Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47341142G>ACA474218147MYBPC3c.1893C>T (p.Phe631=)
c.1875C>T (p.Phe625=)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47341142G>CCA380323567MYBPC3c.1893C>G (p.Phe631Leu)
c.1875C>G (p.Phe625Leu)
11g.47341142G=CA1969334604MYBPC3c.1893C= (p.Phe631=)
c.1875C= (p.Phe625=)
11g.47341142G>TCA380323570MYBPC3c.1893C>A (p.Phe631Leu)
c.1875C>A (p.Phe625Leu)
gnomAD v4 COSMIC COSMIC
11g.47341142_47341143delinsGACA1969334605MYBPC3c.1892_1893delinsTC (p.Phe631=)
c.1874_1875delinsTC (p.Phe625=)
11g.47341143A>CCA380323573MYBPC3c.1892T>G (p.Phe631Cys)
c.1874T>G (p.Phe625Cys)
11g.47341143A>GCA380323580MYBPC3c.1892T>C (p.Phe631Ser)
c.1874T>C (p.Phe625Ser)
11g.47341143A>TCA380323582MYBPC3c.1892T>A (p.Phe631Tyr)
c.1874T>A (p.Phe625Tyr)
gnomAD v4
11g.47341144delCA011401MYBPC3c.1892del (p.Phe631SerfsTer?)
c.1874del (p.Phe625SerfsTer?)
ClinVar dbSNP
11g.47341144A>CCA380323607MYBPC3c.1891T>G (p.Phe631Val)
c.1873T>G (p.Phe625Val)
11g.47341144A>GCA380323604MYBPC3c.1891T>C (p.Phe631Leu)
c.1873T>C (p.Phe625Leu)
11g.47341144A>TCA380323585MYBPC3c.1891T>A (p.Phe631Ile)
c.1873T>A (p.Phe625Ile)
11g.47341144_47341145delinsAGCA1969334607MYBPC3c.1890_1891delinsCT (p.His630=)
c.1872_1873delinsCT (p.His624=)
11g.47341145delCA913190278MYBPC3c.1890del (p.Phe631SerfsTer?)
c.1872del (p.Phe625SerfsTer?)
ClinVar dbSNP
11g.47341145G>ACA474218153MYBPC3c.1890C>T (p.His630=)
c.1872C>T (p.His624=)
gnomAD v4
11g.47341145G>CCA380323609MYBPC3c.1890C>G (p.His630Gln)
c.1872C>G (p.His624Gln)
gnomAD v4
11g.47341145G>TCA380323612MYBPC3c.1890C>A (p.His630Gln)
c.1872C>A (p.His624Gln)
11g.47341146T>ACA078356MYBPC3c.1889A>T (p.His630Leu)
c.1871A>T (p.His624Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341146T>CCA380323618MYBPC3c.1889A>G (p.His630Arg)
c.1871A>G (p.His624Arg)
gnomAD v4
11g.47341146T>GCA380323619MYBPC3c.1889A>C (p.His630Pro)
c.1871A>C (p.His624Pro)
11g.47341146T=CA1969334610MYBPC3c.1889A= (p.His630=)
c.1871A= (p.His624=)
11g.47341147G>ACA380323621MYBPC3c.1888C>T (p.His630Tyr)
c.1870C>T (p.His624Tyr)
dbSNP gnomAD v4
11g.47341147G>CCA380323625MYBPC3c.1888C>G (p.His630Asp)
c.1870C>G (p.His624Asp)
gnomAD v4
11g.47341147G=CA1969334611MYBPC3c.1888C= (p.His630=)
c.1870C= (p.His624=)
11g.47341147G>TCA380323628MYBPC3c.1888C>A (p.His630Asn)
c.1870C>A (p.His624Asn)
11g.47341148G>ACA474218157MYBPC3c.1887C>T (p.Leu629=)
c.1869C>T (p.Leu623=)
dbSNP gnomAD v2 gnomAD v4
11g.47341148G>CCA474218156MYBPC3c.1887C>G (p.Leu629=)
c.1869C>G (p.Leu623=)
11g.47341148G=CA1969334613MYBPC3c.1887C= (p.Leu629=)
c.1869C= (p.Leu623=)
11g.47341148G>TCA474218155MYBPC3c.1887C>A (p.Leu629=)
c.1869C>A (p.Leu623=)
gnomAD v4
11g.47341149_47341205dupCA2573147067MYBPC3c.1831_1887dup (p.Leu629_His630insGluAlaAspTyrSerPheValProGluGlyPheAlaCysAsnLeuSerAlaLysLeu)
c.1813_1869dup (p.Leu623_His624insGluAlaAspTyrSerPheValProGluGlyPheAlaCysAsnLeuSerAlaLysLeu)
ClinVar dbSNP
11g.47341149A=CA1969334615MYBPC3c.1886T= (p.Leu629=)
c.1868T= (p.Leu623=)
11g.47341149A>CCA380323630MYBPC3c.1886T>G (p.Leu629Arg)
c.1868T>G (p.Leu623Arg)
11g.47341149A>GCA011389MYBPC3c.1886T>C (p.Leu629Pro)
c.1868T>C (p.Leu623Pro)
ClinVar dbSNP gnomAD v4
11g.47341149A>TCA380323633MYBPC3c.1886T>A (p.Leu629His)
c.1868T>A (p.Leu623His)
11g.47341150G>ACA380323641MYBPC3c.1885C>T (p.Leu629Phe)
c.1867C>T (p.Leu623Phe)
ClinVar
11g.47341150G>CCA380323639MYBPC3c.1885C>G (p.Leu629Val)
c.1867C>G (p.Leu623Val)
11g.47341150G>TCA380323636MYBPC3c.1885C>A (p.Leu629Ile)
c.1867C>A (p.Leu623Ile)
gnomAD v4
11g.47341151C>ACA380323646MYBPC3c.1884G>T (p.Lys628Asn)
c.1866G>T (p.Lys622Asn)
gnomAD v4
11g.47341151C=CA1969334617MYBPC3c.1884G= (p.Lys628=)
c.1866G= (p.Lys622=)
11g.47341151C>GCA380323648MYBPC3c.1884G>C (p.Lys628Asn)
c.1866G>C (p.Lys622Asn)
11g.47341151C>TCA474218161MYBPC3c.1884G>A (p.Lys628=)
c.1866G>A (p.Lys622=)
ClinVar dbSNP
11g.47341152T>ACA380323654MYBPC3c.1883A>T (p.Lys628Met)
c.1865A>T (p.Lys622Met)
gnomAD v4
11g.47341152T>CCA380323656MYBPC3c.1883A>G (p.Lys628Arg)
c.1865A>G (p.Lys622Arg)
gnomAD v4
11g.47341152T>GCA380323659MYBPC3c.1883A>C (p.Lys628Thr)
c.1865A>C (p.Lys622Thr)
11g.47341153T>ACA380323661MYBPC3c.1882A>T (p.Lys628Ter)
c.1864A>T (p.Lys622Ter)
11g.47341153T>CCA380323663MYBPC3c.1882A>G (p.Lys628Glu)
c.1864A>G (p.Lys622Glu)
11g.47341153T>GCA380323666MYBPC3c.1882A>C (p.Lys628Gln)
c.1864A>C (p.Lys622Gln)
11g.47341154G>ACA474218163MYBPC3c.1881C>T (p.Ala627=)
c.1863C>T (p.Ala621=)
11g.47341154G>CCA474218164MYBPC3c.1881C>G (p.Ala627=)
c.1863C>G (p.Ala621=)
dbSNP
11g.47341154G=CA1969334619MYBPC3c.1881C= (p.Ala627=)
c.1863C= (p.Ala621=)
11g.47341154G>TCA474218165MYBPC3c.1881C>A (p.Ala627=)
c.1863C>A (p.Ala621=)
ClinVar dbSNP gnomAD v4
11g.47341154_47341156delCA2613398141MYBPC3c.1879_1881del (p.Ala627del)
c.1861_1863del (p.Ala621del)
gnomAD v4
11g.47341154_47341155insTTTTTTTTTTTAATCA2613398152MYBPC3c.1880_1881insATTAAAAAAAAAAA (p.Lys628LeufsTer?)
c.1862_1863insATTAAAAAAAAAAA (p.Lys622LeufsTer?)
gnomAD v4
11g.47341155G>ACA380323669MYBPC3c.1880C>T (p.Ala627Val)
c.1862C>T (p.Ala621Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47341155G>CCA380323672MYBPC3c.1880C>G (p.Ala627Gly)
c.1862C>G (p.Ala621Gly)
ClinVar dbSNP
11g.47341155G=CA1969334621MYBPC3c.1880C= (p.Ala627=)
c.1862C= (p.Ala621=)
11g.47341155G>TCA380323674MYBPC3c.1880C>A (p.Ala627Asp)
c.1862C>A (p.Ala621Asp)
gnomAD v4
11g.47341155_47341156insTTTTTTTTTTACA2613398161MYBPC3c.1879_1880insTAAAAAAAAAA (p.Ala627ValfsTer?)
c.1861_1862insTAAAAAAAAAA (p.Ala621ValfsTer?)
gnomAD v4
11g.47341155_47341156insTTTTTTTTTTTACA2791323288MYBPC3c.1879_1880insTAAAAAAAAAAA (p.Ala627delinsValLysLysLysThr)
c.1861_1862insTAAAAAAAAAAA (p.Ala621delinsValLysLysLysThr)
11g.47341156C>ACA380323684MYBPC3c.1879G>T (p.Ala627Ser)
c.1861G>T (p.Ala621Ser)
gnomAD v4
11g.47341156C=CA1969334622MYBPC3c.1879G= (p.Ala627=)
c.1861G= (p.Ala621=)
11g.47341156C>GCA380323680MYBPC3c.1879G>C (p.Ala627Pro)
c.1861G>C (p.Ala621Pro)
11g.47341156C>TCA380323678MYBPC3c.1879G>A (p.Ala627Thr)
c.1861G>A (p.Ala621Thr)
dbSNP gnomAD v3 gnomAD v4
11g.47341157T>ACA474218167MYBPC3c.1878A>T (p.Ser626=)
c.1860A>T (p.Ser620=)
dbSNP COSMIC COSMIC
11g.47341157T>CCA474218168MYBPC3c.1878A>G (p.Ser626=)
c.1860A>G (p.Ser620=)
11g.47341157T>GCA474218169MYBPC3c.1878A>C (p.Ser626=)
c.1860A>C (p.Ser620=)
11g.47341157T=CA1969334624MYBPC3c.1878A= (p.Ser626=)
c.1860A= (p.Ser620=)
11g.47341157_47341158insTATTTTTTAATCA2613398166MYBPC3c.1878_1879insTTAAAAAATAA (p.Ala627LeufsTer?)
c.1860_1861insTTAAAAAATAA (p.Ala621LeufsTer?)
gnomAD v4
11g.47341157_47341158insTTTTTTTTAATCA2791323290MYBPC3c.1878_1879insTTAAAAAAAAA (p.Ala627LeufsTer?)
c.1860_1861insTTAAAAAAAAA (p.Ala621LeufsTer?)
