Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47339622T>CCA937669907MYBPC3c.2067+29A>G (n.2067+29A>G)
c.2049+29A>G (n.2049+29A>G)
dbSNP gnomAD v3 gnomAD v4
11g.47339622T>GCA599374374MYBPC3c.2067+29A>C (n.2067+29A>C)
c.2049+29A>C (n.2049+29A>C)
dbSNP gnomAD v2 gnomAD v4
11g.47339622T=CA1969333349MYBPC3c.2067+29A= (n.2067+29A=)
c.2049+29A= (n.2049+29A=)
11g.47339626dupCA221691068MYBPC3c.2067+28dup (n.2067+28dup)
c.2049+28dup (n.2049+28dup)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339624G>ACA2574816200MYBPC3c.2067+27C>T (n.2067+27C>T)
c.2049+27C>T (n.2049+27C>T)
11g.47339624G>TCA2574816201MYBPC3c.2067+27C>A (n.2067+27C>A)
c.2049+27C>A (n.2049+27C>A)
gnomAD v4
11g.47339625G>CCA078497MYBPC3c.2067+26C>G (n.2067+26C>G)
c.2049+26C>G (n.2049+26C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47339625G=CA1969333351MYBPC3c.2067+26C= (n.2067+26C=)
c.2049+26C= (n.2049+26C=)
11g.47339626G>ACA599374375MYBPC3c.2067+25C>T (n.2067+25C>T)
c.2049+25C>T (n.2049+25C>T)
dbSNP gnomAD v2
11g.47339626G=CA1969333352MYBPC3c.2067+25C= (n.2067+25C=)
c.2049+25C= (n.2049+25C=)
11g.47339628G>CCA048045MYBPC3c.2067+23C>G (n.2067+23C>G)
c.2049+23C>G (n.2049+23C>G)
dbSNP
11g.47339628G=CA1969333353MYBPC3c.2067+23C= (n.2067+23C=)
c.2049+23C= (n.2049+23C=)
11g.47339630C>ACA2613395244MYBPC3c.2067+21G>T (n.2067+21G>T)
c.2049+21G>T (n.2049+21G>T)
gnomAD v4
11g.47339630C>TCA2613395246MYBPC3c.2067+21G>A (n.2067+21G>A)
c.2049+21G>A (n.2049+21G>A)
gnomAD v4
11g.47339631T>ACA2613395248MYBPC3c.2067+20A>T (n.2067+20A>T)
c.2049+20A>T (n.2049+20A>T)
gnomAD v4
11g.47339632G>CCA599374376MYBPC3c.2067+19C>G (n.2067+19C>G)
c.2049+19C>G (n.2049+19C>G)
dbSNP gnomAD v2 gnomAD v4
11g.47339632G=CA1969333354MYBPC3c.2067+19C= (n.2067+19C=)
c.2049+19C= (n.2049+19C=)
11g.47339636A>GCA2511473089MYBPC3c.2067+15T>C (n.2067+15T>C)
c.2049+15T>C (n.2049+15T>C)
11g.47339637G>ACA599374377MYBPC3c.2067+14C>T (n.2067+14C>T)
c.2049+14C>T (n.2049+14C>T)
dbSNP gnomAD v2 gnomAD v4
11g.47339637G>CCA2613395292MYBPC3c.2067+14C>G (n.2067+14C>G)
c.2049+14C>G (n.2049+14C>G)
gnomAD v4
11g.47339637G=CA1969333356MYBPC3c.2067+14C= (n.2067+14C=)
c.2049+14C= (n.2049+14C=)
11g.47339638G>ACA2613395294MYBPC3c.2067+13C>T (n.2067+13C>T)
c.2049+13C>T (n.2049+13C>T)
gnomAD v4
11g.47339639G>CCA676997206MYBPC3c.2067+12C>G (n.2067+12C>G)
c.2049+12C>G (n.2049+12C>G)
dbSNP gnomAD v3 gnomAD v4
11g.47339639G=CA1969333357MYBPC3c.2067+12C= (n.2067+12C=)
c.2049+12C= (n.2049+12C=)
11g.47339639G>TCA2613395296MYBPC3c.2067+12C>A (n.2067+12C>A)
c.2049+12C>A (n.2049+12C>A)
gnomAD v4
11g.47339640_47339664delCA2573051214MYBPC3c.2054_2067+11del
c.2036_2049+11del
11g.47339641C>ACA2613395299MYBPC3c.2067+10G>T (n.2067+10G>T)
c.2049+10G>T (n.2049+10G>T)
gnomAD v4
11g.47339641C>TCA2613395300MYBPC3c.2067+10G>A (n.2067+10G>A)
c.2049+10G>A (n.2049+10G>A)
gnomAD v4
11g.47339643C>ACA2613395303MYBPC3c.2067+8G>T (n.2067+8G>T)
c.2049+8G>T (n.2049+8G>T)
gnomAD v4
11g.47339646A=CA1969333358MYBPC3c.2067+5T= (n.2067+5T=)
c.2049+5T= (n.2049+5T=)
11g.47339646A>CCA078500MYBPC3c.2067+5T>G (n.2067+5T>G)
c.2049+5T>G (n.2049+5T>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47339646A>GCA2613395305MYBPC3c.2067+5T>C (n.2067+5T>C)
c.2049+5T>C (n.2049+5T>C)
gnomAD v4
11g.47339647G>CCA1969333360MYBPC3c.2067+4C>G (n.2067+4C>G)
c.2049+4C>G (n.2049+4C>G)
ClinVar dbSNP
11g.47339647G=CA1969333359MYBPC3c.2067+4C= (n.2067+4C=)
c.2049+4C= (n.2049+4C=)
11g.47339649delCA2580084190MYBPC3c.2067+2del (n.2067+2del)
c.2049+2del (n.2049+2del)
ClinVar
11g.47339649A=CA1969333362MYBPC3c.2067+2T= (n.2067+2T=)
c.2049+2T= (n.2049+2T=)
11g.47339649A>CCA048063MYBPC3c.2067+2T>G (n.2067+2T>G)
c.2049+2T>G (n.2049+2T>G)
dbSNP
11g.47339649A>GCA380321273MYBPC3c.2067+2T>C (n.2067+2T>C)
c.2049+2T>C (n.2049+2T>C)
11g.47339649A>TCA380321276MYBPC3c.2067+2T>A (n.2067+2T>A)
c.2049+2T>A (n.2049+2T>A)
