Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47337729A=CA1969331587MYBPC3c.2374T= (p.Trp792=)
c.2356T= (p.Trp786=)
c.2293T= (p.Trp765=)
11g.47337729A>CCA221688921MYBPC3c.2374T>G (p.Trp792Gly)
c.2356T>G (p.Trp786Gly)
c.2293T>G (p.Trp765Gly)
 dbSNP
11g.47337729A>GCA012147MYBPC3c.2374T>C (p.Trp792Arg)
c.2356T>C (p.Trp786Arg)
c.2293T>C (p.Trp765Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337729A>TCA380318738MYBPC3c.2374T>A (p.Trp792Arg)
c.2356T>A (p.Trp786Arg)
c.2293T>A (p.Trp765Arg)
 ClinVar dbSNP
11g.47337730C>ACA380318741MYBPC3c.2373G>T (p.Gln791His)
c.2355G>T (p.Gln785His)
c.2292G>T (p.Gln764His)
 gnomAD v4
11g.47337730C=CA1969331588MYBPC3c.2373G= (p.Gln791=)
c.2355G= (p.Gln785=)
c.2292G= (p.Gln764=)
11g.47337730C>GCA380318743MYBPC3c.2373G>C (p.Gln791His)
c.2355G>C (p.Gln785His)
c.2292G>C (p.Gln764His)
11g.47337730C>TCA474216081MYBPC3c.2373G>A (p.Gln791=)
c.2355G>A (p.Gln785=)
c.2292G>A (p.Gln764=)
 gnomAD v4
11g.47337730dupCA012139MYBPC3c.2373dup (p.Trp792ValfsTer?)
c.2373dup (p.Trp792ValfsTer16)
c.2355dup (p.Trp786ValfsTer?)
c.2292dup (p.Trp765ValfsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337731T>ACA380318752MYBPC3c.2372A>T (p.Gln791Leu)
c.2354A>T (p.Gln785Leu)
c.2291A>T (p.Gln764Leu)
 gnomAD v4
11g.47337731T>CCA078668MYBPC3c.2372A>G (p.Gln791Arg)
c.2354A>G (p.Gln785Arg)
c.2291A>G (p.Gln764Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47337731T>GCA380318756MYBPC3c.2372A>C (p.Gln791Pro)
c.2354A>C (p.Gln785Pro)
c.2291A>C (p.Gln764Pro)
 ClinVar dbSNP
11g.47337731T=CA1969331589MYBPC3c.2372A= (p.Gln791=)
c.2354A= (p.Gln785=)
c.2291A= (p.Gln764=)
11g.47337731dupCA221688928MYBPC3c.2372dup (p.Trp792ValfsTer?)
c.2372dup (p.Trp792ValfsTer16)
c.2354dup (p.Trp786ValfsTer?)
c.2291dup (p.Trp765ValfsTer?)
 dbSNP
11g.47337732G>ACA279318MYBPC3c.2371C>T (p.Gln791Ter)
c.2353C>T (p.Gln785Ter)
c.2290C>T (p.Gln764Ter)
 ClinVar dbSNP gnomAD v4
11g.47337732G>CCA380318760MYBPC3c.2371C>G (p.Gln791Glu)
c.2353C>G (p.Gln785Glu)
c.2290C>G (p.Gln764Glu)
11g.47337732G=CA1969331590MYBPC3c.2371C= (p.Gln791=)
c.2353C= (p.Gln785=)
c.2290C= (p.Gln764=)
11g.47337732G>TCA380318763MYBPC3c.2371C>A (p.Gln791Lys)
c.2353C>A (p.Gln785Lys)
c.2290C>A (p.Gln764Lys)
11g.47337733T>ACA474216097MYBPC3c.2370A>T (p.Val790=)
c.2352A>T (p.Val784=)
c.2289A>T (p.Val763=)
11g.47337733T>CCA474216098MYBPC3c.2370A>G (p.Val790=)
c.2352A>G (p.Val784=)
c.2289A>G (p.Val763=)
 ClinVar dbSNP
11g.47337733T>GCA474216101MYBPC3c.2370A>C (p.Val790=)
c.2352A>C (p.Val784=)
c.2289A>C (p.Val763=)
11g.47337733T=CA1969331591MYBPC3c.2370A= (p.Val790=)
c.2352A= (p.Val784=)
c.2289A= (p.Val763=)
11g.47337734A>CCA380318768MYBPC3c.2369T>G (p.Val790Gly)
c.2351T>G (p.Val784Gly)
c.2288T>G (p.Val763Gly)
11g.47337734A>GCA380318771MYBPC3c.2369T>C (p.Val790Ala)
c.2351T>C (p.Val784Ala)
c.2288T>C (p.Val763Ala)
 gnomAD v4 COSMIC
11g.47337734A>TCA380318774MYBPC3c.2369T>A (p.Val790Glu)
c.2351T>A (p.Val784Glu)
c.2288T>A (p.Val763Glu)
 gnomAD v4
11g.47337735C>ACA380318777MYBPC3c.2368G>T (p.Val790Leu)
c.2350G>T (p.Val784Leu)
c.2287G>T (p.Val763Leu)
11g.47337735C=CA1969331592MYBPC3c.2368G= (p.Val790=)
c.2350G= (p.Val784=)
c.2287G= (p.Val763=)
11g.47337735C>GCA380318780MYBPC3c.2368G>C (p.Val790Leu)
c.2350G>C (p.Val784Leu)
c.2287G>C (p.Val763Leu)
 dbSNP
11g.47337735C>TCA380318782MYBPC3c.2368G>A (p.Val790Ile)
c.2350G>A (p.Val784Ile)
c.2287G>A (p.Val763Ile)
 gnomAD v4
11g.47337736T>ACA474216124MYBPC3c.2367A>T (p.Thr789=)
c.2349A>T (p.Thr783=)
c.2286A>T (p.Thr762=)
 gnomAD v4
11g.47337736T>CCA474216118MYBPC3c.2367A>G (p.Thr789=)
c.2349A>G (p.Thr783=)
c.2286A>G (p.Thr762=)
 gnomAD v4
11g.47337736T>GCA474216121MYBPC3c.2367A>C (p.Thr789=)
c.2349A>C (p.Thr783=)
c.2286A>C (p.Thr762=)
 gnomAD v4
11g.47337736dupCA913187723MYBPC3c.2367dup (p.Val790SerfsTer?)
c.2367dup (p.Val790SerfsTer18)
c.2349dup (p.Val784SerfsTer?)
c.2286dup (p.Val763SerfsTer?)