11g.47341158delCA2791323291MYBPC3c.1877del (p.Ser626Ter)
c.1859del (p.Ser620Ter)
11g.47341158G>ACA380323686MYBPC3c.1877C>T (p.Ser626Leu)
c.1859C>T (p.Ser620Leu)
gnomAD v4
11g.47341158G>CCA380323690MYBPC3c.1877C>G (p.Ser626Ter)
c.1859C>G (p.Ser620Ter)
ClinVar
11g.47341158G>TCA380323691MYBPC3c.1877C>A (p.Ser626Ter)
c.1859C>A (p.Ser620Ter)
gnomAD v4
11g.47341159A>CCA380323693MYBPC3c.1876T>G (p.Ser626Ala)
c.1858T>G (p.Ser620Ala)
11g.47341159A>GCA380323696MYBPC3c.1876T>C (p.Ser626Pro)
c.1858T>C (p.Ser620Pro)
11g.47341159A>TCA380323697MYBPC3c.1876T>A (p.Ser626Thr)
c.1858T>A (p.Ser620Thr)
gnomAD v4
11g.47341159_47341163delinsACAGGCA1969334625MYBPC3c.1872_1876delinsCCTGT (p.Asn624=)
c.1854_1858delinsCCTGT (p.Asn618=)
11g.47341160C>ACA474218172MYBPC3c.1875G>T (p.Leu625=)
c.1857G>T (p.Leu619=)
gnomAD v4
11g.47341160C=CA1969334628MYBPC3c.1875G= (p.Leu625=)
c.1857G= (p.Leu619=)
11g.47341160C>GCA474218173MYBPC3c.1875G>C (p.Leu625=)
c.1857G>C (p.Leu619=)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47341160C>TCA474218174MYBPC3c.1875G>A (p.Leu625=)
c.1857G>A (p.Leu619=)
dbSNP gnomAD v2 gnomAD v4
11g.47341160_47341162delCA2613398190MYBPC3c.1873_1875del (p.Leu625del)
c.1855_1857del (p.Leu619del)
gnomAD v4
11g.47341160_47341163delCA599374428MYBPC3c.1872_1875del (p.Leu625GlnfsTer?)
c.1854_1857del (p.Leu619GlnfsTer?)
dbSNP gnomAD v2 gnomAD v4
11g.47341160_47341164delCA2613398189MYBPC3c.1871_1875del (p.Asn624IlefsTer12)
c.1853_1857del (p.Asn618IlefsTer12)
gnomAD v4
11g.47341160_47341161insTTTTTACA2613398199MYBPC3c.1874_1875insTAAAAA (p.Leu625_Ser626insLysLys)
c.1856_1857insTAAAAA (p.Leu619_Ser620insLysLys)
gnomAD v4
11g.47341161A>CCA380323700MYBPC3c.1874T>G (p.Leu625Arg)
c.1856T>G (p.Leu619Arg)
gnomAD v4
11g.47341161A>GCA380323702MYBPC3c.1874T>C (p.Leu625Pro)
c.1856T>C (p.Leu619Pro)
gnomAD v4
11g.47341161A>TCA380323704MYBPC3c.1874T>A (p.Leu625Gln)
c.1856T>A (p.Leu619Gln)
gnomAD v4
11g.47341161_47341163delCA2613398200MYBPC3c.1872_1874del (p.Asn624_Leu625delinsLys)
c.1854_1856del (p.Asn618_Leu619delinsLys)
gnomAD v4
11g.47341161_47341168delCA2613398201MYBPC3c.1867_1874del (p.Cys623ValfsTer12)
c.1849_1856del (p.Cys617ValfsTer12)
gnomAD v4
11g.47341162G>ACA474218175MYBPC3c.1873C>T (p.Leu625=)
c.1855C>T (p.Leu619=)
gnomAD v4
11g.47341162G>CCA380323706MYBPC3c.1873C>G (p.Leu625Val)
c.1855C>G (p.Leu619Val)
11g.47341162G>TCA380323709MYBPC3c.1873C>A (p.Leu625Met)
c.1855C>A (p.Leu619Met)
gnomAD v4
11g.47341162_47341163delCA2613398207MYBPC3c.1872_1873del (p.Leu625ValfsTer12)
c.1854_1855del (p.Leu619ValfsTer12)
gnomAD v4
11g.47341163G>ACA474218176MYBPC3c.1872C>T (p.Asn624=)
c.1854C>T (p.Asn618=)
11g.47341163G>CCA380323712MYBPC3c.1872C>G (p.Asn624Lys)
c.1854C>G (p.Asn618Lys)
11g.47341163G>TCA380323714MYBPC3c.1872C>A (p.Asn624Lys)
c.1854C>A (p.Asn618Lys)
gnomAD v4
11g.47341164T>ACA380323723MYBPC3c.1871A>T (p.Asn624Ile)
c.1853A>T (p.Asn618Ile)
gnomAD v4
11g.47341164T>CCA078354MYBPC3c.1871A>G (p.Asn624Ser)
c.1853A>G (p.Asn618Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341164T>GCA380323718MYBPC3c.1871A>C (p.Asn624Thr)
c.1853A>C (p.Asn618Thr)
11g.47341164T=CA1969334630MYBPC3c.1871A= (p.Asn624=)
c.1853A= (p.Asn618=)
11g.47341165T>ACA380323728MYBPC3c.1870A>T (p.Asn624Tyr)
c.1852A>T (p.Asn618Tyr)
11g.47341165T>CCA380323726MYBPC3c.1870A>G (p.Asn624Asp)
c.1852A>G (p.Asn618Asp)
gnomAD v4
11g.47341165T>GCA380323731MYBPC3c.1870A>C (p.Asn624His)
c.1852A>C (p.Asn618His)
11g.47341165_47341166insTTTACTCA2613398223MYBPC3c.1870_1871insGTAAAA (p.Cys623_Asn624insSerLys)
c.1852_1853insGTAAAA (p.Cys617_Asn618insSerLys)
gnomAD v4
11g.47341165_47341166insTTTTAATCA599374429MYBPC3c.1870_1871insTTAAAAA (p.Asn624IlefsTer16)
c.1852_1853insTTAAAAA (p.Asn618IlefsTer16)
gnomAD v2 gnomAD v4
11g.47341165_47341166insTTTTACTCA2613398225MYBPC3c.1870_1871insGTAAAAA (p.Asn624SerfsTer16)
c.1852_1853insGTAAAAA (p.Asn618SerfsTer16)
gnomAD v4
11g.47341166G>ACA011380MYBPC3c.1869C>T (p.Cys623=)
c.1851C>T (p.Cys617=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341166G>CCA380323737MYBPC3c.1869C>G (p.Cys623Trp)
c.1851C>G (p.Cys617Trp)
11g.47341166G=CA1969334631MYBPC3c.1869C= (p.Cys623=)
c.1851C= (p.Cys617=)
11g.47341166G>TCA011370MYBPC3c.1869C>A (p.Cys623Ter)
c.1851C>A (p.Cys617Ter)
ClinVar dbSNP gnomAD v4
11g.47341166_47341167delCA2613398236MYBPC3c.1868_1869del (p.Cys623Ter)
c.1850_1851del (p.Cys617Ter)
gnomAD v4
11g.47341166_47341167insACA2613398245MYBPC3c.1868_1869insT (p.Asn624GlnfsTer14)
c.1850_1851insT (p.Asn618GlnfsTer14)
gnomAD v4
11g.47341166_47341167insTTAATGATACA2613398244MYBPC3c.1868_1869insTATCATTAA (p.Cys623_Asn624insIleIleAsn)
c.1850_1851insTATCATTAA (p.Cys617_Asn618insIleIleAsn)
gnomAD v4
11g.47341167delCA599374430MYBPC3c.1868del (p.Cys623SerfsTer?)
c.1850del (p.Cys617SerfsTer?)
gnomAD v2 gnomAD v4
11g.47341167C>ACA380323742MYBPC3c.1868G>T (p.Cys623Phe)
c.1850G>T (p.Cys617Phe)
gnomAD v4
11g.47341167C>GCA380323746MYBPC3c.1868G>C (p.Cys623Ser)
c.1850G>C (p.Cys617Ser)
11g.47341167C>TCA380323749MYBPC3c.1868G>A (p.Cys623Tyr)
c.1850G>A (p.Cys617Tyr)
gnomAD v4
11g.47341168delCA2613398250MYBPC3c.1867del (p.Cys623AlafsTer?)
c.1849del (p.Cys617AlafsTer?)
gnomAD v4
11g.47341168A=CA1969334634MYBPC3c.1867T= (p.Cys623=)
c.1849T= (p.Cys617=)
11g.47341168A>CCA380323752MYBPC3c.1867T>G (p.Cys623Gly)
c.1849T>G (p.Cys617Gly)
11g.47341168A>GCA380323756MYBPC3c.1867T>C (p.Cys623Arg)
c.1849T>C (p.Cys617Arg)
gnomAD v4
11g.47341168A>TCA047282MYBPC3c.1867T>A (p.Cys623Ser)
c.1849T>A (p.Cys617Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341168_47341169insCCA2613398268MYBPC3c.1866_1867insG (p.Cys623ValfsTer15)
c.1848_1849insG (p.Cys617ValfsTer15)
gnomAD v4
11g.47341168_47341169insTACCA599374431MYBPC3c.1866_1867insGTA (p.Ala622_Cys623insVal)
c.1848_1849insGTA (p.Ala616_Cys617insVal)
gnomAD v2 gnomAD v4
11g.47341168_47341169insTGATACCA2613398260MYBPC3c.1866_1867insGTATCA (p.Ala622_Cys623insValSer)
c.1848_1849insGTATCA (p.Ala616_Cys617insValSer)
gnomAD v4
11g.47341168_47341169insATGATACCA2613398269MYBPC3c.1866_1867insGTATCAT (p.Cys623ValfsTer17)
c.1848_1849insGTATCAT (p.Cys617ValfsTer17)
gnomAD v4
11g.47341169G>ACA047066MYBPC3c.1866C>T (p.Ala622=)
c.1848C>T (p.Ala616=)
gnomAD v4
11g.47341169G>CCA474218181MYBPC3c.1866C>G (p.Ala622=)
c.1848C>G (p.Ala616=)
11g.47341169G>TCA474218180MYBPC3c.1866C>A (p.Ala622=)
c.1848C>A (p.Ala616=)
ClinVar gnomAD v4
11g.47341170delCA2613398265MYBPC3c.1866del (p.Cys623AlafsTer?)
