| 15 | g.73367677G>A | CA491479527 | HCN4 | c.594C>T (p.Asp198=)
| dbSNP gnomAD v2 |
| 15 | g.73367677G>C | CA272700157 | HCN4 | c.594C>G (p.Asp198Glu)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367677G= | CA2187194493 | HCN4 | c.594C= (p.Asp198=)
| |
| 15 | g.73367677G>T | CA393097535 | HCN4 | c.594C>A (p.Asp198Glu)
| |
| 15 | g.73367678T>A | CA393097538 | HCN4 | c.593A>T (p.Asp198Val)
| gnomAD v4 |
| 15 | g.73367678T>C | CA393097541 | HCN4 | c.593A>G (p.Asp198Gly)
| |
| 15 | g.73367678T>G | CA393097540 | HCN4 | c.593A>C (p.Asp198Ala)
| |
| 15 | g.73367679C>A | CA393097542 | HCN4 | c.592G>T (p.Asp198Tyr)
| ClinVar gnomAD v4 |
| 15 | g.73367679C= | CA2187194494 | HCN4 | c.592G= (p.Asp198=)
| |
| 15 | g.73367679C>G | CA393097543 | HCN4 | c.592G>C (p.Asp198His)
| |
| 15 | g.73367679C>T | CA393097544 | HCN4 | c.592G>A (p.Asp198Asn)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367680G>A | CA491479528 | HCN4 | c.591C>T (p.Gly197=)
| gnomAD v4 |
| 15 | g.73367680G>C | CA491479529 | HCN4 | c.591C>G (p.Gly197=)
| |
| 15 | g.73367680G>T | CA491479530 | HCN4 | c.591C>A (p.Gly197=)
| gnomAD v4 |
| 15 | g.73367681C>A | CA393097545 | HCN4 | c.590G>T (p.Gly197Val)
| |
| 15 | g.73367681C>G | CA393097547 | HCN4 | c.590G>C (p.Gly197Ala)
| ClinVar dbSNP |
| 15 | g.73367681C>T | CA393097548 | HCN4 | c.590G>A (p.Gly197Asp)
| gnomAD v4 |
| 15 | g.73367682C>A | CA393097550 | HCN4 | c.589G>T (p.Gly197Cys)
| |
| 15 | g.73367682C>G | CA393097551 | HCN4 | c.589G>C (p.Gly197Arg)
| |
| 15 | g.73367682C>T | CA393097552 | HCN4 | c.589G>A (p.Gly197Ser)
| |
| 15 | g.73367683_73367685del | CA645583576 | HCN4 | c.587_589del (p.Ala196del)
| COSMIC |
| 15 | g.73367683G>A | CA491479531 | HCN4 | c.588C>T (p.Ala196=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367683G>C | CA491479532 | HCN4 | c.588C>G (p.Ala196=)
| ClinVar gnomAD v4 |
| 15 | g.73367683G= | CA2187194495 | HCN4 | c.588C= (p.Ala196=)
| |
| 15 | g.73367683G>T | CA491479533 | HCN4 | c.588C>A (p.Ala196=)
| |
| 15 | g.73367684G>A | CA393097554 | HCN4 | c.587C>T (p.Ala196Val)
| dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73367684G>C | CA7649454 | HCN4 | c.587C>G (p.Ala196Gly)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367684G= | CA2187194496 | HCN4 | c.587C= (p.Ala196=)
| |
| 15 | g.73367684G>T | CA393097556 | HCN4 | c.587C>A (p.Ala196Asp)
| gnomAD v4 |
| 15 | g.73367685C>A | CA393097560 | HCN4 | c.586G>T (p.Ala196Ser)
| |
| 15 | g.73367685C= | CA2187194497 | HCN4 | c.586G= (p.Ala196=)
| |
| 15 | g.73367685C>G | CA393097557 | HCN4 | c.586G>C (p.Ala196Pro)
| |
| 15 | g.73367685C>T | CA393097559 | HCN4 | c.586G>A (p.Ala196Thr)
| dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73367686A= | CA2187194498 | HCN4 | c.585T= (p.Ala195=)
| |
| 15 | g.73367686A>C | CA7649455 | HCN4 | c.585T>G (p.Ala195=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367686A>G | CA491479534 | HCN4 | c.585T>C (p.Ala195=)
| |
| 15 | g.73367686A>T | CA491479535 | HCN4 | c.585T>A (p.Ala195=)
| |
| 15 | g.73367687G>A | CA235705 | HCN4 | c.584C>T (p.Ala195Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367687G>C | CA393097563 | HCN4 | c.584C>G (p.Ala195Gly)
| |
| 15 | g.73367687G= | CA2187194499 | HCN4 | c.584C= (p.Ala195=)
| |
| 15 | g.73367687G>T | CA393097564 | HCN4 | c.584C>A (p.Ala195Asp)
| |
| 15 | g.73367688C>A | CA393097565 | HCN4 | c.583G>T (p.Ala195Ser)
| gnomAD v4 |
| 15 | g.73367688C= | CA2187194500 | HCN4 | c.583G= (p.Ala195=)
