| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.38622398_38622401del | CA2665117246 | SCN5A | c.482+3_482+6del n.677+3_677+6del | gnomAD v4 |
| 3 | g.38622398_38622408del | CA2573136278 | SCN5A | c.475_482+3del n.670_677+3del | ClinVar dbSNP |
| 3 | g.38622401C>A | CA352154487 | SCN5A | c.481G>T (p.Glu161Ter) n.676G>T | dbSNP gnomAD v4 |
| 3 | g.38622401C= | CA1358592992 | SCN5A | c.481G= (p.Glu161=) n.676G= | |
| 3 | g.38622401C>G | CA018595 | SCN5A | c.481G>C (p.Glu161Gln) n.676G>C | ClinVar dbSNP |
| 3 | g.38622401C>T | CA018588 | SCN5A | c.481G>A (p.Glu161Lys) n.676G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
| 3 | g.38622402G>A | CA063654 | SCN5A | c.480C>T (p.Val160=) n.675C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
| 3 | g.38622402G>C | CA433139144 | SCN5A | c.480C>G (p.Val160=) n.675C>G | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.38622402G= | CA1358592993 | SCN5A | c.480C= (p.Val160=) n.675C= | |
| 3 | g.38622402G>T | CA433139145 | SCN5A | c.480C>A (p.Val160=) n.675C>A | dbSNP gnomAD v4 |
| 3 | g.38622403A>C | CA352154491 | SCN5A | c.479T>G (p.Val160Gly) n.674T>G | |
| 3 | g.38622403A>G | CA352154493 | SCN5A | c.479T>C (p.Val160Ala) n.674T>C | |
| 3 | g.38622403A>T | CA352154496 | SCN5A | c.479T>A (p.Val160Asp) n.674T>A | |
| 3 | g.38622404C>A | CA352154498 | SCN5A | c.478G>T (p.Val160Phe) n.673G>T | dbSNP gnomAD v2 |
| 3 | g.38622404C= | CA1358592994 | SCN5A | c.478G= (p.Val160=) n.673G= | |
| 3 | g.38622404C>G | CA352154500 | SCN5A | c.478G>C (p.Val160Leu) n.673G>C | |
| 3 | g.38622404C>T | CA352154502 | SCN5A | c.478G>A (p.Val160Ile) n.673G>A | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.38622405A= | CA1358592995 | SCN5A | c.477T= (p.Tyr159=) n.672T= | |
| 3 | g.38622405A>C | CA352154504 | SCN5A | c.477T>G (p.Tyr159Ter) n.672T>G | ClinVar dbSNP |
| 3 | g.38622405A>G | CA433139146 | SCN5A | c.477T>C (p.Tyr159=) n.672T>C | gnomAD v4 |
| 3 | g.38622405A>T | CA352154505 | SCN5A | c.477T>A (p.Tyr159Ter) n.672T>A | |
| 3 | g.38622406T>A | CA352154507 | SCN5A | c.476A>T (p.Tyr159Phe) n.671A>T | |
| 3 | g.38622406T>C | CA063590 | SCN5A | c.476A>G (p.Tyr159Cys) n.671A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622406T>G | CA352154509 | SCN5A | c.476A>C (p.Tyr159Ser) n.671A>C | |
| 3 | g.38622406T= | CA1358592996 | SCN5A | c.476A= (p.Tyr159=) n.671A= | |
| 3 | g.38622407A>C | CA352154513 | SCN5A | c.475T>G (p.Tyr159Asp) n.670T>G | |
| 3 | g.38622407A>G | CA352154519 | SCN5A | c.475T>C (p.Tyr159His) n.670T>C | |
| 3 | g.38622407A>T | CA352154517 | SCN5A | c.475T>A (p.Tyr159Asn) n.670T>A | gnomAD v4 |
| 3 | g.38622408del | CA2697550811 | SCN5A | c.474del (p.Lys158AsnfsTer?) n.669del c.474del (p.Lys158AsnfsTer27) | ClinVar |
| 3 | g.38622408C>A | CA352154522 | SCN5A | c.474G>T (p.Lys158Asn) n.669G>T | gnomAD v4 |
| 3 | g.38622408C>G | CA352154523 | SCN5A | c.474G>C (p.Lys158Asn) n.669G>C | |
| 3 | g.38622408C>T | CA433139147 | SCN5A | c.474G>A (p.Lys158=) n.669G>A | |
| 3 | g.38622409T>A | CA352154526 | SCN5A | c.473A>T (p.Lys158Met) n.668A>T | |
| 3 | g.38622409T>C | CA352154530 | SCN5A | c.473A>G (p.Lys158Arg) n.668A>G | dbSNP |
| 3 | g.38622409T>G | CA352154527 | SCN5A | c.473A>C (p.Lys158Thr) n.668A>C | dbSNP gnomAD v2 |
| 3 | g.38622409T= | CA1358592997 | SCN5A | c.473A= (p.Lys158=) n.668A= | |
| 3 | g.38622410T>A | CA352154532 | SCN5A | c.472A>T (p.Lys158Ter) n.667A>T | dbSNP |
| 3 | g.38622410T>C | CA352154534 | SCN5A | c.472A>G (p.Lys158Glu) n.667A>G | |
| 3 | g.38622410T>G | CA352154533 | SCN5A | c.472A>C (p.Lys158Gln) n.667A>C | |
| 3 | g.38622410T= | CA1358592998 | SCN5A | c.472A= (p.Lys158=) n.667A= | |
| 3 | g.38622411G>A | CA433139148 | SCN5A | c.471C>T (p.Thr157=) n.666C>T | ClinVar gnomAD v4 |
| 3 | g.38622411G>C | CA433139149 | SCN5A | c.471C>G (p.Thr157=) n.666C>G | |
| 3 | g.38622411G>T | CA433139150 | SCN5A | c.471C>A (p.Thr157=) n.666C>A | gnomAD v4 |
