Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23417583T>ACA389040271MHRT,MYH7c.4273A>T (p.Ile1425Phe)
n.864T>A
gnomAD v4
14g.23417583T>CCA389040272MHRT,MYH7c.4273A>G (p.Ile1425Val)
n.864T>C
14g.23417583T>GCA389040273MHRT,MYH7c.4273A>C (p.Ile1425Leu)
n.864T>G
14g.23417584C>ACA389040274MHRT,MYH7c.4272G>T (p.Glu1424Asp)
n.865C>A
14g.23417584C>GCA389040275MHRT,MYH7c.4272G>C (p.Glu1424Asp)
n.865C>G
14g.23417584C>TCA485617815MHRT,MYH7c.4272G>A (p.Glu1424=)
n.865C>T
14g.23417585T>ACA389040277MHRT,MYH7c.4271A>T (p.Glu1424Val)
n.866T>A
ClinVar
14g.23417585T>CCA389040278MHRT,MYH7c.4271A>G (p.Glu1424Gly)
n.866T>C
14g.23417585T>GCA389040279MHRT,MYH7c.4271A>C (p.Glu1424Ala)
n.866T>G
14g.23417586C>ACA389040281MHRT,MYH7c.4270G>T (p.Glu1424Ter)
n.867C>A
14g.23417586C=CA2123469604MHRT,MYH7c.4270G= (p.Glu1424=)
n.867C=
14g.23417586C>GCA389040283MHRT,MYH7c.4270G>C (p.Glu1424Gln)
n.867C>G
14g.23417586C>TCA014734MHRT,MYH7c.4270G>A (p.Glu1424Lys)
n.867C>T
ClinVar dbSNP COSMIC
14g.23417587A=CA2123469610MHRT,MYH7c.4269T= (p.Asn1423=)
n.868A=
14g.23417587A>CCA389040285MHRT,MYH7c.4269T>G (p.Asn1423Lys)
n.868A>C
dbSNP gnomAD v4
14g.23417587A>GCA485617819MHRT,MYH7c.4269T>C (p.Asn1423=)
n.868A>G
dbSNP
14g.23417587A>TCA389040286MHRT,MYH7c.4269T>A (p.Asn1423Lys)
n.868A>T
14g.23417588T>ACA389040288MHRT,MYH7c.4268A>T (p.Asn1423Ile)
n.869T>A
14g.23417588T>CCA389040290MHRT,MYH7c.4268A>G (p.Asn1423Ser)
n.869T>C
14g.23417588T>GCA389040291MHRT,MYH7c.4268A>C (p.Asn1423Thr)
n.869T>G
14g.23417589T>ACA389040293MHRT,MYH7c.4267A>T (p.Asn1423Tyr)
n.870T>A
14g.23417589T>CCA389040294MHRT,MYH7c.4267A>G (p.Asn1423Asp)
n.870T>C
14g.23417589T>GCA389040296MHRT,MYH7c.4267A>C (p.Asn1423His)
n.870T>G
14g.23417590C>ACA389040297MHRT,MYH7c.4266G>T (p.Gln1422His)
n.871C>A
14g.23417590C>GCA389040299MHRT,MYH7c.4266G>C (p.Gln1422His)
n.871C>G
14g.23417590C>TCA485617820MHRT,MYH7c.4266G>A (p.Gln1422=)
n.871C>T
14g.23417591T>ACA389040300MHRT,MYH7c.4265A>T (p.Gln1422Leu)
n.872T>A
14g.23417591T>CCA389040302MHRT,MYH7c.4265A>G (p.Gln1422Arg)
n.872T>C
14g.23417591T>GCA389040304MHRT,MYH7c.4265A>C (p.Gln1422Pro)
n.872T>G
14g.23417592G>ACA389040306MHRT,MYH7c.4264C>T (p.Gln1422Ter)
n.873G>A
14g.23417592G>CCA389040308MHRT,MYH7c.4264C>G (p.Gln1422Glu)
n.873G>C
14g.23417592G>TCA389040307MHRT,MYH7c.4264C>A (p.Gln1422Lys)
n.873G>T
ClinVar
14g.23417593T>ACA485617821MHRT,MYH7c.4263A>T (p.Leu1421=)
n.874T>A
14g.23417593T>CCA485617822MHRT,MYH7c.4263A>G (p.Leu1421=)
n.874T>C
dbSNP
14g.23417593T>GCA485617823MHRT,MYH7c.4263A>C (p.Leu1421=)
n.874T>G
14g.23417593T=CA2123469616MHRT,MYH7c.4263A= (p.Leu1421=)
n.874T=
14g.23417594A>CCA389040310MHRT,MYH7c.4262T>G (p.Leu1421Arg)
n.875A>C
14g.23417594A>GCA389040314MHRT,MYH7c.4262T>C (p.Leu1421Pro)
n.875A>G
14g.23417594A>TCA389040312MHRT,MYH7c.4262T>A (p.Leu1421Gln)
n.875A>T