| |
| 15 | g.73367688C>G | CA393097567 | HCN4 | c.583G>C (p.Ala195Pro)
| |
| 15 | g.73367688C>T | CA272700177 | HCN4 | c.583G>A (p.Ala195Thr)
| dbSNP gnomAD v4 |
| 15 | g.73367689C>A | CA491479536 | HCN4 | c.582G>T (p.Ala194=)
| gnomAD v4 |
| 15 | g.73367689C= | CA2187194501 | HCN4 | c.582G= (p.Ala194=)
| |
| 15 | g.73367689C>G | CA491479537 | HCN4 | c.582G>C (p.Ala194=)
| |
| 15 | g.73367689C>T | CA491479538 | HCN4 | c.582G>A (p.Ala194=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73367690G>A | CA7649457 | HCN4 | c.581C>T (p.Ala194Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367690G>C | CA393097569 | HCN4 | c.581C>G (p.Ala194Gly)
| |
| 15 | g.73367690G= | CA2187194502 | HCN4 | c.581C= (p.Ala194=)
| |
| 15 | g.73367690G>T | CA7649456 | HCN4 | c.581C>A (p.Ala194Glu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367690_73367691delinsAA | CA2739269583 | HCN4 | c.580_581delinsTT (p.Ala194Leu)
| ClinVar |
| 15 | g.73367691C>A | CA393097574 | HCN4 | c.580G>T (p.Ala194Ser)
| gnomAD v4 |
| 15 | g.73367691C>G | CA393097572 | HCN4 | c.580G>C (p.Ala194Pro)
| |
| 15 | g.73367691C>T | CA393097571 | HCN4 | c.580G>A (p.Ala194Thr)
| gnomAD v4 |
| 15 | g.73367692G>A | CA491479539 | HCN4 | c.579C>T (p.Gly193=)
| ClinVar gnomAD v4 COSMIC |
| 15 | g.73367692G>C | CA491479540 | HCN4 | c.579C>G (p.Gly193=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367692G= | CA2187194503 | HCN4 | c.579C= (p.Gly193=)
| |
| 15 | g.73367692G>T | CA7649458 | HCN4 | c.579C>A (p.Gly193=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367693C>A | CA393097576 | HCN4 | c.578G>T (p.Gly193Val)
| |
| 15 | g.73367693C>G | CA393097578 | HCN4 | c.578G>C (p.Gly193Ala)
| |
| 15 | g.73367693C>T | CA393097579 | HCN4 | c.578G>A (p.Gly193Asp)
| |
| 15 | g.73367694C>A | CA393097580 | HCN4 | c.577G>T (p.Gly193Cys)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73367694C= | CA2187194504 | HCN4 | c.577G= (p.Gly193=)
| |
| 15 | g.73367694C>G | CA393097581 | HCN4 | c.577G>C (p.Gly193Arg)
| |
| 15 | g.73367694C>T | CA393097583 | HCN4 | c.577G>A (p.Gly193Ser)
| |
| 15 | g.73367695T>A | CA491479541 | HCN4 | c.576A>T (p.Gly192=)
| |
| 15 | g.73367695T>C | CA491479542 | HCN4 | c.576A>G (p.Gly192=)
| ClinVar dbSNP |
| 15 | g.73367695T>G | CA491479543 | HCN4 | c.576A>C (p.Gly192=)
| |
| 15 | g.73367695T= | CA2187194505 | HCN4 | c.576A= (p.Gly192=)
| |
| 15 | g.73367696C>A | CA393097585 | HCN4 | c.575G>T (p.Gly192Val)
| dbSNP gnomAD v2 |
| 15 | g.73367696C= | CA2187194506 | HCN4 | c.575G= (p.Gly192=)
| |
| 15 | g.73367696C>G | CA393097586 | HCN4 | c.575G>C (p.Gly192Ala)
| |
| 15 | g.73367696C>T | CA393097588 | HCN4 | c.575G>A (p.Gly192Glu)
| gnomAD v4 |
| 15 | g.73367697C>A | CA393097589 | HCN4 | c.574G>T (p.Gly192Ter)
| |
| 15 | g.73367697C= | CA2187194507 | HCN4 | c.574G= (p.Gly192=)
| |
| 15 | g.73367697C>G | CA393097590 | HCN4 | c.574G>C (p.Gly192Arg)
| |
| 15 | g.73367697C>T | CA393097592 | HCN4 | c.574G>A (p.Gly192Arg)
| dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367698C>A | CA393097593 | HCN4 | c.573G>T (p.Glu191Asp)
| |
| 15 | g.73367698C>G | CA393097595 | HCN4 | c.573G>C (p.Glu191Asp)
| |
| 15 | g.73367698C>T | CA491479544 | HCN4 | c.573G>A (p.Glu191=)
| |
| 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.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.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.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 |
