Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.55151790_55151802delinsTTCCTCAGGGCCCCA2343272649TNNI3c.*32_*44delinsGGGCCCTGAGGAA (n.*32_*44delinsGGGCCCTGAGGAA)
n.664_676delinsGGGCCCTGAGGAA
n.493_505delinsGGGCCCTGAGGAA
19g.55151801_55151812dupCA633870094TNNI3c.*32_*43dup (n.*32_*43dup)
n.664_675dup
n.493_504dup
 dbSNP gnomAD v2 gnomAD v4
19g.55151801_55151812delCA9667715TNNI3c.*32_*43del (n.*32_*43del)
n.664_675del
n.493_504del
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151795C>ACA2587243137TNNI3c.*39G>T (n.*39G>T)
n.671G>T
n.500G>T
 gnomAD v4
19g.55151795C=CA2343272364TNNI3c.*39G= (n.*39G=)
n.671G=
n.500G=
19g.55151795C>TCA051553TNNI3c.*39G>A (n.*39G>A)
n.671G>A
n.500G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151798_55151820delCA2587243136TNNI3c.*17_*39del (n.*17_*39del)
n.649_671del
n.478_500del
 gnomAD v4
19g.55151796A>GCA2587243138TNNI3c.*38T>C (n.*38T>C)
n.670T>C
n.499T>C
 gnomAD v4
19g.55151797G>ACA997245774TNNI3c.*37C>T (n.*37C>T)
n.669C>T
n.498C>T
 dbSNP gnomAD v3 gnomAD v4
19g.55151797G=CA2343272366TNNI3c.*37C= (n.*37C=)
n.669C=
n.498C=
19g.55151798G>ACA2587243139TNNI3c.*36C>T (n.*36C>T)
n.668C>T
n.497C>T
 gnomAD v4
19g.55151799G>ACA021540TNNI3c.*35C>T (n.*35C>T)
n.667C>T
n.496C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151799G=CA2343272376TNNI3c.*35C= (n.*35C=)
n.667C=
n.496C=
19g.55151799G>TCA2576892605TNNI3c.*35C>A (n.*35C>A)
n.667C>A
n.496C>A
 gnomAD v4
19g.55151800C>ACA2587243140TNNI3c.*34G>T (n.*34G>T)
n.666G>T
n.495G>T
 gnomAD v4
19g.55151801C=CA2343272380TNNI3c.*33G= (n.*33G=)
n.665G=
n.494G=
19g.55151801C>GCA051270TNNI3c.*33G>C (n.*33G>C)
n.665G>C
n.494G>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151802C=CA2343272382TNNI3c.*32G= (n.*32G=)
n.664G=
n.493G=
19g.55151802C>GCA2587243141TNNI3c.*32G>C (n.*32G>C)
n.664G>C
n.493G>C
 gnomAD v4
19g.55151802C>TCA310144788TNNI3c.*32G>A (n.*32G>A)
n.664G>A
n.493G>A
 dbSNP gnomAD v4
19g.55151803T>ACA2587243142TNNI3c.*31A>T (n.*31A>T)
n.663A>T
n.492A>T
 gnomAD v4
19g.55151803T>CCA633870104TNNI3c.*31A>G (n.*31A>G)
n.663A>G
n.492A>G
 dbSNP gnomAD v2 gnomAD v4
19g.55151803T>GCA2587243143TNNI3c.*31A>C (n.*31A>C)
n.663A>C
n.492A>C
 gnomAD v4
19g.55151803T=CA2343272383TNNI3c.*31A= (n.*31A=)
n.663A=
n.492A=
19g.55151804C>TCA2587243144TNNI3c.*30G>A (n.*30G>A)
n.662G>A
n.491G>A
 gnomAD v4
19g.55151805C>ACA2587243145TNNI3c.*29G>T (n.*29G>T)
n.661G>T
n.490G>T
 gnomAD v4
19g.55151806T>ACA310144793TNNI3c.*28A>T (n.*28A>T)
n.660A>T
n.489A>T
 dbSNP gnomAD v3 gnomAD v4
19g.55151806T>GCA2735891733TNNI3c.*28A>C (n.*28A>C)
n.660A>C
n.489A>C
 dbSNP
19g.55151806T=CA2343272385TNNI3c.*28A= (n.*28A=)
n.660A=
n.489A=
19g.55151808A=CA2343272389TNNI3c.*26T= (n.*26T=)
n.658T=
n.487T=
19g.55151808A>GCA997245794TNNI3c.*26T>C (n.*26T>C)
n.658T>C
n.487T>C
 dbSNP gnomAD v3 gnomAD v4
19g.55151808A>TCA2343272390TNNI3c.*26T>A (n.*26T>A)
n.658T>A
n.487T>A
 dbSNP
19g.55151815_55151820delCA2576892606TNNI3c.*20_*25del (n.*20_*25del)
n.652_657del
n.481_486del
19g.55151810G>ACA633870107TNNI3c.*24C>T (n.*24C>T)
n.656C>T
n.485C>T
 dbSNP gnomAD v2 gnomAD v4
19g.55151810G=CA2343272392TNNI3c.*24C= (n.*24C=)
n.656C=
n.485C=
19g.55151810G>TCA2587243146TNNI3c.*24C>A (n.*24C>A)
n.656C>A
n.485C>A
 gnomAD v4
19g.55151811G>ACA633870109TNNI3c.*23C>T (n.*23C>T)
n.655C>T
n.484C>T
 dbSNP gnomAD v2 gnomAD v4
19g.55151811G=CA2343272395TNNI3c.*23C= (n.*23C=)
n.655C=
n.484C=
19g.55151811G>TCA050729TNNI3c.*23C>A (n.*23C>A)
n.655C>A
n.484C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151812C>ACA2587243147TNNI3c.*22G>T (n.*22G>T)
n.654G>T
n.483G>T
 gnomAD v4
19g.55151812C=CA2343272400TNNI3c.*22G= (n.*22G=)
n.654G=
n.483G=
19g.55151812C>TCA310144798TNNI3c.*22G>A (n.*22G>A)