14g.23417595G>ACA485617824MHRT,MYH7c.4261C>T (p.Leu1421=)
n.876G>A
14g.23417595G>CCA389040315MHRT,MYH7c.4261C>G (p.Leu1421Val)
n.876G>C
14g.23417595G=CA2123469625MHRT,MYH7c.4261C= (p.Leu1421=)
n.876G=
14g.23417595G>TCA389040317MHRT,MYH7c.4261C>A (p.Leu1421Ile)
n.876G>T
gnomAD v4
14g.23417596C>ACA485617831MYH7c.4260G>T (p.Arg1420=)
14g.23417596C>GCA485617829MYH7c.4260G>C (p.Arg1420=)
dbSNP
14g.23417596C>TCA485617830MYH7c.4260G>A (p.Arg1420=)
14g.23417597C>ACA389040319MYH7c.4259G>T (p.Arg1420Leu)
COSMIC
14g.23417597C=CA2123441084MYH7c.4259G= (p.Arg1420=)
14g.23417597C>GCA389040321MYH7c.4259G>C (p.Arg1420Pro)
ClinVar dbSNP
14g.23417597C>TCA014728MYH7c.4259G>A (p.Arg1420Gln)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23417598G>ACA014718MYH7c.4258C>T (p.Arg1420Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417598G>CCA389040324MYH7c.4258C>G (p.Arg1420Gly)
14g.23417598G=CA2123441092MYH7c.4258C= (p.Arg1420=)
14g.23417598G>TCA485617833MYH7c.4258C>A (p.Arg1420=)
ClinVar dbSNP gnomAD v4
14g.23417599G>ACA485617834MYH7c.4257C>T (p.His1419=)
ClinVar dbSNP
14g.23417599G>CCA389040326MYH7c.4257C>G (p.His1419Gln)
14g.23417599G=CA2123441098MYH7c.4257C= (p.His1419=)
14g.23417599G>TCA389040327MYH7c.4257C>A (p.His1419Gln)
gnomAD v4
14g.23417600T>ACA389040328MYH7c.4256A>T (p.His1419Leu)
ClinVar
14g.23417600T>CCA014711MYH7c.4256A>G (p.His1419Arg)
ClinVar dbSNP
14g.23417600T>GCA389040329MYH7c.4256A>C (p.His1419Pro)
14g.23417600T=CA2123441104MYH7c.4256A= (p.His1419=)
14g.23417601G>ACA389040331MYH7c.4255C>T (p.His1419Tyr)
14g.23417601G>CCA389040335MYH7c.4255C>G (p.His1419Asp)
14g.23417601G>TCA389040333MYH7c.4255C>A (p.His1419Asn)
14g.23417602C>ACA389040336MYH7c.4254G>T (p.Lys1418Asn)
14g.23417602C>GCA389040337MYH7c.4254G>C (p.Lys1418Asn)
14g.23417602C>TCA485617838MYH7c.4254G>A (p.Lys1418=)
14g.23417603T>ACA389040339MYH7c.4253A>T (p.Lys1418Met)
14g.23417603T>CCA389040341MYH7c.4253A>G (p.Lys1418Arg)
14g.23417603T>GCA389040343MYH7c.4253A>C (p.Lys1418Thr)
14g.23417604T>ACA389040344MYH7c.4252A>T (p.Lys1418Ter)
14g.23417604T>CCA389040346MYH7c.4252A>G (p.Lys1418Glu)
14g.23417604T>GCA389040347MYH7c.4252A>C (p.Lys1418Gln)
COSMIC
14g.23417605G>ACA485617843MYH7c.4251C>T (p.Thr1417=)
ClinVar dbSNP gnomAD v4
14g.23417605G>CCA041415MYH7c.4251C>G (p.Thr1417=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417605G=CA2123441114MYH7c.4251C= (p.Thr1417=)
14g.23417605G>TCA485617844MYH7c.4251C>A (p.Thr1417=)
dbSNP gnomAD v2
14g.23417606G>ACA16606529MYH7c.4250C>T (p.Thr1417Ile)
ClinVar dbSNP gnomAD v4
14g.23417606G>CCA389040351MYH7c.4250C>G (p.Thr1417Ser)
gnomAD v4
14g.23417606G=CA2123441127MYH7c.4250C= (p.Thr1417=)
14g.23417606G>TCA389040349MYH7c.4250C>A (p.Thr1417Asn)
14g.23417607T>ACA389040354MYH7c.4249A>T (p.Thr1417Ser)
14g.23417607T>CCA389040355MYH7c.4249A>G (p.Thr1417Ala)
14g.23417607T>GCA389040357MYH7c.4249A>C (p.Thr1417Pro)
14g.23417608C>ACA389040358MYH7c.4248G>T (p.Lys1416Asn)
14g.23417608C=CA2123441134MYH7c.4248G= (p.Lys1416=)
14g.23417608C>GCA389040360MYH7c.4248G>C (p.Lys1416Asn)
dbSNP gnomAD v2 gnomAD v4
14g.23417608C>TCA485617849MYH7c.4248G>A (p.Lys1416=)
14g.23417609T>ACA389040362MYH7c.4247A>T (p.Lys1416Met)
14g.23417609T>CCA389040364MYH7c.4247A>G (p.Lys1416Arg)
14g.23417609T>GCA389040365MYH7c.4247A>C (p.Lys1416Thr)
14g.23417610T>ACA389040367MYH7c.4246A>T (p.Lys1416Ter)
14g.23417610T>CCA041397MYH7c.4246A>G (p.Lys1416Glu)
ClinVar dbSNP ExAC gnomAD v2
14g.23417610T>GCA389040369MYH7c.4246A>C (p.Lys1416Gln)
14g.23417610T=CA2123441143MYH7c.4246A= (p.Lys1416=)
14g.23417611C>ACA389040372MYH7c.4245G>T (p.Glu1415Asp)
14g.23417611C=CA2123441155MYH7c.4245G= (p.Glu1415=)
14g.23417611C>GCA389040371MYH7c.4245G>C (p.Glu1415Asp)
14g.23417611C>TCA041383MYH7c.4245G>A (p.Glu1415=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417612T>ACA389040374MYH7c.4244A>T (p.Glu1415Val)
14g.23417612T>CCA389040375MYH7c.4244A>G (p.Glu1415Gly)
14g.23417612T>GCA389040377MYH7c.4244A>C (p.Glu1415Ala)
14g.23417613C>ACA389040378MYH7c.4243G>T (p.Glu1415Ter)
COSMIC
14g.23417613C=CA2123441162MYH7c.4243G= (p.Glu1415=)
14g.23417613C>GCA389040379MYH7c.4243G>C (p.Glu1415Gln)
dbSNP gnomAD v2 gnomAD v4 COSMIC
14g.23417613C>TCA389040380MYH7c.4243G>A (p.Glu1415Lys)
14g.23417613_23417614delinsAACA645581324MYH7c.4242_4243delinsTT (p.Leu1415Ter)
COSMIC
14g.23417614C>ACA485617858MYH7c.4242G>T (p.Leu1414=)
14g.23417614C>GCA485617860MYH7c.4242G>C (p.Leu1414=)
14g.23417614C>TCA485617863MYH7c.4242G>A (p.Leu1414=)
gnomAD v4
14g.23417615A>CCA389040381MYH7c.4241T>G (p.Leu1414Arg)
14g.23417615A>GCA389040382MYH7c.4241T>C (p.Leu1414Pro)
14g.23417615A>TCA389040383MYH7c.4241T>A (p.Leu1414Gln)
14g.23417616G>ACA485617865MYH7c.4240C>T (p.Leu1414=)
14g.23417616G>CCA389040384MYH7c.4240C>G (p.Leu1414Val)
14g.23417616G=CA2123441171MYH7c.4240C= (p.Leu1414=)
14g.23417616G>TCA014704MYH7c.4240C>A (p.Leu1414Met)
ClinVar dbSNP gnomAD v4
14g.23417617C>ACA485617866MYH7c.4239G>T (p.Ser1413=)
dbSNP
14g.23417617C=CA2123441180MYH7c.4239G= (p.Ser1413=)
14g.23417617C>GCA041354MYH7c.4239G>C (p.Ser1413=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417617C>TCA014697MYH7c.4239G>A (p.Ser1413=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417618G>ACA014687MYH7c.4238C>T (p.Ser1413Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23417618G>CCA389040391MYH7c.4238C>G (p.Ser1413Trp)
14g.23417618G=CA2123441197MYH7c.4238C= (p.Ser1413=)
14g.23417618G>TCA257813292MYH7c.4238C>A (p.Ser1413Ter)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23417619A=CA2123441208MYH7c.4237T= (p.Ser1413=)
14g.23417619A>CCA389040394MYH7c.4237T>G (p.Ser1413Ala)
14g.23417619A>GCA389040392MYH7c.4237T>C (p.Ser1413Pro)
14g.23417619A>TCA389040395MYH7c.4237T>A (p.Ser1413Thr)
dbSNP gnomAD v3 gnomAD v4
14g.23417620G>ACA485617870MYH7c.4236C>T (p.Ser1412=)
ClinVar gnomAD v4
14g.23417620G>CCA485617872MYH7c.4236C>G (p.Ser1412=)
ClinVar
14g.23417620G>TCA485617874MYH7c.4236C>A (p.Ser1412=)
14g.23417621G>ACA389040397MYH7c.4235C>T (p.Ser1412Phe)
gnomAD v4
14g.23417621G>CCA389040399MYH7c.4235C>G (p.Ser1412Cys)
14g.23417621G=CA2123441212MYH7c.4235C= (p.Ser1412=)
14g.23417621G>TCA389040400MYH7c.4235C>A (p.Ser1412Tyr)
dbSNP
14g.23417622A>CCA389040402MYH7c.4234T>G (p.Ser1412Ala)
14g.23417622A>GCA389040403MYH7c.4234T>C (p.Ser1412Pro)
ClinVar
14g.23417622A>TCA389040405MYH7c.4234T>A (p.Ser1412Thr)
14g.23417623G>ACA485617876MYH7c.4233C>T (p.Cys1411=)
gnomAD v4
14g.23417623G>CCA389040407MYH7c.4233C>G (p.Cys1411Trp)
14g.23417623G>TCA389040408MYH7c.4233C>A (p.Cys1411Ter)
ClinVar gnomAD v4
14g.23417624delCA2573149778MYH7c.4232del (p.Cys1411SerfsTer18)
ClinVar dbSNP gnomAD v4
14g.23417624C>ACA389040410MYH7c.4232G>T (p.Cys1411Phe)
14g.23417624C>GCA389040412MYH7c.4232G>C (p.Cys1411Ser)
14g.23417624C>TCA389040413MYH7c.4232G>A (p.Cys1411Tyr)
ClinVar
14g.23417625A=CA2123441220MYH7c.4231T= (p.Cys1411=)
14g.23417625A>CCA389040418MYH7c.4231T>G (p.Cys1411Gly)
14g.23417625A>GCA389040416MYH7c.4231T>C (p.Cys1411Arg)
dbSNP gnomAD v3 gnomAD v4
14g.23417625A>TCA389040415MYH7c.4231T>A (p.Cys1411Ser)
14g.23417626C>ACA389040419MYH7c.4230G>T (p.Lys1410Asn)
14g.23417626C>GCA389040421MYH7c.4230G>C (p.Lys1410Asn)
14g.23417626C>TCA485617881MYH7c.4230G>A (p.Lys1410=)
14g.23417627T>ACA389040423MYH7c.4229A>T (p.Lys1410Met)
14g.23417627T>CCA389040424MYH7c.4229A>G (p.Lys1410Arg)
14g.23417627T>GCA389040426MYH7c.4229A>C (p.Lys1410Thr)
14g.23417628T>ACA389040428MYH7c.4228A>T (p.Lys1410Ter)
14g.23417628T>CCA389040430MYH7c.4228A>G (p.Lys1410Glu)
14g.23417628T>GCA389040431MYH7c.4228A>C (p.Lys1410Gln)
14g.23417629G>ACA485617885MYH7c.4227C>T (p.Ala1409=)
14g.23417629G>CCA014683MYH7c.4227C>G (p.Ala1409=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417629G=CA2123441225MYH7c.4227C= (p.Ala1409=)
14g.23417629G>TCA485617886MYH7c.4227C>A (p.Ala1409=)
14g.23417630G>ACA389040434MYH7c.4226C>T (p.Ala1409Val)
14g.23417630G>CCA389040436MYH7c.4226C>G (p.Ala1409Gly)
14g.23417630G>TCA389040437MYH7c.4226C>A (p.Ala1409Asp)
14g.23417631C>ACA389040441MYH7c.4225G>T (p.Ala1409Ser)
gnomAD v4
14g.23417631C=CA2123441234MYH7c.4225G= (p.Ala1409=)
14g.23417631C>GCA389040440MYH7c.4225G>C (p.Ala1409Pro)
14g.23417631C>TCA389040438MYH7c.4225G>A (p.Ala1409Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
14g.23417632A=CA2123441243MYH7c.4224T= (p.Asn1408=)
14g.23417632A>CCA389040443MYH7c.4224T>G (p.Asn1408Lys)
ClinVar dbSNP
14g.23417632A>GCA041314MYH7c.4224T>C (p.Asn1408=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417632A>TCA389040445MYH7c.4224T>A (p.Asn1408Lys)
ClinVar dbSNP
14g.23417633T>ACA389040447MYH7c.4223A>T (p.Asn1408Ile)
14g.23417633T>CCA389040448MYH7c.4223A>G (p.Asn1408Ser)
14g.23417633T>GCA389040450MYH7c.4223A>C (p.Asn1408Thr)
14g.23417634T>ACA389040452MYH7c.4222A>T (p.Asn1408Tyr)
14g.23417634T>CCA389040453MYH7c.4222A>G (p.Asn1408Asp)
ClinVar
14g.23417634T>GCA389040454MYH7c.4222A>C (p.Asn1408His)
gnomAD v4
14g.23417635A=CA2123441249MYH7c.4221T= (p.Val1407=)
14g.23417635A>CCA485617891MYH7c.4221T>G (p.Val1407=)
14g.23417635A>GCA485617892MYH7c.4221T>C (p.Val1407=)
dbSNP
14g.23417635A>TCA485617893MYH7c.4221T>A (p.Val1407=)
ClinVar gnomAD v4
14g.23417636A>CCA389040456MYH7c.4220T>G (p.Val1407Gly)
14g.23417636A>GCA389040458MYH7c.4220T>C (p.Val1407Ala)
gnomAD v4
14g.23417636A>TCA389040459MYH7c.4220T>A (p.Val1407Asp)
14g.23417637C>ACA389040463MYH7c.4219G>T (p.Val1407Phe)
14g.23417637C=CA2123441253MYH7c.4219G= (p.Val1407=)
14g.23417637C>GCA389040461MYH7c.4219G>C (p.Val1407Leu)
14g.23417637C>TCA014677MYH7c.4219G>A (p.Val1407Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417638A=CA2123441261MYH7c.4218T= (p.Ala1406=)
14g.23417638A>CCA485617898MYH7c.4218T>G (p.Ala1406=)
14g.23417638A>GCA485617899MYH7c.4218T>C (p.Ala1406=)
dbSNP
14g.23417638A>TCA485617900MYH7c.4218T>A (p.Ala1406=)
14g.23417639G>ACA389040465MYH7c.4217C>T (p.Ala1406Val)
COSMIC
14g.23417639G>CCA389040467MYH7c.4217C>G (p.Ala1406Gly)
14g.23417639G>TCA389040468MYH7c.4217C>A (p.Ala1406Asp)
14g.23417645_23417653delCA2741360400MYH7c.4209_4217del (p.Val1404_Ala1406del)
14g.23417640C>ACA389040470MYH7c.4216G>T (p.Ala1406Ser)
ClinVar
14g.23417640C=CA2123441264MYH7c.4216G= (p.Ala1406=)
14g.23417640C>GCA389040472MYH7c.4216G>C (p.Ala1406Pro)
14g.23417640C>TCA041281MYH7c.4216G>A (p.Ala1406Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417641C>ACA389040474MYH7c.4215G>T (p.Glu1405Asp)
14g.23417641C=CA2123441268MYH7c.4215G= (p.Glu1405=)
14g.23417641C>GCA389040476MYH7c.4215G>C (p.Glu1405Asp)
14g.23417641C>TCA014667MYH7c.4215G>A (p.Glu1405=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417642T>ACA389040479MYH7c.4214A>T (p.Glu1405Val)
14g.23417642T>CCA389040480MYH7c.4214A>G (p.Glu1405Gly)
14g.23417642T>GCA389040481MYH7c.4214A>C (p.Glu1405Ala)
14g.23417643C>ACA389040485MYH7c.4213G>T (p.Glu1405Ter)
14g.23417643C=CA2123441275MYH7c.4213G= (p.Glu1405=)
14g.23417643C>GCA389040487MYH7c.4213G>C (p.Glu1405Gln)
14g.23417643C>TCA389040483MYH7c.4213G>A (p.Glu1405Lys)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23417644C>ACA014656MYH7c.4212G>T (p.Val1404=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417644C=CA2123441285MYH7c.4212G= (p.Val1404=)
14g.23417644C>GCA485617914MYH7c.4212G>C (p.Val1404=)
dbSNP
14g.23417644C>TCA041248MYH7c.4212G>A (p.Val1404=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417645A>CCA389040490MYH7c.4211T>G (p.Val1404Gly)
14g.23417645A>GCA389040491MYH7c.4211T>C (p.Val1404Ala)
14g.23417645A>TCA389040492MYH7c.4211T>A (p.Val1404Glu)
14g.23417646C>ACA389040493MYH7c.4210G>T (p.Val1404Leu)
gnomAD v4
14g.23417646C=CA2123441293MYH7c.4210G= (p.Val1404=)
14g.23417646C>GCA389040494MYH7c.4210G>C (p.Val1404Leu)
14g.23417646C>TCA014652MYH7c.4210G>A (p.Val1404Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417647G>ACA041215MYH7c.4209C>T (p.Ala1403=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417647G>CCA485617916MYH7c.4209C>G (p.Ala1403=)
14g.23417647G=CA2123441295MYH7c.4209C= (p.Ala1403=)
14g.23417647G>TCA485617918MYH7c.4209C>A (p.Ala1403=)
dbSNP gnomAD v4
14g.23417648G>ACA389040497MYH7c.4208C>T (p.Ala1403Val)
14g.23417648G>CCA389040498MYH7c.4208C>G (p.Ala1403Gly)
gnomAD v4
14g.23417648G=CA2123441314MYH7c.4208C= (p.Ala1403=)
14g.23417648G>TCA014643MYH7c.4208C>A (p.Ala1403Asp)
ClinVar dbSNP gnomAD v4
14g.23417649C>ACA389040501MYH7c.4207G>T (p.Ala1403Ser)
ClinVar dbSNP gnomAD v4
14g.23417649C>GCA389040502MYH7c.4207G>C (p.Ala1403Pro)
14g.23417649C>TCA389040504MYH7c.4207G>A (p.Ala1403Thr)
14g.23417650C>ACA389040505MYH7c.4206G>T (p.Glu1402Asp)
14g.23417650C>GCA389040506MYH7c.4206G>C (p.Glu1402Asp)
14g.23417650C>TCA485617919MYH7c.4206G>A (p.Glu1402=)
14g.23417651T>ACA389040508MYH7c.4205A>T (p.Glu1402Val)
14g.23417651T>CCA389040510MYH7c.4205A>G (p.Glu1402Gly)
14g.23417651T>GCA389040512MYH7c.4205A>C (p.Glu1402Ala)
ClinVar
14g.23417652C>ACA389040513MYH7c.4204G>T (p.Glu1402Ter)
14g.23417652C=CA2123441324MYH7c.4204G= (p.Glu1402=)
14g.23417652C>GCA389040514MYH7c.4204G>C (p.Glu1402Gln)
14g.23417652C>TCA014639MYH7c.4204G>A (p.Glu1402Lys)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23417653C>ACA389040516MYH7c.4203G>T (p.Glu1401Asp)
ClinVar dbSNP
14g.23417653C=CA2123441328MYH7c.4203G= (p.Glu1401=)
14g.23417653C>GCA389040518MYH7c.4203G>C (p.Glu1401Asp)
14g.23417653C>TCA041206MYH7c.4203G>A (p.Glu1401=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417654T>ACA389040520MYH7c.4202A>T (p.Glu1401Val)
14g.23417654T>CCA389040521MYH7c.4202A>G (p.Glu1401Gly)
14g.23417654T>GCA389040523MYH7c.4202A>C (p.Glu1401Ala)
14g.23417655C>ACA389040527MYH7c.4201G>T (p.Glu1401Ter)
14g.23417655C>GCA389040526MYH7c.4201G>C (p.Glu1401Gln)
14g.23417655C>TCA389040525MYH7c.4201G>A (p.Glu1401Lys)
ClinVar dbSNP
14g.23417656A=CA2123441334MYH7c.4200T= (p.Ala1400=)
14g.23417656A>CCA485617922MYH7c.4200T>G (p.Ala1400=)
14g.23417656A>GCA041186MYH7c.4200T>C (p.Ala1400=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417656A>TCA485617923MYH7c.4200T>A (p.Ala1400=)
14g.23417657G>ACA389040530MYH7c.4199C>T (p.Ala1400Val)
14g.23417657G>CCA014630MYH7c.4199C>G (p.Ala1400Gly)
ClinVar dbSNP
14g.23417657G=CA2123441346MYH7c.4199C= (p.Ala1400=)
14g.23417657G>TCA389040533MYH7c.4199C>A (p.Ala1400Asp)
ClinVar dbSNP
14g.23417658C>ACA389040534MYH7c.4198G>T (p.Ala1400Ser)
14g.23417658C>GCA389040536MYH7c.4198G>C (p.Ala1400Pro)
14g.23417658C>TCA389040537MYH7c.4198G>A (p.Ala1400Thr)
14g.23417659T>ACA014617MYH7c.4197A>T (p.Glu1399Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417659T>CCA485617925MYH7c.4197A>G (p.Glu1399=)
gnomAD v4
14g.23417659T>GCA389040539MYH7c.4197A>C (p.Glu1399Asp)
dbSNP
14g.23417659T=CA2123441367MYH7c.4197A= (p.Glu1399=)
14g.23417660T>ACA389040541MYH7c.4196A>T (p.Glu1399Val)
14g.23417660T>CCA041145MYH7c.4196A>G (p.Glu1399Gly)
dbSNP ExAC gnomAD v2
14g.23417660T>GCA389040543MYH7c.4196A>C (p.Glu1399Ala)
14g.23417660T=CA2123441375MYH7c.4196A= (p.Glu1399=)
14g.23417661C>ACA389040545MYH7c.4195G>T (p.Glu1399Ter)
14g.23417661C>GCA389040547MYH7c.4195G>C (p.Glu1399Gln)
14g.23417661C>TCA389040548MYH7c.4195G>A (p.Glu1399Lys)
14g.23417662C>ACA389040549MYH7c.4194G>T (p.Gln1398His)
14g.23417662C=CA2123441382MYH7c.4194G= (p.Gln1398=)
14g.23417662C>GCA389040554MYH7c.4194G>C (p.Gln1398His)
14g.23417662C>TCA041133MYH7c.4194G>A (p.Gln1398=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417663T>ACA389040556MYH7c.4193A>T (p.Gln1398Leu)
14g.23417663T>CCA389040558MYH7c.4193A>G (p.Gln1398Arg)
14g.23417663T>GCA389040559MYH7c.4193A>C (p.Gln1398Pro)
14g.23417663_23417666delinsTGCACA2123441392MYH7c.4190_4193delinsTGCA (p.Leu1397=)
14g.23417664G>ACA389040561MYH7c.4192C>T (p.Gln1398Ter)
ClinVar
14g.23417664G>CCA389040563MYH7c.4192C>G (p.Gln1398Glu)
14g.23417664G>TCA389040564MYH7c.4192C>A (p.Gln1398Lys)
14g.23417666_23417668delCA014612MYH7c.4190_4192del (p.Leu1397del)
ClinVar dbSNP
14g.23417665C>ACA485617932MYH7c.4191G>T (p.Leu1397=)
dbSNP
14g.23417665C=CA2123441407MYH7c.4191G= (p.Leu1397=)
14g.23417665C>GCA485617931MYH7c.4191G>C (p.Leu1397=)
14g.23417665C>TCA485617933MYH7c.4191G>A (p.Leu1397=)
ClinVar dbSNP
14g.23417666A=CA2123441410MYH7c.4190T= (p.Leu1397=)
14g.23417666A>CCA389040567MYH7c.4190T>G (p.Leu1397Arg)
14g.23417666A>GCA389040568MYH7c.4190T>C (p.Leu1397Pro)
ClinVar dbSNP
14g.23417666A>TCA389040569MYH7c.4190T>A (p.Leu1397Gln)
14g.23417667G>ACA485617935MYH7c.4189C>T (p.Leu1397=)
14g.23417667G>CCA389040571MYH7c.4189C>G (p.Leu1397Val)
14g.23417667G>TCA389040573MYH7c.4189C>A (p.Leu1397Met)
14g.23417668C>ACA014602MYH7c.4188G>T (p.Arg1396=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417668C=CA2123441420MYH7c.4188G= (p.Arg1396=)
14g.23417668C>GCA485617936MYH7c.4188G>C (p.Arg1396=)
14g.23417668C>TCA014595MYH7c.4188G>A (p.Arg1396=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417669C>ACA389040574MYH7c.4187G>T (p.Arg1396Leu)
ClinVar dbSNP
14g.23417669C=CA2123441437MYH7c.4187G= (p.Arg1396=)
14g.23417669C>GCA389040576MYH7c.4187G>C (p.Arg1396Pro)
14g.23417669C>TCA014586MYH7c.4187G>A (p.Arg1396Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417670G>ACA014576MYH7c.4186C>T (p.Arg1396Trp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23417670G>CCA389040578MYH7c.4186C>G (p.Arg1396Gly)
14g.23417670G=CA2123441444MYH7c.4186C= (p.Arg1396=)
14g.23417670G>TCA485617937MYH7c.4186C>A (p.Arg1396=)
ClinVar dbSNP gnomAD v4
14g.23417671C>ACA389040579MYH7c.4185G>T (p.Gln1395His)
14g.23417671C>GCA389040581MYH7c.4185G>C (p.Gln1395His)
gnomAD v4
14g.23417671C>TCA485617938MYH7c.4185G>A (p.Gln1395=)
14g.23417672T>ACA389040583MYH7c.4184A>T (p.Gln1395Leu)
14g.23417672T>CCA389040584MYH7c.4184A>G (p.Gln1395Arg)
14g.23417672T>GCA389040585MYH7c.4184A>C (p.Gln1395Pro)
14g.23417673G>ACA389040587MYH7c.4183C>T (p.Gln1395Ter)
dbSNP
14g.23417673G>CCA389040589MYH7c.4183C>G (p.Gln1395Glu)
gnomAD v4
14g.23417673G>TCA389040591MYH7c.4183C>A (p.Gln1395Lys)
14g.23417674G>ACA014568MYH7c.4182C>T (p.Ala1394=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417674G>CCA485617942MYH7c.4182C>G (p.Ala1394=)
14g.23417674G=CA2123441451MYH7c.4182C= (p.Ala1394=)
14g.23417674G>TCA485617943MYH7c.4182C>A (p.Ala1394=)
14g.23417675G>ACA389040593MYH7c.4181C>T (p.Ala1394Val)
ClinVar dbSNP COSMIC
14g.23417675G>CCA389040595MYH7c.4181C>G (p.Ala1394Gly)
14g.23417675G>TCA389040596MYH7c.4181C>A (p.Ala1394Asp)
14g.23417676C>ACA389040597MYH7c.4180G>T (p.Ala1394Ser)
gnomAD v4
14g.23417676C=CA2123441457MYH7c.4180G= (p.Ala1394=)
14g.23417676C>GCA389040598MYH7c.4180G>C (p.Ala1394Pro)
14g.23417676C>TCA041079MYH7c.4180G>A (p.Ala1394Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417677C>ACA485617945MYH7c.4179G>T (p.Leu1393=)
14g.23417677C>GCA485617946MYH7c.4179G>C (p.Leu1393=)
14g.23417677C>TCA485617947MYH7c.4179G>A (p.Leu1393=)
gnomAD v4
14g.23417678A>CCA389040600MYH7c.4178T>G (p.Leu1393Arg)
14g.23417678A>GCA389040604MYH7c.4178T>C (p.Leu1393Pro)
ClinVar
14g.23417678A>TCA389040602MYH7c.4178T>A (p.Leu1393Gln)
14g.23417679G>ACA485617948MYH7c.4177C>T (p.Leu1393=)
gnomAD v4
14g.23417679G>CCA389040605MYH7c.4177C>G (p.Leu1393Val)
14g.23417679G>TCA389040606MYH7c.4177C>A (p.Leu1393Met)
gnomAD v4
14g.23417680C>ACA389040608MYH7c.4176G>T (p.Lys1392Asn)
ClinVar
14g.23417680C>GCA389040610MYH7c.4176G>C (p.Lys1392Asn)
14g.23417680C>TCA485617949MYH7c.4176G>A (p.Lys1392=)
14g.23417681T>ACA389040611MYH7c.4175A>T (p.Lys1392Met)
14g.23417681T>CCA389040612MYH7c.4175A>G (p.Lys1392Arg)
14g.23417681T>GCA389040613MYH7c.4175A>C (p.Lys1392Thr)
14g.23417682T>ACA389040615MYH7c.4174A>T (p.Lys1392Ter)
14g.23417682T>CCA389040617MYH7c.4174A>G (p.Lys1392Glu)
14g.23417682T>GCA389040618MYH7c.4174A>C (p.Lys1392Gln)
14g.23417683C>ACA389040622MYH7c.4173G>T (p.Lys1391Asn)
14g.23417683C>GCA389040620MYH7c.4173G>C (p.Lys1391Asn)
14g.23417683C>TCA485617951MYH7c.4173G>A (p.Lys1391=)
gnomAD v4

Number of alleles fetched