>G | CA491478217 | HCN4 | c.2784G>C (p.Pro928=) c.1566G>C (p.Pro522=) | dbSNP gnomAD v4 |
| 15 | g.73323309C>T | CA7648956 | HCN4 | c.2784G>A (p.Pro928=) c.1566G>A (p.Pro522=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323309_73323310delinsCG | CA2187187993 | HCN4 | c.2783_2784delinsCG (p.Pro928=) c.1565_1566delinsCG (p.Pro522=) | |
| 15 | g.73323309_73323319delinsCGGGGTGAGCA | CA2187187995 | HCN4 | c.2774_2784delinsTGCTCACCCCG (p.Leu925=) c.1556_1566delinsTGCTCACCCCG (p.Leu519=) | |
| 15 | g.73323310G>A | CA272664258 | HCN4 | c.2783C>T (p.Pro928Leu) c.1565C>T (p.Pro522Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323310G>C | CA393088017 | HCN4 | c.2783C>G (p.Pro928Arg) c.1565C>G (p.Pro522Arg) | |
| 15 | g.73323310G= | CA2187188010 | HCN4 | c.2783C= (p.Pro928=) c.1565C= (p.Pro522=) | |
| 15 | g.73323310G>T | CA393088020 | HCN4 | c.2783C>A (p.Pro928Gln) c.1565C>A (p.Pro522Gln) | gnomAD v4 |
| 15 | g.73323313del | CA619410581 | HCN4 | c.2783del (p.Pro928ArgfsTer?) c.1565del (p.Pro522ArgfsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323314_73323323del | CA7648957 | HCN4 | c.2774_2783del (p.Leu925ArgfsTer?) c.1556_1565del (p.Leu519ArgfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323311G>A | CA393088024 | HCN4 | c.2782C>T (p.Pro928Ser) c.1564C>T (p.Pro522Ser) | |
| 15 | g.73323311G>C | CA393088027 | HCN4 | c.2782C>G (p.Pro928Ala) c.1564C>G (p.Pro522Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323311G= | CA2187188017 | HCN4 | c.2782C= (p.Pro928=) c.1564C= (p.Pro522=) | |
| 15 | g.73323311G>T | CA393088029 | HCN4 | c.2782C>A (p.Pro928Thr) c.1564C>A (p.Pro522Thr) | gnomAD v4 |
| 15 | g.73323312G>A | CA491478223 | HCN4 | c.2781C>T (p.Thr927=) c.1563C>T (p.Thr521=) | gnomAD v4 |
| 15 | g.73323312G>C | CA491478224 | HCN4 | c.2781C>G (p.Thr927=) c.1563C>G (p.Thr521=) | ClinVar dbSNP |
| 15 | g.73323312G>T | CA491478222 | HCN4 | c.2781C>A (p.Thr927=) c.1563C>A (p.Thr521=) | gnomAD v4 |
| 15 | g.73323313G>A | CA393088036 | HCN4 | c.2780C>T (p.Thr927Ile) c.1562C>T (p.Thr521Ile) | gnomAD v4 |
| 15 | g.73323313G>C | CA393088038 | HCN4 | c.2780C>G (p.Thr927Ser) c.1562C>G (p.Thr521Ser) | |
| 15 | g.73323313G>T | CA393088033 | HCN4 | c.2780C>A (p.Thr927Asn) c.1562C>A (p.Thr521Asn) | gnomAD v4 |
| 15 | g.73323314T>A | CA393088045 | HCN4 | c.2779A>T (p.Thr927Ser) c.1561A>T (p.Thr521Ser) | |
| 15 | g.73323314T>C | CA393088042 | HCN4 | c.2779A>G (p.Thr927Ala) c.1561A>G (p.Thr521Ala) | gnomAD v4 |
| 15 | g.73323314T>G | CA393088048 | HCN4 | c.2779A>C (p.Thr927Pro) c.1561A>C (p.Thr521Pro) | dbSNP gnomAD v4 |
| 15 | g.73323314T= | CA2187188022 | HCN4 | c.2779A= (p.Thr927=) c.1561A= (p.Thr521=) | |
| 15 | g.73323315G>A | CA491478229 | HCN4 | c.2778C>T (p.Leu926=) c.1560C>T (p.Leu520=) | dbSNP |
| 15 | g.73323315G>C | CA491478231 | HCN4 | c.2778C>G (p.Leu926=) c.1560C>G (p.Leu520=) | |
| 15 | g.73323315G= | CA2187188026 | HCN4 | c.2778C= (p.Leu926=) c.1560C= (p.Leu520=) | |
| 15 | g.73323315G>T | CA491478230 | HCN4 | c.2778C>A (p.Leu926=) c.1560C>A (p.Leu520=) | dbSNP gnomAD v4 |
| 15 | g.73323315_73323318delinsGAGC | CA2187188025 | HCN4 | c.2775_2778delinsGCTC (p.Leu925=) c.1557_1560delinsGCTC (p.Leu519=) | |
| 15 | g.73323316A>C | CA393088052 | HCN4 | c.2777T>G (p.Leu926Arg) c.1559T>G (p.Leu520Arg) | |
| 15 | g.73323316A>G | CA393088056 | HCN4 | c.2777T>C (p.Leu926Pro) c.1559T>C (p.Leu520Pro) | gnomAD v4 |
| 15 | g.73323316A>T | CA393088057 | HCN4 | c.2777T>A (p.Leu926His) c.1559T>A (p.Leu520His) | |
| 15 | g.73323318_73323320del | CA7648958 | HCN4 | c.2775_2777del (p.Leu926del) c.1557_1559del (p.Leu520del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323317G>A | CA393088059 | HCN4 | c.2776C>T (p.Leu926Phe) c.1558C>T (p.Leu520Phe) | gnomAD v4 |
| 15 | g.73323317G>C | CA393088061 | HCN4 | c.2776C>G (p.Leu926Val) c.1558C>G (p.Leu520Val) | gnomAD v4 |
| 15 | g.73323317G>T | CA393088063 | HCN4 | c.2776C>A (p.Leu926Ile) c.1558C>A (p.Leu520Ile) | gnomAD v4 |
| 15 | g.73323318C>A | CA491478235 | HCN4 | c.2775G>T (p.Leu925=) c.1557G>T (p.Leu519=) | gnomAD v4 |
| 15 | g.73323318C>G | CA491478237 | HCN4 | c.2775G>C (p.Leu925=) c.1557G>C (p.Leu519=) | |
| 15 | g.73323318C>T | CA491478236 | HCN4 | c.2775G>A (p.Leu925=) c.1557G>A (p.Leu519=) | gnomAD v4 |
| 15 | g.73323319A= | CA2187188033 | HCN4 | c.2774T= (p.Leu925=) c.1556T= (p.Leu519=) | |