| 3 | g.38622412G>A | CA063557 | SCN5A | c.470C>T (p.Thr157Ile) n.665C>T | ClinVar dbSNP ExAC gnomAD v2 |
| 3 | g.38622412G>C | CA352154538 | SCN5A | c.470C>G (p.Thr157Ser) n.665C>G | |
| 3 | g.38622412G= | CA1358592999 | SCN5A | c.470C= (p.Thr157=) n.665C= | |
| 3 | g.38622412G>T | CA352154540 | SCN5A | c.470C>A (p.Thr157Asn) n.665C>A | gnomAD v4 |
| 3 | g.38622412_38622444del | CA2573136280 | SCN5A | c.438_470del (p.Phe147_Thr157del) n.633_665del | ClinVar dbSNP |
| 3 | g.38622413T>A | CA352154542 | SCN5A | c.469A>T (p.Thr157Ser) n.664A>T | |
| 3 | g.38622413T>C | CA352154544 | SCN5A | c.469A>G (p.Thr157Ala) n.664A>G | gnomAD v4 |
| 3 | g.38622413T>G | CA352154546 | SCN5A | c.469A>C (p.Thr157Pro) n.664A>C | |
| 3 | g.38622414C>A | CA352154548 | SCN5A | c.468G>T (p.Trp156Cys) n.663G>T | |
| 3 | g.38622414C= | CA1358593000 | SCN5A | c.468G= (p.Trp156=) n.663G= | |
| 3 | g.38622414C>G | CA352154550 | SCN5A | c.468G>C (p.Trp156Cys) n.663G>C | |
| 3 | g.38622414C>T | CA352154551 | SCN5A | c.468G>A (p.Trp156Ter) n.663G>A | ClinVar dbSNP |
| 3 | g.38622415C>A | CA352154553 | SCN5A | c.467G>T (p.Trp156Leu) n.662G>T | |
| 3 | g.38622415C= | CA1358593001 | SCN5A | c.467G= (p.Trp156=) n.662G= | |
| 3 | g.38622415C>G | CA352154555 | SCN5A | c.467G>C (p.Trp156Ser) n.662G>C | |
| 3 | g.38622415C>T | CA10602880 | SCN5A | c.467G>A (p.Trp156Ter) n.662G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.38622416A= | CA1358593002 | SCN5A | c.466T= (p.Trp156=) n.661T= | |
| 3 | g.38622416A>C | CA352154558 | SCN5A | c.466T>G (p.Trp156Gly) n.661T>G | |
| 3 | g.38622416A>G | CA352154561 | SCN5A | c.466T>C (p.Trp156Arg) n.661T>C | |
| 3 | g.38622416A>T | CA352154559 | SCN5A | c.466T>A (p.Trp156Arg) n.661T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622417G>A | CA433139151 | SCN5A | c.465C>T (p.Pro155=) n.660C>T | gnomAD v4 |
| 3 | g.38622417G>C | CA433139152 | SCN5A | c.465C>G (p.Pro155=) n.660C>G | gnomAD v4 |
| 3 | g.38622417G>T | CA433139153 | SCN5A | c.465C>A (p.Pro155=) n.660C>A | gnomAD v4 |
| 3 | g.38622418G>A | CA352154564 | SCN5A | c.464C>T (p.Pro155Leu) n.659C>T | dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.38622418G>C | CA352154565 | SCN5A | c.464C>G (p.Pro155Arg) n.659C>G | |
| 3 | g.38622418G= | CA1358593003 | SCN5A | c.464C= (p.Pro155=) n.659C= | |
| 3 | g.38622418G>T | CA352154567 | SCN5A | c.464C>A (p.Pro155His) n.659C>A | |
| 3 | g.38622419G>A | CA352154568 | SCN5A | c.463C>T (p.Pro155Ser) n.658C>T | gnomAD v4 |
| 3 | g.38622419G>C | CA352154569 | SCN5A | c.463C>G (p.Pro155Ala) n.658C>G | |
| 3 | g.38622419G>T | CA352154571 | SCN5A | c.463C>A (p.Pro155Thr) n.658C>A | gnomAD v4 COSMIC COSMIC COSMIC |
| 3 | g.38622420T>A | CA433139154 | SCN5A | c.462A>T (p.Pro154=) n.657A>T | |
| 3 | g.38622420T>C | CA433139155 | SCN5A | c.462A>G (p.Pro154=) n.657A>G | |
| 3 | g.38622420T>G | CA433139156 | SCN5A | c.462A>C (p.Pro154=) n.657A>C | |
| 3 | g.38622421G>A | CA352154573 | SCN5A | c.461C>T (p.Pro154Leu) n.656C>T | dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.38622421G>C | CA352154575 | SCN5A | c.461C>G (p.Pro154Arg) n.656C>G | |
| 3 | g.38622421G= | CA1358593004 | SCN5A | c.461C= (p.Pro154=) n.656C= | |
| 3 | g.38622421G>T | CA352154577 | SCN5A | c.461C>A (p.Pro154Gln) n.656C>A | |
| 3 | g.38622422G>A | CA352154583 | SCN5A | c.460C>T (p.Pro154Ser) n.655C>T | COSMIC COSMIC COSMIC |
| 3 | g.38622422G>C | CA352154582 | SCN5A | c.460C>G (p.Pro154Ala) n.655C>G | |
| 3 | g.38622422G>T | CA352154580 | SCN5A | c.460C>A (p.Pro154Thr) n.655C>A | |
| 3 | g.38622423del | CA2665117248 | SCN5A | c.459del (p.Pro154HisfsTer?) n.654del | gnomAD v4 |
| 3 | g.38622423A>C | CA433139157 | SCN5A | c.459T>G (p.Pro153=) n.654T>G | |
| 3 | g.38622423A>G | CA433139158 | SCN5A | c.459T>C (p.Pro153=) n.654T>C | |
| 3 | g.38622423A>T | CA433139159 | SCN5A | c.459T>A (p.Pro153=) n.654T>A | |
| 3 | g.38622424G>A | CA352154584 | SCN5A | c.458C>T (p.Pro153Leu) n.653C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.38622424G>C | CA352154586 | SCN5A | c.458C>G (p.Pro153Arg) n.653C>G | |
