| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23416168G>A | CA485766545 | MHRT,MYH7 | c.4789C>T (p.Leu1597=) n.429G>A | ClinVar dbSNP |
| 14 | g.23416168G>C | CA389037630 | MHRT,MYH7 | c.4789C>G (p.Leu1597Val) n.429G>C | |
| 14 | g.23416168G= | CA2123465611 | MHRT,MYH7 | c.4789C= (p.Leu1597=) n.429G= | |
| 14 | g.23416168G>T | CA389037631 | MHRT,MYH7 | c.4789C>A (p.Leu1597Met) n.429G>T | |
| 14 | g.23416169C>A | CA485766546 | MHRT,MYH7 | c.4788G>T (p.Ser1596=) n.430C>A | ClinVar |
| 14 | g.23416169C= | CA2123465619 | MHRT,MYH7 | c.4788G= (p.Ser1596=) n.430C= | |
| 14 | g.23416169C>G | CA485766547 | MHRT,MYH7 | c.4788G>C (p.Ser1596=) n.430C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416169C>T | CA015299 | MHRT,MYH7 | c.4788G>A (p.Ser1596=) n.430C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416170G>A | CA043848 | MHRT,MYH7 | c.4787C>T (p.Ser1596Leu) n.431G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416170G>C | CA389037633 | MHRT,MYH7 | c.4787C>G (p.Ser1596Trp) n.431G>C | |
| 14 | g.23416170G= | CA2123465623 | MHRT,MYH7 | c.4787C= (p.Ser1596=) n.431G= | |
| 14 | g.23416170G>T | CA389037632 | MHRT,MYH7 | c.4787C>A (p.Ser1596Ter) n.431G>T | |
| 14 | g.23416171A= | CA2123465630 | MHRT,MYH7 | c.4786T= (p.Ser1596=) n.432A= | |
| 14 | g.23416171A>C | CA389037634 | MHRT,MYH7 | c.4786T>G (p.Ser1596Ala) n.432A>C | |
| 14 | g.23416171A>G | CA043838 | MHRT,MYH7 | c.4786T>C (p.Ser1596Pro) n.432A>G | dbSNP ExAC gnomAD v2 |
| 14 | g.23416171A>T | CA389037635 | MHRT,MYH7 | c.4786T>A (p.Ser1596Thr) n.432A>T | |
| 14 | g.23416172G>A | CA485766548 | MHRT,MYH7 | c.4785C>T (p.Asp1595=) n.433G>A | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416172G>C | CA389037636 | MHRT,MYH7 | c.4785C>G (p.Asp1595Glu) n.433G>C | |
| 14 | g.23416172G= | CA2123465633 | MHRT,MYH7 | c.4785C= (p.Asp1595=) n.433G= | |
| 14 | g.23416172G>T | CA389037637 | MHRT,MYH7 | c.4785C>A (p.Asp1595Glu) n.433G>T | |
| 14 | g.23416173T>A | CA389037638 | MHRT,MYH7 | c.4784A>T (p.Asp1595Val) n.434T>A | |
| 14 | g.23416173T>C | CA389037639 | MHRT,MYH7 | c.4784A>G (p.Asp1595Gly) n.434T>C | |
| 14 | g.23416173T>G | CA389037640 | MHRT,MYH7 | c.4784A>C (p.Asp1595Ala) n.434T>G | |
| 14 | g.23416174C>A | CA389037641 | MHRT,MYH7 | c.4783G>T (p.Asp1595Tyr) n.435C>A | |
| 14 | g.23416174C= | CA2123465636 | MHRT,MYH7 | c.4783G= (p.Asp1595=) n.435C= | |
| 14 | g.23416174C>G | CA389037642 | MHRT,MYH7 | c.4783G>C (p.Asp1595His) n.435C>G | |
| 14 | g.23416174C>T | CA389037643 | MHRT,MYH7 | c.4783G>A (p.Asp1595Asn) n.435C>T | ClinVar dbSNP |
| 14 | g.23416175C>A | CA485766549 | MHRT,MYH7 | c.4782G>T (p.Val1594=) n.436C>A | |
| 14 | g.23416175C>G | CA485766550 | MHRT,MYH7 | c.4782G>C (p.Val1594=) n.436C>G | |
| 14 | g.23416175C>T | CA485766551 | MHRT,MYH7 | c.4782G>A (p.Val1594=) n.436C>T | |
| 14 | g.23416176A= | CA2123465652 | MHRT,MYH7 | c.4781T= (p.Val1594=) n.437A= | |
| 14 | g.23416176A>C | CA389037644 | MHRT,MYH7 | c.4781T>G (p.Val1594Gly) n.437A>C | dbSNP |
| 14 | g.23416176A>G | CA389037645 | MHRT,MYH7 | c.4781T>C (p.Val1594Ala) n.437A>G | |
| 14 | g.23416176A>T | CA389037646 | MHRT,MYH7 | c.4781T>A (p.Val1594Glu) n.437A>T | |
| 14 | g.23416177C>A | CA389037648 | MHRT,MYH7 | c.4780G>T (p.Val1594Leu) n.438C>A | gnomAD v4 |
| 14 | g.23416177C= | CA2123465657 | MHRT,MYH7 | c.4780G= (p.Val1594=) n.438C= | |
| 14 | g.23416177C>G | CA043815 | MHRT,MYH7 | c.4780G>C (p.Val1594Leu) n.438C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416177C>T | CA389037647 | MHRT,MYH7 | c.4780G>A (p.Val1594Met) n.438C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416178C>A | CA485766552 | MHRT,MYH7 | c.4779G>T (p.Val1593=) n.439C>A | gnomAD v4 |
| 14 | g.23416178C= | CA2123465662 | MHRT,MYH7 | c.4779G= (p.Val1593=) n.439C= | |
| 14 | g.23416178C>G | CA485766553 | MHRT,MYH7 | c.4779G>C (p.Val1593=) n.439C>G | dbSNP |
| 14 | g.23416178C>T | CA485766554 | MHRT,MYH7 | c.4779G>A (p.Val1593=) n.439C>T | |
| 14 | g.23416179A>C | CA389037649 | MHRT,MYH7 | c.4778T>G (p.Val1593Gly) n.440A>C | |
| 14 | g.23416179A>G | CA389037650 | MHRT,MYH7 | c.4778T>C (p.Val1593Ala) n.440A>G | |
