Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47337581_47337690delCA2791331873MYBPC3c.2413+2_2414del
c.2413+2_2414-68del
c.2395+2_2396del
c.2332+2_2333del
11g.47337691delCA2574816029MYBPC3c.2413+1del
c.2395+1del
c.2332+1del
11g.47337690C>ACA380318579MYBPC3c.2413G>T (p.Gly805Cys)
c.2413G>T (p.Gly805Ter)
c.2395G>T (p.Gly799Cys)
c.2332G>T (p.Gly778Cys)
 gnomAD v4
11g.47337690C=CA1969331563MYBPC3c.2413G= (p.Gly805=)
c.2395G= (p.Gly799=)
c.2332G= (p.Gly778=)
11g.47337690C>GCA380318580MYBPC3c.2413G>C (p.Gly805Arg)
c.2395G>C (p.Gly799Arg)
c.2332G>C (p.Gly778Arg)
11g.47337690C>TCA380318577MYBPC3c.2413G>A (p.Gly805Ser)
c.2413G>A (p.Gly805Arg)
c.2395G>A (p.Gly799Ser)
c.2332G>A (p.Gly778Ser)
 ClinVar dbSNP gnomAD v2
11g.47337691C>ACA474429373MYBPC3c.2412G>T (p.Leu804=)
c.2394G>T (p.Leu798=)
c.2331G>T (p.Leu777=)
11g.47337691C>GCA474429374MYBPC3c.2412G>C (p.Leu804=)
c.2394G>C (p.Leu798=)
c.2331G>C (p.Leu777=)
 gnomAD v4
11g.47337691C>TCA474429375MYBPC3c.2412G>A (p.Leu804=)
c.2394G>A (p.Leu798=)
c.2331G>A (p.Leu777=)
 gnomAD v4
11g.47337692A>CCA380318583MYBPC3c.2411T>G (p.Leu804Arg)
c.2393T>G (p.Leu798Arg)
c.2330T>G (p.Leu777Arg)
11g.47337692A>GCA380318584MYBPC3c.2411T>C (p.Leu804Pro)
c.2393T>C (p.Leu798Pro)
c.2330T>C (p.Leu777Pro)
 ClinVar gnomAD v4
11g.47337692A>TCA380318586MYBPC3c.2411T>A (p.Leu804Gln)
c.2393T>A (p.Leu798Gln)
c.2330T>A (p.Leu777Gln)
 gnomAD v4
11g.47337693G>ACA474429376MYBPC3c.2410C>T (p.Leu804=)
c.2392C>T (p.Leu798=)
c.2329C>T (p.Leu777=)
11g.47337693G>CCA380318588MYBPC3c.2410C>G (p.Leu804Val)
c.2392C>G (p.Leu798Val)
c.2329C>G (p.Leu777Val)
11g.47337693G=CA1969331564MYBPC3c.2410C= (p.Leu804=)
c.2392C= (p.Leu798=)
c.2329C= (p.Leu777=)
11g.47337693G>TCA221688879MYBPC3c.2410C>A (p.Leu804Met)
c.2392C>A (p.Leu798Met)
c.2329C>A (p.Leu777Met)
 dbSNP gnomAD v4
11g.47337694G>ACA474429377MYBPC3c.2409C>T (p.Ile803=)
c.2391C>T (p.Ile797=)
c.2328C>T (p.Ile776=)
 gnomAD v4
11g.47337694G>CCA380318590MYBPC3c.2409C>G (p.Ile803Met)
c.2391C>G (p.Ile797Met)
c.2328C>G (p.Ile776Met)
 ClinVar dbSNP gnomAD v4
11g.47337694G=CA1969331565MYBPC3c.2409C= (p.Ile803=)
c.2391C= (p.Ile797=)
c.2328C= (p.Ile776=)
11g.47337694G>TCA078685MYBPC3c.2409C>A (p.Ile803=)
c.2391C>A (p.Ile797=)
c.2328C>A (p.Ile776=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337695A=CA1969331566MYBPC3c.2408T= (p.Ile803=)
c.2390T= (p.Ile797=)
c.2327T= (p.Ile776=)
11g.47337695A>CCA380318591MYBPC3c.2408T>G (p.Ile803Ser)
c.2390T>G (p.Ile797Ser)
c.2327T>G (p.Ile776Ser)