11g.47339649_47339661delinsACCTGCGTGATAGCA1969333363MYBPC3c.2057_2067+2delinsCTATCACGCAGGT
c.2039_2049+2delinsCTATCACGCAGGT
11g.47339650C>ACA380321280MYBPC3c.2067+1G>T (n.2067+1G>T)
c.2049+1G>T (n.2049+1G>T)
11g.47339650C=CA1969333365MYBPC3c.2067+1G= (n.2067+1G=)
c.2049+1G= (n.2049+1G=)
11g.47339650C>GCA380321283MYBPC3c.2067+1G>C (n.2067+1G>C)
c.2049+1G>C (n.2049+1G>C)
11g.47339650C>TCA380321286MYBPC3c.2067+1G>A (n.2067+1G>A)
c.2049+1G>A (n.2049+1G>A)
ClinVar dbSNP
11g.47339653_47339664delCA599374378MYBPC3c.2057_2067+1del
c.2039_2049+1del
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339651C>ACA380321287MYBPC3c.2067G>T (p.Gln689His)
c.2049G>T (p.Gln683His)
ClinVar gnomAD v4
11g.47339651C>GCA380321289MYBPC3c.2067G>C (p.Gln689His)
c.2049G>C (p.Gln683His)
11g.47339651C>TCA474217445MYBPC3c.2067G>A (p.Gln689=)
c.2049G>A (p.Gln683=)
11g.47339652T>ACA380321296MYBPC3c.2066A>T (p.Gln689Leu)
c.2048A>T (p.Gln683Leu)
11g.47339652T>CCA380321294MYBPC3c.2066A>G (p.Gln689Arg)
c.2048A>G (p.Gln683Arg)
11g.47339652T>GCA380321292MYBPC3c.2066A>C (p.Gln689Pro)
c.2048A>C (p.Gln683Pro)
11g.47339653G>ACA279293MYBPC3c.2065C>T (p.Gln689Ter)
c.2047C>T (p.Gln683Ter)
ClinVar dbSNP
11g.47339653G>CCA380321299MYBPC3c.2065C>G (p.Gln689Glu)
c.2047C>G (p.Gln683Glu)
11g.47339653G=CA1969333366MYBPC3c.2065C= (p.Gln689=)
c.2047C= (p.Gln683=)
11g.47339653G>TCA380321301MYBPC3c.2065C>A (p.Gln689Lys)
c.2047C>A (p.Gln683Lys)
11g.47339654C>ACA474217452MYBPC3c.2064G>T (p.Thr688=)
c.2046G>T (p.Thr682=)
dbSNP gnomAD v3 gnomAD v4
11g.47339654C=CA1969333370MYBPC3c.2064G= (p.Thr688=)
c.2046G= (p.Thr682=)
11g.47339654C>GCA474217454MYBPC3c.2064G>C (p.Thr688=)
c.2046G>C (p.Thr682=)
dbSNP gnomAD v2 gnomAD v4
11g.47339654C>TCA078495MYBPC3c.2064G>A (p.Thr688=)
c.2046G>A (p.Thr682=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47339655delCA2739270438MYBPC3c.2063del (p.Thr688SerfsTer?)
c.2045del (p.Thr682SerfsTer?)
ClinVar
11g.47339655G>ACA221691095MYBPC3c.2063C>T (p.Thr688Met)
c.2045C>T (p.Thr682Met)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47339655G>CCA380321305MYBPC3c.2063C>G (p.Thr688Arg)
c.2045C>G (p.Thr682Arg)
11g.47339655G=CA1969333372MYBPC3c.2063C= (p.Thr688=)
c.2045C= (p.Thr682=)
11g.47339655G>TCA011701MYBPC3c.2063C>A (p.Thr688Lys)
c.2045C>A (p.Thr682Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47339656T>ACA380321309MYBPC3c.2062A>T (p.Thr688Ser)
c.2044A>T (p.Thr682Ser)
11g.47339656T>CCA380321313MYBPC3c.2062A>G (p.Thr688Ala)
c.2044A>G (p.Thr682Ala)
11g.47339656T>GCA380321310MYBPC3c.2062A>C (p.Thr688Pro)
c.2044A>C (p.Thr682Pro)
11g.47339656T=CA1969333373MYBPC3c.2062A= (p.Thr688=)
c.2044A= (p.Thr682=)
11g.47339657G>ACA474217460MYBPC3c.2061C>T (p.Ile687=)
c.2043C>T (p.Ile681=)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
11g.47339657G>CCA048115MYBPC3c.2061C>G (p.Ile687Met)
c.2043C>G (p.Ile681Met)
11g.47339657G=CA1969333376MYBPC3c.2061C= (p.Ile687=)
c.2043C= (p.Ile681=)
11g.47339657G>TCA474217462MYBPC3c.2061C>A (p.Ile687=)
c.2043C>A (p.Ile681=)
11g.47339658_47339661dupCA913190275MYBPC3c.2058_2061dup (p.Thr688TyrfsTer6)
c.2040_2043dup (p.Thr682TyrfsTer6)
c.2058_2061dup (p.Thr688TyrfsTer7)
ClinVar dbSNP
11g.47339658A>CCA380321316MYBPC3c.2060T>G (p.Ile687Ser)
c.2042T>G (p.Ile681Ser)
11g.47339658A>GCA380321317MYBPC3c.2060T>C (p.Ile687Thr)
c.2042T>C (p.Ile681Thr)
11g.47339658A>TCA380321320MYBPC3c.2060T>A (p.Ile687Asn)
c.2042T>A (p.Ile681Asn)
11g.47339659T>ACA380321323MYBPC3c.2059A>T (p.Ile687Phe)
c.2041A>T (p.Ile681Phe)
11g.47339659T>CCA380321329MYBPC3c.2059A>G (p.Ile687Val)
c.2041A>G (p.Ile681Val)
11g.47339659T>GCA380321326MYBPC3c.2059A>C (p.Ile687Leu)
c.2041A>C (p.Ile681Leu)
11g.47339659_47339660delinsTACA1969333379MYBPC3c.2058_2059delinsTA (p.Ala686=)
c.2040_2041delinsTA (p.Ala680=)
11g.47339660delCA16619339MYBPC3c.2058del (p.Ile687SerfsTer?)
c.2040del (p.Ile681SerfsTer?)