 ClinVar
11g.47337737G>ACA380318786MYBPC3c.2366C>T (p.Thr789Ile)
c.2348C>T (p.Thr783Ile)
c.2285C>T (p.Thr762Ile)
 ClinVar dbSNP gnomAD v4
11g.47337737G>CCA380318789MYBPC3c.2366C>G (p.Thr789Arg)
c.2348C>G (p.Thr783Arg)
c.2285C>G (p.Thr762Arg)
 gnomAD v4
11g.47337737G>TCA380318791MYBPC3c.2366C>A (p.Thr789Lys)
c.2348C>A (p.Thr783Lys)
c.2285C>A (p.Thr762Lys)
 gnomAD v4
11g.47337737_47337738insACCAGCTGGGAGATCTCAAGCAGGTCATTTAACTGCTTGGAGCCTGTCA2613392508MYBPC3c.2365_2366insACAGGCTCCAAGCAGTTAAATGACCTGCTTGAGATCTCCCAGCTGGT (p.Thr789AsnfsTer8)
c.2347_2348insACAGGCTCCAAGCAGTTAAATGACCTGCTTGAGATCTCCCAGCTGGT (p.Thr783AsnfsTer8)
c.2284_2285insACAGGCTCCAAGCAGTTAAATGACCTGCTTGAGATCTCCCAGCTGGT (p.Thr762AsnfsTer8)
 gnomAD v4
11g.47337738T>ACA380318796MYBPC3c.2365A>T (p.Thr789Ser)
c.2347A>T (p.Thr783Ser)
c.2284A>T (p.Thr762Ser)
11g.47337738T>CCA380318799MYBPC3c.2365A>G (p.Thr789Ala)
c.2347A>G (p.Thr783Ala)
c.2284A>G (p.Thr762Ala)
 gnomAD v4
11g.47337738T>GCA380318801MYBPC3c.2365A>C (p.Thr789Pro)
c.2347A>C (p.Thr783Pro)
c.2284A>C (p.Thr762Pro)
11g.47337739G>ACA474216146MYBPC3c.2364C>T (p.Cys788=)
c.2346C>T (p.Cys782=)
c.2283C>T (p.Cys761=)
 gnomAD v4
11g.47337739G>CCA380318808MYBPC3c.2364C>G (p.Cys788Trp)
c.2346C>G (p.Cys782Trp)
c.2283C>G (p.Cys761Trp)
11g.47337739G>TCA380318805MYBPC3c.2364C>A (p.Cys788Ter)
c.2346C>A (p.Cys782Ter)
c.2283C>A (p.Cys761Ter)
 ClinVar gnomAD v4
11g.47337740C>ACA078665MYBPC3c.2363G>T (p.Cys788Phe)
c.2345G>T (p.Cys782Phe)
c.2282G>T (p.Cys761Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.47337740C=CA1969331593MYBPC3c.2363G= (p.Cys788=)
c.2345G= (p.Cys782=)
c.2282G= (p.Cys761=)
11g.47337740C>GCA380318809MYBPC3c.2363G>C (p.Cys788Ser)
c.2345G>C (p.Cys782Ser)
c.2282G>C (p.Cys761Ser)
11g.47337740C>TCA380318811MYBPC3c.2363G>A (p.Cys788Tyr)
c.2345G>A (p.Cys782Tyr)
c.2282G>A (p.Cys761Tyr)
 gnomAD v4
11g.47337741A>CCA380318814MYBPC3c.2362T>G (p.Cys788Gly)
c.2344T>G (p.Cys782Gly)
c.2281T>G (p.Cys761Gly)
 gnomAD v4
11g.47337741A>GCA380318816MYBPC3c.2362T>C (p.Cys788Arg)
c.2344T>C (p.Cys782Arg)
c.2281T>C (p.Cys761Arg)
 ClinVar gnomAD v4
11g.47337741A>TCA380318817MYBPC3c.2362T>A (p.Cys788Ser)
c.2344T>A (p.Cys782Ser)
c.2281T>A (p.Cys761Ser)
11g.47337741dupCA923726204MYBPC3c.2362dup (p.Cys788LeufsTer?)
c.2362dup (p.Cys788LeufsTer20)
c.2344dup (p.Cys782LeufsTer?)
c.2281dup (p.Cys761LeufsTer?)
11g.47337743_47337745dupCA913187726MYBPC3c.2360_2362dup (p.Ser787_Cys788insSer)
c.2342_2344dup (p.Ser781_Cys782insSer)
c.2279_2281dup (p.Ser760_Cys761insSer)
 ClinVar dbSNP
11g.47337742G>ACA474216184MYBPC3c.2361C>T (p.Ser787=)
c.2343C>T (p.Ser781=)
c.2280C>T (p.Ser760=)
 gnomAD v4
11g.47337742G>CCA474216187MYBPC3c.2361C>G (p.Ser787=)
c.2343C>G (p.Ser781=)
c.2280C>G (p.Ser760=)
11g.47337742G>TCA474216186MYBPC3c.2361C>A (p.Ser787=)
c.2343C>A (p.Ser781=)
c.2280C>A (p.Ser760=)
 gnomAD v4
11g.47337743G>ACA380318828MYBPC3c.2360C>T (p.Ser787Phe)
c.2342C>T (p.Ser781Phe)
c.2279C>T (p.Ser760Phe)
 gnomAD v4
11g.47337743G>CCA380318822MYBPC3c.2360C>G (p.Ser787Cys)
c.2342C>G (p.Ser781Cys)
c.2279C>G (p.Ser760Cys)
11g.47337743G>TCA380318825MYBPC3c.2360C>A (p.Ser787Tyr)
c.2342C>A (p.Ser781Tyr)
c.2279C>A (p.Ser760Tyr)
 gnomAD v4
11g.47337744A>CCA380318832MYBPC3c.2359T>G (p.Ser787Ala)
c.2341T>G (p.Ser781Ala)
c.2278T>G (p.Ser760Ala)
 gnomAD v4
11g.47337744A>GCA380318834MYBPC3c.2359T>C (p.Ser787Pro)
c.2341T>C (p.Ser781Pro)
c.2278T>C (p.Ser760Pro)
11g.47337744A>TCA380318835MYBPC3c.2359T>A (p.Ser787Thr)
c.2341T>A (p.Ser781Thr)
c.2278T>A (p.Ser760Thr)
11g.47337745G>ACA474216213MYBPC3c.2358C>T (p.Asp786=)
c.2340C>T (p.Asp780=)
c.2277C>T (p.Asp759=)
11g.47337745G>CCA380318840MYBPC3c.2358C>G (p.Asp786Glu)
c.2340C>G (p.Asp780Glu)
c.2277C>G (p.Asp759Glu)
11g.47337745G>TCA380318843MYBPC3c.2358C>A (p.Asp786Glu)
c.2340C>A (p.Asp780Glu)
c.2277C>A (p.Asp759Glu)
 gnomAD v4
11g.47337746T>ACA380318847MYBPC3c.2357A>T (p.Asp786Val)
c.2339A>T (p.Asp780Val)
c.2276A>T (p.Asp759Val)
11g.47337746T>CCA380318853MYBPC3c.2357A>G (p.Asp786Gly)
c.2339A>G (p.Asp780Gly)
c.2276A>G (p.Asp759Gly)
 ClinVar dbSNP gnomAD v4
11g.47337746T>GCA380318850MYBPC3c.2357A>C (p.Asp786Ala)
c.2339A>C (p.Asp780Ala)
c.2276A>C (p.Asp759Ala)
 dbSNP
11g.47337746T=CA1969331594MYBPC3c.2357A= (p.Asp786=)
c.2339A= (p.Asp780=)
c.2276A= (p.Asp759=)
11g.47337748_47337750delCA2724174851MYBPC3c.2355_2357del (p.Glu785del)
c.2337_2339del (p.Glu779del)
c.2274_2276del (p.Glu758del)
 dbSNP
11g.47337749_47337753delCA2573051152MYBPC3c.2353_2357del (p.Glu785LeufsTer?)
c.2353_2357del (p.Glu785LeufsTer21)
c.2335_2339del (p.Glu779LeufsTer?)
c.2272_2276del (p.Glu758LeufsTer?)