11g.47337695A>GCA380318593MYBPC3c.2408T>C (p.Ile803Thr)
c.2390T>C (p.Ile797Thr)
c.2327T>C (p.Ile776Thr)
11g.47337695A>TCA380318594MYBPC3c.2408T>A (p.Ile803Asn)
c.2390T>A (p.Ile797Asn)
c.2327T>A (p.Ile776Asn)
 ClinVar dbSNP
11g.47337696T>ACA380318596MYBPC3c.2407A>T (p.Ile803Phe)
c.2389A>T (p.Ile797Phe)
c.2326A>T (p.Ile776Phe)
11g.47337696T>CCA380318598MYBPC3c.2407A>G (p.Ile803Val)
c.2389A>G (p.Ile797Val)
c.2326A>G (p.Ile776Val)
 gnomAD v4
11g.47337696T>GCA380318600MYBPC3c.2407A>C (p.Ile803Leu)
c.2389A>C (p.Ile797Leu)
c.2326A>C (p.Ile776Leu)
11g.47337697G>ACA474429378MYBPC3c.2406C>T (p.Pro802=)
c.2388C>T (p.Pro796=)
c.2325C>T (p.Pro775=)
 ClinVar
11g.47337697G>CCA474429379MYBPC3c.2406C>G (p.Pro802=)
c.2388C>G (p.Pro796=)
c.2325C>G (p.Pro775=)
11g.47337697G>TCA049578MYBPC3c.2406C>A (p.Pro802=)
c.2388C>A (p.Pro796=)
c.2325C>A (p.Pro775=)
 gnomAD v4
11g.47337699delCA2574816033MYBPC3c.2406del (p.Ile803SerfsTer19)
c.2406del (p.Ile803SerfsTer?)
c.2388del (p.Ile797SerfsTer19)
c.2325del (p.Ile776SerfsTer19)
11g.47337698G>ACA380318602MYBPC3c.2405C>T (p.Pro802Leu)
c.2387C>T (p.Pro796Leu)
c.2324C>T (p.Pro775Leu)
11g.47337698G>CCA380318606MYBPC3c.2405C>G (p.Pro802Arg)
c.2387C>G (p.Pro796Arg)
c.2324C>G (p.Pro775Arg)
11g.47337698G>TCA380318604MYBPC3c.2405C>A (p.Pro802His)
c.2387C>A (p.Pro796His)
c.2324C>A (p.Pro775His)
11g.47337698_47337699insCTGCTTGGAGCCTGTTTCCTCATCTGTAAAATGCGGCTGAGTATCCCCA049813MYBPC3c.2404_2405insGGGATACTCAGCCGCATTTTACAGATGAGGAAACAGGCTCCAAGCAG (p.Pro802ArgfsTer36)
c.2404_2405insGGGATACTCAGCCGCATTTTACAGATGAGGAAACAGGCTCCAAGCAG (p.Pro802ArgfsTer?)
c.2386_2387insGGGATACTCAGCCGCATTTTACAGATGAGGAAACAGGCTCCAAGCAG (p.Pro796ArgfsTer36)
c.2323_2324insGGGATACTCAGCCGCATTTTACAGATGAGGAAACAGGCTCCAAGCAG (p.Pro775ArgfsTer36)
11g.47337699G>ACA380318608MYBPC3c.2404C>T (p.Pro802Ser)
c.2386C>T (p.Pro796Ser)
c.2323C>T (p.Pro775Ser)
 gnomAD v4
11g.47337699G>CCA380318611MYBPC3c.2404C>G (p.Pro802Ala)
c.2386C>G (p.Pro796Ala)
c.2323C>G (p.Pro775Ala)
11g.47337699G=CA1969331567MYBPC3c.2404C= (p.Pro802=)
c.2386C= (p.Pro796=)
c.2323C= (p.Pro775=)
11g.47337699G>TCA380318610MYBPC3c.2404C>A (p.Pro802Thr)
c.2386C>A (p.Pro796Thr)
c.2323C>A (p.Pro775Thr)
 ClinVar dbSNP gnomAD v2
11g.47337700C>ACA380318613MYBPC3c.2403G>T (p.Gln801His)
c.2385G>T (p.Gln795His)
c.2322G>T (p.Gln774His)
 gnomAD v4
11g.47337700C=CA1969331568MYBPC3c.2403G= (p.Gln801=)
c.2385G= (p.Gln795=)
c.2322G= (p.Gln774=)
11g.47337700C>GCA380318614MYBPC3c.2403G>C (p.Gln801His)
c.2385G>C (p.Gln795His)
