Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47330388_47335387delCA2740090117
11g.47335093_47335180dupCA2580084264MYBPC3c.2770_2857dup (p.Gly953AspfsTer?)
c.2752_2839dup (p.Gly947AspfsTer?)
c.2689_2776dup (p.Gly926AspfsTer?)
ClinVar
11g.47335104T>ACA380316306MYBPC3c.2843A>T (p.Asn948Ile)
c.2825A>T (p.Asn942Ile)
c.2762A>T (p.Asn921Ile)
11g.47335104T>CCA380316307MYBPC3c.2843A>G (p.Asn948Ser)
c.2825A>G (p.Asn942Ser)
c.2762A>G (p.Asn921Ser)
dbSNP
11g.47335104T>GCA013042MYBPC3c.2843A>C (p.Asn948Thr)
c.2825A>C (p.Asn942Thr)
c.2762A>C (p.Asn921Thr)
ClinVar dbSNP
11g.47335104T=CA1969337110MYBPC3c.2843A= (p.Asn948=)
c.2825A= (p.Asn942=)
c.2762A= (p.Asn921=)
11g.47335104_47335105delCA2499220963MYBPC3c.2842_2843del (p.Asn948TyrfsTer?)
c.2824_2825del (p.Asn942TyrfsTer?)
c.2761_2762del (p.Asn921TyrfsTer?)
ClinVar dbSNP
11g.47335105T>ACA380316308MYBPC3c.2842A>T (p.Asn948Tyr)
c.2824A>T (p.Asn942Tyr)
c.2761A>T (p.Asn921Tyr)
11g.47335105T>CCA380316309MYBPC3c.2842A>G (p.Asn948Asp)
c.2824A>G (p.Asn942Asp)
c.2761A>G (p.Asn921Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47335105T>GCA380316310MYBPC3c.2842A>C (p.Asn948His)
c.2824A>C (p.Asn942His)
c.2761A>C (p.Asn921His)
11g.47335105T=CA1969337115MYBPC3c.2842A= (p.Asn948=)
c.2824A= (p.Asn942=)
c.2761A= (p.Asn921=)
11g.47335106G>ACA474213003MYBPC3c.2841C>T (p.His947=)
c.2823C>T (p.His941=)
c.2760C>T (p.His920=)
11g.47335106G>CCA380316311MYBPC3c.2841C>G (p.His947Gln)
c.2823C>G (p.His941Gln)
c.2760C>G (p.His920Gln)
dbSNP
11g.47335106G=CA1969337118MYBPC3c.2841C= (p.His947=)
c.2823C= (p.His941=)
c.2760C= (p.His920=)
11g.47335106G>TCA078981MYBPC3c.2841C>A (p.His947Gln)
c.2823C>A (p.His941Gln)
c.2760C>A (p.His920Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47335106_47335111delinsTTGTGTCA2580084265MYBPC3c.2836_2841delinsACACAA (p.Ala946_His947delinsThrGln)
c.2818_2823delinsACACAA (p.Ala940_His941delinsThrGln)
c.2755_2760delinsACACAA (p.Ala919_His920delinsThrGln)
ClinVar
11g.47335107T>ACA380316313MYBPC3c.2840A>T (p.His947Leu)
c.2822A>T (p.His941Leu)
c.2759A>T (p.His920Leu)
dbSNP
11g.47335107T>CCA078979MYBPC3c.2840A>G (p.His947Arg)
c.2822A>G (p.His941Arg)
c.2759A>G (p.His920Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47335107T>GCA380316315MYBPC3c.2840A>C (p.His947Pro)
c.2822A>C (p.His941Pro)
c.2759A>C (p.His920Pro)
11g.47335107T=CA1969337120MYBPC3c.2840A= (p.His947=)
c.2822A= (p.His941=)
c.2759A= (p.His920=)
11g.47335108G>ACA380316319MYBPC3c.2839C>T (p.His947Tyr)
c.2821C>T (p.His941Tyr)
c.2758C>T (p.His920Tyr)
gnomAD v4
11g.47335108G>CCA380316317MYBPC3c.2839C>G (p.His947Asp)
c.2821C>G (p.His941Asp)
c.2758C>G (p.His920Asp)
11g.47335108G=CA1969337122MYBPC3c.2839C= (p.His947=)
c.2821C= (p.His941=)
c.2758C= (p.His920=)
11g.47335108G>TCA013033MYBPC3c.2839C>A (p.His947Asn)
c.2821C>A (p.His941Asn)
c.2758C>A (p.His920Asn)
ClinVar dbSNP
11g.47335109T>ACA474213021MYBPC3c.2838A>T (p.Ala946=)
c.2820A>T (p.Ala940=)
c.2757A>T (p.Ala919=)
11g.47335109T>CCA078976MYBPC3c.2838A>G (p.Ala946=)
c.2820A>G (p.Ala940=)
c.2757A>G (p.Ala919=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47335109T>GCA474213024MYBPC3c.2838A>C (p.Ala946=)
c.2820A>C (p.Ala940=)
c.2757A>C (p.Ala919=)
11g.47335109T=CA1969337124MYBPC3c.2838A= (p.Ala946=)
c.2820A= (p.Ala940=)
c.2757A= (p.Ala919=)
11g.47335110G>ACA380316322MYBPC3c.2837C>T (p.Ala946Val)
c.2819C>T (p.Ala940Val)
c.2756C>T (p.Ala919Val)
11g.47335110G>CCA380316324MYBPC3c.2837C>G (p.Ala946Gly)
c.2819C>G (p.Ala940Gly)
c.2756C>G (p.Ala919Gly)
11g.47335110G>TCA380316325MYBPC3c.2837C>A (p.Ala946Glu)
c.2819C>A (p.Ala940Glu)
c.2756C>A (p.Ala919Glu)
11g.47335111C>ACA380316329MYBPC3c.2836G>T (p.Ala946Ser)
c.2818G>T (p.Ala940Ser)
c.2755G>T (p.Ala919Ser)
11g.47335111C=CA1969337125MYBPC3c.2836G= (p.Ala946=)
c.2818G= (p.Ala940=)
c.2755G= (p.Ala919=)
11g.47335111C>GCA380316330MYBPC3c.2836G>C (p.Ala946Pro)
c.2818G>C (p.Ala940Pro)
c.2755G>C (p.Ala919Pro)
11g.47335111C>TCA380316332MYBPC3c.2836G>A (p.Ala946Thr)
c.2818G>A (p.Ala940Thr)
c.2755G>A (p.Ala919Thr)
ClinVar dbSNP gnomAD v4
11g.47335112C>ACA474213031MYBPC3c.2835G>T (p.Arg945=)
c.2817G>T (p.Arg939=)
c.2754G>T (p.Arg918=)
11g.47335112C>GCA474213032MYBPC3c.2835G>C (p.Arg945=)
c.2817G>C (p.Arg939=)
c.2754G>C (p.Arg918=)
11g.47335112C>TCA474213034MYBPC3c.2835G>A (p.Arg945=)
c.2817G>A (p.Arg939=)
c.2754G>A (p.Arg918=)
11g.47335112_47335114delinsCCGCA1969337126MYBPC3c.2833_2835delinsCGG (p.Arg945=)
c.2815_2817delinsCGG (p.Arg939=)
c.2752_2754delinsCGG (p.Arg918=)
11g.47335113C>ACA380316335MYBPC3c.2834G>T (p.Arg945Leu)
c.2816G>T (p.Arg939Leu)
c.2753G>T (p.Arg918Leu)
dbSNP gnomAD v4
11g.47335113C=CA1969337129MYBPC3c.2834G= (p.Arg945=)
c.2816G= (p.Arg939=)
c.2753G= (p.Arg918=)
11g.47335113C>GCA380316336MYBPC3c.2834G>C (p.Arg945Pro)
c.2816G>C (p.Arg939Pro)
c.2753G>C (p.Arg918Pro)
dbSNP gnomAD v3 gnomAD v4
11g.47335113C>TCA380316338MYBPC3c.2834G>A (p.Arg945Gln)
c.2816G>A (p.Arg939Gln)
c.2753G>A (p.Arg918Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47335114_47335115delCA013018MYBPC3c.2833_2834del (p.Arg945GlyfsTer?)
c.2815_2816del (p.Arg939GlyfsTer?)
c.2752_2753del (p.Arg918GlyfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47335114G>ACA013027MYBPC3c.2833C>T (p.Arg945Trp)
c.2815C>T (p.Arg939Trp)
c.2752C>T (p.Arg918Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47335114G>CCA380316342MYBPC3c.2833C>G (p.Arg945Gly)
c.2815C>G (p.Arg939Gly)
c.2752C>G (p.Arg918Gly)
gnomAD v4
11g.47335114G=CA1969337131MYBPC3c.2833C= (p.Arg945=)
c.2815C= (p.Arg939=)
c.2752C= (p.Arg918=)
11g.47335114G>TCA474213047MYBPC3c.2833C>A (p.Arg945=)
c.2815C>A (p.Arg939=)
c.2752C>A (p.Arg918=)
11g.47335115C>ACA474213049MYBPC3c.2832G>T (p.Val944=)
c.2814G>T (p.Val938=)
c.2751G>T (p.Val917=)
11g.47335115C>GCA474213052MYBPC3c.2832G>C (p.Val944=)
c.2814G>C (p.Val938=)
c.2751G>C (p.Val917=)

Number of alleles fetched