n.654G>A
n.483G>A
 dbSNP gnomAD v4
19g.55151813A>GCA2587243148TNNI3c.*21T>C (n.*21T>C)
n.653T>C
n.482T>C
 gnomAD v4
19g.55151815G>ACA883720149TNNI3c.*19C>T (n.*19C>T)
n.651C>T
n.480C>T
 dbSNP gnomAD v3 gnomAD v4
19g.55151815G=CA2343272404TNNI3c.*19C= (n.*19C=)
n.651C=
n.480C=
19g.55151815G>TCA633870113TNNI3c.*19C>A (n.*19C>A)
n.651C>A
n.480C>A
 dbSNP gnomAD v2 gnomAD v4
19g.55151816G>ACA2343272408TNNI3c.*18C>T (n.*18C>T)
n.650C>T
n.479C>T
 dbSNP
19g.55151816G>CCA2587243149TNNI3c.*18C>G (n.*18C>G)
n.650C>G
n.479C>G
 gnomAD v4
19g.55151816G=CA2343272407TNNI3c.*18C= (n.*18C=)
n.650C=
n.479C=
19g.55151816G>TCA2587243150TNNI3c.*18C>A (n.*18C>A)
n.650C>A
n.479C>A
 gnomAD v4
19g.55151817G>ACA050600TNNI3c.*17C>T (n.*17C>T)
n.649C>T
n.478C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151817G=CA2343272410TNNI3c.*17C= (n.*17C=)
n.649C=
n.478C=
19g.55151818C=CA2343272412TNNI3c.*16G= (n.*16G=)
n.648G=
n.477G=
19g.55151818C>TCA050580TNNI3c.*16G>A (n.*16G>A)
n.648G>A
n.477G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151818_55151819insCTTGCA920140592TNNI3c.*15_*16insCAAG (n.*15_*16insCAAG)
n.647_648insCAAG
n.476_477insCAAG
 dbSNP gnomAD v4
19g.55151819A=CA2343272414TNNI3c.*15T= (n.*15T=)
n.647T=
n.476T=
19g.55151819A>CCA2343272415TNNI3c.*15T>G (n.*15T>G)
n.647T>G
n.476T>G
 dbSNP gnomAD v3 gnomAD v4
19g.55151820G>ACA2587243151TNNI3c.*14C>T (n.*14C>T)
n.646C>T
n.475C>T
 gnomAD v4
19g.55151820G=CA2343272417TNNI3c.*14C= (n.*14C=)
n.646C=
n.475C=
19g.55151820G>TCA633870117TNNI3c.*14C>A (n.*14C>A)
n.646C>A
n.475C>A
 dbSNP gnomAD v2 gnomAD v4
19g.55151821T>GCA2587243152TNNI3c.*13A>C (n.*13A>C)
n.645A>C
n.474A>C
 gnomAD v4
19g.55151824_55151825delinsGCCA2343272418TNNI3c.*9_*10delinsGC (n.*9_*10delinsGC)
n.641_642delinsGC
n.470_471delinsGC
19g.55151825delCA633870121TNNI3c.*9del (n.*9del)
n.641del
n.470del
 dbSNP gnomAD v2 gnomAD v4
19g.55151825_55151826delinsCACA2343272420TNNI3c.*8_*9delinsTG (n.*8_*9delinsTG)
n.640_641delinsTG
n.469_470delinsTG
19g.55151826delCA633870123TNNI3c.*8del (n.*8del)
n.640del
n.469del
 dbSNP gnomAD v2 gnomAD v4
19g.55151827G>ACA657447777TNNI3c.*7C>T (n.*7C>T)
n.639C>T
n.468C>T
 COSMIC
19g.55151831G>ACA913189009TNNI3c.*3C>T (n.*3C>T)
n.635C>T
n.464C>T
 ClinVar dbSNP gnomAD v4
19g.55151831G=CA2343272422TNNI3c.*3C= (n.*3C=)
n.635C=
n.464C=
19g.55151832G>ACA2343272425TNNI3c.*2C>T (n.*2C>T)
n.634C>T
n.463C>T
 dbSNP
19g.55151832G=CA2343272424TNNI3c.*2C= (n.*2C=)
n.634C=
n.463C=
19g.55151832G>TCA2587243153TNNI3c.*2C>A (n.*2C>A)
n.634C>A
n.463C>A
 gnomAD v4
19g.55151833C>ACA2587243154TNNI3c.*1G>T (n.*1G>T)
n.633G>T
n.462G>T
 gnomAD v4
19g.55151834T>ACA407439350TNNI3c.633A>T (p.Ter211Cys)
c.666A>T (p.Ter222Cys)
n.632A>T
c.558A>T (p.Ter186Cys)
n.461A>T
19g.55151834T>CCA407439353TNNI3c.633A>G (p.Ter211Trp)
c.666A>G (p.Ter222Trp)
n.632A>G
c.558A>G (p.Ter186Trp)
n.461A>G
19g.55151834T>GCA407439356TNNI3c.633A>C (p.Ter211Cys)
c.666A>C (p.Ter222Cys)
n.632A>C
c.558A>C (p.Ter186Cys)
n.461A>C
19g.55151835C>ACA022109TNNI3c.632G>T (p.Ter211Leu)
c.665G>T (p.Ter222Leu)
n.631G>T
c.557G>T (p.Ter186Leu)
n.460G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151835C=CA2343272427TNNI3c.632G= (p.Ter211=)
c.665G= (p.Ter222=)
n.631G=
c.557G= (p.Ter186=)
n.460G=
19g.55151835C>GCA407439363TNNI3c.632G>C (p.Ter211Ser)
c.665G>C (p.Ter222Ser)
n.631G>C
c.557G>C (p.Ter186Ser)
n.460G>C
19g.55151835C>TCA508989323TNNI3c.632G>A (p.Ter211=)
c.665G>A (p.Ter222=)
n.631G>A
c.557G>A (p.Ter186=)
n.460G>A
 gnomAD v4
19g.55151836A>CCA407439366TNNI3c.631T>G (p.Ter211Gly)
c.664T>G (p.Ter222Gly)
n.630T>G
c.556T>G (p.Ter186Gly)
n.459T>G
19g.55151836A>GCA407439368TNNI3c.631T>C (p.Ter211Arg)
c.664T>C (p.Ter222Arg)
