Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23419920C>ACA485766658MYH7c.3651G>T (p.Leu1217=)
gnomAD v4
14g.23419920C>GCA485766659MYH7c.3651G>C (p.Leu1217=)
14g.23419920C>TCA485766660MYH7c.3651G>A (p.Leu1217=)
ClinVar
14g.23419921A>CCA389043170MYH7c.3650T>G (p.Leu1217Arg)
14g.23419921A>GCA389043172MYH7c.3650T>C (p.Leu1217Pro)
14g.23419921A>TCA389043173MYH7c.3650T>A (p.Leu1217Gln)
14g.23419922G>ACA485766661MYH7c.3649C>T (p.Leu1217=)
14g.23419922G>CCA389043174MYH7c.3649C>G (p.Leu1217Val)
14g.23419922G>TCA389043175MYH7c.3649C>A (p.Leu1217Met)
14g.23419923C>ACA389043177MYH7c.3648G>T (p.Lys1216Asn)
14g.23419923C=CA2123446179MYH7c.3648G= (p.Lys1216=)
14g.23419923C>GCA389043179MYH7c.3648G>C (p.Lys1216Asn)
14g.23419923C>TCA485766662MYH7c.3648G>A (p.Lys1216=)
ClinVar dbSNP COSMIC
14g.23419924T>ACA389043180MYH7c.3647A>T (p.Lys1216Met)
14g.23419924T>CCA389043182MYH7c.3647A>G (p.Lys1216Arg)
14g.23419924T>GCA389043183MYH7c.3647A>C (p.Lys1216Thr)
gnomAD v4
14g.23419925T>ACA389043185MYH7c.3646A>T (p.Lys1216Ter)
14g.23419925T>CCA389043186MYH7c.3646A>G (p.Lys1216Glu)
14g.23419925T>GCA389043184MYH7c.3646A>C (p.Lys1216Gln)
14g.23419926C>ACA389043188MYH7c.3645G>T (p.Gln1215His)
14g.23419926C=CA2123446186MYH7c.3645G= (p.Gln1215=)
14g.23419926C>GCA279271MYH7c.3645G>C (p.Gln1215His)
ClinVar dbSNP gnomAD v4
14g.23419926C>TCA485766663MYH7c.3645G>A (p.Gln1215=)
ClinVar dbSNP gnomAD v4
14g.23419927T>ACA389043189MYH7c.3644A>T (p.Gln1215Leu)
14g.23419927T>CCA257815434MYH7c.3644A>G (p.Gln1215Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419927T>GCA389043191MYH7c.3644A>C (p.Gln1215Pro)
ClinVar dbSNP
14g.23419927T=CA2123446195MYH7c.3644A= (p.Gln1215=)
14g.23419928G>ACA389043193MYH7c.3643C>T (p.Gln1215Ter)
ClinVar
14g.23419928G>CCA389043195MYH7c.3643C>G (p.Gln1215Glu)
ClinVar dbSNP
14g.23419928G>TCA389043196MYH7c.3643C>A (p.Gln1215Lys)
14g.23419929C>ACA389043197MYH7c.3642G>T (p.Lys1214Asn)
14g.23419929C>GCA389043199MYH7c.3642G>C (p.Lys1214Asn)
dbSNP
14g.23419929C>TCA485766664MYH7c.3642G>A (p.Lys1214=)
14g.23419930T>ACA389043201MYH7c.3641A>T (p.Lys1214Met)
14g.23419930T>CCA389043202MYH7c.3641A>G (p.Lys1214Arg)
14g.23419930T>GCA389043204MYH7c.3641A>C (p.Lys1214Thr)
14g.23419931T>ACA389043205MYH7c.3640A>T (p.Lys1214Ter)
14g.23419931T>CCA389043209MYH7c.3640A>G (p.Lys1214Glu)
14g.23419931T>GCA389043207MYH7c.3640A>C (p.Lys1214Gln)
14g.23419932C>ACA485766665MYH7c.3639G>T (p.Val1213=)
14g.23419932C=CA2123446199MYH7c.3639G= (p.Val1213=)
14g.23419932C>GCA485766666MYH7c.3639G>C (p.Val1213=)
14g.23419932C>TCA485766667MYH7c.3639G>A (p.Val1213=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419933A=CA2123446203MYH7c.3638T= (p.Val1213=)
14g.23419933A>CCA389043210MYH7c.3638T>G (p.Val1213Gly)
dbSNP
14g.23419933A>GCA389043211MYH7c.3638T>C (p.Val1213Ala)
14g.23419933A>TCA389043213MYH7c.3638T>A (p.Val1213Glu)
14g.23419934C>ACA389043214MYH7c.3637G>T (p.Val1213Leu)
