Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47330388_47335387delCA2740090117
11g.47332259_47335041delCA2580084187MYBPC3c.2905+1_3628-1del
c.2887+1_3610-1del
c.2824+1_3547-1del
ClinVar
11g.47332549_47332603delCA2580084192MYBPC3c.3593_3627+20del
c.3575_3609+20del
c.3512_3546+20del
ClinVar
11g.47332588_47332592dupCA2580615677MYBPC3c.3607_3611dup (p.Arg1205LeufsTer?)
c.3589_3593dup (p.Arg1199LeufsTer?)
c.3526_3530dup (p.Arg1178LeufsTer?)
ClinVar
11g.47332583_47332593delinsCAGCACAGCAGCA1969334106MYBPC3c.3600_3610delinsCTGCTGTGCTG (p.Leu1200=)
c.3582_3592delinsCTGCTGTGCTG (p.Leu1194=)
c.3519_3529delinsCTGCTGTGCTG (p.Leu1173=)
11g.47332584A>CCA474428903MYBPC3c.3609T>G (p.Ala1203=)
c.3591T>G (p.Ala1197=)
c.3528T>G (p.Ala1176=)
11g.47332584A>GCA474428904MYBPC3c.3609T>C (p.Ala1203=)
c.3591T>C (p.Ala1197=)
c.3528T>C (p.Ala1176=)
11g.47332584A>TCA474428902MYBPC3c.3609T>A (p.Ala1203=)
c.3591T>A (p.Ala1197=)
c.3528T>A (p.Ala1176=)
11g.47332588_47332597dupCA2580084197MYBPC3c.3600_3609dup (p.Val1204LeufsTer7)
c.3582_3591dup (p.Val1198LeufsTer7)
c.3519_3528dup (p.Val1177LeufsTer7)
ClinVar
11g.47332588_47332597delCA014440MYBPC3c.3600_3609del (p.Cys1201SerfsTer?)
c.3582_3591del (p.Cys1195SerfsTer?)
c.3519_3528del (p.Cys1174SerfsTer?)
ClinVar dbSNP
11g.47332585G>ACA380312282MYBPC3c.3608C>T (p.Ala1203Val)
c.3590C>T (p.Ala1197Val)
c.3527C>T (p.Ala1176Val)
dbSNP gnomAD v2 gnomAD v4
11g.47332585G>CCA380312285MYBPC3c.3608C>G (p.Ala1203Gly)
c.3590C>G (p.Ala1197Gly)
c.3527C>G (p.Ala1176Gly)
11g.47332585G=CA1969334125MYBPC3c.3608C= (p.Ala1203=)
c.3590C= (p.Ala1197=)
c.3527C= (p.Ala1176=)
11g.47332585G>TCA380312287MYBPC3c.3608C>A (p.Ala1203Asp)
c.3590C>A (p.Ala1197Asp)
c.3527C>A (p.Ala1176Asp)
11g.47332586C>ACA380312290MYBPC3c.3607G>T (p.Ala1203Ser)
c.3589G>T (p.Ala1197Ser)
c.3526G>T (p.Ala1176Ser)
gnomAD v4
11g.47332586C>GCA380312292MYBPC3c.3607G>C (p.Ala1203Pro)
c.3589G>C (p.Ala1197Pro)
c.3526G>C (p.Ala1176Pro)
11g.47332586C>TCA380312296MYBPC3c.3607G>A (p.Ala1203Thr)
c.3589G>A (p.Ala1197Thr)
c.3526G>A (p.Ala1176Thr)
11g.47332587A=CA1969334129MYBPC3c.3606T= (p.Cys1202=)
c.3588T= (p.Cys1196=)
c.3525T= (p.Cys1175=)
11g.47332587A>CCA380312298MYBPC3c.3606T>G (p.Cys1202Trp)
c.3588T>G (p.Cys1196Trp)
c.3525T>G (p.Cys1175Trp)
11g.47332587A>GCA221682038MYBPC3c.3606T>C (p.Cys1202=)
c.3588T>C (p.Cys1196=)
c.3525T>C (p.Cys1175=)
ClinVar dbSNP gnomAD v4
11g.47332587A>TCA380312301MYBPC3c.3606T>A (p.Cys1202Ter)
c.3588T>A (p.Cys1196Ter)
c.3525T>A (p.Cys1175Ter)
11g.47332588delCA2573051215MYBPC3c.3605del (p.Cys1202LeufsTer?)
c.3587del (p.Cys1196LeufsTer?)
c.3524del (p.Cys1175LeufsTer?)
11g.47332588C>ACA380312309MYBPC3c.3605G>T (p.Cys1202Phe)
c.3587G>T (p.Cys1196Phe)
c.3524G>T (p.Cys1175Phe)
11g.47332588C=CA1969334138MYBPC3c.3605G= (p.Cys1202=)
c.3587G= (p.Cys1196=)
c.3524G= (p.Cys1175=)
11g.47332588C>GCA16613579MYBPC3c.3605G>C (p.Cys1202Ser)
c.3587G>C (p.Cys1196Ser)
c.3524G>C (p.Cys1175Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47332588C>TCA014449MYBPC3c.3605G>A (p.Cys1202Tyr)
c.3587G>A (p.Cys1196Tyr)
c.3524G>A (p.Cys1175Tyr)
ClinVar dbSNP
11g.47332589A>CCA380312311MYBPC3c.3604T>G (p.Cys1202Gly)
c.3586T>G (p.Cys1196Gly)
c.3523T>G (p.Cys1175Gly)
11g.47332589A>GCA380312314MYBPC3c.3604T>C (p.Cys1202Arg)
c.3586T>C (p.Cys1196Arg)
c.3523T>C (p.Cys1175Arg)
11g.47332589A>TCA380312316MYBPC3c.3604T>A (p.Cys1202Ser)
c.3586T>A (p.Cys1196Ser)
c.3523T>A (p.Cys1175Ser)
11g.47332590G>ACA474428929MYBPC3c.3603C>T (p.Cys1201=)
c.3585C>T (p.Cys1195=)
c.3522C>T (p.Cys1174=)
11g.47332590G>CCA380312320MYBPC3c.3603C>G (p.Cys1201Trp)
c.3585C>G (p.Cys1195Trp)
c.3522C>G (p.Cys1174Trp)
11g.47332590G>TCA380312328MYBPC3c.3603C>A (p.Cys1201Ter)
c.3585C>A (p.Cys1195Ter)
c.3522C>A (p.Cys1174Ter)
11g.47332591C>ACA380312334MYBPC3c.3602G>T (p.Cys1201Phe)
c.3584G>T (p.Cys1195Phe)
c.3521G>T (p.Cys1174Phe)
11g.47332591C=CA1969334146MYBPC3c.3602G= (p.Cys1201=)
c.3584G= (p.Cys1195=)
c.3521G= (p.Cys1174=)
11g.47332591C>GCA380312337MYBPC3c.3602G>C (p.Cys1201Ser)
c.3584G>C (p.Cys1195Ser)
c.3521G>C (p.Cys1174Ser)
gnomAD v4
11g.47332591C>TCA380312340MYBPC3c.3602G>A (p.Cys1201Tyr)
c.3584G>A (p.Cys1195Tyr)
c.3521G>A (p.Cys1174Tyr)
dbSNP
11g.47332592A>CCA380312343MYBPC3c.3601T>G (p.Cys1201Gly)
c.3583T>G (p.Cys1195Gly)
c.3520T>G (p.Cys1174Gly)
11g.47332592A>GCA380312346MYBPC3c.3601T>C (p.Cys1201Arg)
c.3583T>C (p.Cys1195Arg)
c.3520T>C (p.Cys1174Arg)
11g.47332592A>TCA380312348MYBPC3c.3601T>A (p.Cys1201Ser)
c.3583T>A (p.Cys1195Ser)
c.3520T>A (p.Cys1174Ser)
11g.47332593G>ACA054468MYBPC3c.3600C>T (p.Leu1200=)
c.3582C>T (p.Leu1194=)
c.3519C>T (p.Leu1173=)
dbSNP gnomAD v2 gnomAD v4
11g.47332593G>CCA474428930MYBPC3c.3600C>G (p.Leu1200=)
c.3582C>G (p.Leu1194=)
c.3519C>G (p.Leu1173=)
11g.47332593G=CA1969334149MYBPC3c.3600C= (p.Leu1200=)
c.3582C= (p.Leu1194=)
c.3519C= (p.Leu1173=)
11g.47332593G>TCA474428931MYBPC3c.3600C>A (p.Leu1200=)
c.3582C>A (p.Leu1194=)
c.3519C>A (p.Leu1173=)
11g.47332594A=CA1969334154MYBPC3c.3599T= (p.Leu1200=)
c.3581T= (p.Leu1194=)
c.3518T= (p.Leu1173=)
11g.47332594A>CCA380312358MYBPC3c.3599T>G (p.Leu1200Arg)
c.3581T>G (p.Leu1194Arg)
c.3518T>G (p.Leu1173Arg)
11g.47332594A>GCA014395MYBPC3c.3599T>C (p.Leu1200Pro)
c.3581T>C (p.Leu1194Pro)
c.3518T>C (p.Leu1173Pro)
ClinVar dbSNP
11g.47332594A>TCA380312352MYBPC3c.3599T>A (p.Leu1200His)
c.3581T>A (p.Leu1194His)
c.3518T>A (p.Leu1173His)
gnomAD v4
11g.47332595G>ACA380312363MYBPC3c.3598C>T (p.Leu1200Phe)
c.3580C>T (p.Leu1194Phe)
c.3517C>T (p.Leu1173Phe)
11g.47332595G>CCA380312366MYBPC3c.3598C>G (p.Leu1200Val)
c.3580C>G (p.Leu1194Val)
c.3517C>G (p.Leu1173Val)
11g.47332595G>TCA380312369MYBPC3c.3598C>A (p.Leu1200Ile)
c.3580C>A (p.Leu1194Ile)
c.3517C>A (p.Leu1173Ile)

Number of alleles fetched