| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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 |
| 14 | g.23416269A>C | CA389037857 | MHRT,MYH7 | c.4688T>G (p.Leu1563Arg) n.530A>C | |
| 14 | g.23416269A>G | CA389037855 | MHRT,MYH7 | c.4688T>C (p.Leu1563Pro) n.530A>G | |
| 14 | g.23416269A>T | CA389037856 | MHRT,MYH7 | c.4688T>A (p.Leu1563Gln) n.530A>T | |
| 14 | g.23416270G>A | CA485766439 | MHRT,MYH7 | c.4687C>T (p.Leu1563=) n.531G>A | |
| 14 | g.23416270G>C | CA015233 | MHRT,MYH7 | c.4687C>G (p.Leu1563Val) n.531G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416270G= | CA2123465976 | MHRT,MYH7 | c.4687C= (p.Leu1563=) n.531G= | |
| 14 | g.23416270G>T | CA389037858 | MHRT,MYH7 | c.4687C>A (p.Leu1563Met) n.531G>T | |
| 14 | g.23416271C>A | CA389037859 | MHRT,MYH7 | c.4686G>T (p.Gln1562His) n.532C>A | |
| 14 | g.23416271C>G | CA389037860 | MHRT,MYH7 | c.4686G>C (p.Gln1562His) n.532C>G | |
| 14 | g.23416271C>T | CA485766444 | MHRT,MYH7 | c.4686G>A (p.Gln1562=) n.532C>T | ClinVar dbSNP |
| 14 | g.23416271_23416287delinsCTGGGCCCGGAGGATCT | CA2123465986 | MHRT,MYH7 | c.4670_4686delinsAGATCCTCCGGGCCCAG (p.Lys1557=) n.532_548delinsCTGGGCCCGGAGGATCT | |
| 14 | g.23416272T>A | CA389037861 | MHRT,MYH7 | c.4685A>T (p.Gln1562Leu) n.533T>A | |
| 14 | g.23416272T>C | CA389037862 | MHRT,MYH7 | c.4685A>G (p.Gln1562Arg) n.533T>C | |
| 14 | g.23416272T>G | CA389037863 | MHRT,MYH7 | c.4685A>C (p.Gln1562Pro) n.533T>G | |
| 14 | g.23416274_23416289del | CA043479 | MHRT,MYH7 | c.4670_4685del (p.Lys1557SerfsTer?) n.535_550del | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416273G>A | CA389037866 | MHRT,MYH7 | c.4684C>T (p.Gln1562Ter) n.534G>A | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416273G>C | CA389037865 | MHRT,MYH7 | c.4684C>G (p.Gln1562Glu) n.534G>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416273G= | CA2123465994 | MHRT,MYH7 | c.4684C= (p.Gln1562=) n.534G= | |
| 14 | g.23416273G>T | CA389037864 | MHRT,MYH7 | c.4684C>A (p.Gln1562Lys) n.534G>T | gnomAD v4 |
| 14 | g.23416274G>A | CA485766450 | MHRT,MYH7 | c.4683C>T (p.Ala1561=) n.535G>A | gnomAD v4 |
| 14 | g.23416274G>C | CA485766451 | MHRT,MYH7 | c.4683C>G (p.Ala1561=) n.535G>C | |
| 14 | g.23416274G= | CA2123465998 | MHRT,MYH7 | c.4683C= (p.Ala1561=) n.535G= | |
| 14 | g.23416274G>T | CA043625 | MHRT,MYH7 | c.4683C>A (p.Ala1561=) n.535G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416275G>A | CA389037867 | MHRT,MYH7 | c.4682C>T (p.Ala1561Val) n.536G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416275G>C | CA389037868 | MHRT,MYH7 | c.4682C>G (p.Ala1561Gly) n.536G>C | |
| 14 | g.23416275G= | CA2123466004 | MHRT,MYH7 | c.4682C= (p.Ala1561=) n.536G= | |
| 14 | g.23416275G>T | CA389037869 | MHRT,MYH7 | c.4682C>A (p.Ala1561Asp) n.536G>T | gnomAD v4 |
| 14 | g.23416275_23416276delinsGC | CA2123466007 | MHRT,MYH7 | c.4681_4682delinsGC (p.Ala1561=) n.536_537delinsGC | |