c.1848del (p.Cys617AlafsTer?)
gnomAD v4
11g.47341170G>ACA380323765MYBPC3c.1865C>T (p.Ala622Val)
c.1847C>T (p.Ala616Val)
11g.47341170G>CCA380323767MYBPC3c.1865C>G (p.Ala622Gly)
c.1847C>G (p.Ala616Gly)
11g.47341170G>TCA380323769MYBPC3c.1865C>A (p.Ala622Asp)
c.1847C>A (p.Ala616Asp)
11g.47341171C>ACA380323777MYBPC3c.1864G>T (p.Ala622Ser)
c.1846G>T (p.Ala616Ser)
gnomAD v4
11g.47341171C=CA1969334637MYBPC3c.1864G= (p.Ala622=)
c.1846G= (p.Ala616=)
11g.47341171C>GCA380323772MYBPC3c.1864G>C (p.Ala622Pro)
c.1846G>C (p.Ala616Pro)
11g.47341171C>TCA380323774MYBPC3c.1864G>A (p.Ala622Thr)
c.1846G>A (p.Ala616Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47341171_47341172delinsCGCA1969334635MYBPC3c.1863_1864delinsCG (p.Phe621=)
c.1845_1846delinsCG (p.Phe615=)
11g.47341172delCA011363MYBPC3c.1863del (p.Phe621LeufsTer?)
c.1845del (p.Phe615LeufsTer?)
ClinVar dbSNP
11g.47341172G>ACA011356MYBPC3c.1863C>T (p.Phe621=)
c.1845C>T (p.Phe615=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341172G>CCA380323782MYBPC3c.1863C>G (p.Phe621Leu)
c.1845C>G (p.Phe615Leu)
dbSNP gnomAD v3 gnomAD v4
11g.47341172G=CA1969334640MYBPC3c.1863C= (p.Phe621=)
c.1845C= (p.Phe615=)
11g.47341172G>TCA380323784MYBPC3c.1863C>A (p.Phe621Leu)
c.1845C>A (p.Phe615Leu)
gnomAD v4
11g.47341173_47341175delCA2613398299MYBPC3c.1861_1863del (p.Phe621del)
c.1843_1845del (p.Phe615del)
gnomAD v4
11g.47341173A>CCA380323789MYBPC3c.1862T>G (p.Phe621Cys)
c.1844T>G (p.Phe615Cys)
11g.47341173A>GCA380323793MYBPC3c.1862T>C (p.Phe621Ser)
c.1844T>C (p.Phe615Ser)
11g.47341173A>TCA380323795MYBPC3c.1862T>A (p.Phe621Tyr)
c.1844T>A (p.Phe615Tyr)
11g.47341173_47341175delinsAAGCA1969334642MYBPC3c.1860_1862delinsCTT (p.Gly620=)
c.1842_1844delinsCTT (p.Gly614=)
11g.47341173_47341174insCCACCGCA2613398340MYBPC3c.1861_1862insCGGTGG (p.Phe621delinsSerValVal)
c.1843_1844insCGGTGG (p.Phe615delinsSerValVal)
gnomAD v4
11g.47341174A=CA1969334643MYBPC3c.1861T= (p.Phe621=)
c.1843T= (p.Phe615=)
11g.47341174A>CCA380323799MYBPC3c.1861T>G (p.Phe621Val)
c.1843T>G (p.Phe615Val)
11g.47341174A>GCA380323800MYBPC3c.1861T>C (p.Phe621Leu)
c.1843T>C (p.Phe615Leu)
dbSNP gnomAD v4
11g.47341174A>TCA380323803MYBPC3c.1861T>A (p.Phe621Ile)
c.1843T>A (p.Phe615Ile)
11g.47341174_47341175delCA599374432MYBPC3c.1860_1861del (p.Phe621ArgfsTer16)
c.1842_1843del (p.Phe615ArgfsTer16)
dbSNP gnomAD v2 gnomAD v4
11g.47341175G>ACA047032MYBPC3c.1860C>T (p.Gly620=)
c.1842C>T (p.Gly614=)
11g.47341175G>CCA078346MYBPC3c.1860C>G (p.Gly620=)
c.1842C>G (p.Gly614=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341175G=CA1969334645MYBPC3c.1860C= (p.Gly620=)
c.1842C= (p.Gly614=)
11g.47341175G>TCA474218186MYBPC3c.1860C>A (p.Gly620=)
c.1842C>A (p.Gly614=)
gnomAD v4
11g.47341175_47341176insATCTACA2613398409MYBPC3c.1859_1860insTAGAT (p.Phe621ArgfsTer?)
c.1841_1842insTAGAT (p.Phe615ArgfsTer?)
gnomAD v4
11g.47341176C>ACA011345MYBPC3c.1859G>T (p.Gly620Val)
c.1841G>T (p.Gly614Val)
ClinVar dbSNP gnomAD v4
11g.47341176C=CA1969334649MYBPC3c.1859G= (p.Gly620=)
c.1841G= (p.Gly614=)
11g.47341176C>GCA380323812MYBPC3c.1859G>C (p.Gly620Ala)
c.1841G>C (p.Gly614Ala)
11g.47341176C>TCA380323808MYBPC3c.1859G>A (p.Gly620Asp)
c.1841G>A (p.Gly614Asp)
ClinVar
11g.47341176_47341183delinsCCCTCGGGCA1969334647MYBPC3c.1852_1859delinsCCCGAGGG (p.Pro618=)
c.1834_1841delinsCCCGAGGG (p.Pro612=)
11g.47341177C>ACA380323815MYBPC3c.1858G>T (p.Gly620Cys)
c.1840G>T (p.Gly614Cys)
dbSNP gnomAD v2 gnomAD v4
11g.47341177C=CA1969334652MYBPC3c.1858G= (p.Gly620=)
c.1840G= (p.Gly614=)
11g.47341177C>GCA380323817MYBPC3c.1858G>C (p.Gly620Arg)
c.1840G>C (p.Gly614Arg)
11g.47341177C>TCA380323820MYBPC3c.1858G>A (p.Gly620Ser)
c.1840G>A (p.Gly614Ser)
gnomAD v4
11g.47341178_47341184delCA599374433MYBPC3c.1852_1858del (p.Pro618AlafsTer?)
c.1834_1840del (p.Pro612AlafsTer?)
dbSNP gnomAD v2 gnomAD v4
11g.47341177_47341178insACCGAGATCA2791323296MYBPC3c.1857_1858insATCTCGGT (p.Gly620IlefsTer?)
c.1839_1840insATCTCGGT (p.Gly614IlefsTer?)
11g.47341178C>ACA380323824MYBPC3c.1857G>T (p.Glu619Asp)
c.1839G>T (p.Glu613Asp)
dbSNP gnomAD v2 gnomAD v4
11g.47341178C=CA1969334654MYBPC3c.1857G= (p.Glu619=)
c.1839G= (p.Glu613=)
11g.47341178C>GCA380323826MYBPC3c.1857G>C (p.Glu619Asp)
c.1839G>C (p.Glu613Asp)
ClinVar
11g.47341178C>TCA078343MYBPC3c.1857G>A (p.Glu619=)
c.1839G>A (p.Glu613=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341179_47341184delCA2791323297MYBPC3c.1852_1857del (p.Pro618_Glu619del)
c.1834_1839del (p.Pro612_Glu613del)
11g.47341179T>ACA380323829MYBPC3c.1856A>T (p.Glu619Val)
c.1838A>T (p.Glu613Val)
11g.47341179T>CCA380323832MYBPC3c.1856A>G (p.Glu619Gly)
c.1838A>G (p.Glu613Gly)
dbSNP gnomAD v2 gnomAD v4
11g.47341179T>GCA380323834MYBPC3c.1856A>C (p.Glu619Ala)
c.1838A>C (p.Glu613Ala)
11g.47341179T=CA1969334657MYBPC3c.1856A= (p.Glu619=)
c.1838A= (p.Glu613=)
11g.47341180C>ACA380323837MYBPC3c.1855G>T (p.Glu619Ter)
c.1837G>T (p.Glu613Ter)
gnomAD v4 COSMIC COSMIC
11g.47341180C=CA1969334659MYBPC3c.1855G= (p.Glu619=)
c.1837G= (p.Glu613=)
11g.47341180C>GCA380323839MYBPC3c.1855G>C (p.Glu619Gln)
c.1837G>C (p.Glu613Gln)
11g.47341180C>TCA011336MYBPC3c.1855G>A (p.Glu619Lys)
c.1837G>A (p.Glu613Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341181G>ACA474218188MYBPC3c.1854C>T (p.Pro618=)
c.1836C>T (p.Pro612=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47341181G>CCA474218189MYBPC3c.1854C>G (p.Pro618=)
c.1836C>G (p.Pro612=)
dbSNP gnomAD v4
11g.47341181G=CA1969334661MYBPC3c.1854C= (p.Pro618=)
c.1836C= (p.Pro612=)
11g.47341181G>TCA474218190MYBPC3c.1854C>A (p.Pro618=)
c.1836C>A (p.Pro612=)
gnomAD v4
11g.47341181_47341183delCA2613398480MYBPC3c.1852_1854del (p.Pro618del)
c.1834_1836del (p.Pro612del)
gnomAD v4
11g.47341183delCA2695212779MYBPC3c.1854del (p.Glu619ArgfsTer?)
c.1836del (p.Glu613ArgfsTer?)
11g.47341182G>ACA380323846MYBPC3c.1853C>T (p.Pro618Leu)
c.1835C>T (p.Pro612Leu)
dbSNP gnomAD v2 gnomAD v4
11g.47341182G>CCA380323849MYBPC3c.1853C>G (p.Pro618Arg)
c.1835C>G (p.Pro612Arg)
gnomAD v4
11g.47341182G=CA1969334662MYBPC3c.1853C= (p.Pro618=)
c.1835C= (p.Pro612=)
11g.47341182G>TCA047341MYBPC3c.1853C>A (p.Pro618His)
c.1835C>A (p.Pro612His)
gnomAD v4
11g.47341183G>ACA380323851MYBPC3c.1852C>T (p.Pro618Ser)
c.1834C>T (p.Pro612Ser)
gnomAD v4
11g.47341183G>CCA380323854MYBPC3c.1852C>G (p.Pro618Ala)
c.1834C>G (p.Pro612Ala)
11g.47341183G=CA1969334664MYBPC3c.1852C= (p.Pro618=)
c.1834C= (p.Pro612=)
11g.47341183G>TCA380323856MYBPC3c.1852C>A (p.Pro618Thr)
c.1834C>A (p.Pro612Thr)
gnomAD v4
11g.47341183_47341184insATCA599374434MYBPC3c.1851_1852insAT (p.Pro618IlefsTer?)
c.1833_1834insAT (p.Pro612IlefsTer?)
gnomAD v2 gnomAD v4
11g.47341183_47341184insATCTACA599374435MYBPC3c.1851_1852insTAGAT (p.Pro618Ter)
c.1833_1834insTAGAT (p.Pro612Ter)
gnomAD v2 gnomAD v4
11g.47341184C>ACA474218192MYBPC3c.1851G>T (p.Val617=)
c.1833G>T (p.Val611=)
gnomAD v4
11g.47341184C=CA1969334668MYBPC3c.1851G= (p.Val617=)
c.1833G= (p.Val611=)
11g.47341184C>GCA474218193MYBPC3c.1851G>C (p.Val617=)
c.1833G>C (p.Val611=)
gnomAD v4
11g.47341184C>TCA474218194MYBPC3c.1851G>A (p.Val617=)
c.1833G>A (p.Val611=)
gnomAD v4
11g.47341184dupCA913190279MYBPC3c.1851dup (p.Pro618AlafsTer20)
c.1833dup (p.Pro612AlafsTer20)
ClinVar dbSNP
11g.47341184_47341185insTCA599374436MYBPC3c.1850_1851insA (p.Pro618AlafsTer20)
c.1832_1833insA (p.Pro612AlafsTer20)
dbSNP gnomAD v2 gnomAD v4
11g.47341185A=CA1969334671MYBPC3c.1850T= (p.Val617=)
c.1832T= (p.Val611=)
11g.47341185A>CCA221694135MYBPC3c.1850T>G (p.Val617Gly)
c.1832T>G (p.Val611Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47341185A>GCA380323860MYBPC3c.1850T>C (p.Val617Ala)
c.1832T>C (p.Val611Ala)
ClinVar dbSNP
11g.47341185A>TCA380323863MYBPC3c.1850T>A (p.Val617Glu)
c.1832T>A (p.Val611Glu)
11g.47341186C>ACA380323867MYBPC3c.1849G>T (p.Val617Leu)
c.1831G>T (p.Val611Leu)
gnomAD v4
11g.47341186C>GCA380323871MYBPC3c.1849G>C (p.Val617Leu)
c.1831G>C (p.Val611Leu)
11g.47341186C>TCA380323870MYBPC3c.1849G>A (p.Val617Met)
c.1831G>A (p.Val611Met)
gnomAD v4
11g.47341186_47341190delinsCAAAGCA1969334673MYBPC3c.1845_1849delinsCTTTG (p.Ser615=)
c.1827_1831delinsCTTTG (p.Ser609=)
11g.47341187A>CCA380323874MYBPC3c.1848T>G (p.Phe616Leu)
c.1830T>G (p.Phe610Leu)
gnomAD v4
11g.47341187A>GCA474218199MYBPC3c.1848T>C (p.Phe616=)
c.1830T>C (p.Phe610=)
gnomAD v4
11g.47341187A>TCA380323876MYBPC3c.1848T>A (p.Phe616Leu)
c.1830T>A (p.Phe610Leu)
11g.47341187_47341189delCA2613398565MYBPC3c.1846_1848del (p.Phe616del)
c.1828_1830del (p.Phe610del)
gnomAD v4
11g.47341189delCA2613398568MYBPC3c.1848del (p.Phe616LeufsTer?)
c.1830del (p.Phe610LeufsTer?)
gnomAD v4
11g.47341187_47341190delCA599374437MYBPC3c.1845_1848del (p.Ser615ArgfsTer?)
c.1827_1830del (p.Ser609ArgfsTer?)
dbSNP gnomAD v2 gnomAD v4
11g.47341187_47341193delCA2613398562MYBPC3c.1842_1848del (p.Tyr614Ter)
c.1824_1830del (p.Tyr608Ter)
gnomAD v4
11g.47341187_47341196delCA2613398559MYBPC3c.1839_1848del (p.Asp613GlufsTer?)
c.1821_1830del (p.Asp607GlufsTer?)
gnomAD v4
11g.47341188A>CCA380323878MYBPC3c.1847T>G (p.Phe616Cys)
c.1829T>G (p.Phe610Cys)
gnomAD v4
11g.47341188A>GCA047354MYBPC3c.1847T>C (p.Phe616Ser)
c.1829T>C (p.Phe610Ser)
gnomAD v4
11g.47341188A>TCA380323882MYBPC3c.1847T>A (p.Phe616Tyr)
c.1829T>A (p.Phe610Tyr)
11g.47341188_47341190delCA2613398579MYBPC3c.1845_1847del (p.Phe616del)
c.1827_1829del (p.Phe610del)
gnomAD v4
11g.47341188_47341193delCA2613398581MYBPC3c.1842_1847del (p.Ser615_Phe616del)
c.1824_1829del (p.Ser609_Phe610del)
gnomAD v4
11g.47341188_47341196delCA2613398582MYBPC3c.1839_1847del (p.Tyr614_Phe616del)
c.1821_1829del (p.Tyr608_Phe610del)
gnomAD v4
11g.47341188_47341208delinsAAGCTGTAGTCAGCCTCGTCGCA1969334674MYBPC3c.1827_1847delinsCGACGAGGCTGACTACAGCTT (p.Ala609=)
c.1809_1829delinsCGACGAGGCTGACTACAGCTT (p.Ala603=)
11g.47341189A=CA1969334675MYBPC3c.1846T= (p.Phe616=)
c.1828T= (p.Phe610=)
11g.47341189A>CCA380323888MYBPC3c.1846T>G (p.Phe616Val)
c.1828T>G (p.Phe610Val)
11g.47341189A>GCA380323891MYBPC3c.1846T>C (p.Phe616Leu)
c.1828T>C (p.Phe610Leu)
11g.47341189A>TCA380323885MYBPC3c.1846T>A (p.Phe616Ile)
c.1828T>A (p.Phe610Ile)
ClinVar dbSNP gnomAD v4
11g.47341189_47341190delCA2613398601MYBPC3c.1845_1846del (p.Phe616CysfsTer21)
c.1827_1828del (p.Phe610CysfsTer21)
gnomAD v4
11g.47341189_47341191delCA2613398602MYBPC3c.1844_1846del (p.Ser615_Phe616delinsIle)
c.1826_1828del (p.Ser609_Phe610delinsIle)
gnomAD v4
11g.47341189_47341196delCA2613398603MYBPC3c.1839_1846del (p.Tyr614CysfsTer21)
c.1821_1828del (p.Tyr608CysfsTer21)
gnomAD v4
11g.47341189_47341201delCA2613398605MYBPC3c.1834_1846del (p.Ala612LeufsTer?)
c.1816_1828del (p.Ala606LeufsTer?)
gnomAD v4
11g.47341189_47341208delinsGCTGTACA658797629MYBPC3c.1827_1846delinsTACAGC (p.Asp610ThrfsTer23)
c.1809_1828delinsTACAGC (p.Asp604ThrfsTer23)
ClinVar dbSNP
11g.47341190G>ACA474218201MYBPC3c.1845C>T (p.Ser615=)
c.1827C>T (p.Ser609=)
dbSNP gnomAD v4
11g.47341190G>CCA380323894MYBPC3c.1845C>G (p.Ser615Arg)
c.1827C>G (p.Ser609Arg)
ClinVar
11g.47341190G=CA1969334676MYBPC3c.1845C= (p.Ser615=)
c.1827C= (p.Ser609=)
11g.47341190G>TCA380323897MYBPC3c.1845C>A (p.Ser615Arg)
c.1827C>A (p.Ser609Arg)
gnomAD v4
11g.47341191_47341193delCA2613398624MYBPC3c.1843_1845del (p.Ser615del)
c.1825_1827del (p.Ser609del)
gnomAD v4
11g.47341190_47341196delCA2613398620MYBPC3c.1839_1845del (p.Tyr614LeufsTer?)
c.1821_1827del (p.Tyr608LeufsTer?)
gnomAD v4
11g.47341190_47341191insTACA2613398625MYBPC3c.1844_1845insTA (p.Phe616ThrfsTer?)
c.1826_1827insTA (p.Phe610ThrfsTer?)
gnomAD v4
11g.47341191C>ACA380323901MYBPC3c.1844G>T (p.Ser615Ile)
c.1826G>T (p.Ser609Ile)
dbSNP gnomAD v2 gnomAD v4
11g.47341191C=CA1969334678MYBPC3c.1844G= (p.Ser615=)
c.1826G= (p.Ser609=)
11g.47341191C>GCA380323909MYBPC3c.1844G>C (p.Ser615Thr)
c.1826G>C (p.Ser609Thr)
11g.47341191C>TCA380323906MYBPC3c.1844G>A (p.Ser615Asn)
c.1826G>A (p.Ser609Asn)
11g.47341192T>ACA380323911MYBPC3c.1843A>T (p.Ser615Cys)
c.1825A>T (p.Ser609Cys)
11g.47341192T>CCA380323913MYBPC3c.1843A>G (p.Ser615Gly)
c.1825A>G (p.Ser609Gly)
ClinVar dbSNP gnomAD v4
11g.47341192T>GCA380323917MYBPC3c.1843A>C (p.Ser615Arg)
c.1825A>C (p.Ser609Arg)
11g.47341192T=CA1969334679MYBPC3c.1843A= (p.Ser615=)
c.1825A= (p.Ser609=)
11g.47341193_47341194delCA2613398628MYBPC3c.1842_1843del (p.Tyr614Ter)
c.1824_1825del (p.Tyr608Ter)
gnomAD v4
11g.47341193_47341197delCA2613398630MYBPC3c.1839_1843del (p.Asp613GlufsTer23)
c.1821_1825del (p.Asp607GlufsTer23)
gnomAD v4
11g.47341192_47341219delinsTGTAGTCAGCCTCGTCGGCAGGTGTGACCA1969334680MYBPC3c.1816_1843delinsGTCACACCTGCCGACGAGGCTGACTACA (p.Val606=)
c.1798_1825delinsGTCACACCTGCCGACGAGGCTGACTACA (p.Val600=)
11g.47341192_47341193insACA2613398650MYBPC3c.1842_1843insT (p.Ser615Ter)
c.1824_1825insT (p.Ser609Ter)
gnomAD v4
11g.47341193delCA2580084220MYBPC3c.1842del (p.Tyr614Ter)
c.1824del (p.Tyr608Ter)
ClinVar gnomAD v4
11g.47341193G>ACA078339MYBPC3c.1842C>T (p.Tyr614=)
c.1824C>T (p.Tyr608=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341193G>CCA380323922MYBPC3c.1842C>G (p.Tyr614Ter)
c.1824C>G (p.Tyr608Ter)
dbSNP gnomAD v3 gnomAD v4
11g.47341193G=CA1969334682MYBPC3c.1842C= (p.Tyr614=)
c.1824C= (p.Tyr608=)
11g.47341193G>TCA380323925MYBPC3c.1842C>A (p.Tyr614Ter)
c.1824C>A (p.Tyr608Ter)
gnomAD v4
11g.47341193_47341196delCA2613398656MYBPC3c.1839_1842del (p.Asp613GlufsTer?)
c.1821_1824del (p.Asp607GlufsTer?)
gnomAD v4
11g.47341195_47341221delCA915948153MYBPC3c.1816_1842del (p.Val606_Tyr614del)
c.1798_1824del (p.Val600_Tyr608del)
ClinVar dbSNP
11g.47341193_47341194insCACA2613398683MYBPC3c.1841_1842insTG (p.Ser615AlafsTer?)
c.1823_1824insTG (p.Ser609AlafsTer?)
gnomAD v4
11g.47341193_47341194insGCCA2613398680MYBPC3c.1841_1842insGC (p.Tyr614Ter)
c.1823_1824insGC (p.Tyr608Ter)
gnomAD v4
11g.47341194delCA2613398674MYBPC3c.1841del (p.Tyr614SerfsTer?)
c.1823del (p.Tyr608SerfsTer?)
gnomAD v4
11g.47341194T>ACA380323928MYBPC3c.1841A>T (p.Tyr614Phe)
c.1823A>T (p.Tyr608Phe)
11g.47341194T>CCA011318MYBPC3c.1841A>G (p.Tyr614Cys)
c.1823A>G (p.Tyr608Cys)
ClinVar dbSNP
11g.47341194T>GCA380323929MYBPC3c.1841A>C (p.Tyr614Ser)
c.1823A>C (p.Tyr608Ser)
11g.47341194T=CA1969334684MYBPC3c.1841A= (p.Tyr614=)
c.1823A= (p.Tyr608=)
11g.47341194_47341195delCA2613398678MYBPC3c.1840_1841del (p.Tyr614GlnfsTer23)
c.1822_1823del (p.Tyr608GlnfsTer23)
gnomAD v4
11g.47341194_47341201delCA2613398676MYBPC3c.1834_1841del (p.Ala612GlnfsTer23)
c.1816_1823del (p.Ala606GlnfsTer23)
gnomAD v4
11g.47341195A>CCA380323930MYBPC3c.1840T>G (p.Tyr614Asp)
c.1822T>G (p.Tyr608Asp)
COSMIC COSMIC
11g.47341195A>GCA380323931MYBPC3c.1840T>C (p.Tyr614His)
c.1822T>C (p.Tyr608His)
gnomAD v4
11g.47341195A>TCA380323932MYBPC3c.1840T>A (p.Tyr614Asn)
c.1822T>A (p.Tyr608Asn)
11g.47341195_47341197delinsAGTCA1969334685MYBPC3c.1838_1840delinsACT (p.Asp613=)
c.1820_1822delinsACT (p.Asp607=)
11g.47341195_47341200delCA2791323304MYBPC3c.1835_1840del (p.Ala612_Tyr614delinsAsp)
c.1817_1822del (p.Ala606_Tyr608delinsAsp)
11g.47341195_47341196insCACCA2613398709MYBPC3c.1839_1840insGTG (p.Asp613_Tyr614insVal)
c.1821_1822insGTG (p.Asp607_Tyr608insVal)
gnomAD v4
11g.47341195_47341196insCACCCA2613398711MYBPC3c.1839_1840insGGTG (p.Tyr614GlyfsTer25)
c.1821_1822insGGTG (p.Tyr608GlyfsTer25)
gnomAD v4
11g.47341196delCA2499220970MYBPC3c.1839del (p.Tyr614ThrfsTer?)
c.1821del (p.Tyr608ThrfsTer?)
ClinVar dbSNP gnomAD v4
11g.47341196G>ACA046979MYBPC3c.1839C>T (p.Asp613=)
c.1821C>T (p.Asp607=)
gnomAD v4
11g.47341196G>CCA380323933MYBPC3c.1839C>G (p.Asp613Glu)
c.1821C>G (p.Asp607Glu)
gnomAD v4
11g.47341196G=CA1969334687MYBPC3c.1839C= (p.Asp613=)
c.1821C= (p.Asp607=)
11g.47341196G>TCA380323935MYBPC3c.1839C>A (p.Asp613Glu)
c.1821C>A (p.Asp607Glu)
dbSNP gnomAD v2 gnomAD v4
11g.47341196_47341197delCA599374438MYBPC3c.1838_1839del (p.Asp613ValfsTer24)
c.1820_1821del (p.Asp607ValfsTer24)
dbSNP gnomAD v2 gnomAD v4
11g.47341196_47341198delCA2613398729MYBPC3c.1837_1839del (p.Asp613del)
c.1819_1821del (p.Asp607del)
gnomAD v4
11g.47341196_47341202delCA2613398733MYBPC3c.1833_1839del (p.Glu611AspfsTer?)
c.1815_1821del (p.Glu605AspfsTer?)
gnomAD v4
11g.47341199_47341207delCA2791323305MYBPC3c.1831_1839del (p.Glu611_Asp613del)
c.1813_1821del (p.Glu605_Asp607del)
11g.47341196_47341197insACA2613398774MYBPC3c.1838_1839insT (p.Tyr614LeufsTer24)
c.1820_1821insT (p.Tyr608LeufsTer24)
gnomAD v4
11g.47341196_47341197insGTCA676998715MYBPC3c.1838_1839insAC (p.Asp613GlufsTer?)
c.1820_1821insAC (p.Asp607GlufsTer?)
11g.47341197delCA2613398756MYBPC3c.1838del (p.Asp613AlafsTer?)
c.1820del (p.Asp607AlafsTer?)
gnomAD v4
11g.47341197T>ACA380323939MYBPC3c.1838A>T (p.Asp613Val)
c.1820A>T (p.Asp607Val)
gnomAD v4
11g.47341197T>CCA380323942MYBPC3c.1838A>G (p.Asp613Gly)
c.1820A>G (p.Asp607Gly)
gnomAD v4
11g.47341197T>GCA380323945MYBPC3c.1838A>C (p.Asp613Ala)
c.1820A>C (p.Asp607Ala)
11g.47341197dupCA277833MYBPC3c.1838dup (p.Asp613GlufsTer25)
c.1820dup (p.Asp607GlufsTer25)
ClinVar dbSNP gnomAD v4
11g.47341197_47341201delCA2613398765MYBPC3c.1834_1838del (p.Ala612LeufsTer24)
c.1816_1820del (p.Ala606LeufsTer24)
gnomAD v4
11g.47341197_47341201delinsTCAGCCA1969334689MYBPC3c.1834_1838delinsGCTGA (p.Ala612=)
c.1816_1820delinsGCTGA (p.Ala606=)
11g.47341198C>ACA380323948MYBPC3c.1837G>T (p.Asp613Tyr)
c.1819G>T (p.Asp607Tyr)
gnomAD v4
11g.47341198C>GCA380323950MYBPC3c.1837G>C (p.Asp613His)
c.1819G>C (p.Asp607His)
11g.47341198C>TCA380323952MYBPC3c.1837G>A (p.Asp613Asn)
c.1819G>A (p.Asp607Asn)
gnomAD v4
11g.47341198dupCA2613398791MYBPC3c.1837dup (p.Asp613GlyfsTer25)
c.1819dup (p.Asp607GlyfsTer25)
gnomAD v4
11g.47341199_47341201delCA2613398794MYBPC3c.1835_1837del (p.Ala612del)
c.1817_1819del (p.Ala606del)
gnomAD v4
11g.47341198_47341202delCA2613398799MYBPC3c.1833_1837del (p.Ala612LeufsTer24)
c.1815_1819del (p.Ala606LeufsTer24)
gnomAD v4
11g.47341199_47341202delCA599374439MYBPC3c.1834_1837del (p.Ala612ThrfsTer?)
c.1816_1819del (p.Ala606ThrfsTer?)
dbSNP gnomAD v2 gnomAD v4
11g.47341199delCA2613398814MYBPC3c.1836del (p.Asp613ThrfsTer?)
c.1818del (p.Asp607ThrfsTer?)
gnomAD v4
11g.47341199A>CCA474218208MYBPC3c.1836T>G (p.Ala612=)
c.1818T>G (p.Ala606=)
gnomAD v4
11g.47341199A>GCA474218209MYBPC3c.1836T>C (p.Ala612=)
c.1818T>C (p.Ala606=)
11g.47341199A>TCA474218210MYBPC3c.1836T>A (p.Ala612=)
c.1818T>A (p.Ala606=)
gnomAD v4
11g.47341199_47341200delCA2613398817MYBPC3c.1835_1836del (p.Ala612GlyfsTer25)
c.1817_1818del (p.Ala606GlyfsTer25)
gnomAD v4
11g.47341199_47341200insTCA2613398854MYBPC3c.1835_1836insA (p.Asp613Ter)
c.1817_1818insA (p.Asp607Ter)
gnomAD v4
11g.47341199_47341200insTTCA2613398858MYBPC3c.1835_1836insAA (p.Asp613MetfsTer?)
c.1817_1818insAA (p.Asp607MetfsTer?)
