Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47345814_47346367delCA2580084293MYBPC3c.933_1090+396del
c.915_1072+396del
ClinVar
11g.47346135_47346208delCA2613392479MYBPC3c.1090+13_1090+86del
c.1072+13_1072+86del
gnomAD v4
11g.47346203T>CCA2825002013MYBPC3c.1090+4A>G (n.1090+4A>G)
c.1072+4A>G (n.1072+4A>G)
ClinVar
11g.47346204A>CCA2825002014MYBPC3c.1090+3T>G (n.1090+3T>G)
c.1072+3T>G (n.1072+3T>G)
ClinVar
11g.47346205A=CA1969339415MYBPC3c.1090+2T= (n.1090+2T=)
c.1072+2T= (n.1072+2T=)
11g.47346205A>CCA009758MYBPC3c.1090+2T>G (n.1090+2T>G)
c.1072+2T>G (n.1072+2T>G)
ClinVar dbSNP
11g.47346205A>GCA380330843MYBPC3c.1090+2T>C (n.1090+2T>C)
c.1072+2T>C (n.1072+2T>C)
dbSNP
11g.47346205A>TCA380330848MYBPC3c.1090+2T>A (n.1090+2T>A)
c.1072+2T>A (n.1072+2T>A)
11g.47346206C>ACA009753MYBPC3c.1090+1G>T (n.1090+1G>T)
c.1072+1G>T (n.1072+1G>T)
ClinVar dbSNP gnomAD v2
11g.47346206C=CA1969339416MYBPC3c.1090+1G= (n.1090+1G=)
c.1072+1G= (n.1072+1G=)
11g.47346206C>GCA380330859MYBPC3c.1090+1G>C (n.1090+1G>C)
c.1072+1G>C (n.1072+1G>C)
ClinVar dbSNP
11g.47346206C>TCA009749MYBPC3c.1090+1G>A (n.1090+1G>A)
c.1072+1G>A (n.1072+1G>A)
ClinVar dbSNP gnomAD v4
11g.47346207C>ACA380330864MYBPC3c.1090G>T (p.Ala364Ser)
c.1072G>T (p.Ala358Ser)
11g.47346207C=CA1969339417MYBPC3c.1090G= (p.Ala364=)
c.1072G= (p.Ala358=)
11g.47346207C>GCA009764MYBPC3c.1090G>C (p.Ala364Pro)
c.1072G>C (p.Ala358Pro)
ClinVar dbSNP
11g.47346207C>TCA221700759MYBPC3c.1090G>A (p.Ala364Thr)
c.1072G>A (p.Ala358Thr)
ClinVar dbSNP
11g.47346208T>ACA474220743MYBPC3c.1089A>T (p.Thr363=)
c.1071A>T (p.Thr357=)
11g.47346208T>CCA474220742MYBPC3c.1089A>G (p.Thr363=)
c.1071A>G (p.Thr357=)
gnomAD v4
11g.47346208T>GCA474220741MYBPC3c.1089A>C (p.Thr363=)
c.1071A>C (p.Thr357=)
11g.47346209G>ACA380330877MYBPC3c.1088C>T (p.Thr363Ile)
c.1070C>T (p.Thr357Ile)
11g.47346209G>CCA380330881MYBPC3c.1088C>G (p.Thr363Arg)
c.1070C>G (p.Thr357Arg)
11g.47346209G>TCA380330887MYBPC3c.1088C>A (p.Thr363Lys)
c.1070C>A (p.Thr357Lys)
11g.47346210T>ACA380330892MYBPC3c.1087A>T (p.Thr363Ser)
c.1069A>T (p.Thr357Ser)
11g.47346210T>CCA380330894MYBPC3c.1087A>G (p.Thr363Ala)
c.1069A>G (p.Thr357Ala)
COSMIC COSMIC
11g.47346210T>GCA380330895MYBPC3c.1087A>C (p.Thr363Pro)
c.1069A>C (p.Thr357Pro)
11g.47346211G>ACA474220747MYBPC3c.1086C>T (p.Ser362=)
c.1068C>T (p.Ser356=)
ClinVar
11g.47346211G>CCA380330896MYBPC3c.1086C>G (p.Ser362Arg)
c.1068C>G (p.Ser356Arg)
11g.47346211G>TCA380330897MYBPC3c.1086C>A (p.Ser362Arg)
c.1068C>A (p.Ser356Arg)
COSMIC
11g.47346212C>ACA380330900MYBPC3c.1085G>T (p.Ser362Ile)
c.1067G>T (p.Ser356Ile)
11g.47346212C=CA1969339418MYBPC3c.1085G= (p.Ser362=)
c.1067G= (p.Ser356=)
11g.47346212C>GCA380330903MYBPC3c.1085G>C (p.Ser362Thr)
c.1067G>C (p.Ser356Thr)
gnomAD v4
11g.47346212C>TCA380330913MYBPC3c.1085G>A (p.Ser362Asn)
c.1067G>A (p.Ser356Asn)
gnomAD v4
11g.47346212_47346215delinsCTCTCA1969339419MYBPC3c.1082_1085delinsAGAG (p.Lys361=)
c.1064_1067delinsAGAG (p.Lys355=)
11g.47346213T>ACA380330930MYBPC3c.1084A>T (p.Ser362Cys)
c.1066A>T (p.Ser356Cys)
11g.47346213T>CCA009745MYBPC3c.1084A>G (p.Ser362Gly)
c.1066A>G (p.Ser356Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47346213T>GCA380330923MYBPC3c.1084A>C (p.Ser362Arg)
c.1066A>C (p.Ser356Arg)
ClinVar dbSNP
11g.47346213T=CA1969339420MYBPC3c.1084A= (p.Ser362=)
c.1066A= (p.Ser356=)
11g.47346213dupCA296499MYBPC3c.1084dup (p.Ser362LysfsTer28)
c.1066dup (p.Ser356LysfsTer28)
ClinVar dbSNP
11g.47346219_47346221delCA042311MYBPC3c.1082_1084del (p.Lys361del)
c.1064_1066del (p.Lys355del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346214C>ACA380330936MYBPC3c.1083G>T (p.Lys361Asn)
c.1065G>T (p.Lys355Asn)
11g.47346214C=CA1969339421MYBPC3c.1083G= (p.Lys361=)
c.1065G= (p.Lys355=)
11g.47346214C>GCA380330939MYBPC3c.1083G>C (p.Lys361Asn)
c.1065G>C (p.Lys355Asn)
11g.47346214C>TCA221700782MYBPC3c.1083G>A (p.Lys361=)
c.1065G>A (p.Lys355=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47346215T>ACA380330942MYBPC3c.1082A>T (p.Lys361Met)
c.1064A>T (p.Lys355Met)
11g.47346215T>CCA380330944MYBPC3c.1082A>G (p.Lys361Arg)
c.1064A>G (p.Lys355Arg)
ClinVar dbSNP
11g.47346215T>GCA380330946MYBPC3c.1082A>C (p.Lys361Thr)