| 14 | g.23416276C>A | CA389037870 | MHRT,MYH7 | c.4681G>T (p.Ala1561Ser) n.537C>A | ClinVar gnomAD v4 |
| 14 | g.23416276C= | CA2123466015 | MHRT,MYH7 | c.4681G= (p.Ala1561=) n.537C= | |
| 14 | g.23416276C>G | CA16619846 | MHRT,MYH7 | c.4681G>C (p.Ala1561Pro) n.537C>G | ClinVar dbSNP |
| 14 | g.23416276C>T | CA389037871 | MHRT,MYH7 | c.4681G>A (p.Ala1561Thr) n.537C>T | |
| 14 | g.23416278del | CA613317654 | MHRT,MYH7 | c.4681del (p.Ala1561ProfsTer?) n.539del | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416277C>A | CA485766457 | MHRT,MYH7 | c.4680G>T (p.Arg1560=) n.538C>A | |
| 14 | g.23416277C= | CA2123466023 | MHRT,MYH7 | c.4680G= (p.Arg1560=) n.538C= | |
| 14 | g.23416277C>G | CA485766458 | MHRT,MYH7 | c.4680G>C (p.Arg1560=) n.538C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23416277C>T | CA043587 | MHRT,MYH7 | c.4680G>A (p.Arg1560=) n.538C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416278C>A | CA389037872 | MHRT,MYH7 | c.4679G>T (p.Arg1560Leu) n.539C>A | |
| 14 | g.23416278C= | CA2123466037 | MHRT,MYH7 | c.4679G= (p.Arg1560=) n.539C= | |
| 14 | g.23416278C>G | CA389037873 | MHRT,MYH7 | c.4679G>C (p.Arg1560Pro) n.539C>G | ClinVar dbSNP |
| 14 | g.23416278C>T | CA015224 | MHRT,MYH7 | c.4679G>A (p.Arg1560Gln) n.539C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416279G>A | CA043564 | MHRT,MYH7 | c.4678C>T (p.Arg1560Trp) n.540G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23416279G>C | CA389037874 | MHRT,MYH7 | c.4678C>G (p.Arg1560Gly) n.540G>C | |
| 14 | g.23416279G= | CA2123466049 | MHRT,MYH7 | c.4678C= (p.Arg1560=) n.540G= | |
| 14 | g.23416279G>T | CA043550 | MHRT,MYH7 | c.4678C>A (p.Arg1560=) n.540G>T | dbSNP ExAC gnomAD v2 |
| 14 | g.23416280G>A | CA043534 | MHRT,MYH7 | c.4677C>T (p.Leu1559=) n.541G>A | dbSNP ExAC gnomAD v2 |
| 14 | g.23416280G>C | CA485766462 | MHRT,MYH7 | c.4677C>G (p.Leu1559=) n.541G>C | gnomAD v4 |
| 14 | g.23416280G= | CA2123466057 | MHRT,MYH7 | c.4677C= (p.Leu1559=) n.541G= | |
| 14 | g.23416280G>T | CA043517 | MHRT,MYH7 | c.4677C>A (p.Leu1559=) n.541G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416281A>C | CA389037875 | MHRT,MYH7 | c.4676T>G (p.Leu1559Arg) n.542A>C | |
| 14 | g.23416281A>G | CA389037876 | MHRT,MYH7 | c.4676T>C (p.Leu1559Pro) n.542A>G | |
| 14 | g.23416281A>T | CA389037877 | MHRT,MYH7 | c.4676T>A (p.Leu1559His) n.542A>T | |
| 14 | g.23416282G>A | CA389037878 | MHRT,MYH7 | c.4675C>T (p.Leu1559Phe) n.543G>A | |
| 14 | g.23416282G>C | CA389037879 | MHRT,MYH7 | c.4675C>G (p.Leu1559Val) n.543G>C | |
| 14 | g.23416282G>T | CA389037880 | MHRT,MYH7 | c.4675C>A (p.Leu1559Ile) n.543G>T | |
| 14 | g.23416283G>A | CA485766464 | MHRT,MYH7 | c.4674C>T (p.Ile1558=) n.544G>A | ClinVar dbSNP COSMIC |
| 14 | g.23416283G>C | CA389037881 | MHRT,MYH7 | c.4674C>G (p.Ile1558Met) n.544G>C | gnomAD v4 |
| 14 | g.23416283G>T | CA485766465 | MHRT,MYH7 | c.4674C>A (p.Ile1558=) n.544G>T | |
| 14 | g.23416284A= | CA2123466069 | MHRT,MYH7 | c.4673T= (p.Ile1558=) n.545A= | |
