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.47332574T>ACA380312215MYBPC3c.3619A>T (p.Ser1207Cys)
c.3601A>T (p.Ser1201Cys)
c.3538A>T (p.Ser1180Cys)
11g.47332574T>CCA380312221MYBPC3c.3619A>G (p.Ser1207Gly)
c.3601A>G (p.Ser1201Gly)
c.3538A>G (p.Ser1180Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47332574T>GCA380312218MYBPC3c.3619A>C (p.Ser1207Arg)
c.3601A>C (p.Ser1201Arg)
c.3538A>C (p.Ser1180Arg)
11g.47332574T=CA1969334056MYBPC3c.3619A= (p.Ser1207=)
c.3601A= (p.Ser1201=)
c.3538A= (p.Ser1180=)
11g.47332575A>CCA474428892MYBPC3c.3618T>G (p.Gly1206=)
c.3600T>G (p.Gly1200=)
c.3537T>G (p.Gly1179=)
11g.47332575A>GCA474428893MYBPC3c.3618T>C (p.Gly1206=)
c.3600T>C (p.Gly1200=)
c.3537T>C (p.Gly1179=)
gnomAD v4
11g.47332575A>TCA474428894MYBPC3c.3618T>A (p.Gly1206=)
c.3600T>A (p.Gly1200=)
c.3537T>A (p.Gly1179=)
gnomAD v4
11g.47332575_47332576delCA2695213904MYBPC3c.3617_3618del (p.Gly1206GlufsTer?)
c.3599_3600del (p.Gly1200GlufsTer?)
c.3536_3537del (p.Gly1179GlufsTer?)
11g.47332575_47332576delinsACCA1969334059MYBPC3c.3617_3618delinsGT (p.Gly1206=)
c.3599_3600delinsGT (p.Gly1200=)
c.3536_3537delinsGT (p.Gly1179=)
11g.47332576C>ACA054375MYBPC3c.3617G>T (p.Gly1206Val)
c.3599G>T (p.Gly1200Val)
c.3536G>T (p.Gly1179Val)
ClinVar dbSNP
11g.47332576C=CA1969334064MYBPC3c.3617G= (p.Gly1206=)
c.3599G= (p.Gly1200=)
c.3536G= (p.Gly1179=)
11g.47332576C>GCA380312229MYBPC3c.3617G>C (p.Gly1206Ala)
c.3599G>C (p.Gly1200Ala)
c.3536G>C (p.Gly1179Ala)
11g.47332576C>TCA16042795MYBPC3c.3617G>A (p.Gly1206Asp)
c.3599G>A (p.Gly1200Asp)
c.3536G>A (p.Gly1179Asp)
ClinVar dbSNP gnomAD v4
11g.47332576_47332577delinsTTCA2580084194MYBPC3c.3616_3617delinsAA (p.Gly1206Asn)
c.3598_3599delinsAA (p.Gly1200Asn)
c.3535_3536delinsAA (p.Gly1179Asn)
ClinVar
11g.47332579delCA16613343MYBPC3c.3617del (p.Gly1206ValfsTer?)
c.3599del (p.Gly1200ValfsTer?)
c.3536del (p.Gly1179ValfsTer?)
ClinVar dbSNP
11g.47332577C>ACA380312232MYBPC3c.3616G>T (p.Gly1206Cys)
c.3598G>T (p.Gly1200Cys)
c.3535G>T (p.Gly1179Cys)
11g.47332577C>GCA380312235MYBPC3c.3616G>C (p.Gly1206Arg)
c.3598G>C (p.Gly1200Arg)
c.3535G>C (p.Gly1179Arg)
11g.47332577C>TCA380312237MYBPC3c.3616G>A (p.Gly1206Ser)
c.3598G>A (p.Gly1200Ser)
c.3535G>A (p.Gly1179Ser)
11g.47332578C>ACA474428895MYBPC3c.3615G>T (p.Arg1205=)
c.3597G>T (p.Arg1199=)
c.3534G>T (p.Arg1178=)
dbSNP
11g.47332578C=CA1969334069MYBPC3c.3615G= (p.Arg1205=)
c.3597G= (p.Arg1199=)
c.3534G= (p.Arg1178=)
11g.47332578C>GCA474428896MYBPC3c.3615G>C (p.Arg1205=)
c.3597G>C (p.Arg1199=)
c.3534G>C (p.Arg1178=)
ClinVar dbSNP gnomAD v4
11g.47332578C>TCA079448MYBPC3c.3615G>A (p.Arg1205=)
c.3597G>A (p.Arg1199=)
c.3534G>A (p.Arg1178=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47332579C>ACA380312245MYBPC3c.3614G>T (p.Arg1205Leu)
c.3596G>T (p.Arg1199Leu)
c.3533G>T (p.Arg1178Leu)
11g.47332579C=CA1969334075MYBPC3c.3614G= (p.Arg1205=)
c.3596G= (p.Arg1199=)
c.3533G= (p.Arg1178=)
11g.47332579C>GCA380312247MYBPC3c.3614G>C (p.Arg1205Pro)
c.3596G>C (p.Arg1199Pro)
c.3533G>C (p.Arg1178Pro)
ClinVar dbSNP
11g.47332579C>TCA014478MYBPC3c.3614G>A (p.Arg1205Gln)
c.3596G>A (p.Arg1199Gln)
c.3533G>A (p.Arg1178Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332580G>ACA014469MYBPC3c.3613C>T (p.Arg1205Trp)
c.3595C>T (p.Arg1199Trp)
c.3532C>T (p.Arg1178Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332580G>CCA054456MYBPC3c.3613C>G (p.Arg1205Gly)
c.3595C>G (p.Arg1199Gly)
c.3532C>G (p.Arg1178Gly)
11g.47332580G=CA1969334088MYBPC3c.3613C= (p.Arg1205=)
c.3595C= (p.Arg1199=)
c.3532C= (p.Arg1178=)
11g.47332580G>TCA474428897MYBPC3c.3613C>A (p.Arg1205=)
c.3595C>A (p.Arg1199=)
c.3532C>A (p.Arg1178=)
gnomAD v4
11g.47332581G>ACA474428898MYBPC3c.3612C>T (p.Val1204=)
c.3594C>T (p.Val1198=)
c.3531C>T (p.Val1177=)
11g.47332581G>CCA474428899MYBPC3c.3612C>G (p.Val1204=)
c.3594C>G (p.Val1198=)
c.3531C>G (p.Val1177=)
11g.47332581G>TCA474428900MYBPC3c.3612C>A (p.Val1204=)
c.3594C>A (p.Val1198=)
c.3531C>A (p.Val1177=)
gnomAD v4
11g.47332582A=CA1969334096MYBPC3c.3611T= (p.Val1204=)
c.3593T= (p.Val1198=)
c.3530T= (p.Val1177=)
11g.47332582A>CCA380312258MYBPC3c.3611T>G (p.Val1204Gly)
c.3593T>G (p.Val1198Gly)
c.3530T>G (p.Val1177Gly)
11g.47332582A>GCA014459MYBPC3c.3611T>C (p.Val1204Ala)
c.3593T>C (p.Val1198Ala)
c.3530T>C (p.Val1177Ala)
ClinVar dbSNP
11g.47332582A>TCA380312264MYBPC3c.3611T>A (p.Val1204Asp)
c.3593T>A (p.Val1198Asp)
c.3530T>A (p.Val1177Asp)
11g.47332588_47332592dupCA2580615677MYBPC3c.3607_3611dup (p.Arg1205LeufsTer?)
c.3589_3593dup (p.Arg1199LeufsTer?)
c.3526_3530dup (p.Arg1178LeufsTer?)
ClinVar
11g.47332583C>ACA380312268MYBPC3c.3610G>T (p.Val1204Phe)
c.3592G>T (p.Val1198Phe)
c.3529G>T (p.Val1177Phe)
11g.47332583C=CA1969334108MYBPC3c.3610G= (p.Val1204=)
c.3592G= (p.Val1198=)
c.3529G= (p.Val1177=)
11g.47332583C>GCA380312274MYBPC3c.3610G>C (p.Val1204Leu)
c.3592G>C (p.Val1198Leu)
c.3529G>C (p.Val1177Leu)
11g.47332583C>TCA380312272MYBPC3c.3610G>A (p.Val1204Ile)
c.3592G>A (p.Val1198Ile)
c.3529G>A (p.Val1177Ile)
dbSNP
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)
11g.47332596C>ACA380312372MYBPC3c.3597G>T (p.Met1199Ile)
c.3579G>T (p.Met1193Ile)
c.3516G>T (p.Met1172Ile)
11g.47332596C=CA1969334160MYBPC3c.3597G= (p.Met1199=)
c.3579G= (p.Met1193=)
c.3516G= (p.Met1172=)
11g.47332596C>GCA380312376MYBPC3c.3597G>C (p.Met1199Ile)
c.3579G>C (p.Met1193Ile)
c.3516G>C (p.Met1172Ile)
dbSNP
11g.47332596C>TCA380312377MYBPC3c.3597G>A (p.Met1199Ile)
c.3579G>A (p.Met1193Ile)
c.3516G>A (p.Met1172Ile)
gnomAD v4
11g.47332597A>CCA380312382MYBPC3c.3596T>G (p.Met1199Arg)
c.3578T>G (p.Met1193Arg)
c.3515T>G (p.Met1172Arg)
11g.47332597A>GCA380312386MYBPC3c.3596T>C (p.Met1199Thr)
c.3578T>C (p.Met1193Thr)
c.3515T>C (p.Met1172Thr)
ClinVar
11g.47332597A>TCA380312388MYBPC3c.3596T>A (p.Met1199Lys)
c.3578T>A (p.Met1193Lys)
c.3515T>A (p.Met1172Lys)
11g.47332598_47332599delCA2697548541MYBPC3c.3595_3596del (p.Met1199AlafsTer8)
c.3577_3578del (p.Met1193AlafsTer8)
c.3514_3515del (p.Met1172AlafsTer8)
ClinVar
11g.47332598T>ACA380312394MYBPC3c.3595A>T (p.Met1199Leu)
c.3577A>T (p.Met1193Leu)
c.3514A>T (p.Met1172Leu)
11g.47332598T>CCA380312396MYBPC3c.3595A>G (p.Met1199Val)
c.3577A>G (p.Met1193Val)
c.3514A>G (p.Met1172Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47332598T>GCA380312400MYBPC3c.3595A>C (p.Met1199Leu)
c.3577A>C (p.Met1193Leu)
c.3514A>C (p.Met1172Leu)
11g.47332598T=CA1969334164MYBPC3c.3595A= (p.Met1199=)
c.3577A= (p.Met1193=)
c.3514A= (p.Met1172=)
11g.47332599A=CA1969334168MYBPC3c.3594T= (p.Ala1198=)
c.3576T= (p.Ala1192=)
c.3513T= (p.Ala1171=)
11g.47332599A>CCA474428932MYBPC3c.3594T>G (p.Ala1198=)
c.3576T>G (p.Ala1192=)
c.3513T>G (p.Ala1171=)
11g.47332599A>GCA474428933MYBPC3c.3594T>C (p.Ala1198=)
c.3576T>C (p.Ala1192=)
c.3513T>C (p.Ala1171=)
dbSNP gnomAD v4
11g.47332599A>TCA474428934MYBPC3c.3594T>A (p.Ala1198=)
c.3576T>A (p.Ala1192=)
c.3513T>A (p.Ala1171=)
11g.47332599_47332611delinsAGCAGTGTAGCCCCA1969334167MYBPC3c.3582_3594delinsGGGCTACACTGCT (p.Ala1194=)
c.3564_3576delinsGGGCTACACTGCT (p.Ala1188=)
c.3501_3513delinsGGGCTACACTGCT (p.Ala1167=)
11g.47332600G>ACA10582915MYBPC3c.3593C>T (p.Ala1198Val)
c.3575C>T (p.Ala1192Val)
c.3512C>T (p.Ala1171Val)
ClinVar dbSNP gnomAD v4
11g.47332600G>CCA380312408MYBPC3c.3593C>G (p.Ala1198Gly)
c.3575C>G (p.Ala1192Gly)
c.3512C>G (p.Ala1171Gly)
11g.47332600G=CA1969334175MYBPC3c.3593C= (p.Ala1198=)
c.3575C= (p.Ala1192=)
c.3512C= (p.Ala1171=)
11g.47332600G>TCA380312403MYBPC3c.3593C>A (p.Ala1198Asp)
c.3575C>A (p.Ala1192Asp)
c.3512C>A (p.Ala1171Asp)
11g.47332602_47332613delCA677013759MYBPC3c.3582_3593del (p.Gly1195_Ala1198del)
c.3564_3575del (p.Gly1189_Ala1192del)
c.3501_3512del (p.Gly1168_Ala1171del)
dbSNP gnomAD v4
11g.47332601C>ACA380312420MYBPC3c.3592G>T (p.Ala1198Ser)
c.3574G>T (p.Ala1192Ser)
c.3511G>T (p.Ala1171Ser)
11g.47332601C>GCA380312414MYBPC3c.3592G>C (p.Ala1198Pro)
c.3574G>C (p.Ala1192Pro)
c.3511G>C (p.Ala1171Pro)
11g.47332601C>TCA380312417MYBPC3c.3592G>A (p.Ala1198Thr)
c.3574G>A (p.Ala1192Thr)
c.3511G>A (p.Ala1171Thr)
gnomAD v4
11g.47332601dupCA16616723MYBPC3c.3592dup (p.Ala1198GlyfsTer10)
c.3574dup (p.Ala1192GlyfsTer10)
c.3511dup (p.Ala1171GlyfsTer10)
11g.47332602A>CCA474428935MYBPC3c.3591T>G (p.Thr1197=)
c.3573T>G (p.Thr1191=)
c.3510T>G (p.Thr1170=)
11g.47332602A>GCA474428936MYBPC3c.3591T>C (p.Thr1197=)
c.3573T>C (p.Thr1191=)
c.3510T>C (p.Thr1170=)
11g.47332602A>TCA474428937MYBPC3c.3591T>A (p.Thr1197=)
c.3573T>A (p.Thr1191=)
c.3510T>A (p.Thr1170=)
11g.47332603G>ACA380312425MYBPC3c.3590C>T (p.Thr1197Ile)
c.3572C>T (p.Thr1191Ile)
c.3509C>T (p.Thr1170Ile)
gnomAD v4
11g.47332603G>CCA380312427MYBPC3c.3590C>G (p.Thr1197Ser)
c.3572C>G (p.Thr1191Ser)
c.3509C>G (p.Thr1170Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47332603G=CA1969334182MYBPC3c.3590C= (p.Thr1197=)
c.3572C= (p.Thr1191=)
c.3509C= (p.Thr1170=)
11g.47332603G>TCA380312429MYBPC3c.3590C>A (p.Thr1197Asn)
c.3572C>A (p.Thr1191Asn)
c.3509C>A (p.Thr1170Asn)
dbSNP
11g.47332604T>ACA380312432MYBPC3c.3589A>T (p.Thr1197Ser)
c.3571A>T (p.Thr1191Ser)
c.3508A>T (p.Thr1170Ser)
11g.47332604T>CCA380312434MYBPC3c.3589A>G (p.Thr1197Ala)
c.3571A>G (p.Thr1191Ala)
c.3508A>G (p.Thr1170Ala)
11g.47332604T>GCA380312437MYBPC3c.3589A>C (p.Thr1197Pro)
c.3571A>C (p.Thr1191Pro)
c.3508A>C (p.Thr1170Pro)
11g.47332605G>ACA474428938MYBPC3c.3588C>T (p.Tyr1196=)
c.3570C>T (p.Tyr1190=)
c.3507C>T (p.Tyr1169=)
dbSNP gnomAD v2 gnomAD v4
11g.47332605G>CCA380312439MYBPC3c.3588C>G (p.Tyr1196Ter)
c.3570C>G (p.Tyr1190Ter)
c.3507C>G (p.Tyr1169Ter)
11g.47332605G=CA1969334188MYBPC3c.3588C= (p.Tyr1196=)
c.3570C= (p.Tyr1190=)
c.3507C= (p.Tyr1169=)
11g.47332605G>TCA380312440MYBPC3c.3588C>A (p.Tyr1196Ter)
c.3570C>A (p.Tyr1190Ter)
c.3507C>A (p.Tyr1169Ter)
ClinVar dbSNP
11g.47332606T>ACA380312441MYBPC3c.3587A>T (p.Tyr1196Phe)
c.3569A>T (p.Tyr1190Phe)
c.3506A>T (p.Tyr1169Phe)
11g.47332606T>CCA380312443MYBPC3c.3587A>G (p.Tyr1196Cys)
c.3569A>G (p.Tyr1190Cys)
c.3506A>G (p.Tyr1169Cys)
11g.47332606T>GCA380312446MYBPC3c.3587A>C (p.Tyr1196Ser)
c.3569A>C (p.Tyr1190Ser)
c.3506A>C (p.Tyr1169Ser)
11g.47332607A>CCA380312449MYBPC3c.3586T>G (p.Tyr1196Asp)
c.3568T>G (p.Tyr1190Asp)
c.3505T>G (p.Tyr1169Asp)
dbSNP
11g.47332607A>GCA380312453MYBPC3c.3586T>C (p.Tyr1196His)
c.3568T>C (p.Tyr1190His)
c.3505T>C (p.Tyr1169His)
11g.47332607A>TCA380312451MYBPC3c.3586T>A (p.Tyr1196Asn)
c.3568T>A (p.Tyr1190Asn)
c.3505T>A (p.Tyr1169Asn)
11g.47332608G>ACA474428939MYBPC3c.3585C>T (p.Gly1195=)
c.3567C>T (p.Gly1189=)
c.3504C>T (p.Gly1168=)
dbSNP
11g.47332608G>CCA474428940MYBPC3c.3585C>G (p.Gly1195=)
c.3567C>G (p.Gly1189=)
c.3504C>G (p.Gly1168=)
11g.47332608G=CA1969334195MYBPC3c.3585C= (p.Gly1195=)
c.3567C= (p.Gly1189=)
c.3504C= (p.Gly1168=)
11g.47332608G>TCA014386MYBPC3c.3585C>A (p.Gly1195=)
c.3567C>A (p.Gly1189=)
c.3504C>A (p.Gly1168=)
ClinVar dbSNP
11g.47332609C>ACA014378MYBPC3c.3584G>T (p.Gly1195Val)
c.3566G>T (p.Gly1189Val)
c.3503G>T (p.Gly1168Val)
ClinVar dbSNP
11g.47332609C=CA1969334203MYBPC3c.3584G= (p.Gly1195=)
c.3566G= (p.Gly1189=)
c.3503G= (p.Gly1168=)
11g.47332609C>GCA380312459MYBPC3c.3584G>C (p.Gly1195Ala)
c.3566G>C (p.Gly1189Ala)
c.3503G>C (p.Gly1168Ala)
dbSNP gnomAD v4
11g.47332609C>TCA380312461MYBPC3c.3584G>A (p.Gly1195Asp)
c.3566G>A (p.Gly1189Asp)
c.3503G>A (p.Gly1168Asp)
ClinVar dbSNP
11g.47332610C>ACA380312464MYBPC3c.3583G>T (p.Gly1195Cys)
c.3565G>T (p.Gly1189Cys)
c.3502G>T (p.Gly1168Cys)
11g.47332610C>GCA380312466MYBPC3c.3583G>C (p.Gly1195Arg)
c.3565G>C (p.Gly1189Arg)
c.3502G>C (p.Gly1168Arg)
ClinVar
11g.47332610C>TCA380312468MYBPC3c.3583G>A (p.Gly1195Ser)
c.3565G>A (p.Gly1189Ser)
c.3502G>A (p.Gly1168Ser)
gnomAD v4
11g.47332611C>ACA474428941MYBPC3c.3582G>T (p.Ala1194=)
c.3564G>T (p.Ala1188=)
c.3501G>T (p.Ala1167=)
11g.47332611C=CA1969334208MYBPC3c.3582G= (p.Ala1194=)
c.3564G= (p.Ala1188=)
c.3501G= (p.Ala1167=)
11g.47332611C>GCA474428942MYBPC3c.3582G>C (p.Ala1194=)
c.3564G>C (p.Ala1188=)
c.3501G>C (p.Ala1167=)
11g.47332611C>TCA079444MYBPC3c.3582G>A (p.Ala1194=)
c.3564G>A (p.Ala1188=)
c.3501G>A (p.Ala1167=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332612G>ACA014370MYBPC3c.3581C>T (p.Ala1194Val)
c.3563C>T (p.Ala1188Val)
c.3500C>T (p.Ala1167Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332612G>CCA380312474MYBPC3c.3581C>G (p.Ala1194Gly)
c.3563C>G (p.Ala1188Gly)
c.3500C>G (p.Ala1167Gly)
11g.47332612G=CA1969334219MYBPC3c.3581C= (p.Ala1194=)
c.3563C= (p.Ala1188=)
c.3500C= (p.Ala1167=)
11g.47332612G>TCA380312476MYBPC3c.3581C>A (p.Ala1194Glu)
c.3563C>A (p.Ala1188Glu)
c.3500C>A (p.Ala1167Glu)
ClinVar dbSNP COSMIC
11g.47332613C>ACA380312480MYBPC3c.3580G>T (p.Ala1194Ser)
c.3562G>T (p.Ala1188Ser)
c.3499G>T (p.Ala1167Ser)
11g.47332613C=CA1969334232MYBPC3c.3580G= (p.Ala1194=)
c.3562G= (p.Ala1188=)
c.3499G= (p.Ala1167=)
11g.47332613C>GCA380312481MYBPC3c.3580G>C (p.Ala1194Pro)
c.3562G>C (p.Ala1188Pro)
c.3499G>C (p.Ala1167Pro)
11g.47332613C>TCA014361MYBPC3c.3580G>A (p.Ala1194Thr)
c.3562G>A (p.Ala1188Thr)
c.3499G>A (p.Ala1167Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332613dupCA915940852MYBPC3c.3580dup (p.Ala1194GlyfsTer14)
c.3562dup (p.Ala1188GlyfsTer14)
c.3499dup (p.Ala1167GlyfsTer14)
11g.47332614delCA054510MYBPC3c.3579del (p.Ile1193MetfsTer?)
c.3561del (p.Ile1187MetfsTer?)
c.3498del (p.Ile1166MetfsTer?)
11g.47332614G>ACA079441MYBPC3c.3579C>T (p.Ile1193=)
c.3561C>T (p.Ile1187=)
c.3498C>T (p.Ile1166=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332614G>CCA221682060MYBPC3c.3579C>G (p.Ile1193Met)
c.3561C>G (p.Ile1187Met)
c.3498C>G (p.Ile1166Met)
dbSNP
11g.47332614G=CA1969334239MYBPC3c.3579C= (p.Ile1193=)
c.3561C= (p.Ile1187=)
c.3498C= (p.Ile1166=)
11g.47332614G>TCA474428943MYBPC3c.3579C>A (p.Ile1193=)
c.3561C>A (p.Ile1187=)
c.3498C>A (p.Ile1166=)
11g.47332615A=CA1969334242MYBPC3c.3578T= (p.Ile1193=)
c.3560T= (p.Ile1187=)
c.3497T= (p.Ile1166=)
11g.47332615A>CCA380312486MYBPC3c.3578T>G (p.Ile1193Ser)
c.3560T>G (p.Ile1187Ser)
c.3497T>G (p.Ile1166Ser)
ClinVar
11g.47332615A>GCA221682063MYBPC3c.3578T>C (p.Ile1193Thr)
c.3560T>C (p.Ile1187Thr)
c.3497T>C (p.Ile1166Thr)
dbSNP
11g.47332615A>TCA380312490MYBPC3c.3578T>A (p.Ile1193Asn)
c.3560T>A (p.Ile1187Asn)
c.3497T>A (p.Ile1166Asn)
11g.47332616T>ACA380312492MYBPC3c.3577A>T (p.Ile1193Phe)
c.3559A>T (p.Ile1187Phe)
c.3496A>T (p.Ile1166Phe)
11g.47332616T>CCA380312494MYBPC3c.3577A>G (p.Ile1193Val)
c.3559A>G (p.Ile1187Val)
c.3496A>G (p.Ile1166Val)
11g.47332616T>GCA380312495MYBPC3c.3577A>C (p.Ile1193Leu)
c.3559A>C (p.Ile1187Leu)
c.3496A>C (p.Ile1166Leu)
11g.47332617G>ACA054294MYBPC3c.3576C>T (p.Val1192=)
c.3558C>T (p.Val1186=)
c.3495C>T (p.Val1165=)
11g.47332617G>CCA474428945MYBPC3c.3576C>G (p.Val1192=)
c.3558C>G (p.Val1186=)
c.3495C>G (p.Val1165=)
11g.47332617G>TCA474428944MYBPC3c.3576C>A (p.Val1192=)
c.3558C>A (p.Val1186=)
c.3495C>A (p.Val1165=)
11g.47332618A>CCA380312497MYBPC3c.3575T>G (p.Val1192Gly)
c.3557T>G (p.Val1186Gly)
c.3494T>G (p.Val1165Gly)
11g.47332618A>GCA380312498MYBPC3c.3575T>C (p.Val1192Ala)
c.3557T>C (p.Val1186Ala)
c.3494T>C (p.Val1165Ala)
11g.47332618A>TCA380312499MYBPC3c.3575T>A (p.Val1192Asp)
c.3557T>A (p.Val1186Asp)
c.3494T>A (p.Val1165Asp)
11g.47332618_47332619insTCCA054552MYBPC3c.3574_3575insGA (p.Val1192GlyfsTer?)
c.3556_3557insGA (p.Val1186GlyfsTer?)
c.3493_3494insGA (p.Val1165GlyfsTer?)
11g.47332619C>ACA380312502MYBPC3c.3574G>T (p.Val1192Phe)
c.3556G>T (p.Val1186Phe)
c.3493G>T (p.Val1165Phe)
11g.47332619C=CA1969334245MYBPC3c.3574G= (p.Val1192=)
c.3556G= (p.Val1186=)
c.3493G= (p.Val1165=)
11g.47332619C>GCA380312504MYBPC3c.3574G>C (p.Val1192Leu)
c.3556G>C (p.Val1186Leu)
c.3493G>C (p.Val1165Leu)
ClinVar gnomAD v4
11g.47332619C>TCA380312506MYBPC3c.3574G>A (p.Val1192Ile)
c.3556G>A (p.Val1186Ile)
c.3493G>A (p.Val1165Ile)
dbSNP gnomAD v4
11g.47332619_47332623delinsCCGAGCA1969334246MYBPC3c.3570_3574delinsCTCGG (p.Arg1190=)
c.3552_3556delinsCTCGG (p.Arg1184=)
c.3489_3493delinsCTCGG (p.Arg1163=)
11g.47332620C>ACA474428947MYBPC3c.3573G>T (p.Ser1191=)
c.3555G>T (p.Ser1185=)
c.3492G>T (p.Ser1164=)
11g.47332620C=CA1969334254MYBPC3c.3573G= (p.Ser1191=)
c.3555G= (p.Ser1185=)
c.3492G= (p.Ser1164=)
11g.47332620C>GCA474428946MYBPC3c.3573G>C (p.Ser1191=)
c.3555G>C (p.Ser1185=)
c.3492G>C (p.Ser1164=)
dbSNP gnomAD v4
11g.47332620C>TCA079439MYBPC3c.3573G>A (p.Ser1191=)
c.3555G>A (p.Ser1185=)
c.3492G>A (p.Ser1164=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.47332622_47332625delCA915948128MYBPC3c.3570_3573del (p.Val1192SerfsTer?)
c.3552_3555del (p.Val1186SerfsTer?)
c.3489_3492del (p.Val1165SerfsTer?)
ClinVar dbSNP
11g.47332621G>ACA079437MYBPC3c.3572C>T (p.Ser1191Leu)
c.3554C>T (p.Ser1185Leu)
c.3491C>T (p.Ser1164Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332621G>CCA380312513MYBPC3c.3572C>G (p.Ser1191Trp)
c.3554C>G (p.Ser1185Trp)
c.3491C>G (p.Ser1164Trp)
11g.47332621G=CA1969334264MYBPC3c.3572C= (p.Ser1191=)
c.3554C= (p.Ser1185=)
c.3491C= (p.Ser1164=)
11g.47332621G>TCA380312515MYBPC3c.3572C>A (p.Ser1191Ter)
c.3554C>A (p.Ser1185Ter)
c.3491C>A (p.Ser1164Ter)
ClinVar dbSNP
11g.47332622A>CCA380312516MYBPC3c.3571T>G (p.Ser1191Ala)
c.3553T>G (p.Ser1185Ala)
c.3490T>G (p.Ser1164Ala)
11g.47332622A>GCA380312517MYBPC3c.3571T>C (p.Ser1191Pro)
c.3553T>C (p.Ser1185Pro)
c.3490T>C (p.Ser1164Pro)
11g.47332622A>TCA380312519MYBPC3c.3571T>A (p.Ser1191Thr)
c.3553T>A (p.Ser1185Thr)
c.3490T>A (p.Ser1164Thr)
11g.47332623G>ACA474428948MYBPC3c.3570C>T (p.Arg1190=)
c.3552C>T (p.Arg1184=)
c.3489C>T (p.Arg1163=)
11g.47332623G>CCA474428950MYBPC3c.3570C>G (p.Arg1190=)
c.3552C>G (p.Arg1184=)
c.3489C>G (p.Arg1163=)
11g.47332623G>TCA474428949MYBPC3c.3570C>A (p.Arg1190=)
c.3552C>A (p.Arg1184=)
c.3489C>A (p.Arg1163=)
11g.47332624C>ACA054274MYBPC3c.3569G>T (p.Arg1190Leu)
c.3551G>T (p.Arg1184Leu)
c.3488G>T (p.Arg1163Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47332624C=CA1969334274MYBPC3c.3569G= (p.Arg1190=)
c.3551G= (p.Arg1184=)
c.3488G= (p.Arg1163=)
11g.47332624C>GCA380312523MYBPC3c.3569G>C (p.Arg1190Pro)
c.3551G>C (p.Arg1184Pro)
c.3488G>C (p.Arg1163Pro)
11g.47332624C>TCA014352MYBPC3c.3569G>A (p.Arg1190His)
c.3551G>A (p.Arg1184His)
c.3488G>A (p.Arg1163His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332625G>ACA079432MYBPC3c.3568C>T (p.Arg1190Cys)
c.3550C>T (p.Arg1184Cys)
c.3487C>T (p.Arg1163Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47332625G>CCA380312527MYBPC3c.3568C>G (p.Arg1190Gly)
c.3550C>G (p.Arg1184Gly)
c.3487C>G (p.Arg1163Gly)
11g.47332625G=CA1969334277MYBPC3c.3568C= (p.Arg1190=)
c.3550C= (p.Arg1184=)
c.3487C= (p.Arg1163=)
11g.47332625G>TCA380312529MYBPC3c.3568C>A (p.Arg1190Ser)
c.3550C>A (p.Arg1184Ser)
c.3487C>A (p.Arg1163Ser)
11g.47332626G>ACA474428951MYBPC3c.3567C>T (p.Asn1189=)
c.3549C>T (p.Asn1183=)
c.3486C>T (p.Asn1162=)
ClinVar
11g.47332626G>CCA380312533MYBPC3c.3567C>G (p.Asn1189Lys)
c.3549C>G (p.Asn1183Lys)
c.3486C>G (p.Asn1162Lys)
11g.47332626G>TCA380312535MYBPC3c.3567C>A (p.Asn1189Lys)
c.3549C>A (p.Asn1183Lys)
c.3486C>A (p.Asn1162Lys)
11g.47332626_47332628dupCA2574815724MYBPC3c.3565_3567dup (p.Asn1189_Arg1190insAsn)
c.3547_3549dup (p.Asn1183_Arg1184insAsn)
c.3484_3486dup (p.Asn1162_Arg1163insAsn)
ClinVar gnomAD v4
11g.47332627T>ACA380312542MYBPC3c.3566A>T (p.Asn1189Ile)
c.3548A>T (p.Asn1183Ile)
c.3485A>T (p.Asn1162Ile)
11g.47332627T>CCA380312540MYBPC3c.3566A>G (p.Asn1189Ser)
c.3548A>G (p.Asn1183Ser)
c.3485A>G (p.Asn1162Ser)
11g.47332627T>GCA380312537MYBPC3c.3566A>C (p.Asn1189Thr)
c.3548A>C (p.Asn1183Thr)
c.3485A>C (p.Asn1162Thr)
11g.47332628T>ACA380312545MYBPC3c.3565A>T (p.Asn1189Tyr)
c.3547A>T (p.Asn1183Tyr)
c.3484A>T (p.Asn1162Tyr)
11g.47332628T>CCA380312550MYBPC3c.3565A>G (p.Asn1189Asp)
c.3547A>G (p.Asn1183Asp)
c.3484A>G (p.Asn1162Asp)
11g.47332628T>GCA380312547MYBPC3c.3565A>C (p.Asn1189His)
c.3547A>C (p.Asn1183His)
c.3484A>C (p.Asn1162His)
11g.47332629C>ACA474428952MYBPC3c.3564G>T (p.Val1188=)
c.3546G>T (p.Val1182=)
c.3483G>T (p.Val1161=)
ClinVar dbSNP
11g.47332629C=CA1969334281MYBPC3c.3564G= (p.Val1188=)
c.3546G= (p.Val1182=)
c.3483G= (p.Val1161=)
11g.47332629C>GCA474428953MYBPC3c.3564G>C (p.Val1188=)
c.3546G>C (p.Val1182=)
c.3483G>C (p.Val1161=)
11g.47332629C>TCA474428954MYBPC3c.3564G>A (p.Val1188=)
c.3546G>A (p.Val1182=)
c.3483G>A (p.Val1161=)
dbSNP gnomAD v4
11g.47332630A=CA1969334282MYBPC3c.3563T= (p.Val1188=)
c.3545T= (p.Val1182=)
c.3482T= (p.Val1161=)
11g.47332630A>CCA380312553MYBPC3c.3563T>G (p.Val1188Gly)
c.3545T>G (p.Val1182Gly)
c.3482T>G (p.Val1161Gly)
11g.47332630A>GCA380312556MYBPC3c.3563T>C (p.Val1188Ala)
c.3545T>C (p.Val1182Ala)
c.3482T>C (p.Val1161Ala)
dbSNP gnomAD v2 gnomAD v4
11g.47332630A>TCA380312555MYBPC3c.3563T>A (p.Val1188Glu)
c.3545T>A (p.Val1182Glu)
c.3482T>A (p.Val1161Glu)
11g.47332631C>ACA380312559MYBPC3c.3562G>T (p.Val1188Leu)
c.3544G>T (p.Val1182Leu)
c.3481G>T (p.Val1161Leu)
11g.47332631C=CA1969334284MYBPC3c.3562G= (p.Val1188=)
c.3544G= (p.Val1182=)
c.3481G= (p.Val1161=)
11g.47332631C>GCA380312561MYBPC3c.3562G>C (p.Val1188Leu)
c.3544G>C (p.Val1182Leu)
c.3481G>C (p.Val1161Leu)
11g.47332631C>TCA380312563MYBPC3c.3562G>A (p.Val1188Met)
c.3544G>A (p.Val1182Met)
c.3481G>A (p.Val1161Met)
dbSNP gnomAD v4
11g.47332632C>ACA474428955MYBPC3c.3561G>T (p.Leu1187=)
c.3543G>T (p.Leu1181=)
c.3480G>T (p.Leu1160=)
11g.47332632C>GCA474428956MYBPC3c.3561G>C (p.Leu1187=)
c.3543G>C (p.Leu1181=)
c.3480G>C (p.Leu1160=)
11g.47332632C>TCA474428957MYBPC3c.3561G>A (p.Leu1187=)
c.3543G>A (p.Leu1181=)
c.3480G>A (p.Leu1160=)
gnomAD v4
11g.47332632_47332633delinsCACA1969334285MYBPC3c.3560_3561delinsTG (p.Leu1187=)
c.3542_3543delinsTG (p.Leu1181=)
c.3479_3480delinsTG (p.Leu1160=)
11g.47332633delCA1139659386MYBPC3c.3560del (p.Leu1187ArgfsTer2)
c.3542del (p.Leu1181ArgfsTer2)
c.3479del (p.Leu1160ArgfsTer2)
ClinVar dbSNP
11g.47332633A>CCA380312565MYBPC3c.3560T>G (p.Leu1187Arg)
c.3542T>G (p.Leu1181Arg)
c.3479T>G (p.Leu1160Arg)
11g.47332633A>GCA380312567MYBPC3c.3560T>C (p.Leu1187Pro)
c.3542T>C (p.Leu1181Pro)
c.3479T>C (p.Leu1160Pro)
ClinVar gnomAD v4
11g.47332633A>TCA380312569MYBPC3c.3560T>A (p.Leu1187Gln)
c.3542T>A (p.Leu1181Gln)
c.3479T>A (p.Leu1160Gln)
11g.47332633_47332634delinsAGCA1969334292MYBPC3c.3559_3560delinsCT (p.Leu1187=)
c.3541_3542delinsCT (p.Leu1181=)
c.3478_3479delinsCT (p.Leu1160=)
11g.47332634G>ACA474428958MYBPC3c.3559C>T (p.Leu1187=)
c.3541C>T (p.Leu1181=)
c.3478C>T (p.Leu1160=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47332634G>CCA380312571MYBPC3c.3559C>G (p.Leu1187Val)
c.3541C>G (p.Leu1181Val)
c.3478C>G (p.Leu1160Val)
11g.47332634G=CA1969334300MYBPC3c.3559C= (p.Leu1187=)
c.3541C= (p.Leu1181=)
c.3478C= (p.Leu1160=)
11g.47332634G>TCA380312573MYBPC3c.3559C>A (p.Leu1187Met)
c.3541C>A (p.Leu1181Met)
c.3478C>A (p.Leu1160Met)
11g.47332637delCA645372894MYBPC3c.3559del (p.Leu1187TrpfsTer2)
c.3541del (p.Leu1181TrpfsTer2)
c.3478del (p.Leu1160TrpfsTer2)
ClinVar dbSNP
11g.47332635G>ACA474428959MYBPC3c.3558C>T (p.Pro1186=)
c.3540C>T (p.Pro1180=)
c.3477C>T (p.Pro1159=)
dbSNP gnomAD v2 gnomAD v4
11g.47332635G>CCA079431MYBPC3c.3558C>G (p.Pro1186=)
c.3540C>G (p.Pro1180=)
c.3477C>G (p.Pro1159=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332635G=CA1969334306MYBPC3c.3558C= (p.Pro1186=)
c.3540C= (p.Pro1180=)
c.3477C= (p.Pro1159=)
11g.47332635G>TCA474428960MYBPC3c.3558C>A (p.Pro1186=)
c.3540C>A (p.Pro1180=)
c.3477C>A (p.Pro1159=)
11g.47332636G>ACA380312582MYBPC3c.3557C>T (p.Pro1186Leu)
c.3539C>T (p.Pro1180Leu)
c.3476C>T (p.Pro1159Leu)
11g.47332636G>CCA380312580MYBPC3c.3557C>G (p.Pro1186Arg)
c.3539C>G (p.Pro1180Arg)
c.3476C>G (p.Pro1159Arg)
11g.47332636G>TCA380312577MYBPC3c.3557C>A (p.Pro1186His)
c.3539C>A (p.Pro1180His)
c.3476C>A (p.Pro1159His)
11g.47332637G>ACA380312585MYBPC3c.3556C>T (p.Pro1186Ser)
c.3538C>T (p.Pro1180Ser)
c.3475C>T (p.Pro1159Ser)
gnomAD v4
11g.47332637G>CCA380312586MYBPC3c.3556C>G (p.Pro1186Ala)
c.3538C>G (p.Pro1180Ala)
c.3475C>G (p.Pro1159Ala)
gnomAD v4
11g.47332637G>TCA380312587MYBPC3c.3556C>A (p.Pro1186Thr)
c.3538C>A (p.Pro1180Thr)
c.3475C>A (p.Pro1159Thr)
11g.47332638C>ACA380312588MYBPC3c.3555G>T (p.Gln1185His)
c.3537G>T (p.Gln1179His)
c.3474G>T (p.Gln1158His)
ClinVar dbSNP
11g.47332638C=CA1969334309MYBPC3c.3555G= (p.Gln1185=)
c.3537G= (p.Gln1179=)
c.3474G= (p.Gln1158=)
11g.47332638C>GCA380312589MYBPC3c.3555G>C (p.Gln1185His)
c.3537G>C (p.Gln1179His)
c.3474G>C (p.Gln1158His)
11g.47332638C>TCA474428961MYBPC3c.3555G>A (p.Gln1185=)
c.3537G>A (p.Gln1179=)
c.3474G>A (p.Gln1158=)
gnomAD v4
11g.47332639T>ACA380312590MYBPC3c.3554A>T (p.Gln1185Leu)
c.3536A>T (p.Gln1179Leu)
c.3473A>T (p.Gln1158Leu)
11g.47332639T>CCA380312591MYBPC3c.3554A>G (p.Gln1185Arg)
c.3536A>G (p.Gln1179Arg)
c.3473A>G (p.Gln1158Arg)
11g.47332639T>GCA380312592MYBPC3c.3554A>C (p.Gln1185Pro)
c.3536A>C (p.Gln1179Pro)
c.3473A>C (p.Gln1158Pro)
11g.47332640G>ACA014331MYBPC3c.3553C>T (p.Gln1185Ter)
c.3535C>T (p.Gln1179Ter)
c.3472C>T (p.Gln1158Ter)
ClinVar dbSNP
11g.47332640G>CCA380312593MYBPC3c.3553C>G (p.Gln1185Glu)
c.3535C>G (p.Gln1179Glu)
c.3472C>G (p.Gln1158Glu)
11g.47332640G=CA1969334312MYBPC3c.3553C= (p.Gln1185=)
c.3535C= (p.Gln1179=)
c.3472C= (p.Gln1158=)
11g.47332640G>TCA380312594MYBPC3c.3553C>A (p.Gln1185Lys)
c.3535C>A (p.Gln1179Lys)
c.3472C>A (p.Gln1158Lys)
11g.47332641G>ACA474428962MYBPC3c.3552C>T (p.Thr1184=)
c.3534C>T (p.Thr1178=)
c.3471C>T (p.Thr1157=)
11g.47332641G>CCA474428963MYBPC3c.3552C>G (p.Thr1184=)
c.3534C>G (p.Thr1178=)
c.3471C>G (p.Thr1157=)
11g.47332641G>TCA474428964MYBPC3c.3552C>A (p.Thr1184=)
c.3534C>A (p.Thr1178=)
c.3471C>A (p.Thr1157=)
gnomAD v4
11g.47332642G>ACA380312596MYBPC3c.3551C>T (p.Thr1184Ile)
c.3533C>T (p.Thr1178Ile)
c.3470C>T (p.Thr1157Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47332642G>CCA380312597MYBPC3c.3551C>G (p.Thr1184Ser)
c.3533C>G (p.Thr1178Ser)
c.3470C>G (p.Thr1157Ser)
11g.47332642G=CA1969334316MYBPC3c.3551C= (p.Thr1184=)
c.3533C= (p.Thr1178=)
c.3470C= (p.Thr1157=)
11g.47332642G>TCA380312595MYBPC3c.3551C>A (p.Thr1184Asn)
c.3533C>A (p.Thr1178Asn)
c.3470C>A (p.Thr1157Asn)
gnomAD v4
11g.47332643T>ACA380312598MYBPC3c.3550A>T (p.Thr1184Ser)
c.3532A>T (p.Thr1178Ser)
c.3469A>T (p.Thr1157Ser)
11g.47332643T>CCA380312599MYBPC3c.3550A>G (p.Thr1184Ala)
c.3532A>G (p.Thr1178Ala)
c.3469A>G (p.Thr1157Ala)
ClinVar dbSNP
11g.47332643T>GCA380312601MYBPC3c.3550A>C (p.Thr1184Pro)
c.3532A>C (p.Thr1178Pro)
c.3469A>C (p.Thr1157Pro)
11g.47332643T=CA1969334322MYBPC3c.3550A= (p.Thr1184=)
c.3532A= (p.Thr1178=)
c.3469A= (p.Thr1157=)
11g.47332644G>ACA474428965MYBPC3c.3549C>T (p.Phe1183=)
c.3531C>T (p.Phe1177=)
c.3468C>T (p.Phe1156=)
gnomAD v4
11g.47332644G>CCA380312603MYBPC3c.3549C>G (p.Phe1183Leu)
c.3531C>G (p.Phe1177Leu)
c.3468C>G (p.Phe1156Leu)
11g.47332644G>TCA380312605MYBPC3c.3549C>A (p.Phe1183Leu)
c.3531C>A (p.Phe1177Leu)
c.3468C>A (p.Phe1156Leu)
11g.47332644dupCA913188356MYBPC3c.3549dup (p.Thr1184HisfsTer24)
c.3531dup (p.Thr1178HisfsTer24)
c.3468dup (p.Thr1157HisfsTer24)
ClinVar dbSNP
11g.47332645A=CA1969334330MYBPC3c.3548T= (p.Phe1183=)
c.3530T= (p.Phe1177=)
c.3467T= (p.Phe1156=)
11g.47332645A>CCA014323MYBPC3c.3548T>G (p.Phe1183Cys)
c.3530T>G (p.Phe1177Cys)
c.3467T>G (p.Phe1156Cys)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47332645A>GCA380312608MYBPC3c.3548T>C (p.Phe1183Ser)
c.3530T>C (p.Phe1177Ser)
c.3467T>C (p.Phe1156Ser)
11g.47332645A>TCA380312611MYBPC3c.3548T>A (p.Phe1183Tyr)
c.3530T>A (p.Phe1177Tyr)
c.3467T>A (p.Phe1156Tyr)
11g.47332646A=CA1969334333MYBPC3c.3547T= (p.Phe1183=)
c.3529T= (p.Phe1177=)
c.3466T= (p.Phe1156=)
11g.47332646A>CCA380312616MYBPC3c.3547T>G (p.Phe1183Val)
c.3529T>G (p.Phe1177Val)
c.3466T>G (p.Phe1156Val)
11g.47332646A>GCA014313MYBPC3c.3547T>C (p.Phe1183Leu)
c.3529T>C (p.Phe1177Leu)
c.3466T>C (p.Phe1156Leu)
ClinVar dbSNP
11g.47332646A>TCA380312619MYBPC3c.3547T>A (p.Phe1183Ile)
c.3529T>A (p.Phe1177Ile)
c.3466T>A (p.Phe1156Ile)
11g.47332647G>ACA474428966MYBPC3c.3546C>T (p.Ser1182=)
c.3528C>T (p.Ser1176=)
c.3465C>T (p.Ser1155=)
11g.47332647G>CCA380312621MYBPC3c.3546C>G (p.Ser1182Arg)
c.3528C>G (p.Ser1176Arg)
c.3465C>G (p.Ser1155Arg)
11g.47332647G>TCA380312624MYBPC3c.3546C>A (p.Ser1182Arg)
c.3528C>A (p.Ser1176Arg)
c.3465C>A (p.Ser1155Arg)
11g.47332648C>ACA380312627MYBPC3c.3545G>T (p.Ser1182Ile)
c.3527G>T (p.Ser1176Ile)
c.3464G>T (p.Ser1155Ile)
11g.47332648C=CA1969334338MYBPC3c.3545G= (p.Ser1182=)
c.3527G= (p.Ser1176=)
c.3464G= (p.Ser1155=)
11g.47332648C>GCA380312630MYBPC3c.3545G>C (p.Ser1182Thr)
c.3527G>C (p.Ser1176Thr)
c.3464G>C (p.Ser1155Thr)
ClinVar dbSNP gnomAD v2
11g.47332648C>TCA380312629MYBPC3c.3545G>A (p.Ser1182Asn)
c.3527G>A (p.Ser1176Asn)
c.3464G>A (p.Ser1155Asn)
11g.47332649T>ACA380312632MYBPC3c.3544A>T (p.Ser1182Cys)
c.3526A>T (p.Ser1176Cys)
c.3463A>T (p.Ser1155Cys)
11g.47332649T>CCA380312634MYBPC3c.3544A>G (p.Ser1182Gly)
c.3526A>G (p.Ser1176Gly)
c.3463A>G (p.Ser1155Gly)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47332649T>GCA380312637MYBPC3c.3544A>C (p.Ser1182Arg)
c.3526A>C (p.Ser1176Arg)
c.3463A>C (p.Ser1155Arg)
ClinVar dbSNP
11g.47332649T=CA1969334343MYBPC3c.3544A= (p.Ser1182=)
c.3526A= (p.Ser1176=)
c.3463A= (p.Ser1155=)
11g.47332650T>ACA474428967MYBPC3c.3543A>T (p.Pro1181=)
c.3525A>T (p.Pro1175=)
c.3462A>T (p.Pro1154=)
11g.47332650T>CCA474428969MYBPC3c.3543A>G (p.Pro1181=)
c.3525A>G (p.Pro1175=)
c.3462A>G (p.Pro1154=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47332650T>GCA474428968MYBPC3c.3543A>C (p.Pro1181=)
c.3525A>C (p.Pro1175=)
c.3462A>C (p.Pro1154=)
11g.47332650T=CA1969334348MYBPC3c.3543A= (p.Pro1181=)
c.3525A= (p.Pro1175=)
c.3462A= (p.Pro1154=)
11g.47332651G>ACA380312640MYBPC3c.3542C>T (p.Pro1181Leu)
c.3524C>T (p.Pro1175Leu)
c.3461C>T (p.Pro1154Leu)
11g.47332651G>CCA380312641MYBPC3c.3542C>G (p.Pro1181Arg)
c.3524C>G (p.Pro1175Arg)
c.3461C>G (p.Pro1154Arg)
11g.47332651G>TCA380312644MYBPC3c.3542C>A (p.Pro1181Gln)
c.3524C>A (p.Pro1175Gln)
c.3461C>A (p.Pro1154Gln)
11g.47332652G>ACA380312647MYBPC3c.3541C>T (p.Pro1181Ser)
c.3523C>T (p.Pro1175Ser)
c.3460C>T (p.Pro1154Ser)
11g.47332652G>CCA014307MYBPC3c.3541C>G (p.Pro1181Ala)
c.3523C>G (p.Pro1175Ala)
c.3460C>G (p.Pro1154Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47332652G=CA1969334353MYBPC3c.3541C= (p.Pro1181=)
c.3523C= (p.Pro1175=)
c.3460C= (p.Pro1154=)
11g.47332652G>TCA380312649MYBPC3c.3541C>A (p.Pro1181Thr)
c.3523C>A (p.Pro1175Thr)
c.3460C>A (p.Pro1154Thr)
11g.47332653G>ACA474428970MYBPC3c.3540C>T (p.Ala1180=)
c.3522C>T (p.Ala1174=)
c.3459C>T (p.Ala1153=)
11g.47332653G>CCA474428971MYBPC3c.3540C>G (p.Ala1180=)
c.3522C>G (p.Ala1174=)
c.3459C>G (p.Ala1153=)
gnomAD v4
11g.47332653G>TCA474428972MYBPC3c.3540C>A (p.Ala1180=)
c.3522C>A (p.Ala1174=)
c.3459C>A (p.Ala1153=)
11g.47332654G>ACA380312652MYBPC3c.3539C>T (p.Ala1180Val)
c.3521C>T (p.Ala1174Val)
c.3458C>T (p.Ala1153Val)
dbSNP
11g.47332654G>CCA380312654MYBPC3c.3539C>G (p.Ala1180Gly)
c.3521C>G (p.Ala1174Gly)
c.3458C>G (p.Ala1153Gly)
11g.47332654G=CA1969334359MYBPC3c.3539C= (p.Ala1180=)
c.3521C= (p.Ala1174=)
c.3458C= (p.Ala1153=)
11g.47332654G>TCA380312656MYBPC3c.3539C>A (p.Ala1180Asp)
c.3521C>A (p.Ala1174Asp)
c.3458C>A (p.Ala1153Asp)
11g.47332655C>ACA380312662MYBPC3c.3538G>T (p.Ala1180Ser)
c.3520G>T (p.Ala1174Ser)
c.3457G>T (p.Ala1153Ser)
11g.47332655C>GCA380312667MYBPC3c.3538G>C (p.Ala1180Pro)
c.3520G>C (p.Ala1174Pro)
c.3457G>C (p.Ala1153Pro)
11g.47332655C>TCA380312660MYBPC3c.3538G>A (p.Ala1180Thr)
c.3520G>A (p.Ala1174Thr)
c.3457G>A (p.Ala1153Thr)
ClinVar dbSNP
11g.47332656C>ACA380312673MYBPC3c.3537G>T (p.Glu1179Asp)
c.3519G>T (p.Glu1173Asp)
c.3456G>T (p.Glu1152Asp)
11g.47332656C=CA1969334363MYBPC3c.3537G= (p.Glu1179=)
c.3519G= (p.Glu1173=)
c.3456G= (p.Glu1152=)
11g.47332656C>GCA380312671MYBPC3c.3537G>C (p.Glu1179Asp)
c.3519G>C (p.Glu1173Asp)
c.3456G>C (p.Glu1152Asp)
11g.47332656C>TCA474428973MYBPC3c.3537G>A (p.Glu1179=)
c.3519G>A (p.Glu1173=)
c.3456G>A (p.Glu1152=)
dbSNP gnomAD v4
11g.47332657T>ACA380312676MYBPC3c.3536A>T (p.Glu1179Val)
c.3518A>T (p.Glu1173Val)
c.3455A>T (p.Glu1152Val)
11g.47332657T>CCA380312679MYBPC3c.3536A>G (p.Glu1179Gly)
c.3518A>G (p.Glu1173Gly)
c.3455A>G (p.Glu1152Gly)
11g.47332657T>GCA380312681MYBPC3c.3536A>C (p.Glu1179Ala)
c.3518A>C (p.Glu1173Ala)
c.3455A>C (p.Glu1152Ala)
11g.47332658C>ACA380312684MYBPC3c.3535G>T (p.Glu1179Ter)
c.3517G>T (p.Glu1173Ter)
c.3454G>T (p.Glu1152Ter)
dbSNP gnomAD v2 gnomAD v4
11g.47332658C=CA1969334368MYBPC3c.3535G= (p.Glu1179=)
c.3517G= (p.Glu1173=)
c.3454G= (p.Glu1152=)
11g.47332658C>GCA380312686MYBPC3c.3535G>C (p.Glu1179Gln)
c.3517G>C (p.Glu1173Gln)
c.3454G>C (p.Glu1152Gln)
11g.47332658C>TCA014298MYBPC3c.3535G>A (p.Glu1179Lys)
c.3517G>A (p.Glu1173Lys)
c.3454G>A (p.Glu1152Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332659G>ACA079428MYBPC3c.3534C>T (p.Ser1178=)
c.3516C>T (p.Ser1172=)
c.3453C>T (p.Ser1151=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47332659G>CCA474428974MYBPC3c.3534C>G (p.Ser1178=)
c.3516C>G (p.Ser1172=)
c.3453C>G (p.Ser1151=)
11g.47332659G=CA1969334372MYBPC3c.3534C= (p.Ser1178=)
c.3516C= (p.Ser1172=)
c.3453C= (p.Ser1151=)
11g.47332659G>TCA474428975MYBPC3c.3534C>A (p.Ser1178=)
c.3516C>A (p.Ser1172=)
c.3453C>A (p.Ser1151=)
11g.47332660G>ACA380312692MYBPC3c.3533C>T (p.Ser1178Phe)
c.3515C>T (p.Ser1172Phe)
c.3452C>T (p.Ser1151Phe)
11g.47332660G>CCA380312694MYBPC3c.3533C>G (p.Ser1178Cys)
c.3515C>G (p.Ser1172Cys)
c.3452C>G (p.Ser1151Cys)
11g.47332660G>TCA380312696MYBPC3c.3533C>A (p.Ser1178Tyr)
c.3515C>A (p.Ser1172Tyr)
c.3452C>A (p.Ser1151Tyr)
11g.47332661A>CCA380312704MYBPC3c.3532T>G (p.Ser1178Ala)
c.3514T>G (p.Ser1172Ala)
c.3451T>G (p.Ser1151Ala)
11g.47332661A>GCA380312702MYBPC3c.3532T>C (p.Ser1178Pro)
c.3514T>C (p.Ser1172Pro)
c.3451T>C (p.Ser1151Pro)
ClinVar gnomAD v4
11g.47332661A>TCA380312700MYBPC3c.3532T>A (p.Ser1178Thr)
c.3514T>A (p.Ser1172Thr)
c.3451T>A (p.Ser1151Thr)
11g.47332662G>ACA054207MYBPC3c.3531C>T (p.Phe1177=)
c.3513C>T (p.Phe1171=)
c.3450C>T (p.Phe1150=)
11g.47332662G>CCA380312706MYBPC3c.3531C>G (p.Phe1177Leu)
c.3513C>G (p.Phe1171Leu)
c.3450C>G (p.Phe1150Leu)
ClinVar dbSNP
11g.47332662G=CA1969334377MYBPC3c.3531C= (p.Phe1177=)
c.3513C= (p.Phe1171=)
c.3450C= (p.Phe1150=)
11g.47332662G>TCA380312708MYBPC3c.3531C>A (p.Phe1177Leu)
c.3513C>A (p.Phe1171Leu)
c.3450C>A (p.Phe1150Leu)
11g.47332663A>CCA380312711MYBPC3c.3530T>G (p.Phe1177Cys)
c.3512T>G (p.Phe1171Cys)
c.3449T>G (p.Phe1150Cys)
11g.47332663A>GCA380312714MYBPC3c.3530T>C (p.Phe1177Ser)
c.3512T>C (p.Phe1171Ser)
c.3449T>C (p.Phe1150Ser)
11g.47332663A>TCA380312715MYBPC3c.3530T>A (p.Phe1177Tyr)
c.3512T>A (p.Phe1171Tyr)
c.3449T>A (p.Phe1150Tyr)
11g.47332664A>CCA380312719MYBPC3c.3529T>G (p.Phe1177Val)
c.3511T>G (p.Phe1171Val)
c.3448T>G (p.Phe1150Val)
11g.47332664A>GCA380312720MYBPC3c.3529T>C (p.Phe1177Leu)
c.3511T>C (p.Phe1171Leu)
c.3448T>C (p.Phe1150Leu)
11g.47332664A>TCA380312722MYBPC3c.3529T>A (p.Phe1177Ile)
c.3511T>A (p.Phe1171Ile)
c.3448T>A (p.Phe1150Ile)
11g.47332665G>ACA474428976MYBPC3c.3528C>T (p.Asp1176=)
c.3510C>T (p.Asp1170=)
c.3447C>T (p.Asp1149=)
gnomAD v4
11g.47332665G>CCA380312725MYBPC3c.3528C>G (p.Asp1176Glu)
c.3510C>G (p.Asp1170Glu)
c.3447C>G (p.Asp1149Glu)
dbSNP
11g.47332665G=CA1969334381MYBPC3c.3528C= (p.Asp1176=)
c.3510C= (p.Asp1170=)
c.3447C= (p.Asp1149=)
11g.47332665G>TCA380312727MYBPC3c.3528C>A (p.Asp1176Glu)
c.3510C>A (p.Asp1170Glu)
c.3447C>A (p.Asp1149Glu)
11g.47332666T>ACA380312728MYBPC3c.3527A>T (p.Asp1176Val)
c.3509A>T (p.Asp1170Val)
c.3446A>T (p.Asp1149Val)
gnomAD v4
11g.47332666T>CCA380312731MYBPC3c.3527A>G (p.Asp1176Gly)
c.3509A>G (p.Asp1170Gly)
c.3446A>G (p.Asp1149Gly)
dbSNP
11g.47332666T>GCA380312732MYBPC3c.3527A>C (p.Asp1176Ala)
c.3509A>C (p.Asp1170Ala)
c.3446A>C (p.Asp1149Ala)
11g.47332666T=CA1969334383MYBPC3c.3527A= (p.Asp1176=)
c.3509A= (p.Asp1170=)
c.3446A= (p.Asp1149=)
11g.47332667C>ACA380312738MYBPC3c.3526G>T (p.Asp1176Tyr)
c.3508G>T (p.Asp1170Tyr)
c.3445G>T (p.Asp1149Tyr)
11g.47332667C>GCA380312740MYBPC3c.3526G>C (p.Asp1176His)
c.3508G>C (p.Asp1170His)
c.3445G>C (p.Asp1149His)
11g.47332667C>TCA380312735MYBPC3c.3526G>A (p.Asp1176Asn)
c.3508G>A (p.Asp1170Asn)
c.3445G>A (p.Asp1149Asn)
ClinVar gnomAD v4
11g.47332668C>ACA474428977MYBPC3c.3525G>T (p.Leu1175=)
c.3507G>T (p.Leu1169=)
c.3444G>T (p.Leu1148=)
11g.47332668C>GCA474428978MYBPC3c.3525G>C (p.Leu1175=)
c.3507G>C (p.Leu1169=)
c.3444G>C (p.Leu1148=)
11g.47332668C>TCA474428979MYBPC3c.3525G>A (p.Leu1175=)
c.3507G>A (p.Leu1169=)
c.3444G>A (p.Leu1148=)
11g.47332669A>CCA380312743MYBPC3c.3524T>G (p.Leu1175Arg)
c.3506T>G (p.Leu1169Arg)
c.3443T>G (p.Leu1148Arg)
11g.47332669A>GCA380312745MYBPC3c.3524T>C (p.Leu1175Pro)
c.3506T>C (p.Leu1169Pro)
c.3443T>C (p.Leu1148Pro)
gnomAD v4
11g.47332669A>TCA380312748MYBPC3c.3524T>A (p.Leu1175Gln)
c.3506T>A (p.Leu1169Gln)
c.3443T>A (p.Leu1148Gln)
11g.47332670G>ACA474428980MYBPC3c.3523C>T (p.Leu1175=)
c.3505C>T (p.Leu1169=)
c.3442C>T (p.Leu1148=)
gnomAD v4
11g.47332670G>CCA079425MYBPC3c.3523C>G (p.Leu1175Val)
c.3505C>G (p.Leu1169Val)
c.3442C>G (p.Leu1148Val)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47332670G=CA1969334385MYBPC3c.3523C= (p.Leu1175=)
c.3505C= (p.Leu1169=)
c.3442C= (p.Leu1148=)
11g.47332670G>TCA380312752MYBPC3c.3523C>A (p.Leu1175Met)
c.3505C>A (p.Leu1169Met)
c.3442C>A (p.Leu1148Met)
11g.47332672dupCA2697548542MYBPC3c.3523dup (p.Leu1175ProfsTer?)
c.3505dup (p.Leu1169ProfsTer?)
c.3442dup (p.Leu1148ProfsTer?)
ClinVar
11g.47332671G>ACA474428981MYBPC3c.3522C>T (p.Ala1174=)
c.3504C>T (p.Ala1168=)
c.3441C>T (p.Ala1147=)
ClinVar gnomAD v4
11g.47332671G>CCA474428983MYBPC3c.3522C>G (p.Ala1174=)
c.3504C>G (p.Ala1168=)
c.3441C>G (p.Ala1147=)
11g.47332671G>TCA474428982MYBPC3c.3522C>A (p.Ala1174=)
c.3504C>A (p.Ala1168=)
c.3441C>A (p.Ala1147=)
11g.47332672G>ACA380312755MYBPC3c.3521C>T (p.Ala1174Val)
c.3503C>T (p.Ala1168Val)
c.3440C>T (p.Ala1147Val)
gnomAD v4
11g.47332672G>CCA380312757MYBPC3c.3521C>G (p.Ala1174Gly)
c.3503C>G (p.Ala1168Gly)
c.3440C>G (p.Ala1147Gly)
11g.47332672G>TCA380312759MYBPC3c.3521C>A (p.Ala1174Asp)
c.3503C>A (p.Ala1168Asp)
c.3440C>A (p.Ala1147Asp)
gnomAD v4
11g.47332672_47332675delinsGCCTCA1969334387MYBPC3c.3518_3521delinsAGGC (p.Lys1173=)
c.3500_3503delinsAGGC (p.Lys1167=)
c.3437_3440delinsAGGC (p.Lys1146=)
11g.47332673C>ACA380312762MYBPC3c.3520G>T (p.Ala1174Ser)
c.3502G>T (p.Ala1168Ser)
c.3439G>T (p.Ala1147Ser)
11g.47332673C>GCA380312765MYBPC3c.3520G>C (p.Ala1174Pro)
c.3502G>C (p.Ala1168Pro)
c.3439G>C (p.Ala1147Pro)
11g.47332673C>TCA380312767MYBPC3c.3520G>A (p.Ala1174Thr)
c.3502G>A (p.Ala1168Thr)
c.3439G>A (p.Ala1147Thr)
11g.47332673_47332675delCA079423MYBPC3c.3518_3520del (p.Lys1173_Ala1174delinsThr)
c.3500_3502del (p.Lys1167_Ala1168delinsThr)
c.3437_3439del (p.Lys1146_Ala1147delinsThr)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47332673_47332676delinsTGGCTCCA2695213907MYBPC3c.3517_3520delinsGAGCCA (p.Lys1173GlufsTer17)
c.3499_3502delinsGAGCCA (p.Lys1167GlufsTer17)
c.3436_3439delinsGAGCCA (p.Lys1146GlufsTer17)
11g.47332674C>ACA380312771MYBPC3c.3519G>T (p.Lys1173Asn)
c.3501G>T (p.Lys1167Asn)
c.3438G>T (p.Lys1146Asn)
ClinVar dbSNP
11g.47332674C=CA1969334393MYBPC3c.3519G= (p.Lys1173=)
c.3501G= (p.Lys1167=)
c.3438G= (p.Lys1146=)
11g.47332674C>GCA380312773MYBPC3c.3519G>C (p.Lys1173Asn)
c.3501G>C (p.Lys1167Asn)
c.3438G>C (p.Lys1146Asn)
11g.47332674C>TCA474428984MYBPC3c.3519G>A (p.Lys1173=)
c.3501G>A (p.Lys1167=)
c.3438G>A (p.Lys1146=)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.47332677_47333963delCA2573051316MYBPC3c.2956_3519del
c.2938_3501del
c.2875_3438del

Number of alleles fetched