| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.45645426C>A | CA359707528 | HCN1 | c.608G>T (p.Ser203Ile) | |
| 5 | g.45645426C>G | CA359707529 | HCN1 | c.608G>C (p.Ser203Thr) | |
| 5 | g.45645426C>T | CA359707530 | HCN1 | c.608G>A (p.Ser203Asn) | |
| 5 | g.45645427T>A | CA359707531 | HCN1 | c.607A>T (p.Ser203Cys) | |
| 5 | g.45645427T>C | CA359707532 | HCN1 | c.607A>G (p.Ser203Gly) | dbSNP gnomAD v4 |
| 5 | g.45645427T>G | CA359707533 | HCN1 | c.607A>C (p.Ser203Arg) | |
| 5 | g.45645427T= | CA1543790606 | HCN1 | c.607A= (p.Ser203=) | |
| 5 | g.45645428G>A | CA444401827 | HCN1 | c.606C>T (p.Asp202=) | COSMIC |
| 5 | g.45645428G>C | CA359707534 | HCN1 | c.606C>G (p.Asp202Glu) | |
| 5 | g.45645428G>T | CA359707535 | HCN1 | c.606C>A (p.Asp202Glu) | |
| 5 | g.45645429T>A | CA359707536 | HCN1 | c.605A>T (p.Asp202Val) | |
| 5 | g.45645429T>C | CA359707538 | HCN1 | c.605A>G (p.Asp202Gly) | |
| 5 | g.45645429T>G | CA359707537 | HCN1 | c.605A>C (p.Asp202Ala) | |
| 5 | g.45645430C>A | CA359707539 | HCN1 | c.604G>T (p.Asp202Tyr) | |
| 5 | g.45645430C>G | CA359707540 | HCN1 | c.604G>C (p.Asp202His) | |
| 5 | g.45645430C>T | CA359707541 | HCN1 | c.604G>A (p.Asp202Asn) | |
| 5 | g.45645431T>A | CA359707542 | HCN1 | c.603A>T (p.Glu201Asp) | |
| 5 | g.45645431T>C | CA444401828 | HCN1 | c.603A>G (p.Glu201=) | |
| 5 | g.45645431T>G | CA359707543 | HCN1 | c.603A>C (p.Glu201Asp) | |
| 5 | g.45645432T>A | CA359707544 | HCN1 | c.602A>T (p.Glu201Val) | |
| 5 | g.45645432T>C | CA359707545 | HCN1 | c.602A>G (p.Glu201Gly) | |
| 5 | g.45645432T>G | CA359707546 | HCN1 | c.602A>C (p.Glu201Ala) | |
| 5 | g.45645433C>A | CA359707547 | HCN1 | c.601G>T (p.Glu201Ter) | |
| 5 | g.45645433C>G | CA359707548 | HCN1 | c.601G>C (p.Glu201Gln) | |
| 5 | g.45645433C>T | CA359707549 | HCN1 | c.601G>A (p.Glu201Lys) | COSMIC |
| 5 | g.45645434A>C | CA359707550 | HCN1 | c.600T>G (p.Asn200Lys) | |
| 5 | g.45645434A>G | CA444401829 | HCN1 | c.600T>C (p.Asn200=) | |
| 5 | g.45645434A>T | CA359707551 | HCN1 | c.600T>A (p.Asn200Lys) | |
| 5 | g.45645435T>A | CA359707553 | HCN1 | c.599A>T (p.Asn200Ile) | gnomAD v4 |
| 5 | g.45645435T>C | CA3259429 | HCN1 | c.599A>G (p.Asn200Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645435T>G | CA359707552 | HCN1 | c.599A>C (p.Asn200Thr) | |
| 5 | g.45645435T= | CA1543790612 | HCN1 | c.599A= (p.Asn200=) | |
| 5 | g.45645436T>A | CA359707554 | HCN1 | c.598A>T (p.Asn200Tyr) | |
| 5 | g.45645436T>C | CA359707555 | HCN1 | c.598A>G (p.Asn200Asp) | |
| 5 | g.45645436T>G | CA359707556 | HCN1 | c.598A>C (p.Asn200His) | |
| 5 | g.45645437G>A | CA118324610 | HCN1 | c.597C>T (p.Val199=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.45645437G>C | CA444401830 | HCN1 | c.597C>G (p.Val199=) | |
| 5 | g.45645437G= | CA1543790616 | HCN1 | c.597C= (p.Val199=) | |
| 5 | g.45645437G>T | CA444401831 | HCN1 | c.597C>A (p.Val199=) | |
| 5 | g.45645438A>C | CA359707557 | HCN1 | c.596T>G (p.Val199Gly) | |
| 5 | g.45645438A>G | CA359707558 | HCN1 | c.596T>C (p.Val199Ala) | |
| 5 | g.45645438A>T | CA359707559 | HCN1 | c.596T>A (p.Val199Asp) | |
| 5 | g.45645439C>A | CA359707560 | HCN1 | c.595G>T (p.Val199Phe) | |
| 5 | g.45645439C>G | CA359707561 | HCN1 | c.595G>C (p.Val199Leu) | |
| 5 | g.45645439C>T | CA359707562 | HCN1 | c.595G>A (p.Val199Ile) | |
| 5 | g.45645440A>C | CA444401832 | HCN1 | c.594T>G (p.Thr198=) | |
| 5 | g.45645440A>G | CA444401834 | HCN1 | c.594T>C (p.Thr198=) | |
| 5 | g.45645440A>T | CA444401833 | HCN1 | c.594T>A (p.Thr198=) | |
| 5 | g.45645441G>A | CA359707563 | HCN1 | c.593C>T (p.Thr198Ile) | COSMIC |
| 5 | g.45645441G>C | CA359707564 | HCN1 | c.593C>G (p.Thr198Ser) | |
| 5 | g.45645441G>T | CA359707565 | HCN1 | c.593C>A (p.Thr198Asn) | |
| 5 | g.45645442T>A | CA359707568 | HCN1 | c.592A>T (p.Thr198Ser) | |
| 5 | g.45645442T>C | CA359707567 | HCN1 | c.592A>G (p.Thr198Ala) | gnomAD v4 |
| 5 | g.45645442T>G | CA359707566 | HCN1 | c.592A>C (p.Thr198Pro) | |
| 5 | g.45645443C>A | CA444401835 | HCN1 | c.591G>T (p.Gly197=) | |
| 5 | g.45645443C>G | CA444401836 | HCN1 | c.591G>C (p.Gly197=) | |
| 5 | g.45645443C>T | CA444401837 | HCN1 | c.591G>A (p.Gly197=) | |
| 5 | g.45645444C>A | CA359707569 | HCN1 | c.590G>T (p.Gly197Val) | COSMIC |
| 5 | g.45645444C>G | CA359707571 | HCN1 | c.590G>C (p.Gly197Ala) | gnomAD v4 |
| 5 | g.45645444C>T | CA359707570 | HCN1 | c.590G>A (p.Gly197Glu) | |
| 5 | g.45645445C>A | CA359707572 | HCN1 | c.589G>T (p.Gly197Trp) | |
| 5 | g.45645445C>G | CA359707574 | HCN1 | c.589G>C (p.Gly197Arg) | COSMIC |
| 5 | g.45645445C>T | CA359707573 | HCN1 | c.589G>A (p.Gly197Arg) | |
| 5 | g.45645446del | CA2673782209 | HCN1 | c.588del (p.Thr198LeufsTer15) | gnomAD v4 |
| 5 | g.45645446A= | CA1543790619 | HCN1 | c.588T= (p.Thr196=) | |
| 5 | g.45645446A>C | CA444401838 | HCN1 | c.588T>G (p.Thr196=) | |
| 5 | g.45645446A>G | CA444401839 | HCN1 | c.588T>C (p.Thr196=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645446A>T | CA444401840 | HCN1 | c.588T>A (p.Thr196=) | |
| 5 | g.45645447G>A | CA359707575 | HCN1 | c.587C>T (p.Thr196Ile) | |
| 5 | g.45645447G>C | CA359707576 | HCN1 | c.587C>G (p.Thr196Ser) | |
| 5 | g.45645447G>T | CA359707577 | HCN1 | c.587C>A (p.Thr196Asn) | |
| 5 | g.45645448T>A | CA359707578 | HCN1 | c.586A>T (p.Thr196Ser) | |
| 5 | g.45645448T>C | CA359707579 | HCN1 | c.586A>G (p.Thr196Ala) | |
| 5 | g.45645448T>G | CA359707580 | HCN1 | c.586A>C (p.Thr196Pro) | |
| 5 | g.45645449C>A | CA359707581 | HCN1 | c.585G>T (p.Arg195Ser) | ClinVar COSMIC |
| 5 | g.45645449C>G | CA359707582 | HCN1 | c.585G>C (p.Arg195Ser) | |
| 5 | g.45645449C>T | CA444401841 | HCN1 | c.585G>A (p.Arg195=) | |
| 5 | g.45645450C>A | CA359707583 | HCN1 | c.584G>T (p.Arg195Met) | |
| 5 | g.45645450C>G | CA359707584 | HCN1 | c.584G>C (p.Arg195Thr) | |
| 5 | g.45645450C>T | CA359707585 | HCN1 | c.584G>A (p.Arg195Lys) | |
| 5 | g.45645451T>A | CA359707586 | HCN1 | c.583A>T (p.Arg195Trp) | |
| 5 | g.45645451T>C | CA359707587 | HCN1 | c.583A>G (p.Arg195Gly) | |
| 5 | g.45645451T>G | CA444401842 | HCN1 | c.583A>C (p.Arg195=) | COSMIC |
| 5 | g.45645452A>C | CA359707588 | HCN1 | c.582T>G (p.Phe194Leu) | |
| 5 | g.45645452A>G | CA444401843 | HCN1 | c.582T>C (p.Phe194=) | COSMIC |
| 5 | g.45645452A>T | CA359707589 | HCN1 | c.582T>A (p.Phe194Leu) | |
| 5 | g.45645453A>C | CA359707590 | HCN1 | c.581T>G (p.Phe194Cys) | |
| 5 | g.45645453A>G | CA359707591 | HCN1 | c.581T>C (p.Phe194Ser) | |
| 5 | g.45645453A>T | CA359707592 | HCN1 | c.581T>A (p.Phe194Tyr) | |
| 5 | g.45645454A>C | CA359707593 | HCN1 | c.580T>G (p.Phe194Val) | |
| 5 | g.45645454A>G | CA359707594 | HCN1 | c.580T>C (p.Phe194Leu) | |
| 5 | g.45645454A>T | CA359707595 | HCN1 | c.580T>A (p.Phe194Ile) | |
| 5 | g.45645455A>C | CA359707596 | HCN1 | c.579T>G (p.Asn193Lys) | |
| 5 | g.45645455A>G | CA444401844 | HCN1 | c.579T>C (p.Asn193=) | |
| 5 | g.45645455A>T | CA359707597 | HCN1 | c.579T>A (p.Asn193Lys) | |
| 5 | g.45645456T>A | CA359707599 | HCN1 | c.578A>T (p.Asn193Ile) | |
| 5 | g.45645456T>C | CA359707600 | HCN1 | c.578A>G (p.Asn193Ser) | |
| 5 | g.45645456T>G | CA359707598 | HCN1 | c.578A>C (p.Asn193Thr) | |
| 5 | g.45645457T>A | CA359707601 | HCN1 | c.577A>T (p.Asn193Tyr) | |
| 5 | g.45645457T>C | CA359707602 | HCN1 | c.577A>G (p.Asn193Asp) | |
| 5 | g.45645457T>G | CA359707603 | HCN1 | c.577A>C (p.Asn193His) | ClinVar |
| 5 | g.45645458C>A | CA359707604 | HCN1 | c.576G>T (p.Met192Ile) | |
| 5 | g.45645458C>G | CA359707605 | HCN1 | c.576G>C (p.Met192Ile) | COSMIC |
| 5 | g.45645458C>T | CA359707606 | HCN1 | c.576G>A (p.Met192Ile) | COSMIC |
| 5 | g.45645459A>C | CA359707607 | HCN1 | c.575T>G (p.Met192Arg) | |
| 5 | g.45645459A>G | CA359707608 | HCN1 | c.575T>C (p.Met192Thr) | |
| 5 | g.45645459A>T | CA359707609 | HCN1 | c.575T>A (p.Met192Lys) | |
| 5 | g.45645460T>A | CA359707610 | HCN1 | c.574A>T (p.Met192Leu) | gnomAD v4 |
| 5 | g.45645460T>C | CA359707611 | HCN1 | c.574A>G (p.Met192Val) | |
| 5 | g.45645460T>G | CA359707612 | HCN1 | c.574A>C (p.Met192Leu) | |
| 5 | g.45645461G>A | CA444401845 | HCN1 | c.573C>T (p.Ile191=) | COSMIC |
| 5 | g.45645461G>C | CA359707613 | HCN1 | c.573C>G (p.Ile191Met) | |
| 5 | g.45645461G= | CA1543790625 | HCN1 | c.573C= (p.Ile191=) | |
| 5 | g.45645461G>T | CA3259430 | HCN1 | c.573C>A (p.Ile191=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645462A>C | CA359707614 | HCN1 | c.572T>G (p.Ile191Ser) | |
| 5 | g.45645462A>G | CA359707615 | HCN1 | c.572T>C (p.Ile191Thr) | |
| 5 | g.45645462A>T | CA359707616 | HCN1 | c.572T>A (p.Ile191Asn) | |
| 5 | g.45645463T>A | CA359707617 | HCN1 | c.571A>T (p.Ile191Phe) | gnomAD v4 |
| 5 | g.45645463T>C | CA359707618 | HCN1 | c.571A>G (p.Ile191Val) | |
| 5 | g.45645463T>G | CA359707619 | HCN1 | c.571A>C (p.Ile191Leu) | gnomAD v4 |
| 5 | g.45645464C>A | CA444401846 | HCN1 | c.570G>T (p.Leu190=) | |
| 5 | g.45645464C= | CA1543790633 | HCN1 | c.570G= (p.Leu190=) | |
| 5 | g.45645464C>G | CA444401847 | HCN1 | c.570G>C (p.Leu190=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645464C>T | CA3259431 | HCN1 | c.570G>A (p.Leu190=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 5 | g.45645465A>C | CA359707620 | HCN1 | c.569T>G (p.Leu190Arg) | |
| 5 | g.45645465A>G | CA359707621 | HCN1 | c.569T>C (p.Leu190Pro) | |
| 5 | g.45645465A>T | CA359707622 | HCN1 | c.569T>A (p.Leu190Gln) | |
| 5 | g.45645466G>A | CA444401848 | HCN1 | c.568C>T (p.Leu190=) | |
| 5 | g.45645466G>C | CA359707623 | HCN1 | c.568C>G (p.Leu190Val) | |
| 5 | g.45645466G>T | CA359707624 | HCN1 | c.568C>A (p.Leu190Met) | |
| 5 | g.45645467G>A | CA444401849 | HCN1 | c.567C>T (p.Asp189=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.45645467G>C | CA359707625 | HCN1 | c.567C>G (p.Asp189Glu) | |
| 5 | g.45645467G= | CA1543790639 | HCN1 | c.567C= (p.Asp189=) | |
| 5 | g.45645467G>T | CA359707626 | HCN1 | c.567C>A (p.Asp189Glu) | |
| 5 | g.45645468T>A | CA359707629 | HCN1 | c.566A>T (p.Asp189Val) | |
| 5 | g.45645468T>C | CA359707628 | HCN1 | c.566A>G (p.Asp189Gly) | |
| 5 | g.45645468T>G | CA359707627 | HCN1 | c.566A>C (p.Asp189Ala) | |
| 5 | g.45645469C>A | CA359707631 | HCN1 | c.565G>T (p.Asp189Tyr) | |
| 5 | g.45645469C>G | CA359707630 | HCN1 | c.565G>C (p.Asp189His) | |
| 5 | g.45645469C>T | CA359707632 | HCN1 | c.565G>A (p.Asp189Asn) | |
| 5 | g.45645470C>A | CA359707633 | HCN1 | c.564G>T (p.Leu188Phe) | dbSNP |
| 5 | g.45645470C= | CA1543790641 | HCN1 | c.564G= (p.Leu188=) | |
| 5 | g.45645470C>G | CA359707634 | HCN1 | c.564G>C (p.Leu188Phe) | |
| 5 | g.45645470C>T | CA444401850 | HCN1 | c.564G>A (p.Leu188=) | ClinVar gnomAD v4 |
| 5 | g.45645471A>C | CA359707635 | HCN1 | c.563T>G (p.Leu188Trp) | |
| 5 | g.45645471A>G | CA359707636 | HCN1 | c.563T>C (p.Leu188Ser) | |
| 5 | g.45645471A>T | CA359707637 | HCN1 | c.563T>A (p.Leu188Ter) | |
| 5 | g.45645472A>C | CA359707638 | HCN1 | c.562T>G (p.Leu188Val) | |
| 5 | g.45645472A>G | CA444401851 | HCN1 | c.562T>C (p.Leu188=) | gnomAD v4 |
| 5 | g.45645472A>T | CA359707639 | HCN1 | c.562T>A (p.Leu188Met) | |
| 5 | g.45645473T>A | CA444401852 | HCN1 | c.561A>T (p.Leu187=) | gnomAD v4 |
| 5 | g.45645473T>C | CA3259432 | HCN1 | c.561A>G (p.Leu187=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645473T>G | CA444401853 | HCN1 | c.561A>C (p.Leu187=) | |
| 5 | g.45645473T= | CA1543790643 | HCN1 | c.561A= (p.Leu187=) | |
| 5 | g.45645474A>C | CA359707640 | HCN1 | c.560T>G (p.Leu187Arg) | COSMIC |
| 5 | g.45645474A>G | CA359707641 | HCN1 | c.560T>C (p.Leu187Pro) | COSMIC |
| 5 | g.45645474A>T | CA359707642 | HCN1 | c.560T>A (p.Leu187Gln) | |
| 5 | g.45645475G>A | CA444401854 | HCN1 | c.559C>T (p.Leu187=) | |
| 5 | g.45645475G>C | CA359707643 | HCN1 | c.559C>G (p.Leu187Val) | |
| 5 | g.45645475G>T | CA359707644 | HCN1 | c.559C>A (p.Leu187Ile) | |
| 5 | g.45645476G>A | CA444401855 | HCN1 | c.558C>T (p.Phe186=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 5 | g.45645476G>C | CA16611854 | HCN1 | c.558C>G (p.Phe186Leu) | ClinVar dbSNP |
| 5 | g.45645476G= | CA1543790651 | HCN1 | c.558C= (p.Phe186=) | |
| 5 | g.45645476G>T | CA359707645 | HCN1 | c.558C>A (p.Phe186Leu) | |
| 5 | g.45645477A>C | CA359707646 | HCN1 | c.557T>G (p.Phe186Cys) | |
| 5 | g.45645477A>G | CA359707647 | HCN1 | c.557T>C (p.Phe186Ser) | |
| 5 | g.45645477A>T | CA359707648 | HCN1 | c.557T>A (p.Phe186Tyr) | |
| 5 | g.45645478A>C | CA359707649 | HCN1 | c.556T>G (p.Phe186Val) | |
| 5 | g.45645478A>G | CA359707650 | HCN1 | c.556T>C (p.Phe186Leu) | |
| 5 | g.45645478A>T | CA359707651 | HCN1 | c.556T>A (p.Phe186Ile) | COSMIC |
| 5 | g.45645479A>C | CA444401858 | HCN1 | c.555T>G (p.Val185=) | |
| 5 | g.45645479A>G | CA444401856 | HCN1 | c.555T>C (p.Val185=) | |
| 5 | g.45645479A>T | CA444401857 | HCN1 | c.555T>A (p.Val185=) | |
| 5 | g.45645480A>C | CA359707652 | HCN1 | c.554T>G (p.Val185Gly) | |
| 5 | g.45645480A>G | CA359707653 | HCN1 | c.554T>C (p.Val185Ala) | |
| 5 | g.45645480A>T | CA359707654 | HCN1 | c.554T>A (p.Val185Asp) | |
| 5 | g.45645481C>A | CA359707655 | HCN1 | c.553G>T (p.Val185Phe) | |
| 5 | g.45645481C>G | CA359707656 | HCN1 | c.553G>C (p.Val185Leu) | |
| 5 | g.45645481C>T | CA359707657 | HCN1 | c.553G>A (p.Val185Ile) | |
| 5 | g.45645482T>A | CA444401859 | HCN1 | c.552A>T (p.Thr184=) | |
| 5 | g.45645482T>C | CA444401861 | HCN1 | c.552A>G (p.Thr184=) | |
| 5 | g.45645482T>G | CA444401860 | HCN1 | c.552A>C (p.Thr184=) | |
| 5 | g.45645483G>A | CA359707660 | HCN1 | c.551C>T (p.Thr184Ile) | |
| 5 | g.45645483G>C | CA359707659 | HCN1 | c.551C>G (p.Thr184Arg) | |
| 5 | g.45645483G>T | CA359707658 | HCN1 | c.551C>A (p.Thr184Lys) | |
| 5 | g.45645484T>A | CA359707661 | HCN1 | c.550A>T (p.Thr184Ser) | |
| 5 | g.45645484T>C | CA359707662 | HCN1 | c.550A>G (p.Thr184Ala) | |
| 5 | g.45645484T>G | CA359707663 | HCN1 | c.550A>C (p.Thr184Pro) | |
| 5 | g.45645485A= | CA1543790657 | HCN1 | c.549T= (p.Asp183=) | |
| 5 | g.45645485A>C | CA359707664 | HCN1 | c.549T>G (p.Asp183Glu) | |
| 5 | g.45645485A>G | CA118324611 | HCN1 | c.549T>C (p.Asp183=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.45645485A>T | CA359707665 | HCN1 | c.549T>A (p.Asp183Glu) | |
| 5 | g.45645486T>A | CA359707666 | HCN1 | c.548A>T (p.Asp183Val) | |
| 5 | g.45645486T>C | CA359707667 | HCN1 | c.548A>G (p.Asp183Gly) | |
| 5 | g.45645486T>G | CA359707668 | HCN1 | c.548A>C (p.Asp183Ala) | |
| 5 | g.45645487C>A | CA359707669 | HCN1 | c.547G>T (p.Asp183Tyr) | |
| 5 | g.45645487C>G | CA359707670 | HCN1 | c.547G>C (p.Asp183His) | COSMIC |
| 5 | g.45645487C>T | CA359707671 | HCN1 | c.547G>A (p.Asp183Asn) | COSMIC |
| 5 | g.45645488T>A | CA444401393 | HCN1 | c.546A>T (p.Ser182=) | |
| 5 | g.45645488T>C | CA3259433 | HCN1 | c.546A>G (p.Ser182=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645488T>G | CA444401395 | HCN1 | c.546A>C (p.Ser182=) | |
| 5 | g.45645488T= | CA1543790662 | HCN1 | c.546A= (p.Ser182=) | |
| 5 | g.45645489G>A | CA359707674 | HCN1 | c.545C>T (p.Ser182Leu) | |
| 5 | g.45645489G>C | CA359707673 | HCN1 | c.545C>G (p.Ser182Ter) | |
| 5 | g.45645489G>T | CA359707672 | HCN1 | c.545C>A (p.Ser182Ter) | |
| 5 | g.45645490A>C | CA359707675 | HCN1 | c.544T>G (p.Ser182Ala) | |
| 5 | g.45645490A>G | CA359707676 | HCN1 | c.544T>C (p.Ser182Pro) | |
| 5 | g.45645490A>T | CA359707677 | HCN1 | c.544T>A (p.Ser182Thr) | |
| 5 | g.45645491T>A | CA444401398 | HCN1 | c.543A>T (p.Ala181=) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.45645491T>C | CA3259434 | HCN1 | c.543A>G (p.Ala181=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.45645491T>G | CA444401399 | HCN1 | c.543A>C (p.Ala181=) | |
| 5 | g.45645491T= | CA1543790667 | HCN1 | c.543A= (p.Ala181=) | |
| 5 | g.45645492G>A | CA359707678 | HCN1 | c.542C>T (p.Ala181Val) | |
| 5 | g.45645492G>C | CA359707679 | HCN1 | c.542C>G (p.Ala181Gly) | |
| 5 | g.45645492G>T | CA359707680 | HCN1 | c.542C>A (p.Ala181Glu) | |
| 5 | g.45645493C>A | CA359707681 | HCN1 | c.541G>T (p.Ala181Ser) | dbSNP gnomAD v4 COSMIC |
| 5 | g.45645493C= | CA1543790672 | HCN1 | c.541G= (p.Ala181=) | |
| 5 | g.45645493C>G | CA359707682 | HCN1 | c.541G>C (p.Ala181Pro) | |
| 5 | g.45645493C>T | CA359707683 | HCN1 | c.541G>A (p.Ala181Thr) | |
| 5 | g.45645494C>A | CA444401401 | HCN1 | c.540G>T (p.Val180=) | |
| 5 | g.45645494C>G | CA444401403 | HCN1 | c.540G>C (p.Val180=) | |
| 5 | g.45645494C>T | CA444401405 | HCN1 | c.540G>A (p.Val180=) | gnomAD v4 COSMIC |
| 5 | g.45645495A>C | CA359707684 | HCN1 | c.539T>G (p.Val180Gly) | |
| 5 | g.45645495A>G | CA359707685 | HCN1 | c.539T>C (p.Val180Ala) | |
| 5 | g.45645495A>T | CA359707686 | HCN1 | c.539T>A (p.Val180Glu) | |
| 5 | g.45645496C>A | CA359707688 | HCN1 | c.538G>T (p.Val180Leu) | dbSNP |
| 5 | g.45645496C>G | CA359707689 | HCN1 | c.538G>C (p.Val180Leu) | |
| 5 | g.45645496C>T | CA359707687 | HCN1 | c.538G>A (p.Val180Met) | |
| 5 | g.45645497A= | CA1543790679 | HCN1 | c.537T= (p.Asn179=) | |
| 5 | g.45645497A>C | CA359707690 | HCN1 | c.537T>G (p.Asn179Lys) | |
| 5 | g.45645497A>G | CA118324612 | HCN1 | c.537T>C (p.Asn179=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645497A>T | CA359707691 | HCN1 | c.537T>A (p.Asn179Lys) | |
| 5 | g.45645498T>A | CA359707692 | HCN1 | c.536A>T (p.Asn179Ile) | |
| 5 | g.45645498T>C | CA359707693 | HCN1 | c.536A>G (p.Asn179Ser) | dbSNP |
| 5 | g.45645498T>G | CA359707694 | HCN1 | c.536A>C (p.Asn179Thr) | |
| 5 | g.45645498T= | CA1543790694 | HCN1 | c.536A= (p.Asn179=) | |
| 5 | g.45645499T>A | CA359707695 | HCN1 | c.535A>T (p.Asn179Tyr) | ClinVar |
| 5 | g.45645499T>C | CA359707696 | HCN1 | c.535A>G (p.Asn179Asp) | |
| 5 | g.45645499T>G | CA359707697 | HCN1 | c.535A>C (p.Asn179His) | |
| 5 | g.45645500G>A | CA444401412 | HCN1 | c.534C>T (p.Phe178=) | |
| 5 | g.45645500G>C | CA359707698 | HCN1 | c.534C>G (p.Phe178Leu) | |
| 5 | g.45645500G>T | CA359707699 | HCN1 | c.534C>A (p.Phe178Leu) | |
| 5 | g.45645501A>C | CA359707700 | HCN1 | c.533T>G (p.Phe178Cys) | |
| 5 | g.45645501A>G | CA359707702 | HCN1 | c.533T>C (p.Phe178Ser) | |
| 5 | g.45645501A>T | CA359707701 | HCN1 | c.533T>A (p.Phe178Tyr) | |
| 5 | g.45645502A>C | CA359707703 | HCN1 | c.532T>G (p.Phe178Val) | |
| 5 | g.45645502A>G | CA359707704 | HCN1 | c.532T>C (p.Phe178Leu) | |
| 5 | g.45645502A>T | CA359707705 | HCN1 | c.532T>A (p.Phe178Ile) | |
| 5 | g.45645503A>C | CA359707706 | HCN1 | c.531T>G (p.Ile177Met) | |
| 5 | g.45645503A>G | CA444401415 | HCN1 | c.531T>C (p.Ile177=) | |
| 5 | g.45645503A>T | CA444401416 | HCN1 | c.531T>A (p.Ile177=) | |
| 5 | g.45645504A>C | CA359707707 | HCN1 | c.530T>G (p.Ile177Ser) | |
| 5 | g.45645504A>G | CA359707709 | HCN1 | c.530T>C (p.Ile177Thr) | ClinVar |
| 5 | g.45645504A>T | CA359707708 | HCN1 | c.530T>A (p.Ile177Asn) | |
| 5 | g.45645505T>A | CA359707710 | HCN1 | c.529A>T (p.Ile177Phe) | |
| 5 | g.45645505T>C | CA359707711 | HCN1 | c.529A>G (p.Ile177Val) | |
| 5 | g.45645505T>G | CA359707712 | HCN1 | c.529A>C (p.Ile177Leu) | |
| 5 | g.45645506A= | CA1543790702 | HCN1 | c.528T= (p.Ile176=) | |
| 5 | g.45645506A>C | CA359707713 | HCN1 | c.528T>G (p.Ile176Met) | |
| 5 | g.45645506A>G | CA232345 | HCN1 | c.528T>C (p.Ile176=) | ClinVar dbSNP |
| 5 | g.45645506A>T | CA444401421 | HCN1 | c.528T>A (p.Ile176=) | |
| 5 | g.45645507A>C | CA359707714 | HCN1 | c.527T>G (p.Ile176Ser) | |
| 5 | g.45645507A>G | CA359707715 | HCN1 | c.527T>C (p.Ile176Thr) | |
| 5 | g.45645507A>T | CA359707716 | HCN1 | c.527T>A (p.Ile176Asn) | |
| 5 | g.45645508T>A | CA359707717 | HCN1 | c.526A>T (p.Ile176Phe) | |
| 5 | g.45645508T>C | CA359707718 | HCN1 | c.526A>G (p.Ile176Val) | COSMIC |
| 5 | g.45645508T>G | CA359707719 | HCN1 | c.526A>C (p.Ile176Leu) | |
| 5 | g.45645509C>A | CA359707720 | HCN1 | c.525G>T (p.Trp175Cys) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.45645509C= | CA1543790712 | HCN1 | c.525G= (p.Trp175=) | |
| 5 | g.45645509C>G | CA359707722 | HCN1 | c.525G>C (p.Trp175Cys) | |
| 5 | g.45645509C>T | CA359707721 | HCN1 | c.525G>A (p.Trp175Ter) | COSMIC |
| 5 | g.45645510C>A | CA359707723 | HCN1 | c.524G>T (p.Trp175Leu) | |
| 5 | g.45645510C>G | CA359707724 | HCN1 | c.524G>C (p.Trp175Ser) | |
| 5 | g.45645510C>T | CA359707725 | HCN1 | c.524G>A (p.Trp175Ter) | COSMIC |
| 5 | g.45645511A>C | CA359707726 | HCN1 | c.523T>G (p.Trp175Gly) | |
| 5 | g.45645511A>G | CA359707727 | HCN1 | c.523T>C (p.Trp175Arg) | ClinVar |
| 5 | g.45645511A>T | CA359707728 | HCN1 | c.523T>A (p.Trp175Arg) | |
| 5 | g.45645512T>A | CA444401428 | HCN1 | c.522A>T (p.Pro174=) | |
| 5 | g.45645512T>C | CA444401429 | HCN1 | c.522A>G (p.Pro174=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645512T>G | CA444401430 | HCN1 | c.522A>C (p.Pro174=) | |
| 5 | g.45645512T= | CA1543790717 | HCN1 | c.522A= (p.Pro174=) | |
| 5 | g.45645513G>A | CA359707729 | HCN1 | c.521C>T (p.Pro174Leu) | gnomAD v4 |
| 5 | g.45645513G>C | CA359707730 | HCN1 | c.521C>G (p.Pro174Arg) | |
| 5 | g.45645513G>T | CA359707731 | HCN1 | c.521C>A (p.Pro174Gln) | |
| 5 | g.45645514G>A | CA359707732 | HCN1 | c.520C>T (p.Pro174Ser) | gnomAD v4 COSMIC |
| 5 | g.45645514G>C | CA359707733 | HCN1 | c.520C>G (p.Pro174Ala) | |
| 5 | g.45645514G>T | CA359707734 | HCN1 | c.520C>A (p.Pro174Thr) | gnomAD v4 |
| 5 | g.45645515T>A | CA118324613 | HCN1 | c.519A>T (p.Thr173=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645515T>C | CA444401434 | HCN1 | c.519A>G (p.Thr173=) | |
| 5 | g.45645515T>G | CA444401435 | HCN1 | c.519A>C (p.Thr173=) | |
| 5 | g.45645515T= | CA1543790723 | HCN1 | c.519A= (p.Thr173=) | |
| 5 | g.45645522_45645524del | CA2578305118 | HCN1 | c.517_519del (p.Thr173del) | |
| 5 | g.45645516G>A | CA359707737 | HCN1 | c.518C>T (p.Thr173Ile) | |
| 5 | g.45645516G>C | CA359707735 | HCN1 | c.518C>G (p.Thr173Arg) | |
| 5 | g.45645516G>T | CA359707736 | HCN1 | c.518C>A (p.Thr173Lys) | gnomAD v4 |
| 5 | g.45645517T>A | CA359707738 | HCN1 | c.517A>T (p.Thr173Ser) | |
| 5 | g.45645517T>C | CA359707739 | HCN1 | c.517A>G (p.Thr173Ala) | dbSNP |
| 5 | g.45645517T>G | CA359707740 | HCN1 | c.517A>C (p.Thr173Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645517T= | CA1543790726 | HCN1 | c.517A= (p.Thr173=) | |
| 5 | g.45645518T>A | CA444401438 | HCN1 | c.516A>T (p.Thr172=) | |
| 5 | g.45645518T>C | CA444401439 | HCN1 | c.516A>G (p.Thr172=) | |
| 5 | g.45645518T>G | CA444401440 | HCN1 | c.516A>C (p.Thr172=) | |
| 5 | g.45645519G>A | CA359707741 | HCN1 | c.515C>T (p.Thr172Ile) | |
| 5 | g.45645519G>C | CA359707742 | HCN1 | c.515C>G (p.Thr172Arg) | |
| 5 | g.45645519G>T | CA359707743 | HCN1 | c.515C>A (p.Thr172Lys) | gnomAD v4 |
| 5 | g.45645520T>A | CA359707744 | HCN1 | c.514A>T (p.Thr172Ser) | |
| 5 | g.45645520T>C | CA359707745 | HCN1 | c.514A>G (p.Thr172Ala) | dbSNP gnomAD v4 |
| 5 | g.45645520T>G | CA359707746 | HCN1 | c.514A>C (p.Thr172Pro) | |
| 5 | g.45645520T= | CA1543790729 | HCN1 | c.514A= (p.Thr172=) | |
| 5 | g.45645521T>A | CA444401443 | HCN1 | c.513A>T (p.Thr171=) | |
| 5 | g.45645521T>C | CA444401444 | HCN1 | c.513A>G (p.Thr171=) | |
| 5 | g.45645521T>G | CA444401445 | HCN1 | c.513A>C (p.Thr171=) | |
| 5 | g.45645522G>A | CA359707747 | HCN1 | c.512C>T (p.Thr171Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645522G>C | CA359707748 | HCN1 | c.512C>G (p.Thr171Arg) | |
| 5 | g.45645522G= | CA1543790733 | HCN1 | c.512C= (p.Thr171=) | |
| 5 | g.45645522G>T | CA359707749 | HCN1 | c.512C>A (p.Thr171Lys) | |
| 5 | g.45645523T>A | CA359707752 | HCN1 | c.511A>T (p.Thr171Ser) | |
| 5 | g.45645523T>C | CA359707751 | HCN1 | c.511A>G (p.Thr171Ala) | |
| 5 | g.45645523T>G | CA359707750 | HCN1 | c.511A>C (p.Thr171Pro) | |
| 5 | g.45645524T>A | CA359707754 | HCN1 | c.510A>T (p.Gln170His) | |
| 5 | g.45645524T>C | CA444401446 | HCN1 | c.510A>G (p.Gln170=) | dbSNP gnomAD v4 |
| 5 | g.45645524T>G | CA359707753 | HCN1 | c.510A>C (p.Gln170His) | |
| 5 | g.45645524T= | CA1543790740 | HCN1 | c.510A= (p.Gln170=) | |
| 5 | g.45645525T>A | CA359707757 | HCN1 | c.509A>T (p.Gln170Leu) | |
| 5 | g.45645525T>C | CA359707755 | HCN1 | c.509A>G (p.Gln170Arg) | |
| 5 | g.45645525T>G | CA359707756 | HCN1 | c.509A>C (p.Gln170Pro) | |
| 5 | g.45645526G>A | CA359707758 | HCN1 | c.508C>T (p.Gln170Ter) | |
| 5 | g.45645526G>C | CA359707759 | HCN1 | c.508C>G (p.Gln170Glu) | |
| 5 | g.45645526G>T | CA359707760 | HCN1 | c.508C>A (p.Gln170Lys) | ClinVar gnomAD v4 |