14g.23419934C=CA2123446205MYH7c.3637G= (p.Val1213=)
14g.23419934C>GCA389043216MYH7c.3637G>C (p.Val1213Leu)
14g.23419934C>TCA013913MYH7c.3637G>A (p.Val1213Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419935C>ACA485766668MYH7c.3636G>T (p.Arg1212=)
14g.23419935C>GCA485766669MYH7c.3636G>C (p.Arg1212=)
14g.23419935C>TCA485766670MYH7c.3636G>A (p.Arg1212=)
ClinVar dbSNP
14g.23419936C>ACA389043217MYH7c.3635G>T (p.Arg1212Leu)
14g.23419936C=CA2123446211MYH7c.3635G= (p.Arg1212=)
14g.23419936C>GCA389043218MYH7c.3635G>C (p.Arg1212Pro)
14g.23419936C>TCA389043219MYH7c.3635G>A (p.Arg1212Gln)
ClinVar dbSNP gnomAD v4
14g.23419937G>ACA389043221MYH7c.3634C>T (p.Arg1212Trp)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23419937G>CCA389043223MYH7c.3634C>G (p.Arg1212Gly)
14g.23419937G=CA2123446213MYH7c.3634C= (p.Arg1212=)
14g.23419937G>TCA485766671MYH7c.3634C>A (p.Arg1212=)
14g.23419938C>ACA389043225MYH7c.3633G>T (p.Gln1211His)
14g.23419938C>GCA389043226MYH7c.3633G>C (p.Gln1211His)
14g.23419938C>TCA485766672MYH7c.3633G>A (p.Gln1211=)
14g.23419939T>ACA389043227MYH7c.3632A>T (p.Gln1211Leu)
14g.23419939T>CCA389043231MYH7c.3632A>G (p.Gln1211Arg)
14g.23419939T>GCA389043229MYH7c.3632A>C (p.Gln1211Pro)
14g.23419940G>ACA389043232MYH7c.3631C>T (p.Gln1211Ter)
ClinVar dbSNP
14g.23419940G>CCA389043234MYH7c.3631C>G (p.Gln1211Glu)
ClinVar dbSNP
14g.23419940G=CA2123446218MYH7c.3631C= (p.Gln1211=)
14g.23419940G>TCA389043235MYH7c.3631C>A (p.Gln1211Lys)
14g.23419941C>ACA485766673MYH7c.3630G>T (p.Leu1210=)
14g.23419941C>GCA485766674MYH7c.3630G>C (p.Leu1210=)
14g.23419941C>TCA485766675MYH7c.3630G>A (p.Leu1210=)
ClinVar
14g.23419942delCA2575504281MYH7c.3629del (p.Leu1210ArgfsTer4)
14g.23419942A>CCA389043237MYH7c.3629T>G (p.Leu1210Arg)
14g.23419942A>GCA389043238MYH7c.3629T>C (p.Leu1210Pro)
14g.23419942A>TCA389043240MYH7c.3629T>A (p.Leu1210Gln)
14g.23419943G>ACA038206MYH7c.3628C>T (p.Leu1210=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419943G>CCA389043242MYH7c.3628C>G (p.Leu1210Val)
14g.23419943G=CA2123446221MYH7c.3628C= (p.Leu1210=)
14g.23419943G>TCA389043243MYH7c.3628C>A (p.Leu1210Met)
14g.23419944G>ACA485766676MYH7c.3627C>T (p.Asn1209=)
ClinVar gnomAD v4
14g.23419944G>CCA013908MYH7c.3627C>G (p.Asn1209Lys)
ClinVar dbSNP
14g.23419944G=CA2123446224MYH7c.3627C= (p.Asn1209=)
14g.23419944G>TCA389043244MYH7c.3627C>A (p.Asn1209Lys)
14g.23419945T>ACA389043247MYH7c.3626A>T (p.Asn1209Ile)
14g.23419945T>CCA013898MYH7c.3626A>G (p.Asn1209Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419945T>GCA038184MYH7c.3626A>C (p.Asn1209Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419945T=CA2123446233MYH7c.3626A= (p.Asn1209=)
14g.23419946T>ACA389043248MYH7c.3625A>T (p.Asn1209Tyr)
14g.23419946T>CCA389043249MYH7c.3625A>G (p.Asn1209Asp)
14g.23419946T>GCA389043251MYH7c.3625A>C (p.Asn1209His)
14g.23419947G>ACA485766677MYH7c.3624C>T (p.Asp1208=)