11g.47337747C>ACA380318856MYBPC3c.2356G>T (p.Asp786Tyr)
c.2338G>T (p.Asp780Tyr)
c.2275G>T (p.Asp759Tyr)
 ClinVar dbSNP gnomAD v4
11g.47337747C>GCA380318858MYBPC3c.2356G>C (p.Asp786His)
c.2338G>C (p.Asp780His)
c.2275G>C (p.Asp759His)
11g.47337747C>TCA380318861MYBPC3c.2356G>A (p.Asp786Asn)
c.2338G>A (p.Asp780Asn)
c.2275G>A (p.Asp759Asn)
11g.47337748C>ACA380318865MYBPC3c.2355G>T (p.Glu785Asp)
c.2337G>T (p.Glu779Asp)
c.2274G>T (p.Glu758Asp)
 gnomAD v4
11g.47337748C=CA1969331595MYBPC3c.2355G= (p.Glu785=)
c.2337G= (p.Glu779=)
c.2274G= (p.Glu758=)
11g.47337748C>GCA380318867MYBPC3c.2355G>C (p.Glu785Asp)
c.2337G>C (p.Glu779Asp)
c.2274G>C (p.Glu758Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47337748C>TCA474216263MYBPC3c.2355G>A (p.Glu785=)
c.2337G>A (p.Glu779=)
c.2274G>A (p.Glu758=)
 gnomAD v4
11g.47337749T>ACA380318871MYBPC3c.2354A>T (p.Glu785Val)
c.2336A>T (p.Glu779Val)
c.2273A>T (p.Glu758Val)
11g.47337749T>CCA380318874MYBPC3c.2354A>G (p.Glu785Gly)
c.2336A>G (p.Glu779Gly)
c.2273A>G (p.Glu758Gly)
 gnomAD v4
11g.47337749T>GCA380318877MYBPC3c.2354A>C (p.Glu785Ala)
c.2336A>C (p.Glu779Ala)
c.2273A>C (p.Glu758Ala)
11g.47337750C>ACA380318881MYBPC3c.2353G>T (p.Glu785Ter)
c.2335G>T (p.Glu779Ter)
c.2272G>T (p.Glu758Ter)
 gnomAD v4
11g.47337750C=CA1969331596MYBPC3c.2353G= (p.Glu785=)
c.2335G= (p.Glu779=)
c.2272G= (p.Glu758=)
11g.47337750C>GCA380318883MYBPC3c.2353G>C (p.Glu785Gln)
c.2335G>C (p.Glu779Gln)
c.2272G>C (p.Glu758Gln)
11g.47337750C>TCA380318891MYBPC3c.2353G>A (p.Glu785Lys)
c.2335G>A (p.Glu779Lys)
c.2272G>A (p.Glu758Lys)
 dbSNP
11g.47337751T>ACA474216280MYBPC3c.2352A>T (p.Gly784=)
c.2334A>T (p.Gly778=)
c.2271A>T (p.Gly757=)
11g.47337751T>CCA078663MYBPC3c.2352A>G (p.Gly784=)
c.2334A>G (p.Gly778=)
c.2271A>G (p.Gly757=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47337751T>GCA474216299MYBPC3c.2352A>C (p.Gly784=)
c.2334A>C (p.Gly778=)
c.2271A>C (p.Gly757=)
11g.47337751T=CA1969331597MYBPC3c.2352A= (p.Gly784=)
c.2334A= (p.Gly778=)
c.2271A= (p.Gly757=)
11g.47337752C>ACA380318902MYBPC3c.2351G>T (p.Gly784Val)
c.2333G>T (p.Gly778Val)
c.2270G>T (p.Gly757Val)
 gnomAD v4
11g.47337752C=CA1969331598MYBPC3c.2351G= (p.Gly784=)
c.2333G= (p.Gly778=)
c.2270G= (p.Gly757=)
11g.47337752C>GCA380318905MYBPC3c.2351G>C (p.Gly784Ala)
c.2333G>C (p.Gly778Ala)
c.2270G>C (p.Gly757Ala)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47337752C>TCA221688960MYBPC3c.2351G>A (p.Gly784Glu)
c.2333G>A (p.Gly778Glu)
c.2270G>A (p.Gly757Glu)
 ClinVar dbSNP gnomAD v4
11g.47337754delCA2574816039MYBPC3c.2351del (p.Gly784GlufsTer?)
c.2333del (p.Gly778GlufsTer?)
c.2270del (p.Gly757GlufsTer?)
11g.47337753C>ACA380318908MYBPC3c.2350G>T (p.Gly784Ter)
c.2332G>T (p.Gly778Ter)
c.2269G>T (p.Gly757Ter)
 gnomAD v4
11g.47337753C=CA1969331599MYBPC3c.2350G= (p.Gly784=)
c.2332G= (p.Gly778=)
c.2269G= (p.Gly757=)
11g.47337753C>GCA380318913MYBPC3c.2350G>C (p.Gly784Arg)
c.2332G>C (p.Gly778Arg)
c.2269G>C (p.Gly757Arg)
11g.47337753C>TCA380318910MYBPC3c.2350G>A (p.Gly784Arg)
c.2332G>A (p.Gly778Arg)
c.2269G>A (p.Gly757Arg)
 ClinVar dbSNP gnomAD v2
11g.47337754C>ACA474216328MYBPC3c.2349G>T (p.Val783=)
c.2331G>T (p.Val777=)
c.2268G>T (p.Val756=)
 gnomAD v4
11g.47337754C>GCA474216330MYBPC3c.2349G>C (p.Val783=)
c.2331G>C (p.Val777=)
c.2268G>C (p.Val756=)
11g.47337754C>TCA474216333MYBPC3c.2349G>A (p.Val783=)
c.2331G>A (p.Val777=)
c.2268G>A (p.Val756=)
 gnomAD v4
11g.47337755A=CA1969331600MYBPC3c.2348T= (p.Val783=)
c.2330T= (p.Val777=)
c.2267T= (p.Val756=)
11g.47337755A>CCA380318917MYBPC3c.2348T>G (p.Val783Gly)
c.2330T>G (p.Val777Gly)
c.2267T>G (p.Val756Gly)
11g.47337755A>GCA380318923MYBPC3c.2348T>C (p.Val783Ala)
c.2330T>C (p.Val777Ala)
c.2267T>C (p.Val756Ala)
 dbSNP gnomAD v4
11g.47337755A>TCA380318920MYBPC3c.2348T>A (p.Val783Glu)
c.2330T>A (p.Val777Glu)
c.2267T>A (p.Val756Glu)
11g.47337756C>ACA16609755MYBPC3c.2347G>T (p.Val783Leu)
c.2329G>T (p.Val777Leu)
c.2266G>T (p.Val756Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337756C=CA1969331601MYBPC3c.2347G= (p.Val783=)
c.2329G= (p.Val777=)
c.2266G= (p.Val756=)
11g.47337756C>GCA380318929MYBPC3c.2347G>C (p.Val783Leu)
c.2329G>C (p.Val777Leu)
c.2266G>C (p.Val756Leu)
11g.47337756C>TCA380318933MYBPC3c.2347G>A (p.Val783Met)
c.2329G>A (p.Val777Met)
c.2266G>A (p.Val756Met)
 ClinVar dbSNP gnomAD v4
11g.47337757G>ACA078662MYBPC3c.2346C>T (p.Asn782=)
c.2328C>T (p.Asn776=)
c.2265C>T (p.Asn755=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.47337757G>CCA380318939MYBPC3c.2346C>G (p.Asn782Lys)
c.2328C>G (p.Asn776Lys)
c.2265C>G (p.Asn755Lys)
11g.47337757G=CA1969331602MYBPC3c.2346C= (p.Asn782=)
c.2328C= (p.Asn776=)
c.2265C= (p.Asn755=)
11g.47337757G>TCA380318942MYBPC3c.2346C>A (p.Asn782Lys)
c.2328C>A (p.Asn776Lys)
c.2265C>A (p.Asn755Lys)
 dbSNP gnomAD v3 gnomAD v4
11g.47337758T>ACA380318946MYBPC3c.2345A>T (p.Asn782Ile)
c.2327A>T (p.Asn776Ile)
c.2264A>T (p.Asn755Ile)
11g.47337758T>CCA078660MYBPC3c.2345A>G (p.Asn782Ser)
c.2327A>G (p.Asn776Ser)
c.2264A>G (p.Asn755Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337758T>GCA380318951MYBPC3c.2345A>C (p.Asn782Thr)