ClinVar dbSNP
11g.47339660A>CCA474217467MYBPC3c.2058T>G (p.Ala686=)
c.2040T>G (p.Ala680=)
11g.47339660A>GCA474217469MYBPC3c.2058T>C (p.Ala686=)
c.2040T>C (p.Ala680=)
11g.47339660A>TCA474217471MYBPC3c.2058T>A (p.Ala686=)
c.2040T>A (p.Ala680=)
ClinVar
11g.47339661G>ACA380321333MYBPC3c.2057C>T (p.Ala686Val)
c.2039C>T (p.Ala680Val)
dbSNP gnomAD v3 gnomAD v4
11g.47339661G>CCA380321335MYBPC3c.2057C>G (p.Ala686Gly)
c.2039C>G (p.Ala680Gly)
11g.47339661G=CA1969333381MYBPC3c.2057C= (p.Ala686=)
c.2039C= (p.Ala680=)
11g.47339661G>TCA380321337MYBPC3c.2057C>A (p.Ala686Asp)
c.2039C>A (p.Ala680Asp)
11g.47339662C>ACA380321341MYBPC3c.2056G>T (p.Ala686Ser)
c.2038G>T (p.Ala680Ser)
gnomAD v4
11g.47339662C=CA1969333382MYBPC3c.2056G= (p.Ala686=)
c.2038G= (p.Ala680=)
11g.47339662C>GCA078493MYBPC3c.2056G>C (p.Ala686Pro)
c.2038G>C (p.Ala680Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47339662C>TCA078490MYBPC3c.2056G>A (p.Ala686Thr)
c.2038G>A (p.Ala680Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47339663C>ACA380321346MYBPC3c.2055G>T (p.Lys685Asn)
c.2037G>T (p.Lys679Asn)
11g.47339663C>GCA380321349MYBPC3c.2055G>C (p.Lys685Asn)
c.2037G>C (p.Lys679Asn)
11g.47339663C>TCA474217478MYBPC3c.2055G>A (p.Lys685=)
c.2037G>A (p.Lys679=)
11g.47339664T>ACA380321354MYBPC3c.2054A>T (p.Lys685Met)
c.2036A>T (p.Lys679Met)
11g.47339664T>CCA380321356MYBPC3c.2054A>G (p.Lys685Arg)
c.2036A>G (p.Lys679Arg)
11g.47339664T>GCA380321360MYBPC3c.2054A>C (p.Lys685Thr)
c.2036A>C (p.Lys679Thr)
11g.47339665T>ACA380321366MYBPC3c.2053A>T (p.Lys685Ter)
c.2035A>T (p.Lys679Ter)
11g.47339665T>CCA380321363MYBPC3c.2053A>G (p.Lys685Glu)
c.2035A>G (p.Lys679Glu)
11g.47339665T>GCA380321362MYBPC3c.2053A>C (p.Lys685Gln)
c.2035A>C (p.Lys679Gln)
11g.47339666C>ACA380321367MYBPC3c.2052G>T (p.Gln684His)
c.2034G>T (p.Gln678His)
11g.47339666C=CA1969333384MYBPC3c.2052G= (p.Gln684=)
c.2034G= (p.Gln678=)
11g.47339666C>GCA380321368MYBPC3c.2052G>C (p.Gln684His)
c.2034G>C (p.Gln678His)
11g.47339666C>TCA474217493MYBPC3c.2052G>A (p.Gln684=)
c.2034G>A (p.Gln678=)
dbSNP gnomAD v2 gnomAD v4
11g.47339667T>ACA380321369MYBPC3c.2051A>T (p.Gln684Leu)
c.2033A>T (p.Gln678Leu)
11g.47339667T>CCA380321371MYBPC3c.2051A>G (p.Gln684Arg)
c.2033A>G (p.Gln678Arg)
11g.47339667T>GCA380321370MYBPC3c.2051A>C (p.Gln684Pro)
c.2033A>C (p.Gln678Pro)
11g.47339668G>ACA380321374MYBPC3c.2050C>T (p.Gln684Ter)
c.2032C>T (p.Gln678Ter)
ClinVar gnomAD v4
11g.47339668G>CCA380321378MYBPC3c.2050C>G (p.Gln684Glu)
c.2032C>G (p.Gln678Glu)
11g.47339668G=CA1969333386MYBPC3c.2050C= (p.Gln684=)
c.2032C= (p.Gln678=)
11g.47339668G>TCA380321375MYBPC3c.2050C>A (p.Gln684Lys)
c.2032C>A (p.Gln678Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339669C>ACA380321381MYBPC3c.2049G>T (p.Trp683Cys)
c.2031G>T (p.Trp677Cys)
gnomAD v4
11g.47339669C>GCA380321386MYBPC3c.2049G>C (p.Trp683Cys)
c.2031G>C (p.Trp677Cys)
11g.47339669C>TCA380321383MYBPC3c.2049G>A (p.Trp683Ter)
c.2031G>A (p.Trp677Ter)
11g.47339670C>ACA380321389MYBPC3c.2048G>T (p.Trp683Leu)
c.2030G>T (p.Trp677Leu)
11g.47339670C=CA1969333388MYBPC3c.2048G= (p.Trp683=)
c.2030G= (p.Trp677=)
11g.47339670C>GCA380321394MYBPC3c.2048G>C (p.Trp683Ser)
c.2030G>C (p.Trp677Ser)
ClinVar dbSNP
11g.47339670C>TCA011693MYBPC3c.2048G>A (p.Trp683Ter)
c.2030G>A (p.Trp677Ter)
ClinVar dbSNP gnomAD v4
11g.47339671delCA2697548571MYBPC3c.2047del (p.Trp683GlyfsTer?)
c.2029del (p.Trp677GlyfsTer?)
