15 | g.73367699T>A | CA393097596 | HCN4 | c.572A>T (p.Glu191Val)
| |
15 | g.73367699T>C | CA393097597 | HCN4 | c.572A>G (p.Glu191Gly)
| ClinVar |
15 | g.73367699T>G | CA393097598 | HCN4 | c.572A>C (p.Glu191Ala)
| |
15 | g.73367700C>A | CA393097600 | HCN4 | c.571G>T (p.Glu191Ter)
| |
15 | g.73367700C>G | CA393097602 | HCN4 | c.571G>C (p.Glu191Gln)
| ClinVar dbSNP |
15 | g.73367700C>T | CA393097604 | HCN4 | c.571G>A (p.Glu191Lys)
| |
15 | g.73367701del | CA2841625088 | HCN4 | c.571del (p.Glu191ArgfsTer?)
| |
15 | g.73367701C>A | CA491479545 | HCN4 | c.570G>T (p.Val190=)
| gnomAD v4 |
15 | g.73367701C>G | CA491479547 | HCN4 | c.570G>C (p.Val190=)
| |
15 | g.73367701C>T | CA491479546 | HCN4 | c.570G>A (p.Val190=)
| |
15 | g.73367702A= | CA2187194508 | HCN4 | c.569T= (p.Val190=)
| |
15 | g.73367702A>C | CA393097605 | HCN4 | c.569T>G (p.Val190Gly)
| ClinVar gnomAD v4 |
15 | g.73367702A>G | CA393097606 | HCN4 | c.569T>C (p.Val190Ala)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367702A>T | CA236707 | HCN4 | c.569T>A (p.Val190Glu)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367703C>A | CA393097608 | HCN4 | c.568G>T (p.Val190Leu)
| |
15 | g.73367703C= | CA2187194509 | HCN4 | c.568G= (p.Val190=)
| |
15 | g.73367703C>G | CA393097610 | HCN4 | c.568G>C (p.Val190Leu)
| |
15 | g.73367703C>T | CA393097612 | HCN4 | c.568G>A (p.Val190Met)
| dbSNP |
15 | g.73367704T>A | CA393097615 | HCN4 | c.567A>T (p.Lys189Asn)
| |
15 | g.73367704T>C | CA491479548 | HCN4 | c.567A>G (p.Lys189=)
| |
15 | g.73367704T>G | CA393097613 | HCN4 | c.567A>C (p.Lys189Asn)
| ClinVar dbSNP |
15 | g.73367704T= | CA2187194510 | HCN4 | c.567A= (p.Lys189=)
| |
15 | g.73367706del | CA2841625089 | HCN4 | c.567del (p.Val190TrpfsTer?)
| |
15 | g.73367705T>A | CA393097617 | HCN4 | c.566A>T (p.Lys189Ile)
| |
15 | g.73367705T>C | CA7649459 | HCN4 | c.566A>G (p.Lys189Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367705T>G | CA393097618 | HCN4 | c.566A>C (p.Lys189Thr)
| |
15 | g.73367705T= | CA2187194511 | HCN4 | c.566A= (p.Lys189=)
| |
15 | g.73367706T>A | CA393097621 | HCN4 | c.565A>T (p.Lys189Ter)
| |
15 | g.73367706T>C | CA393097623 | HCN4 | c.565A>G (p.Lys189Glu)
| ClinVar gnomAD v4 |
15 | g.73367706T>G | CA393097624 | HCN4 | c.565A>C (p.Lys189Gln)
| dbSNP gnomAD v4 |
15 | g.73367706T= | CA2187194512 | HCN4 | c.565A= (p.Lys189=)
| |
15 | g.73367707G>A | CA491479549 | HCN4 | c.564C>T (p.Ile188=)
| |
15 | g.73367707G>C | CA393097625 | HCN4 | c.564C>G (p.Ile188Met)
| gnomAD v4 |
15 | g.73367707G>T | CA491479550 | HCN4 | c.564C>A (p.Ile188=)
| |
15 | g.73367708A>C | CA393097628 | HCN4 | c.563T>G (p.Ile188Ser)
| |
15 | g.73367708A>G | CA393097629 | HCN4 | c.563T>C (p.Ile188Thr)
| |
15 | g.73367708A>T | CA393097631 | HCN4 | c.563T>A (p.Ile188Asn)
| |
15 | g.73367709T>A | CA393097632 | HCN4 | c.562A>T (p.Ile188Phe)
| |
15 | g.73367709T>C | CA7649460 | HCN4 | c.562A>G (p.Ile188Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73367709T>G | CA393097634 | HCN4 | c.562A>C (p.Ile188Leu)
| |
15 | g.73367709T= | CA2187194513 | HCN4 | c.562A= (p.Ile188=)
| |
15 | g.73367710A= | CA2187194514 | HCN4 | c.561T= (p.Ala187=)
| |
15 | g.73367710A>C | CA491479551 | HCN4 | c.561T>G (p.Ala187=)
| |
15 | g.73367710A>G | CA7649461 | HCN4 | c.561T>C (p.Ala187=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367710A>T | CA491479552 | HCN4 | c.561T>A (p.Ala187=)
| |
15 | g.73367711G>A | CA393097639 | HCN4 | c.560C>T (p.Ala187Val)
| dbSNP |
15 | g.73367711G>C | CA393097637 | HCN4 | c.560C>G (p.Ala187Gly)
| |
15 | g.73367711G= | CA2187194515 | HCN4 | c.560C= (p.Ala187=)
| |
15 | g.73367711G>T | CA7649462 | HCN4 | c.560C>A (p.Ala187Asp)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73367712C>A | CA393097641 | HCN4 | c.559G>T (p.Ala187Ser)
