Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47341149_47341205dupCA2573147067MYBPC3c.1831_1887dup (p.Leu629_His630insGluAlaAspTyrSerPheValProGluGlyPheAlaCysAsnLeuSerAlaLysLeu)
c.1813_1869dup (p.Leu623_His624insGluAlaAspTyrSerPheValProGluGlyPheAlaCysAsnLeuSerAlaLysLeu)
ClinVar dbSNP
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.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.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

Number of alleles fetched