Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23418301C>ACA389041005MYH7c.4078G>T (p.Val1360Phe)
14g.23418301C=CA2123442629MYH7c.4078G= (p.Val1360=)
14g.23418301C>GCA389041006MYH7c.4078G>C (p.Val1360Leu)
14g.23418301C>TCA014435MYH7c.4078G>A (p.Val1360Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418302G>ACA014428MYH7c.4077C>T (p.Arg1359=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418302G>CCA485618458MYH7c.4077C>G (p.Arg1359=)
14g.23418302G=CA2123442636MYH7c.4077C= (p.Arg1359=)
14g.23418302G>TCA485618460MYH7c.4077C>A (p.Arg1359=)
dbSNP
14g.23418303C>ACA389041011MYH7c.4076G>T (p.Arg1359Leu)
ClinVar dbSNP gnomAD v4
14g.23418303C=CA2123442642MYH7c.4076G= (p.Arg1359=)
14g.23418303C>GCA389041009MYH7c.4076G>C (p.Arg1359Pro)
14g.23418303C>TCA040309MYH7c.4076G>A (p.Arg1359His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23418304G>ACA014422MYH7c.4075C>T (p.Arg1359Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418304G>CCA389041014MYH7c.4075C>G (p.Arg1359Gly)
14g.23418304G=CA2123442651MYH7c.4075C= (p.Arg1359=)
14g.23418304G>TCA014415MYH7c.4075C>A (p.Arg1359Ser)
ClinVar dbSNP gnomAD v4
14g.23418305C>ACA389041016MYH7c.4074G>T (p.Gln1358His)
14g.23418305C=CA2123442661MYH7c.4074G= (p.Gln1358=)
14g.23418305C>GCA389041018MYH7c.4074G>C (p.Gln1358His)
dbSNP gnomAD v3 gnomAD v4
14g.23418305C>TCA040283MYH7c.4074G>A (p.Gln1358=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418306T>ACA389041020MYH7c.4073A>T (p.Gln1358Leu)
14g.23418306T>CCA389041021MYH7c.4073A>G (p.Gln1358Arg)
gnomAD v4
14g.23418306T>GCA389041023MYH7c.4073A>C (p.Gln1358Pro)
gnomAD v4
14g.23418307G>ACA389041026MYH7c.4072C>T (p.Gln1358Ter)
14g.23418307G>CCA389041027MYH7c.4072C>G (p.Gln1358Glu)
14g.23418307G>TCA389041029MYH7c.4072C>A (p.Gln1358Lys)
14g.23418308C>ACA485618481MYH7c.4071G>T (p.Leu1357=)
ClinVar dbSNP gnomAD v4
14g.23418308C=CA2123442666MYH7c.4071G= (p.Leu1357=)
14g.23418308C>GCA485618483MYH7c.4071G>C (p.Leu1357=)
14g.23418308C>TCA485618486MYH7c.4071G>A (p.Leu1357=)
14g.23418309A=CA2123442671MYH7c.4070T= (p.Leu1357=)
14g.23418309A>CCA389041031MYH7c.4070T>G (p.Leu1357Arg)
ClinVar gnomAD v4
14g.23418309A>GCA014407MYH7c.4070T>C (p.Leu1357Pro)
ClinVar dbSNP
14g.23418309A>TCA389041032MYH7c.4070T>A (p.Leu1357Gln)
14g.23418310G>ACA485618489MYH7c.4069C>T (p.Leu1357=)
gnomAD v4
14g.23418310G>CCA389041033MYH7c.4069C>G (p.Leu1357Val)
14g.23418310G>TCA389041035MYH7c.4069C>A (p.Leu1357Met)
14g.23418311delCA2800863450MYH7c.4068del (p.Glu1356AspfsTer?)
14g.23418311C>ACA389041036MYH7c.4068G>T (p.Glu1356Asp)
14g.23418311C>GCA389041038MYH7c.4068G>C (p.Glu1356Asp)
14g.23418311C>TCA485618494MYH7c.4068G>A (p.Glu1356=)
14g.23418312T>ACA389041039MYH7c.4067A>T (p.Glu1356Val)
14g.23418312T>CCA389041040MYH7c.4067A>G (p.Glu1356Gly)
14g.23418312T>GCA389041041MYH7c.4067A>C (p.Glu1356Ala)
14g.23418313C>ACA389041043MYH7c.4066G>T (p.Glu1356Ter)
14g.23418313C=CA2123442677MYH7c.4066G= (p.Glu1356=)
14g.23418313C>GCA389041045MYH7c.4066G>C (p.Glu1356Gln)
14g.23418313C>TCA014400MYH7c.4066G>A (p.Glu1356Lys)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.23418314G>ACA040268MYH7c.4065C>T (p.Ala1355=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418314G>CCA485618504MYH7c.4065C>G (p.Ala1355=)
gnomAD v4
14g.23418314G=CA2123442686MYH7c.4065C= (p.Ala1355=)
14g.23418314G>TCA485618506MYH7c.4065C>A (p.Ala1355=)
14g.23418315G>ACA389041051MYH7c.4064C>T (p.Ala1355Val)
dbSNP gnomAD v3 gnomAD v4
14g.23418315G>CCA389041050MYH7c.4064C>G (p.Ala1355Gly)
14g.23418315G=CA2123442689MYH7c.4064C= (p.Ala1355=)
14g.23418315G>TCA389041048MYH7c.4064C>A (p.Ala1355Asp)
ClinVar dbSNP gnomAD v4
14g.23418316C>ACA389041053MYH7c.4063G>T (p.Ala1355Ser)
14g.23418316C=CA2123442699MYH7c.4063G= (p.Ala1355=)
14g.23418316C>GCA389041054MYH7c.4063G>C (p.Ala1355Pro)
14g.23418316C>TCA040248MYH7c.4063G>A (p.Ala1355Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418317C>ACA389041055MYH7c.4062G>T (p.Lys1354Asn)
14g.23418317C>GCA389041056MYH7c.4062G>C (p.Lys1354Asn)
14g.23418317C>TCA485618517MYH7c.4062G>A (p.Lys1354=)
14g.23418318T>ACA389041058MYH7c.4061A>T (p.Lys1354Met)
14g.23418318T>CCA040229MYH7c.4061A>G (p.Lys1354Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418318T>GCA389041061MYH7c.4061A>C (p.Lys1354Thr)
14g.23418318T=CA2123442712MYH7c.4061A= (p.Lys1354=)
14g.23418319delCA2729049585MYH7c.4061del (p.Lys1354ArgfsTer?)
dbSNP
14g.23418319T>ACA389041063MYH7c.4060A>T (p.Lys1354Ter)
14g.23418319T>CCA389041064MYH7c.4060A>G (p.Lys1354Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23418319T>GCA389041067MYH7c.4060A>C (p.Lys1354Gln)
14g.23418319T=CA2123442718MYH7c.4060A= (p.Lys1354=)
14g.23418320G>ACA485618530MYH7c.4059C>T (p.Ala1353=)
14g.23418320G>CCA485618525MYH7c.4059C>G (p.Ala1353=)
14g.23418320G>TCA485618527MYH7c.4059C>A (p.Ala1353=)
14g.23418321G>ACA257813833MYH7c.4058C>T (p.Ala1353Val)
ClinVar dbSNP gnomAD v4
14g.23418321G>CCA389041070MYH7c.4058C>G (p.Ala1353Gly)
14g.23418321G=CA2123442724MYH7c.4058C= (p.Ala1353=)
14g.23418321G>TCA389041069MYH7c.4058C>A (p.Ala1353Asp)
COSMIC
14g.23418322C>ACA389041072MYH7c.4057G>T (p.Ala1353Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23418322C=CA2123442727MYH7c.4057G= (p.Ala1353=)
14g.23418322C>GCA389041075MYH7c.4057G>C (p.Ala1353Pro)
14g.23418322C>TCA389041074MYH7c.4057G>A (p.Ala1353Thr)
ClinVar dbSNP gnomAD v4
14g.23418322_23418323insATGACA2800863453MYH7c.4056_4057insTCAT (p.Ala1353SerfsTer25)
14g.23418323C>ACA389041077MYH7c.4056G>T (p.Glu1352Asp)
14g.23418323C>GCA389041078MYH7c.4056G>C (p.Glu1352Asp)
14g.23418323C>TCA485618542MYH7c.4056G>A (p.Glu1352=)
ClinVar gnomAD v4
14g.23418324T>ACA389041079MYH7c.4055A>T (p.Glu1352Val)
14g.23418324T>CCA389041081MYH7c.4055A>G (p.Glu1352Gly)
14g.23418324T>GCA389041082MYH7c.4055A>C (p.Glu1352Ala)
14g.23418325C>ACA389041084MYH7c.4054G>T (p.Glu1352Ter)
14g.23418325C>GCA389041086MYH7c.4054G>C (p.Glu1352Gln)
gnomAD v4
14g.23418325C>TCA389041089MYH7c.4054G>A (p.Glu1352Lys)
14g.23418326C>ACA485618554MYH7c.4053G>T (p.Thr1351=)
dbSNP gnomAD v2
14g.23418326C=CA2123442734MYH7c.4053G= (p.Thr1351=)
14g.23418326C>GCA485618551MYH7c.4053G>C (p.Thr1351=)
gnomAD v4
14g.23418326C>TCA014397MYH7c.4053G>A (p.Thr1351=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418327G>ACA014388MYH7c.4052C>T (p.Thr1351Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418327G>CCA389041092MYH7c.4052C>G (p.Thr1351Arg)
14g.23418327G=CA2123442744MYH7c.4052C= (p.Thr1351=)
14g.23418327G>TCA389041094MYH7c.4052C>A (p.Thr1351Lys)
14g.23418328T>ACA389041096MYH7c.4051A>T (p.Thr1351Ser)
14g.23418328T>CCA389041097MYH7c.4051A>G (p.Thr1351Ala)
14g.23418328T>GCA389041099MYH7c.4051A>C (p.Thr1351Pro)
14g.23418328_23418331delinsTCTCCA2123442750MYH7c.4048_4051delinsGAGA (p.Glu1350=)
14g.23418329C>ACA389041100MYH7c.4050G>T (p.Glu1350Asp)
14g.23418329C=CA2123442756MYH7c.4050G= (p.Glu1350=)
14g.23418329C>GCA389041102MYH7c.4050G>C (p.Glu1350Asp)
14g.23418329C>TCA485618561MYH7c.4050G>A (p.Glu1350=)
dbSNP
14g.23418335_23418337delCA913184874MYH7c.4048_4050del (p.Glu1350del)
ClinVar dbSNP gnomAD v4
14g.23418330T>ACA389041104MYH7c.4049A>T (p.Glu1350Val)
14g.23418330T>CCA389041105MYH7c.4049A>G (p.Glu1350Gly)
ClinVar
14g.23418330T>GCA389041106MYH7c.4049A>C (p.Glu1350Ala)
14g.23418330_23418340delCA2800863455MYH7c.4039_4049del (p.Tyr1347AspfsTer26)
14g.23418331C>ACA389041108MYH7c.4048G>T (p.Glu1350Ter)
14g.23418331C=CA2123442760MYH7c.4048G= (p.Glu1350=)
14g.23418331C>GCA389041110MYH7c.4048G>C (p.Glu1350Gln)
14g.23418331C>TCA389041112MYH7c.4048G>A (p.Glu1350Lys)
ClinVar dbSNP COSMIC
14g.23418332C>ACA389041113MYH7c.4047G>T (p.Glu1349Asp)
14g.23418332C=CA2123442764MYH7c.4047G= (p.Glu1349=)
14g.23418332C>GCA389041114MYH7c.4047G>C (p.Glu1349Asp)
14g.23418332C>TCA485618573MYH7c.4047G>A (p.Glu1349=)
dbSNP
14g.23418333T>ACA389041116MYH7c.4046A>T (p.Glu1349Val)
14g.23418333T>CCA389041118MYH7c.4046A>G (p.Glu1349Gly)
ClinVar
14g.23418333T>GCA389041119MYH7c.4046A>C (p.Glu1349Ala)
14g.23418334C>ACA389041123MYH7c.4045G>T (p.Glu1349Ter)
gnomAD v4
14g.23418334C=CA2123442770MYH7c.4045G= (p.Glu1349=)
14g.23418334C>GCA389041122MYH7c.4045G>C (p.Glu1349Gln)
14g.23418334C>TCA389041121MYH7c.4045G>A (p.Glu1349Lys)
ClinVar dbSNP
14g.23418335C>ACA389041125MYH7c.4044G>T (p.Glu1348Asp)
14g.23418335C=CA2123442773MYH7c.4044G= (p.Glu1348=)
14g.23418335C>GCA389041127MYH7c.4044G>C (p.Glu1348Asp)
14g.23418335C>TCA485618584MYH7c.4044G>A (p.Glu1348=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23418336T>ACA389041128MYH7c.4043A>T (p.Glu1348Val)
gnomAD v4
14g.23418336T>CCA389041130MYH7c.4043A>G (p.Glu1348Gly)
COSMIC
14g.23418336T>GCA389041132MYH7c.4043A>C (p.Glu1348Ala)
14g.23418337C>ACA389041133MYH7c.4042G>T (p.Glu1348Ter)
14g.23418337C=CA2123442781MYH7c.4042G= (p.Glu1348=)
14g.23418337C>GCA389041135MYH7c.4042G>C (p.Glu1348Gln)
ClinVar dbSNP
14g.23418337C>TCA389041136MYH7c.4042G>A (p.Glu1348Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418338G>ACA485618592MYH7c.4041C>T (p.Tyr1347=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23418338G>CCA389041137MYH7c.4041C>G (p.Tyr1347Ter)
14g.23418338G=CA2123442789MYH7c.4041C= (p.Tyr1347=)
14g.23418338G>TCA389041138MYH7c.4041C>A (p.Tyr1347Ter)
gnomAD v4
14g.23418339T>ACA389041140MYH7c.4040A>T (p.Tyr1347Phe)
14g.23418339T>CCA040155MYH7c.4040A>G (p.Tyr1347Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418339T>GCA389041141MYH7c.4040A>C (p.Tyr1347Ser)
14g.23418339T=CA2123442794MYH7c.4040A= (p.Tyr1347=)
14g.23418340A>CCA389041142MYH7c.4039T>G (p.Tyr1347Asp)
14g.23418340A>GCA389041145MYH7c.4039T>C (p.Tyr1347His)
14g.23418340A>TCA389041143MYH7c.4039T>A (p.Tyr1347Asn)
14g.23418341C>ACA389041146MYH7c.4038G>T (p.Gln1346His)
14g.23418341C=CA2123442798MYH7c.4038G= (p.Gln1346=)
14g.23418341C>GCA389041147MYH7c.4038G>C (p.Gln1346His)
14g.23418341C>TCA485618603MYH7c.4038G>A (p.Gln1346=)
ClinVar dbSNP
14g.23418342T>ACA389041149MYH7c.4037A>T (p.Gln1346Leu)
14g.23418342T>CCA389041150MYH7c.4037A>G (p.Gln1346Arg)
gnomAD v4
14g.23418342T>GCA389041152MYH7c.4037A>C (p.Gln1346Pro)
14g.23418343G>ACA389041153MYH7c.4036C>T (p.Gln1346Ter)
ClinVar
14g.23418343G>CCA10577505MYH7c.4036C>G (p.Gln1346Glu)
ClinVar dbSNP COSMIC
14g.23418343G=CA2123442809MYH7c.4036C= (p.Gln1346=)
14g.23418343G>TCA014382MYH7c.4036C>A (p.Gln1346Lys)
ClinVar dbSNP
14g.23418343_23418344delinsTTCA2573149779MYH7c.4035_4036delinsAA (p.Gln1346Lys)
ClinVar dbSNP
14g.23418344C>ACA389041156MYH7c.4035G>T (p.Glu1345Asp)
14g.23418344C=CA2123442818MYH7c.4035G= (p.Glu1345=)
14g.23418344C>GCA389041158MYH7c.4035G>C (p.Glu1345Asp)
14g.23418344C>TCA485618615MYH7c.4035G>A (p.Glu1345=)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23418345T>ACA389041162MYH7c.4034A>T (p.Glu1345Val)
14g.23418345T>CCA389041160MYH7c.4034A>G (p.Glu1345Gly)
14g.23418345T>GCA389041159MYH7c.4034A>C (p.Glu1345Ala)
14g.23418346C>ACA389041164MYH7c.4033G>T (p.Glu1345Ter)
14g.23418346C>GCA389041167MYH7c.4033G>C (p.Glu1345Gln)
14g.23418346C>TCA389041165MYH7c.4033G>A (p.Glu1345Lys)
ClinVar
14g.23418347C>ACA485618619MYH7c.4032G>T (p.Arg1344=)
14g.23418347C>GCA485618621MYH7c.4032G>C (p.Arg1344=)
14g.23418347C>TCA485618623MYH7c.4032G>A (p.Arg1344=)
14g.23418348C>ACA389041168MYH7c.4031G>T (p.Arg1344Leu)
COSMIC
14g.23418348C=CA2123442830MYH7c.4031G= (p.Arg1344=)
14g.23418348C>GCA389041170MYH7c.4031G>C (p.Arg1344Pro)
14g.23418348C>TCA276011MYH7c.4031G>A (p.Arg1344Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23418353_23418362delCA2573149780MYH7c.4022_4031del (p.Asp1341GlyfsTer?)
ClinVar dbSNP
14g.23418349G>ACA014372MYH7c.4030C>T (p.Arg1344Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418349G>CCA389041173MYH7c.4030C>G (p.Arg1344Gly)
14g.23418349G=CA2123442837MYH7c.4030C= (p.Arg1344=)
14g.23418349G>TCA040133MYH7c.4030C>A (p.Arg1344=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418350C>ACA485618636MYH7c.4029G>T (p.Leu1343=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23418350C=CA2123442846MYH7c.4029G= (p.Leu1343=)
14g.23418350C>GCA485618637MYH7c.4029G>C (p.Leu1343=)
14g.23418350C>TCA485618639MYH7c.4029G>A (p.Leu1343=)
ClinVar dbSNP gnomAD v4
14g.23418351A>CCA389041176MYH7c.4028T>G (p.Leu1343Arg)
14g.23418351A>GCA389041177MYH7c.4028T>C (p.Leu1343Pro)
14g.23418351A>TCA389041179MYH7c.4028T>A (p.Leu1343Gln)
gnomAD v4
14g.23418352G>ACA485618642MYH7c.4027C>T (p.Leu1343=)
14g.23418352G>CCA389041180MYH7c.4027C>G (p.Leu1343Val)
gnomAD v4
14g.23418352G=CA2123442848MYH7c.4027C= (p.Leu1343=)
14g.23418352G>TCA257813893MYH7c.4027C>A (p.Leu1343Met)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23418353C>ACA485618646MYH7c.4026G>T (p.Leu1342=)
14g.23418353C>GCA485618647MYH7c.4026G>C (p.Leu1342=)
14g.23418353C>TCA485618649MYH7c.4026G>A (p.Leu1342=)
ClinVar
14g.23418354A>CCA389041186MYH7c.4025T>G (p.Leu1342Arg)
ClinVar
14g.23418354A>GCA389041183MYH7c.4025T>C (p.Leu1342Pro)
14g.23418354A>TCA389041184MYH7c.4025T>A (p.Leu1342Gln)
14g.23418355G>ACA485618654MYH7c.4024C>T (p.Leu1342=)
dbSNP
14g.23418355G>CCA389041187MYH7c.4024C>G (p.Leu1342Val)
14g.23418355G=CA2123442852MYH7c.4024C= (p.Leu1342=)
14g.23418355G>TCA389041188MYH7c.4024C>A (p.Leu1342Met)
14g.23418356G>ACA485618660MYH7c.4023C>T (p.Asp1341=)
gnomAD v4
14g.23418356G>CCA389041189MYH7c.4023C>G (p.Asp1341Glu)
14g.23418356G=CA2123442855MYH7c.4023C= (p.Asp1341=)
14g.23418356G>TCA040117MYH7c.4023C>A (p.Asp1341Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418357T>ACA389041192MYH7c.4022A>T (p.Asp1341Val)
14g.23418357T>CCA389041193MYH7c.4022A>G (p.Asp1341Gly)
14g.23418357T>GCA389041195MYH7c.4022A>C (p.Asp1341Ala)
14g.23418358C>ACA040099MYH7c.4021G>T (p.Asp1341Tyr)
dbSNP ExAC gnomAD v2
14g.23418358C=CA2123442863MYH7c.4021G= (p.Asp1341=)
14g.23418358C>GCA389041196MYH7c.4021G>C (p.Asp1341His)
dbSNP gnomAD v2 gnomAD v4
14g.23418358C>TCA040080MYH7c.4021G>A (p.Asp1341Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418359G>ACA040071MYH7c.4020C>T (p.Cys1340=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418359G>CCA389041202MYH7c.4020C>G (p.Cys1340Trp)
14g.23418359G=CA2123442870MYH7c.4020C= (p.Cys1340=)
14g.23418359G>TCA389041199MYH7c.4020C>A (p.Cys1340Ter)
14g.23418360delCA2800863459MYH7c.4019del (p.Cys1340SerfsTer?)
14g.23418360C>ACA389041204MYH7c.4019G>T (p.Cys1340Phe)
ClinVar dbSNP
14g.23418360C>GCA389041206MYH7c.4019G>C (p.Cys1340Ser)
14g.23418360C>TCA389041207MYH7c.4019G>A (p.Cys1340Tyr)
gnomAD v4
14g.23418361A=CA2123442872MYH7c.4018T= (p.Cys1340=)
14g.23418361A>CCA389041209MYH7c.4018T>G (p.Cys1340Gly)
14g.23418361A>GCA040058MYH7c.4018T>C (p.Cys1340Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418361A>TCA389041212MYH7c.4018T>A (p.Cys1340Ser)
14g.23418362G>ACA040047MYH7c.4017C>T (p.Asp1339=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418362G>CCA389041213MYH7c.4017C>G (p.Asp1339Glu)
14g.23418362G=CA2123442879MYH7c.4017C= (p.Asp1339=)
14g.23418362G>TCA389041215MYH7c.4017C>A (p.Asp1339Glu)
14g.23418363T>ACA389041217MYH7c.4016A>T (p.Asp1339Val)
14g.23418363T>CCA389041218MYH7c.4016A>G (p.Asp1339Gly)
14g.23418363T>GCA389041220MYH7c.4016A>C (p.Asp1339Ala)
14g.23418364C>ACA389041224MYH7c.4015G>T (p.Asp1339Tyr)
14g.23418364C>GCA389041225MYH7c.4015G>C (p.Asp1339His)
14g.23418364C>TCA389041223MYH7c.4015G>A (p.Asp1339Asn)
14g.23418365delCA2580088017MYH7c.4014del (p.His1338GlnfsTer?)
ClinVar
14g.23418365A>CCA389041227MYH7c.4014T>G (p.His1338Gln)
ClinVar
14g.23418365A>GCA485618691MYH7c.4014T>C (p.His1338=)
14g.23418365A>TCA389041228MYH7c.4014T>A (p.His1338Gln)
14g.23418366T>ACA389041230MYH7c.4013A>T (p.His1338Leu)
14g.23418366T>CCA389041231MYH7c.4013A>G (p.His1338Arg)
gnomAD v4
14g.23418366T>GCA389041232MYH7c.4013A>C (p.His1338Pro)
ClinVar dbSNP
14g.23418366T=CA2123442886MYH7c.4013A= (p.His1338=)
14g.23418367G>ACA389041235MYH7c.4012C>T (p.His1338Tyr)
14g.23418367G>CCA389041233MYH7c.4012C>G (p.His1338Asp)
14g.23418367G>TCA389041234MYH7c.4012C>A (p.His1338Asn)
14g.23418368C>ACA485618699MYH7c.4011G>T (p.Arg1337=)
14g.23418368C=CA2123442892MYH7c.4011G= (p.Arg1337=)
14g.23418368C>GCA485618702MYH7c.4011G>C (p.Arg1337=)
gnomAD v4
14g.23418368C>TCA485618701MYH7c.4011G>A (p.Arg1337=)
dbSNP
14g.23418369C>ACA389041236MYH7c.4010G>T (p.Arg1337Leu)
14g.23418369C=CA2123442899MYH7c.4010G= (p.Arg1337=)
14g.23418369C>GCA389041237MYH7c.4010G>C (p.Arg1337Pro)
ClinVar dbSNP
14g.23418369C>TCA014363MYH7c.4010G>A (p.Arg1337Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418370_23418380dupCA7116296MYH7c.4000_4010dup (p.His1338SerfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418370G>ACA040023MYH7c.4009C>T (p.Arg1337Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418370G>CCA389041239MYH7c.4009C>G (p.Arg1337Gly)
14g.23418370G=CA2123442908MYH7c.4009C= (p.Arg1337=)
14g.23418370G>TCA485618712MYH7c.4009C>A (p.Arg1337=)
14g.23418371G>ACA485618713MYH7c.4008C>T (p.Ala1336=)
14g.23418371G>CCA485618714MYH7c.4008C>G (p.Ala1336=)
14g.23418371G>TCA485618716MYH7c.4008C>A (p.Ala1336=)
14g.23418372G>ACA389041242MYH7c.4007C>T (p.Ala1336Val)
14g.23418372G>CCA389041243MYH7c.4007C>G (p.Ala1336Gly)
14g.23418372G>TCA389041240MYH7c.4007C>A (p.Ala1336Asp)
14g.23418373C>ACA389041248MYH7c.4006G>T (p.Ala1336Ser)
14g.23418373C=CA2123442915MYH7c.4006G= (p.Ala1336=)
14g.23418373C>GCA389041245MYH7c.4006G>C (p.Ala1336Pro)
ClinVar
14g.23418373C>TCA389041246MYH7c.4006G>A (p.Ala1336Thr)
ClinVar dbSNP
14g.23418374C>ACA485618725MYH7c.4005G>T (p.Ser1335=)
gnomAD v4
14g.23418374C=CA2123442923MYH7c.4005G= (p.Ser1335=)
14g.23418374C>GCA485618727MYH7c.4005G>C (p.Ser1335=)
ClinVar
14g.23418374C>TCA014353MYH7c.4005G>A (p.Ser1335=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418375G>ACA014343MYH7c.4004C>T (p.Ser1335Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418375G>CCA389041250MYH7c.4004C>G (p.Ser1335Trp)
14g.23418375G=CA2123442933MYH7c.4004C= (p.Ser1335=)
14g.23418375G>TCA389041252MYH7c.4004C>A (p.Ser1335Ter)
14g.23418376A=CA2123442942MYH7c.4003T= (p.Ser1335=)
14g.23418376A>CCA039982MYH7c.4003T>G (p.Ser1335Ala)
ClinVar dbSNP ExAC gnomAD v2
14g.23418376A>GCA389041254MYH7c.4003T>C (p.Ser1335Pro)
14g.23418376A>TCA389041255MYH7c.4003T>A (p.Ser1335Thr)
14g.23418377delCA2697553849MYH7c.4002del (p.Gln1334HisfsTer?)
ClinVar
14g.23418377C>ACA389041257MYH7c.4002G>T (p.Gln1334His)
14g.23418377C>GCA389041259MYH7c.4002G>C (p.Gln1334His)
14g.23418377C>TCA485618736MYH7c.4002G>A (p.Gln1334=)
ClinVar dbSNP gnomAD v4
14g.23418378T>ACA389041260MYH7c.4001A>T (p.Gln1334Leu)
ClinVar
14g.23418378T>CCA389041261MYH7c.4001A>G (p.Gln1334Arg)
14g.23418378T>GCA389041263MYH7c.4001A>C (p.Gln1334Pro)
14g.23418379G>ACA389041268MYH7c.4000C>T (p.Gln1334Ter)
ClinVar dbSNP gnomAD v4
14g.23418379G>CCA389041267MYH7c.4000C>G (p.Gln1334Glu)
14g.23418379G=CA2123442956MYH7c.4000C= (p.Gln1334=)
14g.23418379G>TCA389041265MYH7c.4000C>A (p.Gln1334Lys)
gnomAD v4
14g.23418380C>ACA485618748MYH7c.3999G>T (p.Leu1333=)
gnomAD v4
14g.23418380C>GCA485618750MYH7c.3999G>C (p.Leu1333=)
14g.23418380C>TCA485618752MYH7c.3999G>A (p.Leu1333=)
14g.23418381A>CCA389041269MYH7c.3998T>G (p.Leu1333Arg)
14g.23418381A>GCA389041271MYH7c.3998T>C (p.Leu1333Pro)
14g.23418381A>TCA389041272MYH7c.3998T>A (p.Leu1333Gln)
14g.23418382G>ACA485618759MYH7c.3997C>T (p.Leu1333=)
14g.23418382G>CCA257813922MYH7c.3997C>G (p.Leu1333Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23418382G=CA2123442960MYH7c.3997C= (p.Leu1333=)
14g.23418382G>TCA389041275MYH7c.3997C>A (p.Leu1333Met)
gnomAD v4
14g.23418383T>ACA485618761MYH7c.3996A>T (p.Ala1332=)
14g.23418383T>CCA485618763MYH7c.3996A>G (p.Ala1332=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23418383T>GCA485618765MYH7c.3996A>C (p.Ala1332=)
dbSNP
14g.23418383T=CA2123442966MYH7c.3996A= (p.Ala1332=)
14g.23418384G>ACA389041276MYH7c.3995C>T (p.Ala1332Val)
14g.23418384G>CCA389041277MYH7c.3995C>G (p.Ala1332Gly)
gnomAD v4
14g.23418384G>TCA389041279MYH7c.3995C>A (p.Ala1332Glu)
gnomAD v4
14g.23418385C>ACA389041281MYH7c.3994G>T (p.Ala1332Ser)
ClinVar dbSNP gnomAD v4
14g.23418385C=CA2123442973MYH7c.3994G= (p.Ala1332=)
14g.23418385C>GCA389041282MYH7c.3994G>C (p.Ala1332Pro)
gnomAD v4
14g.23418385C>TCA014334MYH7c.3994G>A (p.Ala1332Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418386G>ACA014326MYH7c.3993C>T (p.His1331=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418386G>CCA389041284MYH7c.3993C>G (p.His1331Gln)
14g.23418386G=CA2123442996MYH7c.3993C= (p.His1331=)
14g.23418386G>TCA389041286MYH7c.3993C>A (p.His1331Gln)
14g.23418387T>ACA389041290MYH7c.3992A>T (p.His1331Leu)
14g.23418387T>CCA389041291MYH7c.3992A>G (p.His1331Arg)
14g.23418387T>GCA389041288MYH7c.3992A>C (p.His1331Pro)
gnomAD v4
14g.23418388G>ACA389041292MYH7c.3991C>T (p.His1331Tyr)
14g.23418388G>CCA16042848MYH7c.3991C>G (p.His1331Asp)
ClinVar dbSNP
14g.23418388G=CA2123443004MYH7c.3991C= (p.His1331=)
14g.23418388G>TCA389041295MYH7c.3991C>A (p.His1331Asn)
14g.23418389G>ACA485618782MYH7c.3990C>T (p.Ala1330=)
dbSNP gnomAD v2 gnomAD v4
14g.23418389G>CCA485618784MYH7c.3990C>G (p.Ala1330=)
14g.23418389G=CA2123443013MYH7c.3990C= (p.Ala1330=)
14g.23418389G>TCA485618786MYH7c.3990C>A (p.Ala1330=)
gnomAD v4
14g.23418390G>ACA389041296MYH7c.3989C>T (p.Ala1330Val)
14g.23418390G>CCA389041298MYH7c.3989C>G (p.Ala1330Gly)
14g.23418390G=CA2123443020MYH7c.3989C= (p.Ala1330=)
14g.23418390G>TCA389041300MYH7c.3989C>A (p.Ala1330Asp)
dbSNP gnomAD v2 gnomAD v4
14g.23418391C>ACA389041301MYH7c.3988G>T (p.Ala1330Ser)
gnomAD v4 COSMIC
14g.23418391C=CA2123443027MYH7c.3988G= (p.Ala1330=)
14g.23418391C>GCA389041303MYH7c.3988G>C (p.Ala1330Pro)
14g.23418391C>TCA257813942MYH7c.3988G>A (p.Ala1330Thr)
ClinVar dbSNP
14g.23418392C>ACA485618795MYH7c.3987G>T (p.Leu1329=)
14g.23418392C=CA2123443033MYH7c.3987G= (p.Leu1329=)
14g.23418392C>GCA039931MYH7c.3987G>C (p.Leu1329=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418392C>TCA039914MYH7c.3987G>A (p.Leu1329=)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418393A=CA2123443037MYH7c.3986T= (p.Leu1329=)
14g.23418393A>CCA389041306MYH7c.3986T>G (p.Leu1329Arg)
14g.23418393A>GCA389041308MYH7c.3986T>C (p.Leu1329Pro)
14g.23418393A>TCA389041309MYH7c.3986T>A (p.Leu1329Gln)
14g.23418394G>ACA485618803MYH7c.3985C>T (p.Leu1329=)
dbSNP
14g.23418394G>CCA389041311MYH7c.3985C>G (p.Leu1329Val)
gnomAD v4
14g.23418394G=CA2123443047MYH7c.3985C= (p.Leu1329=)
14g.23418394G>TCA389041313MYH7c.3985C>A (p.Leu1329Met)
14g.23418396dupCA913190599MYH7c.3985dup (p.Leu1329ProfsTer11)
ClinVar dbSNP
14g.23418395G>ACA485618807MYH7c.3984C>T (p.Ala1328=)
14g.23418395G>CCA485618808MYH7c.3984C>G (p.Ala1328=)
COSMIC
14g.23418395G>TCA485618811MYH7c.3984C>A (p.Ala1328=)
14g.23418396G>ACA389041314MYH7c.3983C>T (p.Ala1328Val)
dbSNP gnomAD v2
14g.23418396G>CCA389041315MYH7c.3983C>G (p.Ala1328Gly)
14g.23418396G=CA2123443048MYH7c.3983C= (p.Ala1328=)
14g.23418396G>TCA389041316MYH7c.3983C>A (p.Ala1328Asp)
gnomAD v4
14g.23418397C>ACA389041318MYH7c.3982G>T (p.Ala1328Ser)
gnomAD v4 COSMIC
14g.23418397C=CA2123443053MYH7c.3982G= (p.Ala1328=)
14g.23418397C>GCA389041320MYH7c.3982G>C (p.Ala1328Pro)
14g.23418397C>TCA014317MYH7c.3982G>A (p.Ala1328Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418398G>ACA039873MYH7c.3981C>T (p.Asn1327=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418398G>CCA389041322MYH7c.3981C>G (p.Asn1327Lys)
gnomAD v4
14g.23418398G=CA2123443061MYH7c.3981C= (p.Asn1327=)
14g.23418398G>TCA014310MYH7c.3981C>A (p.Asn1327Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23418399T>ACA389041325MYH7c.3980A>T (p.Asn1327Ile)
14g.23418399T>CCA389041327MYH7c.3980A>G (p.Asn1327Ser)
14g.23418399T>GCA389041328MYH7c.3980A>C (p.Asn1327Thr)
14g.23418400T>ACA389041330MYH7c.3979A>T (p.Asn1327Tyr)
14g.23418400T>CCA389041333MYH7c.3979A>G (p.Asn1327Asp)
14g.23418400T>GCA389041332MYH7c.3979A>C (p.Asn1327His)
14g.23418401C>ACA389041335MYH7c.3978G>T (p.Lys1326Asn)
14g.23418401C=CA2123443070MYH7c.3978G= (p.Lys1326=)
14g.23418401C>GCA389041337MYH7c.3978G>C (p.Lys1326Asn)
dbSNP gnomAD v2 gnomAD v4
14g.23418401C>TCA485618832MYH7c.3978G>A (p.Lys1326=)

Number of alleles fetched