c.1064A>C (p.Lys355Thr)
11g.47346215T=CA1969339423MYBPC3c.1082A= (p.Lys361=)
c.1064A= (p.Lys355=)
11g.47346216T>ACA380330950MYBPC3c.1081A>T (p.Lys361Ter)
c.1063A>T (p.Lys355Ter)
gnomAD v4
11g.47346216T>CCA380330956MYBPC3c.1081A>G (p.Lys361Glu)
c.1063A>G (p.Lys355Glu)
11g.47346216T>GCA380330955MYBPC3c.1081A>C (p.Lys361Gln)
c.1063A>C (p.Lys355Gln)
11g.47346217C>ACA380330958MYBPC3c.1080G>T (p.Lys360Asn)
c.1062G>T (p.Lys354Asn)
11g.47346217C=CA1969339426MYBPC3c.1080G= (p.Lys360=)
c.1062G= (p.Lys354=)
11g.47346217C>GCA009741MYBPC3c.1080G>C (p.Lys360Asn)
c.1062G>C (p.Lys354Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346217C>TCA474220757MYBPC3c.1080G>A (p.Lys360=)
c.1062G>A (p.Lys354=)
11g.47346218T>ACA380330963MYBPC3c.1079A>T (p.Lys360Met)
c.1061A>T (p.Lys354Met)
11g.47346218T>CCA380330964MYBPC3c.1079A>G (p.Lys360Arg)
c.1061A>G (p.Lys354Arg)
gnomAD v4
11g.47346218T>GCA380330969MYBPC3c.1079A>C (p.Lys360Thr)
c.1061A>C (p.Lys354Thr)
11g.47346219T>ACA380330972MYBPC3c.1078A>T (p.Lys360Ter)
c.1060A>T (p.Lys354Ter)
11g.47346219T>CCA380330974MYBPC3c.1078A>G (p.Lys360Glu)
c.1060A>G (p.Lys354Glu)
ClinVar
11g.47346219T>GCA380330978MYBPC3c.1078A>C (p.Lys360Gln)
c.1060A>C (p.Lys354Gln)
dbSNP gnomAD v2
11g.47346219T=CA1969339427MYBPC3c.1078A= (p.Lys360=)
c.1060A= (p.Lys354=)
11g.47346219_47346222delinsTCTCCA1969339428MYBPC3c.1075_1078delinsGAGA (p.Glu359=)
c.1057_1060delinsGAGA (p.Glu353=)
11g.47346220C>ACA380330980MYBPC3c.1077G>T (p.Glu359Asp)
c.1059G>T (p.Glu353Asp)
11g.47346220C>GCA380330982MYBPC3c.1077G>C (p.Glu359Asp)
c.1059G>C (p.Glu353Asp)
11g.47346220C>TCA474220767MYBPC3c.1077G>A (p.Glu359=)
c.1059G>A (p.Glu353=)
ClinVar gnomAD v4 COSMIC COSMIC
11g.47346220_47346222delCA1969339430MYBPC3c.1075_1077del (p.Glu359del)
c.1057_1059del (p.Glu353del)
dbSNP
11g.47346221T>ACA380330993MYBPC3c.1076A>T (p.Glu359Val)
c.1058A>T (p.Glu353Val)
11g.47346221T>CCA380330989MYBPC3c.1076A>G (p.Glu359Gly)
c.1058A>G (p.Glu353Gly)
ClinVar dbSNP
11g.47346221T>GCA380330988MYBPC3c.1076A>C (p.Glu359Ala)
c.1058A>C (p.Glu353Ala)
11g.47346221T=CA1969339432MYBPC3c.1076A= (p.Glu359=)
c.1058A= (p.Glu353=)
11g.47346222C>ACA10576892MYBPC3c.1075G>T (p.Glu359Ter)
c.1057G>T (p.Glu353Ter)
ClinVar dbSNP
11g.47346222C=CA1969339438MYBPC3c.1075G= (p.Glu359=)
c.1057G= (p.Glu353=)
11g.47346222C>GCA380330998MYBPC3c.1075G>C (p.Glu359Gln)
c.1057G>C (p.Glu353Gln)
11g.47346222C>TCA380331001MYBPC3c.1075G>A (p.Glu359Lys)
c.1057G>A (p.Glu353Lys)
dbSNP gnomAD v4
11g.47346223A=CA1969339444MYBPC3c.1074T= (p.Asp358=)
c.1056T= (p.Asp352=)
11g.47346223A>CCA380331003MYBPC3c.1074T>G (p.Asp358Glu)
c.1056T>G (p.Asp352Glu)
11g.47346223A>GCA474220774MYBPC3c.1074T>C (p.Asp358=)
c.1056T>C (p.Asp352=)
dbSNP gnomAD v2
11g.47346223A>TCA042264MYBPC3c.1074T>A (p.Asp358Glu)
c.1056T>A (p.Asp352Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346224T>ACA380331010MYBPC3c.1073A>T (p.Asp358Val)
c.1055A>T (p.Asp352Val)
11g.47346224T>CCA380331007MYBPC3c.1073A>G (p.Asp358Gly)
c.1055A>G (p.Asp352Gly)
11g.47346224T>GCA380331005MYBPC3c.1073A>C (p.Asp358Ala)
c.1055A>C (p.Asp352Ala)
COSMIC COSMIC
11g.47346224_47346228delinsTCGCGCA1969339447MYBPC3c.1069_1073delinsCGCGA (p.Arg357=)
c.1051_1055delinsCGCGA (p.Arg351=)
11g.47346225C>ACA380331012MYBPC3c.1072G>T (p.Asp358Tyr)
c.1054G>T (p.Asp352Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47346225C=CA1969339453MYBPC3c.1072G= (p.Asp358=)
c.1054G= (p.Asp352=)
11g.47346225C>GCA380331014MYBPC3c.1072G>C (p.Asp358His)
c.1054G>C (p.Asp352His)
11g.47346225C>TCA042250MYBPC3c.1072G>A (p.Asp358Asn)
c.1054G>A (p.Asp352Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346225_47346228delinsGCCA009733MYBPC3c.1069_1072delinsGC (p.Arg357AlafsTer2)
c.1051_1054delinsGC (p.Arg351AlafsTer2)
ClinVar dbSNP
11g.47346226G>ACA042236MYBPC3c.1071C>T (p.Arg357=)
c.1053C>T (p.Arg351=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346226G>CCA474220780MYBPC3c.1071C>G (p.Arg357=)
c.1053C>G (p.Arg351=)
dbSNP
11g.47346226G=CA1969339459MYBPC3c.1071C= (p.Arg357=)
c.1053C= (p.Arg351=)
11g.47346226G>TCA042214MYBPC3c.1071C>A (p.Arg357=)
c.1053C>A (p.Arg351=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346227C>ACA380331033MYBPC3c.1070G>T (p.Arg357Leu)