| 3 | g.38622424G= | CA1358593005 | SCN5A | c.458C= (p.Pro153=) n.653C= | |
| 3 | g.38622424G>T | CA352154588 | SCN5A | c.458C>A (p.Pro153His) n.653C>A | gnomAD v4 |
| 3 | g.38622426del | CA2739279609 | SCN5A | c.458del (p.Pro153LeufsTer?) n.653del | ClinVar |
| 3 | g.38622425G>A | CA352154589 | SCN5A | c.457C>T (p.Pro153Ser) n.652C>T | |
| 3 | g.38622425G>C | CA352154590 | SCN5A | c.457C>G (p.Pro153Ala) n.652C>G | dbSNP |
| 3 | g.38622425G= | CA1358593006 | SCN5A | c.457C= (p.Pro153=) n.652C= | |
| 3 | g.38622425G>T | CA352154591 | SCN5A | c.457C>A (p.Pro153Thr) n.652C>A | |
| 3 | g.38622426G>A | CA063435 | SCN5A | c.456C>T (p.Asp152=) n.651C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622426G>C | CA352154594 | SCN5A | c.456C>G (p.Asp152Glu) n.651C>G | |
| 3 | g.38622426G= | CA1358593007 | SCN5A | c.456C= (p.Asp152=) n.651C= | |
| 3 | g.38622426G>T | CA352154596 | SCN5A | c.456C>A (p.Asp152Glu) n.651C>A | ClinVar dbSNP |
| 3 | g.38622427T>A | CA352154599 | SCN5A | c.455A>T (p.Asp152Val) n.650A>T | |
| 3 | g.38622427T>C | CA352154601 | SCN5A | c.455A>G (p.Asp152Gly) n.650A>G | gnomAD v4 |
| 3 | g.38622427T>G | CA352154603 | SCN5A | c.455A>C (p.Asp152Ala) n.650A>C | |
| 3 | g.38622428C>A | CA352154606 | SCN5A | c.454G>T (p.Asp152Tyr) n.649G>T | ClinVar dbSNP gnomAD v4 |
| 3 | g.38622428C= | CA1358593008 | SCN5A | c.454G= (p.Asp152=) n.649G= | |
| 3 | g.38622428C>G | CA352154605 | SCN5A | c.454G>C (p.Asp152His) n.649G>C | gnomAD v4 |
| 3 | g.38622428C>T | CA063420 | SCN5A | c.454G>A (p.Asp152Asn) n.649G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.38622429G>A | CA063325 | SCN5A | c.453C>T (p.His151=) n.648C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622429G>C | CA352154607 | SCN5A | c.453C>G (p.His151Gln) n.648C>G | |
| 3 | g.38622429G= | CA1358593009 | SCN5A | c.453C= (p.His151=) n.648C= | |
| 3 | g.38622429G>T | CA352154609 | SCN5A | c.453C>A (p.His151Gln) n.648C>A | |
| 3 | g.38622430T>A | CA352154611 | SCN5A | c.452A>T (p.His151Leu) n.647A>T | |
| 3 | g.38622430T>C | CA352154613 | SCN5A | c.452A>G (p.His151Arg) n.647A>G | |
| 3 | g.38622430T>G | CA352154614 | SCN5A | c.452A>C (p.His151Pro) n.647A>C | |
| 3 | g.38622431G>A | CA352154617 | SCN5A | c.451C>T (p.His151Tyr) n.646C>T | ClinVar gnomAD v4 |
| 3 | g.38622431G>C | CA352154618 | SCN5A | c.451C>G (p.His151Asp) n.646C>G | ClinVar dbSNP |
| 3 | g.38622431G= | CA1358593010 | SCN5A | c.451C= (p.His151=) n.646C= | |
| 3 | g.38622431G>T | CA352154620 | SCN5A | c.451C>A (p.His151Asn) n.646C>A | |
| 3 | g.38622432C>A | CA352154622 | SCN5A | c.450G>T (p.Gln150His) n.645G>T | |
| 3 | g.38622432C>G | CA352154624 | SCN5A | c.450G>C (p.Gln150His) n.645G>C | |
| 3 | g.38622432C>T | CA433139160 | SCN5A | c.450G>A (p.Gln150=) n.645G>A | |
| 3 | g.38622433T>A | CA352154627 | SCN5A | c.449A>T (p.Gln150Leu) n.644A>T | |
| 3 | g.38622433T>C | CA352154629 | SCN5A | c.449A>G (p.Gln150Arg) n.644A>G | |
| 3 | g.38622433T>G | CA352154626 | SCN5A | c.449A>C (p.Gln150Pro) n.644A>C | |
| 3 | g.38622434G>A | CA352154634 | SCN5A | c.448C>T (p.Gln150Ter) n.643C>T | |
| 3 | g.38622434G>C | CA352154631 | SCN5A | c.448C>G (p.Gln150Glu) n.643C>G | |
| 3 | g.38622434G>T | CA352154633 | SCN5A | c.448C>A (p.Gln150Lys) n.643C>A | |
| 3 | g.38622435G>A | CA433139161 | SCN5A | c.447C>T (p.Ala149=) n.642C>T | |
| 3 | g.38622435G>C | CA433139163 | SCN5A | c.447C>G (p.Ala149=) n.642C>G | |
| 3 | g.38622435G>T | CA433139162 | SCN5A | c.447C>A (p.Ala149=) n.642C>A | |
| 3 | g.38622436G>A | CA352154636 | SCN5A | c.446C>T (p.Ala149Val) n.641C>T | ClinVar dbSNP |
| 3 | g.38622436G>C | CA352154638 | SCN5A | c.446C>G (p.Ala149Gly) n.641C>G | |
| 3 | g.38622436G= | CA1358593011 | SCN5A | c.446C= (p.Ala149=) n.641C= | |
| 3 | g.38622436G>T | CA352154639 | SCN5A | c.446C>A (p.Ala149Asp) n.641C>A | |
| 3 | g.38622437C>A | CA352154645 | SCN5A | c.445G>T (p.Ala149Ser) n.640G>T | gnomAD v4 |