| 15 | g.73323319A>C | CA393088066 | HCN4 | c.2774T>G (p.Leu925Arg) c.1556T>G (p.Leu519Arg) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323319A>G | CA7648959 | HCN4 | c.2774T>C (p.Leu925Pro) c.1556T>C (p.Leu519Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323319A>T | CA393088068 | HCN4 | c.2774T>A (p.Leu925Gln) c.1556T>A (p.Leu519Gln) | |
| 15 | g.73323320G>A | CA491478240 | HCN4 | c.2773C>T (p.Leu925=) c.1555C>T (p.Leu519=) | gnomAD v4 COSMIC |
| 15 | g.73323320G>C | CA393088071 | HCN4 | c.2773C>G (p.Leu925Val) c.1555C>G (p.Leu519Val) | ClinVar gnomAD v4 |
| 15 | g.73323320G>T | CA393088073 | HCN4 | c.2773C>A (p.Leu925Met) c.1555C>A (p.Leu519Met) | gnomAD v4 |
| 15 | g.73323323del | CA2629370564 | HCN4 | c.2773del (p.Leu925CysfsTer?) c.1555del (p.Leu519CysfsTer?) | gnomAD v4 |
| 15 | g.73323321G>A | CA491478242 | HCN4 | c.2772C>T (p.Pro924=) c.1554C>T (p.Pro518=) | gnomAD v4 |
| 15 | g.73323321G>C | CA491478244 | HCN4 | c.2772C>G (p.Pro924=) c.1554C>G (p.Pro518=) | |
| 15 | g.73323321G>T | CA491478245 | HCN4 | c.2772C>A (p.Pro924=) c.1554C>A (p.Pro518=) | gnomAD v4 |
| 15 | g.73323322G>A | CA393088078 | HCN4 | c.2771C>T (p.Pro924Leu) c.1553C>T (p.Pro518Leu) | gnomAD v4 |
| 15 | g.73323322G>C | CA393088080 | HCN4 | c.2771C>G (p.Pro924Arg) c.1553C>G (p.Pro518Arg) | gnomAD v4 |
| 15 | g.73323322G>T | CA393088081 | HCN4 | c.2771C>A (p.Pro924His) c.1553C>A (p.Pro518His) | gnomAD v4 |
| 15 | g.73323323G>A | CA393088090 | HCN4 | c.2770C>T (p.Pro924Ser) c.1552C>T (p.Pro518Ser) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323323G>C | CA393088084 | HCN4 | c.2770C>G (p.Pro924Ala) c.1552C>G (p.Pro518Ala) | |
| 15 | g.73323323G= | CA2187188037 | HCN4 | c.2770C= (p.Pro924=) c.1552C= (p.Pro518=) | |
| 15 | g.73323323G>T | CA393088086 | HCN4 | c.2770C>A (p.Pro924Thr) c.1552C>A (p.Pro518Thr) | gnomAD v4 |
| 15 | g.73323326_73323327dup | CA2629370565 | HCN4 | c.2769_2770dup (p.Pro924LeufsTer?) c.1551_1552dup (p.Pro518LeufsTer?) | gnomAD v4 |
| 15 | g.73323324A= | CA2187188039 | HCN4 | c.2769T= (p.Ser923=) c.1551T= (p.Ser517=) | |
| 15 | g.73323324A>C | CA491478249 | HCN4 | c.2769T>G (p.Ser923=) c.1551T>G (p.Ser517=) | ClinVar |
| 15 | g.73323324A>G | CA491478252 | HCN4 | c.2769T>C (p.Ser923=) c.1551T>C (p.Ser517=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323324A>T | CA491478250 | HCN4 | c.2769T>A (p.Ser923=) c.1551T>A (p.Ser517=) | |
| 15 | g.73323325G>A | CA393088093 | HCN4 | c.2768C>T (p.Ser923Phe) c.1550C>T (p.Ser517Phe) | dbSNP gnomAD v4 |
| 15 | g.73323325G>C | CA393088096 | HCN4 | c.2768C>G (p.Ser923Cys) c.1550C>G (p.Ser517Cys) | gnomAD v4 |
| 15 | g.73323325G= | CA2187188042 | HCN4 | c.2768C= (p.Ser923=) c.1550C= (p.Ser517=) | |
| 15 | g.73323325G>T | CA393088099 | HCN4 | c.2768C>A (p.Ser923Tyr) c.1550C>A (p.Ser517Tyr) | gnomAD v4 |
| 15 | g.73323326A= | CA2187188044 | HCN4 | c.2767T= (p.Ser923=) c.1549T= (p.Ser517=) | |
| 15 | g.73323326A>C | CA393088101 | HCN4 | c.2767T>G (p.Ser923Ala) c.1549T>G (p.Ser517Ala) | COSMIC |
| 15 | g.73323326A>G | CA393088104 | HCN4 | c.2767T>C (p.Ser923Pro) c.1549T>C (p.Ser517Pro) | gnomAD v4 |
| 15 | g.73323326A>T | CA393088106 | HCN4 | c.2767T>A (p.Ser923Thr) c.1549T>A (p.Ser517Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323327G>A | CA491478254 | HCN4 | c.2766C>T (p.Asp922=) c.1548C>T (p.Asp516=) | dbSNP |
| 15 | g.73323327G>C | CA393088109 | HCN4 | c.2766C>G (p.Asp922Glu) c.1548C>G (p.Asp516Glu) | |
| 15 | g.73323327G= | CA2187188046 | HCN4 | c.2766C= (p.Asp922=) c.1548C= (p.Asp516=) | |
| 15 | g.73323327G>T | CA393088111 | HCN4 | c.2766C>A (p.Asp922Glu) c.1548C>A (p.Asp516Glu) | gnomAD v4 |
| 15 | g.73323328T>A | CA393088114 | HCN4 | c.2765A>T (p.Asp922Val) c.1547A>T (p.Asp516Val) | gnomAD v4 |
| 15 | g.73323328T>C | CA393088116 | HCN4 | c.2765A>G (p.Asp922Gly) c.1547A>G (p.Asp516Gly) | |
| 15 | g.73323328T>G | CA393088118 | HCN4 | c.2765A>C (p.Asp922Ala) c.1547A>C (p.Asp516Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323329C>A | CA393088124 | HCN4 | c.2764G>T (p.Asp922Tyr) c.1546G>T (p.Asp516Tyr) | gnomAD v4 |
| 15 | g.73323329C= | CA2187188053 | HCN4 | c.2764G= (p.Asp922=) c.1546G= (p.Asp516=) | |
| 15 | g.73323329C>G | CA393088122 | HCN4 | c.2764G>C (p.Asp922His) c.1546G>C (p.Asp516His) | |
| 15 | g.73323329C>T | CA272664284 | HCN4 | c.2764G>A (p.Asp922Asn) c.1546G>A (p.Asp516Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323329_73323332delinsCGGA | CA2187188055 | HCN4 | c.2761_2764delinsTCCG (p.Ser921=) c.1543_1546delinsTCCG (p.Ser515=) | |
| 15 | g.73323330G>A | CA7648960 | HCN4 | c.2763C>T (p.Ser921=) c.1545C>T (p.Ser515=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323330G>C | CA491478261 | HCN4 | c.2763C>G (p.Ser921=) c.1545C>G (p.Ser515=) | |
| 15 | g.73323330G= | CA2187188065 | HCN4 | c.2763C= (p.Ser921=) c.1545C= (p.Ser515=) | |
| 15 | g.73323330G>T | CA491478262 | HCN4 | c.2763C>A (p.Ser921=) c.1545C>A (p.Ser515=) | gnomAD v4 |
| 15 | g.73323336_73323338del | CA715544981 | HCN4 | c.2761_2763del (p.Ser921del) c.1543_1545del (p.Ser515del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323331G>A | CA393088130 | HCN4 | c.2762C>T (p.Ser921Phe) c.1544C>T (p.Ser515Phe) | gnomAD v4 |
| 15 | g.73323331G>C | CA393088134 | HCN4 | c.2762C>G (p.Ser921Cys) c.1544C>G (p.Ser515Cys) | |
| 15 | g.73323331G>T | CA393088136 | HCN4 | c.2762C>A (p.Ser921Tyr) c.1544C>A (p.Ser515Tyr) | gnomAD v4 |
| 15 | g.73323332A>C | CA393088140 | HCN4 | c.2761T>G (p.Ser921Ala) c.1543T>G (p.Ser515Ala) | |
| 15 | g.73323332A>G | CA393088142 | HCN4 | c.2761T>C (p.Ser921Pro) c.1543T>C (p.Ser515Pro) | gnomAD v4 |
| 15 | g.73323332A>T | CA393088145 | HCN4 | c.2761T>A (p.Ser921Thr) c.1543T>A (p.Ser515Thr) | |
| 15 | g.73323333G>A | CA491478269 | HCN4 | c.2760C>T (p.Ser920=) c.1542C>T (p.Ser514=) | |
| 15 | g.73323333G>C | CA491478265 | HCN4 | c.2760C>G (p.Ser920=) c.1542C>G (p.Ser514=) | |
| 15 | g.73323333G>T | CA491478267 | HCN4 | c.2760C>A (p.Ser920=) c.1542C>A (p.Ser514=) | gnomAD v4 |
| 15 | g.73323334G>A | CA393088147 | HCN4 | c.2759C>T (p.Ser920Phe) c.1541C>T (p.Ser514Phe) | |
| 15 | g.73323334G>C | CA393088149 | HCN4 | c.2759C>G (p.Ser920Cys) c.1541C>G (p.Ser514Cys) | |
| 15 | g.73323334G>T | CA393088151 | HCN4 | c.2759C>A (p.Ser920Tyr) c.1541C>A (p.Ser514Tyr) | gnomAD v4 |
| 15 | g.73323335A>C | CA393088153 | HCN4 | c.2758T>G (p.Ser920Ala) c.1540T>G (p.Ser514Ala) | |
| 15 | g.73323335A>G | CA393088154 | HCN4 | c.2758T>C (p.Ser920Pro) c.1540T>C (p.Ser514Pro) | gnomAD v4 |
| 15 | g.73323335A>T | CA393088156 | HCN4 | c.2758T>A (p.Ser920Thr) c.1540T>A (p.Ser514Thr) | |
| 15 | g.73323336G>A | CA491478273 | HCN4 | c.2757C>T (p.Ser919=) c.1539C>T (p.Ser513=) | gnomAD v4 COSMIC |
| 15 | g.73323336G>C | CA491478275 | HCN4 | c.2757C>G (p.Ser919=) c.1539C>G (p.Ser513=) | |
| 15 | g.73323336G>T | CA491478277 | HCN4 | c.2757C>A (p.Ser919=) c.1539C>A (p.Ser513=) | gnomAD v4 |
| 15 | g.73323337G>A | CA393088159 | HCN4 | c.2756C>T (p.Ser919Phe) c.1538C>T (p.Ser513Phe) | |
| 15 | g.73323337G>C | CA7648961 | HCN4 | c.2756C>G (p.Ser919Cys) c.1538C>G (p.Ser513Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323337G= | CA2187188068 | HCN4 | c.2756C= (p.Ser919=) c.1538C= (p.Ser513=) | |
| 15 | g.73323337G>T | CA393088157 | HCN4 | c.2756C>A (p.Ser919Tyr) c.1538C>A (p.Ser513Tyr) | gnomAD v4 |
| 15 | g.73323338A>C | CA393088161 | HCN4 | c.2755T>G (p.Ser919Ala) c.1537T>G (p.Ser513Ala) | |
| 15 | g.73323338A>G | CA393088163 | HCN4 | c.2755T>C (p.Ser919Pro) c.1537T>C (p.Ser513Pro) | gnomAD v4 |
| 15 | g.73323338A>T | CA393088164 | HCN4 | c.2755T>A (p.Ser919Thr) c.1537T>A (p.Ser513Thr) | |
| 15 | g.73323339C>A | CA491478279 | HCN4 | c.2754G>T (p.Leu918=) c.1536G>T (p.Leu512=) | gnomAD v4 |
| 15 | g.73323339C>G | CA491478282 | HCN4 | c.2754G>C (p.Leu918=) c.1536G>C (p.Leu512=) | |
| 15 | g.73323339C>T | CA491478285 | HCN4 | c.2754G>A (p.Leu918=) c.1536G>A (p.Leu512=) | |
| 15 | g.73323340A>C | CA393088166 | HCN4 | c.2753T>G (p.Leu918Arg) c.1535T>G (p.Leu512Arg) | |
| 15 | g.73323340A>G | CA393088168 | HCN4 | c.2753T>C (p.Leu918Pro) c.1535T>C (p.Leu512Pro) | gnomAD v4 |
| 15 | g.73323340A>T | CA393088170 | HCN4 | c.2753T>A (p.Leu918Gln) c.1535T>A (p.Leu512Gln) | gnomAD v4 |
| 15 | g.73323341G>A | CA491478291 | HCN4 | c.2752C>T (p.Leu918=) c.1534C>T (p.Leu512=) | |
| 15 | g.73323341G>C | CA393088171 | HCN4 | c.2752C>G (p.Leu918Val) c.1534C>G (p.Leu512Val) | |
| 15 | g.73323341G>T | CA393088172 | HCN4 | c.2752C>A (p.Leu918Met) c.1534C>A (p.Leu512Met) | gnomAD v4 |
| 15 | g.73323342G>A | CA491478292 | HCN4 | c.2751C>T (p.Ser917=) c.1533C>T (p.Ser511=) | gnomAD v4 |
| 15 | g.73323342G>C | CA491478293 | HCN4 | c.2751C>G (p.Ser917=) c.1533C>G (p.Ser511=) | |
| 15 | g.73323342G>T | CA491478294 | HCN4 | c.2751C>A (p.Ser917=) c.1533C>A (p.Ser511=) | gnomAD v4 |
| 15 | g.73323343G>A | CA393088174 | HCN4 | c.2750C>T (p.Ser917Phe) c.1532C>T (p.Ser511Phe) | |
| 15 | g.73323343G>C | CA393088175 | HCN4 | c.2750C>G (p.Ser917Cys) c.1532C>G (p.Ser511Cys) | gnomAD v4 |
| 15 | g.73323343G>T | CA393088177 | HCN4 | c.2750C>A (p.Ser917Tyr) c.1532C>A (p.Ser511Tyr) | gnomAD v4 |
| 15 | g.73323344A>C | CA393088182 | HCN4 | c.2749T>G (p.Ser917Ala) c.1531T>G (p.Ser511Ala) | |
| 15 | g.73323344A>G | CA393088180 | HCN4 | c.2749T>C (p.Ser917Pro) c.1531T>C (p.Ser511Pro) | gnomAD v4 |
| 15 | g.73323344A>T | CA393088179 | HCN4 | c.2749T>A (p.Ser917Thr) c.1531T>A (p.Ser511Thr) | |
| 15 | g.73323345G>A | CA491478300 | HCN4 | c.2748C>T (p.Gly916=) c.1530C>T (p.Gly510=) | gnomAD v4 |
| 15 | g.73323345G>C | CA491478302 | HCN4 | c.2748C>G (p.Gly916=) c.1530C>G (p.Gly510=) | |
| 15 | g.73323345G>T | CA491478304 | HCN4 | c.2748C>A (p.Gly916=) c.1530C>A (p.Gly510=) | gnomAD v4 |
| 15 | g.73323346C>A | CA272664298 | HCN4 | c.2747G>T (p.Gly916Val) c.1529G>T (p.Gly510Val) | dbSNP gnomAD v4 |
| 15 | g.73323346C= | CA2187188072 | HCN4 | c.2747G= (p.Gly916=) c.1529G= (p.Gly510=) | |
| 15 | g.73323346C>G | CA393088189 | HCN4 | c.2747G>C (p.Gly916Ala) c.1529G>C (p.Gly510Ala) | |
| 15 | g.73323346C>T | CA393088185 | HCN4 | c.2747G>A (p.Gly916Asp) c.1529G>A (p.Gly510Asp) | gnomAD v4 |
| 15 | g.73323347C>A | CA393088191 | HCN4 | c.2746G>T (p.Gly916Cys) c.1528G>T (p.Gly510Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323347C= | CA2187188075 | HCN4 | c.2746G= (p.Gly916=) c.1528G= (p.Gly510=) | |
| 15 | g.73323347C>G | CA393088193 | HCN4 | c.2746G>C (p.Gly916Arg) c.1528G>C (p.Gly510Arg) | |
| 15 | g.73323347C>T | CA393088195 | HCN4 | c.2746G>A (p.Gly916Ser) c.1528G>A (p.Gly510Ser) | dbSNP gnomAD v4 |
| 15 | g.73323348A= | CA2187188080 | HCN4 | c.2745T= (p.Gly915=) c.1527T= (p.Gly509=) | |
| 15 | g.73323348A>C | CA491478311 | HCN4 | c.2745T>G (p.Gly915=) c.1527T>G (p.Gly509=) | |
| 15 | g.73323348A>G | CA491478313 | HCN4 | c.2745T>C (p.Gly915=) c.1527T>C (p.Gly509=) | |
| 15 | g.73323348A>T | CA491478314 | HCN4 | c.2745T>A (p.Gly915=) c.1527T>A (p.Gly509=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323348dup | CA2629370566 | HCN4 | c.2745dup (p.Gly916TrpfsTer?) c.1527dup (p.Gly510TrpfsTer?) | gnomAD v4 |
| 15 | g.73323349C>A | CA393088197 | HCN4 | c.2744G>T (p.Gly915Val) c.1526G>T (p.Gly509Val) | |
| 15 | g.73323349C= | CA2187188083 | HCN4 | c.2744G= (p.Gly915=) c.1526G= (p.Gly509=) | |
| 15 | g.73323349C>G | CA393088198 | HCN4 | c.2744G>C (p.Gly915Ala) c.1526G>C (p.Gly509Ala) | |
| 15 | g.73323349C>T | CA393088200 | HCN4 | c.2744G>A (p.Gly915Asp) c.1526G>A (p.Gly509Asp) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323351del | CA2580089981 | HCN4 | c.2744del (p.Gly915ValfsTer?) c.1526del (p.Gly509ValfsTer?) | ClinVar |
| 15 | g.73323350C>A | CA393088202 | HCN4 | c.2743G>T (p.Gly915Cys) c.1525G>T (p.Gly509Cys) | gnomAD v4 |
| 15 | g.73323350C= | CA2187188086 | HCN4 | c.2743G= (p.Gly915=) c.1525G= (p.Gly509=) | |
| 15 | g.73323350C>G | CA393088203 | HCN4 | c.2743G>C (p.Gly915Arg) c.1525G>C (p.Gly509Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323350C>T | CA393088205 | HCN4 | c.2743G>A (p.Gly915Ser) c.1525G>A (p.Gly509Ser) | ClinVar gnomAD v4 |
| 15 | g.73323351C>A | CA491478319 | HCN4 | c.2742G>T (p.Leu914=) c.1524G>T (p.Leu508=) | gnomAD v4 |
| 15 | g.73323351C>G | CA491478320 | HCN4 | c.2742G>C (p.Leu914=) c.1524G>C (p.Leu508=) | |
| 15 | g.73323351C>T | CA491478321 | HCN4 | c.2742G>A (p.Leu914=) c.1524G>A (p.Leu508=) | |
| 15 | g.73323352A>C | CA393088207 | HCN4 | c.2741T>G (p.Leu914Arg) c.1523T>G (p.Leu508Arg) | |
| 15 | g.73323352A>G | CA393088209 | HCN4 | c.2741T>C (p.Leu914Pro) c.1523T>C (p.Leu508Pro) | |
| 15 | g.73323352A>T | CA393088211 | HCN4 | c.2741T>A (p.Leu914Gln) c.1523T>A (p.Leu508Gln) | gnomAD v4 |
| 15 | g.73323353G>A | CA491478332 | HCN4 | c.2740C>T (p.Leu914=) c.1522C>T (p.Leu508=) | gnomAD v4 |
| 15 | g.73323353G>C | CA393088215 | HCN4 | c.2740C>G (p.Leu914Val) c.1522C>G (p.Leu508Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323353G= | CA2187188089 | HCN4 | c.2740C= (p.Leu914=) c.1522C= (p.Leu508=) | |
| 15 | g.73323353G>T | CA393088213 | HCN4 | c.2740C>A (p.Leu914Met) c.1522C>A (p.Leu508Met) | gnomAD v4 |
| 15 | g.73323354C>A | CA491478336 | HCN4 | c.2739G>T (p.Ala913=) c.1521G>T (p.Ala507=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323354C= | CA2187188093 | HCN4 | c.2739G= (p.Ala913=) c.1521G= (p.Ala507=) | |
| 15 | g.73323354C>G | CA491478333 | HCN4 | c.2739G>C (p.Ala913=) c.1521G>C (p.Ala507=) | gnomAD v4 |
| 15 | g.73323354C>T | CA234112 | HCN4 | c.2739G>A (p.Ala913=) c.1521G>A (p.Ala507=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323355G>A | CA7648962 | HCN4 | c.2738C>T (p.Ala913Val) c.1520C>T (p.Ala507Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323355G>C | CA393088218 | HCN4 | c.2738C>G (p.Ala913Gly) c.1520C>G (p.Ala507Gly) | |
| 15 | g.73323355G= | CA2187188097 | HCN4 | c.2738C= (p.Ala913=) c.1520C= (p.Ala507=) | |
| 15 | g.73323355G>T | CA393088220 | HCN4 | c.2738C>A (p.Ala913Glu) c.1520C>A (p.Ala507Glu) | gnomAD v4 |
| 15 | g.73323356C>A | CA393088223 | HCN4 | c.2737G>T (p.Ala913Ser) c.1519G>T (p.Ala507Ser) | dbSNP |
| 15 | g.73323356C= | CA2187188103 | HCN4 | c.2737G= (p.Ala913=) c.1519G= (p.Ala507=) | |
| 15 | g.73323356C>G | CA393088224 | HCN4 | c.2737G>C (p.Ala913Pro) c.1519G>C (p.Ala507Pro) | |
| 15 | g.73323356C>T | CA393088225 | HCN4 | c.2737G>A (p.Ala913Thr) c.1519G>A (p.Ala507Thr) | |
| 15 | g.73323357C>A | CA393088226 | HCN4 | c.2736G>T (p.Lys912Asn) c.1518G>T (p.Lys506Asn) | gnomAD v4 |
| 15 | g.73323357C>G | CA393088227 | HCN4 | c.2736G>C (p.Lys912Asn) c.1518G>C (p.Lys506Asn) | |
| 15 | g.73323357C>T | CA491478346 | HCN4 | c.2736G>A (p.Lys912=) c.1518G>A (p.Lys506=) | |
| 15 | g.73323358T>A | CA393088230 | HCN4 | c.2735A>T (p.Lys912Met) c.1517A>T (p.Lys506Met) | gnomAD v4 COSMIC |
| 15 | g.73323358T>C | CA393088231 | HCN4 | c.2735A>G (p.Lys912Arg) c.1517A>G (p.Lys506Arg) | |
| 15 | g.73323358T>G | CA393088233 | HCN4 | c.2735A>C (p.Lys912Thr) c.1517A>C (p.Lys506Thr) | |
| 15 | g.73323358T= | CA2187188106 | HCN4 | c.2735A= (p.Lys912=) c.1517A= (p.Lys506=) | |
| 15 | g.73323359T>A | CA393088237 | HCN4 | c.2734A>T (p.Lys912Ter) c.1516A>T (p.Lys506Ter) | gnomAD v4 |
| 15 | g.73323359T>C | CA393088236 | HCN4 | c.2734A>G (p.Lys912Glu) c.1516A>G (p.Lys506Glu) | gnomAD v4 |
| 15 | g.73323359T>G | CA393088234 | HCN4 | c.2734A>C (p.Lys912Gln) c.1516A>C (p.Lys506Gln) | gnomAD v4 |
| 15 | g.73323360_73323381dup | CA915946063 | HCN4 | c.2713_2734dup (p.Lys912SerfsTer?) c.1495_1516dup (p.Lys506SerfsTer?) | ClinVar dbSNP |
| 15 | g.73323360G>A | CA7648963 | HCN4 | c.2733C>T (p.His911=) c.1515C>T (p.His505=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323360G>C | CA393088239 | HCN4 | c.2733C>G (p.His911Gln) c.1515C>G (p.His505Gln) | |
| 15 | g.73323360G= | CA2187188116 | HCN4 | c.2733C= (p.His911=) c.1515C= (p.His505=) | |
| 15 | g.73323360G>T | CA393088241 | HCN4 | c.2733C>A (p.His911Gln) c.1515C>A (p.His505Gln) | gnomAD v4 |
| 15 | g.73323361T>A | CA393088243 | HCN4 | c.2732A>T (p.His911Leu) c.1514A>T (p.His505Leu) | |
| 15 | g.73323361T>C | CA393088244 | HCN4 | c.2732A>G (p.His911Arg) c.1514A>G (p.His505Arg) | |
| 15 | g.73323361T>G | CA393088245 | HCN4 | c.2732A>C (p.His911Pro) c.1514A>C (p.His505Pro) | |
| 15 | g.73323362G>A | CA393088249 | HCN4 | c.2731C>T (p.His911Tyr) c.1513C>T (p.His505Tyr) | ClinVar |
| 15 | g.73323362G>C | CA393088247 | HCN4 | c.2731C>G (p.His911Asp) c.1513C>G (p.His505Asp) | |
| 15 | g.73323362G>T | CA393088248 | HCN4 | c.2731C>A (p.His911Asn) c.1513C>A (p.His505Asn) | gnomAD v4 |
| 15 | g.73323363G>A | CA491478364 | HCN4 | c.2730C>T (p.Phe910=) c.1512C>T (p.Phe504=) | ClinVar gnomAD v4 |
| 15 | g.73323363G>C | CA393088250 | HCN4 | c.2730C>G (p.Phe910Leu) c.1512C>G (p.Phe504Leu) | dbSNP |
| 15 | g.73323363G= | CA2187188123 | HCN4 | c.2730C= (p.Phe910=) c.1512C= (p.Phe504=) | |
| 15 | g.73323363G>T | CA7648964 | HCN4 | c.2730C>A (p.Phe910Leu) c.1512C>A (p.Phe504Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323364A>C | CA393088251 | HCN4 | c.2729T>G (p.Phe910Cys) c.1511T>G (p.Phe504Cys) | gnomAD v4 |
| 15 | g.73323364A>G | CA393088253 | HCN4 | c.2729T>C (p.Phe910Ser) c.1511T>C (p.Phe504Ser) | |
| 15 | g.73323364A>T | CA393088254 | HCN4 | c.2729T>A (p.Phe910Tyr) c.1511T>A (p.Phe504Tyr) | |
| 15 | g.73323365A>C | CA393088256 | HCN4 | c.2728T>G (p.Phe910Val) c.1510T>G (p.Phe504Val) | |
| 15 | g.73323365A>G | CA393088260 | HCN4 | c.2728T>C (p.Phe910Leu) c.1510T>C (p.Phe504Leu) | gnomAD v4 |
| 15 | g.73323365A>T | CA393088258 | HCN4 | c.2728T>A (p.Phe910Ile) c.1510T>A (p.Phe504Ile) | |
| 15 | g.73323366G>A | CA491478378 | HCN4 | c.2727C>T (p.His909=) c.1509C>T (p.His503=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323366G>C | CA393088262 | HCN4 | c.2727C>G (p.His909Gln) c.1509C>G (p.His503Gln) | |
| 15 | g.73323366G= | CA2187188131 | HCN4 | c.2727C= (p.His909=) c.1509C= (p.His503=) | |
| 15 | g.73323366G>T | CA393088263 | HCN4 | c.2727C>A (p.His909Gln) c.1509C>A (p.His503Gln) | gnomAD v4 |
| 15 | g.73323367T>A | CA393088265 | HCN4 | c.2726A>T (p.His909Leu) c.1508A>T (p.His503Leu) | |
| 15 | g.73323367T>C | CA393088267 | HCN4 | c.2726A>G (p.His909Arg) c.1508A>G (p.His503Arg) | |
| 15 | g.73323367T>G | CA393088268 | HCN4 | c.2726A>C (p.His909Pro) c.1508A>C (p.His503Pro) | |
| 15 | g.73323368G>A | CA393088270 | HCN4 | c.2725C>T (p.His909Tyr) c.1507C>T (p.His503Tyr) | |
| 15 | g.73323368G>C | CA393088271 | HCN4 | c.2725C>G (p.His909Asp) c.1507C>G (p.His503Asp) | |
| 15 | g.73323368G>T | CA393088273 | HCN4 | c.2725C>A (p.His909Asn) c.1507C>A (p.His503Asn) | gnomAD v4 |
| 15 | g.73323369G>A | CA491478385 | HCN4 | c.2724C>T (p.Gly908=) c.1506C>T (p.Gly502=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323369G>C | CA491478389 | HCN4 | c.2724C>G (p.Gly908=) c.1506C>G (p.Gly502=) | |
| 15 | g.73323369G= | CA2187188133 | HCN4 | c.2724C= (p.Gly908=) c.1506C= (p.Gly502=) | |
| 15 | g.73323369G>T | CA491478390 | HCN4 | c.2724C>A (p.Gly908=) c.1506C>A (p.Gly502=) | |
| 15 | g.73323370C>A | CA393088274 | HCN4 | c.2723G>T (p.Gly908Val) c.1505G>T (p.Gly502Val) | gnomAD v4 |
| 15 | g.73323370C>G | CA393088276 | HCN4 | c.2723G>C (p.Gly908Ala) c.1505G>C (p.Gly502Ala) | |
| 15 | g.73323370C>T | CA393088277 | HCN4 | c.2723G>A (p.Gly908Asp) c.1505G>A (p.Gly502Asp) | gnomAD v4 |
| 15 | g.73323371C>A | CA393088283 | HCN4 | c.2722G>T (p.Gly908Cys) c.1504G>T (p.Gly502Cys) | gnomAD v4 |
| 15 | g.73323371C= | CA2187188135 | HCN4 | c.2722G= (p.Gly908=) c.1504G= (p.Gly502=) | |
| 15 | g.73323371C>G | CA393088281 | HCN4 | c.2722G>C (p.Gly908Arg) c.1504G>C (p.Gly502Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323371C>T | CA393088279 | HCN4 | c.2722G>A (p.Gly908Ser) c.1504G>A (p.Gly502Ser) | |
| 15 | g.73323372A>C | CA393088284 | HCN4 | c.2721T>G (p.Phe907Leu) c.1503T>G (p.Phe501Leu) | |
| 15 | g.73323372A>G | CA491478400 | HCN4 | c.2721T>C (p.Phe907=) c.1503T>C (p.Phe501=) | gnomAD v4 |
| 15 | g.73323372A>T | CA393088286 | HCN4 | c.2721T>A (p.Phe907Leu) c.1503T>A (p.Phe501Leu) | |
| 15 | g.73323373A>C | CA393088288 | HCN4 | c.2720T>G (p.Phe907Cys) c.1502T>G (p.Phe501Cys) | |
| 15 | g.73323373A>G | CA393088290 | HCN4 | c.2720T>C (p.Phe907Ser) c.1502T>C (p.Phe501Ser) | |
| 15 | g.73323373A>T | CA393088291 | HCN4 | c.2720T>A (p.Phe907Tyr) c.1502T>A (p.Phe501Tyr) | |
| 15 | g.73323374A>C | CA393088293 | HCN4 | c.2719T>G (p.Phe907Val) c.1501T>G (p.Phe501Val) | |
| 15 | g.73323374A>G | CA393088294 | HCN4 | c.2719T>C (p.Phe907Leu) c.1501T>C (p.Phe501Leu) | |
| 15 | g.73323374A>T | CA393088296 | HCN4 | c.2719T>A (p.Phe907Ile) c.1501T>A (p.Phe501Ile) | |
| 15 | g.73323375C>A | CA491478409 | HCN4 | c.2718G>T (p.Gly906=) c.1500G>T (p.Gly500=) | COSMIC |
| 15 | g.73323375C= | CA2187188138 | HCN4 | c.2718G= (p.Gly906=) c.1500G= (p.Gly500=) | |
| 15 | g.73323375C>G | CA491478410 | HCN4 | c.2718G>C (p.Gly906=) c.1500G>C (p.Gly500=) | |
| 15 | g.73323375C>T | CA491478412 | HCN4 | c.2718G>A (p.Gly906=) c.1500G>A (p.Gly500=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323376C>A | CA393088298 | HCN4 | c.2717G>T (p.Gly906Val) c.1499G>T (p.Gly500Val) | gnomAD v4 |
| 15 | g.73323376C= | CA2187188140 | HCN4 | c.2717G= (p.Gly906=) c.1499G= (p.Gly500=) | |
| 15 | g.73323376C>G | CA393088302 | HCN4 | c.2717G>C (p.Gly906Ala) c.1499G>C (p.Gly500Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323376C>T | CA393088301 | HCN4 | c.2717G>A (p.Gly906Glu) c.1499G>A (p.Gly500Glu) | gnomAD v4 |
| 15 | g.73323377C>A | CA393088305 | HCN4 | c.2716G>T (p.Gly906Trp) c.1498G>T (p.Gly500Trp) | gnomAD v4 |
| 15 | g.73323377C= | CA2187188146 | HCN4 | c.2716G= (p.Gly906=) c.1498G= (p.Gly500=) | |
| 15 | g.73323377C>G | CA393088306 | HCN4 | c.2716G>C (p.Gly906Arg) c.1498G>C (p.Gly500Arg) | ClinVar dbSNP |
| 15 | g.73323377C>T | CA7648965 | HCN4 | c.2716G>A (p.Gly906Arg) c.1498G>A (p.Gly500Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323378G>A | CA7648966 | HCN4 | c.2715C>T (p.Ala905=) c.1497C>T (p.Ala499=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323378G>C | CA491478419 | HCN4 | c.2715C>G (p.Ala905=) c.1497C>G (p.Ala499=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323378G= | CA2187188158 | HCN4 | c.2715C= (p.Ala905=) c.1497C= (p.Ala499=) | |
| 15 | g.73323378G>T | CA491478420 | HCN4 | c.2715C>A (p.Ala905=) c.1497C>A (p.Ala499=) | |
| 15 | g.73323379G>A | CA272664354 | HCN4 | c.2714C>T (p.Ala905Val) c.1496C>T (p.Ala499Val) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323379G>C | CA393088310 | HCN4 | c.2714C>G (p.Ala905Gly) c.1496C>G (p.Ala499Gly) | |
| 15 | g.73323379G= | CA2187188162 | HCN4 | c.2714C= (p.Ala905=) c.1496C= (p.Ala499=) | |
| 15 | g.73323379G>T | CA393088311 | HCN4 | c.2714C>A (p.Ala905Asp) c.1496C>A (p.Ala499Asp) | gnomAD v4 |
| 15 | g.73323380C>A | CA393088315 | HCN4 | c.2713G>T (p.Ala905Ser) c.1495G>T (p.Ala499Ser) | |
| 15 | g.73323380C>G | CA393088316 | HCN4 | c.2713G>C (p.Ala905Pro) c.1495G>C (p.Ala499Pro) | gnomAD v4 |
| 15 | g.73323380C>T | CA393088318 | HCN4 | c.2713G>A (p.Ala905Thr) c.1495G>A (p.Ala499Thr) | |
| 15 | g.73323381T>A | CA491478432 | HCN4 | c.2712A>T (p.Ile904=) c.1494A>T (p.Ile498=) | |
| 15 | g.73323381T>C | CA393088320 | HCN4 | c.2712A>G (p.Ile904Met) c.1494A>G (p.Ile498Met) | |
| 15 | g.73323381T>G | CA491478428 | HCN4 | c.2712A>C (p.Ile904=) c.1494A>C (p.Ile498=) | |
| 15 | g.73323382A= | CA2187188166 | HCN4 | c.2711T= (p.Ile904=) c.1493T= (p.Ile498=) | |
| 15 | g.73323382A>C | CA393088322 | HCN4 | c.2711T>G (p.Ile904Arg) c.1493T>G (p.Ile498Arg) | |
| 15 | g.73323382A>G | CA393088323 | HCN4 | c.2711T>C (p.Ile904Thr) c.1493T>C (p.Ile498Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323382A>T | CA393088325 | HCN4 | c.2711T>A (p.Ile904Lys) c.1493T>A (p.Ile498Lys) | |
| 15 | g.73323383T>A | CA393088327 | HCN4 | c.2710A>T (p.Ile904Leu) c.1492A>T (p.Ile498Leu) | |
| 15 | g.73323383T>C | CA393088329 | HCN4 | c.2710A>G (p.Ile904Val) c.1492A>G (p.Ile498Val) | dbSNP gnomAD v4 |
| 15 | g.73323383T>G | CA393088330 | HCN4 | c.2710A>C (p.Ile904Leu) c.1492A>C (p.Ile498Leu) | |
| 15 | g.73323383T= | CA2187188172 | HCN4 | c.2710A= (p.Ile904=) c.1492A= (p.Ile498=) | |
| 15 | g.73323389_73323391dup | CA919589489 | HCN4 | c.2708_2710dup (p.Thr903_Ile904insThr) c.1490_1492dup (p.Thr497_Ile498insThr) | dbSNP |
| 15 | g.73323384G>A | CA491478443 | HCN4 | c.2709C>T (p.Thr903=) c.1491C>T (p.Thr497=) | |
| 15 | g.73323384G>C | CA491478442 | HCN4 | c.2709C>G (p.Thr903=) c.1491C>G (p.Thr497=) | |
| 15 | g.73323384G>T | CA491478441 | HCN4 | c.2709C>A (p.Thr903=) c.1491C>A (p.Thr497=) | gnomAD v4 |
| 15 | g.73323385G>A | CA393088332 | HCN4 | c.2708C>T (p.Thr903Ile) c.1490C>T (p.Thr497Ile) | gnomAD v4 |
| 15 | g.73323385G>C | CA393088333 | HCN4 | c.2708C>G (p.Thr903Ser) c.1490C>G (p.Thr497Ser) | |
| 15 | g.73323385G>T | CA393088335 | HCN4 | c.2708C>A (p.Thr903Asn) c.1490C>A (p.Thr497Asn) | |
| 15 | g.73323386T>A | CA393088337 | HCN4 | c.2707A>T (p.Thr903Ser) c.1489A>T (p.Thr497Ser) | |
| 15 | g.73323386T>C | CA393088340 | HCN4 | c.2707A>G (p.Thr903Ala) c.1489A>G (p.Thr497Ala) | |
| 15 | g.73323386T>G | CA393088338 | HCN4 | c.2707A>C (p.Thr903Pro) c.1489A>C (p.Thr497Pro) | |
| 15 | g.73323387G>A | CA491478455 | HCN4 | c.2706C>T (p.Thr902=) c.1488C>T (p.Thr496=) | |
| 15 | g.73323387G>C | CA491478458 | HCN4 | c.2706C>G (p.Thr902=) c.1488C>G (p.Thr496=) | |
| 15 | g.73323387G>T | CA491478457 | HCN4 | c.2706C>A (p.Thr902=) c.1488C>A (p.Thr496=) | |
| 15 | g.73323388G>A | CA393088341 | HCN4 | c.2705C>T (p.Thr902Ile) c.1487C>T (p.Thr496Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323388G>C | CA393088343 | HCN4 | c.2705C>G (p.Thr902Ser) c.1487C>G (p.Thr496Ser) | |
| 15 | g.73323388G= | CA2187188175 | HCN4 | c.2705C= (p.Thr902=) c.1487C= (p.Thr496=) | |
| 15 | g.73323388G>T | CA393088344 | HCN4 | c.2705C>A (p.Thr902Asn) c.1487C>A (p.Thr496Asn) | gnomAD v4 |
| 15 | g.73323389T>A | CA393088346 | HCN4 | c.2704A>T (p.Thr902Ser) c.1486A>T (p.Thr496Ser) | |
| 15 | g.73323389T>C | CA393088348 | HCN4 | c.2704A>G (p.Thr902Ala) c.1486A>G (p.Thr496Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323389T>G | CA393088350 | HCN4 | c.2704A>C (p.Thr902Pro) c.1486A>C (p.Thr496Pro) | |
| 15 | g.73323389T= | CA2187188178 | HCN4 | c.2704A= (p.Thr902=) c.1486A= (p.Thr496=) | |
| 15 | g.73323390G>A | CA7648967 | HCN4 | c.2703C>T (p.Ala901=) c.1485C>T (p.Ala495=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323390G>C | CA491478467 | HCN4 | c.2703C>G (p.Ala901=) c.1485C>G (p.Ala495=) | |
| 15 | g.73323390G= | CA2187188180 | HCN4 | c.2703C= (p.Ala901=) c.1485C= (p.Ala495=) | |
| 15 | g.73323390G>T | CA491478468 | HCN4 | c.2703C>A (p.Ala901=) c.1485C>A (p.Ala495=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323391G>A | CA393088353 | HCN4 | c.2702C>T (p.Ala901Val) c.1484C>T (p.Ala495Val) | |
| 15 | g.73323391G>C | CA393088354 | HCN4 | c.2702C>G (p.Ala901Gly) c.1484C>G (p.Ala495Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323391G= | CA2187188185 | HCN4 | c.2702C= (p.Ala901=) c.1484C= (p.Ala495=) | |
| 15 | g.73323391G>T | CA393088357 | HCN4 | c.2702C>A (p.Ala901Asp) c.1484C>A (p.Ala495Asp) | gnomAD v4 |
| 15 | g.73323392C>A | CA393088358 | HCN4 | c.2701G>T (p.Ala901Ser) c.1483G>T (p.Ala495Ser) | gnomAD v4 |
| 15 | g.73323392C= | CA2187188189 | HCN4 | c.2701G= (p.Ala901=) c.1483G= (p.Ala495=) | |
| 15 | g.73323392C>G | CA393088360 | HCN4 | c.2701G>C (p.Ala901Pro) c.1483G>C (p.Ala495Pro) | dbSNP |
| 15 | g.73323392C>T | CA7648968 | HCN4 | c.2701G>A (p.Ala901Thr) c.1483G>A (p.Ala495Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323393G>A | CA7648970 | HCN4 | c.2700C>T (p.Ala900=) c.1482C>T (p.Ala494=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323393G>C | CA491478477 | HCN4 | c.2700C>G (p.Ala900=) c.1482C>G (p.Ala494=) | |
| 15 | g.73323393G= | CA2187188197 | HCN4 | c.2700C= (p.Ala900=) c.1482C= (p.Ala494=) | |
| 15 | g.73323393G>T | CA7648969 | HCN4 | c.2700C>A (p.Ala900=) c.1482C>A (p.Ala494=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323394G>A | CA393088365 | HCN4 | c.2699C>T (p.Ala900Val) c.1481C>T (p.Ala494Val) | gnomAD v4 |
| 15 | g.73323394G>C | CA393088367 | HCN4 | c.2699C>G (p.Ala900Gly) c.1481C>G (p.Ala494Gly) | |
| 15 | g.73323394G>T | CA393088369 | HCN4 | c.2699C>A (p.Ala900Asp) c.1481C>A (p.Ala494Asp) | gnomAD v4 |
| 15 | g.73323395C>A | CA393088370 | HCN4 | c.2698G>T (p.Ala900Ser) c.1480G>T (p.Ala494Ser) | |
| 15 | g.73323395C= | CA2187188202 | HCN4 | c.2698G= (p.Ala900=) c.1480G= (p.Ala494=) | |
| 15 | g.73323395C>G | CA393088372 | HCN4 | c.2698G>C (p.Ala900Pro) c.1480G>C (p.Ala494Pro) | dbSNP |
| 15 | g.73323395C>T | CA393088374 | HCN4 | c.2698G>A (p.Ala900Thr) c.1480G>A (p.Ala494Thr) | dbSNP gnomAD v4 |
| 15 | g.73323396T>A | CA491478482 | HCN4 | c.2697A>T (p.Val899=) c.1479A>T (p.Val493=) | |
| 15 | g.73323396T>C | CA491478484 | HCN4 | c.2697A>G (p.Val899=) c.1479A>G (p.Val493=) | |
| 15 | g.73323396T>G | CA491478486 | HCN4 | c.2697A>C (p.Val899=) c.1479A>C (p.Val493=) | dbSNP |
| 15 | g.73323396T= | CA2187188205 | HCN4 | c.2697A= (p.Val899=) c.1479A= (p.Val493=) | |
| 15 | g.73323397A>C | CA393088376 | HCN4 | c.2696T>G (p.Val899Gly) c.1478T>G (p.Val493Gly) | ClinVar |
| 15 | g.73323397A>G | CA393088378 | HCN4 | c.2696T>C (p.Val899Ala) c.1478T>C (p.Val493Ala) | dbSNP |
| 15 | g.73323397A>T | CA393088380 | HCN4 | c.2696T>A (p.Val899Glu) c.1478T>A (p.Val493Glu) | |
| 15 | g.73323398C>A | CA393088381 | HCN4 | c.2695G>T (p.Val899Leu) c.1477G>T (p.Val493Leu) | gnomAD v4 |
| 15 | g.73323398C= | CA2187188210 | HCN4 | c.2695G= (p.Val899=) c.1477G= (p.Val493=) | |
| 15 | g.73323398C>G | CA393088383 | HCN4 | c.2695G>C (p.Val899Leu) c.1477G>C (p.Val493Leu) | |
| 15 | g.73323398C>T | CA272664364 | HCN4 | c.2695G>A (p.Val899Ile) c.1477G>A (p.Val493Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323399G>A | CA7648971 | HCN4 | c.2694C>T (p.Gly898=) c.1476C>T (p.Gly492=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323399G>C | CA491478494 | HCN4 | c.2694C>G (p.Gly898=) c.1476C>G (p.Gly492=) | |
| 15 | g.73323399G= | CA2187188217 | HCN4 | c.2694C= (p.Gly898=) c.1476C= (p.Gly492=) | |
| 15 | g.73323399G>T | CA491478495 | HCN4 | c.2694C>A (p.Gly898=) c.1476C>A (p.Gly492=) | ClinVar dbSNP |