| 14 | g.23416179A>T | CA389037651 | MHRT,MYH7 | c.4778T>A (p.Val1593Glu) n.440A>T | |
| 14 | g.23416180C>A | CA389037652 | MHRT,MYH7 | c.4777G>T (p.Val1593Leu) n.441C>A | ClinVar |
| 14 | g.23416180C>G | CA389037653 | MHRT,MYH7 | c.4777G>C (p.Val1593Leu) n.441C>G | |
| 14 | g.23416180C>T | CA389037654 | MHRT,MYH7 | c.4777G>A (p.Val1593Met) n.441C>T | gnomAD v4 |
| 14 | g.23416181C>A | CA485766555 | MHRT,MYH7 | c.4776G>T (p.Arg1592=) n.442C>A | COSMIC |
| 14 | g.23416181C= | CA2123465669 | MHRT,MYH7 | c.4776G= (p.Arg1592=) n.442C= | |
| 14 | g.23416181C>G | CA485766556 | MHRT,MYH7 | c.4776G>C (p.Arg1592=) n.442C>G | dbSNP |
| 14 | g.23416181C>T | CA485766557 | MHRT,MYH7 | c.4776G>A (p.Arg1592=) n.442C>T | |
| 14 | g.23416182C>A | CA389037655 | MHRT,MYH7 | c.4775G>T (p.Arg1592Leu) n.443C>A | dbSNP gnomAD v4 |
| 14 | g.23416182C= | CA2123465676 | MHRT,MYH7 | c.4775G= (p.Arg1592=) n.443C= | |
| 14 | g.23416182C>G | CA389037656 | MHRT,MYH7 | c.4775G>C (p.Arg1592Pro) n.443C>G | |
| 14 | g.23416182C>T | CA389037657 | MHRT,MYH7 | c.4775G>A (p.Arg1592Gln) n.443C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416183G>A | CA389037658 | MHRT,MYH7 | c.4774C>T (p.Arg1592Trp) n.444G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23416183G>C | CA389037659 | MHRT,MYH7 | c.4774C>G (p.Arg1592Gly) n.444G>C | |
| 14 | g.23416183G= | CA2123465685 | MHRT,MYH7 | c.4774C= (p.Arg1592=) n.444G= | |
| 14 | g.23416183G>T | CA485766558 | MHRT,MYH7 | c.4774C>A (p.Arg1592=) n.444G>T | |
| 14 | g.23416184C>A | CA485766559 | MHRT,MYH7 | c.4773G>T (p.Leu1591=) n.445C>A | |
| 14 | g.23416184C= | CA2123465692 | MHRT,MYH7 | c.4773G= (p.Leu1591=) n.445C= | |
| 14 | g.23416184C>G | CA485766561 | MHRT,MYH7 | c.4773G>C (p.Leu1591=) n.445C>G | |
| 14 | g.23416184C>T | CA485766560 | MHRT,MYH7 | c.4773G>A (p.Leu1591=) n.445C>T | dbSNP |
| 14 | g.23416185A= | CA2123465700 | MHRT,MYH7 | c.4772T= (p.Leu1591=) n.446A= | |
| 14 | g.23416185A>C | CA389037660 | MHRT,MYH7 | c.4772T>G (p.Leu1591Arg) n.446A>C | |
| 14 | g.23416185A>G | CA347262 | MHRT,MYH7 | c.4772T>C (p.Leu1591Pro) n.446A>G | ClinVar dbSNP |
| 14 | g.23416185A>T | CA015292 | MHRT,MYH7 | c.4772T>A (p.Leu1591Gln) n.446A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416186G>A | CA485766562 | MHRT,MYH7 | c.4771C>T (p.Leu1591=) n.447G>A | |
| 14 | g.23416186G>C | CA389037661 | MHRT,MYH7 | c.4771C>G (p.Leu1591Val) n.447G>C | |
| 14 | g.23416186G>T | CA389037662 | MHRT,MYH7 | c.4771C>A (p.Leu1591Met) n.447G>T | |
| 14 | g.23416189_23416191del | CA2624234448 | MHRT,MYH7 | c.4769_4771del (p.His1590del) n.450_452del | gnomAD v4 |
| 14 | g.23416187G>A | CA043793 | MHRT,MYH7 | c.4770C>T (p.His1590=) n.448G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416187G>C | CA389037663 | MHRT,MYH7 | c.4770C>G (p.His1590Gln) n.448G>C | |
| 14 | g.23416187G= | CA2123465703 | MHRT,MYH7 | c.4770C= (p.His1590=) n.448G= | |
| 14 | g.23416187G>T | CA389037664 | MHRT,MYH7 | c.4770C>A (p.His1590Gln) n.448G>T | gnomAD v4 |
| 14 | g.23416188T>A | CA389037665 | MHRT,MYH7 | c.4769A>T (p.His1590Leu) n.449T>A | |
| 14 | g.23416188T>C | CA389037666 | MHRT,MYH7 | c.4769A>G (p.His1590Arg) n.449T>C | |
| 14 | g.23416188T>G | CA389037667 | MHRT,MYH7 | c.4769A>C (p.His1590Pro) n.449T>G | |
| 14 | g.23416189G>A | CA389037668 | MHRT,MYH7 | c.4768C>T (p.His1590Tyr) n.450G>A | |
| 14 | g.23416189G>C | CA389037669 | MHRT,MYH7 | c.4768C>G (p.His1590Asp) n.450G>C | |
| 14 | g.23416189G>T | CA389037670 | MHRT,MYH7 | c.4768C>A (p.His1590Asn) n.450G>T | |
| 14 | g.23416190G>A | CA485766563 | MHRT,MYH7 | c.4767C>T (p.Asn1589=) n.451G>A | ClinVar |
| 14 | g.23416190G>C | CA389037671 | MHRT,MYH7 | c.4767C>G (p.Asn1589Lys) n.451G>C | dbSNP |
| 14 | g.23416190G>T | CA389037672 | MHRT,MYH7 | c.4767C>A (p.Asn1589Lys) n.451G>T | COSMIC |
| 14 | g.23416191T>A | CA389037673 | MHRT,MYH7 | c.4766A>T (p.Asn1589Ile) n.452T>A | |
| 14 | g.23416191T>C | CA389037675 | MHRT,MYH7 | c.4766A>G (p.Asn1589Ser) n.452T>C | |
| 14 | g.23416191T>G | CA389037674 | MHRT,MYH7 | c.4766A>C (p.Asn1589Thr) n.452T>G | |