c.2327A>C (p.Asn776Thr)
c.2264A>C (p.Asn755Thr)
11g.47337758T=CA1969331603MYBPC3c.2345A= (p.Asn782=)
c.2327A= (p.Asn776=)
c.2264A= (p.Asn755=)
11g.47337759T>ACA380318954MYBPC3c.2344A>T (p.Asn782Tyr)
c.2326A>T (p.Asn776Tyr)
c.2263A>T (p.Asn755Tyr)
 gnomAD v4
11g.47337759T>CCA380318956MYBPC3c.2344A>G (p.Asn782Asp)
c.2326A>G (p.Asn776Asp)
c.2263A>G (p.Asn755Asp)
 gnomAD v4
11g.47337759T>GCA380318957MYBPC3c.2344A>C (p.Asn782His)
c.2326A>C (p.Asn776His)
c.2263A>C (p.Asn755His)
11g.47337760G>ACA049395MYBPC3c.2343C>T (p.Ser781=)
c.2325C>T (p.Ser775=)
c.2262C>T (p.Ser754=)
 gnomAD v4
11g.47337760G>CCA380318960MYBPC3c.2343C>G (p.Ser781Arg)
c.2325C>G (p.Ser775Arg)
c.2262C>G (p.Ser754Arg)
 gnomAD v4
11g.47337760G>TCA380318963MYBPC3c.2343C>A (p.Ser781Arg)
c.2325C>A (p.Ser775Arg)
c.2262C>A (p.Ser754Arg)
 ClinVar gnomAD v4
11g.47337761C>ACA380318966MYBPC3c.2342G>T (p.Ser781Ile)
c.2324G>T (p.Ser775Ile)
c.2261G>T (p.Ser754Ile)
 gnomAD v4
11g.47337761C=CA1969331604MYBPC3c.2342G= (p.Ser781=)
c.2324G= (p.Ser775=)
c.2261G= (p.Ser754=)
11g.47337761C>GCA380318969MYBPC3c.2342G>C (p.Ser781Thr)
c.2324G>C (p.Ser775Thr)
c.2261G>C (p.Ser754Thr)
11g.47337761C>TCA380318973MYBPC3c.2342G>A (p.Ser781Asn)
c.2324G>A (p.Ser775Asn)
c.2261G>A (p.Ser754Asn)
 dbSNP gnomAD v2 gnomAD v4
11g.47337762T>ACA380318977MYBPC3c.2341A>T (p.Ser781Cys)
c.2323A>T (p.Ser775Cys)
c.2260A>T (p.Ser754Cys)
11g.47337762T>CCA380318988MYBPC3c.2341A>G (p.Ser781Gly)
c.2323A>G (p.Ser775Gly)
c.2260A>G (p.Ser754Gly)
 ClinVar dbSNP gnomAD v4
11g.47337762T>GCA380318989MYBPC3c.2341A>C (p.Ser781Arg)
c.2323A>C (p.Ser775Arg)
c.2260A>C (p.Ser754Arg)
11g.47337762T=CA1969331605MYBPC3c.2341A= (p.Ser781=)
c.2323A= (p.Ser775=)
c.2260A= (p.Ser754=)
11g.47337763G>ACA474216414MYBPC3c.2340C>T (p.Ile780=)
c.2322C>T (p.Ile774=)
c.2259C>T (p.Ile753=)
 gnomAD v4
11g.47337763G>CCA380318995MYBPC3c.2340C>G (p.Ile780Met)
c.2322C>G (p.Ile774Met)
c.2259C>G (p.Ile753Met)
 gnomAD v4
11g.47337763G>TCA474216417MYBPC3c.2340C>A (p.Ile780=)
c.2322C>A (p.Ile774=)
c.2259C>A (p.Ile753=)
 gnomAD v4
11g.47337764A=CA1969331606MYBPC3c.2339T= (p.Ile780=)
c.2321T= (p.Ile774=)
c.2258T= (p.Ile753=)
11g.47337764A>CCA078657MYBPC3c.2339T>G (p.Ile780Ser)
c.2321T>G (p.Ile774Ser)
c.2258T>G (p.Ile753Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337764A>GCA380319000MYBPC3c.2339T>C (p.Ile780Thr)
c.2321T>C (p.Ile774Thr)
c.2258T>C (p.Ile753Thr)
 ClinVar dbSNP gnomAD v4
11g.47337764A>TCA380319003MYBPC3c.2339T>A (p.Ile780Asn)
c.2321T>A (p.Ile774Asn)
c.2258T>A (p.Ile753Asn)
11g.47337765T>ACA380319010MYBPC3c.2338A>T (p.Ile780Phe)
c.2320A>T (p.Ile774Phe)
c.2257A>T (p.Ile753Phe)
 ClinVar
11g.47337765T>CCA380319012MYBPC3c.2338A>G (p.Ile780Val)
c.2320A>G (p.Ile774Val)
c.2257A>G (p.Ile753Val)
 ClinVar COSMIC COSMIC
11g.47337765T>GCA380319008MYBPC3c.2338A>C (p.Ile780Leu)
c.2320A>C (p.Ile774Leu)
c.2257A>C (p.Ile753Leu)
11g.47337766C>ACA078656MYBPC3c.2337G>T (p.Lys779Asn)
c.2319G>T (p.Lys773Asn)
c.2256G>T (p.Lys752Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.47337766C=CA1969331607MYBPC3c.2337G= (p.Lys779=)
c.2319G= (p.Lys773=)
c.2256G= (p.Lys752=)
11g.47337766C>GCA380319018MYBPC3c.2337G>C (p.Lys779Asn)
c.2319G>C (p.Lys773Asn)
c.2256G>C (p.Lys752Asn)
11g.47337766C>TCA474216442MYBPC3c.2337G>A (p.Lys779=)
c.2319G>A (p.Lys773=)
c.2256G>A (p.Lys752=)
11g.47337767T>ACA380319022MYBPC3c.2336A>T (p.Lys779Met)
c.2318A>T (p.Lys773Met)
c.2255A>T (p.Lys752Met)
11g.47337767T>CCA078653MYBPC3c.2336A>G (p.Lys779Arg)
c.2318A>G (p.Lys773Arg)
c.2255A>G (p.Lys752Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337767T>GCA380319028MYBPC3c.2336A>C (p.Lys779Thr)
c.2318A>C (p.Lys773Thr)
c.2255A>C (p.Lys752Thr)
11g.47337767T=CA1969331608MYBPC3c.2336A= (p.Lys779=)
c.2318A= (p.Lys773=)
c.2255A= (p.Lys752=)
11g.47337768T>ACA380319032MYBPC3c.2335A>T (p.Lys779Ter)
c.2317A>T (p.Lys773Ter)
c.2254A>T (p.Lys752Ter)
11g.47337768T>CCA380319034MYBPC3c.2335A>G (p.Lys779Glu)
c.2317A>G (p.Lys773Glu)
c.2254A>G (p.Lys752Glu)
 ClinVar gnomAD v4
11g.47337768T>GCA380319036MYBPC3c.2335A>C (p.Lys779Gln)
c.2317A>C (p.Lys773Gln)
c.2254A>C (p.Lys752Gln)
11g.47337768_47337769delinsTGCA1969331609MYBPC3c.2334_2335delinsCA (p.Pro778=)
c.2316_2317delinsCA (p.Pro772=)
c.2253_2254delinsCA (p.Pro751=)
11g.47337769G>ACA474216451MYBPC3c.2334C>T (p.Pro778=)
c.2316C>T (p.Pro772=)
c.2253C>T (p.Pro751=)
 ClinVar dbSNP gnomAD v4
11g.47337769G>CCA474216454MYBPC3c.2334C>G (p.Pro778=)
c.2316C>G (p.Pro772=)
c.2253C>G (p.Pro751=)
11g.47337769G=CA1969331611MYBPC3c.2334C= (p.Pro778=)
c.2316C= (p.Pro772=)
c.2253C= (p.Pro751=)
11g.47337769G>TCA474216457MYBPC3c.2334C>A (p.Pro778=)
c.2316C>A (p.Pro772=)
c.2253C>A (p.Pro751=)
 gnomAD v4
11g.47337773dupCA1969331610MYBPC3c.2334dup (p.Lys779GlnfsTer?)
c.2334dup (p.Lys779GlnfsTer29)
c.2316dup (p.Lys773GlnfsTer?)
c.2253dup (p.Lys752GlnfsTer?)
 ClinVar dbSNP
11g.47337773delCA16042829MYBPC3c.2334del (p.Lys779ArgfsTer?)
c.2316del (p.Lys773ArgfsTer?)
c.2253del (p.Lys752ArgfsTer?)