14g.23419947G>CCA389043252MYH7c.3624C>G (p.Asp1208Glu)
14g.23419947G>TCA389043254MYH7c.3624C>A (p.Asp1208Glu)
14g.23419948T>ACA389043256MYH7c.3623A>T (p.Asp1208Val)
14g.23419948T>CCA389043257MYH7c.3623A>G (p.Asp1208Gly)
14g.23419948T>GCA389043259MYH7c.3623A>C (p.Asp1208Ala)
14g.23419949C>ACA389043260MYH7c.3622G>T (p.Asp1208Tyr)
14g.23419949C=CA2123446236MYH7c.3622G= (p.Asp1208=)
14g.23419949C>GCA013891MYH7c.3622G>C (p.Asp1208His)
ClinVar dbSNP ExAC gnomAD v2
14g.23419949C>TCA079535MYH7c.3622G>A (p.Asp1208Asn)
ClinVar dbSNP gnomAD v4
14g.23419950G>ACA013881MYH7c.3621C>T (p.Ile1207=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23419950G>CCA038128MYH7c.3621C>G (p.Ile1207Met)
ClinVar dbSNP ExAC gnomAD v4
14g.23419950G=CA2123446245MYH7c.3621C= (p.Ile1207=)
14g.23419950G>TCA038110MYH7c.3621C>A (p.Ile1207=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419951A=CA2123446264MYH7c.3620T= (p.Ile1207=)
14g.23419951A>CCA389043265MYH7c.3620T>G (p.Ile1207Ser)
14g.23419951A>GCA389043267MYH7c.3620T>C (p.Ile1207Thr)
14g.23419951A>TCA013873MYH7c.3620T>A (p.Ile1207Asn)
ClinVar dbSNP gnomAD v4
14g.23419952T>ACA389043270MYH7c.3619A>T (p.Ile1207Phe)
gnomAD v4
14g.23419952T>CCA389043271MYH7c.3619A>G (p.Ile1207Val)
14g.23419952T>GCA389043272MYH7c.3619A>C (p.Ile1207Leu)
14g.23419953C>ACA389043273MYH7c.3618G>T (p.Gln1206His)
14g.23419953C=CA2123446269MYH7c.3618G= (p.Gln1206=)
14g.23419953C>GCA389043275MYH7c.3618G>C (p.Gln1206His)
14g.23419953C>TCA485766678MYH7c.3618G>A (p.Gln1206=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419954T>ACA389043277MYH7c.3617A>T (p.Gln1206Leu)
14g.23419954T>CCA038093MYH7c.3617A>G (p.Gln1206Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419954T>GCA389043281MYH7c.3617A>C (p.Gln1206Pro)
14g.23419954T=CA2123446271MYH7c.3617A= (p.Gln1206=)
14g.23419955G>ACA389043283MYH7c.3616C>T (p.Gln1206Ter)
gnomAD v4
14g.23419955G>CCA389043285MYH7c.3616C>G (p.Gln1206Glu)
14g.23419955G>TCA389043287MYH7c.3616C>A (p.Gln1206Lys)
14g.23419956C>ACA389043288MYH7c.3615G>T (p.Glu1205Asp)
14g.23419956C>GCA389043289MYH7c.3615G>C (p.Glu1205Asp)
14g.23419956C>TCA485766679MYH7c.3615G>A (p.Glu1205=)
14g.23419957T>ACA389043290MYH7c.3614A>T (p.Glu1205Val)
14g.23419957T>CCA16619847MYH7c.3614A>G (p.Glu1205Gly)
ClinVar dbSNP
14g.23419957T>GCA389043292MYH7c.3614A>C (p.Glu1205Ala)
14g.23419957T=CA2123446276MYH7c.3614A= (p.Glu1205=)
14g.23419958C>ACA389043294MYH7c.3613G>T (p.Glu1205Ter)
14g.23419958C=CA2123446285MYH7c.3613G= (p.Glu1205=)
14g.23419958C>GCA389043296MYH7c.3613G>C (p.Glu1205Gln)
14g.23419958C>TCA013863MYH7c.3613G>A (p.Glu1205Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419959G>ACA013856MYH7c.3612C>T (p.Gly1204=)
ClinVar dbSNP
14g.23419959G>CCA485766680MYH7c.3612C>G (p.Gly1204=)
gnomAD v4
14g.23419959G=CA2123446292MYH7c.3612C= (p.Gly1204=)
14g.23419959G>TCA485766681MYH7c.3612C>A (p.Gly1204=)
14g.23419960C>ACA389043298MYH7c.3611G>T (p.Gly1204Val)