| ClinVar |
15 | g.73367712C= | CA2187194516 | HCN4 | c.559G= (p.Ala187=)
| |
15 | g.73367712C>G | CA393097643 | HCN4 | c.559G>C (p.Ala187Pro)
| |
15 | g.73367712C>T | CA087867 | HCN4 | c.559G>A (p.Ala187Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367713G>A | CA491479553 | HCN4 | c.558C>T (p.Thr186=)
| |
15 | g.73367713G>C | CA491479554 | HCN4 | c.558C>G (p.Thr186=)
| ClinVar dbSNP |
15 | g.73367713G>T | CA491479555 | HCN4 | c.558C>A (p.Thr186=)
| dbSNP |
15 | g.73367714G>A | CA393097645 | HCN4 | c.557C>T (p.Thr186Ile)
| gnomAD v4 |
15 | g.73367714G>C | CA393097646 | HCN4 | c.557C>G (p.Thr186Ser)
| |
15 | g.73367714G>T | CA393097647 | HCN4 | c.557C>A (p.Thr186Asn)
| |
15 | g.73367715T>A | CA393097648 | HCN4 | c.556A>T (p.Thr186Ser)
| |
15 | g.73367715T>C | CA393097650 | HCN4 | c.556A>G (p.Thr186Ala)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367715T>G | CA393097651 | HCN4 | c.556A>C (p.Thr186Pro)
| |
15 | g.73367715T= | CA2187194517 | HCN4 | c.556A= (p.Thr186=)
| |
15 | g.73367716G>A | CA272700221 | HCN4 | c.555C>T (p.Asp185=)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367716G>C | CA393097653 | HCN4 | c.555C>G (p.Asp185Glu)
| |
15 | g.73367716G= | CA2187194518 | HCN4 | c.555C= (p.Asp185=)
| |
15 | g.73367716G>T | CA393097654 | HCN4 | c.555C>A (p.Asp185Glu)
| |
15 | g.73367717T>A | CA393097656 | HCN4 | c.554A>T (p.Asp185Val)
| |
15 | g.73367717T>C | CA393097658 | HCN4 | c.554A>G (p.Asp185Gly)
| |
15 | g.73367717T>G | CA393097655 | HCN4 | c.554A>C (p.Asp185Ala)
| |
15 | g.73367718C>A | CA393097660 | HCN4 | c.553G>T (p.Asp185Tyr)
| |
15 | g.73367718C>G | CA393097661 | HCN4 | c.553G>C (p.Asp185His)
| |
15 | g.73367718C>T | CA393097663 | HCN4 | c.553G>A (p.Asp185Asn)
| |
15 | g.73367719C>A | CA491479556 | HCN4 | c.552G>T (p.Val184=)
| |
15 | g.73367719C>G | CA491479557 | HCN4 | c.552G>C (p.Val184=)
| |
15 | g.73367719C>T | CA491479558 | HCN4 | c.552G>A (p.Val184=)
| |
15 | g.73367720A>C | CA393097665 | HCN4 | c.551T>G (p.Val184Gly)
| |
15 | g.73367720A>G | CA393097667 | HCN4 | c.551T>C (p.Val184Ala)
| |
15 | g.73367720A>T | CA393097668 | HCN4 | c.551T>A (p.Val184Glu)
| |
15 | g.73367721C>A | CA393097670 | HCN4 | c.550G>T (p.Val184Leu)
| |
15 | g.73367721C= | CA2187194519 | HCN4 | c.550G= (p.Val184=)
| |
15 | g.73367721C>G | CA393097671 | HCN4 | c.550G>C (p.Val184Leu)
| |
15 | g.73367721C>T | CA393097672 | HCN4 | c.550G>A (p.Val184Met)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73367722C>A | CA7649463 | HCN4 | c.549G>T (p.Ser183=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367722C= | CA2187194520 | HCN4 | c.549G= (p.Ser183=)
| |
15 | g.73367722C>G | CA491479559 | HCN4 | c.549G>C (p.Ser183=)
| |
15 | g.73367722C>T | CA491479560 | HCN4 | c.549G>A (p.Ser183=)
| gnomAD v4 |
15 | g.73367723G>A | CA272700245 | HCN4 | c.548C>T (p.Ser183Leu)
| dbSNP gnomAD v4 |
15 | g.73367723G>C | CA393097674 | HCN4 | c.548C>G (p.Ser183Trp)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73367723G= | CA2187194521 | HCN4 | c.548C= (p.Ser183=)
| |
15 | g.73367723G>T | CA393097676 | HCN4 | c.548C>A (p.Ser183Ter)
| |
15 | g.73367724A>C | CA393097679 | HCN4 | c.547T>G (p.Ser183Ala)
| |
15 | g.73367724A>G | CA393097678 | HCN4 | c.547T>C (p.Ser183Pro)
| |
15 | g.73367724A>T | CA393097677 | HCN4 | c.547T>A (p.Ser183Thr)
| |
15 | g.73367725G>A | CA491479561 | HCN4 | c.546C>T (p.Pro182=)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367725G>C | CA7649464 | HCN4 | c.546C>G (p.Pro182=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73367725G= | CA2187194522 | HCN4 | c.546C= (p.Pro182=)
| |
15 | g.73367725G>T | CA491479562 | HCN4 | c.546C>A (p.Pro182=)
| |
15 | g.73367727del | CA2629389814 | HCN4 | c.546del (p.Ser183ArgfsTer?)