 ClinVar dbSNP gnomAD v4
11g.47337771_47337773delCA2613392572MYBPC3c.2332_2334del (p.Pro778del)
c.2314_2316del (p.Pro772del)
c.2251_2253del (p.Pro751del)
 gnomAD v4
11g.47337770G>ACA380319044MYBPC3c.2333C>T (p.Pro778Leu)
c.2315C>T (p.Pro772Leu)
c.2252C>T (p.Pro751Leu)
 dbSNP gnomAD v2
11g.47337770G>CCA380319045MYBPC3c.2333C>G (p.Pro778Arg)
c.2315C>G (p.Pro772Arg)
c.2252C>G (p.Pro751Arg)
11g.47337770G=CA1969331612MYBPC3c.2333C= (p.Pro778=)
c.2315C= (p.Pro772=)
c.2252C= (p.Pro751=)
11g.47337770G>TCA380319048MYBPC3c.2333C>A (p.Pro778His)
c.2315C>A (p.Pro772His)
c.2252C>A (p.Pro751His)
 gnomAD v4
11g.47337771G>ACA380319054MYBPC3c.2332C>T (p.Pro778Ser)
c.2314C>T (p.Pro772Ser)
c.2251C>T (p.Pro751Ser)
 gnomAD v4
11g.47337771G>CCA380319049MYBPC3c.2332C>G (p.Pro778Ala)
c.2314C>G (p.Pro772Ala)
c.2251C>G (p.Pro751Ala)
11g.47337771G>TCA380319051MYBPC3c.2332C>A (p.Pro778Thr)
c.2314C>A (p.Pro772Thr)
c.2251C>A (p.Pro751Thr)
 gnomAD v4
11g.47337772G>ACA474216477MYBPC3c.2331C>T (p.Ala777=)
c.2313C>T (p.Ala771=)
c.2250C>T (p.Ala750=)
11g.47337772G>CCA474216479MYBPC3c.2331C>G (p.Ala777=)
c.2313C>G (p.Ala771=)
c.2250C>G (p.Ala750=)
11g.47337772G>TCA474216481MYBPC3c.2331C>A (p.Ala777=)
c.2313C>A (p.Ala771=)
c.2250C>A (p.Ala750=)
 gnomAD v4
11g.47337773G>ACA078651MYBPC3c.2330C>T (p.Ala777Val)
c.2312C>T (p.Ala771Val)
c.2249C>T (p.Ala750Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337773G>CCA380319058MYBPC3c.2330C>G (p.Ala777Gly)
c.2312C>G (p.Ala771Gly)
c.2249C>G (p.Ala750Gly)
11g.47337773G=CA1969331613MYBPC3c.2330C= (p.Ala777=)
c.2312C= (p.Ala771=)
c.2249C= (p.Ala750=)
11g.47337773G>TCA380319062MYBPC3c.2330C>A (p.Ala777Asp)
c.2312C>A (p.Ala771Asp)
c.2249C>A (p.Ala750Asp)
 gnomAD v4
11g.47337774C>ACA380319066MYBPC3c.2329G>T (p.Ala777Ser)
c.2311G>T (p.Ala771Ser)
c.2248G>T (p.Ala750Ser)
 gnomAD v4
11g.47337774C>GCA380319069MYBPC3c.2329G>C (p.Ala777Pro)
c.2311G>C (p.Ala771Pro)
c.2248G>C (p.Ala750Pro)
 gnomAD v4
11g.47337774C>TCA380319072MYBPC3c.2329G>A (p.Ala777Thr)
c.2311G>A (p.Ala771Thr)
c.2248G>A (p.Ala750Thr)
 dbSNP
11g.47337775dupCA2573051240MYBPC3c.2329dup (p.Ala777GlyfsTer?)
c.2311dup (p.Ala771GlyfsTer?)
c.2248dup (p.Ala750GlyfsTer?)
11g.47337775C>ACA474216491MYBPC3c.2328G>T (p.Ala776=)
c.2310G>T (p.Ala770=)
c.2247G>T (p.Ala749=)
 gnomAD v4
11g.47337775C=CA1969331614MYBPC3c.2328G= (p.Ala776=)
c.2310G= (p.Ala770=)
c.2247G= (p.Ala749=)
11g.47337775C>GCA474216493MYBPC3c.2328G>C (p.Ala776=)
c.2310G>C (p.Ala770=)
c.2247G>C (p.Ala749=)
11g.47337775C>TCA474216495MYBPC3c.2328G>A (p.Ala776=)
c.2310G>A (p.Ala770=)
c.2247G>A (p.Ala749=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337776G>ACA049319MYBPC3c.2327C>T (p.Ala776Val)
c.2309C>T (p.Ala770Val)
c.2246C>T (p.Ala749Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337776G>CCA380319085MYBPC3c.2327C>G (p.Ala776Gly)
c.2309C>G (p.Ala770Gly)
c.2246C>G (p.Ala749Gly)
11g.47337776G=CA1969331615MYBPC3c.2327C= (p.Ala776=)
c.2309C= (p.Ala770=)
c.2246C= (p.Ala749=)
11g.47337776G>TCA380319089MYBPC3c.2327C>A (p.Ala776Glu)
c.2309C>A (p.Ala770Glu)
c.2246C>A (p.Ala749Glu)
 gnomAD v4
11g.47337777C>ACA380319093MYBPC3c.2326G>T (p.Ala776Ser)
c.2308G>T (p.Ala770Ser)
c.2245G>T (p.Ala749Ser)
 gnomAD v4
11g.47337777C=CA1969331616MYBPC3c.2326G= (p.Ala776=)
c.2308G= (p.Ala770=)
c.2245G= (p.Ala749=)
11g.47337777C>GCA380319095MYBPC3c.2326G>C (p.Ala776Pro)
c.2308G>C (p.Ala770Pro)
c.2245G>C (p.Ala749Pro)
11g.47337777C>TCA380319099MYBPC3c.2326G>A (p.Ala776Thr)
c.2308G>A (p.Ala770Thr)
c.2245G>A (p.Ala749Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47337778A>CCA474216506MYBPC3c.2325T>G (p.Pro775=)
c.2307T>G (p.Pro769=)
c.2244T>G (p.Pro748=)
11g.47337778A>GCA474216510MYBPC3c.2325T>C (p.Pro775=)
c.2307T>C (p.Pro769=)
c.2244T>C (p.Pro748=)
 gnomAD v4
11g.47337778A>TCA474216508MYBPC3c.2325T>A (p.Pro775=)
c.2307T>A (p.Pro769=)
c.2244T>A (p.Pro748=)
 gnomAD v4
11g.47337779G>ACA380319110MYBPC3c.2324C>T (p.Pro775Leu)
c.2306C>T (p.Pro769Leu)
c.2243C>T (p.Pro748Leu)
 gnomAD v4
11g.47337779G>CCA012122MYBPC3c.2324C>G (p.Pro775Arg)
c.2306C>G (p.Pro769Arg)
c.2243C>G (p.Pro748Arg)
 ClinVar dbSNP gnomAD v4
11g.47337779G=CA1969331617MYBPC3c.2324C= (p.Pro775=)
c.2306C= (p.Pro769=)
c.2243C= (p.Pro748=)
11g.47337779G>TCA380319105MYBPC3c.2324C>A (p.Pro775His)
c.2306C>A (p.Pro769His)
c.2243C>A (p.Pro748His)
 gnomAD v4
11g.47337780G>ACA380319115MYBPC3c.2323C>T (p.Pro775Ser)
c.2305C>T (p.Pro769Ser)
c.2242C>T (p.Pro748Ser)
 gnomAD v4
11g.47337780G>CCA380319122MYBPC3c.2323C>G (p.Pro775Ala)
c.2305C>G (p.Pro769Ala)
c.2242C>G (p.Pro748Ala)
11g.47337780G>TCA380319118MYBPC3c.2323C>A (p.Pro775Thr)
c.2305C>A (p.Pro769Thr)
c.2242C>A (p.Pro748Thr)
 gnomAD v4
11g.47337781T>ACA474216515MYBPC3c.2322A>T (p.Ala774=)
c.2304A>T (p.Ala768=)
c.2241A>T (p.Ala747=)
11g.47337781T>CCA474216517MYBPC3c.2322A>G (p.Ala774=)
c.2304A>G (p.Ala768=)
c.2241A>G (p.Ala747=)
 gnomAD v4
11g.47337781T>GCA474216519MYBPC3c.2322A>C (p.Ala774=)
c.2304A>C (p.Ala768=)
c.2241A>C (p.Ala747=)
11g.47337782G>ACA380319125MYBPC3c.2321C>T (p.Ala774Val)
c.2303C>T (p.Ala768Val)
c.2240C>T (p.Ala747Val)
 ClinVar dbSNP gnomAD v4
11g.47337782G>CCA380319128MYBPC3c.2321C>G (p.Ala774Gly)
c.2303C>G (p.Ala768Gly)
c.2240C>G (p.Ala747Gly)
11g.47337782G=CA1969331618MYBPC3c.2321C= (p.Ala774=)
c.2303C= (p.Ala768=)
c.2240C= (p.Ala747=)
11g.47337782G>TCA380319130MYBPC3c.2321C>A (p.Ala774Glu)
c.2303C>A (p.Ala768Glu)
c.2240C>A (p.Ala747Glu)
 gnomAD v4
11g.47337783C>ACA380319134MYBPC3c.2320G>T (p.Ala774Ser)
c.2302G>T (p.Ala768Ser)
c.2239G>T (p.Ala747Ser)
11g.47337783C=CA1969331619MYBPC3c.2320G= (p.Ala774=)
c.2302G= (p.Ala768=)
c.2239G= (p.Ala747=)
11g.47337783C>GCA380319139MYBPC3c.2320G>C (p.Ala774Pro)
c.2302G>C (p.Ala768Pro)
c.2239G>C (p.Ala747Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47337783C>TCA012113MYBPC3c.2320G>A (p.Ala774Thr)
c.2302G>A (p.Ala768Thr)
c.2239G>A (p.Ala747Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337784G>ACA012107MYBPC3c.2319C>T (p.Asp773=)
c.2301C>T (p.Asp767=)
c.2238C>T (p.Asp746=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337784G>CCA380319148MYBPC3c.2319C>G (p.Asp773Glu)
c.2301C>G (p.Asp767Glu)
c.2238C>G (p.Asp746Glu)
11g.47337784G=CA1969331620MYBPC3c.2319C= (p.Asp773=)
c.2301C= (p.Asp767=)
c.2238C= (p.Asp746=)
11g.47337784G>TCA380319163MYBPC3c.2319C>A (p.Asp773Glu)
c.2301C>A (p.Asp767Glu)
c.2238C>A (p.Asp746Glu)
11g.47337785T>ACA380319168MYBPC3c.2318A>T (p.Asp773Val)
c.2300A>T (p.Asp767Val)
c.2237A>T (p.Asp746Val)
 ClinVar dbSNP
11g.47337785T>CCA380319170MYBPC3c.2318A>G (p.Asp773Gly)
c.2300A>G (p.Asp767Gly)
c.2237A>G (p.Asp746Gly)
 gnomAD v4
11g.47337785T>GCA380319173MYBPC3c.2318A>C (p.Asp773Ala)
c.2300A>C (p.Asp767Ala)
c.2237A>C (p.Asp746Ala)
11g.47337786C>ACA380319178MYBPC3c.2317G>T (p.Asp773Tyr)
c.2299G>T (p.Asp767Tyr)
c.2236G>T (p.Asp746Tyr)
 gnomAD v4
11g.47337786C=CA1969331621MYBPC3c.2317G= (p.Asp773=)
c.2299G= (p.Asp767=)
c.2236G= (p.Asp746=)
11g.47337786C>GCA380319183MYBPC3c.2317G>C (p.Asp773His)
c.2299G>C (p.Asp767His)
c.2236G>C (p.Asp746His)
11g.47337786C>TCA049293MYBPC3c.2317G>A (p.Asp773Asn)
c.2299G>A (p.Asp767Asn)
c.2236G>A (p.Asp746Asn)
 dbSNP gnomAD v2
11g.47337787T>ACA474216546MYBPC3c.2316A>T (p.Pro772=)
c.2298A>T (p.Pro766=)
c.2235A>T (p.Pro745=)
11g.47337787T>CCA474216547MYBPC3c.2316A>G (p.Pro772=)
c.2298A>G (p.Pro766=)
c.2235A>G (p.Pro745=)
 dbSNP gnomAD v2 gnomAD v4
11g.47337787T>GCA474216550MYBPC3c.2316A>C (p.Pro772=)
c.2298A>C (p.Pro766=)
c.2235A>C (p.Pro745=)
11g.47337787T=CA1969331622MYBPC3c.2316A= (p.Pro772=)
c.2298A= (p.Pro766=)
c.2235A= (p.Pro745=)
11g.47337788G>ACA380319188MYBPC3c.2315C>T (p.Pro772Leu)
c.2297C>T (p.Pro766Leu)
c.2234C>T (p.Pro745Leu)
11g.47337788G>CCA380319191MYBPC3c.2315C>G (p.Pro772Arg)
c.2297C>G (p.Pro766Arg)
c.2234C>G (p.Pro745Arg)
 gnomAD v4
11g.47337788G>TCA380319194MYBPC3c.2315C>A (p.Pro772Gln)
c.2297C>A (p.Pro766Gln)
c.2234C>A (p.Pro745Gln)
11g.47337789G>ACA380319199MYBPC3c.2314C>T (p.Pro772Ser)
c.2296C>T (p.Pro766Ser)
c.2233C>T (p.Pro745Ser)
 gnomAD v4
11g.47337789G>CCA380319200MYBPC3c.2314C>G (p.Pro772Ala)
c.2296C>G (p.Pro766Ala)
c.2233C>G (p.Pro745Ala)
 dbSNP
11g.47337789G=CA1969331623MYBPC3c.2314C= (p.Pro772=)
c.2296C= (p.Pro766=)
c.2233C= (p.Pro745=)
11g.47337789G>TCA380319204MYBPC3c.2314C>A (p.Pro772Thr)
c.2296C>A (p.Pro766Thr)
c.2233C>A (p.Pro745Thr)
11g.47337789_47337794delCA2739291463MYBPC3c.2309_2314del (p.Asp770_Pro772delinsAla)
c.2291_2296del (p.Asp764_Pro766delinsAla)
c.2228_2233del (p.Asp743_Pro745delinsAla)
11g.47337790C>ACA474216561MYBPC3c.2313G>T (p.Val771=)
c.2295G>T (p.Val765=)
c.2232G>T (p.Val744=)
 gnomAD v4
11g.47337790C=CA1969331624MYBPC3c.2313G= (p.Val771=)
c.2295G= (p.Val765=)
c.2232G= (p.Val744=)
11g.47337790C>GCA474216563MYBPC3c.2313G>C (p.Val771=)
c.2295G>C (p.Val765=)
c.2232G>C (p.Val744=)
11g.47337790C>TCA474216565MYBPC3c.2313G>A (p.Val771=)
c.2295G>A (p.Val765=)
c.2232G>A (p.Val744=)
 dbSNP gnomAD v4
11g.47337791A=CA1969331625MYBPC3c.2312T= (p.Val771=)
c.2294T= (p.Val765=)
c.2231T= (p.Val744=)
11g.47337791A>CCA380319210MYBPC3c.2312T>G (p.Val771Gly)
c.2294T>G (p.Val765Gly)
c.2231T>G (p.Val744Gly)
11g.47337791A>GCA012096MYBPC3c.2312T>C (p.Val771Ala)
c.2294T>C (p.Val765Ala)
c.2231T>C (p.Val744Ala)
 ClinVar dbSNP
11g.47337791A>TCA380319215MYBPC3c.2312T>A (p.Val771Glu)
c.2294T>A (p.Val765Glu)
c.2231T>A (p.Val744Glu)
11g.47337792C>ACA380319231MYBPC3c.2311G>T (p.Val771Leu)
c.2293G>T (p.Val765Leu)
c.2230G>T (p.Val744Leu)
 gnomAD v4
11g.47337792C=CA1969331627MYBPC3c.2311G= (p.Val771=)
c.2293G= (p.Val765=)
c.2230G= (p.Val744=)
11g.47337792C>GCA380319225MYBPC3c.2311G>C (p.Val771Leu)
c.2293G>C (p.Val765Leu)
c.2230G>C (p.Val744Leu)
 gnomAD v4
11g.47337792C>TCA012087MYBPC3c.2311G>A (p.Val771Met)
c.2293G>A (p.Val765Met)
c.2230G>A (p.Val744Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337792dupCA012076MYBPC3c.2311dup (p.Val771GlyfsTer?)
c.2293dup (p.Val765GlyfsTer?)
c.2230dup (p.Val744GlyfsTer?)
 ClinVar dbSNP
11g.47337792_47337793delinsCGCA1969331626MYBPC3c.2310_2311delinsCG (p.Asp770=)
c.2292_2293delinsCG (p.Asp764=)
c.2229_2230delinsCG (p.Asp743=)
11g.47337793delCA658797627MYBPC3c.2310del (p.Asp770GlufsTer?)
c.2292del (p.Asp764GlufsTer?)
c.2229del (p.Asp743GlufsTer?)
 ClinVar dbSNP
11g.47337793G>ACA012068MYBPC3c.2310C>T (p.Asp770=)
c.2292C>T (p.Asp764=)
c.2229C>T (p.Asp743=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337793G>CCA380319237MYBPC3c.2310C>G (p.Asp770Glu)
c.2292C>G (p.Asp764Glu)
c.2229C>G (p.Asp743Glu)
 gnomAD v4
11g.47337793G=CA1969331628MYBPC3c.2310C= (p.Asp770=)
c.2292C= (p.Asp764=)
c.2229C= (p.Asp743=)
11g.47337793G>TCA221689026MYBPC3c.2310C>A (p.Asp770Glu)
c.2292C>A (p.Asp764Glu)
c.2229C>A (p.Asp743Glu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47337794T>ACA380319243MYBPC3c.2309A>T (p.Asp770Val)
c.2291A>T (p.Asp764Val)
c.2228A>T (p.Asp743Val)
11g.47337794T>CCA380319246MYBPC3c.2309A>G (p.Asp770Gly)
c.2291A>G (p.Asp764Gly)
c.2228A>G (p.Asp743Gly)
11g.47337794T>GCA380319248MYBPC3c.2309A>C (p.Asp770Ala)
c.2291A>C (p.Asp764Ala)
c.2228A>C (p.Asp743Ala)
 gnomAD v4
11g.47337795_47337796dupCA2739291464MYBPC3c.2309-1_2309dup
c.2291-1_2291dup
c.2228-1_2228dup
11g.47337795_47338523dupCA916081643MYBPC3c.2306_2309dup
c.2288_2291dup
c.2225_2228dup
11g.47337795C>ACA380319253MYBPC3c.2309-1G>T (n.2309-1G>T)
c.2291-1G>T (n.2291-1G>T)
c.2228-1G>T (n.2228-1G>T)
 gnomAD v4
11g.47337795C=CA1969331629MYBPC3c.2309-1G= (n.2309-1G=)
c.2291-1G= (n.2291-1G=)
c.2228-1G= (n.2228-1G=)
11g.47337795C>GCA380319255MYBPC3c.2309-1G>C (n.2309-1G>C)
c.2291-1G>C (n.2291-1G>C)
c.2228-1G>C (n.2228-1G>C)
11g.47337795C>TCA380319259MYBPC3c.2309-1G>A (n.2309-1G>A)
c.2291-1G>A (n.2291-1G>A)
c.2228-1G>A (n.2228-1G>A)
 dbSNP gnomAD v4
11g.47337796T>ACA380319263MYBPC3c.2309-2A>T (n.2309-2A>T)
c.2291-2A>T (n.2291-2A>T)
c.2228-2A>T (n.2228-2A>T)
 dbSNP
11g.47337796T>CCA012043MYBPC3c.2309-2A>G (n.2309-2A>G)
c.2291-2A>G (n.2291-2A>G)
c.2228-2A>G (n.2228-2A>G)
 ClinVar dbSNP gnomAD v4
11g.47337796T>GCA221689041MYBPC3c.2309-2A>C (n.2309-2A>C)
c.2291-2A>C (n.2291-2A>C)
c.2228-2A>C (n.2228-2A>C)
 dbSNP
11g.47337796T=CA1969331630MYBPC3c.2309-2A= (n.2309-2A=)
c.2291-2A= (n.2291-2A=)
c.2228-2A= (n.2228-2A=)
11g.47337797G>CCA915940854MYBPC3c.2309-3C>G (n.2309-3C>G)
c.2291-3C>G (n.2291-3C>G)
c.2228-3C>G (n.2228-3C>G)
11g.47337798G>ACA221689056MYBPC3c.2309-4C>T (n.2309-4C>T)
c.2291-4C>T (n.2291-4C>T)
c.2228-4C>T (n.2228-4C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337798G=CA1969331631MYBPC3c.2309-4C= (n.2309-4C=)
c.2291-4C= (n.2291-4C=)
c.2228-4C= (n.2228-4C=)
11g.47337798G>TCA2613392583MYBPC3c.2309-4C>A (n.2309-4C>A)
c.2291-4C>A (n.2291-4C>A)
c.2228-4C>A (n.2228-4C>A)
 gnomAD v4
11g.47337800T>CCA2613392584MYBPC3c.2309-6A>G (n.2309-6A>G)
c.2291-6A>G (n.2291-6A>G)
c.2228-6A>G (n.2228-6A>G)
 gnomAD v4
11g.47337801G>ACA2613392585MYBPC3c.2309-7C>T (n.2309-7C>T)
c.2291-7C>T (n.2291-7C>T)
c.2228-7C>T (n.2228-7C>T)
 gnomAD v4
11g.47337801G>TCA2613392586MYBPC3c.2309-7C>A (n.2309-7C>A)
c.2291-7C>A (n.2291-7C>A)
c.2228-7C>A (n.2228-7C>A)
 gnomAD v4
11g.47337804delCA2574816041MYBPC3c.2309-7del (n.2309-7del)
c.2291-7del (n.2291-7del)
c.2228-7del (n.2228-7del)
 gnomAD v4
11g.47337802G>TCA2613392587MYBPC3c.2309-8C>A (n.2309-8C>A)
c.2291-8C>A (n.2291-8C>A)
c.2228-8C>A (n.2228-8C>A)
 gnomAD v4
11g.47337803G>ACA599058478MYBPC3c.2309-9C>T (n.2309-9C>T)
c.2291-9C>T (n.2291-9C>T)
c.2228-9C>T (n.2228-9C>T)
 dbSNP gnomAD v2
11g.47337803G=CA1969331632MYBPC3c.2309-9C= (n.2309-9C=)
c.2291-9C= (n.2291-9C=)
c.2228-9C= (n.2228-9C=)
11g.47337803G>TCA012052MYBPC3c.2309-9C>A (n.2309-9C>A)
c.2291-9C>A (n.2291-9C>A)
c.2228-9C>A (n.2228-9C>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47337804G>ACA599058479MYBPC3c.2309-10C>T (n.2309-10C>T)
c.2291-10C>T (n.2291-10C>T)
c.2228-10C>T (n.2228-10C>T)
 dbSNP gnomAD v2
11g.47337804G=CA1969331633MYBPC3c.2309-10C= (n.2309-10C=)
c.2291-10C= (n.2291-10C=)
c.2228-10C= (n.2228-10C=)
11g.47337804G>TCA2613392588MYBPC3c.2309-10C>A (n.2309-10C>A)
c.2291-10C>A (n.2291-10C>A)
c.2228-10C>A (n.2228-10C>A)
 gnomAD v4
11g.47337805T>GCA1969331635MYBPC3c.2309-11A>C (n.2309-11A>C)
c.2291-11A>C (n.2291-11A>C)
c.2228-11A>C (n.2228-11A>C)
 dbSNP
11g.47337805T=CA1969331634MYBPC3c.2309-11A= (n.2309-11A=)
c.2291-11A= (n.2291-11A=)
c.2228-11A= (n.2228-11A=)
11g.47337806G>ACA2573146816MYBPC3c.2309-12C>T (n.2309-12C>T)
c.2291-12C>T (n.2291-12C>T)
c.2228-12C>T (n.2228-12C>T)
 ClinVar dbSNP
11g.47337808delCA2825002010MYBPC3c.2309-12del (n.2309-12del)
c.2291-12del (n.2291-12del)
c.2228-12del (n.2228-12del)
 ClinVar
11g.47337807G>TCA2613392589MYBPC3c.2309-13C>A (n.2309-13C>A)
c.2291-13C>A (n.2291-13C>A)
c.2228-13C>A (n.2228-13C>A)
 gnomAD v4
11g.47337808G>ACA2613392590MYBPC3c.2309-14C>T (n.2309-14C>T)
c.2291-14C>T (n.2291-14C>T)
c.2228-14C>T (n.2228-14C>T)
 gnomAD v4
11g.47337808G>TCA2574816042MYBPC3c.2309-14C>A (n.2309-14C>A)
c.2291-14C>A (n.2291-14C>A)
c.2228-14C>A (n.2228-14C>A)
 gnomAD v4
11g.47337809A>GCA2613392591MYBPC3c.2309-15T>C (n.2309-15T>C)
c.2291-15T>C (n.2291-15T>C)
c.2228-15T>C (n.2228-15T>C)
 gnomAD v4
11g.47337810T>GCA599058480MYBPC3c.2309-16A>C (n.2309-16A>C)
c.2291-16A>C (n.2291-16A>C)
c.2228-16A>C (n.2228-16A>C)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47337810T=CA1969331636MYBPC3c.2309-16A= (n.2309-16A=)
c.2291-16A= (n.2291-16A=)
c.2228-16A= (n.2228-16A=)
11g.47337811G>ACA2613392592MYBPC3c.2309-17C>T (n.2309-17C>T)
c.2291-17C>T (n.2291-17C>T)
c.2228-17C>T (n.2228-17C>T)
 gnomAD v4
11g.47337812G>ACA2613392593MYBPC3c.2309-18C>T (n.2309-18C>T)
c.2291-18C>T (n.2291-18C>T)
c.2228-18C>T (n.2228-18C>T)
 gnomAD v4
11g.47337812G>TCA2613392594MYBPC3c.2309-18C>A (n.2309-18C>A)
c.2291-18C>A (n.2291-18C>A)
c.2228-18C>A (n.2228-18C>A)
 gnomAD v4
11g.47337813A=CA1969331637MYBPC3c.2309-19T= (n.2309-19T=)
c.2291-19T= (n.2291-19T=)
c.2228-19T= (n.2228-19T=)
11g.47337813A>GCA2613392595MYBPC3c.2309-19T>C (n.2309-19T>C)
c.2291-19T>C (n.2291-19T>C)
c.2228-19T>C (n.2228-19T>C)
 gnomAD v4
11g.47337813A>TCA676995507MYBPC3c.2309-19T>A (n.2309-19T>A)
c.2291-19T>A (n.2291-19T>A)
c.2228-19T>A (n.2228-19T>A)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47337815_47337818delCA2574816043MYBPC3c.2309-22_2309-19del (n.2309-22_2309-19del)
c.2291-22_2291-19del (n.2291-22_2291-19del)
c.2228-22_2228-19del (n.2228-22_2228-19del)
11g.47337814C>ACA2613392597MYBPC3c.2309-20G>T (n.2309-20G>T)
c.2291-20G>T (n.2291-20G>T)
c.2228-20G>T (n.2228-20G>T)
 gnomAD v4
11g.47337814C=CA1969331638MYBPC3c.2309-20G= (n.2309-20G=)
c.2291-20G= (n.2291-20G=)
c.2228-20G= (n.2228-20G=)
11g.47337814C>TCA012025MYBPC3c.2309-20G>A (n.2309-20G>A)
c.2291-20G>A (n.2291-20G>A)
c.2228-20G>A (n.2228-20G>A)
 ClinVar dbSNP gnomAD v4
11g.47337816delCA2613392596MYBPC3c.2309-20del (n.2309-20del)
c.2291-20del (n.2291-20del)
c.2228-20del (n.2228-20del)
 gnomAD v4
11g.47337815C>ACA2613392598MYBPC3c.2309-21G>T (n.2309-21G>T)
c.2291-21G>T (n.2291-21G>T)
c.2228-21G>T (n.2228-21G>T)
 gnomAD v4
11g.47337815C=CA1969331639MYBPC3c.2309-21G= (n.2309-21G=)
c.2291-21G= (n.2291-21G=)
c.2228-21G= (n.2228-21G=)
11g.47337815C>TCA012030MYBPC3c.2309-21G>A (n.2309-21G>A)
c.2291-21G>A (n.2291-21G>A)
c.2228-21G>A (n.2228-21G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.47337816C>GCA2613392599MYBPC3c.2309-22G>C (n.2309-22G>C)
c.2291-22G>C (n.2291-22G>C)
c.2228-22G>C (n.2228-22G>C)
 gnomAD v4
11g.47337817A>CCA2613392600MYBPC3c.2309-23T>G (n.2309-23T>G)
c.2291-23T>G (n.2291-23T>G)
c.2228-23T>G (n.2228-23T>G)
 gnomAD v4
11g.47337818C>TCA2613392601MYBPC3c.2309-24G>A (n.2309-24G>A)
c.2291-24G>A (n.2291-24G>A)
c.2228-24G>A (n.2228-24G>A)
 gnomAD v4
11g.47337820T>CCA10602349MYBPC3c.2309-26A>G (n.2309-26A>G)
c.2291-26A>G (n.2291-26A>G)
c.2228-26A>G (n.2228-26A>G)
 ClinVar dbSNP
11g.47337820T=CA1969331640MYBPC3c.2309-26A= (n.2309-26A=)
c.2291-26A= (n.2291-26A=)
c.2228-26A= (n.2228-26A=)
11g.47337821C=CA1969331641MYBPC3c.2309-27G= (n.2309-27G=)
c.2291-27G= (n.2291-27G=)
c.2228-27G= (n.2228-27G=)
11g.47337821C>TCA012038MYBPC3c.2309-27G>A (n.2309-27G>A)
c.2291-27G>A (n.2291-27G>A)
c.2228-27G>A (n.2228-27G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337823G>ACA2613392602MYBPC3c.2309-29C>T (n.2309-29C>T)
c.2291-29C>T (n.2291-29C>T)
c.2228-29C>T (n.2228-29C>T)
 gnomAD v4
11g.47337823G>TCA2574816044MYBPC3c.2309-29C>A (n.2309-29C>A)
c.2291-29C>A (n.2291-29C>A)
c.2228-29C>A (n.2228-29C>A)
 gnomAD v4
11g.47337824C>TCA2613392603MYBPC3c.2309-30G>A (n.2309-30G>A)
c.2291-30G>A (n.2291-30G>A)
c.2228-30G>A (n.2228-30G>A)
 gnomAD v4
11g.47337825C>ACA2791322965MYBPC3c.2309-31G>T (n.2309-31G>T)
c.2291-31G>T (n.2291-31G>T)
c.2228-31G>T (n.2228-31G>T)
11g.47337825C>TCA2613392604MYBPC3c.2309-31G>A (n.2309-31G>A)
c.2291-31G>A (n.2291-31G>A)
c.2228-31G>A (n.2228-31G>A)
 gnomAD v4
11g.47337826C>ACA2613392605MYBPC3c.2309-32G>T (n.2309-32G>T)
c.2291-32G>T (n.2291-32G>T)
c.2228-32G>T (n.2228-32G>T)
 gnomAD v4
11g.47337828G>ACA2526882580MYBPC3c.2309-34C>T (n.2309-34C>T)
c.2291-34C>T (n.2291-34C>T)
c.2228-34C>T (n.2228-34C>T)
 gnomAD v4
11g.47337828G>TCA2613392606MYBPC3c.2309-34C>A (n.2309-34C>A)
c.2291-34C>A (n.2291-34C>A)
c.2228-34C>A (n.2228-34C>A)
 gnomAD v4
11g.47337829C>ACA676995528MYBPC3c.2309-35G>T (n.2309-35G>T)
c.2291-35G>T (n.2291-35G>T)
c.2228-35G>T (n.2228-35G>T)
 dbSNP gnomAD v3 gnomAD v4
11g.47337829C=CA1969331642MYBPC3c.2309-35G= (n.2309-35G=)
c.2291-35G= (n.2291-35G=)
c.2228-35G= (n.2228-35G=)
11g.47337829C>TCA599058481MYBPC3c.2309-35G>A (n.2309-35G>A)
c.2291-35G>A (n.2291-35G>A)
c.2228-35G>A (n.2228-35G>A)
 dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched