Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47347891C>ACA380333920MYBPC3c.787G>T (p.Gly263Ter)
ClinVar dbSNP gnomAD v4
11g.47347891C=CA1969340644MYBPC3c.787G= (p.Gly263=)
11g.47347891C>GCA380333922MYBPC3c.787G>C (p.Gly263Arg)
dbSNP
11g.47347891C>TCA015857MYBPC3c.787G>A (p.Gly263Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47347892G>ACA015851MYBPC3c.786C>T (p.Thr262=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47347892G>CCA474221324MYBPC3c.786C>G (p.Thr262=)
11g.47347892G=CA1630848685MYBPC3c.786C= (p.Thr262=)
11g.47347892G>TCA474221325MYBPC3c.786C>A (p.Thr262=)
gnomAD v4
11g.47347893G>ACA380333933MYBPC3c.785C>T (p.Thr262Ile)
gnomAD v4
11g.47347893G>CCA015841MYBPC3c.785C>G (p.Thr262Ser)
dbSNP
11g.47347893G=CA1969340645MYBPC3c.785C= (p.Thr262=)
11g.47347893G>TCA380333927MYBPC3c.785C>A (p.Thr262Asn)
gnomAD v4
11g.47347894T>ACA380333937MYBPC3c.784A>T (p.Thr262Ser)
11g.47347894T>CCA380333940MYBPC3c.784A>G (p.Thr262Ala)
dbSNP gnomAD v2
11g.47347894T>GCA380333939MYBPC3c.784A>C (p.Thr262Pro)
11g.47347894T=CA1969340646MYBPC3c.784A= (p.Thr262=)
11g.47347895G>ACA474221326MYBPC3c.783C>T (p.Gly261=)
gnomAD v4
11g.47347895G>CCA474221327MYBPC3c.783C>G (p.Gly261=)
gnomAD v4
11g.47347895G=CA1969340647MYBPC3c.783C= (p.Gly261=)
11g.47347895G>TCA056842MYBPC3c.783C>A (p.Gly261=)
dbSNP ExAC gnomAD v4
11g.47347896C>ACA380333946MYBPC3c.782G>T (p.Gly261Val)
gnomAD v4
11g.47347896C>GCA380333948MYBPC3c.782G>C (p.Gly261Ala)
gnomAD v4
11g.47347896C>TCA380333950MYBPC3c.782G>A (p.Gly261Asp)
gnomAD v4
11g.47347898delCA474221328MYBPC3c.782del (p.Gly261AlafsTer?)
COSMIC COSMIC
11g.47347897C>ACA380333953MYBPC3c.781G>T (p.Gly261Cys)
gnomAD v4 COSMIC COSMIC
11g.47347897C>GCA380333955MYBPC3c.781G>C (p.Gly261Arg)
11g.47347897C>TCA380333956MYBPC3c.781G>A (p.Gly261Ser)
gnomAD v4
11g.47347898C>ACA380333960MYBPC3c.780G>T (p.Met260Ile)
gnomAD v4
11g.47347898C>GCA380333962MYBPC3c.780G>C (p.Met260Ile)
11g.47347898C>TCA380333965MYBPC3c.780G>A (p.Met260Ile)
gnomAD v4
11g.47347898_47347899delinsCACA1969340648MYBPC3c.779_780delinsTG (p.Met260=)
11g.47347899delCA015832MYBPC3c.779del (p.Met260ArgfsTer?)
dbSNP
11g.47347899A=CA1969340649MYBPC3c.779T= (p.Met260=)
11g.47347899A>CCA380333976MYBPC3c.779T>G (p.Met260Arg)
dbSNP gnomAD v2 gnomAD v4
11g.47347899A>GCA380333974MYBPC3c.779T>C (p.Met260Thr)
ClinVar dbSNP gnomAD v4
11g.47347899A>TCA380333968MYBPC3c.779T>A (p.Met260Lys)
gnomAD v4
11g.47347899_47347900insCCA2613394588MYBPC3c.778_779insG (p.Met260SerfsTer26)
gnomAD v4
11g.47347900T>ACA380333979MYBPC3c.778A>T (p.Met260Leu)
gnomAD v4
11g.47347900T>CCA380333981MYBPC3c.778A>G (p.Met260Val)
gnomAD v4
11g.47347900T>GCA380333983MYBPC3c.778A>C (p.Met260Leu)
gnomAD v4
11g.47347901G>ACA474221329MYBPC3c.777C>T (p.Ala259=)
ClinVar dbSNP gnomAD v4
11g.47347901G>CCA474221330MYBPC3c.777C>G (p.Ala259=)
11g.47347901G>TCA474221331MYBPC3c.777C>A (p.Ala259=)
gnomAD v4
11g.47347902dupCA2613394591MYBPC3c.777dup (p.Met260HisfsTer26)
gnomAD v4
11g.47347902G>ACA221702723MYBPC3c.776C>T (p.Ala259Val)
dbSNP gnomAD v3 gnomAD v4
11g.47347902G>CCA380333986MYBPC3c.776C>G (p.Ala259Gly)
ClinVar dbSNP
11g.47347902G=CA1969340650MYBPC3c.776C= (p.Ala259=)
11g.47347902G>TCA380333988MYBPC3c.776C>A (p.Ala259Asp)
gnomAD v4
11g.47347902delinsAACA2695213943MYBPC3c.776delinsTT (p.Ala259ValfsTer27)
11g.47347903C>ACA380333990MYBPC3c.775G>T (p.Ala259Ser)
gnomAD v4

Number of alleles fetched