| gnomAD v4 |
15 | g.73367726G>A | CA7649465 | HCN4 | c.545C>T (p.Pro182Leu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73367726G>C | CA393097681 | HCN4 | c.545C>G (p.Pro182Arg)
| |
15 | g.73367726G= | CA2187194523 | HCN4 | c.545C= (p.Pro182=)
| |
15 | g.73367726G>T | CA393097683 | HCN4 | c.545C>A (p.Pro182His)
| |
15 | g.73367732_73367755dup | CA2629389815 | HCN4 | c.522_545dup (p.Pro182_Ser183insAlaSerAlaSerCysGluGlnPro)
| gnomAD v4 |
15 | g.73367727G>A | CA393097685 | HCN4 | c.544C>T (p.Pro182Ser)
| gnomAD v4 |
15 | g.73367727G>C | CA393097687 | HCN4 | c.544C>G (p.Pro182Ala)
| |
15 | g.73367727G>T | CA393097688 | HCN4 | c.544C>A (p.Pro182Thr)
| |
15 | g.73367728C>A | CA393097689 | HCN4 | c.543G>T (p.Gln181His)
| gnomAD v4 |
15 | g.73367728C>G | CA393097691 | HCN4 | c.543G>C (p.Gln181His)
| |
15 | g.73367728C>T | CA491479563 | HCN4 | c.543G>A (p.Gln181=)
| dbSNP gnomAD v4 |
15 | g.73367729T>A | CA393097693 | HCN4 | c.542A>T (p.Gln181Leu)
| ClinVar dbSNP |
15 | g.73367729T>C | CA393097695 | HCN4 | c.542A>G (p.Gln181Arg)
| |
15 | g.73367729T>G | CA393097696 | HCN4 | c.542A>C (p.Gln181Pro)
| |
15 | g.73367729T= | CA2187194524 | HCN4 | c.542A= (p.Gln181=)
| |
15 | g.73367730G>A | CA393097699 | HCN4 | c.541C>T (p.Gln181Ter)
| gnomAD v4 |
15 | g.73367730G>C | CA393097698 | HCN4 | c.541C>G (p.Gln181Glu)
| ClinVar dbSNP |
15 | g.73367730G>T | CA393097697 | HCN4 | c.541C>A (p.Gln181Lys)
| gnomAD v4 |
15 | g.73367731C>A | CA393097700 | HCN4 | c.540G>T (p.Glu180Asp)
| |
15 | g.73367731C>G | CA393097702 | HCN4 | c.540G>C (p.Glu180Asp)
| |
15 | g.73367731C>T | CA491479564 | HCN4 | c.540G>A (p.Glu180=)
| |
15 | g.73367732T>A | CA393097703 | HCN4 | c.539A>T (p.Glu180Val)
| |
15 | g.73367732T>C | CA393097704 | HCN4 | c.539A>G (p.Glu180Gly)
| |
15 | g.73367732T>G | CA7649466 | HCN4 | c.539A>C (p.Glu180Ala)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73367732T= | CA2187194525 | HCN4 | c.539A= (p.Glu180=)
| |
15 | g.73367733C>A | CA393097706 | HCN4 | c.538G>T (p.Glu180Ter)
| dbSNP COSMIC |
15 | g.73367733C= | CA2187194526 | HCN4 | c.538G= (p.Glu180=)
| |
15 | g.73367733C>G | CA393097707 | HCN4 | c.538G>C (p.Glu180Gln)
| |
15 | g.73367733C>T | CA393097709 | HCN4 | c.538G>A (p.Glu180Lys)
| COSMIC |
15 | g.73367734G>A | CA7649467 | HCN4 | c.537C>T (p.Cys179=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367734G>C | CA393097710 | HCN4 | c.537C>G (p.Cys179Trp)
| dbSNP gnomAD v3 gnomAD v4 |
15 | g.73367734G= | CA2187194527 | HCN4 | c.537C= (p.Cys179=)
| |
15 | g.73367734G>T | CA393097712 | HCN4 | c.537C>A (p.Cys179Ter)
| |
15 | g.73367735C>A | CA393097714 | HCN4 | c.536G>T (p.Cys179Phe)
| |
15 | g.73367735C>G | CA393097716 | HCN4 | c.536G>C (p.Cys179Ser)
| |
15 | g.73367735C>T | CA393097717 | HCN4 | c.536G>A (p.Cys179Tyr)
| |
15 | g.73367736A>C | CA393097721 | HCN4 | c.535T>G (p.Cys179Gly)
| |
15 | g.73367736A>G | CA393097720 | HCN4 | c.535T>C (p.Cys179Arg)
| |
15 | g.73367736A>T | CA393097719 | HCN4 | c.535T>A (p.Cys179Ser)
| |
15 | g.73367737G>A | CA272700289 | HCN4 | c.534C>T (p.Ser178=)
| dbSNP gnomAD v4 |
15 | g.73367737G>C | CA491479565 | HCN4 | c.534C>G (p.Ser178=)
| |
15 | g.73367737G= | CA2187194528 | HCN4 | c.534C= (p.Ser178=)
| |
15 | g.73367737G>T | CA491479566 | HCN4 | c.534C>A (p.Ser178=)
| |
15 | g.73367738G>A | CA393097722 | HCN4 | c.533C>T (p.Ser178Phe)
| |
15 | g.73367738G>C | CA393097724 | HCN4 | c.533C>G (p.Ser178Cys)
| |
15 | g.73367738G>T | CA393097725 | HCN4 | c.533C>A (p.Ser178Tyr)
| gnomAD v4 |
15 | g.73367739A>C | CA393097727 | HCN4 | c.532T>G (p.Ser178Ala)
| |
15 | g.73367739A>G | CA393097728 | HCN4 | c.532T>C (p.Ser178Pro)
| |
