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.73322487A>C | CA393084607 | HCN4 | c.3606T>G (p.Asn1202Lys) c.2388T>G (p.Asn796Lys) | |
| 15 | g.73322487A>G | CA491477748 | HCN4 | c.3606T>C (p.Asn1202=) c.2388T>C (p.Asn796=) | |
| 15 | g.73322487A>T | CA393084608 | HCN4 | c.3606T>A (p.Asn1202Lys) c.2388T>A (p.Asn796Lys) | |
| 15 | g.73322488T>A | CA393084609 | HCN4 | c.3605A>T (p.Asn1202Ile) c.2387A>T (p.Asn796Ile) | |
| 15 | g.73322488T>C | CA7648790 | HCN4 | c.3605A>G (p.Asn1202Ser) c.2387A>G (p.Asn796Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73322488T>G | CA393084610 | HCN4 | c.3605A>C (p.Asn1202Thr) c.2387A>C (p.Asn796Thr) | |
| 15 | g.73322488T= | CA2187186022 | HCN4 | c.3605A= (p.Asn1202=) c.2387A= (p.Asn796=) | |
| 15 | g.73322489T>A | CA393084611 | HCN4 | c.3604A>T (p.Asn1202Tyr) c.2386A>T (p.Asn796Tyr) | gnomAD v4 |
| 15 | g.73322489T>C | CA393084613 | HCN4 | c.3604A>G (p.Asn1202Asp) c.2386A>G (p.Asn796Asp) | |
| 15 | g.73322489T>G | CA393084612 | HCN4 | c.3604A>C (p.Asn1202His) c.2386A>C (p.Asn796His) | gnomAD v4 |
| 15 | g.73322490G>A | CA491477749 | HCN4 | c.3603C>T (p.Ser1201=) c.2385C>T (p.Ser795=) | gnomAD v4 |
| 15 | g.73322490G>C | CA491477750 | HCN4 | c.3603C>G (p.Ser1201=) c.2385C>G (p.Ser795=) | |
| 15 | g.73322490G>T | CA491477751 | HCN4 | c.3603C>A (p.Ser1201=) c.2385C>A (p.Ser795=) | gnomAD v4 |
| 15 | g.73322491G>A | CA393084614 | HCN4 | c.3602C>T (p.Ser1201Phe) c.2384C>T (p.Ser795Phe) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322491G>C | CA393084615 | HCN4 | c.3602C>G (p.Ser1201Cys) c.2384C>G (p.Ser795Cys) | |
| 15 | g.73322491G= | CA2187186026 | HCN4 | c.3602C= (p.Ser1201=) c.2384C= (p.Ser795=) | |
| 15 | g.73322491G>T | CA393084616 | HCN4 | c.3602C>A (p.Ser1201Tyr) c.2384C>A (p.Ser795Tyr) | COSMIC |
| 15 | g.73322491_73322493delinsAAC | CA2580613289 | HCN4 | c.3600_3602delinsGTT (p.Ser1201Phe) c.2382_2384delinsGTT (p.Ser795Phe) | ClinVar |
| 15 | g.73322492A>C | CA393084618 | HCN4 | c.3601T>G (p.Ser1201Ala) c.2383T>G (p.Ser795Ala) | |
| 15 | g.73322492A>G | CA393084619 | HCN4 | c.3601T>C (p.Ser1201Pro) c.2383T>C (p.Ser795Pro) | |
| 15 | g.73322492A>T | CA393084621 | HCN4 | c.3601T>A (p.Ser1201Thr) c.2383T>A (p.Ser795Thr) | |
| 15 | g.73322493T>A | CA7648791 | HCN4 | c.3600A>T (p.Pro1200=) c.2382A>T (p.Pro794=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322493T>C | CA148388 | HCN4 | c.3600A>G (p.Pro1200=) c.2382A>G (p.Pro794=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322493T>G | CA491477752 | HCN4 | c.3600A>C (p.Pro1200=) c.2382A>C (p.Pro794=) | gnomAD v4 |
| 15 | g.73322493T= | CA2187186037 | HCN4 | c.3600A= (p.Pro1200=) c.2382A= (p.Pro794=) | |
| 15 | g.73322493_73322494delinsCA | CA891844154 | HCN4 | c.3599_3600delinsTG (p.Pro1200Leu) c.2381_2382delinsTG (p.Pro794Leu) | ClinVar |
| 15 | g.73322494G>A | CA7648792 | HCN4 | c.3599C>T (p.Pro1200Leu) c.2381C>T (p.Pro794Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322494G>C | CA393084627 | HCN4 | c.3599C>G (p.Pro1200Arg) c.2381C>G (p.Pro794Arg) | |
| 15 | g.73322494G= | CA2187186049 | HCN4 | c.3599C= (p.Pro1200=) c.2381C= (p.Pro794=) | |
| 15 | g.73322494G>T | CA7648793 | HCN4 | c.3599C>A (p.Pro1200Gln) c.2381C>A (p.Pro794Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322495del | CA2629370522 | HCN4 | c.3599del (p.Pro1200HisfsTer29) c.2381del (p.Pro794HisfsTer29) | gnomAD v4 |
| 15 | g.73322495G>A | CA393084631 | HCN4 | c.3598C>T (p.Pro1200Ser) c.2380C>T (p.Pro794Ser) | gnomAD v4 |
| 15 | g.73322495G>C | CA393084636 | HCN4 | c.3598C>G (p.Pro1200Ala) c.2380C>G (p.Pro794Ala) | gnomAD v4 |
| 15 | g.73322495G>T | CA393084633 | HCN4 | c.3598C>A (p.Pro1200Thr) c.2380C>A (p.Pro794Thr) | gnomAD v4 |
| 15 | g.73322496C>A | CA491477753 | HCN4 | c.3597G>T (p.Leu1199=) c.2379G>T (p.Leu793=) | gnomAD v4 |
| 15 | g.73322496C>G | CA491477754 | HCN4 | c.3597G>C (p.Leu1199=) c.2379G>C (p.Leu793=) | |
| 15 | g.73322496C>T | CA491477755 | HCN4 | c.3597G>A (p.Leu1199=) c.2379G>A (p.Leu793=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322497A= | CA2187186059 | HCN4 | c.3596T= (p.Leu1199=) c.2378T= (p.Leu793=) | |
| 15 | g.73322497A>C | CA393084639 | HCN4 | c.3596T>G (p.Leu1199Arg) c.2378T>G (p.Leu793Arg) | |
| 15 | g.73322497A>G | CA393084642 | HCN4 | c.3596T>C (p.Leu1199Pro) c.2378T>C (p.Leu793Pro) | |
| 15 | g.73322497A>T | CA272662970 | HCN4 | c.3596T>A (p.Leu1199Gln) c.2378T>A (p.Leu793Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322498G>A | CA491477756 | HCN4 | c.3595C>T (p.Leu1199=) c.2377C>T (p.Leu793=) | |
| 15 | g.73322498G>C | CA393084645 | HCN4 | c.3595C>G (p.Leu1199Val) c.2377C>G (p.Leu793Val) | |
| 15 | g.73322498G= | CA2187186066 | HCN4 | c.3595C= (p.Leu1199=) c.2377C= (p.Leu793=) | |
| 15 | g.73322498G>T | CA7648794 | HCN4 | c.3595C>A (p.Leu1199Met) c.2377C>A (p.Leu793Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322499T>A | CA393084650 | HCN4 | c.3594A>T (p.Lys1198Asn) c.2376A>T (p.Lys792Asn) | |
| 15 | g.73322499T>C | CA491477757 | HCN4 | c.3594A>G (p.Lys1198=) c.2376A>G (p.Lys792=) | |
| 15 | g.73322499T>G | CA393084652 | HCN4 | c.3594A>C (p.Lys1198Asn) c.2376A>C (p.Lys792Asn) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322499T= | CA2187186072 | HCN4 | c.3594A= (p.Lys1198=) c.2376A= (p.Lys792=) | |
| 15 | g.73322500T>A | CA393084655 | HCN4 | c.3593A>T (p.Lys1198Ile) c.2375A>T (p.Lys792Ile) | |
| 15 | g.73322500T>C | CA393084658 | HCN4 | c.3593A>G (p.Lys1198Arg) c.2375A>G (p.Lys792Arg) | |
| 15 | g.73322500T>G | CA393084661 | HCN4 | c.3593A>C (p.Lys1198Thr) c.2375A>C (p.Lys792Thr) | gnomAD v4 |
| 15 | g.73322501T>A | CA393084663 | HCN4 | c.3592A>T (p.Lys1198Ter) c.2374A>T (p.Lys792Ter) | |
| 15 | g.73322501T>C | CA393084666 | HCN4 | c.3592A>G (p.Lys1198Glu) c.2374A>G (p.Lys792Glu) | gnomAD v4 |
| 15 | g.73322501T>G | CA393084668 | HCN4 | c.3592A>C (p.Lys1198Gln) c.2374A>C (p.Lys792Gln) | |
| 15 | g.73322502G>A | CA491477758 | HCN4 | c.3591C>T (p.Ser1197=) c.2373C>T (p.Ser791=) | |
| 15 | g.73322502G>C | CA491477760 | HCN4 | c.3591C>G (p.Ser1197=) c.2373C>G (p.Ser791=) | |
| 15 | g.73322502G>T | CA491477759 | HCN4 | c.3591C>A (p.Ser1197=) c.2373C>A (p.Ser791=) | gnomAD v4 |
| 15 | g.73322503G>A | CA7648796 | HCN4 | c.3590C>T (p.Ser1197Phe) c.2372C>T (p.Ser791Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322503G>C | CA7648795 | HCN4 | c.3590C>G (p.Ser1197Cys) c.2372C>G (p.Ser791Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322503G= | CA2187186076 | HCN4 | c.3590C= (p.Ser1197=) c.2372C= (p.Ser791=) | |
| 15 | g.73322503G>T | CA393084676 | HCN4 | c.3590C>A (p.Ser1197Tyr) c.2372C>A (p.Ser791Tyr) | gnomAD v4 |
| 15 | g.73322504A>C | CA393084679 | HCN4 | c.3589T>G (p.Ser1197Ala) c.2371T>G (p.Ser791Ala) | |
| 15 | g.73322504A>G | CA393084681 | HCN4 | c.3589T>C (p.Ser1197Pro) c.2371T>C (p.Ser791Pro) | gnomAD v4 |
| 15 | g.73322504A>T | CA393084684 | HCN4 | c.3589T>A (p.Ser1197Thr) c.2371T>A (p.Ser791Thr) | gnomAD v4 |
| 15 | g.73322505G>A | CA491477813 | HCN4 | c.3588C>T (p.Arg1196=) c.2370C>T (p.Arg790=) | gnomAD v4 |
| 15 | g.73322505G>C | CA491477815 | HCN4 | c.3588C>G (p.Arg1196=) c.2370C>G (p.Arg790=) | |
| 15 | g.73322505G>T | CA491477816 | HCN4 | c.3588C>A (p.Arg1196=) c.2370C>A (p.Arg790=) | gnomAD v4 |
| 15 | g.73322506C>A | CA393084692 | HCN4 | c.3587G>T (p.Arg1196Leu) c.2369G>T (p.Arg790Leu) | gnomAD v4 |
| 15 | g.73322506C= | CA2187186080 | HCN4 | c.3587G= (p.Arg1196=) c.2369G= (p.Arg790=) | |
| 15 | g.73322506C>G | CA393084688 | HCN4 | c.3587G>C (p.Arg1196Pro) c.2369G>C (p.Arg790Pro) | |
| 15 | g.73322506C>T | CA203629 | HCN4 | c.3587G>A (p.Arg1196His) c.2369G>A (p.Arg790His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322507G>A | CA7648797 | HCN4 | c.3586C>T (p.Arg1196Cys) c.2368C>T (p.Arg790Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73322507G>C | CA393084696 | HCN4 | c.3586C>G (p.Arg1196Gly) c.2368C>G (p.Arg790Gly) | |
| 15 | g.73322507G= | CA2187186093 | HCN4 | c.3586C= (p.Arg1196=) c.2368C= (p.Arg790=) | |
| 15 | g.73322507G>T | CA393084699 | HCN4 | c.3586C>A (p.Arg1196Ser) c.2368C>A (p.Arg790Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73322508C>A | CA491477819 | HCN4 | c.3585G>T (p.Val1195=) c.2367G>T (p.Val789=) | gnomAD v4 |
| 15 | g.73322508C>G | CA491477820 | HCN4 | c.3585G>C (p.Val1195=) c.2367G>C (p.Val789=) | |
| 15 | g.73322508C>T | CA491477821 | HCN4 | c.3585G>A (p.Val1195=) c.2367G>A (p.Val789=) | |
| 15 | g.73322509A>C | CA393084701 | HCN4 | c.3584T>G (p.Val1195Gly) c.2366T>G (p.Val789Gly) | |
| 15 | g.73322509A>G | CA393084704 | HCN4 | c.3584T>C (p.Val1195Ala) c.2366T>C (p.Val789Ala) | |
| 15 | g.73322509A>T | CA393084707 | HCN4 | c.3584T>A (p.Val1195Glu) c.2366T>A (p.Val789Glu) | gnomAD v4 |
| 15 | g.73322510C>A | CA7648798 | HCN4 | c.3583G>T (p.Val1195Leu) c.2365G>T (p.Val789Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322510C= | CA2187186098 | HCN4 | c.3583G= (p.Val1195=) c.2365G= (p.Val789=) | |
| 15 | g.73322510C>G | CA393084711 | HCN4 | c.3583G>C (p.Val1195Leu) c.2365G>C (p.Val789Leu) | |
| 15 | g.73322510C>T | CA393084714 | HCN4 | c.3583G>A (p.Val1195Met) c.2365G>A (p.Val789Met) | gnomAD v4 |
| 15 | g.73322511T>A | CA491477824 | HCN4 | c.3582A>T (p.Pro1194=) c.2364A>T (p.Pro788=) | |
| 15 | g.73322511T>C | CA7648799 | HCN4 | c.3582A>G (p.Pro1194=) c.2364A>G (p.Pro788=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322511T>G | CA491477825 | HCN4 | c.3582A>C (p.Pro1194=) c.2364A>C (p.Pro788=) | |
| 15 | g.73322511T= | CA2187186104 | HCN4 | c.3582A= (p.Pro1194=) c.2364A= (p.Pro788=) | |
| 15 | g.73322512G>A | CA7648800 | HCN4 | c.3581C>T (p.Pro1194Leu) c.2363C>T (p.Pro788Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322512G>C | CA393084720 | HCN4 | c.3581C>G (p.Pro1194Arg) c.2363C>G (p.Pro788Arg) | |
| 15 | g.73322512G= | CA2187186109 | HCN4 | c.3581C= (p.Pro1194=) c.2363C= (p.Pro788=) | |
| 15 | g.73322512G>T | CA393084719 | HCN4 | c.3581C>A (p.Pro1194Gln) c.2363C>A (p.Pro788Gln) | gnomAD v4 |
| 15 | g.73322513G>A | CA393084725 | HCN4 | c.3580C>T (p.Pro1194Ser) c.2362C>T (p.Pro788Ser) | gnomAD v4 |
| 15 | g.73322513G>C | CA393084726 | HCN4 | c.3580C>G (p.Pro1194Ala) c.2362C>G (p.Pro788Ala) | |
| 15 | g.73322513G>T | CA393084728 | HCN4 | c.3580C>A (p.Pro1194Thr) c.2362C>A (p.Pro788Thr) | gnomAD v4 |
| 15 | g.73322514C>A | CA393084731 | HCN4 | c.3579G>T (p.Glu1193Asp) c.2361G>T (p.Glu787Asp) | |
| 15 | g.73322514C= | CA2187186111 | HCN4 | c.3579G= (p.Glu1193=) c.2361G= (p.Glu787=) | |
| 15 | g.73322514C>G | CA393084734 | HCN4 | c.3579G>C (p.Glu1193Asp) c.2361G>C (p.Glu787Asp) | |
| 15 | g.73322514C>T | CA491477830 | HCN4 | c.3579G>A (p.Glu1193=) c.2361G>A (p.Glu787=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322515T>A | CA393084737 | HCN4 | c.3578A>T (p.Glu1193Val) c.2360A>T (p.Glu787Val) | |
| 15 | g.73322515T>C | CA393084740 | HCN4 | c.3578A>G (p.Glu1193Gly) c.2360A>G (p.Glu787Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322515T>G | CA393084742 | HCN4 | c.3578A>C (p.Glu1193Ala) c.2360A>C (p.Glu787Ala) | |
| 15 | g.73322515T= | CA2187186117 | HCN4 | c.3578A= (p.Glu1193=) c.2360A= (p.Glu787=) | |
| 15 | g.73322516C>A | CA7648801 | HCN4 | c.3577G>T (p.Glu1193Ter) c.2359G>T (p.Glu787Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322516C= | CA2187186128 | HCN4 | c.3577G= (p.Glu1193=) c.2359G= (p.Glu787=) | |
| 15 | g.73322516C>G | CA236695 | HCN4 | c.3577G>C (p.Glu1193Gln) c.2359G>C (p.Glu787Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73322516C>T | CA393084748 | HCN4 | c.3577G>A (p.Glu1193Lys) c.2359G>A (p.Glu787Lys) | gnomAD v4 |
| 15 | g.73322517A>C | CA491477832 | HCN4 | c.3576T>G (p.Pro1192=) c.2358T>G (p.Pro786=) | |
| 15 | g.73322517A>G | CA491477833 | HCN4 | c.3576T>C (p.Pro1192=) c.2358T>C (p.Pro786=) | |
| 15 | g.73322517A>T | CA491477834 | HCN4 | c.3576T>A (p.Pro1192=) c.2358T>A (p.Pro786=) | |
| 15 | g.73322518G>A | CA7648802 | HCN4 | c.3575C>T (p.Pro1192Leu) c.2357C>T (p.Pro786Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322518G>C | CA393084754 | HCN4 | c.3575C>G (p.Pro1192Arg) c.2357C>G (p.Pro786Arg) | ClinVar |
| 15 | g.73322518G= | CA2187186131 | HCN4 | c.3575C= (p.Pro1192=) c.2357C= (p.Pro786=) | |
| 15 | g.73322518G>T | CA393084751 | HCN4 | c.3575C>A (p.Pro1192His) c.2357C>A (p.Pro786His) | gnomAD v4 |
| 15 | g.73322519G>A | CA7648803 | HCN4 | c.3574C>T (p.Pro1192Ser) c.2356C>T (p.Pro786Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322519G>C | CA393084759 | HCN4 | c.3574C>G (p.Pro1192Ala) c.2356C>G (p.Pro786Ala) | gnomAD v4 |
| 15 | g.73322519G= | CA2187186138 | HCN4 | c.3574C= (p.Pro1192=) c.2356C= (p.Pro786=) | |
| 15 | g.73322519G>T | CA393084761 | HCN4 | c.3574C>A (p.Pro1192Thr) c.2356C>A (p.Pro786Thr) | gnomAD v4 |
| 15 | g.73322520C>A | CA393084764 | HCN4 | c.3573G>T (p.Arg1191Ser) c.2355G>T (p.Arg785Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322520C= | CA2187186142 | HCN4 | c.3573G= (p.Arg1191=) c.2355G= (p.Arg785=) | |
| 15 | g.73322520C>G | CA393084767 | HCN4 | c.3573G>C (p.Arg1191Ser) c.2355G>C (p.Arg785Ser) | |
| 15 | g.73322520C>T | CA491477837 | HCN4 | c.3573G>A (p.Arg1191=) c.2355G>A (p.Arg785=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322521C>A | CA393084769 | HCN4 | c.3572G>T (p.Arg1191Met) c.2354G>T (p.Arg785Met) | gnomAD v4 |
| 15 | g.73322521C= | CA2187186145 | HCN4 | c.3572G= (p.Arg1191=) c.2354G= (p.Arg785=) | |
| 15 | g.73322521C>G | CA393084772 | HCN4 | c.3572G>C (p.Arg1191Thr) c.2354G>C (p.Arg785Thr) | dbSNP gnomAD v4 |
| 15 | g.73322521C>T | CA393084774 | HCN4 | c.3572G>A (p.Arg1191Lys) c.2354G>A (p.Arg785Lys) | gnomAD v4 |
| 15 | g.73322522T>A | CA393084776 | HCN4 | c.3571A>T (p.Arg1191Trp) c.2353A>T (p.Arg785Trp) | |
| 15 | g.73322522T>C | CA393084777 | HCN4 | c.3571A>G (p.Arg1191Gly) c.2353A>G (p.Arg785Gly) | dbSNP gnomAD v4 |
| 15 | g.73322522T>G | CA491477839 | HCN4 | c.3571A>C (p.Arg1191=) c.2353A>C (p.Arg785=) | |
| 15 | g.73322522T= | CA2187186149 | HCN4 | c.3571A= (p.Arg1191=) c.2353A= (p.Arg785=) | |
| 15 | g.73322523G>A | CA491477840 | HCN4 | c.3570C>T (p.Ala1190=) c.2352C>T (p.Ala784=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322523G>C | CA491477841 | HCN4 | c.3570C>G (p.Ala1190=) c.2352C>G (p.Ala784=) | |
| 15 | g.73322523G>T | CA491477842 | HCN4 | c.3570C>A (p.Ala1190=) c.2352C>A (p.Ala784=) | |
| 15 | g.73322524G>A | CA393084780 | HCN4 | c.3569C>T (p.Ala1190Val) c.2351C>T (p.Ala784Val) | gnomAD v4 |
| 15 | g.73322524G>C | CA393084783 | HCN4 | c.3569C>G (p.Ala1190Gly) c.2351C>G (p.Ala784Gly) | |
| 15 | g.73322524G>T | CA393084786 | HCN4 | c.3569C>A (p.Ala1190Asp) c.2351C>A (p.Ala784Asp) | gnomAD v4 |
| 15 | g.73322525C>A | CA393084787 | HCN4 | c.3568G>T (p.Ala1190Ser) c.2350G>T (p.Ala784Ser) | ClinVar gnomAD v4 |
| 15 | g.73322525C= | CA2187186155 | HCN4 | c.3568G= (p.Ala1190=) c.2350G= (p.Ala784=) | |
| 15 | g.73322525C>G | CA393084790 | HCN4 | c.3568G>C (p.Ala1190Pro) c.2350G>C (p.Ala784Pro) | |
| 15 | g.73322525C>T | CA16614725 | HCN4 | c.3568G>A (p.Ala1190Thr) c.2350G>A (p.Ala784Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322526C>A | CA491477844 | HCN4 | c.3567G>T (p.Gly1189=) c.2349G>T (p.Gly783=) | gnomAD v4 |
| 15 | g.73322526C= | CA2187186158 | HCN4 | c.3567G= (p.Gly1189=) c.2349G= (p.Gly783=) | |
| 15 | g.73322526C>G | CA491477845 | HCN4 | c.3567G>C (p.Gly1189=) c.2349G>C (p.Gly783=) | gnomAD v4 |
| 15 | g.73322526C>T | CA7648804 | HCN4 | c.3567G>A (p.Gly1189=) c.2349G>A (p.Gly783=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322527C>A | CA393084794 | HCN4 | c.3566G>T (p.Gly1189Val) c.2348G>T (p.Gly783Val) | gnomAD v4 |
| 15 | g.73322527C= | CA2187186161 | HCN4 | c.3566G= (p.Gly1189=) c.2348G= (p.Gly783=) | |
| 15 | g.73322527C>G | CA393084797 | HCN4 | c.3566G>C (p.Gly1189Ala) c.2348G>C (p.Gly783Ala) | |
| 15 | g.73322527C>T | CA393084800 | HCN4 | c.3566G>A (p.Gly1189Glu) c.2348G>A (p.Gly783Glu) | dbSNP gnomAD v2 |
| 15 | g.73322528C>A | CA393084804 | HCN4 | c.3565G>T (p.Gly1189Trp) c.2347G>T (p.Gly783Trp) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322528C= | CA2187186164 | HCN4 | c.3565G= (p.Gly1189=) c.2347G= (p.Gly783=) | |
| 15 | g.73322528C>G | CA393084806 | HCN4 | c.3565G>C (p.Gly1189Arg) c.2347G>C (p.Gly783Arg) | |
| 15 | g.73322528C>T | CA393084810 | HCN4 | c.3565G>A (p.Gly1189Arg) c.2347G>A (p.Gly783Arg) | |
| 15 | g.73322529A>C | CA491477851 | HCN4 | c.3564T>G (p.Pro1188=) c.2346T>G (p.Pro782=) | |
| 15 | g.73322529A>G | CA491477849 | HCN4 | c.3564T>C (p.Pro1188=) c.2346T>C (p.Pro782=) | ClinVar |
| 15 | g.73322529A>T | CA491477850 | HCN4 | c.3564T>A (p.Pro1188=) c.2346T>A (p.Pro782=) | |
| 15 | g.73322530G>A | CA393084813 | HCN4 | c.3563C>T (p.Pro1188Leu) c.2345C>T (p.Pro782Leu) | COSMIC |
| 15 | g.73322530G>C | CA393084815 | HCN4 | c.3563C>G (p.Pro1188Arg) c.2345C>G (p.Pro782Arg) | gnomAD v4 |
| 15 | g.73322530G>T | CA393084816 | HCN4 | c.3563C>A (p.Pro1188His) c.2345C>A (p.Pro782His) | |
| 15 | g.73322531G>A | CA393084819 | HCN4 | c.3562C>T (p.Pro1188Ser) c.2344C>T (p.Pro782Ser) | |
| 15 | g.73322531G>C | CA393084821 | HCN4 | c.3562C>G (p.Pro1188Ala) c.2344C>G (p.Pro782Ala) | |
| 15 | g.73322531G>T | CA393084824 | HCN4 | c.3562C>A (p.Pro1188Thr) c.2344C>A (p.Pro782Thr) | gnomAD v4 |
| 15 | g.73322532T>A | CA393084828 | HCN4 | c.3561A>T (p.Glu1187Asp) c.2343A>T (p.Glu781Asp) | |
| 15 | g.73322532T>C | CA491477855 | HCN4 | c.3561A>G (p.Glu1187=) c.2343A>G (p.Glu781=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322532T>G | CA393084825 | HCN4 | c.3561A>C (p.Glu1187Asp) c.2343A>C (p.Glu781Asp) | |
| 15 | g.73322532T= | CA2187186167 | HCN4 | c.3561A= (p.Glu1187=) c.2343A= (p.Glu781=) | |
| 15 | g.73322533T>A | CA393084831 | HCN4 | c.3560A>T (p.Glu1187Val) c.2342A>T (p.Glu781Val) | |
| 15 | g.73322533T>C | CA393084834 | HCN4 | c.3560A>G (p.Glu1187Gly) c.2342A>G (p.Glu781Gly) | |
| 15 | g.73322533T>G | CA393084835 | HCN4 | c.3560A>C (p.Glu1187Ala) c.2342A>C (p.Glu781Ala) | |
| 15 | g.73322534C>A | CA393084839 | HCN4 | c.3559G>T (p.Glu1187Ter) c.2341G>T (p.Glu781Ter) | |
| 15 | g.73322534C>G | CA393084842 | HCN4 | c.3559G>C (p.Glu1187Gln) c.2341G>C (p.Glu781Gln) | |
| 15 | g.73322534C>T | CA393084844 | HCN4 | c.3559G>A (p.Glu1187Lys) c.2341G>A (p.Glu781Lys) | |
| 15 | g.73322535C>A | CA393084849 | HCN4 | c.3558G>T (p.Arg1186Ser) c.2340G>T (p.Arg780Ser) | |
| 15 | g.73322535C>G | CA393084850 | HCN4 | c.3558G>C (p.Arg1186Ser) c.2340G>C (p.Arg780Ser) | |
| 15 | g.73322535C>T | CA491477858 | HCN4 | c.3558G>A (p.Arg1186=) c.2340G>A (p.Arg780=) | ClinVar gnomAD v4 |
| 15 | g.73322536C>A | CA393084851 | HCN4 | c.3557G>T (p.Arg1186Met) c.2339G>T (p.Arg780Met) | |
| 15 | g.73322536C= | CA2187186169 | HCN4 | c.3557G= (p.Arg1186=) c.2339G= (p.Arg780=) | |
| 15 | g.73322536C>G | CA393084853 | HCN4 | c.3557G>C (p.Arg1186Thr) c.2339G>C (p.Arg780Thr) | |
| 15 | g.73322536C>T | CA393084855 | HCN4 | c.3557G>A (p.Arg1186Lys) c.2339G>A (p.Arg780Lys) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322537T>A | CA393084858 | HCN4 | c.3556A>T (p.Arg1186Trp) c.2338A>T (p.Arg780Trp) | |
| 15 | g.73322537T>C | CA393084859 | HCN4 | c.3556A>G (p.Arg1186Gly) c.2338A>G (p.Arg780Gly) | |
| 15 | g.73322537T>G | CA491477862 | HCN4 | c.3556A>C (p.Arg1186=) c.2338A>C (p.Arg780=) | |
| 15 | g.73322538C>A | CA393084867 | HCN4 | c.3555G>T (p.Gln1185His) c.2337G>T (p.Gln779His) | gnomAD v4 |
| 15 | g.73322538C>G | CA393084864 | HCN4 | c.3555G>C (p.Gln1185His) c.2337G>C (p.Gln779His) | |
| 15 | g.73322538C>T | CA491477863 | HCN4 | c.3555G>A (p.Gln1185=) c.2337G>A (p.Gln779=) | ClinVar gnomAD v4 |
| 15 | g.73322539T>A | CA393084870 | HCN4 | c.3554A>T (p.Gln1185Leu) c.2336A>T (p.Gln779Leu) | dbSNP |
| 15 | g.73322539T>C | CA393084871 | HCN4 | c.3554A>G (p.Gln1185Arg) c.2336A>G (p.Gln779Arg) | |
| 15 | g.73322539T>G | CA393084873 | HCN4 | c.3554A>C (p.Gln1185Pro) c.2336A>C (p.Gln779Pro) | |
| 15 | g.73322539T= | CA2187186172 | HCN4 | c.3554A= (p.Gln1185=) c.2336A= (p.Gln779=) | |
| 15 | g.73322540G>A | CA393084876 | HCN4 | c.3553C>T (p.Gln1185Ter) c.2335C>T (p.Gln779Ter) | |
| 15 | g.73322540G>C | CA393084879 | HCN4 | c.3553C>G (p.Gln1185Glu) c.2335C>G (p.Gln779Glu) | |
| 15 | g.73322540G>T | CA393084882 | HCN4 | c.3553C>A (p.Gln1185Lys) c.2335C>A (p.Gln779Lys) | gnomAD v4 |
| 15 | g.73322541G>A | CA491477866 | HCN4 | c.3552C>T (p.Pro1184=) c.2334C>T (p.Pro778=) | dbSNP gnomAD v2 |
| 15 | g.73322541G>C | CA491477867 | HCN4 | c.3552C>G (p.Pro1184=) c.2334C>G (p.Pro778=) | |
| 15 | g.73322541G= | CA2187186175 | HCN4 | c.3552C= (p.Pro1184=) c.2334C= (p.Pro778=) | |
| 15 | g.73322541G>T | CA491477868 | HCN4 | c.3552C>A (p.Pro1184=) c.2334C>A (p.Pro778=) | |
| 15 | g.73322542G>A | CA393084890 | HCN4 | c.3551C>T (p.Pro1184Leu) c.2333C>T (p.Pro778Leu) | dbSNP |
| 15 | g.73322542G>C | CA393084887 | HCN4 | c.3551C>G (p.Pro1184Arg) c.2333C>G (p.Pro778Arg) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322542G= | CA2187186183 | HCN4 | c.3551C= (p.Pro1184=) c.2333C= (p.Pro778=) | |
| 15 | g.73322542G>T | CA393084884 | HCN4 | c.3551C>A (p.Pro1184His) c.2333C>A (p.Pro778His) | gnomAD v4 |
| 15 | g.73322543G>A | CA393084893 | HCN4 | c.3550C>T (p.Pro1184Ser) c.2332C>T (p.Pro778Ser) | gnomAD v4 COSMIC |
| 15 | g.73322543G>C | CA393084895 | HCN4 | c.3550C>G (p.Pro1184Ala) c.2332C>G (p.Pro778Ala) | ClinVar |
| 15 | g.73322543G= | CA2187186186 | HCN4 | c.3550C= (p.Pro1184=) c.2332C= (p.Pro778=) | |
| 15 | g.73322543G>T | CA272663044 | HCN4 | c.3550C>A (p.Pro1184Thr) c.2332C>A (p.Pro778Thr) | dbSNP gnomAD v4 |
| 15 | g.73322544T>A | CA491477872 | HCN4 | c.3549A>T (p.Gly1183=) c.2331A>T (p.Gly777=) | |
| 15 | g.73322544T>C | CA491477873 | HCN4 | c.3549A>G (p.Gly1183=) c.2331A>G (p.Gly777=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322544T>G | CA491477874 | HCN4 | c.3549A>C (p.Gly1183=) c.2331A>C (p.Gly777=) | |
| 15 | g.73322544T= | CA2187186189 | HCN4 | c.3549A= (p.Gly1183=) c.2331A= (p.Gly777=) | |
| 15 | g.73322545C>A | CA393084900 | HCN4 | c.3548G>T (p.Gly1183Val) c.2330G>T (p.Gly777Val) | |
| 15 | g.73322545C>G | CA393084905 | HCN4 | c.3548G>C (p.Gly1183Ala) c.2330G>C (p.Gly777Ala) | |
| 15 | g.73322545C>T | CA393084906 | HCN4 | c.3548G>A (p.Gly1183Glu) c.2330G>A (p.Gly777Glu) | |
| 15 | g.73322546C>A | CA393084909 | HCN4 | c.3547G>T (p.Gly1183Ter) c.2329G>T (p.Gly777Ter) | |
| 15 | g.73322546C= | CA2187186194 | HCN4 | c.3547G= (p.Gly1183=) c.2329G= (p.Gly777=) | |
| 15 | g.73322546C>G | CA393084915 | HCN4 | c.3547G>C (p.Gly1183Arg) c.2329G>C (p.Gly777Arg) | |
| 15 | g.73322546C>T | CA393084912 | HCN4 | c.3547G>A (p.Gly1183Arg) c.2329G>A (p.Gly777Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322547A>C | CA491477878 | HCN4 | c.3546T>G (p.Ala1182=) c.2328T>G (p.Ala776=) | |
| 15 | g.73322547A>G | CA491477879 | HCN4 | c.3546T>C (p.Ala1182=) c.2328T>C (p.Ala776=) | gnomAD v4 |
| 15 | g.73322547A>T | CA491477880 | HCN4 | c.3546T>A (p.Ala1182=) c.2328T>A (p.Ala776=) | |
| 15 | g.73322548G>A | CA393084916 | HCN4 | c.3545C>T (p.Ala1182Val) c.2327C>T (p.Ala776Val) | dbSNP gnomAD v2 |
| 15 | g.73322548G>C | CA393084919 | HCN4 | c.3545C>G (p.Ala1182Gly) c.2327C>G (p.Ala776Gly) | |
| 15 | g.73322548G= | CA2187186202 | HCN4 | c.3545C= (p.Ala1182=) c.2327C= (p.Ala776=) | |
| 15 | g.73322548G>T | CA393084921 | HCN4 | c.3545C>A (p.Ala1182Asp) c.2327C>A (p.Ala776Asp) | |
| 15 | g.73322549C>A | CA7648805 | HCN4 | c.3544G>T (p.Ala1182Ser) c.2326G>T (p.Ala776Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322549C= | CA2187186205 | HCN4 | c.3544G= (p.Ala1182=) c.2326G= (p.Ala776=) | |
| 15 | g.73322549C>G | CA393084926 | HCN4 | c.3544G>C (p.Ala1182Pro) c.2326G>C (p.Ala776Pro) | |
| 15 | g.73322549C>T | CA393084929 | HCN4 | c.3544G>A (p.Ala1182Thr) c.2326G>A (p.Ala776Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73322552_73322555del | CA2580089966 | HCN4 | c.3541_3544del (p.Thr1181LeufsTer?) c.2323_2326del (p.Thr775LeufsTer?) | ClinVar |
| 15 | g.73322550A>C | CA491477882 | HCN4 | c.3543T>G (p.Thr1181=) c.2325T>G (p.Thr775=) | |
| 15 | g.73322550A>G | CA491477883 | HCN4 | c.3543T>C (p.Thr1181=) c.2325T>C (p.Thr775=) | |
| 15 | g.73322550A>T | CA491477881 | HCN4 | c.3543T>A (p.Thr1181=) c.2325T>A (p.Thr775=) | |
| 15 | g.73322551G>A | CA393084932 | HCN4 | c.3542C>T (p.Thr1181Ile) c.2324C>T (p.Thr775Ile) | |
| 15 | g.73322551G>C | CA393084933 | HCN4 | c.3542C>G (p.Thr1181Ser) c.2324C>G (p.Thr775Ser) | |
| 15 | g.73322551G>T | CA393084934 | HCN4 | c.3542C>A (p.Thr1181Asn) c.2324C>A (p.Thr775Asn) | |
| 15 | g.73322552T>A | CA393084935 | HCN4 | c.3541A>T (p.Thr1181Ser) c.2323A>T (p.Thr775Ser) | |
| 15 | g.73322552T>C | CA393084937 | HCN4 | c.3541A>G (p.Thr1181Ala) c.2323A>G (p.Thr775Ala) | gnomAD v4 |
| 15 | g.73322552T>G | CA7648806 | HCN4 | c.3541A>C (p.Thr1181Pro) c.2323A>C (p.Thr775Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322552T= | CA2187186213 | HCN4 | c.3541A= (p.Thr1181=) c.2323A= (p.Thr775=) | |
| 15 | g.73322553C>A | CA491477886 | HCN4 | c.3540G>T (p.Leu1180=) c.2322G>T (p.Leu774=) | gnomAD v4 |
| 15 | g.73322553C= | CA2187186214 | HCN4 | c.3540G= (p.Leu1180=) c.2322G= (p.Leu774=) | |
| 15 | g.73322553C>G | CA491477884 | HCN4 | c.3540G>C (p.Leu1180=) c.2322G>C (p.Leu774=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322553C>T | CA491477885 | HCN4 | c.3540G>A (p.Leu1180=) c.2322G>A (p.Leu774=) | |
| 15 | g.73322557_73322570del | CA2580089967 | HCN4 | c.3527_3540del (p.Gly1176AspfsTer13) c.2309_2322del (p.Gly770AspfsTer13) | ClinVar |
| 15 | g.73322554A>C | CA393084947 | HCN4 | c.3539T>G (p.Leu1180Arg) c.2321T>G (p.Leu774Arg) | |
| 15 | g.73322554A>G | CA393084944 | HCN4 | c.3539T>C (p.Leu1180Pro) c.2321T>C (p.Leu774Pro) | |
| 15 | g.73322554A>T | CA393084943 | HCN4 | c.3539T>A (p.Leu1180Gln) c.2321T>A (p.Leu774Gln) | |
| 15 | g.73322555G>A | CA491477887 | HCN4 | c.3538C>T (p.Leu1180=) c.2320C>T (p.Leu774=) | |
| 15 | g.73322555G>C | CA393084953 | HCN4 | c.3538C>G (p.Leu1180Val) c.2320C>G (p.Leu774Val) | |
| 15 | g.73322555G>T | CA393084952 | HCN4 | c.3538C>A (p.Leu1180Met) c.2320C>A (p.Leu774Met) | |
| 15 | g.73322556A= | CA2187186218 | HCN4 | c.3537T= (p.Pro1179=) c.2319T= (p.Pro773=) | |
| 15 | g.73322556A>C | CA491477889 | HCN4 | c.3537T>G (p.Pro1179=) c.2319T>G (p.Pro773=) | |
| 15 | g.73322556A>G | CA491477890 | HCN4 | c.3537T>C (p.Pro1179=) c.2319T>C (p.Pro773=) | |
| 15 | g.73322556A>T | CA491477888 | HCN4 | c.3537T>A (p.Pro1179=) c.2319T>A (p.Pro773=) | |
| 15 | g.73322557G>A | CA393084961 | HCN4 | c.3536C>T (p.Pro1179Leu) c.2318C>T (p.Pro773Leu) | ClinVar COSMIC |
| 15 | g.73322557G>C | CA393084958 | HCN4 | c.3536C>G (p.Pro1179Arg) c.2318C>G (p.Pro773Arg) | |
| 15 | g.73322557G>T | CA393084960 | HCN4 | c.3536C>A (p.Pro1179His) c.2318C>A (p.Pro773His) | |
| 15 | g.73322561dup | CA619410583 | HCN4 | c.3536dup (p.Leu1180SerfsTer14) c.2318dup (p.Leu774SerfsTer14) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322561del | CA645586806 | HCN4 | c.3536del (p.Pro1179LeufsTer2) c.2318del (p.Pro773LeufsTer2) | COSMIC |
| 15 | g.73322558G>A | CA393084963 | HCN4 | c.3535C>T (p.Pro1179Ser) c.2317C>T (p.Pro773Ser) | gnomAD v4 |
| 15 | g.73322558G>C | CA393084965 | HCN4 | c.3535C>G (p.Pro1179Ala) c.2317C>G (p.Pro773Ala) | |
| 15 | g.73322558G>T | CA393084966 | HCN4 | c.3535C>A (p.Pro1179Thr) c.2317C>A (p.Pro773Thr) | |
| 15 | g.73322559G>A | CA491477891 | HCN4 | c.3534C>T (p.Pro1178=) c.2316C>T (p.Pro772=) | |
| 15 | g.73322559G>C | CA491477892 | HCN4 | c.3534C>G (p.Pro1178=) c.2316C>G (p.Pro772=) | |
| 15 | g.73322559G>T | CA491477894 | HCN4 | c.3534C>A (p.Pro1178=) c.2316C>A (p.Pro772=) | |
| 15 | g.73322560G>A | CA393084972 | HCN4 | c.3533C>T (p.Pro1178Leu) c.2315C>T (p.Pro772Leu) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73322560G>C | CA393084971 | HCN4 | c.3533C>G (p.Pro1178Arg) c.2315C>G (p.Pro772Arg) | |
| 15 | g.73322560G= | CA2187186226 | HCN4 | c.3533C= (p.Pro1178=) c.2315C= (p.Pro772=) | |
| 15 | g.73322560G>T | CA393084969 | HCN4 | c.3533C>A (p.Pro1178His) c.2315C>A (p.Pro772His) | |
| 15 | g.73322561G>A | CA393084975 | HCN4 | c.3532C>T (p.Pro1178Ser) c.2314C>T (p.Pro772Ser) | ClinVar dbSNP |
| 15 | g.73322561G>C | CA393084978 | HCN4 | c.3532C>G (p.Pro1178Ala) c.2314C>G (p.Pro772Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322561G= | CA2187186232 | HCN4 | c.3532C= (p.Pro1178=) c.2314C= (p.Pro772=) | |
| 15 | g.73322561G>T | CA393084980 | HCN4 | c.3532C>A (p.Pro1178Thr) c.2314C>A (p.Pro772Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322561_73322562delinsGC | CA2187186231 | HCN4 | c.3531_3532delinsGC (p.Gly1177=) c.2313_2314delinsGC (p.Gly771=) | |
| 15 | g.73322562C>A | CA7648808 | HCN4 | c.3531G>T (p.Gly1177=) c.2313G>T (p.Gly771=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322562C= | CA2187186243 | HCN4 | c.3531G= (p.Gly1177=) c.2313G= (p.Gly771=) | |
| 15 | g.73322562C>G | CA7648809 | HCN4 | c.3531G>C (p.Gly1177=) c.2313G>C (p.Gly771=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322562C>T | CA491477900 | HCN4 | c.3531G>A (p.Gly1177=) c.2313G>A (p.Gly771=) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73322567dup | CA619410584 | HCN4 | c.3531dup (p.Pro1178AlafsTer16) c.2313dup (p.Pro772AlafsTer16) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73322567del | CA7648807 | HCN4 | c.3531del (p.Pro1179LeufsTer2) c.2313del (p.Pro773LeufsTer2) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73322562_73322563insG | CA491477901 | HCN4 | c.3530_3531insC (p.Pro1178AlafsTer16) c.2312_2313insC (p.Pro772AlafsTer16) | |
| 15 | g.73322563C>A | CA393084994 | HCN4 | c.3530G>T (p.Gly1177Val) c.2312G>T (p.Gly771Val) | ClinVar |
| 15 | g.73322563C= | CA2187186249 | HCN4 | c.3530G= (p.Gly1177=) c.2312G= (p.Gly771=) | |
| 15 | g.73322563C>G | CA393084992 | HCN4 | c.3530G>C (p.Gly1177Ala) c.2312G>C (p.Gly771Ala) | |
| 15 | g.73322563C>T | CA7648810 | HCN4 | c.3530G>A (p.Gly1177Glu) c.2312G>A (p.Gly771Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322564C>A | CA393084997 | HCN4 | c.3529G>T (p.Gly1177Trp) c.2311G>T (p.Gly771Trp) | |
| 15 | g.73322564C>G | CA393084998 | HCN4 | c.3529G>C (p.Gly1177Arg) c.2311G>C (p.Gly771Arg) | |
| 15 | g.73322564C>T | CA393085000 | HCN4 | c.3529G>A (p.Gly1177Arg) c.2311G>A (p.Gly771Arg) | ClinVar dbSNP |
| 15 | g.73322565C>A | CA491477905 | HCN4 | c.3528G>T (p.Gly1176=) c.2310G>T (p.Gly770=) | dbSNP |
| 15 | g.73322565C>G | CA491477906 | HCN4 | c.3528G>C (p.Gly1176=) c.2310G>C (p.Gly770=) | |
| 15 | g.73322565C>T | CA491477907 | HCN4 | c.3528G>A (p.Gly1176=) c.2310G>A (p.Gly770=) | COSMIC |
| 15 | g.73322566C>A | CA393085001 | HCN4 | c.3527G>T (p.Gly1176Val) c.2309G>T (p.Gly770Val) | gnomAD v4 |
| 15 | g.73322566C= | CA2187186255 | HCN4 | c.3527G= (p.Gly1176=) c.2309G= (p.Gly770=) | |
| 15 | g.73322566C>G | CA393085003 | HCN4 | c.3527G>C (p.Gly1176Ala) c.2309G>C (p.Gly770Ala) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322566C>T | CA393085004 | HCN4 | c.3527G>A (p.Gly1176Glu) c.2309G>A (p.Gly770Glu) | |
| 15 | g.73322567C>A | CA393085007 | HCN4 | c.3526G>T (p.Gly1176Trp) c.2308G>T (p.Gly770Trp) | ClinVar gnomAD v4 |
| 15 | g.73322567C= | CA2187186261 | HCN4 | c.3526G= (p.Gly1176=) c.2308G= (p.Gly770=) | |
| 15 | g.73322567C>G | CA16614912 | HCN4 | c.3526G>C (p.Gly1176Arg) c.2308G>C (p.Gly770Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322567C>T | CA393085008 | HCN4 | c.3526G>A (p.Gly1176Arg) c.2308G>A (p.Gly770Arg) | |
| 15 | g.73322568A>C | CA491477911 | HCN4 | c.3525T>G (p.Ser1175=) c.2307T>G (p.Ser769=) | |
| 15 | g.73322568A>G | CA491477912 | HCN4 | c.3525T>C (p.Ser1175=) c.2307T>C (p.Ser769=) | gnomAD v4 |
| 15 | g.73322568A>T | CA491477913 | HCN4 | c.3525T>A (p.Ser1175=) c.2307T>A (p.Ser769=) | |
| 15 | g.73322569G>A | CA393085009 | HCN4 | c.3524C>T (p.Ser1175Phe) c.2306C>T (p.Ser769Phe) | gnomAD v4 |
| 15 | g.73322569G>C | CA393085010 | HCN4 | c.3524C>G (p.Ser1175Cys) c.2306C>G (p.Ser769Cys) | |
| 15 | g.73322569G>T | CA393085011 | HCN4 | c.3524C>A (p.Ser1175Tyr) c.2306C>A (p.Ser769Tyr) | ClinVar |
| 15 | g.73322570A>C | CA393085014 | HCN4 | c.3523T>G (p.Ser1175Ala) c.2305T>G (p.Ser769Ala) | |
| 15 | g.73322570A>G | CA393085017 | HCN4 | c.3523T>C (p.Ser1175Pro) c.2305T>C (p.Ser769Pro) | |
| 15 | g.73322570A>T | CA393085015 | HCN4 | c.3523T>A (p.Ser1175Thr) c.2305T>A (p.Ser769Thr) | |
| 15 | g.73322571A= | CA2187186263 | HCN4 | c.3522T= (p.Ser1174=) c.2304T= (p.Ser768=) | |
| 15 | g.73322571A>C | CA491477916 | HCN4 | c.3522T>G (p.Ser1174=) c.2304T>G (p.Ser768=) | gnomAD v4 |
| 15 | g.73322571A>G | CA491477917 | HCN4 | c.3522T>C (p.Ser1174=) c.2304T>C (p.Ser768=) | dbSNP gnomAD v4 |
| 15 | g.73322571A>T | CA491477919 | HCN4 | c.3522T>A (p.Ser1174=) c.2304T>A (p.Ser768=) | |
| 15 | g.73322572G>A | CA393085018 | HCN4 | c.3521C>T (p.Ser1174Phe) c.2303C>T (p.Ser768Phe) | |
| 15 | g.73322572G>C | CA393085021 | HCN4 | c.3521C>G (p.Ser1174Cys) c.2303C>G (p.Ser768Cys) | |
| 15 | g.73322572G>T | CA393085023 | HCN4 | c.3521C>A (p.Ser1174Tyr) c.2303C>A (p.Ser768Tyr) | |
| 15 | g.73322573A>C | CA393085024 | HCN4 | c.3520T>G (p.Ser1174Ala) c.2302T>G (p.Ser768Ala) | |
| 15 | g.73322573A>G | CA393085026 | HCN4 | c.3520T>C (p.Ser1174Pro) c.2302T>C (p.Ser768Pro) | |
| 15 | g.73322573A>T | CA393085027 | HCN4 | c.3520T>A (p.Ser1174Thr) c.2302T>A (p.Ser768Thr) | |
| 15 | g.73322574G>A | CA7648811 | HCN4 | c.3519C>T (p.Thr1173=) c.2301C>T (p.Thr767=) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 15 | g.73322574G>C | CA491477921 | HCN4 | c.3519C>G (p.Thr1173=) c.2301C>G (p.Thr767=) | |
| 15 | g.73322574G= | CA2187186266 | HCN4 | c.3519C= (p.Thr1173=) c.2301C= (p.Thr767=) | |
| 15 | g.73322574G>T | CA491477923 | HCN4 | c.3519C>A (p.Thr1173=) c.2301C>A (p.Thr767=) | gnomAD v4 |
| 15 | g.73322575G>A | CA393085030 | HCN4 | c.3518C>T (p.Thr1173Ile) c.2300C>T (p.Thr767Ile) | gnomAD v4 |
| 15 | g.73322575G>C | CA393085032 | HCN4 | c.3518C>G (p.Thr1173Ser) c.2300C>G (p.Thr767Ser) | |
| 15 | g.73322575G>T | CA393085034 | HCN4 | c.3518C>A (p.Thr1173Asn) c.2300C>A (p.Thr767Asn) | gnomAD v4 |
| 15 | g.73322576T>A | CA393085036 | HCN4 | c.3517A>T (p.Thr1173Ser) c.2299A>T (p.Thr767Ser) | |
| 15 | g.73322576T>C | CA393085038 | HCN4 | c.3517A>G (p.Thr1173Ala) c.2299A>G (p.Thr767Ala) | |
| 15 | g.73322576T>G | CA393085039 | HCN4 | c.3517A>C (p.Thr1173Pro) c.2299A>C (p.Thr767Pro) | |
| 15 | g.73322577G>A | CA491477927 | HCN4 | c.3516C>T (p.Ala1172=) c.2298C>T (p.Ala766=) | |
| 15 | g.73322577G>C | CA491477928 | HCN4 | c.3516C>G (p.Ala1172=) c.2298C>G (p.Ala766=) | |
| 15 | g.73322577G>T | CA491477926 | HCN4 | c.3516C>A (p.Ala1172=) c.2298C>A (p.Ala766=) | |
| 15 | g.73322578G>A | CA393085040 | HCN4 | c.3515C>T (p.Ala1172Val) c.2297C>T (p.Ala766Val) | |
| 15 | g.73322578G>C | CA393085043 | HCN4 | c.3515C>G (p.Ala1172Gly) c.2297C>G (p.Ala766Gly) | |
| 15 | g.73322578G>T | CA393085042 | HCN4 | c.3515C>A (p.Ala1172Asp) c.2297C>A (p.Ala766Asp) | |
| 15 | g.73322579C>A | CA393085045 | HCN4 | c.3514G>T (p.Ala1172Ser) c.2296G>T (p.Ala766Ser) | |
| 15 | g.73322579C>G | CA393085047 | HCN4 | c.3514G>C (p.Ala1172Pro) c.2296G>C (p.Ala766Pro) | |
| 15 | g.73322579C>T | CA393085049 | HCN4 | c.3514G>A (p.Ala1172Thr) c.2296G>A (p.Ala766Thr) | gnomAD v4 |
| 15 | g.73322580T>A | CA393085051 | HCN4 | c.3513A>T (p.Arg1171Ser) c.2295A>T (p.Arg765Ser) | |
| 15 | g.73322580T>C | CA491477930 | HCN4 | c.3513A>G (p.Arg1171=) c.2295A>G (p.Arg765=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322580T>G | CA393085052 | HCN4 | c.3513A>C (p.Arg1171Ser) c.2295A>C (p.Arg765Ser) | gnomAD v4 |
| 15 | g.73322580T= | CA2187186274 | HCN4 | c.3513A= (p.Arg1171=) c.2295A= (p.Arg765=) | |
| 15 | g.73322581C>A | CA301975 | HCN4 | c.3512G>T (p.Arg1171Ile) c.2294G>T (p.Arg765Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322581C= | CA2187186281 | HCN4 | c.3512G= (p.Arg1171=) c.2294G= (p.Arg765=) | |
| 15 | g.73322581C>G | CA393085054 | HCN4 | c.3512G>C (p.Arg1171Thr) c.2294G>C (p.Arg765Thr) | |
| 15 | g.73322581C>T | CA393085055 | HCN4 | c.3512G>A (p.Arg1171Lys) c.2294G>A (p.Arg765Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73322582T>A | CA393085056 | HCN4 | c.3511A>T (p.Arg1171Ter) c.2293A>T (p.Arg765Ter) | |
| 15 | g.73322582T>C | CA393085057 | HCN4 | c.3511A>G (p.Arg1171Gly) c.2293A>G (p.Arg765Gly) | |
| 15 | g.73322582T>G | CA491477934 | HCN4 | c.3511A>C (p.Arg1171=) c.2293A>C (p.Arg765=) | |
| 15 | g.73322583T>A | CA491477937 | HCN4 | c.3510A>T (p.Ala1170=) c.2292A>T (p.Ala764=) | |
| 15 | g.73322583T>C | CA491477935 | HCN4 | c.3510A>G (p.Ala1170=) c.2292A>G (p.Ala764=) | |
| 15 | g.73322583T>G | CA491477936 | HCN4 | c.3510A>C (p.Ala1170=) c.2292A>C (p.Ala764=) | |
| 15 | g.73322584G>A | CA393085062 | HCN4 | c.3509C>T (p.Ala1170Val) c.2291C>T (p.Ala764Val) | |
| 15 | g.73322584G>C | CA393085060 | HCN4 | c.3509C>G (p.Ala1170Gly) c.2291C>G (p.Ala764Gly) | |
| 15 | g.73322584G>T | CA393085059 | HCN4 | c.3509C>A (p.Ala1170Glu) c.2291C>A (p.Ala764Glu) | |
| 15 | g.73322585C>A | CA393085064 | HCN4 | c.3508G>T (p.Ala1170Ser) c.2290G>T (p.Ala764Ser) | |
| 15 | g.73322585C= | CA2187186285 | HCN4 | c.3508G= (p.Ala1170=) c.2290G= (p.Ala764=) | |
| 15 | g.73322585C>G | CA393085067 | HCN4 | c.3508G>C (p.Ala1170Pro) c.2290G>C (p.Ala764Pro) | |
| 15 | g.73322585C>T | CA393085066 | HCN4 | c.3508G>A (p.Ala1170Thr) c.2290G>A (p.Ala764Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73322586C>A | CA491477939 | HCN4 | c.3507G>T (p.Gly1169=) c.2289G>T (p.Gly763=) | |
| 15 | g.73322586C>G | CA491477940 | HCN4 | c.3507G>C (p.Gly1169=) c.2289G>C (p.Gly763=) | |
| 15 | g.73322586C>T | CA491477941 | HCN4 | c.3507G>A (p.Gly1169=) c.2289G>A (p.Gly763=) | COSMIC |
| 15 | g.73322587C>A | CA393085069 | HCN4 | c.3506G>T (p.Gly1169Val) c.2288G>T (p.Gly763Val) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322587C= | CA2187186289 | HCN4 | c.3506G= (p.Gly1169=) c.2288G= (p.Gly763=) | |
| 15 | g.73322587C>G | CA393085070 | HCN4 | c.3506G>C (p.Gly1169Ala) c.2288G>C (p.Gly763Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322587C>T | CA393085071 | HCN4 | c.3506G>A (p.Gly1169Glu) c.2288G>A (p.Gly763Glu) | |
| 15 | g.73322587_73322590del | CA2629370523 | HCN4 | c.3503_3506del (p.Phe1168TrpfsTer12) c.2285_2288del (p.Phe762TrpfsTer12) | gnomAD v4 |
| 15 | g.73322587_73322591delinsCCAAA | CA2187186288 | HCN4 | c.3502_3506delinsTTTGG (p.Phe1168=) c.2284_2288delinsTTTGG (p.Phe762=) |