ClinVar
11g.47339671A>CCA380321398MYBPC3c.2047T>G (p.Trp683Gly)
c.2029T>G (p.Trp677Gly)
11g.47339671A>GCA380321404MYBPC3c.2047T>C (p.Trp683Arg)
c.2029T>C (p.Trp677Arg)
11g.47339671A>TCA380321400MYBPC3c.2047T>A (p.Trp683Arg)
c.2029T>A (p.Trp677Arg)
ClinVar dbSNP
11g.47339672G>ACA048081MYBPC3c.2046C>T (p.Ile682=)
c.2028C>T (p.Ile676=)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47339672G>CCA380321407MYBPC3c.2046C>G (p.Ile682Met)
c.2028C>G (p.Ile676Met)
11g.47339672G=CA1969333390MYBPC3c.2046C= (p.Ile682=)
c.2028C= (p.Ile676=)
11g.47339672G>TCA474217514MYBPC3c.2046C>A (p.Ile682=)
c.2028C>A (p.Ile676=)
11g.47339673A>CCA380321418MYBPC3c.2045T>G (p.Ile682Ser)
c.2027T>G (p.Ile676Ser)
11g.47339673A>GCA380321413MYBPC3c.2045T>C (p.Ile682Thr)
c.2027T>C (p.Ile676Thr)
11g.47339673A>TCA380321416MYBPC3c.2045T>A (p.Ile682Asn)
c.2027T>A (p.Ile676Asn)
11g.47339674T>ACA380321421MYBPC3c.2044A>T (p.Ile682Phe)
c.2026A>T (p.Ile676Phe)
11g.47339674T>CCA380321423MYBPC3c.2044A>G (p.Ile682Val)
c.2026A>G (p.Ile676Val)
gnomAD v4
11g.47339674T>GCA380321424MYBPC3c.2044A>C (p.Ile682Leu)
c.2026A>C (p.Ile676Leu)
11g.47339675C>ACA474217523MYBPC3c.2043G>T (p.Val681=)
c.2025G>T (p.Val675=)
11g.47339675C=CA1969333391MYBPC3c.2043G= (p.Val681=)
c.2025G= (p.Val675=)
11g.47339675C>GCA474217527MYBPC3c.2043G>C (p.Val681=)
c.2025G>C (p.Val675=)
11g.47339675C>TCA474217525MYBPC3c.2043G>A (p.Val681=)
c.2025G>A (p.Val675=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47339676A>CCA380321428MYBPC3c.2042T>G (p.Val681Gly)
c.2024T>G (p.Val675Gly)
11g.47339676A>GCA380321429MYBPC3c.2042T>C (p.Val681Ala)
c.2024T>C (p.Val675Ala)
11g.47339676A>TCA380321433MYBPC3c.2042T>A (p.Val681Glu)
c.2024T>A (p.Val675Glu)
11g.47339677C>ACA380321435MYBPC3c.2041G>T (p.Val681Leu)
c.2023G>T (p.Val675Leu)
11g.47339677C=CA1969333393MYBPC3c.2041G= (p.Val681=)
c.2023G= (p.Val675=)
11g.47339677C>GCA380321440MYBPC3c.2041G>C (p.Val681Leu)
c.2023G>C (p.Val675Leu)
11g.47339677C>TCA078488MYBPC3c.2041G>A (p.Val681Met)
c.2023G>A (p.Val675Met)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47339678A>CCA048096MYBPC3c.2040T>G (p.Thr680=)
c.2022T>G (p.Thr674=)
11g.47339678A>GCA474217538MYBPC3c.2040T>C (p.Thr680=)
c.2022T>C (p.Thr674=)
ClinVar dbSNP
11g.47339678A>TCA474217541MYBPC3c.2040T>A (p.Thr680=)
c.2022T>A (p.Thr674=)
11g.47339678dupCA011684MYBPC3c.2040dup (p.Val681CysfsTer12)
c.2022dup (p.Val675CysfsTer12)
c.2040dup (p.Val681CysfsTer13)
ClinVar dbSNP
11g.47339679G>ACA380321446MYBPC3c.2039C>T (p.Thr680Ile)
c.2021C>T (p.Thr674Ile)
ClinVar dbSNP
11g.47339679G>CCA380321448MYBPC3c.2039C>G (p.Thr680Ser)
c.2021C>G (p.Thr674Ser)
11g.47339679G>TCA380321451MYBPC3c.2039C>A (p.Thr680Asn)
c.2021C>A (p.Thr674Asn)
11g.47339680T>ACA380321454MYBPC3c.2038A>T (p.Thr680Ser)
c.2020A>T (p.Thr674Ser)
11g.47339680T>CCA380321458MYBPC3c.2038A>G (p.Thr680Ala)
c.2020A>G (p.Thr674Ala)
11g.47339680T>GCA380321456MYBPC3c.2038A>C (p.Thr680Pro)
c.2020A>C (p.Thr674Pro)
11g.47339681G>ACA474217561MYBPC3c.2037C>T (p.Pro679=)
c.2019C>T (p.Pro673=)
11g.47339681G>CCA474217563MYBPC3c.2037C>G (p.Pro679=)
c.2019C>G (p.Pro673=)
11g.47339681G=CA1969333394MYBPC3c.2037C= (p.Pro679=)
c.2019C= (p.Pro673=)
11g.47339681G>TCA078486MYBPC3c.2037C>A (p.Pro679=)
c.2019C>A (p.Pro673=)
ClinVar dbSNP ExAC gnomAD v4
11g.47339682G>ACA380321463MYBPC3c.2036C>T (p.Pro679Leu)
c.2018C>T (p.Pro673Leu)
11g.47339682G>CCA380321466MYBPC3c.2036C>G (p.Pro679Arg)
c.2018C>G (p.Pro673Arg)
gnomAD v4
11g.47339682G>TCA380321469MYBPC3c.2036C>A (p.Pro679His)
c.2018C>A (p.Pro673His)
11g.47339683G>ACA011676MYBPC3c.2035C>T (p.Pro679Ser)