c.1052G>T (p.Arg351Leu)
11g.47346227C=CA1969339465MYBPC3c.1070G= (p.Arg357=)
c.1052G= (p.Arg351=)
11g.47346227C>GCA380331029MYBPC3c.1070G>C (p.Arg357Pro)
c.1052G>C (p.Arg351Pro)
11g.47346227C>TCA009737MYBPC3c.1070G>A (p.Arg357His)
c.1052G>A (p.Arg351His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47346228G>ACA380331037MYBPC3c.1069C>T (p.Arg357Cys)
c.1051C>T (p.Arg351Cys)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
11g.47346228G>CCA380331038MYBPC3c.1069C>G (p.Arg357Gly)
c.1051C>G (p.Arg351Gly)
11g.47346228G=CA1969339469MYBPC3c.1069C= (p.Arg357=)
c.1051C= (p.Arg351=)
11g.47346228G>TCA380331039MYBPC3c.1069C>A (p.Arg357Ser)
c.1051C>A (p.Arg351Ser)
11g.47346229C>ACA380331040MYBPC3c.1068G>T (p.Arg356Ser)
c.1050G>T (p.Arg350Ser)
11g.47346229C=CA1969339471MYBPC3c.1068G= (p.Arg356=)
c.1050G= (p.Arg350=)
11g.47346229C>GCA380331041MYBPC3c.1068G>C (p.Arg356Ser)
c.1050G>C (p.Arg350Ser)
11g.47346229C>TCA474220786MYBPC3c.1068G>A (p.Arg356=)
c.1050G>A (p.Arg350=)
ClinVar dbSNP gnomAD v4
11g.47346230C>ACA380331043MYBPC3c.1067G>T (p.Arg356Met)
c.1049G>T (p.Arg350Met)
dbSNP COSMIC COSMIC
11g.47346230C=CA1969339475MYBPC3c.1067G= (p.Arg356=)
c.1049G= (p.Arg350=)
11g.47346230C>GCA380331045MYBPC3c.1067G>C (p.Arg356Thr)
c.1049G>C (p.Arg350Thr)
11g.47346230C>TCA380331053MYBPC3c.1067G>A (p.Arg356Lys)
c.1049G>A (p.Arg350Lys)
dbSNP
11g.47346231T>ACA380331056MYBPC3c.1066A>T (p.Arg356Trp)
c.1048A>T (p.Arg350Trp)
11g.47346231T>CCA380331060MYBPC3c.1066A>G (p.Arg356Gly)
c.1048A>G (p.Arg350Gly)
11g.47346231T>GCA474220790MYBPC3c.1066A>C (p.Arg356=)
c.1048A>C (p.Arg350=)
11g.47346232C>ACA380331068MYBPC3c.1065G>T (p.Met355Ile)
c.1047G>T (p.Met349Ile)
11g.47346232C>GCA380331071MYBPC3c.1065G>C (p.Met355Ile)
c.1047G>C (p.Met349Ile)
11g.47346232C>TCA380331072MYBPC3c.1065G>A (p.Met355Ile)
c.1047G>A (p.Met349Ile)
11g.47346233A>CCA380331075MYBPC3c.1064T>G (p.Met355Arg)
c.1046T>G (p.Met349Arg)
11g.47346233A>GCA380331080MYBPC3c.1064T>C (p.Met355Thr)
c.1046T>C (p.Met349Thr)
11g.47346233A>TCA380331077MYBPC3c.1064T>A (p.Met355Lys)
c.1046T>A (p.Met349Lys)
11g.47346234T>ACA380331083MYBPC3c.1063A>T (p.Met355Leu)
c.1045A>T (p.Met349Leu)
11g.47346234T>CCA380331085MYBPC3c.1063A>G (p.Met355Val)
c.1045A>G (p.Met349Val)
ClinVar dbSNP gnomAD v4
11g.47346234T>GCA380331086MYBPC3c.1063A>C (p.Met355Leu)
c.1045A>C (p.Met349Leu)
11g.47346234T=CA1969339481MYBPC3c.1063A= (p.Met355=)
c.1045A= (p.Met349=)
11g.47346235G>ACA474220796MYBPC3c.1062C>T (p.Gly354=)
c.1044C>T (p.Gly348=)
dbSNP
11g.47346235G>CCA474220797MYBPC3c.1062C>G (p.Gly354=)
c.1044C>G (p.Gly348=)
11g.47346235G=CA1969339484MYBPC3c.1062C= (p.Gly354=)
c.1044C= (p.Gly348=)
11g.47346235G>TCA474220795MYBPC3c.1062C>A (p.Gly354=)
c.1044C>A (p.Gly348=)
ClinVar dbSNP gnomAD v4
11g.47346236C>ACA380331089MYBPC3c.1061G>T (p.Gly354Val)
c.1043G>T (p.Gly348Val)
ClinVar
11g.47346236C=CA1969339488MYBPC3c.1061G= (p.Gly354=)
c.1043G= (p.Gly348=)
11g.47346236C>GCA380331091MYBPC3c.1061G>C (p.Gly354Ala)
c.1043G>C (p.Gly348Ala)
dbSNP gnomAD v2 gnomAD v4
11g.47346236C>TCA380331093MYBPC3c.1061G>A (p.Gly354Asp)
c.1043G>A (p.Gly348Asp)
11g.47346237C>ACA380331105MYBPC3c.1060G>T (p.Gly354Cys)
c.1042G>T (p.Gly348Cys)
11g.47346237C=CA1969339490MYBPC3c.1060G= (p.Gly354=)
c.1042G= (p.Gly348=)
11g.47346237C>GCA380331095MYBPC3c.1060G>C (p.Gly354Arg)
c.1042G>C (p.Gly348Arg)
11g.47346237C>TCA380331103MYBPC3c.1060G>A (p.Gly354Ser)
c.1042G>A (p.Gly348Ser)
dbSNP gnomAD v4
11g.47346238C>ACA380331109MYBPC3c.1059G>T (p.Lys353Asn)
c.1041G>T (p.Lys347Asn)
11g.47346238C>GCA380331111MYBPC3c.1059G>C (p.Lys353Asn)
c.1041G>C (p.Lys347Asn)
11g.47346238C>TCA474220800MYBPC3c.1059G>A (p.Lys353=)
c.1041G>A (p.Lys347=)
11g.47346239T>ACA380331113MYBPC3c.1058A>T (p.Lys353Met)
c.1040A>T (p.Lys347Met)
11g.47346239T>CCA380331115MYBPC3c.1058A>G (p.Lys353Arg)
c.1040A>G (p.Lys347Arg)
11g.47346239T>GCA380331119MYBPC3c.1058A>C (p.Lys353Thr)
c.1040A>C (p.Lys347Thr)
11g.47346240delCA2580084165MYBPC3c.1058del (p.Lys353ArgfsTer3)
c.1040del (p.Lys347ArgfsTer3)
ClinVar
11g.47346240T>ACA380331122MYBPC3c.1057A>T (p.Lys353Ter)
c.1039A>T (p.Lys347Ter)
11g.47346240T>CCA380331129MYBPC3c.1057A>G (p.Lys353Glu)
c.1039A>G (p.Lys347Glu)
11g.47346240T>GCA380331126MYBPC3c.1057A>C (p.Lys353Gln)
c.1039A>C (p.Lys347Gln)
11g.47346241G>ACA474220808MYBPC3c.1056C>T (p.Leu352=)
c.1038C>T (p.Leu346=)
11g.47346241G>CCA042179MYBPC3c.1056C>G (p.Leu352=)
c.1038C>G (p.Leu346=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346241G=CA1969339495MYBPC3c.1056C= (p.Leu352=)
c.1038C= (p.Leu346=)
11g.47346241G>TCA474220805MYBPC3c.1056C>A (p.Leu352=)
c.1038C>A (p.Leu346=)
11g.47346242A=CA1969339500MYBPC3c.1055T= (p.Leu352=)
c.1037T= (p.Leu346=)
11g.47346242A>CCA380331135MYBPC3c.1055T>G (p.Leu352Arg)
c.1037T>G (p.Leu346Arg)
11g.47346242A>GCA380331137MYBPC3c.1055T>C (p.Leu352Pro)
c.1037T>C (p.Leu346Pro)
ClinVar dbSNP
11g.47346242A>TCA380331140MYBPC3c.1055T>A (p.Leu352His)
c.1037T>A (p.Leu346His)
11g.47346242_47346313delinsAGCCTCTTTAGCATGCCGCGCAGGTCAGTGACGCCGTACTGGAAGGCGATGCGCTCGTACTCAGATGGGGGTCA1969339501MYBPC3c.984_1055delinsACCCCCATCTGAGTACGAGCGCATCGCCTTCCAGTACGGCGTCACTGACCTGCGCGGCATGCTAAAGAGGCT (p.Ala328=)
c.966_1037delinsACCCCCATCTGAGTACGAGCGCATCGCCTTCCAGTACGGCGTCACTGACCTGCGCGGCATGCTAAAGAGGCT (p.Ala322=)
11g.47346243G>ACA380331142MYBPC3c.1054C>T (p.Leu352Phe)
c.1036C>T (p.Leu346Phe)
11g.47346243G>CCA380331144MYBPC3c.1054C>G (p.Leu352Val)
c.1036C>G (p.Leu346Val)
dbSNP gnomAD v3 gnomAD v4
11g.47346243G=CA1969339505MYBPC3c.1054C= (p.Leu352=)
c.1036C= (p.Leu346=)
11g.47346243G>TCA380331146MYBPC3c.1054C>A (p.Leu352Ile)
c.1036C>A (p.Leu346Ile)
11g.47346243_47346244delinsAACA2695213926MYBPC3c.1053_1054delinsTT (p.Arg351_Leu352delinsSerPhe)
c.1035_1036delinsTT (p.Arg345_Leu346delinsSerPhe)
11g.47346247_47346317delCA016227MYBPC3c.984_1054del (p.Pro329GlnfsTer7)
c.966_1036del (p.Pro323GlnfsTer7)
ClinVar dbSNP
11g.47346243_47346244insAACA2573051161MYBPC3c.1053_1054insTT (p.Leu352PhefsTer5)
c.1035_1036insTT (p.Leu346PhefsTer5)
11g.47346244C>ACA380331156MYBPC3c.1053G>T (p.Arg351Ser)
c.1035G>T (p.Arg345Ser)
11g.47346244C=CA1969339508MYBPC3c.1053G= (p.Arg351=)
c.1035G= (p.Arg345=)
11g.47346244C>GCA380331159MYBPC3c.1053G>C (p.Arg351Ser)
c.1035G>C (p.Arg345Ser)
ClinVar
11g.47346244C>TCA474220811MYBPC3c.1053G>A (p.Arg351=)
c.1035G>A (p.Arg345=)
ClinVar
11g.47346245C>ACA380331162MYBPC3c.1052G>T (p.Arg351Met)
c.1034G>T (p.Arg345Met)
11g.47346245C>GCA380331165MYBPC3c.1052G>C (p.Arg351Thr)
c.1034G>C (p.Arg345Thr)
11g.47346245C>TCA380331163MYBPC3c.1052G>A (p.Arg351Lys)
c.1034G>A (p.Arg345Lys)
gnomAD v4
11g.47346246T>ACA380331168MYBPC3c.1051A>T (p.Arg351Trp)
c.1033A>T (p.Arg345Trp)
gnomAD v4
11g.47346246T>CCA380331170MYBPC3c.1051A>G (p.Arg351Gly)
c.1033A>G (p.Arg345Gly)
ClinVar
11g.47346246T>GCA474220816MYBPC3c.1051A>C (p.Arg351=)
c.1033A>C (p.Arg345=)
11g.47346247C>ACA380331173MYBPC3c.1050G>T (p.Lys350Asn)
c.1032G>T (p.Lys344Asn)
11g.47346247C=CA1969339512MYBPC3c.1050G= (p.Lys350=)
c.1032G= (p.Lys344=)
11g.47346247C>GCA380331179MYBPC3c.1050G>C (p.Lys350Asn)
c.1032G>C (p.Lys344Asn)
dbSNP gnomAD v2 gnomAD v4
11g.47346247C>TCA474220817MYBPC3c.1050G>A (p.Lys350=)
c.1032G>A (p.Lys344=)
COSMIC COSMIC
11g.47346248T>ACA380331181MYBPC3c.1049A>T (p.Lys350Met)
c.1031A>T (p.Lys344Met)
gnomAD v4
11g.47346248T>CCA380331185MYBPC3c.1049A>G (p.Lys350Arg)
c.1031A>G (p.Lys344Arg)
11g.47346248T>GCA380331186MYBPC3c.1049A>C (p.Lys350Thr)
c.1031A>C (p.Lys344Thr)
11g.47346250delCA2580084166MYBPC3c.1049del (p.Lys350ArgfsTer6)
c.1031del (p.Lys344ArgfsTer6)
ClinVar
11g.47346249_47346250delCA2499220980MYBPC3c.1048_1049del (p.Lys350GlufsTer9)
c.1030_1031del (p.Lys344GlufsTer9)
ClinVar dbSNP
11g.47346249T>ACA380331190MYBPC3c.1048A>T (p.Lys350Ter)
c.1030A>T (p.Lys344Ter)
gnomAD v4
11g.47346249T>CCA380331191MYBPC3c.1048A>G (p.Lys350Glu)
c.1030A>G (p.Lys344Glu)
11g.47346249T>GCA380331192MYBPC3c.1048A>C (p.Lys350Gln)
c.1030A>C (p.Lys344Gln)
11g.47346250T>ACA474220822MYBPC3c.1047A>T (p.Leu349=)
c.1029A>T (p.Leu343=)
11g.47346250T>CCA474220823MYBPC3c.1047A>G (p.Leu349=)
c.1029A>G (p.Leu343=)
gnomAD v4
11g.47346250T>GCA474220824MYBPC3c.1047A>C (p.Leu349=)
c.1029A>C (p.Leu343=)
11g.47346251A=CA1969339517MYBPC3c.1046T= (p.Leu349=)
c.1028T= (p.Leu343=)
11g.47346251A>CCA380331193MYBPC3c.1046T>G (p.Leu349Arg)
c.1028T>G (p.Leu343Arg)
11g.47346251A>GCA380331195MYBPC3c.1046T>C (p.Leu349Pro)
c.1028T>C (p.Leu343Pro)
dbSNP
11g.47346251A>TCA380331197MYBPC3c.1046T>A (p.Leu349Gln)
c.1028T>A (p.Leu343Gln)
11g.47346252G>ACA474220826MYBPC3c.1045C>T (p.Leu349=)
c.1027C>T (p.Leu343=)
11g.47346252G>CCA380331198MYBPC3c.1045C>G (p.Leu349Val)
c.1027C>G (p.Leu343Val)
11g.47346252G>TCA380331199MYBPC3c.1045C>A (p.Leu349Ile)
c.1027C>A (p.Leu343Ile)
11g.47346253C>ACA380331200MYBPC3c.1044G>T (p.Met348Ile)
c.1026G>T (p.Met342Ile)
11g.47346253C>GCA380331202MYBPC3c.1044G>C (p.Met348Ile)
c.1026G>C (p.Met342Ile)
11g.47346253C>TCA380331204MYBPC3c.1044G>A (p.Met348Ile)
c.1026G>A (p.Met342Ile)
11g.47346254A=CA1969339518MYBPC3c.1043T= (p.Met348=)
c.1025T= (p.Met342=)
11g.47346254A>CCA380331209MYBPC3c.1043T>G (p.Met348Arg)
c.1025T>G (p.Met342Arg)
11g.47346254A>GCA380331208MYBPC3c.1043T>C (p.Met348Thr)
c.1025T>C (p.Met342Thr)
ClinVar dbSNP gnomAD v4
11g.47346254A>TCA380331207MYBPC3c.1043T>A (p.Met348Lys)
c.1025T>A (p.Met342Lys)
11g.47346255T>ACA380331213MYBPC3c.1042A>T (p.Met348Leu)
c.1024A>T (p.Met342Leu)
11g.47346255T>CCA380331217MYBPC3c.1042A>G (p.Met348Val)
c.1024A>G (p.Met342Val)
11g.47346255T>GCA380331220MYBPC3c.1042A>C (p.Met348Leu)
c.1024A>C (p.Met342Leu)
11g.47346255_47346259dupCA273429MYBPC3c.1038_1042dup (p.Met348ThrfsTer4)
c.1020_1024dup (p.Met342ThrfsTer4)
ClinVar dbSNP ExAC gnomAD v2
11g.47346256G>ACA474220832MYBPC3c.1041C>T (p.Gly347=)
c.1023C>T (p.Gly341=)
11g.47346256G>CCA474220835MYBPC3c.1041C>G (p.Gly347=)
c.1023C>G (p.Gly341=)
11g.47346256G>TCA474220834MYBPC3c.1041C>A (p.Gly347=)
c.1023C>A (p.Gly341=)
11g.47346257C>ACA380331226MYBPC3c.1040G>T (p.Gly347Val)
c.1022G>T (p.Gly341Val)
ClinVar dbSNP
11g.47346257C=CA1969339526MYBPC3c.1040G= (p.Gly347=)
c.1022G= (p.Gly341=)
11g.47346257C>GCA380331232MYBPC3c.1040G>C (p.Gly347Ala)
c.1022G>C (p.Gly341Ala)
11g.47346257C>TCA380331234MYBPC3c.1040G>A (p.Gly347Asp)
c.1022G>A (p.Gly341Asp)
ClinVar dbSNP
11g.47346258C>ACA380331236MYBPC3c.1039G>T (p.Gly347Cys)
c.1021G>T (p.Gly341Cys)
gnomAD v4
11g.47346258C=CA1969339530MYBPC3c.1039G= (p.Gly347=)
c.1021G= (p.Gly341=)
11g.47346258C>GCA380331238MYBPC3c.1039G>C (p.Gly347Arg)
c.1021G>C (p.Gly341Arg)
ClinVar dbSNP
11g.47346258C>TCA009719MYBPC3c.1039G>A (p.Gly347Ser)
c.1021G>A (p.Gly341Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346258_47346259insTGCCGCA2739291479MYBPC3c.1038_1039insCGGCA (p.Gly347ArgfsTer5)
c.1020_1021insCGGCA (p.Gly341ArgfsTer5)
11g.47346259G>ACA042114MYBPC3c.1038C>T (p.Arg346=)
c.1020C>T (p.Arg340=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346259G>CCA474220842MYBPC3c.1038C>G (p.Arg346=)
c.1020C>G (p.Arg340=)
11g.47346259G=CA1969339535MYBPC3c.1038C= (p.Arg346=)
c.1020C= (p.Arg340=)
11g.47346259G>TCA474220843MYBPC3c.1038C>A (p.Arg346=)
c.1020C>A (p.Arg340=)
11g.47346260C>ACA380331244MYBPC3c.1037G>T (p.Arg346Leu)
c.1019G>T (p.Arg340Leu)
11g.47346260C=CA1969339539MYBPC3c.1037G= (p.Arg346=)
c.1019G= (p.Arg340=)
11g.47346260C>GCA380331248MYBPC3c.1037G>C (p.Arg346Pro)
c.1019G>C (p.Arg340Pro)
11g.47346260C>TCA009714MYBPC3c.1037G>A (p.Arg346His)
c.1019G>A (p.Arg340His)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47346261G>ACA380331260MYBPC3c.1036C>T (p.Arg346Cys)
c.1018C>T (p.Arg340Cys)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.47346261G>CCA380331264MYBPC3c.1036C>G (p.Arg346Gly)
c.1018C>G (p.Arg340Gly)
ClinVar dbSNP
11g.47346261G=CA1969339543MYBPC3c.1036C= (p.Arg346=)
c.1018C= (p.Arg340=)
11g.47346261G>TCA380331255MYBPC3c.1036C>A (p.Arg346Ser)
c.1018C>A (p.Arg340Ser)
ClinVar dbSNP
11g.47346262C>ACA474220846MYBPC3c.1035G>T (p.Leu345=)
c.1017G>T (p.Leu339=)
11g.47346262C=CA1969339548MYBPC3c.1035G= (p.Leu345=)
c.1017G= (p.Leu339=)
11g.47346262C>GCA474220848MYBPC3c.1035G>C (p.Leu345=)
c.1017G>C (p.Leu339=)
11g.47346262C>TCA042085MYBPC3c.1035G>A (p.Leu345=)
c.1017G>A (p.Leu339=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47346263A=CA1969339551MYBPC3c.1034T= (p.Leu345=)
c.1016T= (p.Leu339=)
11g.47346263A>CCA380331267MYBPC3c.1034T>G (p.Leu345Arg)
c.1016T>G (p.Leu339Arg)
11g.47346263A>GCA380331268MYBPC3c.1034T>C (p.Leu345Pro)
c.1016T>C (p.Leu339Pro)
ClinVar dbSNP
11g.47346263A>TCA380331269MYBPC3c.1034T>A (p.Leu345Gln)
c.1016T>A (p.Leu339Gln)
11g.47346264G>ACA474220850MYBPC3c.1033C>T (p.Leu345=)
c.1015C>T (p.Leu339=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47346264G>CCA380331270MYBPC3c.1033C>G (p.Leu345Val)
c.1015C>G (p.Leu339Val)
ClinVar
11g.47346264G=CA1969339554MYBPC3c.1033C= (p.Leu345=)
c.1015C= (p.Leu339=)
11g.47346264G>TCA380331271MYBPC3c.1033C>A (p.Leu345Met)
c.1015C>A (p.Leu339Met)
11g.47346264_47346268delinsGGTCACA1969339556MYBPC3c.1029_1033delinsTGACC (p.Thr343=)
c.1011_1015delinsTGACC (p.Thr337=)
11g.47346265G>ACA474220851MYBPC3c.1032C>T (p.Asp344=)
c.1014C>T (p.Asp338=)
ClinVar dbSNP gnomAD v4
11g.47346265G>CCA380331273MYBPC3c.1032C>G (p.Asp344Glu)
c.1014C>G (p.Asp338Glu)
11g.47346265G=CA1969339560MYBPC3c.1032C= (p.Asp344=)
c.1014C= (p.Asp338=)
11g.47346265G>TCA380331272MYBPC3c.1032C>A (p.Asp344Glu)
c.1014C>A (p.Asp338Glu)
ClinVar dbSNP
11g.47346267_47346270delCA915948162MYBPC3c.1029_1032del (p.Asp344CysfsTer5)
c.1011_1014del (p.Asp338CysfsTer5)
ClinVar dbSNP
11g.47346266T>ACA380331274MYBPC3c.1031A>T (p.Asp344Val)
c.1013A>T (p.Asp338Val)
11g.47346266T>CCA380331275MYBPC3c.1031A>G (p.Asp344Gly)
c.1013A>G (p.Asp338Gly)
ClinVar dbSNP
11g.47346266T>GCA380331276MYBPC3c.1031A>C (p.Asp344Ala)
c.1013A>C (p.Asp338Ala)
11g.47346266T=CA1969339565MYBPC3c.1031A= (p.Asp344=)
c.1013A= (p.Asp338=)
11g.47346267C>ACA380331278MYBPC3c.1030G>T (p.Asp344Tyr)
c.1012G>T (p.Asp338Tyr)
11g.47346267C=CA1969339567MYBPC3c.1030G= (p.Asp344=)
c.1012G= (p.Asp338=)
11g.47346267C>GCA380331279MYBPC3c.1030G>C (p.Asp344His)
c.1012G>C (p.Asp338His)
dbSNP gnomAD v4
11g.47346267C>TCA380331284MYBPC3c.1030G>A (p.Asp344Asn)
c.1012G>A (p.Asp338Asn)
gnomAD v4
11g.47346268A>CCA474220858MYBPC3c.1029T>G (p.Thr343=)
c.1011T>G (p.Thr337=)
11g.47346268A>GCA474220860MYBPC3c.1029T>C (p.Thr343=)
c.1011T>C (p.Thr337=)
11g.47346268A>TCA474220862MYBPC3c.1029T>A (p.Thr343=)
c.1011T>A (p.Thr337=)
11g.47346268_47346269delinsAGCA1969339569MYBPC3c.1028_1029delinsCT (p.Thr343=)
c.1010_1011delinsCT (p.Thr337=)
11g.47346269delCA009708MYBPC3c.1028del (p.Thr343MetfsTer7)
c.1010del (p.Thr337MetfsTer7)
ClinVar dbSNP gnomAD v4
11g.47346269G>ACA380331288MYBPC3c.1028C>T (p.Thr343Ile)
c.1010C>T (p.Thr337Ile)
ClinVar
11g.47346269G>CCA380331290MYBPC3c.1028C>G (p.Thr343Ser)
c.1010C>G (p.Thr337Ser)
11g.47346269G>TCA380331289MYBPC3c.1028C>A (p.Thr343Asn)
c.1010C>A (p.Thr337Asn)
11g.47346271_47346278delCA2695213930MYBPC3c.1021_1028del (p.Gly341Ter)
c.1003_1010del (p.Gly335Ter)
11g.47346270T>ACA380331292MYBPC3c.1027A>T (p.Thr343Ser)
c.1009A>T (p.Thr337Ser)
11g.47346270T>CCA380331296MYBPC3c.1027A>G (p.Thr343Ala)
c.1009A>G (p.Thr337Ala)
11g.47346270T>GCA380331297MYBPC3c.1027A>C (p.Thr343Pro)
c.1009A>C (p.Thr337Pro)
11g.47346271G>ACA474220872MYBPC3c.1026C>T (p.Val342=)
c.1008C>T (p.Val336=)
11g.47346271G>CCA474220869MYBPC3c.1026C>G (p.Val342=)
c.1008C>G (p.Val336=)
11g.47346271G>TCA474220868MYBPC3c.1026C>A (p.Val342=)
c.1008C>A (p.Val336=)
11g.47346272A=CA1969339572MYBPC3c.1025T= (p.Val342=)
c.1007T= (p.Val336=)
11g.47346272A>CCA380331298MYBPC3c.1025T>G (p.Val342Gly)
c.1007T>G (p.Val336Gly)
11g.47346272A>GCA380331299MYBPC3c.1025T>C (p.Val342Ala)
c.1007T>C (p.Val336Ala)
gnomAD v4
11g.47346272A>TCA009704MYBPC3c.1025T>A (p.Val342Asp)
c.1007T>A (p.Val336Asp)
dbSNP
11g.47346273C>ACA380331301MYBPC3c.1024G>T (p.Val342Phe)
c.1006G>T (p.Val336Phe)
11g.47346273C=CA1969339574MYBPC3c.1024G= (p.Val342=)
c.1006G= (p.Val336=)
11g.47346273C>GCA380331312MYBPC3c.1024G>C (p.Val342Leu)
c.1006G>C (p.Val336Leu)
11g.47346273C>TCA009698MYBPC3c.1024G>A (p.Val342Ile)
c.1006G>A (p.Val336Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346274G>ACA042054MYBPC3c.1023C>T (p.Gly341=)
c.1005C>T (p.Gly335=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346274G>CCA474220880MYBPC3c.1023C>G (p.Gly341=)
c.1005C>G (p.Gly335=)
11g.47346274G=CA1969339578MYBPC3c.1023C= (p.Gly341=)
c.1005C= (p.Gly335=)
11g.47346274G>TCA474220881MYBPC3c.1023C>A (p.Gly341=)
c.1005C>A (p.Gly335=)
11g.47346275C>ACA380331320MYBPC3c.1022G>T (p.Gly341Val)
c.1004G>T (p.Gly335Val)