14g.23419960C=CA2123446295MYH7c.3611G= (p.Gly1204=)
14g.23419960C>GCA389043300MYH7c.3611G>C (p.Gly1204Ala)
14g.23419960C>TCA038065MYH7c.3611G>A (p.Gly1204Asp)
dbSNP ExAC gnomAD v2
14g.23419961C>ACA389043302MYH7c.3610G>T (p.Gly1204Cys)
14g.23419961C=CA2123446298MYH7c.3610G= (p.Gly1204=)
14g.23419961C>GCA013846MYH7c.3610G>C (p.Gly1204Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419961C>TCA038038MYH7c.3610G>A (p.Gly1204Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419962C>ACA485766682MYH7c.3609G>T (p.Leu1203=)
ClinVar dbSNP
14g.23419962C=CA2123446304MYH7c.3609G= (p.Leu1203=)
14g.23419962C>GCA485766683MYH7c.3609G>C (p.Leu1203=)
14g.23419962C>TCA485766684MYH7c.3609G>A (p.Leu1203=)
14g.23419963A>CCA389043305MYH7c.3608T>G (p.Leu1203Arg)
14g.23419963A>GCA389043307MYH7c.3608T>C (p.Leu1203Pro)
14g.23419963A>TCA389043306MYH7c.3608T>A (p.Leu1203Gln)
14g.23419964G>ACA485766685MYH7c.3607C>T (p.Leu1203=)
ClinVar gnomAD v4
14g.23419964G>CCA389043309MYH7c.3607C>G (p.Leu1203Val)
14g.23419964G>TCA389043310MYH7c.3607C>A (p.Leu1203Met)
14g.23419965C>ACA389043312MYH7c.3606G>T (p.Glu1202Asp)
14g.23419965C=CA2123446308MYH7c.3606G= (p.Glu1202=)
14g.23419965C>GCA038018MYH7c.3606G>C (p.Glu1202Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419965C>TCA485766686MYH7c.3606G>A (p.Glu1202=)
ClinVar dbSNP
14g.23419966T>ACA389043315MYH7c.3605A>T (p.Glu1202Val)
14g.23419966T>CCA389043316MYH7c.3605A>G (p.Glu1202Gly)
14g.23419966T>GCA389043318MYH7c.3605A>C (p.Glu1202Ala)
14g.23419967C>ACA037993MYH7c.3604G>T (p.Glu1202Ter)
dbSNP ExAC gnomAD v2
14g.23419967C=CA2123446310MYH7c.3604G= (p.Glu1202=)
14g.23419967C>GCA389043319MYH7c.3604G>C (p.Glu1202Gln)
14g.23419967C>TCA389043320MYH7c.3604G>A (p.Glu1202Lys)
ClinVar dbSNP
14g.23419968G>ACA485766688MYH7c.3603C>T (p.Ala1201=)
ClinVar dbSNP gnomAD v4
14g.23419968G>CCA013836MYH7c.3603C>G (p.Ala1201=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23419968G=CA2123446318MYH7c.3603C= (p.Ala1201=)
14g.23419968G>TCA485766687MYH7c.3603C>A (p.Ala1201=)
dbSNP
14g.23419969G>ACA389043323MYH7c.3602C>T (p.Ala1201Val)
14g.23419969G>CCA389043325MYH7c.3602C>G (p.Ala1201Gly)
gnomAD v4
14g.23419969G>TCA389043326MYH7c.3602C>A (p.Ala1201Asp)
14g.23419970C>ACA389043332MYH7c.3601G>T (p.Ala1201Ser)
14g.23419970C>GCA389043330MYH7c.3601G>C (p.Ala1201Pro)
14g.23419970C>TCA389043328MYH7c.3601G>A (p.Ala1201Thr)
14g.23419971dupCA2697553857MYH7c.3601dup (p.Ala1201GlyfsTer30)
ClinVar
14g.23419971C>ACA485766691MYH7c.3600G>T (p.Val1200=)
14g.23419971C>GCA485766690MYH7c.3600G>C (p.Val1200=)
14g.23419971C>TCA485766689MYH7c.3600G>A (p.Val1200=)
14g.23419972A>CCA389043333MYH7c.3599T>G (p.Val1200Gly)
14g.23419972A>GCA389043334MYH7c.3599T>C (p.Val1200Ala)
gnomAD v4
14g.23419972A>TCA389043336MYH7c.3599T>A (p.Val1200Glu)
14g.23419973C>ACA389043338MYH7c.3598G>T (p.Val1200Leu)
14g.23419973C=CA2123446331MYH7c.3598G= (p.Val1200=)
14g.23419973C>GCA389043340MYH7c.3598G>C (p.Val1200Leu)
14g.23419973C>TCA037979MYH7c.3598G>A (p.Val1200Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419974G>ACA485766692MYH7c.3597C>T (p.Ser1199=)
ClinVar dbSNP gnomAD v4
14g.23419974G>CCA013829MYH7c.3597C>G (p.Ser1199Arg)
ClinVar dbSNP
14g.23419974G=CA2123446338MYH7c.3597C= (p.Ser1199=)
14g.23419974G>TCA389043342MYH7c.3597C>A (p.Ser1199Arg)
ClinVar gnomAD v4
14g.23419975C>ACA389043344MYH7c.3596G>T (p.Ser1199Ile)
14g.23419975C=CA2123446345MYH7c.3596G= (p.Ser1199=)
14g.23419975C>GCA389043346MYH7c.3596G>C (p.Ser1199Thr)
dbSNP gnomAD v2 gnomAD v4
14g.23419975C>TCA389043347MYH7c.3596G>A (p.Ser1199Asn)
dbSNP gnomAD v2 gnomAD v4
14g.23419976T>ACA389043349MYH7c.3595A>T (p.Ser1199Cys)
14g.23419976T>CCA389043350MYH7c.3595A>G (p.Ser1199Gly)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23419976T>GCA389043348MYH7c.3595A>C (p.Ser1199Arg)
14g.23419976T=CA2123446351MYH7c.3595A= (p.Ser1199=)
14g.23419977G>ACA485766693MYH7c.3594C>T (p.Asp1198=)
14g.23419977G>CCA389043351MYH7c.3594C>G (p.Asp1198Glu)
gnomAD v4
14g.23419977G>TCA389043352MYH7c.3594C>A (p.Asp1198Glu)
14g.23419978delCA2697553858MYH7c.3593del (p.Asp1198AlafsTer16)
ClinVar
14g.23419978T>ACA389043354MYH7c.3593A>T (p.Asp1198Val)
14g.23419978T>CCA389043355MYH7c.3593A>G (p.Asp1198Gly)
dbSNP gnomAD v2 gnomAD v4
14g.23419978T>GCA389043356MYH7c.3593A>C (p.Asp1198Ala)
14g.23419978T=CA2123446369MYH7c.3593A= (p.Asp1198=)
14g.23419978_23419979delinsTCCA2123446355MYH7c.3592_3593delinsGA (p.Asp1198=)
14g.23419978_23419980delinsTCGCA2123446359MYH7c.3591_3593delinsCGA (p.Ala1197=)
14g.23419979delCA037972MYH7c.3592del (p.Asp1198ThrfsTer16)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419979C>ACA389043359MYH7c.3592G>T (p.Asp1198Tyr)
ClinVar dbSNP gnomAD v4
14g.23419979C=CA2123446387MYH7c.3592G= (p.Asp1198=)
14g.23419979C>GCA389043360MYH7c.3592G>C (p.Asp1198His)
14g.23419979C>TCA013820MYH7c.3592G>A (p.Asp1198Asn)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23419979_23419980delinsGCTTCTTCA10576954MYH7c.3591_3592delinsAAGAAGC (p.Asp1198ArgfsTer18)
ClinVar dbSNP
14g.23419980G>ACA257815584MYH7c.3591C>T (p.Ala1197=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419980G>CCA485766694MYH7c.3591C>G (p.Ala1197=)
ClinVar
14g.23419980G=CA2123446404MYH7c.3591C= (p.Ala1197=)
14g.23419980G>TCA485766695MYH7c.3591C>A (p.Ala1197=)
14g.23419980_23419981insCTTCTTCA037944MYH7c.3590_3591insAAGAAG (p.Ala1197_Asp1198insArgSer)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419981G>ACA389043366MYH7c.3590C>T (p.Ala1197Val)
14g.23419981G>CCA389043365MYH7c.3590C>G (p.Ala1197Gly)
14g.23419981G>TCA389043363MYH7c.3590C>A (p.Ala1197Asp)
14g.23419982C>ACA389043368MYH7c.3589G>T (p.Ala1197Ser)
14g.23419982C=CA2123446411MYH7c.3589G= (p.Ala1197=)
14g.23419982C>GCA389043370MYH7c.3589G>C (p.Ala1197Pro)
14g.23419982C>TCA389043371MYH7c.3589G>A (p.Ala1197Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419983G>ACA037926MYH7c.3588C>T (p.His1196=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419983G>CCA389043373MYH7c.3588C>G (p.His1196Gln)
gnomAD v4
14g.23419983G=CA2123446416MYH7c.3588C= (p.His1196=)
14g.23419983G>TCA389043375MYH7c.3588C>A (p.His1196Gln)
14g.23419984T>ACA389043377MYH7c.3587A>T (p.His1196Leu)
14g.23419984T>CCA389043380MYH7c.3587A>G (p.His1196Arg)
14g.23419984T>GCA389043378MYH7c.3587A>C (p.His1196Pro)
14g.23419985G>ACA389043383MYH7c.3586C>T (p.His1196Tyr)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419985G>CCA389043384MYH7c.3586C>G (p.His1196Asp)
14g.23419985G=CA2123446417MYH7c.3586C= (p.His1196=)
14g.23419985G>TCA389043385MYH7c.3586C>A (p.His1196Asn)
14g.23419986C>ACA389043387MYH7c.3585G>T (p.Lys1195Asn)
14g.23419986C>GCA389043389MYH7c.3585G>C (p.Lys1195Asn)
14g.23419986C>TCA485766696MYH7c.3585G>A (p.Lys1195=)
14g.23419987T>ACA389043392MYH7c.3584A>T (p.Lys1195Met)
14g.23419987T>CCA389043394MYH7c.3584A>G (p.Lys1195Arg)
14g.23419987T>GCA389043391MYH7c.3584A>C (p.Lys1195Thr)
14g.23419988T>ACA389043399MYH7c.3583A>T (p.Lys1195Ter)
14g.23419988T>CCA389043395MYH7c.3583A>G (p.Lys1195Glu)
14g.23419988T>GCA389043397MYH7c.3583A>C (p.Lys1195Gln)
gnomAD v4
14g.23419989C>ACA389043400MYH7c.3582G>T (p.Lys1194Asn)
14g.23419989C>GCA389043401MYH7c.3582G>C (p.Lys1194Asn)
14g.23419989C>TCA485766697MYH7c.3582G>A (p.Lys1194=)
14g.23419990T>ACA389043403MYH7c.3581A>T (p.Lys1194Met)
14g.23419990T>CCA389043404MYH7c.3581A>G (p.Lys1194Arg)
14g.23419990T>GCA389043406MYH7c.3581A>C (p.Lys1194Thr)
14g.23419991T>ACA389043408MYH7c.3580A>T (p.Lys1194Ter)
14g.23419991T>CCA389043409MYH7c.3580A>G (p.Lys1194Glu)
14g.23419991T>GCA389043410MYH7c.3580A>C (p.Lys1194Gln)
14g.23419992G>ACA485766698MYH7c.3579C>T (p.Arg1193=)
14g.23419992G>CCA485766699MYH7c.3579C>G (p.Arg1193=)
gnomAD v4
14g.23419992G>TCA485766700MYH7c.3579C>A (p.Arg1193=)
14g.23419993C>ACA389043412MYH7c.3578G>T (p.Arg1193Leu)
14g.23419993C=CA2123446419MYH7c.3578G= (p.Arg1193=)
14g.23419993C>GCA389043413MYH7c.3578G>C (p.Arg1193Pro)
14g.23419993C>TCA013815MYH7c.3578G>A (p.Arg1193His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23419994G>ACA389043416MYH7c.3577C>T (p.Arg1193Cys)
ClinVar dbSNP
14g.23419994G>CCA389043415MYH7c.3577C>G (p.Arg1193Gly)
ClinVar
14g.23419994G=CA2123446428MYH7c.3577C= (p.Arg1193=)
14g.23419994G>TCA10587766MYH7c.3577C>A (p.Arg1193Ser)
ClinVar dbSNP gnomAD v4
14g.23419995delCA2697553860MYH7c.3576del (p.Arg1193AlafsTer21)
ClinVar
14g.23419995C>ACA485766701MYH7c.3576G>T (p.Leu1192=)
14g.23419995C=CA2123446436MYH7c.3576G= (p.Leu1192=)
14g.23419995C>GCA485766702MYH7c.3576G>C (p.Leu1192=)
14g.23419995C>TCA037902MYH7c.3576G>A (p.Leu1192=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419996A>CCA389043419MYH7c.3575T>G (p.Leu1192Arg)
ClinVar
14g.23419996A>GCA389043421MYH7c.3575T>C (p.Leu1192Pro)
14g.23419996A>TCA389043422MYH7c.3575T>A (p.Leu1192Gln)
14g.23419997G>ACA485766703MYH7c.3574C>T (p.Leu1192=)
14g.23419997G>CCA389043424MYH7c.3574C>G (p.Leu1192Val)
14g.23419997G>TCA389043425MYH7c.3574C>A (p.Leu1192Met)
14g.23419999_23420011delCA2695219244MYH7c.3562_3574del (p.Thr1188CysfsTer22)
14g.23419998G>ACA485766704MYH7c.3573C>T (p.Ala1191=)
gnomAD v4
14g.23419998G>CCA485766705MYH7c.3573C>G (p.Ala1191=)
gnomAD v4
14g.23419998G>TCA485766706MYH7c.3573C>A (p.Ala1191=)
14g.23419998_23419999insCCACTCA2697553861MYH7c.3572_3573insAGTGG (p.Leu1192ValfsTer24)
ClinVar
14g.23419999G>ACA389043427MYH7c.3572C>T (p.Ala1191Val)
ClinVar dbSNP
14g.23419999G>CCA389043429MYH7c.3572C>G (p.Ala1191Gly)
14g.23419999G=CA2123446443MYH7c.3572C= (p.Ala1191=)
14g.23419999G>TCA389043430MYH7c.3572C>A (p.Ala1191Asp)
ClinVar dbSNP COSMIC
14g.23420000C>ACA389043431MYH7c.3571G>T (p.Ala1191Ser)
14g.23420000C=CA2123446445MYH7c.3571G= (p.Ala1191=)
14g.23420000C>GCA389043433MYH7c.3571G>C (p.Ala1191Pro)
14g.23420000C>TCA037869MYH7c.3571G>A (p.Ala1191Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23420001C>ACA485766707MYH7c.3570G>T (p.Ala1190=)
14g.23420001C=CA2123446450MYH7c.3570G= (p.Ala1190=)
14g.23420001C>GCA485766708MYH7c.3570G>C (p.Ala1190=)
ClinVar dbSNP gnomAD v4
14g.23420001C>TCA037849MYH7c.3570G>A (p.Ala1190=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23420002G>ACA389043439MYH7c.3569C>T (p.Ala1190Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23420002G>CCA389043436MYH7c.3569C>G (p.Ala1190Gly)
14g.23420002G=CA2123446453MYH7c.3569C= (p.Ala1190=)
14g.23420002G>TCA389043438MYH7c.3569C>A (p.Ala1190Glu)
gnomAD v4
14g.23420003C>ACA389043441MYH7c.3568G>T (p.Ala1190Ser)
ClinVar
14g.23420003C>GCA389043442MYH7c.3568G>C (p.Ala1190Pro)
14g.23420003C>TCA389043443MYH7c.3568G>A (p.Ala1190Thr)
ClinVar gnomAD v4
14g.23420004G>ACA485766711MYH7c.3567C>T (p.Ala1189=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23420004G>CCA485766710MYH7c.3567C>G (p.Ala1189=)
ClinVar dbSNP gnomAD v4
14g.23420004G=CA2123446463MYH7c.3567C= (p.Ala1189=)
14g.23420004G>TCA485766709MYH7c.3567C>A (p.Ala1189=)
14g.23420005G>ACA389043445MYH7c.3566C>T (p.Ala1189Val)
14g.23420005G>CCA389043447MYH7c.3566C>G (p.Ala1189Gly)
14g.23420005G>TCA389043448MYH7c.3566C>A (p.Ala1189Asp)
14g.23420005_23420006insGAGTGGCCTCGTGCTGCA2624231696MYH7c.3566_3567insAGCACGAGGCCACTCC (p.Ala1191ArgfsTer?)
gnomAD v4
14g.23420006C>ACA389043452MYH7c.3565G>T (p.Ala1189Ser)
14g.23420006C>GCA389043454MYH7c.3565G>C (p.Ala1189Pro)
14g.23420006C>TCA389043455MYH7c.3565G>A (p.Ala1189Thr)
gnomAD v4
14g.23420007A=CA2123446472MYH7c.3564T= (p.Thr1188=)
14g.23420007A>CCA485766712MYH7c.3564T>G (p.Thr1188=)
14g.23420007A>GCA013805MYH7c.3564T>C (p.Thr1188=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23420007A>TCA485766713MYH7c.3564T>A (p.Thr1188=)
dbSNP
14g.23420007_23420011delCA2697553862MYH7c.3560_3564del (p.Ala1187GlyfsTer?)
ClinVar
14g.23420008G>ACA389043459MYH7c.3563C>T (p.Thr1188Ile)
ClinVar dbSNP
14g.23420008G>CCA389043460MYH7c.3563C>G (p.Thr1188Ser)
ClinVar dbSNP gnomAD v4
14g.23420008G=CA2123446483MYH7c.3563C= (p.Thr1188=)
14g.23420008G>TCA389043458MYH7c.3563C>A (p.Thr1188Asn)
14g.23420009T>ACA389043462MYH7c.3562A>T (p.Thr1188Ser)
14g.23420009T>CCA389043464MYH7c.3562A>G (p.Thr1188Ala)
dbSNP gnomAD v4
14g.23420009T>GCA389043465MYH7c.3562A>C (p.Thr1188Pro)
gnomAD v4
14g.23420009T=CA2123446489MYH7c.3562A= (p.Thr1188=)
14g.23420010G>ACA485766714MYH7c.3561C>T (p.Ala1187=)
14g.23420010G>CCA485766716MYH7c.3561C>G (p.Ala1187=)
14g.23420010G>TCA485766715MYH7c.3561C>A (p.Ala1187=)
14g.23420011G>ACA389043467MYH7c.3560C>T (p.Ala1187Val)
ClinVar gnomAD v4
14g.23420011G>CCA389043468MYH7c.3560C>G (p.Ala1187Gly)
14g.23420011G>TCA389043469MYH7c.3560C>A (p.Ala1187Asp)
14g.23420012C>ACA389043471MYH7c.3559G>T (p.Ala1187Ser)
14g.23420012C>GCA389043475MYH7c.3559G>C (p.Ala1187Pro)
14g.23420012C>TCA389043473MYH7c.3559G>A (p.Ala1187Thr)
14g.23420013C>ACA389043481MYH7c.3558G>T (p.Glu1186Asp)
14g.23420013C=CA2123446496MYH7c.3558G= (p.Glu1186=)
14g.23420013C>GCA389043482MYH7c.3558G>C (p.Glu1186Asp)
14g.23420013C>TCA485766717MYH7c.3558G>A (p.Glu1186=)
ClinVar dbSNP gnomAD v4
14g.23420014T>ACA389043484MYH7c.3557A>T (p.Glu1186Val)
14g.23420014T>CCA389043486MYH7c.3557A>G (p.Glu1186Gly)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23420014T>GCA389043487MYH7c.3557A>C (p.Glu1186Ala)
14g.23420014T=CA2123446503MYH7c.3557A= (p.Glu1186=)
14g.23420014_23420015insGCA2697553864MYH7c.3556_3557insC (p.Glu1186AlafsTer?)
ClinVar
14g.23420015C>ACA389043490MYH7c.3556G>T (p.Glu1186Ter)
dbSNP gnomAD v2 gnomAD v4
14g.23420015C=CA2123446511MYH7c.3556G= (p.Glu1186=)
14g.23420015C>GCA389043492MYH7c.3556G>C (p.Glu1186Gln)
ClinVar dbSNP
14g.23420015C>TCA389043489MYH7c.3556G>A (p.Glu1186Lys)
dbSNP gnomAD v3 gnomAD v4
14g.23420016G>ACA485766718MYH7c.3555C>T (p.His1185=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23420016G>CCA389043495MYH7c.3555C>G (p.His1185Gln)
ClinVar gnomAD v4
14g.23420016G=CA2123446517MYH7c.3555C= (p.His1185=)
14g.23420016G>TCA389043493MYH7c.3555C>A (p.His1185Gln)
14g.23420016_23420017insCAAGAAGCACA2697553865MYH7c.3554_3555insTGCTTCTTG (p.His1185_Glu1186insAlaSerCys)
ClinVar
14g.23420017T>ACA389043497MYH7c.3554A>T (p.His1185Leu)
14g.23420017T>CCA389043496MYH7c.3554A>G (p.His1185Arg)
ClinVar
14g.23420017T>GCA389043499MYH7c.3554A>C (p.His1185Pro)
ClinVar gnomAD v4
14g.23420018G>ACA389043501MYH7c.3553C>T (p.His1185Tyr)
14g.23420018G>CCA389043504MYH7c.3553C>G (p.His1185Asp)
14g.23420018G>TCA389043503MYH7c.3553C>A (p.His1185Asn)
14g.23420019C>ACA389043505MYH7c.3552G>T (p.Gln1184His)
14g.23420019C>GCA389043506MYH7c.3552G>C (p.Gln1184His)
14g.23420019C>TCA485766719MYH7c.3552G>A (p.Gln1184=)
14g.23420020T>ACA013801MYH7c.3551A>T (p.Gln1184Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23420020T>CCA389043509MYH7c.3551A>G (p.Gln1184Arg)
ClinVar dbSNP
14g.23420020T>GCA389043511MYH7c.3551A>C (p.Gln1184Pro)
14g.23420020T=CA2123446531MYH7c.3551A= (p.Gln1184=)

Number of alleles fetched