gnomAD v4
11g.47341199_47341200insCTTCTTCA2613398849MYBPC3c.1835_1836insAAGAAG (p.Ala612_Asp613insArgSer)
c.1817_1818insAAGAAG (p.Ala606_Asp607insArgSer)
gnomAD v4
11g.47341200delCA2613398844MYBPC3c.1835del (p.Ala612ValfsTer?)
c.1817del (p.Ala606ValfsTer?)
gnomAD v4
11g.47341200G>ACA380323954MYBPC3c.1835C>T (p.Ala612Val)
c.1817C>T (p.Ala606Val)
gnomAD v4
11g.47341200G>CCA380323956MYBPC3c.1835C>G (p.Ala612Gly)
c.1817C>G (p.Ala606Gly)
gnomAD v4
11g.47341200G>TCA380323958MYBPC3c.1835C>A (p.Ala612Asp)
c.1817C>A (p.Ala606Asp)
gnomAD v4
11g.47341200_47341201delCA2613398846MYBPC3c.1834_1835del (p.Ala612Ter)
c.1816_1817del (p.Ala606Ter)
gnomAD v4
11g.47341200_47341201insTCA2613398867MYBPC3c.1834_1835insA (p.Ala612AspfsTer2)
c.1816_1817insA (p.Ala606AspfsTer2)
gnomAD v4
11g.47341201C>ACA380323963MYBPC3c.1834G>T (p.Ala612Ser)
c.1816G>T (p.Ala606Ser)
dbSNP gnomAD v2 gnomAD v4
11g.47341201C=CA1969334690MYBPC3c.1834G= (p.Ala612=)
c.1816G= (p.Ala606=)
11g.47341201C>GCA380323962MYBPC3c.1834G>C (p.Ala612Pro)
c.1816G>C (p.Ala606Pro)
gnomAD v4
11g.47341201C>TCA380323961MYBPC3c.1834G>A (p.Ala612Thr)
c.1816G>A (p.Ala606Thr)
gnomAD v4
11g.47341201_47341202delCA2613398874MYBPC3c.1833_1834del (p.Glu611AspfsTer2)
c.1815_1816del (p.Glu605AspfsTer2)
gnomAD v4
11g.47341202delCA2613398873MYBPC3c.1834del (p.Ala612LeufsTer?)
c.1816del (p.Ala606LeufsTer?)
gnomAD v4
11g.47341201_47341202insGCA2613398906MYBPC3c.1833_1834insC (p.Ala612ArgfsTer2)
c.1815_1816insC (p.Ala606ArgfsTer2)
gnomAD v4
11g.47341201_47341202insATCA2613398909MYBPC3c.1833_1834insAT (p.Ala612MetfsTer?)
c.1815_1816insAT (p.Ala606MetfsTer?)
gnomAD v4
11g.47341201_47341202insAATCA2613398885MYBPC3c.1833_1834insATT (p.Glu611_Ala612insIle)
c.1815_1816insATT (p.Glu605_Ala606insIle)
gnomAD v4
11g.47341201_47341202insACGATTCA2613398913MYBPC3c.1833_1834insAATCGT (p.Glu611_Ala612insAsnArg)
c.1815_1816insAATCGT (p.Glu605_Ala606insAsnArg)
gnomAD v4
11g.47341201_47341202insGAACTTCA2613398902MYBPC3c.1833_1834insAAGTTC (p.Glu611_Ala612insLysPhe)
c.1815_1816insAAGTTC (p.Glu605_Ala606insLysPhe)
gnomAD v4
11g.47341201_47341202insGACTCTCA2613398898MYBPC3c.1833_1834insAGAGTC (p.Glu611_Ala612insArgVal)
c.1815_1816insAGAGTC (p.Glu605_Ala606insArgVal)
gnomAD v4
11g.47341201_47341202insGTCTCTCA2613398893MYBPC3c.1833_1834insAGAGAC (p.Glu611_Ala612insArgAsp)
c.1815_1816insAGAGAC (p.Glu605_Ala606insArgAsp)
gnomAD v4
11g.47341201_47341202insTTGAATCA2613398888MYBPC3c.1833_1834insATTCAA (p.Glu611_Ala612insIleGln)
c.1815_1816insATTCAA (p.Glu605_Ala606insIleGln)
gnomAD v4
11g.47341201_47341202insGGATTAACA2613398970MYBPC3c.1833_1834insTTAATCC (p.Ala612LeufsTer4)
c.1815_1816insTTAATCC (p.Ala606LeufsTer4)
gnomAD v4
11g.47341201_47341202insTCCACTTCA2613398890MYBPC3c.1833_1834insAAGTGGA (p.Ala612LysfsTer4)
c.1815_1816insAAGTGGA (p.Ala606LysfsTer4)
gnomAD v4
11g.47341202C>ACA380323964MYBPC3c.1833G>T (p.Glu611Asp)
c.1815G>T (p.Glu605Asp)
gnomAD v4
11g.47341202C=CA1969334692MYBPC3c.1833G= (p.Glu611=)
c.1815G= (p.Glu605=)
11g.47341202C>GCA380323965MYBPC3c.1833G>C (p.Glu611Asp)
c.1815G>C (p.Glu605Asp)
11g.47341202C>TCA078337MYBPC3c.1833G>A (p.Glu611=)
c.1815G>A (p.Glu605=)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341204_47341205insTAACTCCA2613398907MYBPC3c.1833_1834insTTAGAG (p.Glu611_Ala612insLeuGlu)
c.1815_1816insTTAGAG (p.Glu605_Ala606insLeuGlu)
gnomAD v4
11g.47341202_47341203insGACA2613399017MYBPC3c.1832_1833insTC (p.Glu611AspfsTer?)
c.1814_1815insTC (p.Glu605AspfsTer?)
gnomAD v4
11g.47341202_47341203insAACTAACA2613399022MYBPC3c.1832_1833insTTAGTT (p.Glu611AspfsTer2)
c.1814_1815insTTAGTT (p.Glu605AspfsTer2)
gnomAD v4
11g.47341202_47341203insATCACACA2613399021MYBPC3c.1832_1833insTGTGAT (p.Glu611delinsAspValMet)
c.1814_1815insTGTGAT (p.Glu605delinsAspValMet)
gnomAD v4
11g.47341203T>ACA380323966MYBPC3c.1832A>T (p.Glu611Val)
c.1814A>T (p.Glu605Val)
11g.47341203T>CCA380323967MYBPC3c.1832A>G (p.Glu611Gly)
c.1814A>G (p.Glu605Gly)
ClinVar dbSNP
11g.47341203T>GCA380323968MYBPC3c.1832A>C (p.Glu611Ala)
c.1814A>C (p.Glu605Ala)
11g.47341203_47341204insATCA2791323306MYBPC3c.1832_1833insTA (p.Glu611AspfsTer?)
c.1814_1815insTA (p.Glu605AspfsTer?)
11g.47341203_47341204insAATCA2613398995MYBPC3c.1832_1833insTTA (p.Glu611AspfsTer2)
c.1814_1815insTTA (p.Glu605AspfsTer2)
gnomAD v4
11g.47341203_47341204insTAATCA2613399001MYBPC3c.1832_1833insTTAA (p.Glu611AspfsTer2)
c.1814_1815insTTAA (p.Glu605AspfsTer2)
gnomAD v4
11g.47341203_47341204insACATTGTCA2613399003MYBPC3c.1832_1833insCAATGTA (p.Glu611AspfsTer5)
c.1814_1815insCAATGTA (p.Glu605AspfsTer5)
gnomAD v4
11g.47341203dupCA2613399005MYBPC3c.1832dup (p.Ala612GlyfsTer2)
c.1814dup (p.Ala606GlyfsTer2)
gnomAD v4
11g.47341206_47341208delCA2580615683MYBPC3c.1830_1832del (p.Asp610del)
c.1812_1814del (p.Asp604del)
ClinVar dbSNP
11g.47341204C>ACA380323969MYBPC3c.1831G>T (p.Glu611Ter)
c.1813G>T (p.Glu605Ter)
ClinVar dbSNP gnomAD v4
11g.47341204C=CA1969334693MYBPC3c.1831G= (p.Glu611=)
c.1813G= (p.Glu605=)
11g.47341204C>GCA380323970MYBPC3c.1831G>C (p.Glu611Gln)
c.1813G>C (p.Glu605Gln)
11g.47341204C>TCA011308MYBPC3c.1831G>A (p.Glu611Lys)
c.1813G>A (p.Glu605Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47341204_47341212delinsCGTCGGCAGCA1969334694MYBPC3c.1823_1831delinsCTGCCGACG (p.Pro608=)
c.1805_1813delinsCTGCCGACG (p.Pro602=)
11g.47341205G>ACA078334MYBPC3c.1830C>T (p.Asp610=)
c.1812C>T (p.Asp604=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341205G>CCA380323971MYBPC3c.1830C>G (p.Asp610Glu)
c.1812C>G (p.Asp604Glu)
ClinVar dbSNP gnomAD v4
11g.47341205G=CA1969334697MYBPC3c.1830C= (p.Asp610=)
c.1812C= (p.Asp604=)
11g.47341205G>TCA380323972MYBPC3c.1830C>A (p.Asp610Glu)
c.1812C>A (p.Asp604Glu)
dbSNP
11g.47341205_47341212delinsTCA645372896MYBPC3c.1823_1830delinsA (p.Pro608GlnfsTer?)
c.1805_1812delinsA (p.Pro602GlnfsTer?)
ClinVar dbSNP
11g.47341206T>ACA011292MYBPC3c.1829A>T (p.Asp610Val)
c.1811A>T (p.Asp604Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47341206T>CCA380323973MYBPC3c.1829A>G (p.Asp610Gly)
c.1811A>G (p.Asp604Gly)
11g.47341206T>GCA380323974MYBPC3c.1829A>C (p.Asp610Ala)
c.1811A>C (p.Asp604Ala)
11g.47341206T=CA1969334701MYBPC3c.1829A= (p.Asp610=)
c.1811A= (p.Asp604=)
11g.47341207delCA2697548577MYBPC3c.1828del (p.Asp610ThrfsTer?)
c.1810del (p.Asp604ThrfsTer?)