| 14 | g.23416284A>C | CA257810745 | MHRT,MYH7 | c.4673T>G (p.Ile1558Ser) n.545A>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416284A>G | CA389037882 | MHRT,MYH7 | c.4673T>C (p.Ile1558Thr) n.545A>G | |
| 14 | g.23416284A>T | CA389037883 | MHRT,MYH7 | c.4673T>A (p.Ile1558Asn) n.545A>T | |
| 14 | g.23416285T>A | CA043503 | MHRT,MYH7 | c.4672A>T (p.Ile1558Phe) n.546T>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416285T>C | CA389037884 | MHRT,MYH7 | c.4672A>G (p.Ile1558Val) n.546T>C | |
| 14 | g.23416285T>G | CA389037885 | MHRT,MYH7 | c.4672A>C (p.Ile1558Leu) n.546T>G | |
| 14 | g.23416285T= | CA2123466077 | MHRT,MYH7 | c.4672A= (p.Ile1558=) n.546T= | |
| 14 | g.23416286C>A | CA389037886 | MHRT,MYH7 | c.4671G>T (p.Lys1557Asn) n.547C>A | ClinVar COSMIC |
| 14 | g.23416286C= | CA2123466087 | MHRT,MYH7 | c.4671G= (p.Lys1557=) n.547C= | |
| 14 | g.23416286C>G | CA389037887 | MHRT,MYH7 | c.4671G>C (p.Lys1557Asn) n.547C>G | |
| 14 | g.23416286C>T | CA015216 | MHRT,MYH7 | c.4671G>A (p.Lys1557=) n.547C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416287T>A | CA389037888 | MHRT,MYH7 | c.4670A>T (p.Lys1557Met) n.548T>A | |
| 14 | g.23416287T>C | CA389037889 | MHRT,MYH7 | c.4670A>G (p.Lys1557Arg) n.548T>C | ClinVar dbSNP |
| 14 | g.23416287T>G | CA389037890 | MHRT,MYH7 | c.4670A>C (p.Lys1557Thr) n.548T>G | |
| 14 | g.23416287T= | CA2123466096 | MHRT,MYH7 | c.4670A= (p.Lys1557=) n.548T= | |
| 14 | g.23416288T>A | CA389037891 | MHRT,MYH7 | c.4669A>T (p.Lys1557Ter) n.549T>A | |
| 14 | g.23416288T>C | CA389037892 | MHRT,MYH7 | c.4669A>G (p.Lys1557Glu) n.549T>C | |
| 14 | g.23416288T>G | CA389037893 | MHRT,MYH7 | c.4669A>C (p.Lys1557Gln) n.549T>G | |
| 14 | g.23416289G>A | CA485766468 | MHRT,MYH7 | c.4668C>T (p.Gly1556=) n.550G>A | |
| 14 | g.23416289G>C | CA485766471 | MHRT,MYH7 | c.4668C>G (p.Gly1556=) n.550G>C | |
| 14 | g.23416289G= | CA2123466101 | MHRT,MYH7 | c.4668C= (p.Gly1556=) n.550G= | |
| 14 | g.23416289G>T | CA043470 | MHRT,MYH7 | c.4668C>A (p.Gly1556=) n.550G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416290C>A | CA389037894 | MHRT,MYH7 | c.4667G>T (p.Gly1556Val) n.551C>A | |
| 14 | g.23416290C= | CA2123466109 | MHRT,MYH7 | c.4667G= (p.Gly1556=) n.551C= | |
| 14 | g.23416290C>G | CA389037895 | MHRT,MYH7 | c.4667G>C (p.Gly1556Ala) n.551C>G | |
| 14 | g.23416290C>T | CA389037896 | MHRT,MYH7 | c.4667G>A (p.Gly1556Asp) n.551C>T | ClinVar dbSNP |
| 14 | g.23416291C>A | CA389037898 | MHRT,MYH7 | c.4666G>T (p.Gly1556Cys) n.552C>A | dbSNP |
| 14 | g.23416291C= | CA2123466118 | MHRT,MYH7 | c.4666G= (p.Gly1556=) n.552C= | |
| 14 | g.23416291C>G | CA389037899 | MHRT,MYH7 | c.4666G>C (p.Gly1556Arg) n.552C>G | |
| 14 | g.23416291C>T | CA389037897 | MHRT,MYH7 | c.4666G>A (p.Gly1556Ser) n.552C>T | |
| 14 | g.23416292C>A | CA389037901 | MHRT,MYH7 | c.4665G>T (p.Glu1555Asp) n.553C>A | |
| 14 | g.23416292C= | CA2123466125 | MHRT,MYH7 | c.4665G= (p.Glu1555=) n.553C= | |
| 14 | g.23416292C>G | CA389037900 | MHRT,MYH7 | c.4665G>C (p.Glu1555Asp) n.553C>G | |
| 14 | g.23416292C>T | CA485766473 | MHRT,MYH7 | c.4665G>A (p.Glu1555=) n.553C>T | ClinVar dbSNP |
| 14 | g.23416293T>A | CA389037902 | MHRT,MYH7 | c.4664A>T (p.Glu1555Val) n.554T>A | |
| 14 | g.23416293T>C | CA015211 | MHRT,MYH7 | c.4664A>G (p.Glu1555Gly) n.554T>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416293T>G | CA389037903 | MHRT,MYH7 | c.4664A>C (p.Glu1555Ala) n.554T>G | |
| 14 | g.23416293T= | CA2123466131 | MHRT,MYH7 | c.4664A= (p.Glu1555=) n.554T= | |
| 14 | g.23416294C>A | CA389037904 | MHRT,MYH7 | c.4663G>T (p.Glu1555Ter) n.555C>A | |
| 14 | g.23416294C= | CA2123466138 | MHRT,MYH7 | c.4663G= (p.Glu1555=) n.555C= | |
| 14 | g.23416294C>G | CA015206 | MHRT,MYH7 | c.4663G>C (p.Glu1555Gln) n.555C>G | ClinVar dbSNP |
| 14 | g.23416294C>T | CA389037905 | MHRT,MYH7 | c.4663G>A (p.Glu1555Lys) n.555C>T | ClinVar dbSNP COSMIC |
| 14 | g.23416295C>A | CA389037906 | MHRT,MYH7 | c.4662G>T (p.Glu1554Asp) n.556C>A | |
| 14 | g.23416295C= | CA2123466147 | MHRT,MYH7 | c.4662G= (p.Glu1554=) n.556C= | |
| 14 | g.23416295C>G | CA389037907 | MHRT,MYH7 | c.4662G>C (p.Glu1554Asp) n.556C>G | |
| 14 | g.23416295C>T | CA043454 | MHRT,MYH7 | c.4662G>A (p.Glu1554=) n.556C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416296T>A | CA389037908 | MHRT,MYH7 | c.4661A>T (p.Glu1554Val) n.557T>A | |
| 14 | g.23416296T>C | CA389037909 | MHRT,MYH7 | c.4661A>G (p.Glu1554Gly) n.557T>C | |
| 14 | g.23416296T>G | CA389037910 | MHRT,MYH7 | c.4661A>C (p.Glu1554Ala) n.557T>G | |
| 14 | g.23416297C>A | CA389037911 | MHRT,MYH7 | c.4660G>T (p.Glu1554Ter) n.558C>A | |
| 14 | g.23416297C= | CA2123466153 | MHRT,MYH7 | c.4660G= (p.Glu1554=) n.558C= | |
| 14 | g.23416297C>G | CA043434 | MHRT,MYH7 | c.4660G>C (p.Glu1554Gln) n.558C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416297C>T | CA389037912 | MHRT,MYH7 | c.4660G>A (p.Glu1554Lys) n.558C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416298G>A | CA043411 | MHRT,MYH7 | c.4659C>T (p.His1553=) n.558+1G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416298G>C | CA389037913 | MHRT,MYH7 | c.4659C>G (p.His1553Gln) n.558+1G>C | ClinVar |
| 14 | g.23416298G= | CA2123466161 | MHRT,MYH7 | c.4659C= (p.His1553=) n.558+1G= | |
| 14 | g.23416298G>T | CA389037914 | MHRT,MYH7 | c.4659C>A (p.His1553Gln) n.558+1G>T | |
| 14 | g.23416299T>A | CA389037915 | MHRT,MYH7 | c.4658A>T (p.His1553Leu) n.558+2T>A | |
| 14 | g.23416299T>C | CA389037916 | MHRT,MYH7 | c.4658A>G (p.His1553Arg) n.558+2T>C | |
| 14 | g.23416299T>G | CA389037917 | MHRT,MYH7 | c.4658A>C (p.His1553Pro) n.558+2T>G | |
| 14 | g.23416300G>A | CA389037918 | MHRT,MYH7 | c.4657C>T (p.His1553Tyr) n.558+3G>A | |
| 14 | g.23416300G>C | CA389037919 | MHRT,MYH7 | c.4657C>G (p.His1553Asp) n.558+3G>C | |
| 14 | g.23416300G>T | CA389037920 | MHRT,MYH7 | c.4657C>A (p.His1553Asn) n.558+3G>T |