ClinVar dbSNP gnomAD v2
11g.47346275C=CA1969339584MYBPC3c.1022G= (p.Gly341=)
c.1004G= (p.Gly335=)
11g.47346275C>GCA380331326MYBPC3c.1022G>C (p.Gly341Ala)
c.1004G>C (p.Gly335Ala)
11g.47346275C>TCA380331324MYBPC3c.1022G>A (p.Gly341Asp)
c.1004G>A (p.Gly335Asp)
dbSNP COSMIC COSMIC
11g.47346276C>ACA380331329MYBPC3c.1021G>T (p.Gly341Cys)
c.1003G>T (p.Gly335Cys)
11g.47346276C=CA1969339586MYBPC3c.1021G= (p.Gly341=)
c.1003G= (p.Gly335=)
11g.47346276C>GCA380331331MYBPC3c.1021G>C (p.Gly341Arg)
c.1003G>C (p.Gly335Arg)
11g.47346276C>TCA009692MYBPC3c.1021G>A (p.Gly341Ser)
c.1003G>A (p.Gly335Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47346277delCA2697548548MYBPC3c.1020del (p.Tyr340Ter)
c.1002del (p.Tyr334Ter)
ClinVar
11g.47346277G>ACA042025MYBPC3c.1020C>T (p.Tyr340=)
c.1002C>T (p.Tyr334=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47346277G>CCA380331334MYBPC3c.1020C>G (p.Tyr340Ter)
c.1002C>G (p.Tyr334Ter)
11g.47346277G=CA1969339595MYBPC3c.1020C= (p.Tyr340=)
c.1002C= (p.Tyr334=)
11g.47346277G>TCA380331336MYBPC3c.1020C>A (p.Tyr340Ter)
c.1002C>A (p.Tyr334Ter)
11g.47346278T>ACA380331339MYBPC3c.1019A>T (p.Tyr340Phe)
c.1001A>T (p.Tyr334Phe)
11g.47346278T>CCA380331342MYBPC3c.1019A>G (p.Tyr340Cys)
c.1001A>G (p.Tyr334Cys)
11g.47346278T>GCA380331349MYBPC3c.1019A>C (p.Tyr340Ser)
c.1001A>C (p.Tyr334Ser)
11g.47346279A>CCA380331354MYBPC3c.1018T>G (p.Tyr340Asp)
c.1000T>G (p.Tyr334Asp)
11g.47346279A>GCA380331358MYBPC3c.1018T>C (p.Tyr340His)
c.1000T>C (p.Tyr334His)
11g.47346279A>TCA380331360MYBPC3c.1018T>A (p.Tyr340Asn)
c.1000T>A (p.Tyr334Asn)
11g.47346280C>ACA380331363MYBPC3c.1017G>T (p.Gln339His)
c.999G>T (p.Gln333His)
dbSNP
11g.47346280C=CA1969339603MYBPC3c.1017G= (p.Gln339=)
c.999G= (p.Gln333=)
11g.47346280C>GCA380331367MYBPC3c.1017G>C (p.Gln339His)
c.999G>C (p.Gln333His)
ClinVar
11g.47346280C>TCA474220890MYBPC3c.1017G>A (p.Gln339=)
c.999G>A (p.Gln333=)
ClinVar dbSNP gnomAD v4
11g.47346281T>ACA380331376MYBPC3c.1016A>T (p.Gln339Leu)
c.998A>T (p.Gln333Leu)
11g.47346281T>CCA380331368MYBPC3c.1016A>G (p.Gln339Arg)
c.998A>G (p.Gln333Arg)
11g.47346281T>GCA380331371MYBPC3c.1016A>C (p.Gln339Pro)
c.998A>C (p.Gln333Pro)
11g.47346282G>ACA009690MYBPC3c.1015C>T (p.Gln339Ter)
c.997C>T (p.Gln333Ter)
ClinVar dbSNP
11g.47346282G>CCA380331386MYBPC3c.1015C>G (p.Gln339Glu)
c.997C>G (p.Gln333Glu)
11g.47346282G=CA1969339608MYBPC3c.1015C= (p.Gln339=)
c.997C= (p.Gln333=)
11g.47346282G>TCA380331389MYBPC3c.1015C>A (p.Gln339Lys)
c.997C>A (p.Gln333Lys)
11g.47346283G>ACA474220894MYBPC3c.1014C>T (p.Phe338=)
c.996C>T (p.Phe332=)
11g.47346283G>CCA380331392MYBPC3c.1014C>G (p.Phe338Leu)
c.996C>G (p.Phe332Leu)
11g.47346283G>TCA380331393MYBPC3c.1014C>A (p.Phe338Leu)
c.996C>A (p.Phe332Leu)
11g.47346284A>CCA380331396MYBPC3c.1013T>G (p.Phe338Cys)
c.995T>G (p.Phe332Cys)
11g.47346284A>GCA380331399MYBPC3c.1013T>C (p.Phe338Ser)
c.995T>C (p.Phe332Ser)
11g.47346284A>TCA380331400MYBPC3c.1013T>A (p.Phe338Tyr)
c.995T>A (p.Phe332Tyr)
11g.47346285A>CCA380331402MYBPC3c.1012T>G (p.Phe338Val)
c.994T>G (p.Phe332Val)
11g.47346285A>GCA380331405MYBPC3c.1012T>C (p.Phe338Leu)
c.994T>C (p.Phe332Leu)
11g.47346285A>TCA380331407MYBPC3c.1012T>A (p.Phe338Ile)
c.994T>A (p.Phe332Ile)
11g.47346286G>ACA474220899MYBPC3c.1011C>T (p.Ala337=)
c.993C>T (p.Ala331=)
11g.47346286G>CCA474220900MYBPC3c.1011C>G (p.Ala337=)
c.993C>G (p.Ala331=)
ClinVar dbSNP
11g.47346286G>TCA474220901MYBPC3c.1011C>A (p.Ala337=)
c.993C>A (p.Ala331=)
11g.47346287G>ACA380331416MYBPC3c.1010C>T (p.Ala337Val)
c.992C>T (p.Ala331Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47346287G>CCA380331420MYBPC3c.1010C>G (p.Ala337Gly)
c.992C>G (p.Ala331Gly)
COSMIC COSMIC
11g.47346287G=CA1969339611MYBPC3c.1010C= (p.Ala337=)
c.992C= (p.Ala331=)
11g.47346287G>TCA380331413MYBPC3c.1010C>A (p.Ala337Asp)
c.992C>A (p.Ala331Asp)
11g.47346288C>ACA380331426MYBPC3c.1009G>T (p.Ala337Ser)
c.991G>T (p.Ala331Ser)
11g.47346288C=CA1969339615MYBPC3c.1009G= (p.Ala337=)
c.991G= (p.Ala331=)
11g.47346288C>GCA380331428MYBPC3c.1009G>C (p.Ala337Pro)
c.991G>C (p.Ala331Pro)
11g.47346288C>TCA042017MYBPC3c.1009G>A (p.Ala337Thr)
c.991G>A (p.Ala331Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346289G>ACA009683MYBPC3c.1008C>T (p.Ile336=)
c.990C>T (p.Ile330=)
ClinVar dbSNP gnomAD v4
11g.47346289G>CCA380331441MYBPC3c.1008C>G (p.Ile336Met)
c.990C>G (p.Ile330Met)
ClinVar dbSNP
11g.47346289G=CA1969339618MYBPC3c.1008C= (p.Ile336=)
c.990C= (p.Ile330=)
11g.47346289G>TCA474220904MYBPC3c.1008C>A (p.Ile336=)
c.990C>A (p.Ile330=)
dbSNP gnomAD v2
11g.47346290A>CCA380331446MYBPC3c.1007T>G (p.Ile336Ser)
c.989T>G (p.Ile330Ser)
11g.47346290A>GCA380331444MYBPC3c.1007T>C (p.Ile336Thr)
c.989T>C (p.Ile330Thr)
11g.47346290A>TCA380331443MYBPC3c.1007T>A (p.Ile336Asn)
c.989T>A (p.Ile330Asn)
11g.47346291T>ACA042000MYBPC3c.1006A>T (p.Ile336Phe)
c.988A>T (p.Ile330Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47346291T>CCA380331451MYBPC3c.1006A>G (p.Ile336Val)
c.988A>G (p.Ile330Val)
ClinVar dbSNP gnomAD v4
11g.47346291T>GCA380331453MYBPC3c.1006A>C (p.Ile336Leu)
c.988A>C (p.Ile330Leu)
11g.47346291T=CA1969339620MYBPC3c.1006A= (p.Ile336=)
c.988A= (p.Ile330=)
11g.47346292G>ACA474220910MYBPC3c.1005C>T (p.Arg335=)
c.987C>T (p.Arg329=)
11g.47346292G>CCA474220908MYBPC3c.1005C>G (p.Arg335=)
c.987C>G (p.Arg329=)
11g.47346292G>TCA474220909MYBPC3c.1005C>A (p.Arg335=)
c.987C>A (p.Arg329=)
11g.47346293C>ACA380331454MYBPC3c.1004G>T (p.Arg335Leu)
c.986G>T (p.Arg329Leu)
ClinVar gnomAD v4
11g.47346293C>GCA380331458MYBPC3c.1004G>C (p.Arg335Pro)
c.986G>C (p.Arg329Pro)
11g.47346293C>TCA380331459MYBPC3c.1004G>A (p.Arg335His)
c.986G>A (p.Arg329His)
gnomAD v4
11g.47346294G>ACA009677MYBPC3c.1003C>T (p.Arg335Cys)
c.985C>T (p.Arg329Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47346294G>CCA380331461MYBPC3c.1003C>G (p.Arg335Gly)
c.985C>G (p.Arg329Gly)
11g.47346294G=CA1969339623MYBPC3c.1003C= (p.Arg335=)
c.985C= (p.Arg329=)
11g.47346294G>TCA380331460MYBPC3c.1003C>A (p.Arg335Ser)
c.985C>A (p.Arg329Ser)
dbSNP gnomAD v2 gnomAD v4
11g.47346295C>ACA380331463MYBPC3c.1002G>T (p.Glu334Asp)
c.984G>T (p.Glu328Asp)
11g.47346295C>GCA380331466MYBPC3c.1002G>C (p.Glu334Asp)
c.984G>C (p.Glu328Asp)
11g.47346295C>TCA474220913MYBPC3c.1002G>A (p.Glu334=)
c.984G>A (p.Glu328=)
gnomAD v4 COSMIC COSMIC
11g.47346296T>ACA380331470MYBPC3c.1001A>T (p.Glu334Val)
c.983A>T (p.Glu328Val)
11g.47346296T>CCA380331473MYBPC3c.1001A>G (p.Glu334Gly)
c.983A>G (p.Glu328Gly)
11g.47346296T>GCA380331479MYBPC3c.1001A>C (p.Glu334Ala)
c.983A>C (p.Glu328Ala)
11g.47346297C>ACA009672MYBPC3c.1000G>T (p.Glu334Ter)
c.982G>T (p.Glu328Ter)
ClinVar dbSNP gnomAD v4
11g.47346297C=CA1969339628MYBPC3c.1000G= (p.Glu334=)
c.982G= (p.Glu328=)
11g.47346297C>GCA380331485MYBPC3c.1000G>C (p.Glu334Gln)
c.982G>C (p.Glu328Gln)
11g.47346297C>TCA009667MYBPC3c.1000G>A (p.Glu334Lys)
c.982G>A (p.Glu328Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47346298delCA2697548549MYBPC3c.999del (p.Tyr333Ter)
c.981del (p.Tyr327Ter)
ClinVar
11g.47346298G>ACA057719MYBPC3c.999C>T (p.Tyr333=)
c.981C>T (p.Tyr327=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47346298G>CCA016252MYBPC3c.999C>G (p.Tyr333Ter)
c.981C>G (p.Tyr327Ter)
ClinVar dbSNP
11g.47346298G=CA1969339631MYBPC3c.999C= (p.Tyr333=)
c.981C= (p.Tyr327=)
11g.47346298G>TCA380331492MYBPC3c.999C>A (p.Tyr333Ter)
c.981C>A (p.Tyr327Ter)
ClinVar dbSNP
11g.47346299T>ACA380331496MYBPC3c.998A>T (p.Tyr333Phe)
c.980A>T (p.Tyr327Phe)
11g.47346299T>CCA380331502MYBPC3c.998A>G (p.Tyr333Cys)
c.980A>G (p.Tyr327Cys)
11g.47346299T>GCA380331500MYBPC3c.998A>C (p.Tyr333Ser)
c.980A>C (p.Tyr327Ser)
11g.47346300A>CCA380331504MYBPC3c.997T>G (p.Tyr333Asp)
c.979T>G (p.Tyr327Asp)
11g.47346300A>GCA380331508MYBPC3c.997T>C (p.Tyr333His)
c.979T>C (p.Tyr327His)
11g.47346300A>TCA380331506MYBPC3c.997T>A (p.Tyr333Asn)
c.979T>A (p.Tyr327Asn)
11g.47346301C>ACA380331511MYBPC3c.996G>T (p.Glu332Asp)
c.978G>T (p.Glu326Asp)
11g.47346301C>GCA380331513MYBPC3c.996G>C (p.Glu332Asp)
c.978G>C (p.Glu326Asp)
11g.47346301C>TCA474220921MYBPC3c.996G>A (p.Glu332=)
c.978G>A (p.Glu326=)
11g.47346302T>ACA380331515MYBPC3c.995A>T (p.Glu332Val)
c.977A>T (p.Glu326Val)
11g.47346302T>CCA380331517MYBPC3c.995A>G (p.Glu332Gly)
c.977A>G (p.Glu326Gly)
11g.47346302T>GCA380331519MYBPC3c.995A>C (p.Glu332Ala)
c.977A>C (p.Glu326Ala)

Number of alleles fetched