ClinVar
11g.47341207C>ACA380323975MYBPC3c.1828G>T (p.Asp610Tyr)
c.1810G>T (p.Asp604Tyr)
ClinVar dbSNP gnomAD v4
11g.47341207C=CA1969334703MYBPC3c.1828G= (p.Asp610=)
c.1810G= (p.Asp604=)
11g.47341207C>GCA011286MYBPC3c.1828G>C (p.Asp610His)
c.1810G>C (p.Asp604His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341207C>TCA011276MYBPC3c.1828G>A (p.Asp610Asn)
c.1810G>A (p.Asp604Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341208G>ACA046957MYBPC3c.1827C>T (p.Ala609=)
c.1809C>T (p.Ala603=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341208G>CCA078328MYBPC3c.1827C>G (p.Ala609=)
c.1809C>G (p.Ala603=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341208G=CA1969334706MYBPC3c.1827C= (p.Ala609=)
c.1809C= (p.Ala603=)
11g.47341208G>TCA474218212MYBPC3c.1827C>A (p.Ala609=)
c.1809C>A (p.Ala603=)
gnomAD v4
11g.47341209dupCA2695212780MYBPC3c.1827dup (p.Asp610ArgfsTer4)
c.1809dup (p.Asp604ArgfsTer4)
11g.47341209G>ACA011267MYBPC3c.1826C>T (p.Ala609Val)
c.1808C>T (p.Ala603Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341209G>CCA380323976MYBPC3c.1826C>G (p.Ala609Gly)
c.1808C>G (p.Ala603Gly)
11g.47341209G=CA1969334709MYBPC3c.1826C= (p.Ala609=)
c.1808C= (p.Ala603=)
11g.47341209G>TCA380323977MYBPC3c.1826C>A (p.Ala609Asp)
c.1808C>A (p.Ala603Asp)
11g.47341210C>ACA380323978MYBPC3c.1825G>T (p.Ala609Ser)
c.1807G>T (p.Ala603Ser)
11g.47341210C>GCA046947MYBPC3c.1825G>C (p.Ala609Pro)
c.1807G>C (p.Ala603Pro)
11g.47341210C>TCA046933MYBPC3c.1825G>A (p.Ala609Thr)
c.1807G>A (p.Ala603Thr)
gnomAD v4
11g.47341211A>CCA474218216MYBPC3c.1824T>G (p.Pro608=)
c.1806T>G (p.Pro602=)
11g.47341211A>GCA474218217MYBPC3c.1824T>C (p.Pro608=)
c.1806T>C (p.Pro602=)
ClinVar dbSNP
11g.47341211A>TCA474218218MYBPC3c.1824T>A (p.Pro608=)
c.1806T>A (p.Pro602=)
gnomAD v4
11g.47341212G>ACA046897MYBPC3c.1823C>T (p.Pro608Leu)
c.1805C>T (p.Pro602Leu)
dbSNP
11g.47341212G>CCA078324MYBPC3c.1823C>G (p.Pro608Arg)
c.1805C>G (p.Pro602Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341212G=CA1969334711MYBPC3c.1823C= (p.Pro608=)
c.1805C= (p.Pro602=)
11g.47341212G>TCA380323979MYBPC3c.1823C>A (p.Pro608His)
c.1805C>A (p.Pro602His)
11g.47341213G>ACA011258MYBPC3c.1822C>T (p.Pro608Ser)
c.1804C>T (p.Pro602Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341213G>CCA380323980MYBPC3c.1822C>G (p.Pro608Ala)
c.1804C>G (p.Pro602Ala)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47341213G=CA1969334714MYBPC3c.1822C= (p.Pro608=)
c.1804C= (p.Pro602=)
11g.47341213G>TCA380323981MYBPC3c.1822C>A (p.Pro608Thr)
c.1804C>A (p.Pro602Thr)
gnomAD v4
11g.47341216_47341217delCA2580615684MYBPC3c.1821_1822del (p.Pro608CysfsTer5)
c.1803_1804del (p.Pro602CysfsTer5)
ClinVar dbSNP
11g.47341214T>ACA474218220MYBPC3c.1821A>T (p.Thr607=)
c.1803A>T (p.Thr601=)
11g.47341214T>CCA078320MYBPC3c.1821A>G (p.Thr607=)
c.1803A>G (p.Thr601=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341214T>GCA474218221MYBPC3c.1821A>C (p.Thr607=)
c.1803A>C (p.Thr601=)
dbSNP
11g.47341214T=CA1969334718MYBPC3c.1821A= (p.Thr607=)
c.1803A= (p.Thr601=)
11g.47341216_47341229delCA2580084222MYBPC3c.1808_1821del (p.Ile603ThrfsTer6)
c.1790_1803del (p.Ile597ThrfsTer6)
ClinVar
11g.47341215G>ACA078317MYBPC3c.1820C>T (p.Thr607Ile)
c.1802C>T (p.Thr601Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341215G>CCA046882MYBPC3c.1820C>G (p.Thr607Arg)
c.1802C>G (p.Thr601Arg)
11g.47341215G=CA1969334719MYBPC3c.1820C= (p.Thr607=)
c.1802C= (p.Thr601=)
11g.47341215G>TCA380323982MYBPC3c.1820C>A (p.Thr607Lys)
c.1802C>A (p.Thr601Lys)
11g.47341216T>ACA380323983MYBPC3c.1819A>T (p.Thr607Ser)
c.1801A>T (p.Thr601Ser)
ClinVar dbSNP
11g.47341216T>CCA380323984MYBPC3c.1819A>G (p.Thr607Ala)
c.1801A>G (p.Thr601Ala)
gnomAD v4
11g.47341216T>GCA380323985MYBPC3c.1819A>C (p.Thr607Pro)
c.1801A>C (p.Thr601Pro)
11g.47341216T=CA1969334721MYBPC3c.1819A= (p.Thr607=)
c.1801A= (p.Thr601=)
11g.47341217G>ACA474218225MYBPC3c.1818C>T (p.Val606=)
c.1800C>T (p.Val600=)
11g.47341217G>CCA474218226MYBPC3c.1818C>G (p.Val606=)
c.1800C>G (p.Val600=)
11g.47341217G>TCA474218227MYBPC3c.1818C>A (p.Val606=)
c.1800C>A (p.Val600=)
11g.47341218A=CA1969334722MYBPC3c.1817T= (p.Val606=)
c.1799T= (p.Val600=)
11g.47341218A>CCA380323986MYBPC3c.1817T>G (p.Val606Gly)
c.1799T>G (p.Val600Gly)
11g.47341218A>GCA380323987MYBPC3c.1817T>C (p.Val606Ala)
c.1799T>C (p.Val600Ala)
dbSNP gnomAD v4
11g.47341218A>TCA380323988MYBPC3c.1817T>A (p.Val606Asp)
c.1799T>A (p.Val600Asp)
11g.47341218_47341221delinsACGTCA1969334723MYBPC3c.1814_1817delinsACGT (p.Asp605=)
c.1796_1799delinsACGT (p.Asp599=)
11g.47341219C>ACA380323994MYBPC3c.1816G>T (p.Val606Phe)
c.1798G>T (p.Val600Phe)
gnomAD v4
11g.47341219C=CA1969334725MYBPC3c.1816G= (p.Val606=)
c.1798G= (p.Val600=)
11g.47341219C>GCA380323990MYBPC3c.1816G>C (p.Val606Leu)
c.1798G>C (p.Val600Leu)
11g.47341219C>TCA011251MYBPC3c.1816G>A (p.Val606Ile)
c.1798G>A (p.Val600Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341223_47341225delCA011234MYBPC3c.1814_1816del (p.Asp605del)
c.1796_1798del (p.Asp599del)
ClinVar dbSNP
11g.47341219_47341220insATTGACA2613399319MYBPC3c.1815_1816insTCAAT (p.Val606SerfsTer?)
c.1797_1798insTCAAT (p.Val600SerfsTer?)
gnomAD v4
11g.47341220G>ACA078314MYBPC3c.1815C>T (p.Asp605=)
c.1797C>T (p.Asp599=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.47341220G>CCA380323996MYBPC3c.1815C>G (p.Asp605Glu)
c.1797C>G (p.Asp599Glu)
11g.47341220G=CA1969334728MYBPC3c.1815C= (p.Asp605=)
c.1797C= (p.Asp599=)
11g.47341220G>TCA380323998MYBPC3c.1815C>A (p.Asp605Glu)
c.1797C>A (p.Asp599Glu)
11g.47341221T>ACA380324000MYBPC3c.1814A>T (p.Asp605Val)
c.1796A>T (p.Asp599Val)
11g.47341221T>CCA011239MYBPC3c.1814A>G (p.Asp605Gly)
c.1796A>G (p.Asp599Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341221T>GCA380324003MYBPC3c.1814A>C (p.Asp605Ala)
c.1796A>C (p.Asp599Ala)
11g.47341221T=CA1969334732MYBPC3c.1814A= (p.Asp605=)
c.1796A= (p.Asp599=)
11g.47341222C>ACA380324006MYBPC3c.1813G>T (p.Asp605Tyr)
c.1795G>T (p.Asp599Tyr)
gnomAD v4
11g.47341222C=CA1969334735MYBPC3c.1813G= (p.Asp605=)
c.1795G= (p.Asp599=)
11g.47341222C>GCA380324008MYBPC3c.1813G>C (p.Asp605His)
c.1795G>C (p.Asp599His)
11g.47341222C>TCA011225MYBPC3c.1813G>A (p.Asp605Asn)
c.1795G>A (p.Asp599Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341222_47341223dupCA5975372MYBPC3c.1812_1813dup (p.Asp605AlafsTer?)
c.1794_1795dup (p.Asp599AlafsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341223G>ACA011214MYBPC3c.1812C>T (p.Asp604=)
c.1794C>T (p.Asp598=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341223G>CCA380324012MYBPC3c.1812C>G (p.Asp604Glu)
c.1794C>G (p.Asp598Glu)
11g.47341223G=CA1969334737MYBPC3c.1812C= (p.Asp604=)
c.1794C= (p.Asp598=)
11g.47341223G>TCA380324009MYBPC3c.1812C>A (p.Asp604Glu)
c.1794C>A (p.Asp598Glu)
gnomAD v4
11g.47341224T>ACA380324014MYBPC3c.1811A>T (p.Asp604Val)
c.1793A>T (p.Asp598Val)
dbSNP
11g.47341224T>CCA046789MYBPC3c.1811A>G (p.Asp604Gly)
c.1793A>G (p.Asp598Gly)
gnomAD v4
11g.47341224T>GCA380324017MYBPC3c.1811A>C (p.Asp604Ala)
c.1793A>C (p.Asp598Ala)
11g.47341224T=CA1969334739MYBPC3c.1811A= (p.Asp604=)
c.1793A= (p.Asp598=)
11g.47341225C>ACA380324020MYBPC3c.1810G>T (p.Asp604Tyr)
c.1792G>T (p.Asp598Tyr)
gnomAD v4
11g.47341225C>GCA380324021MYBPC3c.1810G>C (p.Asp604His)
c.1792G>C (p.Asp598His)
11g.47341225C>TCA046766MYBPC3c.1810G>A (p.Asp604Asn)
c.1792G>A (p.Asp598Asn)
gnomAD v4
11g.47341225_47341226delinsCACA1969334740MYBPC3c.1809_1810delinsTG (p.Ile603=)
c.1791_1792delinsTG (p.Ile597=)
11g.47341226A=CA1969334742MYBPC3c.1809T= (p.Ile603=)
c.1791T= (p.Ile597=)
11g.47341226A>CCA078307MYBPC3c.1809T>G (p.Ile603Met)
c.1791T>G (p.Ile597Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341226A>GCA474218239MYBPC3c.1809T>C (p.Ile603=)
c.1791T>C (p.Ile597=)
ClinVar dbSNP gnomAD v4
11g.47341226A>TCA474218240MYBPC3c.1809T>A (p.Ile603=)
c.1791T>A (p.Ile597=)
11g.47341227delCA16619340MYBPC3c.1809del (p.Ile603MetfsTer?)
c.1791del (p.Ile597MetfsTer?)