c.2322G>C (p.Gln774His)
 dbSNP
11g.47337700C>TCA474429380MYBPC3c.2403G>A (p.Gln801=)
c.2385G>A (p.Gln795=)
c.2322G>A (p.Gln774=)
 gnomAD v4
11g.47337701T>ACA380318616MYBPC3c.2402A>T (p.Gln801Leu)
c.2384A>T (p.Gln795Leu)
c.2321A>T (p.Gln774Leu)
11g.47337701T>CCA380318619MYBPC3c.2402A>G (p.Gln801Arg)
c.2384A>G (p.Gln795Arg)
c.2321A>G (p.Gln774Arg)
 dbSNP gnomAD v2
11g.47337701T>GCA380318617MYBPC3c.2402A>C (p.Gln801Pro)
c.2384A>C (p.Gln795Pro)
c.2321A>C (p.Gln774Pro)
11g.47337701T=CA1969331569MYBPC3c.2402A= (p.Gln801=)
c.2384A= (p.Gln795=)
c.2321A= (p.Gln774=)
11g.47337702G>ACA380318621MYBPC3c.2401C>T (p.Gln801Ter)
c.2383C>T (p.Gln795Ter)
c.2320C>T (p.Gln774Ter)
11g.47337702G>CCA380318625MYBPC3c.2401C>G (p.Gln801Glu)
c.2383C>G (p.Gln795Glu)
c.2320C>G (p.Gln774Glu)
 gnomAD v4
11g.47337702G>TCA380318623MYBPC3c.2401C>A (p.Gln801Lys)
c.2383C>A (p.Gln795Lys)
c.2320C>A (p.Gln774Lys)
11g.47337703C>ACA474429381MYBPC3c.2400G>T (p.Gly800=)
c.2382G>T (p.Gly794=)
c.2319G>T (p.Gly773=)
11g.47337703C>GCA474429382MYBPC3c.2400G>C (p.Gly800=)
c.2382G>C (p.Gly794=)
c.2319G>C (p.Gly773=)
 gnomAD v4
11g.47337703C>TCA474429383MYBPC3c.2400G>A (p.Gly800=)
c.2382G>A (p.Gly794=)
c.2319G>A (p.Gly773=)
11g.47337704C>ACA380318627MYBPC3c.2399G>T (p.Gly800Val)
c.2381G>T (p.Gly794Val)
c.2318G>T (p.Gly773Val)
 ClinVar dbSNP gnomAD v4
11g.47337704C=CA1969331570MYBPC3c.2399G= (p.Gly800=)
c.2381G= (p.Gly794=)
c.2318G= (p.Gly773=)
11g.47337704C>GCA380318629MYBPC3c.2399G>C (p.Gly800Ala)
c.2381G>C (p.Gly794Ala)
c.2318G>C (p.Gly773Ala)
11g.47337704C>TCA380318631MYBPC3c.2399G>A (p.Gly800Glu)
c.2381G>A (p.Gly794Glu)
c.2318G>A (p.Gly773Glu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.47337705C>ACA380318633MYBPC3c.2398G>T (p.Gly800Trp)
c.2380G>T (p.Gly794Trp)
c.2317G>T (p.Gly773Trp)
 gnomAD v4
11g.47337705C=CA1969331571MYBPC3c.2398G= (p.Gly800=)
c.2380G= (p.Gly794=)
c.2317G= (p.Gly773=)
11g.47337705C>GCA380318635MYBPC3c.2398G>C (p.Gly800Arg)
c.2380G>C (p.Gly794Arg)
c.2317G>C (p.Gly773Arg)
11g.47337705C>TCA012214MYBPC3c.2398G>A (p.Gly800Arg)
c.2380G>A (p.Gly794Arg)
c.2317G>A (p.Gly773Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337706G>ACA078681MYBPC3c.2397C>T (p.Gly799=)
c.2379C>T (p.Gly793=)
c.2316C>T (p.Gly772=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337706G>CCA474215832MYBPC3c.2397C>G (p.Gly799=)
c.2379C>G (p.Gly793=)
c.2316C>G (p.Gly772=)
11g.47337706G=CA1969331572MYBPC3c.2397C= (p.Gly799=)
c.2379C= (p.Gly793=)
c.2316C= (p.Gly772=)