15 | g.73367739A>T | CA393097730 | HCN4 | c.532T>A (p.Ser178Thr)
| |
15 | g.73367740G>A | CA491479567 | HCN4 | c.531C>T (p.Ala177=)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367740G>C | CA491479568 | HCN4 | c.531C>G (p.Ala177=)
| |
15 | g.73367740G>T | CA491479569 | HCN4 | c.531C>A (p.Ala177=)
| |
15 | g.73367741G>A | CA7649468 | HCN4 | c.530C>T (p.Ala177Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367741G>C | CA393097732 | HCN4 | c.530C>G (p.Ala177Gly)
| |
15 | g.73367741G= | CA2187194529 | HCN4 | c.530C= (p.Ala177=)
| |
15 | g.73367741G>T | CA393097733 | HCN4 | c.530C>A (p.Ala177Asp)
| |
15 | g.73367742C>A | CA393097734 | HCN4 | c.529G>T (p.Ala177Ser)
| ClinVar dbSNP |
15 | g.73367742C= | CA2187194530 | HCN4 | c.529G= (p.Ala177=)
| |
15 | g.73367742C>G | CA393097736 | HCN4 | c.529G>C (p.Ala177Pro)
| |
15 | g.73367742C>T | CA393097737 | HCN4 | c.529G>A (p.Ala177Thr)
| gnomAD v4 |
15 | g.73367743G>A | CA7649469 | HCN4 | c.528C>T (p.Ser176=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367743G>C | CA491479570 | HCN4 | c.528C>G (p.Ser176=)
| gnomAD v4 |
15 | g.73367743G= | CA2187194531 | HCN4 | c.528C= (p.Ser176=)
| |
15 | g.73367743G>T | CA491479571 | HCN4 | c.528C>A (p.Ser176=)
| dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367744G>A | CA393097741 | HCN4 | c.527C>T (p.Ser176Phe)
| gnomAD v4 |
15 | g.73367744G>C | CA393097742 | HCN4 | c.527C>G (p.Ser176Cys)
| |
15 | g.73367744G>T | CA393097740 | HCN4 | c.527C>A (p.Ser176Tyr)
| |
15 | g.73367745_73367750dup | CA2629389816 | HCN4 | c.522_527dup (p.Ser176_Ala177insAlaSer)
| gnomAD v4 |
15 | g.73367745A= | CA2187194532 | HCN4 | c.526T= (p.Ser176=)
| |
15 | g.73367745A>C | CA393097743 | HCN4 | c.526T>G (p.Ser176Ala)
| ClinVar gnomAD v4 |
15 | g.73367745A>G | CA393097744 | HCN4 | c.526T>C (p.Ser176Pro)
| gnomAD v4 |
15 | g.73367745A>T | CA393097746 | HCN4 | c.526T>A (p.Ser176Thr)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367746G>A | CA491479572 | HCN4 | c.525C>T (p.Ala175=)
| |
15 | g.73367746G>C | CA491479573 | HCN4 | c.525C>G (p.Ala175=)
| gnomAD v4 |
15 | g.73367746G>T | CA491479574 | HCN4 | c.525C>A (p.Ala175=)
| |
15 | g.73367747G>A | CA393097748 | HCN4 | c.524C>T (p.Ala175Val)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367747G>C | CA393097749 | HCN4 | c.524C>G (p.Ala175Gly)
| |
15 | g.73367747G= | CA2187194533 | HCN4 | c.524C= (p.Ala175=)
| |
15 | g.73367747G>T | CA393097751 | HCN4 | c.524C>A (p.Ala175Asp)
| |
15 | g.73367748C>A | CA393097752 | HCN4 | c.523G>T (p.Ala175Ser)
| gnomAD v4 |
15 | g.73367748C>G | CA393097753 | HCN4 | c.523G>C (p.Ala175Pro)
| |
15 | g.73367748C>T | CA393097755 | HCN4 | c.523G>A (p.Ala175Thr)
| gnomAD v4 |
15 | g.73367749C>A | CA491479575 | HCN4 | c.522G>T (p.Pro174=)
| dbSNP gnomAD v2 |
15 | g.73367749C= | CA2187194534 | HCN4 | c.522G= (p.Pro174=)
| |
15 | g.73367749C>G | CA491479576 | HCN4 | c.522G>C (p.Pro174=)
| |
15 | g.73367749C>T | CA491479577 | HCN4 | c.522G>A (p.Pro174=)
| ClinVar dbSNP |
15 | g.73367750G>A | CA393097757 | HCN4 | c.521C>T (p.Pro174Leu)
| gnomAD v4 |
15 | g.73367750G>C | CA393097758 | HCN4 | c.521C>G (p.Pro174Arg)
| gnomAD v4 |
15 | g.73367750G>T | CA393097760 | HCN4 | c.521C>A (p.Pro174Gln)
| |
15 | g.73367751G>A | CA301971 | HCN4 | c.520C>T (p.Pro174Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367751G>C | CA393097763 | HCN4 | c.520C>G (p.Pro174Ala)
| ClinVar dbSNP |
15 | g.73367751G= | CA2187194535 | HCN4 | c.520C= (p.Pro174=)
| |
15 | g.73367751G>T | CA393097761 | HCN4 | c.520C>A (p.Pro174Thr)
| |
15 | g.73367752C>A | CA393097764 | HCN4 | c.519G>T (p.Gln173His)
| |
15 | g.73367752C>G | CA393097766 | HCN4 | c.519G>C (p.Gln173His)
| |
15 | g.73367752C>T | CA491479578 | HCN4 | c.519G>A (p.Gln173=)
| gnomAD v4 |
15 | g.73367753T>A | CA393097768 | HCN4 | c.518A>T (p.Gln173Leu)
| |
15 | g.73367753T>C | CA393097769 | HCN4 | c.518A>G (p.Gln173Arg)
| |
15 | g.73367753T>G | CA393097771 | HCN4 | c.518A>C (p.Gln173Pro)
| dbSNP COSMIC |
15 | g.73367753T= | CA2187194536 | HCN4 | c.518A= (p.Gln173=)
| |
15 | g.73367754G>A | CA393097774 | HCN4 | c.517C>T (p.Gln173Ter)
| |
15 | g.73367754G>C | CA393097772 | HCN4 | c.517C>G (p.Gln173Glu)
| |
15 | g.73367754G>T | CA393097773 | HCN4 | c.517C>A (p.Gln173Lys)
| gnomAD v4 |
15 | g.73367755C>A | CA7649471 | HCN4 | c.516G>T (p.Pro172=)
| dbSNP ExAC gnomAD v2 |
15 | g.73367755C= | CA2187194537 | HCN4 | c.516G= (p.Pro172=)
| |
15 | g.73367755C>G | CA491479579 | HCN4 | c.516G>C (p.Pro172=)
| |
15 | g.73367755C>T | CA7649470 | HCN4 | c.516G>A (p.Pro172=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367756G>A | CA393097777 | HCN4 | c.515C>T (p.Pro172Leu)
| gnomAD v4 |
15 | g.73367756G>C | CA7649472 | HCN4 | c.515C>G (p.Pro172Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367756G= | CA2187194538 | HCN4 | c.515C= (p.Pro172=)
| |
15 | g.73367756G>T | CA393097779 | HCN4 | c.515C>A (p.Pro172Gln)
| gnomAD v4 |
15 | g.73367757G>A | CA393097781 | HCN4 | c.514C>T (p.Pro172Ser)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367757G>C | CA393097784 | HCN4 | c.514C>G (p.Pro172Ala)
| |
15 | g.73367757G= | CA2187194539 | HCN4 | c.514C= (p.Pro172=)
| |
15 | g.73367757G>T | CA393097782 | HCN4 | c.514C>A (p.Pro172Thr)
| gnomAD v4 |
15 | g.73367758T>A | CA491479580 | HCN4 | c.513A>T (p.Pro171=)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367758T>C | CA491479581 | HCN4 | c.513A>G (p.Pro171=)
| ClinVar |
15 | g.73367758T>G | CA491479582 | HCN4 | c.513A>C (p.Pro171=)
| |
15 | g.73367758_73367767delinsTGGCTGCTGG | CA2187194540 | HCN4 | c.504_513delinsCCAGCAGCCA (p.Pro168=)
| |
15 | g.73367759G>A | CA393097786 | HCN4 | c.512C>T (p.Pro171Leu)
| gnomAD v4 |
15 | g.73367759G>C | CA393097788 | HCN4 | c.512C>G (p.Pro171Arg)
| |
15 | g.73367759G= | CA2187194541 | HCN4 | c.512C= (p.Pro171=)
| |
15 | g.73367759G>T | CA393097787 | HCN4 | c.512C>A (p.Pro171Gln)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367760del | CA2841625090 | HCN4 | c.512del (p.Pro171HisfsTer?)
| |
15 | g.73367762_73367770del | CA919589361 | HCN4 | c.504_512del (p.Gln169_Pro171del)
| dbSNP |
15 | g.73367760G>A | CA393097790 | HCN4 | c.511C>T (p.Pro171Ser)
| dbSNP gnomAD v3 gnomAD v4 |
15 | g.73367760G>C | CA393097792 | HCN4 | c.511C>G (p.Pro171Ala)
| |
15 | g.73367760G= | CA2187194542 | HCN4 | c.511C= (p.Pro171=)
| |
15 | g.73367760G>T | CA393097793 | HCN4 | c.511C>A (p.Pro171Thr)
| gnomAD v4 |
15 | g.73367761C>A | CA393097795 | HCN4 | c.510G>T (p.Gln170His)
| gnomAD v4 |
15 | g.73367761C>G | CA393097796 | HCN4 | c.510G>C (p.Gln170His)
| gnomAD v4 |
15 | g.73367761C>T | CA491479583 | HCN4 | c.510G>A (p.Gln170=)
| |
15 | g.73367762T>A | CA393097797 | HCN4 | c.509A>T (p.Gln170Leu)
| |
15 | g.73367762T>C | CA393097798 | HCN4 | c.509A>G (p.Gln170Arg)
| gnomAD v4 |
15 | g.73367762T>G | CA393097800 | HCN4 | c.509A>C (p.Gln170Pro)
| |
15 | g.73367763G>A | CA393097802 | HCN4 | c.508C>T (p.Gln170Ter)
| dbSNP gnomAD v2 |
15 | g.73367763G>C | CA393097804 | HCN4 | c.508C>G (p.Gln170Glu)
| |
15 | g.73367763G= | CA2187194543 | HCN4 | c.508C= (p.Gln170=)
| |
15 | g.73367763G>T | CA393097805 | HCN4 | c.508C>A (p.Gln170Lys)
| |
15 | g.73367764C>A | CA393097806 | HCN4 | c.507G>T (p.Gln169His)
| |
15 | g.73367764C>G | CA393097808 | HCN4 | c.507G>C (p.Gln169His)
| |
15 | g.73367764C>T | CA491479584 | HCN4 | c.507G>A (p.Gln169=)
| gnomAD v4 |
15 | g.73367765T>A | CA393097810 | HCN4 | c.506A>T (p.Gln169Leu)
| |
15 | g.73367765T>C | CA393097812 | HCN4 | c.506A>G (p.Gln169Arg)
| gnomAD v4 |
15 | g.73367765T>G | CA393097811 | HCN4 | c.506A>C (p.Gln169Pro)
| dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367765T= | CA2187194544 | HCN4 | c.506A= (p.Gln169=)
| |
15 | g.73367766G>A | CA393097815 | HCN4 | c.505C>T (p.Gln169Ter)
| |
15 | g.73367766G>C | CA393097816 | HCN4 | c.505C>G (p.Gln169Glu)
| |
15 | g.73367766G>T | CA393097817 | HCN4 | c.505C>A (p.Gln169Lys)
| gnomAD v4 |
15 | g.73367767G>A | CA491479585 | HCN4 | c.504C>T (p.Pro168=)
| gnomAD v4 |
15 | g.73367767G>C | CA491479586 | HCN4 | c.504C>G (p.Pro168=)
| |
15 | g.73367767G>T | CA491479587 | HCN4 | c.504C>A (p.Pro168=)
| |
15 | g.73367767_73367770delinsGGGC | CA2187194545 | HCN4 | c.501_504delinsGCCC (p.Pro167=)
| |
15 | g.73367768G>A | CA393097822 | HCN4 | c.503C>T (p.Pro168Leu)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367768G>C | CA393097824 | HCN4 | c.503C>G (p.Pro168Arg)
| |
15 | g.73367768G= | CA2187194547 | HCN4 | c.503C= (p.Pro168=)
| |
15 | g.73367768G>T | CA393097826 | HCN4 | c.503C>A (p.Pro168His)
| |
15 | g.73367778_73367780dup | CA2187194546 | HCN4 | c.501_503dup (p.Pro168_Gln169insPro)
| dbSNP gnomAD v4 |
15 | g.73367775_73367780dup | CA2575784034 | HCN4 | c.498_503dup (p.Pro168_Gln169insProPro)
| |
15 | g.73367778_73367780del | CA619410711 | HCN4 | c.501_503del (p.Pro168del)
| dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367775_73367780del | CA2575784033 | HCN4 | c.498_503del (p.Pro167_Pro168del)
| |
15 | g.73367769G>A | CA272700296 | HCN4 | c.502C>T (p.Pro168Ser)
| dbSNP gnomAD v4 |
15 | g.73367769G>C | CA393097827 | HCN4 | c.502C>G (p.Pro168Ala)
| |
15 | g.73367769G= | CA2187194548 | HCN4 | c.502C= (p.Pro168=)
| |
15 | g.73367769G>T | CA393097829 | HCN4 | c.502C>A (p.Pro168Thr)
| |
15 | g.73367770C>A | CA491479588 | HCN4 | c.501G>T (p.Pro167=)
| dbSNP |
15 | g.73367770C= | CA2187194549 | HCN4 | c.501G= (p.Pro167=)
| |
15 | g.73367770C>G | CA491479589 | HCN4 | c.501G>C (p.Pro167=)
| |
15 | g.73367770C>T | CA491479590 | HCN4 | c.501G>A (p.Pro167=)
| dbSNP gnomAD v4 |
15 | g.73367771G>A | CA393097834 | HCN4 | c.500C>T (p.Pro167Leu)
| gnomAD v4 |
15 | g.73367771G>C | CA393097833 | HCN4 | c.500C>G (p.Pro167Arg)
| |
15 | g.73367771G>T | CA393097831 | HCN4 | c.500C>A (p.Pro167Gln)
| |
15 | g.73367774_73367791dup | CA272700301 | HCN4 | c.483_500dup (p.Pro167_Pro168insAlaAlaSerProProPro)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367774_73367791del | CA2595918209 | HCN4 | c.483_500del (p.Ala162_Pro167del)
| gnomAD v3 gnomAD v4 |
15 | g.73367772G>A | CA393097836 | HCN4 | c.499C>T (p.Pro167Ser)
| |
15 | g.73367772G>C | CA393097837 | HCN4 | c.499C>G (p.Pro167Ala)
| ClinVar |
15 | g.73367772G>T | CA393097839 | HCN4 | c.499C>A (p.Pro167Thr)
| |
15 | g.73367772_73367773delinsTA | CA2697549205 | HCN4 | c.498_499delinsTA (p.Pro167Thr)
| ClinVar |
15 | g.73367773C>A | CA491479591 | HCN4 | c.498G>T (p.Pro166=)
| ClinVar |
15 | g.73367773C>G | CA491479592 | HCN4 | c.498G>C (p.Pro166=)
| |
15 | g.73367773C>T | CA491479593 | HCN4 | c.498G>A (p.Pro166=)
| ClinVar gnomAD v4 |
15 | g.73367774G>A | CA7649473 | HCN4 | c.497C>T (p.Pro166Leu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367774G>C | CA393097841 | HCN4 | c.497C>G (p.Pro166Arg)
| |
15 | g.73367774G= | CA2187194550 | HCN4 | c.497C= (p.Pro166=)
| |
15 | g.73367774G>T | CA393097843 | HCN4 | c.497C>A (p.Pro166Gln)
| ClinVar dbSNP |
15 | g.73367777_73367784dup | CA2573151175 | HCN4 | c.490_497dup (p.Pro167ArgfsTer?)
| ClinVar dbSNP |
15 | g.73367778_73367803dup | CA2629389817 | HCN4 | c.472_497dup (p.Pro167ArgfsTer?)
| gnomAD v4 |
15 | g.73367775G>A | CA393097844 | HCN4 | c.496C>T (p.Pro166Ser)
| gnomAD v4 |
15 | g.73367775G>C | CA393097846 | HCN4 | c.496C>G (p.Pro166Ala)
| |
15 | g.73367775G>T | CA393097848 | HCN4 | c.496C>A (p.Pro166Thr)
| |
15 | g.73367776C>A | CA491479599 | HCN4 | c.495G>T (p.Pro165=)
| gnomAD v4 |
15 | g.73367776C>G | CA491479598 | HCN4 | c.495G>C (p.Pro165=)
| |
15 | g.73367776C>T | CA491479597 | HCN4 | c.495G>A (p.Pro165=)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367777G>A | CA393097849 | HCN4 | c.494C>T (p.Pro165Leu)
| dbSNP gnomAD v4 |
15 | g.73367777G>C | CA393097850 | HCN4 | c.494C>G (p.Pro165Arg)
| gnomAD v4 |
15 | g.73367777G= | CA2187194551 | HCN4 | c.494C= (p.Pro165=)
| |
15 | g.73367777G>T | CA393097851 | HCN4 | c.494C>A (p.Pro165Gln)
| ClinVar gnomAD v4 |
15 | g.73367778G>A | CA393097856 | HCN4 | c.493C>T (p.Pro165Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367778G>C | CA393097855 | HCN4 | c.493C>G (p.Pro165Ala)
| |
15 | g.73367778G= | CA2187194552 | HCN4 | c.493C= (p.Pro165=)
| |
15 | g.73367778G>T | CA393097853 | HCN4 | c.493C>A (p.Pro165Thr)
| |
15 | g.73367779C>A | CA491479606 | HCN4 | c.492G>T (p.Ser164=)
| |
15 | g.73367779C>G | CA491479605 | HCN4 | c.492G>C (p.Ser164=)
| |
15 | g.73367779C>T | CA491479604 | HCN4 | c.492G>A (p.Ser164=)
| ClinVar |
15 | g.73367785_73367802dup | CA2573151176 | HCN4 | c.475_492dup (p.Ser164_Pro165insAlaGlnProAlaAlaSer)
| ClinVar dbSNP |
15 | g.73367780G>A | CA393097857 | HCN4 | c.491C>T (p.Ser164Leu)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367780G>C | CA393097858 | HCN4 | c.491C>G (p.Ser164Trp)
| ClinVar |
15 | g.73367780G= | CA2187194553 | HCN4 | c.491C= (p.Ser164=)
| |
15 | g.73367780G>T | CA393097859 | HCN4 | c.491C>A (p.Ser164Ter)
| gnomAD v4 |
15 | g.73367781A>C | CA393097860 | HCN4 | c.490T>G (p.Ser164Ala)
| |
15 | g.73367781A>G | CA393097861 | HCN4 | c.490T>C (p.Ser164Pro)
| dbSNP |
15 | g.73367781A>T | CA393097863 | HCN4 | c.490T>A (p.Ser164Thr)
| |
15 | g.73367782G>A | CA491479610 | HCN4 | c.489C>T (p.Ala163=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367782G>C | CA491479612 | HCN4 | c.489C>G (p.Ala163=)
| |
15 | g.73367782G= | CA2187194554 | HCN4 | c.489C= (p.Ala163=)
| |
15 | g.73367782G>T | CA491479611 | HCN4 | c.489C>A (p.Ala163=)
| gnomAD v4 |
15 | g.73367783G>A | CA393097868 | HCN4 | c.488C>T (p.Ala163Val)
| gnomAD v4 |
15 | g.73367783G>C | CA393097869 | HCN4 | c.488C>G (p.Ala163Gly)
| |
15 | g.73367783G>T | CA393097870 | HCN4 | c.488C>A (p.Ala163Asp)
| gnomAD v4 |
15 | g.73367784C>A | CA393097871 | HCN4 | c.487G>T (p.Ala163Ser)
| ClinVar gnomAD v4 |
15 | g.73367784C>G | CA393097872 | HCN4 | c.487G>C (p.Ala163Pro)
| |
15 | g.73367784C>T | CA393097874 | HCN4 | c.487G>A (p.Ala163Thr)
| ClinVar gnomAD v4 |
15 | g.73367785T>A | CA491479614 | HCN4 | c.486A>T (p.Ala162=)
| |
15 | g.73367785T>C | CA491479615 | HCN4 | c.486A>G (p.Ala162=)
| |
15 | g.73367785T>G | CA491479616 | HCN4 | c.486A>C (p.Ala162=)
| |
15 | g.73367786G>A | CA393097879 | HCN4 | c.485C>T (p.Ala162Val)
| dbSNP gnomAD v4 |
15 | g.73367786G>C | CA393097877 | HCN4 | c.485C>G (p.Ala162Gly)
| |
15 | g.73367786G= | CA2187194555 | HCN4 | c.485C= (p.Ala162=)
| |
15 | g.73367786G>T | CA393097875 | HCN4 | c.485C>A (p.Ala162Glu)
| |
15 | g.73367787C>A | CA393097880 | HCN4 | c.484G>T (p.Ala162Ser)
| dbSNP gnomAD v4 |
15 | g.73367787C= | CA2187194556 | HCN4 | c.484G= (p.Ala162=)
| |
15 | g.73367787C>G | CA393097883 | HCN4 | c.484G>C (p.Ala162Pro)
| |
15 | g.73367787C>T | CA393097881 | HCN4 | c.484G>A (p.Ala162Thr)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73367788G>A | CA491479620 | HCN4 | c.483C>T (p.Pro161=)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367788G>C | CA491479621 | HCN4 | c.483C>G (p.Pro161=)
| ClinVar gnomAD v4 |
15 | g.73367788G= | CA2187194557 | HCN4 | c.483C= (p.Pro161=)
| |
15 | g.73367788G>T | CA491479622 | HCN4 | c.483C>A (p.Pro161=)
| gnomAD v4 |
15 | g.73367789G>A | CA393097885 | HCN4 | c.482C>T (p.Pro161Leu)
| |
15 | g.73367789G>C | CA393097888 | HCN4 | c.482C>G (p.Pro161Arg)
| |
15 | g.73367789G>T | CA393097886 | HCN4 | c.482C>A (p.Pro161His)
| |
15 | g.73367790G>A | CA393097889 | HCN4 | c.481C>T (p.Pro161Ser)
| ClinVar gnomAD v4 |
15 | g.73367790G>C | CA393097890 | HCN4 | c.481C>G (p.Pro161Ala)
| |
15 | g.73367790G= | CA2187194558 | HCN4 | c.481C= (p.Pro161=)
| |
15 | g.73367790G>T | CA393097892 | HCN4 | c.481C>A (p.Pro161Thr)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73367791C>A | CA393097893 | HCN4 | c.480G>T (p.Gln160His)
| ClinVar gnomAD v4 |
15 | g.73367791C>G | CA393097894 | HCN4 | c.480G>C (p.Gln160His)
| |
15 | g.73367791C>T | CA491479624 | HCN4 | c.480G>A (p.Gln160=)
| ClinVar |
15 | g.73367792T>A | CA393097896 | HCN4 | c.479A>T (p.Gln160Leu)
| |
15 | g.73367792T>C | CA393097897 | HCN4 | c.479A>G (p.Gln160Arg)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367792T>G | CA393097899 | HCN4 | c.479A>C (p.Gln160Pro)
| dbSNP |
15 | g.73367792T= | CA2187194559 | HCN4 | c.479A= (p.Gln160=)
| |
15 | g.73367793G>A | CA393097901 | HCN4 | c.478C>T (p.Gln160Ter)
| |
15 | g.73367793G>C | CA393097903 | HCN4 | c.478C>G (p.Gln160Glu)
| |
15 | g.73367793G>T | CA393097904 | HCN4 | c.478C>A (p.Gln160Lys)
| |
15 | g.73367799_73367806dup | CA2629389818 | HCN4 | c.471_478dup (p.Gln160ProfsTer?)
| gnomAD v4 |
15 | g.73367794C>A | CA491479625 | HCN4 | c.477G>T (p.Ala159=)
| gnomAD v4 |
15 | g.73367794C>G | CA491479627 | HCN4 | c.477G>C (p.Ala159=)
| |
15 | g.73367794C>T | CA491479629 | HCN4 | c.477G>A (p.Ala159=)
| gnomAD v4 |
15 | g.73367795G>A | CA393097908 | HCN4 | c.476C>T (p.Ala159Val)
| gnomAD v4 |
15 | g.73367795G>C | CA393097906 | HCN4 | c.476C>G (p.Ala159Gly)
| |
15 | g.73367795G>T | CA393097905 | HCN4 | c.476C>A (p.Ala159Glu)
| |
15 | g.73367796C>A | CA393097913 | HCN4 | c.475G>T (p.Ala159Ser)
| gnomAD v4 |
15 | g.73367796C= | CA2187194560 | HCN4 | c.475G= (p.Ala159=)
| |
15 | g.73367796C>G | CA393097914 | HCN4 | c.475G>C (p.Ala159Pro)
| dbSNP |
15 | g.73367796C>T | CA393097915 | HCN4 | c.475G>A (p.Ala159Thr)
| |
15 | g.73367797C>A | CA491479631 | HCN4 | c.474G>T (p.Ser158=)
| gnomAD v4 |
15 | g.73367797C= | CA2187194561 | HCN4 | c.474G= (p.Ser158=)
| |
15 | g.73367797C>G | CA491479632 | HCN4 | c.474G>C (p.Ser158=)
| ClinVar dbSNP gnomAD v4 |
15 | g.73367797C>T | CA491479634 | HCN4 | c.474G>A (p.Ser158=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73367798G>A | CA393097918 | HCN4 | c.473C>T (p.Ser158Leu)
| gnomAD v4 |
15 | g.73367798G>C | CA393097919 | HCN4 | c.473C>G (p.Ser158Trp)
| dbSNP |
15 | g.73367798G= | CA2187194562 | HCN4 | c.473C= (p.Ser158=)
| |
15 | g.73367798G>T | CA393097920 | HCN4 | c.473C>A (p.Ser158Ter)
| gnomAD v4 |
15 | g.73367799A>C | CA393097922 | HCN4 | c.472T>G (p.Ser158Ala)
| |
15 | g.73367799A>G | CA393097923 | HCN4 | c.472T>C (p.Ser158Pro)
| dbSNP |
15 | g.73367799A>T | CA393097925 | HCN4 | c.472T>A (p.Ser158Thr)
| |