c.2017C>T (p.Pro673Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339683G>CCA380321473MYBPC3c.2035C>G (p.Pro679Ala)
c.2017C>G (p.Pro673Ala)
11g.47339683G=CA1969333397MYBPC3c.2035C= (p.Pro679=)
c.2017C= (p.Pro673=)
11g.47339683G>TCA380321476MYBPC3c.2035C>A (p.Pro679Thr)
c.2017C>A (p.Pro673Thr)
ClinVar dbSNP
11g.47339684A=CA1969333399MYBPC3c.2034T= (p.Ala678=)
c.2016T= (p.Ala672=)
11g.47339684A>CCA474217584MYBPC3c.2034T>G (p.Ala678=)
c.2016T>G (p.Ala672=)
11g.47339684A>GCA078484MYBPC3c.2034T>C (p.Ala678=)
c.2016T>C (p.Ala672=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47339684A>TCA474217581MYBPC3c.2034T>A (p.Ala678=)
c.2016T>A (p.Ala672=)
11g.47339685G>ACA380321481MYBPC3c.2033C>T (p.Ala678Val)
c.2015C>T (p.Ala672Val)
gnomAD v4
11g.47339685G>CCA380321483MYBPC3c.2033C>G (p.Ala678Gly)
c.2015C>G (p.Ala672Gly)
gnomAD v4
11g.47339685G=CA1969333401MYBPC3c.2033C= (p.Ala678=)
c.2015C= (p.Ala672=)
11g.47339685G>TCA078482MYBPC3c.2033C>A (p.Ala678Asp)
c.2015C>A (p.Ala672Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47339686C>ACA380321487MYBPC3c.2032G>T (p.Ala678Ser)
c.2014G>T (p.Ala672Ser)
11g.47339686C>GCA380321493MYBPC3c.2032G>C (p.Ala678Pro)
c.2014G>C (p.Ala672Pro)
11g.47339686C>TCA380321490MYBPC3c.2032G>A (p.Ala678Thr)
c.2014G>A (p.Ala672Thr)
ClinVar gnomAD v4
11g.47339689_47339697delCA2573051234MYBPC3c.2024_2032del (p.Gly675_Pro677del)
c.2006_2014del (p.Gly669_Pro671del)
11g.47339687A>CCA474217594MYBPC3c.2031T>G (p.Pro677=)
c.2013T>G (p.Pro671=)
11g.47339687A>GCA047965MYBPC3c.2031T>C (p.Pro677=)
c.2013T>C (p.Pro671=)
11g.47339687A>TCA474217599MYBPC3c.2031T>A (p.Pro677=)
c.2013T>A (p.Pro671=)
11g.47339688G>ACA011667MYBPC3c.2030C>T (p.Pro677Leu)
c.2012C>T (p.Pro671Leu)
ClinVar dbSNP gnomAD v4
11g.47339688G>CCA380321497MYBPC3c.2030C>G (p.Pro677Arg)
c.2012C>G (p.Pro671Arg)
11g.47339688G=CA1969333402MYBPC3c.2030C= (p.Pro677=)
c.2012C= (p.Pro671=)
11g.47339688G>TCA047956MYBPC3c.2030C>A (p.Pro677His)
c.2012C>A (p.Pro671His)
11g.47339689G>ACA221691171MYBPC3c.2029C>T (p.Pro677Ser)
c.2011C>T (p.Pro671Ser)
ClinVar dbSNP
11g.47339689G>CCA380321503MYBPC3c.2029C>G (p.Pro677Ala)
c.2011C>G (p.Pro671Ala)
11g.47339689G=CA1969333404MYBPC3c.2029C= (p.Pro677=)
c.2011C= (p.Pro671=)
11g.47339689G>TCA380321506MYBPC3c.2029C>A (p.Pro677Thr)
c.2011C>A (p.Pro671Thr)
11g.47339690G>ACA474217609MYBPC3c.2028C>T (p.Asp676=)
c.2010C>T (p.Asp670=)
11g.47339690G>CCA380321509MYBPC3c.2028C>G (p.Asp676Glu)
c.2010C>G (p.Asp670Glu)
11g.47339690G>TCA380321512MYBPC3c.2028C>A (p.Asp676Glu)
c.2010C>A (p.Asp670Glu)
11g.47339691T>ACA380321515MYBPC3c.2027A>T (p.Asp676Val)
c.2009A>T (p.Asp670Val)
ClinVar gnomAD v4
11g.47339691T>CCA380321519MYBPC3c.2027A>G (p.Asp676Gly)
c.2009A>G (p.Asp670Gly)
11g.47339691T>GCA380321521MYBPC3c.2027A>C (p.Asp676Ala)
c.2009A>C (p.Asp670Ala)
gnomAD v4
11g.47339692C>ACA221691177MYBPC3c.2026G>T (p.Asp676Tyr)
c.2008G>T (p.Asp670Tyr)
dbSNP gnomAD v3 gnomAD v4
11g.47339692C=CA1969333406MYBPC3c.2026G= (p.Asp676=)
c.2008G= (p.Asp670=)
11g.47339692C>GCA380321527MYBPC3c.2026G>C (p.Asp676His)
c.2008G>C (p.Asp670His)
11g.47339692C>TCA380321524MYBPC3c.2026G>A (p.Asp676Asn)
c.2008G>A (p.Asp670Asn)
11g.47339695dupCA2724175940MYBPC3c.2026dup (p.Asp676GlyfsTer17)
c.2008dup (p.Asp670GlyfsTer17)
c.2026dup (p.Asp676GlyfsTer18)
dbSNP
11g.47339694_47339695delCA2573051153MYBPC3c.2025_2026del (p.Asp676ProfsTer16)
c.2007_2008del (p.Asp670ProfsTer16)
c.2025_2026del (p.Asp676ProfsTer17)
11g.47339693C>ACA474217623MYBPC3c.2025G>T (p.Gly675=)
c.2007G>T (p.Gly669=)
11g.47339693C=CA1969333408MYBPC3c.2025G= (p.Gly675=)
c.2007G= (p.Gly669=)
11g.47339693C>GCA474217625MYBPC3c.2025G>C (p.Gly675=)
c.2007G>C (p.Gly669=)