| 14 | g.23416192del | CA2575486617 | MHRT,MYH7 | c.4766del (p.Asn1589ThrfsTer24) n.453del | |
| 14 | g.23416192T>A | CA389037676 | MHRT,MYH7 | c.4765A>T (p.Asn1589Tyr) n.453T>A | |
| 14 | g.23416192T>C | CA389037678 | MHRT,MYH7 | c.4765A>G (p.Asn1589Asp) n.453T>C | |
| 14 | g.23416192T>G | CA389037677 | MHRT,MYH7 | c.4765A>C (p.Asn1589His) n.453T>G | gnomAD v4 |
| 14 | g.23416193G>A | CA485766564 | MHRT,MYH7 | c.4764C>T (p.Arg1588=) n.454G>A | ClinVar dbSNP |
| 14 | g.23416193G>C | CA485766565 | MHRT,MYH7 | c.4764C>G (p.Arg1588=) n.454G>C | |
| 14 | g.23416193G= | CA2123465708 | MHRT,MYH7 | c.4764C= (p.Arg1588=) n.454G= | |
| 14 | g.23416193G>T | CA485766566 | MHRT,MYH7 | c.4764C>A (p.Arg1588=) n.454G>T | |
| 14 | g.23416194C>A | CA389037679 | MHRT,MYH7 | c.4763G>T (p.Arg1588Leu) n.455C>A | |
| 14 | g.23416194C= | CA2123465723 | MHRT,MYH7 | c.4763G= (p.Arg1588=) n.455C= | |
| 14 | g.23416194C>G | CA347259 | MHRT,MYH7 | c.4763G>C (p.Arg1588Pro) n.455C>G | dbSNP |
| 14 | g.23416194C>T | CA389037680 | MHRT,MYH7 | c.4763G>A (p.Arg1588His) n.455C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23416195G>A | CA389037681 | MHRT,MYH7 | c.4762C>T (p.Arg1588Cys) n.456G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416195G>C | CA389037682 | MHRT,MYH7 | c.4762C>G (p.Arg1588Gly) n.456G>C | gnomAD v4 |
| 14 | g.23416195G= | CA2123465732 | MHRT,MYH7 | c.4762C= (p.Arg1588=) n.456G= | |
| 14 | g.23416195G>T | CA389037683 | MHRT,MYH7 | c.4762C>A (p.Arg1588Ser) n.456G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416196C>A | CA389037684 | MHRT,MYH7 | c.4761G>T (p.Lys1587Asn) n.457C>A | |
| 14 | g.23416196C>G | CA389037685 | MHRT,MYH7 | c.4761G>C (p.Lys1587Asn) n.457C>G | |
| 14 | g.23416196C>T | CA485766567 | MHRT,MYH7 | c.4761G>A (p.Lys1587=) n.457C>T | |
| 14 | g.23416197T>A | CA389037686 | MHRT,MYH7 | c.4760A>T (p.Lys1587Met) n.458T>A | |
| 14 | g.23416197T>C | CA389037687 | MHRT,MYH7 | c.4760A>G (p.Lys1587Arg) n.458T>C | COSMIC |
| 14 | g.23416197T>G | CA389037688 | MHRT,MYH7 | c.4760A>C (p.Lys1587Thr) n.458T>G | |
| 14 | g.23416198T>A | CA389037691 | MHRT,MYH7 | c.4759A>T (p.Lys1587Ter) n.459T>A | |
| 14 | g.23416198T>C | CA389037690 | MHRT,MYH7 | c.4759A>G (p.Lys1587Glu) n.459T>C | |
| 14 | g.23416198T>G | CA389037689 | MHRT,MYH7 | c.4759A>C (p.Lys1587Gln) n.459T>G | |
| 14 | g.23416199G>A | CA485766568 | MHRT,MYH7 | c.4758C>T (p.Ala1586=) n.460G>A | |
| 14 | g.23416199G>C | CA485766569 | MHRT,MYH7 | c.4758C>G (p.Ala1586=) n.460G>C | |
| 14 | g.23416199G>T | CA485766570 | MHRT,MYH7 | c.4758C>A (p.Ala1586=) n.460G>T | |
| 14 | g.23416200G>A | CA389037692 | MHRT,MYH7 | c.4757C>T (p.Ala1586Val) n.461G>A | |
| 14 | g.23416200G>C | CA389037693 | MHRT,MYH7 | c.4757C>G (p.Ala1586Gly) n.461G>C | ClinVar dbSNP |
| 14 | g.23416200G= | CA2123465743 | MHRT,MYH7 | c.4757C= (p.Ala1586=) n.461G= | |
| 14 | g.23416200G>T | CA389037694 | MHRT,MYH7 | c.4757C>A (p.Ala1586Asp) n.461G>T | |
| 14 | g.23416201C>A | CA389037695 | MHRT,MYH7 | c.4756G>T (p.Ala1586Ser) n.462C>A | |
| 14 | g.23416201C= | CA2123465750 | MHRT,MYH7 | c.4756G= (p.Ala1586=) n.462C= | |
| 14 | g.23416201C>G | CA389037696 | MHRT,MYH7 | c.4756G>C (p.Ala1586Pro) n.462C>G | |
| 14 | g.23416201C>T | CA389037697 | MHRT,MYH7 | c.4756G>A (p.Ala1586Thr) n.462C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416202C>A | CA389037698 | MHRT,MYH7 | c.4755G>T (p.Gln1585His) n.463C>A | |
| 14 | g.23416202C>G | CA389037699 | MHRT,MYH7 | c.4755G>C (p.Gln1585His) n.463C>G | gnomAD v4 |
| 14 | g.23416202C>T | CA485766571 | MHRT,MYH7 | c.4755G>A (p.Gln1585=) n.463C>T | |
| 14 | g.23416203T>A | CA389037700 | MHRT,MYH7 | c.4754A>T (p.Gln1585Leu) n.464T>A | |
| 14 | g.23416203T>C | CA389037701 | MHRT,MYH7 | c.4754A>G (p.Gln1585Arg) n.464T>C | |
| 14 | g.23416203T>G | CA389037702 | MHRT,MYH7 | c.4754A>C (p.Gln1585Pro) n.464T>G | |
| 14 | g.23416204G>A | CA389037705 | MHRT,MYH7 | c.4753C>T (p.Gln1585Ter) n.465G>A | gnomAD v4 |
| 14 | g.23416204G>C | CA389037704 | MHRT,MYH7 | c.4753C>G (p.Gln1585Glu) n.465G>C | |
| 14 | g.23416204G>T | CA389037703 | MHRT,MYH7 | c.4753C>A (p.Gln1585Lys) n.465G>T | |
| 14 | g.23416205T>A | CA389037706 | MHRT,MYH7 | c.4752A>T (p.Glu1584Asp) n.466T>A | |
| 14 | g.23416205T>C | CA485766572 | MHRT,MYH7 | c.4752A>G (p.Glu1584=) n.466T>C | ClinVar dbSNP |
| 14 | g.23416205T>G | CA389037707 | MHRT,MYH7 | c.4752A>C (p.Glu1584Asp) n.466T>G | |
| 14 | g.23416205T= | CA2123465758 | MHRT,MYH7 | c.4752A= (p.Glu1584=) n.466T= | |
| 14 | g.23416206T>A | CA389037708 | MHRT,MYH7 | c.4751A>T (p.Glu1584Val) n.467T>A | |
| 14 | g.23416206T>C | CA043766 | MHRT,MYH7 | c.4751A>G (p.Glu1584Gly) n.467T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416206T>G | CA389037709 | MHRT,MYH7 | c.4751A>C (p.Glu1584Ala) n.467T>G | |
| 14 | g.23416206T= | CA2123465762 | MHRT,MYH7 | c.4751A= (p.Glu1584=) n.467T= | |
| 14 | g.23416207C>A | CA389037710 | MHRT,MYH7 | c.4750G>T (p.Glu1584Ter) n.468C>A | |
| 14 | g.23416207C>G | CA389037711 | MHRT,MYH7 | c.4750G>C (p.Glu1584Gln) n.468C>G | |
| 14 | g.23416207C>T | CA389037712 | MHRT,MYH7 | c.4750G>A (p.Glu1584Lys) n.468C>T | |
| 14 | g.23416208C>A | CA389037713 | MHRT,MYH7 | c.4749G>T (p.Met1583Ile) n.469C>A | ClinVar dbSNP |
| 14 | g.23416208C= | CA2123465770 | MHRT,MYH7 | c.4749G= (p.Met1583=) n.469C= | |
| 14 | g.23416208C>G | CA389037714 | MHRT,MYH7 | c.4749G>C (p.Met1583Ile) n.469C>G | |
| 14 | g.23416208C>T | CA389037715 | MHRT,MYH7 | c.4749G>A (p.Met1583Ile) n.469C>T | gnomAD v4 |
| 14 | g.23416209A= | CA2123465776 | MHRT,MYH7 | c.4748T= (p.Met1583=) n.470A= | |
| 14 | g.23416209A>C | CA389037718 | MHRT,MYH7 | c.4748T>G (p.Met1583Arg) n.470A>C | |
| 14 | g.23416209A>G | CA389037717 | MHRT,MYH7 | c.4748T>C (p.Met1583Thr) n.470A>G | dbSNP |
| 14 | g.23416209A>T | CA389037716 | MHRT,MYH7 | c.4748T>A (p.Met1583Lys) n.470A>T | |
| 14 | g.23416210T>A | CA389037719 | MHRT,MYH7 | c.4747A>T (p.Met1583Leu) n.471T>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416210T>C | CA389037720 | MHRT,MYH7 | c.4747A>G (p.Met1583Val) n.471T>C | |
| 14 | g.23416210T>G | CA389037721 | MHRT,MYH7 | c.4747A>C (p.Met1583Leu) n.471T>G | |
| 14 | g.23416210T= | CA2123465782 | MHRT,MYH7 | c.4747A= (p.Met1583=) n.471T= | |
| 14 | g.23416210_23416213delinsTCTC | CA2123465788 | MHRT,MYH7 | c.4744_4747delinsGAGA (p.Glu1582=) n.471_474delinsTCTC | |
| 14 | g.23416211C>A | CA389037722 | MHRT,MYH7 | c.4746G>T (p.Glu1582Asp) n.472C>A | |
| 14 | g.23416211C= | CA2123465797 | MHRT,MYH7 | c.4746G= (p.Glu1582=) n.472C= | |
| 14 | g.23416211C>G | CA389037723 | MHRT,MYH7 | c.4746G>C (p.Glu1582Asp) n.472C>G | ClinVar dbSNP |
| 14 | g.23416211C>T | CA485766573 | MHRT,MYH7 | c.4746G>A (p.Glu1582=) n.472C>T | |
| 14 | g.23416214_23416216del | CA658658244 | MHRT,MYH7 | c.4744_4746del (p.Glu1582del) n.475_477del | ClinVar dbSNP |
| 14 | g.23416212T>A | CA389037724 | MHRT,MYH7 | c.4745A>T (p.Glu1582Val) n.473T>A | |
| 14 | g.23416212T>C | CA389037725 | MHRT,MYH7 | c.4745A>G (p.Glu1582Gly) n.473T>C | |
| 14 | g.23416212T>G | CA389037726 | MHRT,MYH7 | c.4745A>C (p.Glu1582Ala) n.473T>G | |
| 14 | g.23416213C>A | CA389037727 | MHRT,MYH7 | c.4744G>T (p.Glu1582Ter) n.474C>A | COSMIC |
| 14 | g.23416213C= | CA2123465804 | MHRT,MYH7 | c.4744G= (p.Glu1582=) n.474C= | |
| 14 | g.23416213C>G | CA389037728 | MHRT,MYH7 | c.4744G>C (p.Glu1582Gln) n.474C>G | |
| 14 | g.23416213C>T | CA389037729 | MHRT,MYH7 | c.4744G>A (p.Glu1582Lys) n.474C>T | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416214C>A | CA389037730 | MHRT,MYH7 | c.4743G>T (p.Glu1581Asp) n.475C>A | |
| 14 | g.23416214C>G | CA389037731 | MHRT,MYH7 | c.4743G>C (p.Glu1581Asp) n.475C>G | |
| 14 | g.23416214C>T | CA485766574 | MHRT,MYH7 | c.4743G>A (p.Glu1581=) n.475C>T | gnomAD v4 |
| 14 | g.23416215T>A | CA389037733 | MHRT,MYH7 | c.4742A>T (p.Glu1581Val) n.476T>A | |
| 14 | g.23416215T>C | CA389037734 | MHRT,MYH7 | c.4742A>G (p.Glu1581Gly) n.476T>C | |
| 14 | g.23416215T>G | CA389037732 | MHRT,MYH7 | c.4742A>C (p.Glu1581Ala) n.476T>G | |
| 14 | g.23416216C>A | CA389037737 | MHRT,MYH7 | c.4741G>T (p.Glu1581Ter) n.477C>A | |
| 14 | g.23416216C= | CA2123465811 | MHRT,MYH7 | c.4741G= (p.Glu1581=) n.477C= | |
| 14 | g.23416216C>G | CA389037735 | MHRT,MYH7 | c.4741G>C (p.Glu1581Gln) n.477C>G | |
| 14 | g.23416216C>T | CA389037736 | MHRT,MYH7 | c.4741G>A (p.Glu1581Lys) n.477C>T | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.23416217G>A | CA043734 | MHRT,MYH7 | c.4740C>T (p.Asp1580=) n.478G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416217G>C | CA389037738 | MHRT,MYH7 | c.4740C>G (p.Asp1580Glu) n.478G>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416217G= | CA2123465820 | MHRT,MYH7 | c.4740C= (p.Asp1580=) n.478G= | |
| 14 | g.23416217G>T | CA389037739 | MHRT,MYH7 | c.4740C>A (p.Asp1580Glu) n.478G>T | gnomAD v4 |
| 14 | g.23416218T>A | CA389037740 | MHRT,MYH7 | c.4739A>T (p.Asp1580Val) n.479T>A | |
| 14 | g.23416218T>C | CA389037741 | MHRT,MYH7 | c.4739A>G (p.Asp1580Gly) n.479T>C | |
| 14 | g.23416218T>G | CA389037742 | MHRT,MYH7 | c.4739A>C (p.Asp1580Ala) n.479T>G | |
| 14 | g.23416219C>A | CA389037743 | MHRT,MYH7 | c.4738G>T (p.Asp1580Tyr) n.480C>A | |
| 14 | g.23416219C>G | CA389037744 | MHRT,MYH7 | c.4738G>C (p.Asp1580His) n.480C>G | |
| 14 | g.23416219C>T | CA389037745 | MHRT,MYH7 | c.4738G>A (p.Asp1580Asn) n.480C>T | COSMIC |
| 14 | g.23416220C>A | CA389037746 | MHRT,MYH7 | c.4737G>T (p.Lys1579Asn) n.481C>A | |
| 14 | g.23416220C>G | CA389037747 | MHRT,MYH7 | c.4737G>C (p.Lys1579Asn) n.481C>G | |
| 14 | g.23416220C>T | CA485766360 | MHRT,MYH7 | c.4737G>A (p.Lys1579=) n.481C>T | |
| 14 | g.23416222_23416224del | CA2580087877 | MHRT,MYH7 | c.4735_4737del (p.Lys1579del) n.483_485del | ClinVar |
| 14 | g.23416221T>A | CA389037750 | MHRT,MYH7 | c.4736A>T (p.Lys1579Met) n.482T>A | |
| 14 | g.23416221T>C | CA389037749 | MHRT,MYH7 | c.4736A>G (p.Lys1579Arg) n.482T>C | |
| 14 | g.23416221T>G | CA389037748 | MHRT,MYH7 | c.4736A>C (p.Lys1579Thr) n.482T>G | |
| 14 | g.23416222T>A | CA389037751 | MHRT,MYH7 | c.4735A>T (p.Lys1579Ter) n.483T>A | gnomAD v4 |
| 14 | g.23416222T>C | CA389037752 | MHRT,MYH7 | c.4735A>G (p.Lys1579Glu) n.483T>C | |
| 14 | g.23416222T>G | CA389037753 | MHRT,MYH7 | c.4735A>C (p.Lys1579Gln) n.483T>G | |
| 14 | g.23416223C>A | CA389037754 | MHRT,MYH7 | c.4734G>T (p.Glu1578Asp) n.484C>A | |
| 14 | g.23416223C>G | CA389037755 | MHRT,MYH7 | c.4734G>C (p.Glu1578Asp) n.484C>G | |
| 14 | g.23416223C>T | CA485766369 | MHRT,MYH7 | c.4734G>A (p.Glu1578=) n.484C>T | |
| 14 | g.23416224T>A | CA389037756 | MHRT,MYH7 | c.4733A>T (p.Glu1578Val) n.485T>A | |
| 14 | g.23416224T>C | CA389037757 | MHRT,MYH7 | c.4733A>G (p.Glu1578Gly) n.485T>C | |
| 14 | g.23416224T>G | CA389037758 | MHRT,MYH7 | c.4733A>C (p.Glu1578Ala) n.485T>G | |
| 14 | g.23416225C>A | CA389037759 | MHRT,MYH7 | c.4732G>T (p.Glu1578Ter) n.486C>A | COSMIC |
| 14 | g.23416225C>G | CA389037760 | MHRT,MYH7 | c.4732G>C (p.Glu1578Gln) n.486C>G | |
| 14 | g.23416225C>T | CA389037761 | MHRT,MYH7 | c.4732G>A (p.Glu1578Lys) n.486C>T | |
| 14 | g.23416226T>A | CA485766372 | MHRT,MYH7 | c.4731A>T (p.Ala1577=) n.487T>A | |
| 14 | g.23416226T>C | CA485766373 | MHRT,MYH7 | c.4731A>G (p.Ala1577=) n.487T>C | |
| 14 | g.23416226T>G | CA485766374 | MHRT,MYH7 | c.4731A>C (p.Ala1577=) n.487T>G | |
| 14 | g.23416227G>A | CA389037762 | MHRT,MYH7 | c.4730C>T (p.Ala1577Val) n.488G>A | ClinVar gnomAD v4 |
| 14 | g.23416227G>C | CA389037763 | MHRT,MYH7 | c.4730C>G (p.Ala1577Gly) n.488G>C | |
| 14 | g.23416227G>T | CA389037764 | MHRT,MYH7 | c.4730C>A (p.Ala1577Glu) n.488G>T | |
| 14 | g.23416228C>A | CA389037767 | MHRT,MYH7 | c.4729G>T (p.Ala1577Ser) n.489C>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416228C= | CA2123465831 | MHRT,MYH7 | c.4729G= (p.Ala1577=) n.489C= | |
| 14 | g.23416228C>G | CA389037766 | MHRT,MYH7 | c.4729G>C (p.Ala1577Pro) n.489C>G | |
| 14 | g.23416228C>T | CA389037765 | MHRT,MYH7 | c.4729G>A (p.Ala1577Thr) n.489C>T | ClinVar dbSNP |
| 14 | g.23416229C>A | CA485766378 | MHRT,MYH7 | c.4728G>T (p.Leu1576=) n.490C>A | |
| 14 | g.23416229C>G | CA485766379 | MHRT,MYH7 | c.4728G>C (p.Leu1576=) n.490C>G | |
| 14 | g.23416229C>T | CA485766380 | MHRT,MYH7 | c.4728G>A (p.Leu1576=) n.490C>T | |
| 14 | g.23416230A>C | CA389037768 | MHRT,MYH7 | c.4727T>G (p.Leu1576Arg) n.491A>C | |
| 14 | g.23416230A>G | CA389037769 | MHRT,MYH7 | c.4727T>C (p.Leu1576Pro) n.491A>G | |
| 14 | g.23416230A>T | CA389037770 | MHRT,MYH7 | c.4727T>A (p.Leu1576Gln) n.491A>T | |
| 14 | g.23416231G>A | CA485766385 | MHRT,MYH7 | c.4726C>T (p.Leu1576=) n.492G>A | |
| 14 | g.23416231G>C | CA389037771 | MHRT,MYH7 | c.4726C>G (p.Leu1576Val) n.492G>C | dbSNP gnomAD v2 |
| 14 | g.23416231G= | CA2123465835 | MHRT,MYH7 | c.4726C= (p.Leu1576=) n.492G= | |
| 14 | g.23416231G>T | CA389037772 | MHRT,MYH7 | c.4726C>A (p.Leu1576Met) n.492G>T | |
| 14 | g.23416232C>A | CA389037774 | MHRT,MYH7 | c.4725G>T (p.Lys1575Asn) n.493C>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416232C= | CA2123465844 | MHRT,MYH7 | c.4725G= (p.Lys1575=) n.493C= | |
| 14 | g.23416232C>G | CA389037773 | MHRT,MYH7 | c.4725G>C (p.Lys1575Asn) n.493C>G | |
| 14 | g.23416232C>T | CA015268 | MHRT,MYH7 | c.4725G>A (p.Lys1575=) n.493C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416233T>A | CA389037775 | MHRT,MYH7 | c.4724A>T (p.Lys1575Met) n.494T>A | |
| 14 | g.23416233T>C | CA389037776 | MHRT,MYH7 | c.4724A>G (p.Lys1575Arg) n.494T>C | gnomAD v4 |
| 14 | g.23416233T>G | CA389037777 | MHRT,MYH7 | c.4724A>C (p.Lys1575Thr) n.494T>G | |
| 14 | g.23416234T>A | CA389037778 | MHRT,MYH7 | c.4723A>T (p.Lys1575Ter) n.495T>A | |
| 14 | g.23416234T>C | CA389037779 | MHRT,MYH7 | c.4723A>G (p.Lys1575Glu) n.495T>C | |
| 14 | g.23416234T>G | CA389037780 | MHRT,MYH7 | c.4723A>C (p.Lys1575Gln) n.495T>G | |
| 14 | g.23416235C>A | CA485766394 | MHRT,MYH7 | c.4722G>T (p.Arg1574=) n.496C>A | |
| 14 | g.23416235C>G | CA485766393 | MHRT,MYH7 | c.4722G>C (p.Arg1574=) n.496C>G | |
| 14 | g.23416235C>T | CA485766392 | MHRT,MYH7 | c.4722G>A (p.Arg1574=) n.496C>T | |
| 14 | g.23416236del | CA485766391 | MHRT,MYH7 | c.4722del (p.Lys1575SerfsTer?) n.497del | COSMIC |
| 14 | g.23416236C>A | CA389037782 | MHRT,MYH7 | c.4721G>T (p.Arg1574Leu) n.497C>A | |
| 14 | g.23416236C= | CA2123465848 | MHRT,MYH7 | c.4721G= (p.Arg1574=) n.497C= | |
| 14 | g.23416236C>G | CA389037781 | MHRT,MYH7 | c.4721G>C (p.Arg1574Pro) n.497C>G | ClinVar dbSNP |
| 14 | g.23416236C>T | CA043706 | MHRT,MYH7 | c.4721G>A (p.Arg1574Gln) n.497C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416237G>A | CA015258 | MHRT,MYH7 | c.4720C>T (p.Arg1574Trp) n.498G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416237G>C | CA389037783 | MHRT,MYH7 | c.4720C>G (p.Arg1574Gly) n.498G>C | |
| 14 | g.23416237G= | CA2123465857 | MHRT,MYH7 | c.4720C= (p.Arg1574=) n.498G= | |
| 14 | g.23416237G>T | CA485766398 | MHRT,MYH7 | c.4720C>A (p.Arg1574=) n.498G>T | dbSNP gnomAD v4 |
| 14 | g.23416238C>A | CA389037784 | MHRT,MYH7 | c.4719G>T (p.Glu1573Asp) n.499C>A | |
| 14 | g.23416238C= | CA2123465860 | MHRT,MYH7 | c.4719G= (p.Glu1573=) n.499C= | |
| 14 | g.23416238C>G | CA389037785 | MHRT,MYH7 | c.4719G>C (p.Glu1573Asp) n.499C>G | |
| 14 | g.23416238C>T | CA485766401 | MHRT,MYH7 | c.4719G>A (p.Glu1573=) n.499C>T | dbSNP |
| 14 | g.23416239T>A | CA389037786 | MHRT,MYH7 | c.4718A>T (p.Glu1573Val) n.500T>A | |
| 14 | g.23416239T>C | CA389037787 | MHRT,MYH7 | c.4718A>G (p.Glu1573Gly) n.500T>C | |
| 14 | g.23416239T>G | CA389037788 | MHRT,MYH7 | c.4718A>C (p.Glu1573Ala) n.500T>G | |
| 14 | g.23416240C>A | CA389037789 | MHRT,MYH7 | c.4717G>T (p.Glu1573Ter) n.501C>A | |
| 14 | g.23416240C= | CA2123465864 | MHRT,MYH7 | c.4717G= (p.Glu1573=) n.501C= | |
| 14 | g.23416240C>G | CA389037790 | MHRT,MYH7 | c.4717G>C (p.Glu1573Gln) n.501C>G | COSMIC |
| 14 | g.23416240C>T | CA043695 | MHRT,MYH7 | c.4717G>A (p.Glu1573Lys) n.501C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416241G>A | CA015251 | MHRT,MYH7 | c.4716C>T (p.Ile1572=) n.502G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416241G>C | CA389037791 | MHRT,MYH7 | c.4716C>G (p.Ile1572Met) n.502G>C | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416241G= | CA2123465879 | MHRT,MYH7 | c.4716C= (p.Ile1572=) n.502G= | |
| 14 | g.23416241G>T | CA485766404 | MHRT,MYH7 | c.4716C>A (p.Ile1572=) n.502G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416242A>C | CA389037792 | MHRT,MYH7 | c.4715T>G (p.Ile1572Ser) n.503A>C | |
| 14 | g.23416242A>G | CA389037794 | MHRT,MYH7 | c.4715T>C (p.Ile1572Thr) n.503A>G | |
| 14 | g.23416242A>T | CA389037793 | MHRT,MYH7 | c.4715T>A (p.Ile1572Asn) n.503A>T | |
| 14 | g.23416243T>A | CA389037795 | MHRT,MYH7 | c.4714A>T (p.Ile1572Phe) n.504T>A | |
| 14 | g.23416243T>C | CA389037796 | MHRT,MYH7 | c.4714A>G (p.Ile1572Val) n.504T>C | ClinVar |
| 14 | g.23416243T>G | CA389037797 | MHRT,MYH7 | c.4714A>C (p.Ile1572Leu) n.504T>G | |
| 14 | g.23416244C>A | CA389037798 | MHRT,MYH7 | c.4713G>T (p.Glu1571Asp) n.505C>A | gnomAD v4 |
| 14 | g.23416244C>G | CA389037799 | MHRT,MYH7 | c.4713G>C (p.Glu1571Asp) n.505C>G | gnomAD v4 |
| 14 | g.23416244C>T | CA485766410 | MHRT,MYH7 | c.4713G>A (p.Glu1571=) n.505C>T | |
| 14 | g.23416245T>A | CA389037802 | MHRT,MYH7 | c.4712A>T (p.Glu1571Val) n.506T>A | |
| 14 | g.23416245T>C | CA389037801 | MHRT,MYH7 | c.4712A>G (p.Glu1571Gly) n.506T>C | |
| 14 | g.23416245T>G | CA389037800 | MHRT,MYH7 | c.4712A>C (p.Glu1571Ala) n.506T>G | |
| 14 | g.23416246C>A | CA389037803 | MHRT,MYH7 | c.4711G>T (p.Glu1571Ter) n.507C>A | |
| 14 | g.23416246C>G | CA389037804 | MHRT,MYH7 | c.4711G>C (p.Glu1571Gln) n.507C>G | |
| 14 | g.23416246C>T | CA389037805 | MHRT,MYH7 | c.4711G>A (p.Glu1571Lys) n.507C>T | gnomAD v4 |
| 14 | g.23416247T>A | CA485766412 | MHRT,MYH7 | c.4710A>T (p.Ala1570=) n.508T>A | |
| 14 | g.23416247T>C | CA485766413 | MHRT,MYH7 | c.4710A>G (p.Ala1570=) n.508T>C | |
| 14 | g.23416247T>G | CA485766416 | MHRT,MYH7 | c.4710A>C (p.Ala1570=) n.508T>G | |
| 14 | g.23416248G>A | CA389037806 | MHRT,MYH7 | c.4709C>T (p.Ala1570Val) n.509G>A | dbSNP |
| 14 | g.23416248G>C | CA389037807 | MHRT,MYH7 | c.4709C>G (p.Ala1570Gly) n.509G>C | |
| 14 | g.23416248G= | CA2123465892 | MHRT,MYH7 | c.4709C= (p.Ala1570=) n.509G= | |
| 14 | g.23416248G>T | CA015247 | MHRT,MYH7 | c.4709C>A (p.Ala1570Glu) n.509G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416249C>A | CA389037810 | MHRT,MYH7 | c.4708G>T (p.Ala1570Ser) n.510C>A | |
| 14 | g.23416249C>G | CA389037808 | MHRT,MYH7 | c.4708G>C (p.Ala1570Pro) n.510C>G | |
| 14 | g.23416249C>T | CA389037809 | MHRT,MYH7 | c.4708G>A (p.Ala1570Thr) n.510C>T | ClinVar gnomAD v4 |
| 14 | g.23416250C>A | CA015240 | MHRT,MYH7 | c.4707G>T (p.Lys1569Asn) n.511C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416250C= | CA2123465907 | MHRT,MYH7 | c.4707G= (p.Lys1569=) n.511C= | |
| 14 | g.23416250C>G | CA043659 | MHRT,MYH7 | c.4707G>C (p.Lys1569Asn) n.511C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416250C>T | CA485766417 | MHRT,MYH7 | c.4707G>A (p.Lys1569=) n.511C>T | |
| 14 | g.23416251T>A | CA389037811 | MHRT,MYH7 | c.4706A>T (p.Lys1569Met) n.512T>A | |
| 14 | g.23416251T>C | CA389037812 | MHRT,MYH7 | c.4706A>G (p.Lys1569Arg) n.512T>C | |
| 14 | g.23416251T>G | CA389037813 | MHRT,MYH7 | c.4706A>C (p.Lys1569Thr) n.512T>G | |
| 14 | g.23416252T>A | CA389037814 | MHRT,MYH7 | c.4705A>T (p.Lys1569Ter) n.513T>A | |
| 14 | g.23416252T>C | CA389037815 | MHRT,MYH7 | c.4705A>G (p.Lys1569Glu) n.513T>C | |
| 14 | g.23416252T>G | CA389037816 | MHRT,MYH7 | c.4705A>C (p.Lys1569Gln) n.513T>G | |
| 14 | g.23416253G>A | CA485766419 | MHRT,MYH7 | c.4704C>T (p.Ile1568=) n.514G>A | |
| 14 | g.23416253G>C | CA389037817 | MHRT,MYH7 | c.4704C>G (p.Ile1568Met) n.514G>C | |
| 14 | g.23416253G>T | CA485766420 | MHRT,MYH7 | c.4704C>A (p.Ile1568=) n.514G>T | ClinVar |
| 14 | g.23416254A>C | CA389037818 | MHRT,MYH7 | c.4703T>G (p.Ile1568Ser) n.515A>C | |
| 14 | g.23416254A>G | CA389037819 | MHRT,MYH7 | c.4703T>C (p.Ile1568Thr) n.515A>G | |
| 14 | g.23416254A>T | CA389037820 | MHRT,MYH7 | c.4703T>A (p.Ile1568Asn) n.515A>T | |
| 14 | g.23416255T>A | CA389037821 | MHRT,MYH7 | c.4702A>T (p.Ile1568Phe) n.516T>A | |
| 14 | g.23416255T>C | CA389037823 | MHRT,MYH7 | c.4702A>G (p.Ile1568Val) n.516T>C | ClinVar dbSNP |
| 14 | g.23416255T>G | CA389037822 | MHRT,MYH7 | c.4702A>C (p.Ile1568Leu) n.516T>G | |
| 14 | g.23416255T= | CA2123465914 | MHRT,MYH7 | c.4702A= (p.Ile1568=) n.516T= | |
| 14 | g.23416256C>A | CA389037824 | MHRT,MYH7 | c.4701G>T (p.Gln1567His) n.517C>A | |
| 14 | g.23416256C= | CA2123465918 | MHRT,MYH7 | c.4701G= (p.Gln1567=) n.517C= | |
| 14 | g.23416256C>G | CA389037825 | MHRT,MYH7 | c.4701G>C (p.Gln1567His) n.517C>G | ClinVar dbSNP |
| 14 | g.23416256C>T | CA485766422 | MHRT,MYH7 | c.4701G>A (p.Gln1567=) n.517C>T | |
| 14 | g.23416257T>A | CA389037826 | MHRT,MYH7 | c.4700A>T (p.Gln1567Leu) n.518T>A | |
| 14 | g.23416257T>C | CA389037827 | MHRT,MYH7 | c.4700A>G (p.Gln1567Arg) n.518T>C | |
| 14 | g.23416257T>G | CA389037828 | MHRT,MYH7 | c.4700A>C (p.Gln1567Pro) n.518T>G | ClinVar COSMIC |
| 14 | g.23416258G>A | CA389037829 | MHRT,MYH7 | c.4699C>T (p.Gln1567Ter) n.519G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416258G>C | CA389037830 | MHRT,MYH7 | c.4699C>G (p.Gln1567Glu) n.519G>C | |
| 14 | g.23416258G= | CA2123465922 | MHRT,MYH7 | c.4699C= (p.Gln1567=) n.519G= | |
| 14 | g.23416258G>T | CA389037831 | MHRT,MYH7 | c.4699C>A (p.Gln1567Lys) n.519G>T | |
| 14 | g.23416259G>A | CA485766423 | MHRT,MYH7 | c.4698C>T (p.Asn1566=) n.520G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416259G>C | CA389037832 | MHRT,MYH7 | c.4698C>G (p.Asn1566Lys) n.520G>C | |
| 14 | g.23416259G= | CA2123465931 | MHRT,MYH7 | c.4698C= (p.Asn1566=) n.520G= | |
| 14 | g.23416259G>T | CA389037833 | MHRT,MYH7 | c.4698C>A (p.Asn1566Lys) n.520G>T | |
| 14 | g.23416260T>A | CA389037834 | MHRT,MYH7 | c.4697A>T (p.Asn1566Ile) n.521T>A | |
| 14 | g.23416260T>C | CA257810700 | MHRT,MYH7 | c.4697A>G (p.Asn1566Ser) n.521T>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416260T>G | CA389037835 | MHRT,MYH7 | c.4697A>C (p.Asn1566Thr) n.521T>G | |
| 14 | g.23416260T= | CA2123465941 | MHRT,MYH7 | c.4697A= (p.Asn1566=) n.521T= | |
| 14 | g.23416261T>A | CA389037836 | MHRT,MYH7 | c.4696A>T (p.Asn1566Tyr) n.522T>A | |
| 14 | g.23416261T>C | CA389037838 | MHRT,MYH7 | c.4696A>G (p.Asn1566Asp) n.522T>C | |
| 14 | g.23416261T>G | CA389037837 | MHRT,MYH7 | c.4696A>C (p.Asn1566His) n.522T>G | |
| 14 | g.23416262G>A | CA485766428 | MHRT,MYH7 | c.4695C>T (p.Phe1565=) n.523G>A | |
| 14 | g.23416262G>C | CA389037839 | MHRT,MYH7 | c.4695C>G (p.Phe1565Leu) n.523G>C | |
| 14 | g.23416262G>T | CA389037840 | MHRT,MYH7 | c.4695C>A (p.Phe1565Leu) n.523G>T | |
| 14 | g.23416263A>C | CA389037841 | MHRT,MYH7 | c.4694T>G (p.Phe1565Cys) n.524A>C | |
| 14 | g.23416263A>G | CA389037842 | MHRT,MYH7 | c.4694T>C (p.Phe1565Ser) n.524A>G | |
| 14 | g.23416263A>T | CA389037843 | MHRT,MYH7 | c.4694T>A (p.Phe1565Tyr) n.524A>T | |
| 14 | g.23416264A>C | CA389037844 | MHRT,MYH7 | c.4693T>G (p.Phe1565Val) n.525A>C | gnomAD v3 gnomAD v4 |
| 14 | g.23416264A>G | CA389037845 | MHRT,MYH7 | c.4693T>C (p.Phe1565Leu) n.525A>G | gnomAD v4 |
| 14 | g.23416264A>T | CA389037846 | MHRT,MYH7 | c.4693T>A (p.Phe1565Ile) n.525A>T | |
| 14 | g.23416265C>A | CA389037847 | MHRT,MYH7 | c.4692G>T (p.Glu1564Asp) n.526C>A | |
| 14 | g.23416265C>G | CA389037848 | MHRT,MYH7 | c.4692G>C (p.Glu1564Asp) n.526C>G | |
| 14 | g.23416265C>T | CA485766434 | MHRT,MYH7 | c.4692G>A (p.Glu1564=) n.526C>T | |
| 14 | g.23416266T>A | CA389037851 | MHRT,MYH7 | c.4691A>T (p.Glu1564Val) n.527T>A | |
| 14 | g.23416266T>C | CA389037850 | MHRT,MYH7 | c.4691A>G (p.Glu1564Gly) n.527T>C | |
| 14 | g.23416266T>G | CA389037849 | MHRT,MYH7 | c.4691A>C (p.Glu1564Ala) n.527T>G | ClinVar |
| 14 | g.23416267C>A | CA389037852 | MHRT,MYH7 | c.4690G>T (p.Glu1564Ter) n.528C>A | |
| 14 | g.23416267C>G | CA389037854 | MHRT,MYH7 | c.4690G>C (p.Glu1564Gln) n.528C>G | gnomAD v4 |
| 14 | g.23416267C>T | CA389037853 | MHRT,MYH7 | c.4690G>A (p.Glu1564Lys) n.528C>T | |
| 14 | g.23416268C>A | CA485766436 | MHRT,MYH7 | c.4689G>T (p.Leu1563=) n.529C>A | |
| 14 | g.23416268C= | CA2123465965 | MHRT,MYH7 | c.4689G= (p.Leu1563=) n.529C= | |
| 14 | g.23416268C>G | CA485766435 | MHRT,MYH7 | c.4689G>C (p.Leu1563=) n.529C>G | ClinVar dbSNP |
| 14 | g.23416268C>T | CA043646 | MHRT,MYH7 | c.4689G>A (p.Leu1563=) n.529C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |