Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23417495_23417501delCA2800863298MHRT,MYH7c.4353+6_4353+12del (n.4353+6_4353+12del)
n.814-38_814-32del
14g.23417497_23417500delCA2729048594MHRT,MYH7c.4353+3_4353+6del (n.4353+3_4353+6del)
n.814-36_814-33del
dbSNP
14g.23417499C>ACA2624237990MHRT,MYH7c.4353+4G>T (n.4353+4G>T)
n.814-34C>A
gnomAD v4
14g.23417499C>TCA2624237994MHRT,MYH7c.4353+4G>A (n.4353+4G>A)
n.814-34C>T
gnomAD v4
14g.23417500C>ACA041823MHRT,MYH7c.4353+3G>T (n.4353+3G>T)
n.814-33C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417500C=CA2123469221MHRT,MYH7c.4353+3G= (n.4353+3G=)
n.814-33C=
14g.23417500C>TCA041807MHRT,MYH7c.4353+3G>A (n.4353+3G>A)
n.814-33C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417501A>CCA389039967MHRT,MYH7c.4353+2T>G (n.4353+2T>G)
n.814-32A>C
14g.23417501A>GCA389039968MHRT,MYH7c.4353+2T>C (n.4353+2T>C)
n.814-32A>G
14g.23417501A>TCA389039969MHRT,MYH7c.4353+2T>A (n.4353+2T>A)
n.814-32A>T
14g.23417502C>ACA389039971MHRT,MYH7c.4353+1G>T (n.4353+1G>T)
n.814-31C>A
14g.23417502C=CA2123469224MHRT,MYH7c.4353+1G= (n.4353+1G=)
n.814-31C=
14g.23417502C>GCA389039973MHRT,MYH7c.4353+1G>C (n.4353+1G>C)
n.814-31C>G
14g.23417502C>TCA257813140MHRT,MYH7c.4353+1G>A (n.4353+1G>A)
n.814-31C>T
dbSNP
14g.23417503C>ACA389039975MHRT,MYH7c.4353G>T (p.Lys1451Asn)
n.814-30C>A
14g.23417503C>GCA389039976MHRT,MYH7c.4353G>C (p.Lys1451Asn)
n.814-30C>G
14g.23417503C>TCA485617721MHRT,MYH7c.4353G>A (p.Lys1451=)
n.814-30C>T
gnomAD v4
14g.23417504T>ACA389039979MHRT,MYH7c.4352A>T (p.Lys1451Met)
n.814-29T>A
14g.23417504T>CCA389039980MHRT,MYH7c.4352A>G (p.Lys1451Arg)
n.814-29T>C
14g.23417504T>GCA389039982MHRT,MYH7c.4352A>C (p.Lys1451Thr)
n.814-29T>G
ClinVar
14g.23417505T>ACA389039984MHRT,MYH7c.4351A>T (p.Lys1451Ter)
n.814-28T>A
14g.23417505T>CCA389039986MHRT,MYH7c.4351A>G (p.Lys1451Glu)
n.814-28T>C
ClinVar
14g.23417505T>GCA389039987MHRT,MYH7c.4351A>C (p.Lys1451Gln)
n.814-28T>G
14g.23417506G>ACA485617725MHRT,MYH7c.4350C>T (p.Asp1450=)
n.814-27G>A
ClinVar dbSNP gnomAD v4
14g.23417506G>CCA389039988MHRT,MYH7c.4350C>G (p.Asp1450Glu)
n.814-27G>C
14g.23417506G=CA2123469227MHRT,MYH7c.4350C= (p.Asp1450=)
n.814-27G=
14g.23417506G>TCA389039990MHRT,MYH7c.4350C>A (p.Asp1450Glu)
n.814-27G>T
14g.23417507T>ACA389039992MHRT,MYH7c.4349A>T (p.Asp1450Val)
n.814-26T>A
14g.23417507T>CCA389039994MHRT,MYH7c.4349A>G (p.Asp1450Gly)
n.814-26T>C
14g.23417507T>GCA389039995MHRT,MYH7c.4349A>C (p.Asp1450Ala)
n.814-26T>G
14g.23417508C>ACA389039999MHRT,MYH7c.4348G>T (p.Asp1450Tyr)
n.814-25C>A
14g.23417508C=CA2123469235MHRT,MYH7c.4348G= (p.Asp1450=)
n.814-25C=
14g.23417508C>GCA389039996MHRT,MYH7c.4348G>C (p.Asp1450His)
n.814-25C>G
gnomAD v4
14g.23417508C>TCA014834MHRT,MYH7c.4348G>A (p.Asp1450Asn)
n.814-25C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417509G>ACA041696MHRT,MYH7c.4347C>T (p.Phe1449=)
n.814-24G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417509G>CCA389040001MHRT,MYH7c.4347C>G (p.Phe1449Leu)
n.814-24G>C
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23417509G=CA2123469240MHRT,MYH7c.4347C= (p.Phe1449=)
n.814-24G=
14g.23417509G>TCA389040002MHRT,MYH7c.4347C>A (p.Phe1449Leu)
n.814-24G>T
14g.23417510A>CCA389040003MHRT,MYH7c.4346T>G (p.Phe1449Cys)
n.814-23A>C
14g.23417510A>GCA389040005MHRT,MYH7c.4346T>C (p.Phe1449Ser)
n.814-23A>G
14g.23417510A>TCA389040006MHRT,MYH7c.4346T>A (p.Phe1449Tyr)
n.814-23A>T
14g.23417511A>CCA389040008MHRT,MYH7c.4345T>G (p.Phe1449Val)
n.814-22A>C
14g.23417511A>GCA389040009MHRT,MYH7c.4345T>C (p.Phe1449Leu)
n.814-22A>G
14g.23417511A>TCA389040011MHRT,MYH7c.4345T>A (p.Phe1449Ile)
n.814-22A>T
14g.23417512G>ACA485617730MHRT,MYH7c.4344C>T (p.Asn1448=)
n.814-21G>A
dbSNP
14g.23417512G>CCA389040012MHRT,MYH7c.4344C>G (p.Asn1448Lys)
n.814-21G>C
14g.23417512G=CA2123469250MHRT,MYH7c.4344C= (p.Asn1448=)
n.814-21G=
14g.23417512G>TCA389040014MHRT,MYH7c.4344C>A (p.Asn1448Lys)
n.814-21G>T
dbSNP
14g.23417513T>ACA041680MHRT,MYH7c.4343A>T (p.Asn1448Ile)
n.814-20T>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417513T>CCA389040018MHRT,MYH7c.4343A>G (p.Asn1448Ser)
n.814-20T>C
ClinVar dbSNP gnomAD v4
14g.23417513T>GCA389040016MHRT,MYH7c.4343A>C (p.Asn1448Thr)
n.814-20T>G
14g.23417513T=CA2123469261MHRT,MYH7c.4343A= (p.Asn1448=)
n.814-20T=
14g.23417514T>ACA389040020MHRT,MYH7c.4342A>T (p.Asn1448Tyr)
n.814-19T>A
14g.23417514T>CCA389040023MHRT,MYH7c.4342A>G (p.Asn1448Asp)
n.814-19T>C
14g.23417514T>GCA389040021MHRT,MYH7c.4342A>C (p.Asn1448His)
n.814-19T>G
14g.23417515C>ACA389040025MHRT,MYH7c.4341G>T (p.Arg1447Ser)
n.814-18C>A
14g.23417515C=CA2123469270MHRT,MYH7c.4341G= (p.Arg1447=)
n.814-18C=
14g.23417515C>GCA389040027MHRT,MYH7c.4341G>C (p.Arg1447Ser)
n.814-18C>G
14g.23417515C>TCA041669MHRT,MYH7c.4341G>A (p.Arg1447=)
n.814-18C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23417516C>ACA389040029MHRT,MYH7c.4340G>T (p.Arg1447Met)
n.814-17C>A
14g.23417516C>GCA389040031MHRT,MYH7c.4340G>C (p.Arg1447Thr)
n.814-17C>G
14g.23417516C>TCA389040032MHRT,MYH7c.4340G>A (p.Arg1447Lys)
n.814-17C>T
COSMIC
14g.23417517T>ACA389040034MHRT,MYH7c.4339A>T (p.Arg1447Trp)
n.814-16T>A
14g.23417517T>CCA389040037MHRT,MYH7c.4339A>G (p.Arg1447Gly)
n.814-16T>C
14g.23417517T>GCA485617736MHRT,MYH7c.4339A>C (p.Arg1447=)
n.814-16T>G
14g.23417518C>ACA389040039MHRT,MYH7c.4338G>T (p.Gln1446His)
n.814-15C>A
14g.23417518C>GCA389040041MHRT,MYH7c.4338G>C (p.Gln1446His)
n.814-15C>G
14g.23417518C>TCA485617738MHRT,MYH7c.4338G>A (p.Gln1446=)
n.814-15C>T
14g.23417519T>ACA389040043MHRT,MYH7c.4337A>T (p.Gln1446Leu)
n.814-14T>A
14g.23417519T>CCA389040044MHRT,MYH7c.4337A>G (p.Gln1446Arg)
n.814-14T>C
14g.23417519T>GCA389040045MHRT,MYH7c.4337A>C (p.Gln1446Pro)
n.814-14T>G
14g.23417520G>ACA389040051MHRT,MYH7c.4336C>T (p.Gln1446Ter)
n.814-13G>A
14g.23417520G>CCA389040047MHRT,MYH7c.4336C>G (p.Gln1446Glu)
n.814-13G>C
14g.23417520G>TCA389040049MHRT,MYH7c.4336C>A (p.Gln1446Lys)
n.814-13G>T
14g.23417521C>ACA389040052MHRT,MYH7c.4335G>T (p.Lys1445Asn)
n.814-12C>A
14g.23417521C=CA2123469279MHRT,MYH7c.4335G= (p.Lys1445=)
n.814-12C=
14g.23417521C>GCA389040054MHRT,MYH7c.4335G>C (p.Lys1445Asn)
n.814-12C>G
14g.23417521C>TCA485617742MHRT,MYH7c.4335G>A (p.Lys1445=)
n.814-12C>T
ClinVar dbSNP gnomAD v4
14g.23417524_23417526delCA2580616569MHRT,MYH7c.4333_4335del (p.Lys1445del)
n.814-9_814-7del
ClinVar
14g.23417522T>ACA389040056MHRT,MYH7c.4334A>T (p.Lys1445Met)
n.814-11T>A
14g.23417522T>CCA389040058MHRT,MYH7c.4334A>G (p.Lys1445Arg)
n.814-11T>C
14g.23417522T>GCA389040059MHRT,MYH7c.4334A>C (p.Lys1445Thr)
n.814-11T>G
14g.23417523T>ACA389040061MHRT,MYH7c.4333A>T (p.Lys1445Ter)
n.814-10T>A
14g.23417523T>CCA389040063MHRT,MYH7c.4333A>G (p.Lys1445Glu)
n.814-10T>C
14g.23417523T>GCA389040064MHRT,MYH7c.4333A>C (p.Lys1445Gln)
n.814-10T>G
14g.23417524C>ACA389040065MHRT,MYH7c.4332G>T (p.Lys1444Asn)
n.814-9C>A
14g.23417524C=CA2123469288MHRT,MYH7c.4332G= (p.Lys1444=)
n.814-9C=
14g.23417524C>GCA389040066MHRT,MYH7c.4332G>C (p.Lys1444Asn)
n.814-9C>G
14g.23417524C>TCA16621654MHRT,MYH7c.4332G>A (p.Lys1444=)
n.814-9C>T
ClinVar dbSNP gnomAD v4
14g.23417525T>ACA389040070MHRT,MYH7c.4331A>T (p.Lys1444Met)
n.814-8T>A
14g.23417525T>CCA389040071MHRT,MYH7c.4331A>G (p.Lys1444Arg)
n.814-8T>C
14g.23417525T>GCA389040068MHRT,MYH7c.4331A>C (p.Lys1444Thr)
n.814-8T>G
14g.23417526T>ACA389040073MHRT,MYH7c.4330A>T (p.Lys1444Ter)
n.814-7T>A
14g.23417526T>CCA014823MHRT,MYH7c.4330A>G (p.Lys1444Glu)
n.814-7T>C
ClinVar dbSNP
14g.23417526T>GCA389040074MHRT,MYH7c.4330A>C (p.Lys1444Gln)
n.814-7T>G
14g.23417526T=CA2123469308MHRT,MYH7c.4330A= (p.Lys1444=)
n.814-7T=
14g.23417527G>ACA485617746MHRT,MYH7c.4329C>T (p.Asp1443=)
n.814-6G>A
14g.23417527G>CCA389040076MHRT,MYH7c.4329C>G (p.Asp1443Glu)
n.814-6G>C
gnomAD v4
14g.23417527G>TCA389040078MHRT,MYH7c.4329C>A (p.Asp1443Glu)
n.814-6G>T
gnomAD v4
14g.23417528T>ACA389040080MHRT,MYH7c.4328A>T (p.Asp1443Val)
n.814-5T>A
14g.23417528T>CCA389040081MHRT,MYH7c.4328A>G (p.Asp1443Gly)
n.814-5T>C
14g.23417528T>GCA389040083MHRT,MYH7c.4328A>C (p.Asp1443Ala)
n.814-5T>G
14g.23417529C>ACA389040084MHRT,MYH7c.4327G>T (p.Asp1443Tyr)
n.814-4C>A
14g.23417529C>GCA389040086MHRT,MYH7c.4327G>C (p.Asp1443His)
n.814-4C>G
ClinVar dbSNP gnomAD v4
14g.23417529C>TCA389040087MHRT,MYH7c.4327G>A (p.Asp1443Asn)
n.814-4C>T
ClinVar dbSNP gnomAD v4
14g.23417530C>ACA485617750MHRT,MYH7c.4326G>T (p.Leu1442=)
n.814-3C>A
14g.23417530C=CA2123469319MHRT,MYH7c.4326G= (p.Leu1442=)
n.814-3C=
14g.23417530C>GCA485617751MHRT,MYH7c.4326G>C (p.Leu1442=)
n.814-3C>G
ClinVar
14g.23417530C>TCA014816MHRT,MYH7c.4326G>A (p.Leu1442=)
n.814-3C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23417531A>CCA389040093MHRT,MYH7c.4325T>G (p.Leu1442Arg)
n.814-2A>C
14g.23417531A>GCA389040090MHRT,MYH7c.4325T>C (p.Leu1442Pro)
n.814-2A>G
ClinVar dbSNP
14g.23417531A>TCA389040092MHRT,MYH7c.4325T>A (p.Leu1442Gln)
n.814-2A>T
14g.23417532G>ACA485617755MHRT,MYH7c.4324C>T (p.Leu1442=)
n.814-1G>A
14g.23417532G>CCA389040095MHRT,MYH7c.4324C>G (p.Leu1442Val)
n.814-1G>C
14g.23417532G>TCA389040097MHRT,MYH7c.4324C>A (p.Leu1442Met)
n.814-1G>T
14g.23417532_23417534dupCA2580088005MHRT,MYH7c.4322_4324dup (p.Ala1441_Leu1442insPro)
n.814-1_815dup
ClinVar dbSNP
14g.23417533G>ACA041640MHRT,MYH7c.4323C>T (p.Ala1441=)
n.814G>A
dbSNP ExAC
14g.23417533G>CCA485617756MHRT,MYH7c.4323C>G (p.Ala1441=)
n.814G>C
14g.23417533G=CA2123469326MHRT,MYH7c.4323C= (p.Ala1441=)
n.814G=
14g.23417533G>TCA485617757MHRT,MYH7c.4323C>A (p.Ala1441=)
n.814G>T
ClinVar dbSNP
14g.23417534G>ACA389040098MHRT,MYH7c.4322C>T (p.Ala1441Val)
n.815G>A
gnomAD v4
14g.23417534G>CCA389040099MHRT,MYH7c.4322C>G (p.Ala1441Gly)
n.815G>C
14g.23417534G>TCA389040101MHRT,MYH7c.4322C>A (p.Ala1441Asp)
n.815G>T
14g.23417535C>ACA014807MHRT,MYH7c.4321G>T (p.Ala1441Ser)
n.816C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417535C=CA2123469336MHRT,MYH7c.4321G= (p.Ala1441=)
n.816C=
14g.23417535C>GCA389040103MHRT,MYH7c.4321G>C (p.Ala1441Pro)
n.816C>G
14g.23417535C>TCA389040105MHRT,MYH7c.4321G>A (p.Ala1441Thr)
n.816C>T
gnomAD v4
14g.23417536T>ACA485617759MHRT,MYH7c.4320A>T (p.Ala1440=)
n.817T>A
14g.23417536T>CCA041618MHRT,MYH7c.4320A>G (p.Ala1440=)
n.817T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23417536T>GCA485617762MHRT,MYH7c.4320A>C (p.Ala1440=)
n.817T>G
ClinVar dbSNP
14g.23417536T=CA2123469339MHRT,MYH7c.4320A= (p.Ala1440=)
n.817T=
14g.23417537G>ACA389040107MHRT,MYH7c.4319C>T (p.Ala1440Val)
n.818G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23417537G>CCA389040109MHRT,MYH7c.4319C>G (p.Ala1440Gly)
n.818G>C
14g.23417537G=CA2123469345MHRT,MYH7c.4319C= (p.Ala1440=)
n.818G=
14g.23417537G>TCA389040110MHRT,MYH7c.4319C>A (p.Ala1440Glu)
n.818G>T
COSMIC
14g.23417546_23417548dupCA916081707MHRT,MYH7c.4317_4319dup (p.Ala1440_Ala1441insAla)
n.827_829dup
ClinVar dbSNP
14g.23417538C>ACA389040114MHRT,MYH7c.4318G>T (p.Ala1440Ser)
n.819C>A
14g.23417538C>GCA389040115MHRT,MYH7c.4318G>C (p.Ala1440Pro)
n.819C>G
14g.23417538C>TCA389040112MHRT,MYH7c.4318G>A (p.Ala1440Thr)
n.819C>T
14g.23417539A=CA2123469351MHRT,MYH7c.4317T= (p.Ala1439=)
n.820A=
14g.23417539A>CCA485617764MHRT,MYH7c.4317T>G (p.Ala1439=)
n.820A>C
14g.23417539A>GCA485617765MHRT,MYH7c.4317T>C (p.Ala1439=)
n.820A>G
ClinVar dbSNP
14g.23417539A>TCA485617766MHRT,MYH7c.4317T>A (p.Ala1439=)
n.820A>T
gnomAD v4 COSMIC
14g.23417540G>ACA389040120MHRT,MYH7c.4316C>T (p.Ala1439Val)
n.821G>A
14g.23417540G>CCA389040117MHRT,MYH7c.4316C>G (p.Ala1439Gly)
n.821G>C
14g.23417540G>TCA389040118MHRT,MYH7c.4316C>A (p.Ala1439Asp)
n.821G>T
14g.23417541C>ACA389040123MHRT,MYH7c.4315G>T (p.Ala1439Ser)
n.822C>A
14g.23417541C=CA2123469356MHRT,MYH7c.4315G= (p.Ala1439=)
n.822C=
14g.23417541C>GCA347256MHRT,MYH7c.4315G>C (p.Ala1439Pro)
n.822C>G
dbSNP
14g.23417541C>TCA389040124MHRT,MYH7c.4315G>A (p.Ala1439Thr)
n.822C>T
14g.23417542A=CA2123469362MHRT,MYH7c.4314T= (p.Ala1438=)
n.823A=
14g.23417542A>CCA485617768MHRT,MYH7c.4314T>G (p.Ala1438=)
n.823A>C
14g.23417542A>GCA485617770MHRT,MYH7c.4314T>C (p.Ala1438=)
n.823A>G
ClinVar dbSNP
14g.23417542A>TCA485617772MHRT,MYH7c.4314T>A (p.Ala1438=)
n.823A>T
14g.23417543G>ACA389040129MHRT,MYH7c.4313C>T (p.Ala1438Val)
n.824G>A
gnomAD v4
14g.23417543G>CCA389040128MHRT,MYH7c.4313C>G (p.Ala1438Gly)
n.824G>C
14g.23417543G>TCA389040126MHRT,MYH7c.4313C>A (p.Ala1438Asp)
n.824G>T
14g.23417544C>ACA389040131MHRT,MYH7c.4312G>T (p.Ala1438Ser)
n.825C>A
14g.23417544C>GCA389040132MHRT,MYH7c.4312G>C (p.Ala1438Pro)
n.825C>G
ClinVar
14g.23417544C>TCA389040134MHRT,MYH7c.4312G>A (p.Ala1438Thr)
n.825C>T
14g.23417545A=CA2123469373MHRT,MYH7c.4311T= (p.Ala1437=)
n.826A=
14g.23417545A>CCA485617774MHRT,MYH7c.4311T>G (p.Ala1437=)
n.826A>C
ClinVar dbSNP
14g.23417545A>GCA485617775MHRT,MYH7c.4311T>C (p.Ala1437=)
n.826A>G
14g.23417545A>TCA485617777MHRT,MYH7c.4311T>A (p.Ala1437=)
n.826A>T
14g.23417546G>ACA389040136MHRT,MYH7c.4310C>T (p.Ala1437Val)
n.827G>A
14g.23417546G>CCA389040138MHRT,MYH7c.4310C>G (p.Ala1437Gly)
n.827G>C
14g.23417546G>TCA389040139MHRT,MYH7c.4310C>A (p.Ala1437Asp)
n.827G>T
14g.23417547C>ACA389040140MHRT,MYH7c.4309G>T (p.Ala1437Ser)
n.828C>A
14g.23417547C>GCA389040144MHRT,MYH7c.4309G>C (p.Ala1437Pro)
n.828C>G
ClinVar
14g.23417547C>TCA389040142MHRT,MYH7c.4309G>A (p.Ala1437Thr)
n.828C>T
14g.23417548A=CA2123469383MHRT,MYH7c.4308T= (p.Asn1436=)
n.829A=
14g.23417548A>CCA389040145MHRT,MYH7c.4308T>G (p.Asn1436Lys)
n.829A>C
14g.23417548A>GCA485617779MHRT,MYH7c.4308T>C (p.Asn1436=)
n.829A>G
ClinVar dbSNP
14g.23417548A>TCA389040147MHRT,MYH7c.4308T>A (p.Asn1436Lys)
n.829A>T
14g.23417549T>ACA389040149MHRT,MYH7c.4307A>T (p.Asn1436Ile)
n.830T>A
14g.23417549T>CCA389040150MHRT,MYH7c.4307A>G (p.Asn1436Ser)
n.830T>C
ClinVar dbSNP COSMIC
14g.23417549T>GCA389040152MHRT,MYH7c.4307A>C (p.Asn1436Thr)
n.830T>G
14g.23417549T=CA2123469393MHRT,MYH7c.4307A= (p.Asn1436=)
n.830T=
14g.23417550T>ACA389040153MHRT,MYH7c.4306A>T (p.Asn1436Tyr)
n.831T>A
14g.23417550T>CCA389040154MHRT,MYH7c.4306A>G (p.Asn1436Asp)
n.831T>C
ClinVar dbSNP gnomAD v4
14g.23417550T>GCA389040156MHRT,MYH7c.4306A>C (p.Asn1436His)
n.831T>G
14g.23417550T=CA2123469400MHRT,MYH7c.4306A= (p.Asn1436=)
n.831T=
14g.23417551G>ACA485617785MHRT,MYH7c.4305C>T (p.Ser1435=)
n.832G>A
14g.23417551G>CCA485617784MHRT,MYH7c.4305C>G (p.Ser1435=)
n.832G>C
14g.23417551G>TCA485617783MHRT,MYH7c.4305C>A (p.Ser1435=)
n.832G>T
14g.23417552G>ACA389040158MHRT,MYH7c.4304C>T (p.Ser1435Phe)
n.833G>A
gnomAD v4
14g.23417552G>CCA389040160MHRT,MYH7c.4304C>G (p.Ser1435Cys)
n.833G>C
14g.23417552G>TCA389040161MHRT,MYH7c.4304C>A (p.Ser1435Tyr)
n.833G>T
14g.23417553A>CCA389040166MHRT,MYH7c.4303T>G (p.Ser1435Ala)
n.834A>C
14g.23417553A>GCA389040164MHRT,MYH7c.4303T>C (p.Ser1435Pro)
n.834A>G
14g.23417553A>TCA389040163MHRT,MYH7c.4303T>A (p.Ser1435Thr)
n.834A>T
14g.23417554G>ACA257813213MHRT,MYH7c.4302C>T (p.Arg1434=)
n.835G>A
ClinVar dbSNP gnomAD v4
14g.23417554G>CCA485617788MHRT,MYH7c.4302C>G (p.Arg1434=)
n.835G>C
14g.23417554G=CA2123469408MHRT,MYH7c.4302C= (p.Arg1434=)
n.835G=
14g.23417554G>TCA485617786MHRT,MYH7c.4302C>A (p.Arg1434=)
n.835G>T
14g.23417555C>ACA389040168MHRT,MYH7c.4301G>T (p.Arg1434Leu)
n.836C>A
ClinVar
14g.23417555C=CA2123469423MHRT,MYH7c.4301G= (p.Arg1434=)
n.836C=
14g.23417555C>GCA389040170MHRT,MYH7c.4301G>C (p.Arg1434Pro)
n.836C>G
ClinVar dbSNP
14g.23417555C>TCA041602MHRT,MYH7c.4301G>A (p.Arg1434His)
n.836C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417556G>ACA014792MHRT,MYH7c.4300C>T (p.Arg1434Cys)
n.837G>A
ClinVar dbSNP gnomAD v4 COSMIC
14g.23417556G>CCA389040172MHRT,MYH7c.4300C>G (p.Arg1434Gly)
n.837G>C
ClinVar dbSNP
14g.23417556G=CA2123469443MHRT,MYH7c.4300C= (p.Arg1434=)
n.837G=
14g.23417556G>TCA389040173MHRT,MYH7c.4300C>A (p.Arg1434Ser)
n.837G>T
14g.23417557C>ACA389040175MHRT,MYH7c.4299G>T (p.Glu1433Asp)
n.838C>A
14g.23417557C>GCA389040177MHRT,MYH7c.4299G>C (p.Glu1433Asp)
n.838C>G
14g.23417557C>TCA485617789MHRT,MYH7c.4299G>A (p.Glu1433=)
n.838C>T
14g.23417558T>ACA389040178MHRT,MYH7c.4298A>T (p.Glu1433Val)
n.839T>A
14g.23417558T>CCA389040180MHRT,MYH7c.4298A>G (p.Glu1433Gly)
n.839T>C
14g.23417558T>GCA389040181MHRT,MYH7c.4298A>C (p.Glu1433Ala)
n.839T>G
14g.23417559C>ACA389040183MHRT,MYH7c.4297G>T (p.Glu1433Ter)
n.840C>A
14g.23417559C>GCA389040185MHRT,MYH7c.4297G>C (p.Glu1433Gln)
n.840C>G
gnomAD v4
14g.23417559C>TCA389040186MHRT,MYH7c.4297G>A (p.Glu1433Lys)
n.840C>T
COSMIC
14g.23417560T>ACA485617792MHRT,MYH7c.4296A>T (p.Val1432=)
n.841T>A
14g.23417560T>CCA485617793MHRT,MYH7c.4296A>G (p.Val1432=)
n.841T>C
dbSNP
14g.23417560T>GCA485617794MHRT,MYH7c.4296A>C (p.Val1432=)
n.841T>G
dbSNP
14g.23417560T=CA2123469451MHRT,MYH7c.4296A= (p.Val1432=)
n.841T=
14g.23417561A>CCA389040192MHRT,MYH7c.4295T>G (p.Val1432Gly)
n.842A>C
14g.23417561A>GCA389040190MHRT,MYH7c.4295T>C (p.Val1432Ala)
n.842A>G
14g.23417561A>TCA389040188MHRT,MYH7c.4295T>A (p.Val1432Glu)
n.842A>T
14g.23417562C>ACA389040194MHRT,MYH7c.4294G>T (p.Val1432Leu)
n.843C>A
14g.23417562C=CA2123469456MHRT,MYH7c.4294G= (p.Val1432=)
n.843C=
14g.23417562C>GCA389040196MHRT,MYH7c.4294G>C (p.Val1432Leu)
n.843C>G
dbSNP
14g.23417562C>TCA041577MHRT,MYH7c.4294G>A (p.Val1432Ile)
n.843C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417563G>ACA014782MHRT,MYH7c.4293C>T (p.Asp1431=)
n.844G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417563G>CCA389040198MHRT,MYH7c.4293C>G (p.Asp1431Glu)
n.844G>C
14g.23417563G=CA2123469465MHRT,MYH7c.4293C= (p.Asp1431=)
n.844G=
14g.23417563G>TCA389040199MHRT,MYH7c.4293C>A (p.Asp1431Glu)
n.844G>T
dbSNP gnomAD v4
14g.23417564T>ACA389040201MHRT,MYH7c.4292A>T (p.Asp1431Val)
n.845T>A
14g.23417564T>CCA041540MHRT,MYH7c.4292A>G (p.Asp1431Gly)
n.845T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417564T>GCA389040204MHRT,MYH7c.4292A>C (p.Asp1431Ala)
n.845T>G
14g.23417564T=CA2123469480MHRT,MYH7c.4292A= (p.Asp1431=)
n.845T=
14g.23417564_23417567delinsTCCACA2123469477MHRT,MYH7c.4289_4292delinsTGGA (p.Val1430=)
n.845_848delinsTCCA
14g.23417565C>ACA389040206MHRT,MYH7c.4291G>T (p.Asp1431Tyr)
n.846C>A
gnomAD v4
14g.23417565C>GCA389040207MHRT,MYH7c.4291G>C (p.Asp1431His)
n.846C>G
14g.23417565C>TCA389040208MHRT,MYH7c.4291G>A (p.Asp1431Asn)
n.846C>T
14g.23417568_23417570delCA658798184MHRT,MYH7c.4289_4291del (p.Val1430del)
n.849_851del
ClinVar dbSNP
14g.23417566C>ACA041527MHRT,MYH7c.4290G>T (p.Val1430=)
n.847C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417566C=CA2123469491MHRT,MYH7c.4290G= (p.Val1430=)
n.847C=
14g.23417566C>GCA485617799MHRT,MYH7c.4290G>C (p.Val1430=)
n.847C>G
14g.23417566C>TCA485617800MHRT,MYH7c.4290G>A (p.Val1430=)
n.847C>T
14g.23417567A>CCA389040210MHRT,MYH7c.4289T>G (p.Val1430Gly)
n.848A>C
14g.23417567A>GCA389040212MHRT,MYH7c.4289T>C (p.Val1430Ala)
n.848A>G
14g.23417567A>TCA389040209MHRT,MYH7c.4289T>A (p.Val1430Glu)
n.848A>T
14g.23417568C>ACA389040213MHRT,MYH7c.4288G>T (p.Val1430Leu)
n.849C>A
ClinVar
14g.23417568C>GCA389040216MHRT,MYH7c.4288G>C (p.Val1430Leu)
n.849C>G
gnomAD v4
14g.23417568C>TCA389040214MHRT,MYH7c.4288G>A (p.Val1430Met)
n.849C>T
gnomAD v4
14g.23417568_23417571delinsCCATCA2123469498MHRT,MYH7c.4285_4288delinsATGG (p.Met1429=)
n.849_852delinsCCAT
14g.23417569C>ACA389040218MHRT,MYH7c.4287G>T (p.Met1429Ile)
n.850C>A
14g.23417569C=CA2123469518MHRT,MYH7c.4287G= (p.Met1429=)
n.850C=
14g.23417569C>GCA389040221MHRT,MYH7c.4287G>C (p.Met1429Ile)
n.850C>G
14g.23417569C>TCA389040220MHRT,MYH7c.4287G>A (p.Met1429Ile)
n.850C>T
dbSNP gnomAD v2 gnomAD v4
14g.23417571_23417573dupCA1139663374MHRT,MYH7c.4285_4287dup (p.Met1429_Val1430insMet)
n.852_854dup
ClinVar dbSNP
14g.23417571_23417573delCA1139663373MHRT,MYH7c.4285_4287del (p.Met1429del)
n.852_854del
ClinVar dbSNP
14g.23417570A=CA2123469529MHRT,MYH7c.4286T= (p.Met1429=)
n.851A=
14g.23417570A>CCA389040223MHRT,MYH7c.4286T>G (p.Met1429Arg)
n.851A>C
14g.23417570A>GCA041505MHRT,MYH7c.4286T>C (p.Met1429Thr)
n.851A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417570A>TCA389040225MHRT,MYH7c.4286T>A (p.Met1429Lys)
n.851A>T
14g.23417571T>ACA389040227MHRT,MYH7c.4285A>T (p.Met1429Leu)
n.852T>A
ClinVar dbSNP gnomAD v4
14g.23417571T>CCA389040228MHRT,MYH7c.4285A>G (p.Met1429Val)
n.852T>C
gnomAD v4
14g.23417571T>GCA389040230MHRT,MYH7c.4285A>C (p.Met1429Leu)
n.852T>G
14g.23417571T=CA2123469544MHRT,MYH7c.4285A= (p.Met1429=)
n.852T=
14g.23417572C>ACA389040231MHRT,MYH7c.4284G>T (p.Leu1428Phe)
n.853C>A
14g.23417572C=CA2123469548MHRT,MYH7c.4284G= (p.Leu1428=)
n.853C=
14g.23417572C>GCA389040233MHRT,MYH7c.4284G>C (p.Leu1428Phe)
n.853C>G
dbSNP
14g.23417572C>TCA485617805MHRT,MYH7c.4284G>A (p.Leu1428=)
n.853C>T
dbSNP gnomAD v3 gnomAD v4
14g.23417573A=CA2123469558MHRT,MYH7c.4283T= (p.Leu1428=)
n.854A=
14g.23417573A>CCA389040234MHRT,MYH7c.4283T>G (p.Leu1428Trp)
n.854A>C
14g.23417573A>GCA014765MHRT,MYH7c.4283T>C (p.Leu1428Ser)
n.854A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417573A>TCA389040236MHRT,MYH7c.4283T>A (p.Leu1428Ter)
n.854A>T
14g.23417574A=CA2123469567MHRT,MYH7c.4282T= (p.Leu1428=)
n.855A=
14g.23417574A>CCA389040238MHRT,MYH7c.4282T>G (p.Leu1428Val)
n.855A>C
14g.23417574A>GCA485617806MHRT,MYH7c.4282T>C (p.Leu1428=)
n.855A>G
dbSNP
14g.23417574A>TCA389040239MHRT,MYH7c.4282T>A (p.Leu1428Met)
n.855A>T
14g.23417575G>ACA485617808MHRT,MYH7c.4281C>T (p.Asp1427=)
n.856G>A
14g.23417575G>CCA389040241MHRT,MYH7c.4281C>G (p.Asp1427Glu)
n.856G>C
14g.23417575G>TCA389040243MHRT,MYH7c.4281C>A (p.Asp1427Glu)
n.856G>T
gnomAD v4
14g.23417576T>ACA014757MHRT,MYH7c.4280A>T (p.Asp1427Val)
n.857T>A
dbSNP
14g.23417576T>CCA389040247MHRT,MYH7c.4280A>G (p.Asp1427Gly)
n.857T>C
14g.23417576T>GCA389040245MHRT,MYH7c.4280A>C (p.Asp1427Ala)
n.857T>G
14g.23417576T=CA2123469571MHRT,MYH7c.4280A= (p.Asp1427=)
n.857T=
14g.23417577C>ACA389040248MHRT,MYH7c.4279G>T (p.Asp1427Tyr)
n.858C>A
ClinVar
14g.23417577C>GCA389040249MHRT,MYH7c.4279G>C (p.Asp1427His)
n.858C>G
14g.23417577C>TCA389040251MHRT,MYH7c.4279G>A (p.Asp1427Asn)
n.858C>T
ClinVar
14g.23417578C>ACA389040252MHRT,MYH7c.4278G>T (p.Glu1426Asp)
n.859C>A
14g.23417578C=CA2123469577MHRT,MYH7c.4278G= (p.Glu1426=)
n.859C=
14g.23417578C>GCA389040254MHRT,MYH7c.4278G>C (p.Glu1426Asp)
n.859C>G
14g.23417578C>TCA041463MHRT,MYH7c.4278G>A (p.Glu1426=)
n.859C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417579T>ACA389040256MHRT,MYH7c.4277A>T (p.Glu1426Val)
n.860T>A
14g.23417579T>CCA389040257MHRT,MYH7c.4277A>G (p.Glu1426Gly)
n.860T>C
14g.23417579T>GCA389040259MHRT,MYH7c.4277A>C (p.Glu1426Ala)
n.860T>G
14g.23417580C>ACA389040261MHRT,MYH7c.4276G>T (p.Glu1426Ter)
n.861C>A
gnomAD v4
14g.23417580C=CA2123469586MHRT,MYH7c.4276G= (p.Glu1426=)
n.861C=
14g.23417580C>GCA389040263MHRT,MYH7c.4276G>C (p.Glu1426Gln)
n.861C>G
14g.23417580C>TCA014743MHRT,MYH7c.4276G>A (p.Glu1426Lys)
n.861C>T
ClinVar dbSNP COSMIC
14g.23417581G>ACA041447MHRT,MYH7c.4275C>T (p.Ile1425=)
n.862G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417581G>CCA389040265MHRT,MYH7c.4275C>G (p.Ile1425Met)
n.862G>C
14g.23417581G=CA2123469597MHRT,MYH7c.4275C= (p.Ile1425=)
n.862G=
14g.23417581G>TCA041432MHRT,MYH7c.4275C>A (p.Ile1425=)
n.862G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417582A>CCA389040266MHRT,MYH7c.4274T>G (p.Ile1425Ser)
n.863A>C
14g.23417582A>GCA389040268MHRT,MYH7c.4274T>C (p.Ile1425Thr)
n.863A>G
14g.23417582A>TCA389040269MHRT,MYH7c.4274T>A (p.Ile1425Asn)
n.863A>T
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

Number of alleles fetched