11g.47337706G>TCA474215837MYBPC3c.2397C>A (p.Gly799=)
c.2379C>A (p.Gly793=)
c.2316C>A (p.Gly772=)
11g.47337707C>ACA380318642MYBPC3c.2396G>T (p.Gly799Val)
c.2378G>T (p.Gly793Val)
c.2315G>T (p.Gly772Val)
 gnomAD v4
11g.47337707C=CA1969331573MYBPC3c.2396G= (p.Gly799=)
c.2378G= (p.Gly793=)
c.2315G= (p.Gly772=)
11g.47337707C>GCA380318644MYBPC3c.2396G>C (p.Gly799Ala)
c.2378G>C (p.Gly793Ala)
c.2315G>C (p.Gly772Ala)
11g.47337707C>TCA380318646MYBPC3c.2396G>A (p.Gly799Asp)
c.2378G>A (p.Gly793Asp)
c.2315G>A (p.Gly772Asp)
 ClinVar dbSNP
11g.47337708C>ACA380318648MYBPC3c.2395G>T (p.Gly799Cys)
c.2377G>T (p.Gly793Cys)
c.2314G>T (p.Gly772Cys)
11g.47337708C=CA1969331574MYBPC3c.2395G= (p.Gly799=)
c.2377G= (p.Gly793=)
c.2314G= (p.Gly772=)
11g.47337708C>GCA380318650MYBPC3c.2395G>C (p.Gly799Arg)
c.2377G>C (p.Gly793Arg)
c.2314G>C (p.Gly772Arg)
11g.47337708C>TCA049565MYBPC3c.2395G>A (p.Gly799Ser)
c.2377G>A (p.Gly793Ser)
c.2314G>A (p.Gly772Ser)
11g.47337709A=CA1969331575MYBPC3c.2394T= (p.Asp798=)
c.2376T= (p.Asp792=)
c.2313T= (p.Asp771=)
11g.47337709A>CCA380318654MYBPC3c.2394T>G (p.Asp798Glu)
c.2376T>G (p.Asp792Glu)
c.2313T>G (p.Asp771Glu)
11g.47337709A>GCA221688892MYBPC3c.2394T>C (p.Asp798=)
c.2376T>C (p.Asp792=)
c.2313T>C (p.Asp771=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337709A>TCA380318652MYBPC3c.2394T>A (p.Asp798Glu)
c.2376T>A (p.Asp792Glu)
c.2313T>A (p.Asp771Glu)
 gnomAD v4
11g.47337709dupCA012205MYBPC3c.2394dup (p.Gly799TrpfsTer?)
c.2394dup (p.Gly799TrpfsTer9)
c.2376dup (p.Gly793TrpfsTer?)
c.2313dup (p.Gly772TrpfsTer?)
 ClinVar dbSNP
11g.47337710T>ACA380318656MYBPC3c.2393A>T (p.Asp798Val)
c.2375A>T (p.Asp792Val)
c.2312A>T (p.Asp771Val)
11g.47337710T>CCA380318658MYBPC3c.2393A>G (p.Asp798Gly)
c.2375A>G (p.Asp792Gly)
c.2312A>G (p.Asp771Gly)
11g.47337710T>GCA380318660MYBPC3c.2393A>C (p.Asp798Ala)
c.2375A>C (p.Asp792Ala)
c.2312A>C (p.Asp771Ala)
11g.47337711C>ACA380318662MYBPC3c.2392G>T (p.Asp798Tyr)
c.2374G>T (p.Asp792Tyr)
c.2311G>T (p.Asp771Tyr)
 gnomAD v4
11g.47337711C=CA1969331576MYBPC3c.2392G= (p.Asp798=)
c.2374G= (p.Asp792=)
c.2311G= (p.Asp771=)
11g.47337711C>GCA380318664MYBPC3c.2392G>C (p.Asp798His)
c.2374G>C (p.Asp792His)
c.2311G>C (p.Asp771His)
11g.47337711C>TCA078678MYBPC3c.2392G>A (p.Asp798Asn)
c.2374G>A (p.Asp792Asn)
c.2311G>A (p.Asp771Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.47337712G>ACA078676MYBPC3c.2391C>T (p.Tyr797=)
c.2373C>T (p.Tyr791=)
c.2310C>T (p.Tyr770=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337712G>CCA380318667MYBPC3c.2391C>G (p.Tyr797Ter)
c.2373C>G (p.Tyr791Ter)
c.2310C>G (p.Tyr770Ter)
 ClinVar dbSNP
11g.47337712G=CA1969331577MYBPC3c.2391C= (p.Tyr797=)
c.2373C= (p.Tyr791=)
c.2310C= (p.Tyr770=)
11g.47337712G>TCA012195MYBPC3c.2391C>A (p.Tyr797Ter)
c.2373C>A (p.Tyr791Ter)
c.2310C>A (p.Tyr770Ter)
 ClinVar dbSNP gnomAD v4
11g.47337713T>ACA380318672MYBPC3c.2390A>T (p.Tyr797Phe)
c.2372A>T (p.Tyr791Phe)
c.2309A>T (p.Tyr770Phe)
11g.47337713T>CCA380318671MYBPC3c.2390A>G (p.Tyr797Cys)
c.2372A>G (p.Tyr791Cys)
c.2309A>G (p.Tyr770Cys)
 ClinVar gnomAD v4
11g.47337713T>GCA380318670MYBPC3c.2390A>C (p.Tyr797Ser)
c.2372A>C (p.Tyr791Ser)
c.2309A>C (p.Tyr770Ser)
11g.47337714A>CCA380318674MYBPC3c.2389T>G (p.Tyr797Asp)
c.2371T>G (p.Tyr791Asp)
c.2308T>G (p.Tyr770Asp)
11g.47337714A>GCA380318676MYBPC3c.2389T>C (p.Tyr797His)
c.2371T>C (p.Tyr791His)
c.2308T>C (p.Tyr770His)
11g.47337714A>TCA380318678MYBPC3c.2389T>A (p.Tyr797Asn)
c.2371T>A (p.Tyr791Asn)
c.2308T>A (p.Tyr770Asn)
11g.47337715G>ACA049499MYBPC3c.2388C>T (p.Ala796=)
c.2370C>T (p.Ala790=)
c.2307C>T (p.Ala769=)
 gnomAD v4
11g.47337715G>CCA474215938MYBPC3c.2388C>G (p.Ala796=)
c.2370C>G (p.Ala790=)
c.2307C>G (p.Ala769=)
11g.47337715G>TCA474215955MYBPC3c.2388C>A (p.Ala796=)
c.2370C>A (p.Ala790=)
c.2307C>A (p.Ala769=)
11g.47337716G>ACA380318680MYBPC3c.2387C>T (p.Ala796Val)
c.2369C>T (p.Ala790Val)
c.2306C>T (p.Ala769Val)
 gnomAD v4
11g.47337716G>CCA380318682MYBPC3c.2387C>G (p.Ala796Gly)
c.2369C>G (p.Ala790Gly)
c.2306C>G (p.Ala769Gly)
11g.47337716G>TCA380318684MYBPC3c.2387C>A (p.Ala796Asp)
c.2369C>A (p.Ala790Asp)
c.2306C>A (p.Ala769Asp)
 gnomAD v4
11g.47337717C>ACA380318686MYBPC3c.2386G>T (p.Ala796Ser)
c.2368G>T (p.Ala790Ser)
c.2305G>T (p.Ala769Ser)
 gnomAD v4
11g.47337717C>GCA380318688MYBPC3c.2386G>C (p.Ala796Pro)
c.2368G>C (p.Ala790Pro)
c.2305G>C (p.Ala769Pro)
11g.47337717C>TCA380318689MYBPC3c.2386G>A (p.Ala796Thr)
c.2368G>A (p.Ala790Thr)
c.2305G>A (p.Ala769Thr)
11g.47337718A>CCA474215966MYBPC3c.2385T>G (p.Pro795=)
c.2367T>G (p.Pro789=)
c.2304T>G (p.Pro768=)
11g.47337718A>GCA474215963MYBPC3c.2385T>C (p.Pro795=)
c.2367T>C (p.Pro789=)
c.2304T>C (p.Pro768=)
 gnomAD v4
11g.47337718A>TCA474215961MYBPC3c.2385T>A (p.Pro795=)
c.2367T>A (p.Pro789=)
c.2304T>A (p.Pro768=)
11g.47337719G>ACA380318692MYBPC3c.2384C>T (p.Pro795Leu)
c.2366C>T (p.Pro789Leu)
c.2303C>T (p.Pro768Leu)
11g.47337719G>CCA380318694MYBPC3c.2384C>G (p.Pro795Arg)
c.2366C>G (p.Pro789Arg)
c.2303C>G (p.Pro768Arg)
11g.47337719G>TCA380318695MYBPC3c.2384C>A (p.Pro795His)
c.2366C>A (p.Pro789His)
c.2303C>A (p.Pro768His)
 gnomAD v4
11g.47337720G>ACA380318698MYBPC3c.2383C>T (p.Pro795Ser)
c.2365C>T (p.Pro789Ser)
c.2302C>T (p.Pro768Ser)
 gnomAD v4
11g.47337720G>CCA380318696MYBPC3c.2383C>G (p.Pro795Ala)
c.2365C>G (p.Pro789Ala)
c.2302C>G (p.Pro768Ala)
11g.47337720G=CA1969331579MYBPC3c.2383C= (p.Pro795=)
c.2365C= (p.Pro789=)
c.2302C= (p.Pro768=)
11g.47337720G>TCA380318697MYBPC3c.2383C>A (p.Pro795Thr)
c.2365C>A (p.Pro789Thr)
c.2302C>A (p.Pro768Thr)
 dbSNP gnomAD v2 gnomAD v4
11g.47337720_47337721delinsGCCA1969331578MYBPC3c.2382_2383delinsGC (p.Pro794=)
c.2364_2365delinsGC (p.Pro788=)
c.2301_2302delinsGC (p.Pro767=)
11g.47337720_47337727delCA2695212763MYBPC3c.2376_2383del (p.Trp792CysfsTer?)
c.2376_2383del (p.Trp792CysfsTer13)
c.2358_2365del (p.Trp786CysfsTer?)
c.2295_2302del (p.Trp765CysfsTer?)
11g.47337721delCA012182MYBPC3c.2382del (p.Pro795LeufsTer27)
c.2382del (p.Pro795LeufsTer?)
c.2364del (p.Pro789LeufsTer27)
c.2301del (p.Pro768LeufsTer27)
 ClinVar dbSNP
11g.47337721C>ACA474216020MYBPC3c.2382G>T (p.Pro794=)
c.2364G>T (p.Pro788=)
c.2301G>T (p.Pro767=)
 gnomAD v4
11g.47337721C=CA1969331580MYBPC3c.2382G= (p.Pro794=)
c.2364G= (p.Pro788=)
c.2301G= (p.Pro767=)
11g.47337721C>GCA474215992MYBPC3c.2382G>C (p.Pro794=)
c.2364G>C (p.Pro788=)
c.2301G>C (p.Pro767=)
11g.47337721C>TCA474216016MYBPC3c.2382G>A (p.Pro794=)
c.2364G>A (p.Pro788=)
c.2301G>A (p.Pro767=)
 ClinVar dbSNP gnomAD v4
11g.47337722G>ACA012173MYBPC3c.2381C>T (p.Pro794Leu)
c.2363C>T (p.Pro788Leu)
c.2300C>T (p.Pro767Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47337722G>CCA380318702MYBPC3c.2381C>G (p.Pro794Arg)
c.2363C>G (p.Pro788Arg)
c.2300C>G (p.Pro767Arg)
11g.47337722G=CA1969331581MYBPC3c.2381C= (p.Pro794=)
c.2363C= (p.Pro788=)
c.2300C= (p.Pro767=)
11g.47337722G>TCA380318703MYBPC3c.2381C>A (p.Pro794Gln)
c.2363C>A (p.Pro788Gln)
c.2300C>A (p.Pro767Gln)
 gnomAD v4
11g.47337723G>ACA380318706MYBPC3c.2380C>T (p.Pro794Ser)
c.2362C>T (p.Pro788Ser)
c.2299C>T (p.Pro767Ser)
 gnomAD v4
11g.47337723G>CCA380318708MYBPC3c.2380C>G (p.Pro794Ala)
c.2362C>G (p.Pro788Ala)
c.2299C>G (p.Pro767Ala)
11g.47337723G=CA1969331582MYBPC3c.2380C= (p.Pro794=)
c.2362C= (p.Pro788=)
c.2299C= (p.Pro767=)
11g.47337723G>TCA380318710MYBPC3c.2380C>A (p.Pro794Thr)
c.2362C>A (p.Pro788Thr)
c.2299C>A (p.Pro767Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47337724C>ACA380318712MYBPC3c.2379G>T (p.Glu793Asp)
c.2361G>T (p.Glu787Asp)
c.2298G>T (p.Glu766Asp)
11g.47337724C=CA1969331583MYBPC3c.2379G= (p.Glu793=)
c.2361G= (p.Glu787=)
c.2298G= (p.Glu766=)
11g.47337724C>GCA380318714MYBPC3c.2379G>C (p.Glu793Asp)
c.2361G>C (p.Glu787Asp)
c.2298G>C (p.Glu766Asp)
11g.47337724C>TCA474216028MYBPC3c.2379G>A (p.Glu793=)
c.2361G>A (p.Glu787=)
c.2298G>A (p.Glu766=)
 dbSNP gnomAD v3 gnomAD v4
11g.47337725T>ACA380318716MYBPC3c.2378A>T (p.Glu793Val)
c.2360A>T (p.Glu787Val)
c.2297A>T (p.Glu766Val)
11g.47337725T>CCA380318718MYBPC3c.2378A>G (p.Glu793Gly)
c.2360A>G (p.Glu787Gly)
c.2297A>G (p.Glu766Gly)
11g.47337725T>GCA380318720MYBPC3c.2378A>C (p.Glu793Ala)
c.2360A>C (p.Glu787Ala)
c.2297A>C (p.Glu766Ala)
 dbSNP
11g.47337725T=CA1969331584MYBPC3c.2378A= (p.Glu793=)
c.2360A= (p.Glu787=)
c.2297A= (p.Glu766=)
11g.47337726C>ACA380318727MYBPC3c.2377G>T (p.Glu793Ter)
c.2359G>T (p.Glu787Ter)
c.2296G>T (p.Glu766Ter)
 gnomAD v4
11g.47337726C=CA1969331585MYBPC3c.2377G= (p.Glu793=)
c.2359G= (p.Glu787=)
c.2296G= (p.Glu766=)
11g.47337726C>GCA078671MYBPC3c.2377G>C (p.Glu793Gln)
c.2359G>C (p.Glu787Gln)
c.2296G>C (p.Glu766Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.47337726C>TCA380318722MYBPC3c.2377G>A (p.Glu793Lys)
c.2359G>A (p.Glu787Lys)
c.2296G>A (p.Glu766Lys)
 gnomAD v4
11g.47337728dupCA891842473MYBPC3c.2377dup (p.Glu793GlyfsTer?)
c.2377dup (p.Glu793GlyfsTer15)
c.2359dup (p.Glu787GlyfsTer?)
c.2296dup (p.Glu766GlyfsTer?)
 ClinVar dbSNP
11g.47337727C>ACA380318730MYBPC3c.2376G>T (p.Trp792Cys)
c.2358G>T (p.Trp786Cys)
c.2295G>T (p.Trp765Cys)
11g.47337727C=CA1969331586MYBPC3c.2376G= (p.Trp792=)
c.2358G= (p.Trp786=)
c.2295G= (p.Trp765=)
11g.47337727C>GCA380318729MYBPC3c.2376G>C (p.Trp792Cys)
c.2358G>C (p.Trp786Cys)
c.2295G>C (p.Trp765Cys)
11g.47337727C>TCA279280MYBPC3c.2376G>A (p.Trp792Ter)
c.2358G>A (p.Trp786Ter)
c.2295G>A (p.Trp765Ter)
 ClinVar dbSNP
11g.47337728C>ACA049778MYBPC3c.2375G>T (p.Trp792Leu)
c.2357G>T (p.Trp786Leu)
c.2294G>T (p.Trp765Leu)
 ClinVar gnomAD v4
11g.47337728C>GCA380318733MYBPC3c.2375G>C (p.Trp792Ser)
c.2357G>C (p.Trp786Ser)
c.2294G>C (p.Trp765Ser)
11g.47337728C>TCA380318735MYBPC3c.2375G>A (p.Trp792Ter)
c.2357G>A (p.Trp786Ter)
c.2294G>A (p.Trp765Ter)
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)
 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=)
 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?)
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)
 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)
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

Number of alleles fetched