ClinVar dbSNP
11g.47339693C>TCA474217626MYBPC3c.2025G>A (p.Gly675=)
c.2007G>A (p.Gly669=)
11g.47339694C>ACA380321532MYBPC3c.2024G>T (p.Gly675Val)
c.2006G>T (p.Gly669Val)
11g.47339694C>GCA380321535MYBPC3c.2024G>C (p.Gly675Ala)
c.2006G>C (p.Gly669Ala)
11g.47339694C>TCA380321537MYBPC3c.2024G>A (p.Gly675Glu)
c.2006G>A (p.Gly669Glu)
ClinVar dbSNP COSMIC COSMIC
11g.47339695C>ACA380321538MYBPC3c.2023G>T (p.Gly675Trp)
c.2005G>T (p.Gly669Trp)
11g.47339695C>GCA380321539MYBPC3c.2023G>C (p.Gly675Arg)
c.2005G>C (p.Gly669Arg)
11g.47339695C>TCA380321540MYBPC3c.2023G>A (p.Gly675Arg)
c.2005G>A (p.Gly669Arg)
ClinVar
11g.47339696A>CCA474217637MYBPC3c.2022T>G (p.Ser674=)
c.2004T>G (p.Ser668=)
11g.47339696A>GCA474217639MYBPC3c.2022T>C (p.Ser674=)
c.2004T>C (p.Ser668=)
gnomAD v4
11g.47339696A>TCA474217638MYBPC3c.2022T>A (p.Ser674=)
c.2004T>A (p.Ser668=)
11g.47339697G>ACA380321541MYBPC3c.2021C>T (p.Ser674Phe)
c.2003C>T (p.Ser668Phe)
11g.47339697G>CCA380321542MYBPC3c.2021C>G (p.Ser674Cys)
c.2003C>G (p.Ser668Cys)
ClinVar dbSNP
11g.47339697G=CA1969333410MYBPC3c.2021C= (p.Ser674=)
c.2003C= (p.Ser668=)
11g.47339697G>TCA380321543MYBPC3c.2021C>A (p.Ser674Tyr)
c.2003C>A (p.Ser668Tyr)
11g.47339698A>CCA380321544MYBPC3c.2020T>G (p.Ser674Ala)
c.2002T>G (p.Ser668Ala)
11g.47339698A>GCA380321546MYBPC3c.2020T>C (p.Ser674Pro)
c.2002T>C (p.Ser668Pro)
11g.47339698A>TCA380321549MYBPC3c.2020T>A (p.Ser674Thr)
c.2002T>A (p.Ser668Thr)
11g.47339699G>ACA078479MYBPC3c.2019C>T (p.Ile673=)
c.2001C>T (p.Ile667=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47339699G>CCA221691182MYBPC3c.2019C>G (p.Ile673Met)
c.2001C>G (p.Ile667Met)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339699G=CA1969333412MYBPC3c.2019C= (p.Ile673=)
c.2001C= (p.Ile667=)
11g.47339699G>TCA474217642MYBPC3c.2019C>A (p.Ile673=)
c.2001C>A (p.Ile667=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47339700A=CA1969333414MYBPC3c.2018T= (p.Ile673=)
c.2000T= (p.Ile667=)
11g.47339700A>CCA380321554MYBPC3c.2018T>G (p.Ile673Ser)
c.2000T>G (p.Ile667Ser)
11g.47339700A>GCA078477MYBPC3c.2018T>C (p.Ile673Thr)
c.2000T>C (p.Ile667Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47339700A>TCA380321556MYBPC3c.2018T>A (p.Ile673Asn)
c.2000T>A (p.Ile667Asn)
11g.47339701T>ACA380321560MYBPC3c.2017A>T (p.Ile673Phe)
c.1999A>T (p.Ile667Phe)
11g.47339701T>CCA380321562MYBPC3c.2017A>G (p.Ile673Val)
c.1999A>G (p.Ile667Val)
gnomAD v4
11g.47339701T>GCA380321565MYBPC3c.2017A>C (p.Ile673Leu)
c.1999A>C (p.Ile667Leu)
11g.47339701_47339703delinsTAGCA1969333415MYBPC3c.2015_2017delinsCTA (p.Pro672=)
c.1997_1999delinsCTA (p.Pro666=)
11g.47339701_47339705delinsTAGGGCA1969333416MYBPC3c.2013_2017delinsCCCTA (p.Val671=)
c.1995_1999delinsCCCTA (p.Val665=)
11g.47339702A=CA1969333420MYBPC3c.2016T= (p.Pro672=)
c.1998T= (p.Pro666=)
11g.47339702A>CCA474217651MYBPC3c.2016T>G (p.Pro672=)
c.1998T>G (p.Pro666=)
dbSNP
11g.47339702A>GCA078474MYBPC3c.2016T>C (p.Pro672=)
c.1998T>C (p.Pro666=)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47339702A>TCA474217655MYBPC3c.2016T>A (p.Pro672=)
c.1998T>A (p.Pro666=)
11g.47339702_47339703delCA676997349MYBPC3c.2015_2016del (p.Pro672HisfsTer20)
c.1997_1998del (p.Pro666HisfsTer20)
c.2015_2016del (p.Pro672HisfsTer21)
dbSNP
11g.47339702_47339705delinsCCCA011652MYBPC3c.2013_2016delinsGG (p.Pro672AspfsTer20)
c.1995_1998delinsGG (p.Pro666AspfsTer20)
c.2013_2016delinsGG (p.Pro672AspfsTer21)
ClinVar dbSNP
11g.47339703_47339706delCA937669959MYBPC3c.2013_2016del (p.Pro672SerfsTer9)
c.1995_1998del (p.Pro666SerfsTer9)
dbSNP gnomAD v3 gnomAD v4
11g.47339703G>ACA380321575MYBPC3c.2015C>T (p.Pro672Leu)
c.1997C>T (p.Pro666Leu)