ClinVar dbSNP
11g.47341227A=CA1969334745MYBPC3c.1808T= (p.Ile603=)
c.1790T= (p.Ile597=)
11g.47341227A>CCA380324025MYBPC3c.1808T>G (p.Ile603Ser)
c.1790T>G (p.Ile597Ser)
11g.47341227A>GCA011205MYBPC3c.1808T>C (p.Ile603Thr)
c.1790T>C (p.Ile597Thr)
ClinVar dbSNP
11g.47341227A>TCA380324027MYBPC3c.1808T>A (p.Ile603Asn)
c.1790T>A (p.Ile597Asn)
11g.47341227_47341228insATCCA2697548578MYBPC3c.1807_1808insGAT (p.Ile603delinsArgPhe)
c.1789_1790insGAT (p.Ile597delinsArgPhe)
ClinVar
11g.47341228T>ACA380324030MYBPC3c.1807A>T (p.Ile603Phe)
c.1789A>T (p.Ile597Phe)
11g.47341228T>CCA380324032MYBPC3c.1807A>G (p.Ile603Val)
c.1789A>G (p.Ile597Val)
11g.47341228T>GCA380324034MYBPC3c.1807A>C (p.Ile603Leu)
c.1789A>C (p.Ile597Leu)
11g.47341228_47341229delinsTGCA1969334746MYBPC3c.1806_1807delinsCA (p.Thr602=)
c.1788_1789delinsCA (p.Thr596=)
11g.47341229G>ACA474218254MYBPC3c.1806C>T (p.Thr602=)
c.1788C>T (p.Thr596=)
gnomAD v4
11g.47341229G>CCA474218257MYBPC3c.1806C>G (p.Thr602=)
c.1788C>G (p.Thr596=)
gnomAD v4
11g.47341229G=CA1969334749MYBPC3c.1806C= (p.Thr602=)
c.1788C= (p.Thr596=)
11g.47341229G>TCA078304MYBPC3c.1806C>A (p.Thr602=)
c.1788C>A (p.Thr596=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47341230delCA011196MYBPC3c.1806del (p.Ile603LeufsTer?)
c.1788del (p.Ile597LeufsTer?)
ClinVar dbSNP gnomAD v4
11g.47341230G>ACA011188MYBPC3c.1805C>T (p.Thr602Ile)
c.1787C>T (p.Thr596Ile)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47341230G>CCA380324038MYBPC3c.1805C>G (p.Thr602Ser)
c.1787C>G (p.Thr596Ser)
11g.47341230G=CA1969334752MYBPC3c.1805C= (p.Thr602=)
c.1787C= (p.Thr596=)
11g.47341230G>TCA380324040MYBPC3c.1805C>A (p.Thr602Asn)
c.1787C>A (p.Thr596Asn)
11g.47341231T>ACA380324042MYBPC3c.1804A>T (p.Thr602Ser)
c.1786A>T (p.Thr596Ser)
11g.47341231T>CCA380324044MYBPC3c.1804A>G (p.Thr602Ala)
c.1786A>G (p.Thr596Ala)
gnomAD v4
11g.47341231T>GCA380324046MYBPC3c.1804A>C (p.Thr602Pro)
c.1786A>C (p.Thr596Pro)
11g.47341232C>ACA474218266MYBPC3c.1803G>T (p.Leu601=)
c.1785G>T (p.Leu595=)
gnomAD v4
11g.47341232C=CA1969334753MYBPC3c.1803G= (p.Leu601=)
c.1785G= (p.Leu595=)
11g.47341232C>GCA474218264MYBPC3c.1803G>C (p.Leu601=)
c.1785G>C (p.Leu595=)
11g.47341232C>TCA011180MYBPC3c.1803G>A (p.Leu601=)
c.1785G>A (p.Leu595=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47341233A>CCA380324049MYBPC3c.1802T>G (p.Leu601Arg)
c.1784T>G (p.Leu595Arg)
11g.47341233A>GCA380324052MYBPC3c.1802T>C (p.Leu601Pro)
c.1784T>C (p.Leu595Pro)
gnomAD v4
11g.47341233A>TCA380324051MYBPC3c.1802T>A (p.Leu601Gln)
c.1784T>A (p.Leu595Gln)
11g.47341234G>ACA474218271MYBPC3c.1801C>T (p.Leu601=)
c.1783C>T (p.Leu595=)
gnomAD v4
11g.47341234G>CCA380324054MYBPC3c.1801C>G (p.Leu601Val)
c.1783C>G (p.Leu595Val)
11g.47341234G>TCA380324056MYBPC3c.1801C>A (p.Leu601Met)
c.1783C>A (p.Leu595Met)
gnomAD v4
11g.47341234_47341235delinsGTCA1969334755MYBPC3c.1800_1801delinsAC (p.Lys600=)
c.1782_1783delinsAC (p.Lys594=)
11g.47341235T>ACA380324057MYBPC3c.1800A>T (p.Lys600Asn)
c.1782A>T (p.Lys594Asn)
11g.47341235T>CCA474218294MYBPC3c.1800A>G (p.Lys600=)
c.1782A>G (p.Lys594=)
11g.47341235T>GCA380324059MYBPC3c.1800A>C (p.Lys600Asn)
c.1782A>C (p.Lys594Asn)
11g.47341237delCA011173MYBPC3c.1800del (p.Lys600AsnfsTer2)
c.1782del (p.Lys594AsnfsTer2)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47341236T>ACA380324065MYBPC3c.1799A>T (p.Lys600Ile)
c.1781A>T (p.Lys594Ile)
11g.47341236T>CCA380324067MYBPC3c.1799A>G (p.Lys600Arg)
c.1781A>G (p.Lys594Arg)
ClinVar dbSNP gnomAD v4
11g.47341236T>GCA380324063MYBPC3c.1799A>C (p.Lys600Thr)
c.1781A>C (p.Lys594Thr)
ClinVar
11g.47341237T>ACA380324071MYBPC3c.1798A>T (p.Lys600Ter)
c.1780A>T (p.Lys594Ter)
11g.47341237T>CCA380324069MYBPC3c.1798A>G (p.Lys600Glu)
c.1780A>G (p.Lys594Glu)
gnomAD v4
11g.47341237T>GCA380324073MYBPC3c.1798A>C (p.Lys600Gln)
c.1780A>C (p.Lys594Gln)
11g.47341238delCA2695212781MYBPC3c.1797del (p.His599GlnfsTer3)
c.1779del (p.His593GlnfsTer3)
11g.47341238G>ACA474218303MYBPC3c.1797C>T (p.His599=)
c.1779C>T (p.His593=)
dbSNP gnomAD v2
11g.47341238G>CCA380324075MYBPC3c.1797C>G (p.His599Gln)
c.1779C>G (p.His593Gln)
gnomAD v4
11g.47341238G=CA1969334758MYBPC3c.1797C= (p.His599=)
c.1779C= (p.His593=)
11g.47341238G>TCA380324077MYBPC3c.1797C>A (p.His599Gln)
c.1779C>A (p.His593Gln)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47341239T>ACA380324079MYBPC3c.1796A>T (p.His599Leu)
c.1778A>T (p.His593Leu)
11g.47341239T>CCA380324081MYBPC3c.1796A>G (p.His599Arg)
c.1778A>G (p.His593Arg)
11g.47341239T>GCA380324083MYBPC3c.1796A>C (p.His599Pro)
c.1778A>C (p.His593Pro)
11g.47341240G>ACA380324085MYBPC3c.1795C>T (p.His599Tyr)
c.1777C>T (p.His593Tyr)
gnomAD v4
11g.47341240G>CCA380324087MYBPC3c.1795C>G (p.His599Asp)
c.1777C>G (p.His593Asp)
11g.47341240G>TCA380324088MYBPC3c.1795C>A (p.His599Asn)
c.1777C>A (p.His593Asn)
11g.47341241delCA2613399573MYBPC3c.1795del (p.His599ThrfsTer3)
c.1777del (p.His593ThrfsTer3)
gnomAD v4
11g.47341241G>ACA474218318MYBPC3c.1794C>T (p.Val598=)
c.1776C>T (p.Val592=)
11g.47341241G>CCA474218321MYBPC3c.1794C>G (p.Val598=)
c.1776C>G (p.Val592=)
11g.47341241G>TCA474218322MYBPC3c.1794C>A (p.Val598=)
c.1776C>A (p.Val592=)
gnomAD v4
11g.47341242A>CCA380324090MYBPC3c.1793T>G (p.Val598Gly)
c.1775T>G (p.Val592Gly)
11g.47341242A>GCA380324092MYBPC3c.1793T>C (p.Val598Ala)
c.1775T>C (p.Val592Ala)
gnomAD v4
11g.47341242A>TCA380324094MYBPC3c.1793T>A (p.Val598Asp)
c.1775T>A (p.Val592Asp)
gnomAD v4
11g.47341242_47341243delinsACCA1969334760MYBPC3c.1792_1793delinsGT (p.Val598=)
c.1774_1775delinsGT (p.Val592=)

Number of alleles fetched