| 3 | g.38622437C>G | CA352154643 | SCN5A | c.445G>C (p.Ala149Pro) n.640G>C | |
| 3 | g.38622437C>T | CA352154642 | SCN5A | c.445G>A (p.Ala149Thr) n.640G>A | |
| 3 | g.38622438C>A | CA352154647 | SCN5A | c.444G>T (p.Met148Ile) n.639G>T | |
| 3 | g.38622438C>G | CA352154649 | SCN5A | c.444G>C (p.Met148Ile) n.639G>C | |
| 3 | g.38622438C>T | CA352154650 | SCN5A | c.444G>A (p.Met148Ile) n.639G>A | |
| 3 | g.38622439A>C | CA352154651 | SCN5A | c.443T>G (p.Met148Arg) n.638T>G | |
| 3 | g.38622439A>G | CA352154652 | SCN5A | c.443T>C (p.Met148Thr) n.638T>C | |
| 3 | g.38622439A>T | CA352154653 | SCN5A | c.443T>A (p.Met148Lys) n.638T>A | |
| 3 | g.38622440T>A | CA352154656 | SCN5A | c.442A>T (p.Met148Leu) n.637A>T | |
| 3 | g.38622440T>C | CA352154658 | SCN5A | c.442A>G (p.Met148Val) n.637A>G | dbSNP gnomAD v4 |
| 3 | g.38622440T>G | CA352154657 | SCN5A | c.442A>C (p.Met148Leu) n.637A>C | |
| 3 | g.38622440T= | CA1358593012 | SCN5A | c.442A= (p.Met148=) n.637A= | |
| 3 | g.38622441G>A | CA433139164 | SCN5A | c.441C>T (p.Phe147=) n.636C>T | ClinVar |
| 3 | g.38622441G>C | CA352154660 | SCN5A | c.441C>G (p.Phe147Leu) n.636C>G | |
| 3 | g.38622441G>T | CA352154662 | SCN5A | c.441C>A (p.Phe147Leu) n.636C>A | |
| 3 | g.38622442A>C | CA352154664 | SCN5A | c.440T>G (p.Phe147Cys) n.635T>G | |
| 3 | g.38622442A>G | CA352154666 | SCN5A | c.440T>C (p.Phe147Ser) n.635T>C | |
| 3 | g.38622442A>T | CA352154667 | SCN5A | c.440T>A (p.Phe147Tyr) n.635T>A | |
| 3 | g.38622443A>C | CA352154670 | SCN5A | c.439T>G (p.Phe147Val) n.634T>G | |
| 3 | g.38622443A>G | CA352154672 | SCN5A | c.439T>C (p.Phe147Leu) n.634T>C | |
| 3 | g.38622443A>T | CA352154674 | SCN5A | c.439T>A (p.Phe147Ile) n.634T>A | |
| 3 | g.38622444C>A | CA433139165 | SCN5A | c.438G>T (p.Val146=) n.633G>T | |
| 3 | g.38622444C>G | CA433139166 | SCN5A | c.438G>C (p.Val146=) n.633G>C | |
| 3 | g.38622444C>T | CA433139167 | SCN5A | c.438G>A (p.Val146=) n.633G>A | ClinVar |
| 3 | g.38622445A= | CA1358593013 | SCN5A | c.437T= (p.Val146=) n.632T= | |
| 3 | g.38622445A>C | CA352154676 | SCN5A | c.437T>G (p.Val146Gly) n.632T>G | |
| 3 | g.38622445A>G | CA352154677 | SCN5A | c.437T>C (p.Val146Ala) n.632T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.38622445A>T | CA352154678 | SCN5A | c.437T>A (p.Val146Glu) n.632T>A | |
| 3 | g.38622446C>A | CA352154682 | SCN5A | c.436G>T (p.Val146Leu) n.631G>T | |
| 3 | g.38622446C= | CA1358593014 | SCN5A | c.436G= (p.Val146=) n.631G= | |
| 3 | g.38622446C>G | CA352154681 | SCN5A | c.436G>C (p.Val146Leu) n.631G>C | |
| 3 | g.38622446C>T | CA018183 | SCN5A | c.436G>A (p.Val146Met) n.631G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
| 3 | g.38622447G>A | CA018176 | SCN5A | c.435C>T (p.Cys145=) n.630C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
| 3 | g.38622447G>C | CA352154688 | SCN5A | c.435C>G (p.Cys145Trp) n.630C>G | |
| 3 | g.38622447G= | CA1358593015 | SCN5A | c.435C= (p.Cys145=) n.630C= | |
| 3 | g.38622447G>T | CA352154690 | SCN5A | c.435C>A (p.Cys145Ter) n.630C>A | ClinVar dbSNP |
| 3 | g.38622448C>A | CA352154692 | SCN5A | c.434G>T (p.Cys145Phe) n.629G>T | gnomAD v4 |
| 3 | g.38622448C= | CA1358593016 | SCN5A | c.434G= (p.Cys145=) n.629G= | |
| 3 | g.38622448C>G | CA352154694 | SCN5A | c.434G>C (p.Cys145Ser) n.629G>C | |
| 3 | g.38622448C>T | CA352154696 | SCN5A | c.434G>A (p.Cys145Tyr) n.629G>A | dbSNP |
| 3 | g.38622449A= | CA1358593017 | SCN5A | c.433T= (p.Cys145=) n.628T= | |
| 3 | g.38622449A>C | CA352154701 | SCN5A | c.433T>G (p.Cys145Gly) n.628T>G | |
| 3 | g.38622449A>G | CA352154698 | SCN5A | c.433T>C (p.Cys145Arg) n.628T>C | ClinVar dbSNP |
| 3 | g.38622449A>T | CA352154700 | SCN5A | c.433T>A (p.Cys145Ser) n.628T>A | |
| 3 | g.38622450G>A | CA433139168 | SCN5A | c.432C>T (p.Asn144=) n.627C>T | |
| 3 | g.38622450G>C | CA352154703 | SCN5A | c.432C>G (p.Asn144Lys) n.627C>G | |
| 3 | g.38622450G>T | CA352154705 | SCN5A | c.432C>A (p.Asn144Lys) n.627C>A | |
| 3 | g.38622451T>A | CA352154707 | SCN5A | c.431A>T (p.Asn144Ile) n.626A>T | |
| 3 | g.38622451T>C | CA352154709 | SCN5A | c.431A>G (p.Asn144Ser) n.626A>G | gnomAD v4 |
| 3 | g.38622451T>G | CA352154711 | SCN5A | c.431A>C (p.Asn144Thr) n.626A>C | ClinVar gnomAD v4 |
| 3 | g.38622452T>A | CA352154714 | SCN5A | c.430A>T (p.Asn144Tyr) n.625A>T | |
| 3 | g.38622452T>C | CA352154718 | SCN5A | c.430A>G (p.Asn144Asp) n.625A>G | |
| 3 | g.38622452T>G | CA352154716 | SCN5A | c.430A>C (p.Asn144His) n.625A>C | |
| 3 | g.38622453G>A | CA433139169 | SCN5A | c.429C>T (p.Thr143=) n.624C>T | |
| 3 | g.38622453G>C | CA433139171 | SCN5A | c.429C>G (p.Thr143=) n.624C>G | |
| 3 | g.38622453G>T | CA433139170 | SCN5A | c.429C>A (p.Thr143=) n.624C>A | |
| 3 | g.38622454del | CA2586972100 | SCN5A | c.429del (p.Asn144ThrfsTer?) n.624del | |
| 3 | g.38622454G>A | CA352154721 | SCN5A | c.428C>T (p.Thr143Ile) n.623C>T | |
| 3 | g.38622454G>C | CA352154723 | SCN5A | c.428C>G (p.Thr143Ser) n.623C>G | |
| 3 | g.38622454G>T | CA352154725 | SCN5A | c.428C>A (p.Thr143Asn) n.623C>A | gnomAD v4 |
| 3 | g.38622455T>A | CA352154728 | SCN5A | c.427A>T (p.Thr143Ser) n.622A>T | |
| 3 | g.38622455T>C | CA063020 | SCN5A | c.427A>G (p.Thr143Ala) n.622A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.38622455T>G | CA352154731 | SCN5A | c.427A>C (p.Thr143Pro) n.622A>C | |
| 3 | g.38622455T= | CA1358593018 | SCN5A | c.427A= (p.Thr143=) n.622A= | |
| 3 | g.38622456G>A | CA433139172 | SCN5A | c.426C>T (p.Leu142=) n.621C>T | |
| 3 | g.38622456G>C | CA433139173 | SCN5A | c.426C>G (p.Leu142=) n.621C>G | |
| 3 | g.38622456G>T | CA433139174 | SCN5A | c.426C>A (p.Leu142=) n.621C>A | |
| 3 | g.38622457A>C | CA352154734 | SCN5A | c.425T>G (p.Leu142Arg) n.620T>G | |
| 3 | g.38622457A>G | CA352154736 | SCN5A | c.425T>C (p.Leu142Pro) n.620T>C | |
| 3 | g.38622457A>T | CA352154738 | SCN5A | c.425T>A (p.Leu142His) n.620T>A | |
| 3 | g.38622458G>A | CA352154743 | SCN5A | c.424C>T (p.Leu142Phe) n.619C>T | ClinVar dbSNP |
| 3 | g.38622458G>C | CA352154745 | SCN5A | c.424C>G (p.Leu142Val) n.619C>G | |
| 3 | g.38622458G= | CA1358593019 | SCN5A | c.424C= (p.Leu142=) n.619C= | |
| 3 | g.38622458G>T | CA352154747 | SCN5A | c.424C>A (p.Leu142Ile) n.619C>A | |
| 3 | g.38622459G>A | CA433139175 | SCN5A | c.423C>T (p.Ile141=) n.618C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC |
| 3 | g.38622459G>C | CA352154750 | SCN5A | c.423C>G (p.Ile141Met) n.618C>G | |
| 3 | g.38622459G= | CA1358593020 | SCN5A | c.423C= (p.Ile141=) n.618C= | |
| 3 | g.38622459G>T | CA433139176 | SCN5A | c.423C>A (p.Ile141=) n.618C>A | ClinVar |
| 3 | g.38622460A= | CA1358593021 | SCN5A | c.422T= (p.Ile141=) n.617T= | |
| 3 | g.38622460A>C | CA352154755 | SCN5A | c.422T>G (p.Ile141Ser) n.617T>G | |
| 3 | g.38622460A>G | CA352154753 | SCN5A | c.422T>C (p.Ile141Thr) n.617T>C | |
| 3 | g.38622460A>T | CA062954 | SCN5A | c.422T>A (p.Ile141Asn) n.617T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622461T>A | CA017991 | SCN5A | c.421A>T (p.Ile141Phe) n.616A>T | ClinVar dbSNP |
| 3 | g.38622461T>C | CA352154763 | SCN5A | c.421A>G (p.Ile141Val) n.616A>G | ClinVar gnomAD v4 |
| 3 | g.38622461T>G | CA352154760 | SCN5A | c.421A>C (p.Ile141Leu) n.616A>C | |
| 3 | g.38622461T= | CA1358593022 | SCN5A | c.421A= (p.Ile141=) n.616A= | |
| 3 | g.38622462G>A | CA433139177 | SCN5A | c.420C>T (p.Thr140=) n.615C>T | COSMIC COSMIC COSMIC |
| 3 | g.38622462G>C | CA433139178 | SCN5A | c.420C>G (p.Thr140=) n.615C>G | |
| 3 | g.38622462G>T | CA433139179 | SCN5A | c.420C>A (p.Thr140=) n.615C>A | gnomAD v4 |
| 3 | g.38622463G>A | CA352154766 | SCN5A | c.419C>T (p.Thr140Ile) n.614C>T | |
| 3 | g.38622463G>C | CA352154767 | SCN5A | c.419C>G (p.Thr140Ser) n.614C>G | |
| 3 | g.38622463G>T | CA352154769 | SCN5A | c.419C>A (p.Thr140Asn) n.614C>A | |
| 3 | g.38622464T>A | CA352154771 | SCN5A | c.418A>T (p.Thr140Ser) n.613A>T | |
| 3 | g.38622464T>C | CA352154773 | SCN5A | c.418A>G (p.Thr140Ala) n.613A>G | |
| 3 | g.38622464T>G | CA352154775 | SCN5A | c.418A>C (p.Thr140Pro) n.613A>C | |
| 3 | g.38622466_38622474dup | CA2586972101 | SCN5A | c.410_418dup (p.Cys139_Thr140insIleMetCys) n.605_613dup | |
| 3 | g.38622465G>A | CA062917 | SCN5A | c.417C>T (p.Cys139=) n.612C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622465G>C | CA352154779 | SCN5A | c.417C>G (p.Cys139Trp) n.612C>G | |
| 3 | g.38622465G= | CA1358593023 | SCN5A | c.417C= (p.Cys139=) n.612C= | |
| 3 | g.38622465G>T | CA352154780 | SCN5A | c.417C>A (p.Cys139Ter) n.612C>A | dbSNP |
| 3 | g.38622466C>A | CA352154783 | SCN5A | c.416G>T (p.Cys139Phe) n.611G>T | gnomAD v4 |
| 3 | g.38622466C>G | CA352154785 | SCN5A | c.416G>C (p.Cys139Ser) n.611G>C | |
| 3 | g.38622466C>T | CA352154787 | SCN5A | c.416G>A (p.Cys139Tyr) n.611G>A | gnomAD v4 |
| 3 | g.38622467A>C | CA352154794 | SCN5A | c.415T>G (p.Cys139Gly) n.610T>G | |
| 3 | g.38622467A>G | CA352154790 | SCN5A | c.415T>C (p.Cys139Arg) n.610T>C | |
| 3 | g.38622467A>T | CA352154792 | SCN5A | c.415T>A (p.Cys139Ser) n.610T>A | |
| 3 | g.38622468C>A | CA352154796 | SCN5A | c.414G>T (p.Met138Ile) n.609G>T | |
| 3 | g.38622468C= | CA1358593024 | SCN5A | c.414G= (p.Met138=) n.609G= | |
| 3 | g.38622468C>G | CA352154798 | SCN5A | c.414G>C (p.Met138Ile) n.609G>C | |
| 3 | g.38622468C>T | CA017919 | SCN5A | c.414G>A (p.Met138Ile) n.609G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622469A= | CA1358593025 | SCN5A | c.413T= (p.Met138=) n.608T= | |
| 3 | g.38622469A>C | CA352154802 | SCN5A | c.413T>G (p.Met138Arg) n.608T>G | ClinVar dbSNP |
| 3 | g.38622469A>G | CA017907 | SCN5A | c.413T>C (p.Met138Thr) n.608T>C | ClinVar dbSNP |
| 3 | g.38622469A>T | CA352154806 | SCN5A | c.413T>A (p.Met138Lys) n.608T>A | ClinVar dbSNP |
| 3 | g.38622473_38622475del | CA2580614199 | SCN5A | c.411_413del (p.Ile137del) n.606_608del | ClinVar |
| 3 | g.38622470T>A | CA352154809 | SCN5A | c.412A>T (p.Met138Leu) n.607A>T | |
| 3 | g.38622470T>C | CA352154810 | SCN5A | c.412A>G (p.Met138Val) n.607A>G | gnomAD v4 |
| 3 | g.38622470T>G | CA352154812 | SCN5A | c.412A>C (p.Met138Leu) n.607A>C | |
| 3 | g.38622471G>A | CA433139180 | SCN5A | c.411C>T (p.Ile137=) n.606C>T | |
| 3 | g.38622471G>C | CA352154814 | SCN5A | c.411C>G (p.Ile137Met) n.606C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.38622471G= | CA1358593026 | SCN5A | c.411C= (p.Ile137=) n.606C= | |
| 3 | g.38622471G>T | CA433139181 | SCN5A | c.411C>A (p.Ile137=) n.606C>A | |
| 3 | g.38622472A>C | CA352154822 | SCN5A | c.410T>G (p.Ile137Ser) n.605T>G | |
| 3 | g.38622472A>G | CA352154820 | SCN5A | c.410T>C (p.Ile137Thr) n.605T>C | |
| 3 | g.38622472A>T | CA352154818 | SCN5A | c.410T>A (p.Ile137Asn) n.605T>A | |
| 3 | g.38622473T>A | CA352154825 | SCN5A | c.409A>T (p.Ile137Phe) n.604A>T | |
| 3 | g.38622473T>C | CA062833 | SCN5A | c.409A>G (p.Ile137Val) n.604A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.38622473T>G | CA352154828 | SCN5A | c.409A>C (p.Ile137Leu) n.604A>C | gnomAD v4 |
| 3 | g.38622473T= | CA1358593027 | SCN5A | c.409A= (p.Ile137=) n.604A= | |
| 3 | g.38622474G>A | CA72949039 | SCN5A | c.408C>T (p.Leu136=) n.603C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622474G>C | CA433139185 | SCN5A | c.408C>G (p.Leu136=) n.603C>G | |
| 3 | g.38622474G= | CA1358593028 | SCN5A | c.408C= (p.Leu136=) n.603C= | |
| 3 | g.38622474G>T | CA433139186 | SCN5A | c.408C>A (p.Leu136=) n.603C>A | gnomAD v4 |
| 3 | g.38622475A= | CA1358593029 | SCN5A | c.407T= (p.Leu136=) n.602T= | |
| 3 | g.38622475A>C | CA352154831 | SCN5A | c.407T>G (p.Leu136Arg) n.602T>G | |
| 3 | g.38622475A>G | CA017871 | SCN5A | c.407T>C (p.Leu136Pro) n.602T>C | ClinVar dbSNP |
| 3 | g.38622475A>T | CA352154834 | SCN5A | c.407T>A (p.Leu136His) n.602T>A | |
| 3 | g.38622476G>A | CA352154837 | SCN5A | c.406C>T (p.Leu136Phe) n.601C>T | |
| 3 | g.38622476G>C | CA352154838 | SCN5A | c.406C>G (p.Leu136Val) n.601C>G | |
| 3 | g.38622476G>T | CA352154841 | SCN5A | c.406C>A (p.Leu136Ile) n.601C>A | gnomAD v4 |
| 3 | g.38622477C>A | CA352154843 | SCN5A | c.405G>T (p.Met135Ile) n.600G>T | |
| 3 | g.38622477C= | CA1358593030 | SCN5A | c.405G= (p.Met135=) n.600G= | |
| 3 | g.38622477C>G | CA352154844 | SCN5A | c.405G>C (p.Met135Ile) n.600G>C | |
| 3 | g.38622477C>T | CA352154846 | SCN5A | c.405G>A (p.Met135Ile) n.600G>A | ClinVar dbSNP gnomAD v4 |
| 3 | g.38622478A= | CA1358593031 | SCN5A | c.404T= (p.Met135=) n.599T= | |
| 3 | g.38622478A>C | CA352154852 | SCN5A | c.404T>G (p.Met135Arg) n.599T>G | |
| 3 | g.38622478A>G | CA352154851 | SCN5A | c.404T>C (p.Met135Thr) n.599T>C | dbSNP |
| 3 | g.38622478A>T | CA352154849 | SCN5A | c.404T>A (p.Met135Lys) n.599T>A | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.38622479T>A | CA352154854 | SCN5A | c.403A>T (p.Met135Leu) n.598A>T | |
| 3 | g.38622479T>C | CA062751 | SCN5A | c.403A>G (p.Met135Val) n.598A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622479T>G | CA352154858 | SCN5A | c.403A>C (p.Met135Leu) n.598A>C | ClinVar dbSNP |
| 3 | g.38622479T= | CA1358593032 | SCN5A | c.403A= (p.Met135=) n.598A= | |
| 3 | g.38622480G>A | CA062744 | SCN5A | c.402C>T (p.Asn134=) n.597C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.38622480G>C | CA352154861 | SCN5A | c.402C>G (p.Asn134Lys) n.597C>G | |
| 3 | g.38622480G= | CA1358593033 | SCN5A | c.402C= (p.Asn134=) n.597C= | |
| 3 | g.38622480G>T | CA352154863 | SCN5A | c.402C>A (p.Asn134Lys) n.597C>A | |
| 3 | g.38622481T>A | CA352154864 | SCN5A | c.401A>T (p.Asn134Ile) n.596A>T | |
| 3 | g.38622481T>C | CA72949047 | SCN5A | c.401A>G (p.Asn134Ser) n.596A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622481T>G | CA352154867 | SCN5A | c.401A>C (p.Asn134Thr) n.596A>C | |
| 3 | g.38622481T= | CA1358593034 | SCN5A | c.401A= (p.Asn134=) n.596A= | |
| 3 | g.38622482T>A | CA352154870 | SCN5A | c.400A>T (p.Asn134Tyr) n.595A>T | |
| 3 | g.38622482T>C | CA352154872 | SCN5A | c.400A>G (p.Asn134Asp) n.595A>G | |
| 3 | g.38622482T>G | CA352154874 | SCN5A | c.400A>C (p.Asn134His) n.595A>C | |
| 3 | g.38622483G>A | CA062707 | SCN5A | c.399C>T (p.Phe133=) n.594C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.38622483G>C | CA352154879 | SCN5A | c.399C>G (p.Phe133Leu) n.594C>G | |
| 3 | g.38622483G= | CA1358593035 | SCN5A | c.399C= (p.Phe133=) n.594C= | |
| 3 | g.38622483G>T | CA352154877 | SCN5A | c.399C>A (p.Phe133Leu) n.594C>A | |
| 3 | g.38622484A>C | CA352154884 | SCN5A | c.398T>G (p.Phe133Cys) n.593T>G | |
| 3 | g.38622484A>G | CA352154888 | SCN5A | c.398T>C (p.Phe133Ser) n.593T>C | |
| 3 | g.38622484A>T | CA352154886 | SCN5A | c.398T>A (p.Phe133Tyr) n.593T>A | |
| 3 | g.38622485A>C | CA352154891 | SCN5A | c.397T>G (p.Phe133Val) n.592T>G | |
| 3 | g.38622485A>G | CA352154893 | SCN5A | c.397T>C (p.Phe133Leu) n.592T>C | |
| 3 | g.38622485A>T | CA352154895 | SCN5A | c.397T>A (p.Phe133Ile) n.592T>A | |
| 3 | g.38622486G>A | CA433139193 | SCN5A | c.396C>T (p.Leu132=) n.591C>T | ClinVar |
| 3 | g.38622486G>C | CA433139194 | SCN5A | c.396C>G (p.Leu132=) n.591C>G | |
| 3 | g.38622486G>T | CA433139195 | SCN5A | c.396C>A (p.Leu132=) n.591C>A | |
| 3 | g.38622487A= | CA1358593036 | SCN5A | c.395T= (p.Leu132=) n.590T= | |
| 3 | g.38622487A>C | CA352154897 | SCN5A | c.395T>G (p.Leu132Arg) n.590T>G | |
| 3 | g.38622487A>G | CA352154899 | SCN5A | c.395T>C (p.Leu132Pro) n.590T>C | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.38622487A>T | CA352154901 | SCN5A | c.395T>A (p.Leu132His) n.590T>A | |
| 3 | g.38622488G>A | CA352154904 | SCN5A | c.394C>T (p.Leu132Phe) n.589C>T | |
| 3 | g.38622488G>C | CA352154906 | SCN5A | c.394C>G (p.Leu132Val) n.589C>G | |
| 3 | g.38622488G>T | CA352154908 | SCN5A | c.394C>A (p.Leu132Ile) n.589C>A | |
| 3 | g.38622489C>A | CA352154910 | SCN5A | c.393G>T (p.Ser131=) n.588G>T c.394-1G>T (n.394-1G>T) | |
| 3 | g.38622489C= | CA1358593037 | SCN5A | c.393G= (p.Ser131=) n.588G= c.394-1G= (n.394-1G=) | |
| 3 | g.38622489C>G | CA72949051 | SCN5A | c.393G>C (p.Ser131=) n.588G>C c.394-1G>C (n.394-1G>C) | dbSNP gnomAD v4 |
| 3 | g.38622489C>T | CA062566 | SCN5A | c.393G>A (p.Ser131=) n.588G>A c.394-1G>A (n.394-1G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
| 3 | g.38622490G>A | CA062511 | SCN5A | c.393-1C>T (n.393-1C>T) n.588-1C>T c.394-2C>T (n.394-2C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622490G>C | CA352154914 | SCN5A | c.393-1C>G (n.393-1C>G) n.588-1C>G c.394-2C>G (n.394-2C>G) | dbSNP |
| 3 | g.38622490G= | CA1358593038 | SCN5A | c.393-1C= (n.393-1C=) n.588-1C= c.394-2C= (n.394-2C=) | |
| 3 | g.38622490G>T | CA352154917 | SCN5A | c.393-1C>A (n.393-1C>A) n.588-1C>A c.394-2C>A (n.394-2C>A) | |
| 3 | g.38622491T>A | CA352154920 | SCN5A | c.393-2A>T (n.393-2A>T) n.588-2A>T c.394-3A>T (n.394-3A>T) | dbSNP |
| 3 | g.38622491T>C | CA352154923 | SCN5A | c.393-2A>G (n.393-2A>G) n.588-2A>G c.394-3A>G (n.394-3A>G) | ClinVar dbSNP |
| 3 | g.38622491T>G | CA352154925 | SCN5A | c.393-2A>C (n.393-2A>C) n.588-2A>C c.394-3A>C (n.394-3A>C) | |
| 3 | g.38622491T= | CA1358593039 | SCN5A | c.393-2A= (n.393-2A=) n.588-2A= c.394-3A= (n.394-3A=) | |
| 3 | g.38622491dup | CA2665117249 | SCN5A | c.393-2dup (n.393-2dup) n.588-2dup c.394-3dup (n.394-3dup) | gnomAD v4 |
| 3 | g.38622492G>T | CA2665117250 | SCN5A | c.393-3C>A (n.393-3C>A) n.588-3C>A c.394-4C>A (n.394-4C>A) | gnomAD v4 |
| 3 | g.38622493C>A | CA2665117251 | SCN5A | c.393-4G>T (n.393-4G>T) n.588-4G>T c.394-5G>T (n.394-5G>T) | gnomAD v4 |
| 3 | g.38622493C= | CA1358593040 | SCN5A | c.393-4G= (n.393-4G=) n.588-4G= c.394-5G= (n.394-5G=) | |
| 3 | g.38622493C>G | CA2740094357 | SCN5A | c.393-4G>C (n.393-4G>C) n.588-4G>C c.394-5G>C (n.394-5G>C) | ClinVar |
| 3 | g.38622493C>T | CA542274232 | SCN5A | c.393-4G>A (n.393-4G>A) n.588-4G>A c.394-5G>A (n.394-5G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622494G>A | CA062560 | SCN5A | c.393-5C>T (n.393-5C>T) n.588-5C>T c.394-6C>T (n.394-6C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622494G>C | CA2580069741 | SCN5A | c.393-5C>G (n.393-5C>G) n.588-5C>G c.394-6C>G (n.394-6C>G) | ClinVar |
| 3 | g.38622494G= | CA1358593041 | SCN5A | c.393-5C= (n.393-5C=) n.588-5C= c.394-6C= (n.394-6C=) | |
| 3 | g.38622494G>T | CA017645 | SCN5A | c.393-5C>A (n.393-5C>A) n.588-5C>A c.394-6C>A (n.394-6C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.38622496G>T | CA2665117252 | SCN5A | c.393-7C>A (n.393-7C>A) n.588-7C>A c.394-8C>A (n.394-8C>A) | gnomAD v4 |
| 3 | g.38622497G>A | CA1358593043 | SCN5A | c.393-8C>T (n.393-8C>T) n.588-8C>T c.394-9C>T (n.394-9C>T) | dbSNP gnomAD v4 |
| 3 | g.38622497G= | CA1358593042 | SCN5A | c.393-8C= (n.393-8C=) n.588-8C= c.394-9C= (n.394-9C=) | |
| 3 | g.38622497G>T | CA2665117253 | SCN5A | c.393-8C>A (n.393-8C>A) n.588-8C>A c.394-9C>A (n.394-9C>A) | gnomAD v4 |
| 3 | g.38622498G>C | CA72949056 | SCN5A | c.393-9C>G (n.393-9C>G) n.588-9C>G c.394-10C>G (n.394-10C>G) | dbSNP |
| 3 | g.38622498G= | CA1358593044 | SCN5A | c.393-9C= (n.393-9C=) n.588-9C= c.394-10C= (n.394-10C=) | |
| 3 | g.38622498G>T | CA2665117254 | SCN5A | c.393-9C>A (n.393-9C>A) n.588-9C>A c.394-10C>A (n.394-10C>A) | gnomAD v4 |
| 3 | g.38622499G>A | CA542274233 | SCN5A | c.393-10C>T (n.393-10C>T) n.588-10C>T c.394-11C>T (n.394-11C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.38622499G>C | CA72949059 | SCN5A | c.393-10C>G (n.393-10C>G) n.588-10C>G c.394-11C>G (n.394-11C>G) | dbSNP |
| 3 | g.38622499G= | CA1358593045 | SCN5A | c.393-10C= (n.393-10C=) n.588-10C= c.394-11C= (n.394-11C=) | |
| 3 | g.38622499G>T | CA2665117255 | SCN5A | c.393-10C>A (n.393-10C>A) n.588-10C>A c.394-11C>A (n.394-11C>A) | gnomAD v4 |
| 3 | g.38622501C>A | CA2577565894 | SCN5A | c.393-12G>T (n.393-12G>T) n.588-12G>T c.394-13G>T (n.394-13G>T) | gnomAD v4 |
| 3 | g.38622501C>T | CA2573052158 | SCN5A | c.393-12G>A (n.393-12G>A) n.588-12G>A c.394-13G>A (n.394-13G>A) | ClinVar dbSNP |