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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73322734_73322767del | CA2804726812 | HCN4 | c.3331_3364del (p.Glu1111LeufsTer?) c.2113_2146del (p.Glu705LeufsTer?) | |
| 15 | g.73322753C>A | CA393085542 | HCN4 | c.3340G>T (p.Ala1114Ser) c.2122G>T (p.Ala708Ser) | |
| 15 | g.73322753C>G | CA393085537 | HCN4 | c.3340G>C (p.Ala1114Pro) c.2122G>C (p.Ala708Pro) | ClinVar dbSNP |
| 15 | g.73322753C>T | CA393085539 | HCN4 | c.3340G>A (p.Ala1114Thr) c.2122G>A (p.Ala708Thr) | |
| 15 | g.73322754C>A | CA393085544 | HCN4 | c.3339G>T (p.Met1113Ile) c.2121G>T (p.Met707Ile) | |
| 15 | g.73322754C>G | CA393085545 | HCN4 | c.3339G>C (p.Met1113Ile) c.2121G>C (p.Met707Ile) | |
| 15 | g.73322754C>T | CA393085547 | HCN4 | c.3339G>A (p.Met1113Ile) c.2121G>A (p.Met707Ile) | |
| 15 | g.73322755A= | CA2187186653 | HCN4 | c.3338T= (p.Met1113=) c.2120T= (p.Met707=) | |
| 15 | g.73322755A>C | CA393085550 | HCN4 | c.3338T>G (p.Met1113Arg) c.2120T>G (p.Met707Arg) | |
| 15 | g.73322755A>G | CA393085551 | HCN4 | c.3338T>C (p.Met1113Thr) c.2120T>C (p.Met707Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322755A>T | CA393085553 | HCN4 | c.3338T>A (p.Met1113Lys) c.2120T>A (p.Met707Lys) | |
| 15 | g.73322756T>A | CA393085555 | HCN4 | c.3337A>T (p.Met1113Leu) c.2119A>T (p.Met707Leu) | |
| 15 | g.73322756T>C | CA180105 | HCN4 | c.3337A>G (p.Met1113Val) c.2119A>G (p.Met707Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322756T>G | CA393085558 | HCN4 | c.3337A>C (p.Met1113Leu) c.2119A>C (p.Met707Leu) | |
| 15 | g.73322756T= | CA2187186659 | HCN4 | c.3337A= (p.Met1113=) c.2119A= (p.Met707=) | |
| 15 | g.73322757G>A | CA491478166 | HCN4 | c.3336C>T (p.Ser1112=) c.2118C>T (p.Ser706=) | dbSNP |
| 15 | g.73322757G>C | CA491478167 | HCN4 | c.3336C>G (p.Ser1112=) c.2118C>G (p.Ser706=) | |
| 15 | g.73322757G= | CA2187186661 | HCN4 | c.3336C= (p.Ser1112=) c.2118C= (p.Ser706=) | |
| 15 | g.73322757G>T | CA491478168 | HCN4 | c.3336C>A (p.Ser1112=) c.2118C>A (p.Ser706=) | |
| 15 | g.73322758G>A | CA393085560 | HCN4 | c.3335C>T (p.Ser1112Phe) c.2117C>T (p.Ser706Phe) | |
| 15 | g.73322758G>C | CA393085562 | HCN4 | c.3335C>G (p.Ser1112Cys) c.2117C>G (p.Ser706Cys) | |
| 15 | g.73322758G>T | CA393085564 | HCN4 | c.3335C>A (p.Ser1112Tyr) c.2117C>A (p.Ser706Tyr) | |
| 15 | g.73322759A>C | CA393085570 | HCN4 | c.3334T>G (p.Ser1112Ala) c.2116T>G (p.Ser706Ala) | |
| 15 | g.73322759A>G | CA393085568 | HCN4 | c.3334T>C (p.Ser1112Pro) c.2116T>C (p.Ser706Pro) | |
| 15 | g.73322759A>T | CA393085565 | HCN4 | c.3334T>A (p.Ser1112Thr) c.2116T>A (p.Ser706Thr) | |
| 15 | g.73322760C>A | CA393085572 | HCN4 | c.3333G>T (p.Glu1111Asp) c.2115G>T (p.Glu705Asp) | gnomAD v4 |
| 15 | g.73322760C>G | CA393085574 | HCN4 | c.3333G>C (p.Glu1111Asp) c.2115G>C (p.Glu705Asp) | |
| 15 | g.73322760C>T | CA491478169 | HCN4 | c.3333G>A (p.Glu1111=) c.2115G>A (p.Glu705=) | |
| 15 | g.73322761T>A | CA393085576 | HCN4 | c.3332A>T (p.Glu1111Val) c.2114A>T (p.Glu705Val) | |
| 15 | g.73322761T>C | CA393085578 | HCN4 | c.3332A>G (p.Glu1111Gly) c.2114A>G (p.Glu705Gly) | |
| 15 | g.73322761T>G | CA393085580 | HCN4 | c.3332A>C (p.Glu1111Ala) c.2114A>C (p.Glu705Ala) | |
| 15 | g.73322762C>A | CA393085583 | HCN4 | c.3331G>T (p.Glu1111Ter) c.2113G>T (p.Glu705Ter) | gnomAD v4 |
| 15 | g.73322762C>G | CA393085585 | HCN4 | c.3331G>C (p.Glu1111Gln) c.2113G>C (p.Glu705Gln) | |
| 15 | g.73322762C>T | CA393085587 | HCN4 | c.3331G>A (p.Glu1111Lys) c.2113G>A (p.Glu705Lys) | |
| 15 | g.73322765del | CA2629370528 | HCN4 | c.3331del (p.Glu1111SerfsTer?) c.2113del (p.Glu705SerfsTer?) | gnomAD v4 |
| 15 | g.73322763C>A | CA491477761 | HCN4 | c.3330G>T (p.Gly1110=) c.2112G>T (p.Gly704=) | |
| 15 | g.73322763C>G | CA491477762 | HCN4 | c.3330G>C (p.Gly1110=) c.2112G>C (p.Gly704=) | |
| 15 | g.73322763C>T | CA491477763 | HCN4 | c.3330G>A (p.Gly1110=) c.2112G>A (p.Gly704=) | gnomAD v4 COSMIC |
| 15 | g.73322764C>A | CA393085588 | HCN4 | c.3329G>T (p.Gly1110Val) c.2111G>T (p.Gly704Val) | |
| 15 | g.73322764C>G | CA393085590 | HCN4 | c.3329G>C (p.Gly1110Ala) c.2111G>C (p.Gly704Ala) | gnomAD v4 |
| 15 | g.73322764C>T | CA393085592 | HCN4 | c.3329G>A (p.Gly1110Glu) c.2111G>A (p.Gly704Glu) | |
| 15 | g.73322765C>A | CA393085595 | HCN4 | c.3328G>T (p.Gly1110Trp) c.2110G>T (p.Gly704Trp) | gnomAD v4 |
| 15 | g.73322765C>G | CA393085598 | HCN4 | c.3328G>C (p.Gly1110Arg) c.2110G>C (p.Gly704Arg) | |
| 15 | g.73322765C>T | CA393085600 | HCN4 | c.3328G>A (p.Gly1110Arg) c.2110G>A (p.Gly704Arg) | ClinVar dbSNP |
| 15 | g.73322766T>A | CA491477764 | HCN4 | c.3327A>T (p.Ser1109=) c.2109A>T (p.Ser703=) | |
| 15 | g.73322766T>C | CA16607863 | HCN4 | c.3327A>G (p.Ser1109=) c.2109A>G (p.Ser703=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322766T>G | CA491477765 | HCN4 | c.3327A>C (p.Ser1109=) c.2109A>C (p.Ser703=) | |
| 15 | g.73322766T= | CA2187186668 | HCN4 | c.3327A= (p.Ser1109=) c.2109A= (p.Ser703=) | |
| 15 | g.73322766_73322769delinsTGAG | CA2187186666 | HCN4 | c.3324_3327delinsCTCA (p.Ser1108=) c.2106_2109delinsCTCA (p.Ser702=) | |
| 15 | g.73322767G>A | CA393085606 | HCN4 | c.3326C>T (p.Ser1109Leu) c.2108C>T (p.Ser703Leu) | |
| 15 | g.73322767G>C | CA393085602 | HCN4 | c.3326C>G (p.Ser1109Ter) c.2108C>G (p.Ser703Ter) | |
| 15 | g.73322767G>T | CA393085604 | HCN4 | c.3326C>A (p.Ser1109Ter) c.2108C>A (p.Ser703Ter) | gnomAD v4 |
| 15 | g.73322770_73322772del | CA715543212 | HCN4 | c.3324_3326del (p.Ser1109del) c.2106_2108del (p.Ser703del) | dbSNP |
| 15 | g.73322768A>C | CA393085608 | HCN4 | c.3325T>G (p.Ser1109Ala) c.2107T>G (p.Ser703Ala) | |
| 15 | g.73322768A>G | CA393085609 | HCN4 | c.3325T>C (p.Ser1109Pro) c.2107T>C (p.Ser703Pro) | |
| 15 | g.73322768A>T | CA393085611 | HCN4 | c.3325T>A (p.Ser1109Thr) c.2107T>A (p.Ser703Thr) | |
| 15 | g.73322769G>A | CA491477766 | HCN4 | c.3324C>T (p.Ser1108=) c.2106C>T (p.Ser702=) | dbSNP gnomAD v4 COSMIC |
| 15 | g.73322769G>C | CA491477767 | HCN4 | c.3324C>G (p.Ser1108=) c.2106C>G (p.Ser702=) | |
| 15 | g.73322769G= | CA2187186674 | HCN4 | c.3324C= (p.Ser1108=) c.2106C= (p.Ser702=) | |
| 15 | g.73322769G>T | CA491477768 | HCN4 | c.3324C>A (p.Ser1108=) c.2106C>A (p.Ser702=) | |
| 15 | g.73322770G>A | CA393085614 | HCN4 | c.3323C>T (p.Ser1108Phe) c.2105C>T (p.Ser702Phe) | dbSNP gnomAD v2 |
| 15 | g.73322770G>C | CA393085615 | HCN4 | c.3323C>G (p.Ser1108Cys) c.2105C>G (p.Ser702Cys) | |
| 15 | g.73322770G= | CA2187186678 | HCN4 | c.3323C= (p.Ser1108=) c.2105C= (p.Ser702=) | |
| 15 | g.73322770G>T | CA393085617 | HCN4 | c.3323C>A (p.Ser1108Tyr) c.2105C>A (p.Ser702Tyr) | |
| 15 | g.73322771A>C | CA393085620 | HCN4 | c.3322T>G (p.Ser1108Ala) c.2104T>G (p.Ser702Ala) | ClinVar gnomAD v4 |
| 15 | g.73322771A>G | CA393085621 | HCN4 | c.3322T>C (p.Ser1108Pro) c.2104T>C (p.Ser702Pro) | |
| 15 | g.73322771A>T | CA393085624 | HCN4 | c.3322T>A (p.Ser1108Thr) c.2104T>A (p.Ser702Thr) | |
| 15 | g.73322772G>A | CA491477769 | HCN4 | c.3321C>T (p.His1107=) c.2103C>T (p.His701=) | |
| 15 | g.73322772G>C | CA393085626 | HCN4 | c.3321C>G (p.His1107Gln) c.2103C>G (p.His701Gln) | gnomAD v4 |
| 15 | g.73322772G>T | CA393085628 | HCN4 | c.3321C>A (p.His1107Gln) c.2103C>A (p.His701Gln) | gnomAD v4 |
| 15 | g.73322773T>A | CA7648846 | HCN4 | c.3320A>T (p.His1107Leu) c.2102A>T (p.His701Leu) | dbSNP ExAC gnomAD v2 |
| 15 | g.73322773T>C | CA393085632 | HCN4 | c.3320A>G (p.His1107Arg) c.2102A>G (p.His701Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322773T>G | CA393085630 | HCN4 | c.3320A>C (p.His1107Pro) c.2102A>C (p.His701Pro) | |
| 15 | g.73322773T= | CA2187186681 | HCN4 | c.3320A= (p.His1107=) c.2102A= (p.His701=) | |
| 15 | g.73322774G>A | CA393085637 | HCN4 | c.3319C>T (p.His1107Tyr) c.2101C>T (p.His701Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322774G>C | CA393085639 | HCN4 | c.3319C>G (p.His1107Asp) c.2101C>G (p.His701Asp) | |
| 15 | g.73322774G= | CA2187186687 | HCN4 | c.3319C= (p.His1107=) c.2101C= (p.His701=) | |
| 15 | g.73322774G>T | CA393085641 | HCN4 | c.3319C>A (p.His1107Asn) c.2101C>A (p.His701Asn) | gnomAD v4 |
| 15 | g.73322774_73322775delinsGC | CA2187186686 | HCN4 | c.3318_3319delinsGC (p.Pro1106=) c.2100_2101delinsGC (p.Pro700=) | |
| 15 | g.73322775del | CA7648847 | HCN4 | c.3318del (p.His1107ThrfsTer?) c.2100del (p.His701ThrfsTer?) | dbSNP ExAC gnomAD v2 |
| 15 | g.73322775C>A | CA491477772 | HCN4 | c.3318G>T (p.Pro1106=) c.2100G>T (p.Pro700=) | gnomAD v4 |
| 15 | g.73322775C= | CA2187186690 | HCN4 | c.3318G= (p.Pro1106=) c.2100G= (p.Pro700=) | |
| 15 | g.73322775C>G | CA491477770 | HCN4 | c.3318G>C (p.Pro1106=) c.2100G>C (p.Pro700=) | |
| 15 | g.73322775C>T | CA491477771 | HCN4 | c.3318G>A (p.Pro1106=) c.2100G>A (p.Pro700=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322776G>A | CA272663408 | HCN4 | c.3317C>T (p.Pro1106Leu) c.2099C>T (p.Pro700Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322776G>C | CA393085644 | HCN4 | c.3317C>G (p.Pro1106Arg) c.2099C>G (p.Pro700Arg) | gnomAD v4 |
| 15 | g.73322776G= | CA2187186693 | HCN4 | c.3317C= (p.Pro1106=) c.2099C= (p.Pro700=) | |
| 15 | g.73322776G>T | CA393085645 | HCN4 | c.3317C>A (p.Pro1106Gln) c.2099C>A (p.Pro700Gln) | gnomAD v4 |
| 15 | g.73322779del | CA2573151085 | HCN4 | c.3317del (p.Pro1106ArgfsTer?) c.2099del (p.Pro700ArgfsTer?) | ClinVar dbSNP |
| 15 | g.73322777G>A | CA393085647 | HCN4 | c.3316C>T (p.Pro1106Ser) c.2098C>T (p.Pro700Ser) | |
| 15 | g.73322777G>C | CA393085650 | HCN4 | c.3316C>G (p.Pro1106Ala) c.2098C>G (p.Pro700Ala) | |
| 15 | g.73322777G>T | CA393085652 | HCN4 | c.3316C>A (p.Pro1106Thr) c.2098C>A (p.Pro700Thr) | gnomAD v4 |
| 15 | g.73322778G>A | CA491477773 | HCN4 | c.3315C>T (p.Ser1105=) c.2097C>T (p.Ser699=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322778G>C | CA491477774 | HCN4 | c.3315C>G (p.Ser1105=) c.2097C>G (p.Ser699=) | |
| 15 | g.73322778G= | CA2187186697 | HCN4 | c.3315C= (p.Ser1105=) c.2097C= (p.Ser699=) | |
| 15 | g.73322778G>T | CA491477775 | HCN4 | c.3315C>A (p.Ser1105=) c.2097C>A (p.Ser699=) | |
| 15 | g.73322778_73322779insC | CA2187186699 | HCN4 | c.3314_3315insG (p.His1107AlafsTer?) c.2096_2097insG (p.His701AlafsTer?) | dbSNP |
| 15 | g.73322779G>A | CA393085654 | HCN4 | c.3314C>T (p.Ser1105Phe) c.2096C>T (p.Ser699Phe) | gnomAD v4 |
| 15 | g.73322779G>C | CA393085656 | HCN4 | c.3314C>G (p.Ser1105Cys) c.2096C>G (p.Ser699Cys) | |
| 15 | g.73322779G= | CA2187186698 | HCN4 | c.3314C= (p.Ser1105=) c.2096C= (p.Ser699=) | |
| 15 | g.73322779G>T | CA393085657 | HCN4 | c.3314C>A (p.Ser1105Tyr) c.2096C>A (p.Ser699Tyr) | dbSNP gnomAD v2 |
| 15 | g.73322780A>C | CA393085664 | HCN4 | c.3313T>G (p.Ser1105Ala) c.2095T>G (p.Ser699Ala) | COSMIC |
| 15 | g.73322780A>G | CA393085661 | HCN4 | c.3313T>C (p.Ser1105Pro) c.2095T>C (p.Ser699Pro) | gnomAD v4 |
| 15 | g.73322780A>T | CA393085662 | HCN4 | c.3313T>A (p.Ser1105Thr) c.2095T>A (p.Ser699Thr) | |
| 15 | g.73322781G>A | CA491477776 | HCN4 | c.3312C>T (p.Ala1104=) c.2094C>T (p.Ala698=) | dbSNP |
| 15 | g.73322781G>C | CA491477777 | HCN4 | c.3312C>G (p.Ala1104=) c.2094C>G (p.Ala698=) | |
| 15 | g.73322781G>T | CA491477778 | HCN4 | c.3312C>A (p.Ala1104=) c.2094C>A (p.Ala698=) | |
| 15 | g.73322782G>A | CA393085666 | HCN4 | c.3311C>T (p.Ala1104Val) c.2093C>T (p.Ala698Val) | |
| 15 | g.73322782G>C | CA393085668 | HCN4 | c.3311C>G (p.Ala1104Gly) c.2093C>G (p.Ala698Gly) | |
| 15 | g.73322782G>T | CA393085670 | HCN4 | c.3311C>A (p.Ala1104Asp) c.2093C>A (p.Ala698Asp) | gnomAD v4 |
| 15 | g.73322783C>A | CA393085673 | HCN4 | c.3310G>T (p.Ala1104Ser) c.2092G>T (p.Ala698Ser) | gnomAD v4 |
| 15 | g.73322783C= | CA2187186703 | HCN4 | c.3310G= (p.Ala1104=) c.2092G= (p.Ala698=) | |
| 15 | g.73322783C>G | CA393085675 | HCN4 | c.3310G>C (p.Ala1104Pro) c.2092G>C (p.Ala698Pro) | |
| 15 | g.73322783C>T | CA7648848 | HCN4 | c.3310G>A (p.Ala1104Thr) c.2092G>A (p.Ala698Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322784T>A | CA393085679 | HCN4 | c.3309A>T (p.Arg1103Ser) c.2091A>T (p.Arg697Ser) | |
| 15 | g.73322784T>C | CA491477779 | HCN4 | c.3309A>G (p.Arg1103=) c.2091A>G (p.Arg697=) | gnomAD v4 |
| 15 | g.73322784T>G | CA393085681 | HCN4 | c.3309A>C (p.Arg1103Ser) c.2091A>C (p.Arg697Ser) | |
| 15 | g.73322784_73322802delinsTCTGCGGAGAGTCTGCGCC | CA2187186704 | HCN4 | c.3291_3309delinsGGCGCAGACTCTCCGCAGA (p.Gly1097=) c.2073_2091delinsGGCGCAGACTCTCCGCAGA (p.Gly691=) | |
| 15 | g.73322785C>A | CA393085683 | HCN4 | c.3308G>T (p.Arg1103Ile) c.2090G>T (p.Arg697Ile) | gnomAD v4 |
| 15 | g.73322785C>G | CA393085686 | HCN4 | c.3308G>C (p.Arg1103Thr) c.2090G>C (p.Arg697Thr) | |
| 15 | g.73322785C>T | CA393085688 | HCN4 | c.3308G>A (p.Arg1103Lys) c.2090G>A (p.Arg697Lys) | |
| 15 | g.73322786_73322803del | CA7648849 | HCN4 | c.3291_3308del (p.Ala1098_Arg1103del) c.2073_2090del (p.Ala692_Arg697del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322786T>A | CA393085691 | HCN4 | c.3307A>T (p.Arg1103Ter) c.2089A>T (p.Arg697Ter) | |
| 15 | g.73322786T>C | CA10583260 | HCN4 | c.3307A>G (p.Arg1103Gly) c.2089A>G (p.Arg697Gly) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322786T>G | CA491477780 | HCN4 | c.3307A>C (p.Arg1103=) c.2089A>C (p.Arg697=) | |
| 15 | g.73322786T= | CA2187186705 | HCN4 | c.3307A= (p.Arg1103=) c.2089A= (p.Arg697=) | |
| 15 | g.73322787G>A | CA491477781 | HCN4 | c.3306C>T (p.Arg1102=) c.2088C>T (p.Arg696=) | gnomAD v4 |
| 15 | g.73322787G>C | CA491477782 | HCN4 | c.3306C>G (p.Arg1102=) c.2088C>G (p.Arg696=) | dbSNP gnomAD v2 |
| 15 | g.73322787G= | CA2187186707 | HCN4 | c.3306C= (p.Arg1102=) c.2088C= (p.Arg696=) | |
| 15 | g.73322787G>T | CA491477783 | HCN4 | c.3306C>A (p.Arg1102=) c.2088C>A (p.Arg696=) | gnomAD v4 |
| 15 | g.73322788C>A | CA393085694 | HCN4 | c.3305G>T (p.Arg1102Leu) c.2087G>T (p.Arg696Leu) | gnomAD v4 |
| 15 | g.73322788C= | CA2187186710 | HCN4 | c.3305G= (p.Arg1102=) c.2087G= (p.Arg696=) | |
| 15 | g.73322788C>G | CA393085697 | HCN4 | c.3305G>C (p.Arg1102Pro) c.2087G>C (p.Arg696Pro) | |
| 15 | g.73322788C>T | CA7648850 | HCN4 | c.3305G>A (p.Arg1102His) c.2087G>A (p.Arg696His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322789G>A | CA7648851 | HCN4 | c.3304C>T (p.Arg1102Cys) c.2086C>T (p.Arg696Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322789G>C | CA393085702 | HCN4 | c.3304C>G (p.Arg1102Gly) c.2086C>G (p.Arg696Gly) | |
| 15 | g.73322789G= | CA2187186712 | HCN4 | c.3304C= (p.Arg1102=) c.2086C= (p.Arg696=) | |
| 15 | g.73322789G>T | CA393085699 | HCN4 | c.3304C>A (p.Arg1102Ser) c.2086C>A (p.Arg696Ser) | gnomAD v4 |
| 15 | g.73322789_73322790dup | CA2629370529 | HCN4 | c.3303_3304dup (p.Arg1102ProfsTer?) c.2085_2086dup (p.Arg696ProfsTer?) | gnomAD v4 |
| 15 | g.73322790G>A | CA491477784 | HCN4 | c.3303C>T (p.Leu1101=) c.2085C>T (p.Leu695=) | gnomAD v4 |
| 15 | g.73322790G>C | CA491477785 | HCN4 | c.3303C>G (p.Leu1101=) c.2085C>G (p.Leu695=) | |
| 15 | g.73322790G>T | CA491477786 | HCN4 | c.3303C>A (p.Leu1101=) c.2085C>A (p.Leu695=) | gnomAD v4 |
| 15 | g.73322791A>C | CA393085704 | HCN4 | c.3302T>G (p.Leu1101Arg) c.2084T>G (p.Leu695Arg) | |
| 15 | g.73322791A>G | CA393085706 | HCN4 | c.3302T>C (p.Leu1101Pro) c.2084T>C (p.Leu695Pro) | |
| 15 | g.73322791A>T | CA393085709 | HCN4 | c.3302T>A (p.Leu1101His) c.2084T>A (p.Leu695His) | |
| 15 | g.73322792G>A | CA393085712 | HCN4 | c.3301C>T (p.Leu1101Phe) c.2083C>T (p.Leu695Phe) | |
| 15 | g.73322792G>C | CA393085714 | HCN4 | c.3301C>G (p.Leu1101Val) c.2083C>G (p.Leu695Val) | gnomAD v4 |
| 15 | g.73322792G>T | CA393085716 | HCN4 | c.3301C>A (p.Leu1101Ile) c.2083C>A (p.Leu695Ile) | gnomAD v4 |
| 15 | g.73322793A>C | CA491477787 | HCN4 | c.3300T>G (p.Thr1100=) c.2082T>G (p.Thr694=) | |
| 15 | g.73322793A>G | CA491477788 | HCN4 | c.3300T>C (p.Thr1100=) c.2082T>C (p.Thr694=) | ClinVar dbSNP |
| 15 | g.73322793A>T | CA491477789 | HCN4 | c.3300T>A (p.Thr1100=) c.2082T>A (p.Thr694=) | ClinVar dbSNP |
| 15 | g.73322794G>A | CA393085718 | HCN4 | c.3299C>T (p.Thr1100Ile) c.2081C>T (p.Thr694Ile) | gnomAD v4 |
| 15 | g.73322794G>C | CA393085720 | HCN4 | c.3299C>G (p.Thr1100Ser) c.2081C>G (p.Thr694Ser) | dbSNP gnomAD v4 |
| 15 | g.73322794G= | CA2187186713 | HCN4 | c.3299C= (p.Thr1100=) c.2081C= (p.Thr694=) | |
| 15 | g.73322794G>T | CA393085722 | HCN4 | c.3299C>A (p.Thr1100Asn) c.2081C>A (p.Thr694Asn) | gnomAD v4 |
| 15 | g.73322795T>A | CA393085725 | HCN4 | c.3298A>T (p.Thr1100Ser) c.2080A>T (p.Thr694Ser) | |
| 15 | g.73322795T>C | CA393085727 | HCN4 | c.3298A>G (p.Thr1100Ala) c.2080A>G (p.Thr694Ala) | |
| 15 | g.73322795T>G | CA393085728 | HCN4 | c.3298A>C (p.Thr1100Pro) c.2080A>C (p.Thr694Pro) | |
| 15 | g.73322796C>A | CA393085732 | HCN4 | c.3297G>T (p.Gln1099His) c.2079G>T (p.Gln693His) | gnomAD v4 |
| 15 | g.73322796C= | CA2187186714 | HCN4 | c.3297G= (p.Gln1099=) c.2079G= (p.Gln693=) | |
| 15 | g.73322796C>G | CA393085733 | HCN4 | c.3297G>C (p.Gln1099His) c.2079G>C (p.Gln693His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322796C>T | CA491477790 | HCN4 | c.3297G>A (p.Gln1099=) c.2079G>A (p.Gln693=) | gnomAD v4 |
| 15 | g.73322797T>A | CA393085735 | HCN4 | c.3296A>T (p.Gln1099Leu) c.2078A>T (p.Gln693Leu) | gnomAD v4 |
| 15 | g.73322797T>C | CA393085737 | HCN4 | c.3296A>G (p.Gln1099Arg) c.2078A>G (p.Gln693Arg) | gnomAD v4 |
| 15 | g.73322797T>G | CA393085739 | HCN4 | c.3296A>C (p.Gln1099Pro) c.2078A>C (p.Gln693Pro) | gnomAD v4 |
| 15 | g.73322798G>A | CA393085742 | HCN4 | c.3295C>T (p.Gln1099Ter) c.2077C>T (p.Gln693Ter) | gnomAD v4 |
| 15 | g.73322798G>C | CA393085744 | HCN4 | c.3295C>G (p.Gln1099Glu) c.2077C>G (p.Gln693Glu) | |
| 15 | g.73322798G>T | CA393085746 | HCN4 | c.3295C>A (p.Gln1099Lys) c.2077C>A (p.Gln693Lys) | gnomAD v4 |
| 15 | g.73322799C>A | CA491477791 | HCN4 | c.3294G>T (p.Ala1098=) c.2076G>T (p.Ala692=) | gnomAD v4 |
| 15 | g.73322799C= | CA2187186715 | HCN4 | c.3294G= (p.Ala1098=) c.2076G= (p.Ala692=) | |
| 15 | g.73322799C>G | CA491477792 | HCN4 | c.3294G>C (p.Ala1098=) c.2076G>C (p.Ala692=) | |
| 15 | g.73322799C>T | CA7648852 | HCN4 | c.3294G>A (p.Ala1098=) c.2076G>A (p.Ala692=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322800G>A | CA16621676 | HCN4 | c.3293C>T (p.Ala1098Val) c.2075C>T (p.Ala692Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73322800G>C | CA393085750 | HCN4 | c.3293C>G (p.Ala1098Gly) c.2075C>G (p.Ala692Gly) | |
| 15 | g.73322800G= | CA2187186716 | HCN4 | c.3293C= (p.Ala1098=) c.2075C= (p.Ala692=) | |
| 15 | g.73322800G>T | CA393085752 | HCN4 | c.3293C>A (p.Ala1098Glu) c.2075C>A (p.Ala692Glu) | gnomAD v4 |
| 15 | g.73322801C>A | CA393085758 | HCN4 | c.3292G>T (p.Ala1098Ser) c.2074G>T (p.Ala692Ser) | gnomAD v4 |
| 15 | g.73322801C>G | CA393085756 | HCN4 | c.3292G>C (p.Ala1098Pro) c.2074G>C (p.Ala692Pro) | gnomAD v4 |
| 15 | g.73322801C>T | CA393085755 | HCN4 | c.3292G>A (p.Ala1098Thr) c.2074G>A (p.Ala692Thr) | gnomAD v4 |
| 15 | g.73322804del | CA2629370530 | HCN4 | c.3292del (p.Ala1098ArgfsTer?) c.2074del (p.Ala692ArgfsTer?) | gnomAD v4 |
| 15 | g.73322802C>A | CA491477793 | HCN4 | c.3291G>T (p.Gly1097=) c.2073G>T (p.Gly691=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322802C= | CA2187186719 | HCN4 | c.3291G= (p.Gly1097=) c.2073G= (p.Gly691=) | |
| 15 | g.73322802C>G | CA491477794 | HCN4 | c.3291G>C (p.Gly1097=) c.2073G>C (p.Gly691=) | ClinVar |
| 15 | g.73322802C>T | CA491477795 | HCN4 | c.3291G>A (p.Gly1097=) c.2073G>A (p.Gly691=) | gnomAD v4 |
| 15 | g.73322803C>A | CA393085761 | HCN4 | c.3290G>T (p.Gly1097Val) c.2072G>T (p.Gly691Val) | gnomAD v4 |
| 15 | g.73322803C= | CA2187186720 | HCN4 | c.3290G= (p.Gly1097=) c.2072G= (p.Gly691=) | |
| 15 | g.73322803C>G | CA393085763 | HCN4 | c.3290G>C (p.Gly1097Ala) c.2072G>C (p.Gly691Ala) | ClinVar gnomAD v4 |
| 15 | g.73322803C>T | CA393085765 | HCN4 | c.3290G>A (p.Gly1097Glu) c.2072G>A (p.Gly691Glu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322804C>A | CA7648854 | HCN4 | c.3289G>T (p.Gly1097Trp) c.2071G>T (p.Gly691Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322804C= | CA2187186721 | HCN4 | c.3289G= (p.Gly1097=) c.2071G= (p.Gly691=) | |
| 15 | g.73322804C>G | CA393085766 | HCN4 | c.3289G>C (p.Gly1097Arg) c.2071G>C (p.Gly691Arg) | |
| 15 | g.73322804C>T | CA7648853 | HCN4 | c.3289G>A (p.Gly1097Arg) c.2071G>A (p.Gly691Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322805G>A | CA180107 | HCN4 | c.3288C>T (p.Asp1096=) c.2070C>T (p.Asp690=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322805G>C | CA393085772 | HCN4 | c.3288C>G (p.Asp1096Glu) c.2070C>G (p.Asp690Glu) | |
| 15 | g.73322805G= | CA2187186724 | HCN4 | c.3288C= (p.Asp1096=) c.2070C= (p.Asp690=) | |
| 15 | g.73322805G>T | CA393085774 | HCN4 | c.3288C>A (p.Asp1096Glu) c.2070C>A (p.Asp690Glu) | gnomAD v4 |
| 15 | g.73322806T>A | CA393085776 | HCN4 | c.3287A>T (p.Asp1096Val) c.2069A>T (p.Asp690Val) | |
| 15 | g.73322806T>C | CA393085778 | HCN4 | c.3287A>G (p.Asp1096Gly) c.2069A>G (p.Asp690Gly) | gnomAD v4 |
| 15 | g.73322806T>G | CA393085780 | HCN4 | c.3287A>C (p.Asp1096Ala) c.2069A>C (p.Asp690Ala) | |
| 15 | g.73322807C>A | CA393085786 | HCN4 | c.3286G>T (p.Asp1096Tyr) c.2068G>T (p.Asp690Tyr) | gnomAD v4 |
| 15 | g.73322807C>G | CA393085782 | HCN4 | c.3286G>C (p.Asp1096His) c.2068G>C (p.Asp690His) | |
| 15 | g.73322807C>T | CA393085784 | HCN4 | c.3286G>A (p.Asp1096Asn) c.2068G>A (p.Asp690Asn) | |
| 15 | g.73322808C>A | CA393085788 | HCN4 | c.3285G>T (p.Gln1095His) c.2067G>T (p.Gln689His) | gnomAD v4 |
| 15 | g.73322808C>G | CA393085790 | HCN4 | c.3285G>C (p.Gln1095His) c.2067G>C (p.Gln689His) | |
| 15 | g.73322808C>T | CA491477796 | HCN4 | c.3285G>A (p.Gln1095=) c.2067G>A (p.Gln689=) | ClinVar |
| 15 | g.73322809T>A | CA393085791 | HCN4 | c.3284A>T (p.Gln1095Leu) c.2066A>T (p.Gln689Leu) | |
| 15 | g.73322809T>C | CA393085792 | HCN4 | c.3284A>G (p.Gln1095Arg) c.2066A>G (p.Gln689Arg) | gnomAD v4 |
| 15 | g.73322809T>G | CA393085794 | HCN4 | c.3284A>C (p.Gln1095Pro) c.2066A>C (p.Gln689Pro) | |
| 15 | g.73322810G>A | CA393085795 | HCN4 | c.3283C>T (p.Gln1095Ter) c.2065C>T (p.Gln689Ter) | gnomAD v4 |
| 15 | g.73322810G>C | CA393085797 | HCN4 | c.3283C>G (p.Gln1095Glu) c.2065C>G (p.Gln689Glu) | |
| 15 | g.73322810G>T | CA393085799 | HCN4 | c.3283C>A (p.Gln1095Lys) c.2065C>A (p.Gln689Lys) | gnomAD v4 |
| 15 | g.73322811A>C | CA491477797 | HCN4 | c.3282T>G (p.Pro1094=) c.2064T>G (p.Pro688=) | |
| 15 | g.73322811A>G | CA491477798 | HCN4 | c.3282T>C (p.Pro1094=) c.2064T>C (p.Pro688=) | ClinVar gnomAD v4 |
| 15 | g.73322811A>T | CA491477799 | HCN4 | c.3282T>A (p.Pro1094=) c.2064T>A (p.Pro688=) | gnomAD v4 |
| 15 | g.73322812G>A | CA393085802 | HCN4 | c.3281C>T (p.Pro1094Leu) c.2063C>T (p.Pro688Leu) | gnomAD v4 |
| 15 | g.73322812G>C | CA393085803 | HCN4 | c.3281C>G (p.Pro1094Arg) c.2063C>G (p.Pro688Arg) | |
| 15 | g.73322812G>T | CA393085805 | HCN4 | c.3281C>A (p.Pro1094His) c.2063C>A (p.Pro688His) | gnomAD v4 |
| 15 | g.73322813G>A | CA393085809 | HCN4 | c.3280C>T (p.Pro1094Ser) c.2062C>T (p.Pro688Ser) | gnomAD v4 |
| 15 | g.73322813G>C | CA393085811 | HCN4 | c.3280C>G (p.Pro1094Ala) c.2062C>G (p.Pro688Ala) | |
| 15 | g.73322813G>T | CA393085808 | HCN4 | c.3280C>A (p.Pro1094Thr) c.2062C>A (p.Pro688Thr) | gnomAD v4 |
| 15 | g.73322814C>A | CA491477800 | HCN4 | c.3279G>T (p.Leu1093=) c.2061G>T (p.Leu687=) | gnomAD v4 |
| 15 | g.73322814C>G | CA491477801 | HCN4 | c.3279G>C (p.Leu1093=) c.2061G>C (p.Leu687=) | |
| 15 | g.73322814C>T | CA491477802 | HCN4 | c.3279G>A (p.Leu1093=) c.2061G>A (p.Leu687=) | ClinVar gnomAD v4 |
| 15 | g.73322815A>C | CA393085819 | HCN4 | c.3278T>G (p.Leu1093Arg) c.2060T>G (p.Leu687Arg) | |
| 15 | g.73322815A>G | CA393085814 | HCN4 | c.3278T>C (p.Leu1093Pro) c.2060T>C (p.Leu687Pro) | |
| 15 | g.73322815A>T | CA393085816 | HCN4 | c.3278T>A (p.Leu1093Gln) c.2060T>A (p.Leu687Gln) | |
| 15 | g.73322816G>A | CA491477803 | HCN4 | c.3277C>T (p.Leu1093=) c.2059C>T (p.Leu687=) | gnomAD v4 |
| 15 | g.73322816G>C | CA393085820 | HCN4 | c.3277C>G (p.Leu1093Val) c.2059C>G (p.Leu687Val) | |
| 15 | g.73322816G>T | CA393085822 | HCN4 | c.3277C>A (p.Leu1093Met) c.2059C>A (p.Leu687Met) | gnomAD v4 |
| 15 | g.73322817G>A | CA491477805 | HCN4 | c.3276C>T (p.Ala1092=) c.2058C>T (p.Ala686=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322817G>C | CA491477806 | HCN4 | c.3276C>G (p.Ala1092=) c.2058C>G (p.Ala686=) | |
| 15 | g.73322817G= | CA2187186727 | HCN4 | c.3276C= (p.Ala1092=) c.2058C= (p.Ala686=) | |
| 15 | g.73322817G>T | CA491477804 | HCN4 | c.3276C>A (p.Ala1092=) c.2058C>A (p.Ala686=) | gnomAD v4 |
| 15 | g.73322818G>A | CA393085825 | HCN4 | c.3275C>T (p.Ala1092Val) c.2057C>T (p.Ala686Val) | gnomAD v4 |
| 15 | g.73322818G>C | CA393085827 | HCN4 | c.3275C>G (p.Ala1092Gly) c.2057C>G (p.Ala686Gly) | |
| 15 | g.73322818G>T | CA393085828 | HCN4 | c.3275C>A (p.Ala1092Asp) c.2057C>A (p.Ala686Asp) | ClinVar gnomAD v4 |
| 15 | g.73322819C>A | CA393085832 | HCN4 | c.3274G>T (p.Ala1092Ser) c.2056G>T (p.Ala686Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322819C= | CA2187186730 | HCN4 | c.3274G= (p.Ala1092=) c.2056G= (p.Ala686=) | |
| 15 | g.73322819C>G | CA393085834 | HCN4 | c.3274G>C (p.Ala1092Pro) c.2056G>C (p.Ala686Pro) | |
| 15 | g.73322819C>T | CA393085836 | HCN4 | c.3274G>A (p.Ala1092Thr) c.2056G>A (p.Ala686Thr) | gnomAD v4 |
| 15 | g.73322820T>A | CA491477807 | HCN4 | c.3273A>T (p.Pro1091=) c.2055A>T (p.Pro685=) | |
| 15 | g.73322820T>C | CA491477808 | HCN4 | c.3273A>G (p.Pro1091=) c.2055A>G (p.Pro685=) | |
| 15 | g.73322820T>G | CA491477809 | HCN4 | c.3273A>C (p.Pro1091=) c.2055A>C (p.Pro685=) | gnomAD v4 |
| 15 | g.73322821G>A | CA393085838 | HCN4 | c.3272C>T (p.Pro1091Leu) c.2054C>T (p.Pro685Leu) | gnomAD v4 |
| 15 | g.73322821G>C | CA393085840 | HCN4 | c.3272C>G (p.Pro1091Arg) c.2054C>G (p.Pro685Arg) | |
| 15 | g.73322821G>T | CA393085842 | HCN4 | c.3272C>A (p.Pro1091Gln) c.2054C>A (p.Pro685Gln) | gnomAD v4 |
| 15 | g.73322822del | CA2629370531 | HCN4 | c.3272del (p.Pro1091GlnfsTer?) c.2054del (p.Pro685GlnfsTer?) | gnomAD v4 |
| 15 | g.73322822G>A | CA393085847 | HCN4 | c.3271C>T (p.Pro1091Ser) c.2053C>T (p.Pro685Ser) | gnomAD v4 |
| 15 | g.73322822G>C | CA393085844 | HCN4 | c.3271C>G (p.Pro1091Ala) c.2053C>G (p.Pro685Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322822G= | CA2187186734 | HCN4 | c.3271C= (p.Pro1091=) c.2053C= (p.Pro685=) | |
| 15 | g.73322822G>T | CA393085845 | HCN4 | c.3271C>A (p.Pro1091Thr) c.2053C>A (p.Pro685Thr) | gnomAD v4 |
| 15 | g.73322823C>A | CA393085849 | HCN4 | c.3270G>T (p.Gln1090His) c.2052G>T (p.Gln684His) | gnomAD v4 |
| 15 | g.73322823C>G | CA393085851 | HCN4 | c.3270G>C (p.Gln1090His) c.2052G>C (p.Gln684His) | gnomAD v4 |
| 15 | g.73322823C>T | CA491477810 | HCN4 | c.3270G>A (p.Gln1090=) c.2052G>A (p.Gln684=) | gnomAD v4 |
| 15 | g.73322823_73322824del | CA2575783816 | HCN4 | c.3269_3270del (p.Gln1090ProfsTer?) c.2051_2052del (p.Gln684ProfsTer?) | |
| 15 | g.73322824T>A | CA393085853 | HCN4 | c.3269A>T (p.Gln1090Leu) c.2051A>T (p.Gln684Leu) | |
| 15 | g.73322824T>C | CA393085855 | HCN4 | c.3269A>G (p.Gln1090Arg) c.2051A>G (p.Gln684Arg) | gnomAD v4 |
| 15 | g.73322824T>G | CA393085857 | HCN4 | c.3269A>C (p.Gln1090Pro) c.2051A>C (p.Gln684Pro) | |
| 15 | g.73322825G>A | CA393085860 | HCN4 | c.3268C>T (p.Gln1090Ter) c.2050C>T (p.Gln684Ter) | gnomAD v4 |
| 15 | g.73322825G>C | CA393085861 | HCN4 | c.3268C>G (p.Gln1090Glu) c.2050C>G (p.Gln684Glu) | |
| 15 | g.73322825G>T | CA393085864 | HCN4 | c.3268C>A (p.Gln1090Lys) c.2050C>A (p.Gln684Lys) | gnomAD v4 |
| 15 | g.73322826A>C | CA491477811 | HCN4 | c.3267T>G (p.Ser1089=) c.2049T>G (p.Ser683=) | |
| 15 | g.73322826A>G | CA491477812 | HCN4 | c.3267T>C (p.Ser1089=) c.2049T>C (p.Ser683=) | ClinVar gnomAD v4 |
| 15 | g.73322826A>T | CA491477814 | HCN4 | c.3267T>A (p.Ser1089=) c.2049T>A (p.Ser683=) | |
| 15 | g.73322827G>A | CA393085866 | HCN4 | c.3266C>T (p.Ser1089Phe) c.2048C>T (p.Ser683Phe) | gnomAD v4 |
| 15 | g.73322827G>C | CA393085868 | HCN4 | c.3266C>G (p.Ser1089Cys) c.2048C>G (p.Ser683Cys) | |
| 15 | g.73322827G>T | CA393085870 | HCN4 | c.3266C>A (p.Ser1089Tyr) c.2048C>A (p.Ser683Tyr) | gnomAD v4 |
| 15 | g.73322828A>C | CA393085876 | HCN4 | c.3265T>G (p.Ser1089Ala) c.2047T>G (p.Ser683Ala) | |
| 15 | g.73322828A>G | CA393085874 | HCN4 | c.3265T>C (p.Ser1089Pro) c.2047T>C (p.Ser683Pro) | gnomAD v4 |
| 15 | g.73322828A>T | CA393085872 | HCN4 | c.3265T>A (p.Ser1089Thr) c.2047T>A (p.Ser683Thr) | |
| 15 | g.73322829C>A | CA491477817 | HCN4 | c.3264G>T (p.Ala1088=) c.2046G>T (p.Ala682=) | gnomAD v4 |
| 15 | g.73322829C= | CA2187186737 | HCN4 | c.3264G= (p.Ala1088=) c.2046G= (p.Ala682=) | |
| 15 | g.73322829C>G | CA491477818 | HCN4 | c.3264G>C (p.Ala1088=) c.2046G>C (p.Ala682=) | |
| 15 | g.73322829C>T | CA7648855 | HCN4 | c.3264G>A (p.Ala1088=) c.2046G>A (p.Ala682=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73322830G>A | CA7648856 | HCN4 | c.3263C>T (p.Ala1088Val) c.2045C>T (p.Ala682Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322830G>C | CA393085881 | HCN4 | c.3263C>G (p.Ala1088Gly) c.2045C>G (p.Ala682Gly) | |
| 15 | g.73322830G= | CA2187186743 | HCN4 | c.3263C= (p.Ala1088=) c.2045C= (p.Ala682=) | |
| 15 | g.73322830G>T | CA393085883 | HCN4 | c.3263C>A (p.Ala1088Glu) c.2045C>A (p.Ala682Glu) | gnomAD v4 |
| 15 | g.73322831C>A | CA393085885 | HCN4 | c.3262G>T (p.Ala1088Ser) c.2044G>T (p.Ala682Ser) | gnomAD v4 |
| 15 | g.73322831C= | CA2187186752 | HCN4 | c.3262G= (p.Ala1088=) c.2044G= (p.Ala682=) | |
| 15 | g.73322831C>G | CA393085887 | HCN4 | c.3262G>C (p.Ala1088Pro) c.2044G>C (p.Ala682Pro) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322831C>T | CA272663481 | HCN4 | c.3262G>A (p.Ala1088Thr) c.2044G>A (p.Ala682Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322832G>A | CA272663495 | HCN4 | c.3261C>T (p.Ser1087=) c.2043C>T (p.Ser681=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322832G>C | CA491477822 | HCN4 | c.3261C>G (p.Ser1087=) c.2043C>G (p.Ser681=) | ClinVar gnomAD v4 |
| 15 | g.73322832G= | CA2187186756 | HCN4 | c.3261C= (p.Ser1087=) c.2043C= (p.Ser681=) | |
| 15 | g.73322832G>T | CA491477823 | HCN4 | c.3261C>A (p.Ser1087=) c.2043C>A (p.Ser681=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322833G>A | CA393085892 | HCN4 | c.3260C>T (p.Ser1087Phe) c.2042C>T (p.Ser681Phe) | ClinVar gnomAD v4 |
| 15 | g.73322833G>C | CA393085894 | HCN4 | c.3260C>G (p.Ser1087Cys) c.2042C>G (p.Ser681Cys) | |
| 15 | g.73322833G>T | CA393085896 | HCN4 | c.3260C>A (p.Ser1087Tyr) c.2042C>A (p.Ser681Tyr) | gnomAD v4 |
| 15 | g.73322834A= | CA2187186760 | HCN4 | c.3259T= (p.Ser1087=) c.2041T= (p.Ser681=) | |
| 15 | g.73322834A>C | CA393085897 | HCN4 | c.3259T>G (p.Ser1087Ala) c.2041T>G (p.Ser681Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322834A>G | CA393085899 | HCN4 | c.3259T>C (p.Ser1087Pro) c.2041T>C (p.Ser681Pro) | gnomAD v4 |
| 15 | g.73322834A>T | CA393085901 | HCN4 | c.3259T>A (p.Ser1087Thr) c.2041T>A (p.Ser681Thr) | |
| 15 | g.73322835G>A | CA491477826 | HCN4 | c.3258C>T (p.Ile1086=) c.2040C>T (p.Ile680=) | |
| 15 | g.73322835G>C | CA393085903 | HCN4 | c.3258C>G (p.Ile1086Met) c.2040C>G (p.Ile680Met) | |
| 15 | g.73322835G>T | CA491477827 | HCN4 | c.3258C>A (p.Ile1086=) c.2040C>A (p.Ile680=) | gnomAD v4 |
| 15 | g.73322837_73322839dup | CA2580089970 | HCN4 | c.3256_3258dup (p.Ile1086_Ser1087insIle) c.2038_2040dup (p.Ile680_Ser681insIle) | ClinVar |
| 15 | g.73322836_73322847del | CA2697549179 | HCN4 | c.3247_3258del (p.Leu1083_Ile1086del) c.2029_2040del (p.Leu677_Ile680del) | ClinVar |
| 15 | g.73322836A>C | CA393085905 | HCN4 | c.3257T>G (p.Ile1086Ser) c.2039T>G (p.Ile680Ser) | |
| 15 | g.73322836A>G | CA393085907 | HCN4 | c.3257T>C (p.Ile1086Thr) c.2039T>C (p.Ile680Thr) | gnomAD v4 |
| 15 | g.73322836A>T | CA393085909 | HCN4 | c.3257T>A (p.Ile1086Asn) c.2039T>A (p.Ile680Asn) | gnomAD v4 |
| 15 | g.73322837T>A | CA393085912 | HCN4 | c.3256A>T (p.Ile1086Phe) c.2038A>T (p.Ile680Phe) | |
| 15 | g.73322837T>C | CA393085913 | HCN4 | c.3256A>G (p.Ile1086Val) c.2038A>G (p.Ile680Val) | gnomAD v4 |
| 15 | g.73322837T>G | CA393085916 | HCN4 | c.3256A>C (p.Ile1086Leu) c.2038A>C (p.Ile680Leu) | dbSNP gnomAD v4 |
| 15 | g.73322838G>A | CA491477828 | HCN4 | c.3255C>T (p.Leu1085=) c.2037C>T (p.Leu679=) | gnomAD v4 |
| 15 | g.73322838G>C | CA491477831 | HCN4 | c.3255C>G (p.Leu1085=) c.2037C>G (p.Leu679=) | |
| 15 | g.73322838G= | CA2187186765 | HCN4 | c.3255C= (p.Leu1085=) c.2037C= (p.Leu679=) | |
| 15 | g.73322838G>T | CA491477829 | HCN4 | c.3255C>A (p.Leu1085=) c.2037C>A (p.Leu679=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322839A= | CA2187186769 | HCN4 | c.3254T= (p.Leu1085=) c.2036T= (p.Leu679=) | |
| 15 | g.73322839A>C | CA393085918 | HCN4 | c.3254T>G (p.Leu1085Arg) c.2036T>G (p.Leu679Arg) | |
| 15 | g.73322839A>G | CA393085920 | HCN4 | c.3254T>C (p.Leu1085Pro) c.2036T>C (p.Leu679Pro) | gnomAD v4 |
| 15 | g.73322839A>T | CA393085922 | HCN4 | c.3254T>A (p.Leu1085His) c.2036T>A (p.Leu679His) | dbSNP gnomAD v4 |
| 15 | g.73322840G>A | CA7648857 | HCN4 | c.3253C>T (p.Leu1085Phe) c.2035C>T (p.Leu679Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322840G>C | CA393085924 | HCN4 | c.3253C>G (p.Leu1085Val) c.2035C>G (p.Leu679Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322840G= | CA2187186772 | HCN4 | c.3253C= (p.Leu1085=) c.2035C= (p.Leu679=) | |
| 15 | g.73322840G>T | CA393085925 | HCN4 | c.3253C>A (p.Leu1085Ile) c.2035C>A (p.Leu679Ile) | gnomAD v4 |
| 15 | g.73322841C>A | CA393085926 | HCN4 | c.3252G>T (p.Lys1084Asn) c.2034G>T (p.Lys678Asn) | gnomAD v4 |
| 15 | g.73322841C= | CA2187186774 | HCN4 | c.3252G= (p.Lys1084=) c.2034G= (p.Lys678=) | |
| 15 | g.73322841C>G | CA393085927 | HCN4 | c.3252G>C (p.Lys1084Asn) c.2034G>C (p.Lys678Asn) | gnomAD v4 |
| 15 | g.73322841C>T | CA272663516 | HCN4 | c.3252G>A (p.Lys1084=) c.2034G>A (p.Lys678=) | dbSNP gnomAD v4 |
| 15 | g.73322842T>A | CA7648858 | HCN4 | c.3251A>T (p.Lys1084Met) c.2033A>T (p.Lys678Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322842T>C | CA393085929 | HCN4 | c.3251A>G (p.Lys1084Arg) c.2033A>G (p.Lys678Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322842T>G | CA393085928 | HCN4 | c.3251A>C (p.Lys1084Thr) c.2033A>C (p.Lys678Thr) | |
| 15 | g.73322842T= | CA2187186777 | HCN4 | c.3251A= (p.Lys1084=) c.2033A= (p.Lys678=) | |
| 15 | g.73322843T>A | CA393085932 | HCN4 | c.3250A>T (p.Lys1084Ter) c.2032A>T (p.Lys678Ter) | |
| 15 | g.73322843T>C | CA393085930 | HCN4 | c.3250A>G (p.Lys1084Glu) c.2032A>G (p.Lys678Glu) | dbSNP gnomAD v4 |
| 15 | g.73322843T>G | CA393085931 | HCN4 | c.3250A>C (p.Lys1084Gln) c.2032A>C (p.Lys678Gln) | |
| 15 | g.73322843T= | CA2187186778 | HCN4 | c.3250A= (p.Lys1084=) c.2032A= (p.Lys678=) | |
| 15 | g.73322844G>A | CA7648859 | HCN4 | c.3249C>T (p.Leu1083=) c.2031C>T (p.Leu677=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73322844G>C | CA491477835 | HCN4 | c.3249C>G (p.Leu1083=) c.2031C>G (p.Leu677=) | |
| 15 | g.73322844G= | CA2187186780 | HCN4 | c.3249C= (p.Leu1083=) c.2031C= (p.Leu677=) | |
| 15 | g.73322844G>T | CA491477836 | HCN4 | c.3249C>A (p.Leu1083=) c.2031C>A (p.Leu677=) | gnomAD v4 |
| 15 | g.73322845A>C | CA393085933 | HCN4 | c.3248T>G (p.Leu1083Arg) c.2030T>G (p.Leu677Arg) | gnomAD v4 |
| 15 | g.73322845A>G | CA393085934 | HCN4 | c.3248T>C (p.Leu1083Pro) c.2030T>C (p.Leu677Pro) | gnomAD v4 |
| 15 | g.73322845A>T | CA393085935 | HCN4 | c.3248T>A (p.Leu1083His) c.2030T>A (p.Leu677His) | gnomAD v4 |
| 15 | g.73322846G>A | CA393085936 | HCN4 | c.3247C>T (p.Leu1083Phe) c.2029C>T (p.Leu677Phe) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322846G>C | CA393085937 | HCN4 | c.3247C>G (p.Leu1083Val) c.2029C>G (p.Leu677Val) | gnomAD v4 |
| 15 | g.73322846G= | CA2187186782 | HCN4 | c.3247C= (p.Leu1083=) c.2029C= (p.Leu677=) | |
| 15 | g.73322846G>T | CA393085938 | HCN4 | c.3247C>A (p.Leu1083Ile) c.2029C>A (p.Leu677Ile) | gnomAD v4 |
| 15 | g.73322847G>A | CA491477838 | HCN4 | c.3246C>T (p.Asp1082=) c.2028C>T (p.Asp676=) | dbSNP gnomAD v4 |
| 15 | g.73322847G>C | CA393085939 | HCN4 | c.3246C>G (p.Asp1082Glu) c.2028C>G (p.Asp676Glu) | |
| 15 | g.73322847G= | CA2187186784 | HCN4 | c.3246C= (p.Asp1082=) c.2028C= (p.Asp676=) | |
| 15 | g.73322847G>T | CA393085940 | HCN4 | c.3246C>A (p.Asp1082Glu) c.2028C>A (p.Asp676Glu) | gnomAD v4 |
| 15 | g.73322848T>A | CA393085941 | HCN4 | c.3245A>T (p.Asp1082Val) c.2027A>T (p.Asp676Val) | |
| 15 | g.73322848T>C | CA393085942 | HCN4 | c.3245A>G (p.Asp1082Gly) c.2027A>G (p.Asp676Gly) | |
| 15 | g.73322848T>G | CA393085943 | HCN4 | c.3245A>C (p.Asp1082Ala) c.2027A>C (p.Asp676Ala) | |
| 15 | g.73322849C>A | CA393085946 | HCN4 | c.3244G>T (p.Asp1082Tyr) c.2026G>T (p.Asp676Tyr) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322849C= | CA2187186786 | HCN4 | c.3244G= (p.Asp1082=) c.2026G= (p.Asp676=) | |
| 15 | g.73322849C>G | CA393085945 | HCN4 | c.3244G>C (p.Asp1082His) c.2026G>C (p.Asp676His) | |
| 15 | g.73322849C>T | CA393085944 | HCN4 | c.3244G>A (p.Asp1082Asn) c.2026G>A (p.Asp676Asn) | gnomAD v4 |
| 15 | g.73322850C>A | CA393085947 | HCN4 | c.3243G>T (p.Gln1081His) c.2025G>T (p.Gln675His) | gnomAD v4 |
| 15 | g.73322850C= | CA2187186789 | HCN4 | c.3243G= (p.Gln1081=) c.2025G= (p.Gln675=) | |
| 15 | g.73322850C>G | CA393085948 | HCN4 | c.3243G>C (p.Gln1081His) c.2025G>C (p.Gln675His) | |
| 15 | g.73322850C>T | CA491477843 | HCN4 | c.3243G>A (p.Gln1081=) c.2025G>A (p.Gln675=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322851T>A | CA393085949 | HCN4 | c.3242A>T (p.Gln1081Leu) c.2024A>T (p.Gln675Leu) | |
| 15 | g.73322851T>C | CA393085950 | HCN4 | c.3242A>G (p.Gln1081Arg) c.2024A>G (p.Gln675Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322851T>G | CA393085951 | HCN4 | c.3242A>C (p.Gln1081Pro) c.2024A>C (p.Gln675Pro) | |
| 15 | g.73322851T= | CA2187186791 | HCN4 | c.3242A= (p.Gln1081=) c.2024A= (p.Gln675=) | |
| 15 | g.73322852G>A | CA393085952 | HCN4 | c.3241C>T (p.Gln1081Ter) c.2023C>T (p.Gln675Ter) | gnomAD v4 |
| 15 | g.73322852G>C | CA393085953 | HCN4 | c.3241C>G (p.Gln1081Glu) c.2023C>G (p.Gln675Glu) | |
| 15 | g.73322852G>T | CA393085954 | HCN4 | c.3241C>A (p.Gln1081Lys) c.2023C>A (p.Gln675Lys) | gnomAD v4 |
| 15 | g.73322853G>A | CA491477846 | HCN4 | c.3240C>T (p.Thr1080=) c.2022C>T (p.Thr674=) | gnomAD v4 |
| 15 | g.73322853G>C | CA491477847 | HCN4 | c.3240C>G (p.Thr1080=) c.2022C>G (p.Thr674=) | |
| 15 | g.73322853G>T | CA491477848 | HCN4 | c.3240C>A (p.Thr1080=) c.2022C>A (p.Thr674=) | gnomAD v4 |