11g.47339703G>CCA380321577MYBPC3c.2015C>G (p.Pro672Arg)
c.1997C>G (p.Pro666Arg)
11g.47339703G>TCA380321579MYBPC3c.2015C>A (p.Pro672His)
c.1997C>A (p.Pro666His)
11g.47339705delCA2580084196MYBPC3c.2015del (p.Pro672LeufsTer10)
c.1997del (p.Pro666LeufsTer10)
ClinVar
11g.47339704G>ACA380321583MYBPC3c.2014C>T (p.Pro672Ser)
c.1996C>T (p.Pro666Ser)
ClinVar gnomAD v4
11g.47339704G>CCA380321585MYBPC3c.2014C>G (p.Pro672Ala)
c.1996C>G (p.Pro666Ala)
dbSNP
11g.47339704G=CA1969333422MYBPC3c.2014C= (p.Pro672=)
c.1996C= (p.Pro666=)
11g.47339704G>TCA380321589MYBPC3c.2014C>A (p.Pro672Thr)
c.1996C>A (p.Pro666Thr)
11g.47339705G>ACA474217667MYBPC3c.2013C>T (p.Val671=)
c.1995C>T (p.Val665=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339705G>CCA474217666MYBPC3c.2013C>G (p.Val671=)
c.1995C>G (p.Val665=)
dbSNP
11g.47339705G=CA1969333423MYBPC3c.2013C= (p.Val671=)
c.1995C= (p.Val665=)
11g.47339705G>TCA474217664MYBPC3c.2013C>A (p.Val671=)
c.1995C>A (p.Val665=)
11g.47339705_47339706insCCCA937669977MYBPC3c.2012_2013insGG (p.Pro672AlafsTer11)
c.1994_1995insGG (p.Pro666AlafsTer11)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47339706A>CCA380321598MYBPC3c.2012T>G (p.Val671Gly)
c.1994T>G (p.Val665Gly)
11g.47339706A>GCA380321595MYBPC3c.2012T>C (p.Val671Ala)
c.1994T>C (p.Val665Ala)
11g.47339706A>TCA380321593MYBPC3c.2012T>A (p.Val671Asp)
c.1994T>A (p.Val665Asp)
11g.47339707C>ACA380321601MYBPC3c.2011G>T (p.Val671Phe)
c.1993G>T (p.Val665Phe)
ClinVar dbSNP
11g.47339707C=CA1969333425MYBPC3c.2011G= (p.Val671=)
c.1993G= (p.Val665=)
11g.47339707C>GCA380321604MYBPC3c.2011G>C (p.Val671Leu)
c.1993G>C (p.Val665Leu)
11g.47339707C>TCA10576889MYBPC3c.2011G>A (p.Val671Ile)
c.1993G>A (p.Val665Ile)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339708G>ACA078472MYBPC3c.2010C>T (p.Asp670=)
c.1992C>T (p.Asp664=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47339708G>CCA380321609MYBPC3c.2010C>G (p.Asp670Glu)
c.1992C>G (p.Asp664Glu)
11g.47339708G=CA1969333428MYBPC3c.2010C= (p.Asp670=)
c.1992C= (p.Asp664=)
11g.47339708G>TCA380321613MYBPC3c.2010C>A (p.Asp670Glu)
c.1992C>A (p.Asp664Glu)
gnomAD v4
11g.47339709T>ACA380321616MYBPC3c.2009A>T (p.Asp670Val)
c.1991A>T (p.Asp664Val)
11g.47339709T>CCA380321619MYBPC3c.2009A>G (p.Asp670Gly)
c.1991A>G (p.Asp664Gly)
11g.47339709T>GCA380321622MYBPC3c.2009A>C (p.Asp670Ala)
c.1991A>C (p.Asp664Ala)
11g.47339710C>ACA380321626MYBPC3c.2008G>T (p.Asp670Tyr)
c.1990G>T (p.Asp664Tyr)
gnomAD v4
11g.47339710C>GCA380321628MYBPC3c.2008G>C (p.Asp670His)
c.1990G>C (p.Asp664His)
11g.47339710C>TCA380321631MYBPC3c.2008G>A (p.Asp670Asn)
c.1990G>A (p.Asp664Asn)
11g.47339711C>ACA474217685MYBPC3c.2007G>T (p.Leu669=)
c.1989G>T (p.Leu663=)
11g.47339711C>GCA474217687MYBPC3c.2007G>C (p.Leu669=)
c.1989G>C (p.Leu663=)
11g.47339711C>TCA474217689MYBPC3c.2007G>A (p.Leu669=)
c.1989G>A (p.Leu663=)
gnomAD v4
11g.47339712A>CCA380321644MYBPC3c.2006T>G (p.Leu669Arg)
c.1988T>G (p.Leu663Arg)
11g.47339712A>GCA380321642MYBPC3c.2006T>C (p.Leu669Pro)
c.1988T>C (p.Leu663Pro)
11g.47339712A>TCA380321635MYBPC3c.2006T>A (p.Leu669Gln)
c.1988T>A (p.Leu663Gln)
11g.47339713G>ACA474217695MYBPC3c.2005C>T (p.Leu669=)
c.1987C>T (p.Leu663=)
11g.47339713G>CCA380321647MYBPC3c.2005C>G (p.Leu669Val)
c.1987C>G (p.Leu663Val)
dbSNP gnomAD v3 gnomAD v4
11g.47339713G=CA1969333431MYBPC3c.2005C= (p.Leu669=)
c.1987C= (p.Leu663=)
11g.47339713G>TCA380321650MYBPC3c.2005C>A (p.Leu669Met)
c.1987C>A (p.Leu663Met)
ClinVar dbSNP
11g.47339714A=CA1969333433MYBPC3c.2004T= (p.Arg668=)
c.1986T= (p.Arg662=)
11g.47339714A>CCA474217700MYBPC3c.2004T>G (p.Arg668=)
c.1986T>G (p.Arg662=)
11g.47339714A>GCA474217702MYBPC3c.2004T>C (p.Arg668=)
c.1986T>C (p.Arg662=)
dbSNP gnomAD v3 gnomAD v4
11g.47339714A>TCA474217704MYBPC3c.2004T>A (p.Arg668=)
c.1986T>A (p.Arg662=)
dbSNP
11g.47339715C>ACA380321653MYBPC3c.2003G>T (p.Arg668Leu)
c.1985G>T (p.Arg662Leu)
11g.47339715C=CA1969333436MYBPC3c.2003G= (p.Arg668=)
c.1985G= (p.Arg662=)
11g.47339715C>GCA380321656MYBPC3c.2003G>C (p.Arg668Pro)
c.1985G>C (p.Arg662Pro)
ClinVar dbSNP
11g.47339715C>TCA011643MYBPC3c.2003G>A (p.Arg668His)
c.1985G>A (p.Arg662His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47339715dupCA891842475MYBPC3c.2003dup (p.Leu669SerfsTer24)
c.1985dup (p.Leu663SerfsTer24)
c.2003dup (p.Leu669SerfsTer25)
ClinVar dbSNP
11g.47339716G>ACA011634MYBPC3c.2002C>T (p.Arg668Cys)
c.1984C>T (p.Arg662Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47339716G>CCA380321663MYBPC3c.2002C>G (p.Arg668Gly)
c.1984C>G (p.Arg662Gly)
11g.47339716G=CA1969333438MYBPC3c.2002C= (p.Arg668=)
c.1984C= (p.Arg662=)
11g.47339716G>TCA380321666MYBPC3c.2002C>A (p.Arg668Ser)
c.1984C>A (p.Arg662Ser)
11g.47339717T>ACA474217713MYBPC3c.2001A>T (p.Leu667=)
c.1983A>T (p.Leu661=)
11g.47339717T>CCA474217715MYBPC3c.2001A>G (p.Leu667=)
c.1983A>G (p.Leu661=)
ClinVar dbSNP gnomAD v4
11g.47339717T>GCA474217718MYBPC3c.2001A>C (p.Leu667=)
c.1983A>C (p.Leu661=)
11g.47339717T=CA1969333441MYBPC3c.2001A= (p.Leu667=)
c.1983A= (p.Leu661=)
11g.47339717_47339718delinsTACA1969333440MYBPC3c.2000_2001delinsTA (p.Leu667=)
c.1982_1983delinsTA (p.Leu661=)
11g.47339717_47339719delinsTAGCA1969333442MYBPC3c.1999_2001delinsCTA (p.Leu667=)
c.1981_1983delinsCTA (p.Leu661=)
11g.47339718delCA599374383MYBPC3c.2000del (p.Leu667HisfsTer15)
c.1982del (p.Leu661HisfsTer15)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339718A>CCA380321670MYBPC3c.2000T>G (p.Leu667Arg)
c.1982T>G (p.Leu661Arg)
dbSNP
11g.47339718A>GCA380321672MYBPC3c.2000T>C (p.Leu667Pro)
c.1982T>C (p.Leu661Pro)
11g.47339718A>TCA380321675MYBPC3c.2000T>A (p.Leu667Gln)
c.1982T>A (p.Leu661Gln)
11g.47339718_47339719delCA2573051164MYBPC3c.1999_2000del (p.Leu667ThrfsTer25)
c.1981_1982del (p.Leu661ThrfsTer25)
c.1999_2000del (p.Leu667ThrfsTer26)
11g.47339718_47339719delinsCCA011614MYBPC3c.1999_2000delinsG (p.Leu667AspfsTer15)
c.1981_1982delinsG (p.Leu661AspfsTer15)
ClinVar dbSNP
11g.47339718_47339719delinsTCA011607MYBPC3c.1999_2000delinsA (p.Leu667AsnfsTer15)
c.1981_1982delinsA (p.Leu661AsnfsTer15)
dbSNP
11g.47339719G>ACA047863MYBPC3c.1999C>T (p.Leu667=)
c.1981C>T (p.Leu661=)
dbSNP
11g.47339719G>CCA380321683MYBPC3c.1999C>G (p.Leu667Val)
c.1981C>G (p.Leu661Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47339719G=CA1969333447MYBPC3c.1999C= (p.Leu667=)
c.1981C= (p.Leu661=)
11g.47339719G>TCA078466MYBPC3c.1999C>A (p.Leu667Ile)
c.1981C>A (p.Leu661Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47339720C>ACA380321686MYBPC3c.1998G>T (p.Lys666Asn)
c.1980G>T (p.Lys660Asn)
11g.47339720C>GCA380321688MYBPC3c.1998G>C (p.Lys666Asn)
c.1980G>C (p.Lys660Asn)
11g.47339720C>TCA474217744MYBPC3c.1998G>A (p.Lys666=)
c.1980G>A (p.Lys660=)
11g.47339721T>ACA380321691MYBPC3c.1997A>T (p.Lys666Met)
c.1979A>T (p.Lys660Met)
dbSNP
11g.47339721T>CCA380321694MYBPC3c.1997A>G (p.Lys666Arg)
c.1979A>G (p.Lys660Arg)
11g.47339721T>GCA380321697MYBPC3c.1997A>C (p.Lys666Thr)
c.1979A>C (p.Lys660Thr)
11g.47339721T=CA1969333448MYBPC3c.1997A= (p.Lys666=)
c.1979A= (p.Lys660=)
11g.47339722T>ACA380321700MYBPC3c.1996A>T (p.Lys666Ter)
c.1978A>T (p.Lys660Ter)
11g.47339722T>CCA380321702MYBPC3c.1996A>G (p.Lys666Glu)
c.1978A>G (p.Lys660Glu)
11g.47339722T>GCA380321705MYBPC3c.1996A>C (p.Lys666Gln)
c.1978A>C (p.Lys660Gln)

Number of alleles fetched