n.630T>C
c.556T>C (p.Ter186Arg)
n.459T>C
19g.55151836A>TCA407439370TNNI3c.631T>A (p.Ter211Arg)
c.664T>A (p.Ter222Arg)
n.630T>A
c.556T>A (p.Ter186Arg)
n.459T>A
19g.55151837G>ACA508989324TNNI3c.630C>T (p.Ser210=)
c.663C>T (p.Ser221=)
n.629C>T
c.555C>T (p.Ser185=)
n.458C>T
19g.55151837G>CCA407439372TNNI3c.630C>G (p.Ser210Arg)
c.663C>G (p.Ser221Arg)
n.629C>G
c.555C>G (p.Ser185Arg)
n.458C>G
19g.55151837G>TCA407439373TNNI3c.630C>A (p.Ser210Arg)
c.663C>A (p.Ser221Arg)
n.629C>A
c.555C>A (p.Ser185Arg)
n.458C>A
19g.55151838C>ACA407439381TNNI3c.629G>T (p.Ser210Ile)
c.662G>T (p.Ser221Ile)
n.628G>T
c.554G>T (p.Ser185Ile)
n.457G>T
19g.55151838C=CA2343272428TNNI3c.629G= (p.Ser210=)
c.662G= (p.Ser221=)
n.628G=
c.554G= (p.Ser185=)
n.457G=
19g.55151838C>GCA407439379TNNI3c.629G>C (p.Ser210Thr)
c.662G>C (p.Ser221Thr)
n.628G>C
c.554G>C (p.Ser185Thr)
n.457G>C
19g.55151838C>TCA407439376TNNI3c.629G>A (p.Ser210Asn)
c.662G>A (p.Ser221Asn)
n.628G>A
c.554G>A (p.Ser185Asn)
n.457G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55151839T>ACA407439384TNNI3c.628A>T (p.Ser210Cys)
c.661A>T (p.Ser221Cys)
n.627A>T
c.553A>T (p.Ser185Cys)
n.456A>T
19g.55151839T>CCA407439388TNNI3c.628A>G (p.Ser210Gly)
c.661A>G (p.Ser221Gly)
n.627A>G
c.553A>G (p.Ser185Gly)
n.456A>G
 ClinVar dbSNP
19g.55151839T>GCA407439386TNNI3c.628A>C (p.Ser210Arg)
c.661A>C (p.Ser221Arg)
n.627A>C
c.553A>C (p.Ser185Arg)
n.456A>C
19g.55151839T=CA2343272429TNNI3c.628A= (p.Ser210=)
c.661A= (p.Ser221=)
n.627A=
c.553A= (p.Ser185=)
n.456A=
19g.55151840C>ACA407439391TNNI3c.627G>T (p.Glu209Asp)
c.660G>T (p.Glu220Asp)
n.626G>T
c.552G>T (p.Glu184Asp)
n.455G>T
19g.55151840C=CA2343272431TNNI3c.627G= (p.Glu209=)
c.660G= (p.Glu220=)
n.626G=
c.552G= (p.Glu184=)
n.455G=
19g.55151840C>GCA407439393TNNI3c.627G>C (p.Glu209Asp)
c.660G>C (p.Glu220Asp)
n.626G>C
c.552G>C (p.Glu184Asp)
n.455G>C
 ClinVar dbSNP
19g.55151840C>TCA508989325TNNI3c.627G>A (p.Glu209=)
c.660G>A (p.Glu220=)
n.626G>A
c.552G>A (p.Glu184=)
n.455G>A
 gnomAD v4
19g.55151841T>ACA407439397TNNI3c.626A>T (p.Glu209Val)
c.659A>T (p.Glu220Val)
n.625A>T
c.551A>T (p.Glu184Val)
n.454A>T
19g.55151841T>CCA407439399TNNI3c.626A>G (p.Glu209Gly)
c.659A>G (p.Glu220Gly)
n.625A>G
c.551A>G (p.Glu184Gly)
n.454A>G
 dbSNP gnomAD v2 gnomAD v4
19g.55151841T>GCA022103TNNI3c.626A>C (p.Glu209Ala)
c.659A>C (p.Glu220Ala)
n.625A>C
c.551A>C (p.Glu184Ala)
n.454A>C
 ClinVar dbSNP
19g.55151841T=CA2343272433TNNI3c.626A= (p.Glu209=)
c.659A= (p.Glu220=)
n.625A=
c.551A= (p.Glu184=)
n.454A=
19g.55151842C>ACA407439402TNNI3c.625G>T (p.Glu209Ter)
c.658G>T (p.Glu220Ter)
n.624G>T
c.550G>T (p.Glu184Ter)
n.453G>T
 gnomAD v4
19g.55151842C=CA2343272437TNNI3c.625G= (p.Glu209=)
c.658G= (p.Glu220=)
n.624G=
c.550G= (p.Glu184=)
n.453G=
19g.55151842C>GCA407439405TNNI3c.625G>C (p.Glu209Gln)
c.658G>C (p.Glu220Gln)
n.624G>C
c.550G>C (p.Glu184Gln)
n.453G>C
19g.55151842C>TCA022097TNNI3c.625G>A (p.Glu209Lys)
c.658G>A (p.Glu220Lys)
n.624G>A
c.550G>A (p.Glu184Lys)
n.453G>A
 ClinVar dbSNP COSMIC
19g.55151843A=CA2343272443TNNI3c.624T= (p.Phe208=)
c.657T= (p.Phe219=)
n.623T=
c.549T= (p.Phe183=)
n.452T=
19g.55151843A>CCA10577112TNNI3c.624T>G (p.Phe208Leu)
c.657T>G (p.Phe219Leu)
n.623T>G
c.549T>G (p.Phe183Leu)
n.452T>G
 ClinVar dbSNP
19g.55151843A>GCA508989326TNNI3c.624T>C (p.Phe208=)
c.657T>C (p.Phe219=)
n.623T>C
c.549T>C (p.Phe183=)
n.452T>C
19g.55151843A>TCA407439408TNNI3c.624T>A (p.Phe208Leu)
c.657T>A (p.Phe219Leu)
n.623T>A
c.549T>A (p.Phe183Leu)
n.452T>A
19g.55151845dupCA915953048TNNI3c.624dup (p.Glu209Ter)
c.657dup (p.Glu220Ter)
n.623dup
c.549dup (p.Glu184Ter)
n.452dup
 ClinVar dbSNP
19g.55151844A>CCA407439411TNNI3c.623T>G (p.Phe208Cys)
c.656T>G (p.Phe219Cys)
n.622T>G
c.548T>G (p.Phe183Cys)
n.451T>G
19g.55151844A>GCA407439414TNNI3c.623T>C (p.Phe208Ser)
c.656T>C (p.Phe219Ser)
n.622T>C
c.548T>C (p.Phe183Ser)
n.451T>C
19g.55151844A>TCA407439416TNNI3c.623T>A (p.Phe208Tyr)
c.656T>A (p.Phe219Tyr)
n.622T>A
c.548T>A (p.Phe183Tyr)
n.451T>A
19g.55151845A=CA2343272444TNNI3c.622T= (p.Phe208=)
c.655T= (p.Phe219=)
n.621T=
c.547T= (p.Phe183=)
n.450T=
19g.55151845A>CCA407439418TNNI3c.622T>G (p.Phe208Val)
c.655T>G (p.Phe219Val)
n.621T>G
c.547T>G (p.Phe183Val)
n.450T>G
19g.55151845A>GCA407439420TNNI3c.622T>C (p.Phe208Leu)
c.655T>C (p.Phe219Leu)
n.621T>C
c.547T>C (p.Phe183Leu)
n.450T>C
19g.55151845A>TCA10577113TNNI3c.622T>A (p.Phe208Ile)
c.655T>A (p.Phe219Ile)
n.621T>A
c.547T>A (p.Phe183Ile)
n.450T>A
 ClinVar dbSNP
19g.55151846C>ACA407439424TNNI3c.621G>T (p.Lys207Asn)
c.654G>T (p.Lys218Asn)
n.620G>T
c.546G>T (p.Lys182Asn)
n.449G>T
19g.55151846C=CA2343272446TNNI3c.621G= (p.Lys207=)
c.654G= (p.Lys218=)
n.620G=
c.546G= (p.Lys182=)
n.449G=
19g.55151846C>GCA407439426TNNI3c.621G>C (p.Lys207Asn)
c.654G>C (p.Lys218Asn)
n.620G>C
c.546G>C (p.Lys182Asn)
n.449G>C
 ClinVar dbSNP
19g.55151846C>TCA508989327TNNI3c.621G>A (p.Lys207=)
c.654G>A (p.Lys218=)
n.620G>A
c.546G>A (p.Lys182=)
n.449G>A
 gnomAD v4
19g.55151846_55151847delinsCTCA2343272445TNNI3c.620_621delinsAG (p.Lys207=)
c.653_654delinsAG (p.Lys218=)
n.619_620delinsAG
c.545_546delinsAG (p.Lys182=)
n.448_449delinsAG
19g.55151847T>ACA407439428TNNI3c.620A>T (p.Lys207Met)
c.653A>T (p.Lys218Met)
n.619A>T
c.545A>T (p.Lys182Met)
n.448A>T
19g.55151847T>CCA310144831TNNI3c.620A>G (p.Lys207Arg)
c.653A>G (p.Lys218Arg)
n.619A>G
c.545A>G (p.Lys182Arg)
n.448A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55151847T>GCA407439432TNNI3c.620A>C (p.Lys207Thr)
c.653A>C (p.Lys218Thr)
n.619A>C
c.545A>C (p.Lys182Thr)
n.448A>C
19g.55151847T=CA2343272447TNNI3c.620A= (p.Lys207=)
c.653A= (p.Lys218=)
n.619A=
c.545A= (p.Lys182=)
n.448A=
19g.55151851delCA920140594TNNI3c.620del (p.Lys207SerfsTer14)
c.653del (p.Lys218SerfsTer14)
n.619del
c.545del (p.Lys182SerfsTer14)
n.448del
 dbSNP
19g.55151850_55151851delCA2695229153TNNI3c.619_620del (p.Lys207ValfsTer2)
c.652_653del (p.Lys218ValfsTer2)
n.618_619del
c.544_545del (p.Lys182ValfsTer2)
n.447_448del
19g.55151848T>ACA407439439TNNI3c.619A>T (p.Lys207Ter)
c.652A>T (p.Lys218Ter)
n.618A>T
c.544A>T (p.Lys182Ter)
n.447A>T
19g.55151848T>CCA407439437TNNI3c.619A>G (p.Lys207Glu)
c.652A>G (p.Lys218Glu)
n.618A>G
c.544A>G (p.Lys182Glu)
n.447A>G
19g.55151848T>GCA407439436TNNI3c.619A>C (p.Lys207Gln)
c.652A>C (p.Lys218Gln)
n.618A>C
c.544A>C (p.Lys182Gln)
n.447A>C
19g.55151849T>ACA407439440TNNI3c.618A>T (p.Lys206Asn)
c.651A>T (p.Lys217Asn)
n.617A>T
c.543A>T (p.Lys181Asn)
n.446A>T
19g.55151849T>CCA508989328TNNI3c.618A>G (p.Lys206=)
c.651A>G (p.Lys217=)
n.617A>G
c.543A>G (p.Lys181=)
n.446A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55151849T>GCA407439442TNNI3c.618A>C (p.Lys206Asn)
c.651A>C (p.Lys217Asn)
n.617A>C
c.543A>C (p.Lys181Asn)
n.446A>C
19g.55151849T=CA2343272448TNNI3c.618A= (p.Lys206=)
c.651A= (p.Lys217=)
n.617A=
c.543A= (p.Lys181=)
n.446A=
19g.55151850T>ACA022085TNNI3c.617A>T (p.Lys206Ile)
c.650A>T (p.Lys217Ile)
n.616A>T
c.542A>T (p.Lys181Ile)
n.445A>T
 ClinVar dbSNP
19g.55151850T>CCA407439444TNNI3c.617A>G (p.Lys206Arg)
c.650A>G (p.Lys217Arg)
n.616A>G
c.542A>G (p.Lys181Arg)
n.445A>G
19g.55151850T>GCA407439446TNNI3c.617A>C (p.Lys206Thr)
c.650A>C (p.Lys217Thr)
n.616A>C
c.542A>C (p.Lys181Thr)
n.445A>C
19g.55151850T=CA2343272450TNNI3c.617A= (p.Lys206=)
c.650A= (p.Lys217=)
n.616A=
c.542A= (p.Lys181=)
n.445A=
19g.55151851T>ACA407439447TNNI3c.616A>T (p.Lys206Ter)
c.649A>T (p.Lys217Ter)
n.615A>T
c.541A>T (p.Lys181Ter)
n.444A>T
19g.55151851T>CCA022079TNNI3c.616A>G (p.Lys206Glu)
c.649A>G (p.Lys217Glu)
n.615A>G
c.541A>G (p.Lys181Glu)
n.444A>G
 ClinVar dbSNP
19g.55151851T>GCA022072TNNI3c.616A>C (p.Lys206Gln)
c.649A>C (p.Lys217Gln)
n.615A>C
c.541A>C (p.Lys181Gln)
n.444A>C
 ClinVar dbSNP
19g.55151851T=CA2343272459TNNI3c.616A= (p.Lys206=)
c.649A= (p.Lys217=)
n.615A=
c.541A= (p.Lys181=)
n.444A=
19g.55151852C>ACA407439450TNNI3c.615G>T (p.Lys205Asn)
c.648G>T (p.Lys216Asn)
n.614G>T
c.540G>T (p.Lys180Asn)
n.443G>T
 ClinVar
19g.55151852C>GCA407439451TNNI3c.615G>C (p.Lys205Asn)
c.648G>C (p.Lys216Asn)
n.614G>C
c.540G>C (p.Lys180Asn)
n.443G>C
19g.55151852C>TCA508989329TNNI3c.615G>A (p.Lys205=)
c.648G>A (p.Lys216=)
n.614G>A
c.540G>A (p.Lys180=)
n.443G>A
19g.55151853T>ACA407439452TNNI3c.614A>T (p.Lys205Met)
c.647A>T (p.Lys216Met)
n.613A>T
c.539A>T (p.Lys180Met)
n.442A>T
19g.55151853T>CCA407439453TNNI3c.614A>G (p.Lys205Arg)
c.647A>G (p.Lys216Arg)
n.613A>G
c.539A>G (p.Lys180Arg)
n.442A>G
19g.55151853T>GCA407439454TNNI3c.614A>C (p.Lys205Thr)
c.647A>C (p.Lys216Thr)
n.613A>C
c.539A>C (p.Lys180Thr)
n.442A>C
 ClinVar dbSNP
19g.55151853T=CA2343272465TNNI3c.614A= (p.Lys205=)
c.647A= (p.Lys216=)
n.613A=
c.539A= (p.Lys180=)
n.442A=
19g.55151854T>ACA407439456TNNI3c.613A>T (p.Lys205Ter)
c.646A>T (p.Lys216Ter)
n.612A>T
c.538A>T (p.Lys180Ter)
n.441A>T
19g.55151854T>CCA407439457TNNI3c.613A>G (p.Lys205Glu)
c.646A>G (p.Lys216Glu)
n.612A>G
c.538A>G (p.Lys180Glu)
n.441A>G
19g.55151854T>GCA022066TNNI3c.613A>C (p.Lys205Gln)
c.646A>C (p.Lys216Gln)
n.612A>C
c.538A>C (p.Lys180Gln)
n.441A>C
 ClinVar dbSNP
19g.55151854T=CA2343272470TNNI3c.613A= (p.Lys205=)
c.646A= (p.Lys216=)
n.612A=
c.538A= (p.Lys180=)
n.441A=
19g.55151855G>ACA508989332TNNI3c.612C>T (p.Arg204=)
c.645C>T (p.Arg215=)
n.611C>T
c.537C>T (p.Arg179=)
n.440C>T
19g.55151855G>CCA508989330TNNI3c.612C>G (p.Arg204=)
c.645C>G (p.Arg215=)
n.611C>G
c.537C>G (p.Arg179=)
n.440C>G
 ClinVar dbSNP gnomAD v4
19g.55151855G=CA2343272476TNNI3c.612C= (p.Arg204=)
c.645C= (p.Arg215=)
n.611C=
c.537C= (p.Arg179=)
n.440C=
19g.55151855G>TCA508989331TNNI3c.612C>A (p.Arg204=)
c.645C>A (p.Arg215=)
n.611C>A
c.537C>A (p.Arg179=)
n.440C>A
 dbSNP
19g.55151856C>ACA051933TNNI3c.611G>T (p.Arg204Leu)
c.644G>T (p.Arg215Leu)
n.610G>T
c.536G>T (p.Arg179Leu)
n.439G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.55151856C=CA2343272484TNNI3c.611G= (p.Arg204=)
c.644G= (p.Arg215=)
n.610G=
c.536G= (p.Arg179=)
n.439G=
19g.55151856C>GCA407439460TNNI3c.611G>C (p.Arg204Pro)
c.644G>C (p.Arg215Pro)
n.610G>C
c.536G>C (p.Arg179Pro)
n.439G>C
19g.55151856C>TCA022060TNNI3c.611G>A (p.Arg204His)
c.644G>A (p.Arg215His)
n.610G>A
c.536G>A (p.Arg179His)
n.439G>A
 ClinVar dbSNP gnomAD v4
19g.55151857G>ACA022054TNNI3c.610C>T (p.Arg204Cys)
c.643C>T (p.Arg215Cys)
n.609C>T
c.535C>T (p.Arg179Cys)
n.438C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
19g.55151857G>CCA407439463TNNI3c.610C>G (p.Arg204Gly)
c.643C>G (p.Arg215Gly)
n.609C>G
c.535C>G (p.Arg179Gly)
n.438C>G
19g.55151857G=CA2343272490TNNI3c.610C= (p.Arg204=)
c.643C= (p.Arg215=)
n.609C=
c.535C= (p.Arg179=)
n.438C=
19g.55151857G>TCA407439464TNNI3c.610C>A (p.Arg204Ser)
c.643C>A (p.Arg215Ser)
n.609C>A
c.535C>A (p.Arg179Ser)
n.438C>A
 ClinVar dbSNP
19g.55151858G>ACA022049TNNI3c.609C>T (p.Gly203=)
c.642C>T (p.Gly214=)
n.608C>T
c.534C>T (p.Gly178=)
n.437C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55151858G>CCA508989334TNNI3c.609C>G (p.Gly203=)
c.642C>G (p.Gly214=)
n.608C>G
c.534C>G (p.Gly178=)
n.437C>G
19g.55151858G=CA2343272501TNNI3c.609C= (p.Gly203=)
c.642C= (p.Gly214=)
n.608C=
c.534C= (p.Gly178=)
n.437C=
19g.55151858G>TCA508989333TNNI3c.609C>A (p.Gly203=)
c.642C>A (p.Gly214=)
n.608C>A
c.534C>A (p.Gly178=)
n.437C>A
19g.55151859C>ACA407439466TNNI3c.608G>T (p.Gly203Val)
c.641G>T (p.Gly214Val)
n.607G>T
c.533G>T (p.Gly178Val)
n.436G>T
19g.55151859C>GCA407439467TNNI3c.608G>C (p.Gly203Ala)
c.641G>C (p.Gly214Ala)
n.607G>C
c.533G>C (p.Gly178Ala)
n.436G>C
19g.55151859C>TCA407439469TNNI3c.608G>A (p.Gly203Asp)
c.641G>A (p.Gly214Asp)
n.607G>A
c.533G>A (p.Gly178Asp)
n.436G>A
 ClinVar
19g.55151860C>ACA407439470TNNI3c.607G>T (p.Gly203Cys)
c.640G>T (p.Gly214Cys)
n.606G>T
c.532G>T (p.Gly178Cys)
n.435G>T
19g.55151860C=CA2343272506TNNI3c.607G= (p.Gly203=)
c.640G= (p.Gly214=)
n.606G=
c.532G= (p.Gly178=)
n.435G=
19g.55151860C>GCA407439472TNNI3c.607G>C (p.Gly203Arg)
c.640G>C (p.Gly214Arg)
n.606G>C
c.532G>C (p.Gly178Arg)
n.435G>C
19g.55151860C>TCA022043TNNI3c.607G>A (p.Gly203Ser)
c.640G>A (p.Gly214Ser)
n.606G>A
c.532G>A (p.Gly178Ser)
n.435G>A
 ClinVar dbSNP
19g.55151861C>ACA407439474TNNI3c.606G>T (p.Glu202Asp)
c.639G>T (p.Glu213Asp)
n.605G>T
c.531G>T (p.Glu177Asp)
n.434G>T
19g.55151861C=CA2343272513TNNI3c.606G= (p.Glu202=)
c.639G= (p.Glu213=)
n.605G=
c.531G= (p.Glu177=)
n.434G=
19g.55151861C>GCA407439477TNNI3c.606G>C (p.Glu202Asp)
c.639G>C (p.Glu213Asp)
n.605G>C
c.531G>C (p.Glu177Asp)
n.434G>C
19g.55151861C>TCA310144864TNNI3c.606G>A (p.Glu202=)
c.639G>A (p.Glu213=)
n.605G>A
c.531G>A (p.Glu177=)
n.434G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55151862T>ACA407439479TNNI3c.605A>T (p.Glu202Val)
c.638A>T (p.Glu213Val)
n.604A>T
c.530A>T (p.Glu177Val)
n.433A>T
19g.55151862T>CCA407439480TNNI3c.605A>G (p.Glu202Gly)
c.638A>G (p.Glu213Gly)
n.604A>G
c.530A>G (p.Glu177Gly)
n.433A>G
 ClinVar gnomAD v4
19g.55151862T>GCA407439482TNNI3c.605A>C (p.Glu202Ala)
c.638A>C (p.Glu213Ala)
n.604A>C
c.530A>C (p.Glu177Ala)
n.433A>C
 gnomAD v4
19g.55151863C>ACA407439484TNNI3c.604G>T (p.Glu202Ter)
c.637G>T (p.Glu213Ter)
n.603G>T
c.529G>T (p.Glu177Ter)
n.432G>T
 gnomAD v4
19g.55151863C=CA2343272516TNNI3c.604G= (p.Glu202=)
c.637G= (p.Glu213=)
n.603G=
c.529G= (p.Glu177=)
n.432G=
19g.55151863C>GCA407439485TNNI3c.604G>C (p.Glu202Gln)
c.637G>C (p.Glu213Gln)
n.603G>C
c.529G>C (p.Glu177Gln)
n.432G>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55151863C>TCA407439486TNNI3c.604G>A (p.Glu202Lys)
c.637G>A (p.Glu213Lys)
n.603G>A
c.529G>A (p.Glu177Lys)
n.432G>A
19g.55151864C>ACA407439488TNNI3c.603G>T (p.Met201Ile)
c.636G>T (p.Met212Ile)
n.602G>T
c.528G>T (p.Met176Ile)
n.431G>T
19g.55151864C=CA2343272519TNNI3c.603G= (p.Met201=)
c.636G= (p.Met212=)
n.602G=
c.528G= (p.Met176=)
n.431G=
19g.55151864C>GCA051926TNNI3c.603G>C (p.Met201Ile)
c.636G>C (p.Met212Ile)
n.602G>C
c.528G>C (p.Met176Ile)
n.431G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151864C>TCA407439490TNNI3c.603G>A (p.Met201Ile)
c.636G>A (p.Met212Ile)
n.602G>A
c.528G>A (p.Met176Ile)
n.431G>A
 gnomAD v4
19g.55151865A=CA2343272522TNNI3c.602T= (p.Met201=)
c.635T= (p.Met212=)
n.601T=
c.527T= (p.Met176=)
n.430T=
19g.55151865A>CCA407439494TNNI3c.602T>G (p.Met201Arg)
c.635T>G (p.Met212Arg)
n.601T>G
c.527T>G (p.Met176Arg)
n.430T>G
19g.55151865A>GCA022037TNNI3c.602T>C (p.Met201Thr)
c.635T>C (p.Met212Thr)
n.601T>C
c.527T>C (p.Met176Thr)
n.430T>C
 ClinVar dbSNP
19g.55151865A>TCA407439492TNNI3c.602T>A (p.Met201Lys)
c.635T>A (p.Met212Lys)
n.601T>A
c.527T>A (p.Met176Lys)
n.430T>A
19g.55151866T>ACA407439495TNNI3c.601A>T (p.Met201Leu)
c.634A>T (p.Met212Leu)
n.600A>T
c.526A>T (p.Met176Leu)
n.429A>T
19g.55151866T>CCA407439497TNNI3c.601A>G (p.Met201Val)
c.634A>G (p.Met212Val)
n.600A>G
c.526A>G (p.Met176Val)
n.429A>G
 gnomAD v4
19g.55151866T>GCA407439496TNNI3c.601A>C (p.Met201Leu)
c.634A>C (p.Met212Leu)
n.600A>C
c.526A>C (p.Met176Leu)
n.429A>C
19g.55151867T>ACA508989337TNNI3c.600A>T (p.Gly200=)
c.633A>T (p.Gly211=)
n.599A>T
c.525A>T (p.Gly175=)
n.428A>T
19g.55151867T>CCA508989335TNNI3c.600A>G (p.Gly200=)
c.633A>G (p.Gly211=)
n.599A>G
c.525A>G (p.Gly175=)
n.428A>G
19g.55151867T>GCA508989336TNNI3c.600A>C (p.Gly200=)
c.633A>C (p.Gly211=)
n.599A>C
c.525A>C (p.Gly175=)
n.428A>C
19g.55151868C>ACA16616444TNNI3c.599G>T (p.Gly200Val)
c.632G>T (p.Gly211Val)
n.598G>T
c.524G>T (p.Gly175Val)
n.427G>T
 ClinVar dbSNP
19g.55151868C=CA2343272527TNNI3c.599G= (p.Gly200=)
c.632G= (p.Gly211=)
n.598G=
c.524G= (p.Gly175=)
n.427G=
19g.55151868C>GCA407439498TNNI3c.599G>C (p.Gly200Ala)
c.632G>C (p.Gly211Ala)
n.598G>C
c.524G>C (p.Gly175Ala)
n.427G>C
19g.55151868C>TCA10583862TNNI3c.599G>A (p.Gly200Glu)
c.632G>A (p.Gly211Glu)
n.598G>A
c.524G>A (p.Gly175Glu)
n.427G>A
 ClinVar dbSNP
19g.55151869C>ACA407439500TNNI3c.598G>T (p.Gly200Ter)
c.631G>T (p.Gly211Ter)
n.597G>T
c.523G>T (p.Gly175Ter)
n.426G>T
19g.55151869C>GCA407439501TNNI3c.598G>C (p.Gly200Arg)
c.631G>C (p.Gly211Arg)
n.597G>C
c.523G>C (p.Gly175Arg)
n.426G>C
19g.55151869C>TCA407439502TNNI3c.598G>A (p.Gly200Arg)
c.631G>A (p.Gly211Arg)
n.597G>A
c.523G>A (p.Gly175Arg)
n.426G>A
19g.55151870delCA2580097811TNNI3c.597del (p.Ser199ArgfsTer22)
c.630del (p.Ser210ArgfsTer22)
n.596del
c.522del (p.Ser174ArgfsTer22)
n.425del
 ClinVar
19g.55151870A=CA2343272532TNNI3c.597T= (p.Ser199=)
c.630T= (p.Ser210=)
n.596T=
c.522T= (p.Ser174=)
n.425T=
19g.55151870A>CCA407439503TNNI3c.597T>G (p.Ser199Arg)
c.630T>G (p.Ser210Arg)
n.596T>G
c.522T>G (p.Ser174Arg)
n.425T>G
19g.55151870A>GCA508989338TNNI3c.597T>C (p.Ser199=)
c.630T>C (p.Ser210=)
n.596T>C
c.522T>C (p.Ser174=)
n.425T>C
 dbSNP gnomAD v3 gnomAD v4
19g.55151870A>TCA407439505TNNI3c.597T>A (p.Ser199Arg)
c.630T>A (p.Ser210Arg)
n.596T>A
c.522T>A (p.Ser174Arg)
n.425T>A
19g.55151871C>ACA407439507TNNI3c.596G>T (p.Ser199Ile)
c.629G>T (p.Ser210Ile)
n.595G>T
c.521G>T (p.Ser174Ile)
n.424G>T
19g.55151871C=CA2343272536TNNI3c.596G= (p.Ser199=)
c.629G= (p.Ser210=)
n.595G=
c.521G= (p.Ser174=)
n.424G=
19g.55151871C>GCA407439509TNNI3c.596G>C (p.Ser199Thr)
c.629G>C (p.Ser210Thr)
n.595G>C
c.521G>C (p.Ser174Thr)
n.424G>C
19g.55151871C>TCA022024TNNI3c.596G>A (p.Ser199Asn)
c.629G>A (p.Ser210Asn)
n.595G>A
c.521G>A (p.Ser174Asn)
n.424G>A
 ClinVar dbSNP gnomAD v4
19g.55151872T>ACA407439519TNNI3c.595A>T (p.Ser199Cys)
c.628A>T (p.Ser210Cys)
n.594A>T
c.520A>T (p.Ser174Cys)
n.423A>T
 ClinVar dbSNP
19g.55151872T>CCA407439517TNNI3c.595A>G (p.Ser199Gly)
c.628A>G (p.Ser210Gly)
n.594A>G
c.520A>G (p.Ser174Gly)
n.423A>G
 dbSNP
19g.55151872T>GCA407439514TNNI3c.595A>C (p.Ser199Arg)
c.628A>C (p.Ser210Arg)
n.594A>C
c.520A>C (p.Ser174Arg)
n.423A>C
19g.55151872T=CA2343272541TNNI3c.595A= (p.Ser199=)
c.628A= (p.Ser210=)
n.594A=
c.520A= (p.Ser174=)
n.423A=
19g.55151873C>ACA508989341TNNI3c.594G>T (p.Leu198=)
c.627G>T (p.Leu209=)
n.593G>T
c.519G>T (p.Leu173=)
n.422G>T
19g.55151873C=CA2343272544TNNI3c.594G= (p.Leu198=)
c.627G= (p.Leu209=)
n.593G=
c.519G= (p.Leu173=)
n.422G=
19g.55151873C>GCA508989339TNNI3c.594G>C (p.Leu198=)
c.627G>C (p.Leu209=)
n.593G>C
c.519G>C (p.Leu173=)
n.422G>C
 ClinVar dbSNP gnomAD v4
19g.55151873C>TCA508989340TNNI3c.594G>A (p.Leu198=)
c.627G>A (p.Leu209=)
n.593G>A
c.519G>A (p.Leu173=)
n.422G>A
 dbSNP
19g.55151874A>CCA407439521TNNI3c.593T>G (p.Leu198Arg)
c.626T>G (p.Leu209Arg)
n.592T>G
c.518T>G (p.Leu173Arg)
n.421T>G
19g.55151874A>GCA407439523TNNI3c.593T>C (p.Leu198Pro)
c.626T>C (p.Leu209Pro)
n.592T>C
c.518T>C (p.Leu173Pro)
n.421T>C
19g.55151874A>TCA407439525TNNI3c.593T>A (p.Leu198Gln)
c.626T>A (p.Leu209Gln)
n.592T>A
c.518T>A (p.Leu173Gln)
n.421T>A
19g.55151875G>ACA508989342TNNI3c.592C>T (p.Leu198=)
c.625C>T (p.Leu209=)
n.591C>T
c.517C>T (p.Leu173=)
n.420C>T
 dbSNP gnomAD v2 gnomAD v4
19g.55151875G>CCA022019TNNI3c.592C>G (p.Leu198Val)
c.625C>G (p.Leu209Val)
n.591C>G
c.517C>G (p.Leu173Val)
n.420C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.55151875G=CA2343272548TNNI3c.592C= (p.Leu198=)
c.625C= (p.Leu209=)
n.591C=
c.517C= (p.Leu173=)
n.420C=
19g.55151875G>TCA407439529TNNI3c.592C>A (p.Leu198Met)
c.625C>A (p.Leu209Met)
n.591C>A
c.517C>A (p.Leu173Met)
n.420C>A
19g.55151877_55151886delCA2695229154TNNI3c.583_592del (p.Ile195Ter)
c.616_625del (p.Ile206Ter)
n.582_591del
c.508_517del (p.Ile170Ter)
n.411_420del
19g.55151876T>ACA508989344TNNI3c.591A>T (p.Ala197=)
c.624A>T (p.Ala208=)
n.590A>T
c.516A>T (p.Ala172=)
n.419A>T
19g.55151876T>CCA051909TNNI3c.591A>G (p.Ala197=)
c.624A>G (p.Ala208=)
n.590A>G
c.516A>G (p.Ala172=)
n.419A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151876T>GCA508989343TNNI3c.591A>C (p.Ala197=)
c.624A>C (p.Ala208=)
n.590A>C
c.516A>C (p.Ala172=)
n.419A>C
19g.55151876T=CA2343272553TNNI3c.591A= (p.Ala197=)
c.624A= (p.Ala208=)
n.590A=
c.516A= (p.Ala172=)
n.419A=
19g.55151877G>ACA407439533TNNI3c.590C>T (p.Ala197Val)
c.623C>T (p.Ala208Val)
n.589C>T
c.515C>T (p.Ala172Val)
n.418C>T
 dbSNP
19g.55151877G>CCA407439535TNNI3c.590C>G (p.Ala197Gly)
c.623C>G (p.Ala208Gly)
n.589C>G
c.515C>G (p.Ala172Gly)
n.418C>G
19g.55151877G=CA2343272555TNNI3c.590C= (p.Ala197=)
c.623C= (p.Ala208=)
n.589C=
c.515C= (p.Ala172=)
n.418C=
19g.55151877G>TCA407439537TNNI3c.590C>A (p.Ala197Glu)
c.623C>A (p.Ala208Glu)
n.589C>A
c.515C>A (p.Ala172Glu)
n.418C>A
19g.55151878C>ACA407439539TNNI3c.589G>T (p.Ala197Ser)
c.622G>T (p.Ala208Ser)
n.588G>T
c.514G>T (p.Ala172Ser)
n.417G>T
19g.55151878C>GCA407439542TNNI3c.589G>C (p.Ala197Pro)
c.622G>C (p.Ala208Pro)
n.588G>C
c.514G>C (p.Ala172Pro)
n.417G>C
19g.55151878C>TCA407439544TNNI3c.589G>A (p.Ala197Thr)
c.622G>A (p.Ala208Thr)
n.588G>A
c.514G>A (p.Ala172Thr)
n.417G>A
19g.55151879A>CCA407439547TNNI3c.588T>G (p.Asp196Glu)
c.621T>G (p.Asp207Glu)
n.587T>G
c.513T>G (p.Asp171Glu)
n.416T>G
19g.55151879A>GCA508989345TNNI3c.588T>C (p.Asp196=)
c.621T>C (p.Asp207=)
n.587T>C
c.513T>C (p.Asp171=)
n.416T>C
19g.55151879A>TCA407439548TNNI3c.588T>A (p.Asp196Glu)
c.621T>A (p.Asp207Glu)
n.587T>A
c.513T>A (p.Asp171Glu)
n.416T>A
19g.55151880T>ACA407439550TNNI3c.587A>T (p.Asp196Val)
c.620A>T (p.Asp207Val)
n.586A>T
c.512A>T (p.Asp171Val)
n.415A>T
19g.55151880T>CCA407439552TNNI3c.587A>G (p.Asp196Gly)
c.620A>G (p.Asp207Gly)
n.586A>G
c.512A>G (p.Asp171Gly)
n.415A>G
 ClinVar dbSNP
19g.55151880T>GCA407439554TNNI3c.587A>C (p.Asp196Ala)
c.620A>C (p.Asp207Ala)
n.586A>C
c.512A>C (p.Asp171Ala)
n.415A>C
 gnomAD v4
19g.55151881C>ACA022012TNNI3c.586G>T (p.Asp196Tyr)
c.619G>T (p.Asp207Tyr)
n.585G>T
c.511G>T (p.Asp171Tyr)
n.414G>T
 ClinVar dbSNP gnomAD v4
19g.55151881C=CA2343272564TNNI3c.586G= (p.Asp196=)
c.619G= (p.Asp207=)
n.585G=
c.511G= (p.Asp171=)
n.414G=
19g.55151881C>GCA407439559TNNI3c.586G>C (p.Asp196His)
c.619G>C (p.Asp207His)
n.585G>C
c.511G>C (p.Asp171His)
n.414G>C
 ClinVar
19g.55151881C>TCA022006TNNI3c.586G>A (p.Asp196Asn)
c.619G>A (p.Asp207Asn)
n.585G>A
c.511G>A (p.Asp171Asn)
n.414G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151882G>ACA051883TNNI3c.585C>T (p.Ile195=)
c.618C>T (p.Ile206=)
n.584C>T
c.510C>T (p.Ile170=)
n.413C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151882G>CCA407439563TNNI3c.585C>G (p.Ile195Met)
c.618C>G (p.Ile206Met)
n.584C>G
c.510C>G (p.Ile170Met)
n.413C>G
 ClinVar dbSNP
19g.55151882G=CA2343272575TNNI3c.585C= (p.Ile195=)
c.618C= (p.Ile206=)
n.584C=
c.510C= (p.Ile170=)
n.413C=
19g.55151882G>TCA508989346TNNI3c.585C>A (p.Ile195=)
c.618C>A (p.Ile206=)
n.584C>A
c.510C>A (p.Ile170=)
n.413C>A
 gnomAD v4
19g.55151883A>CCA407439565TNNI3c.584T>G (p.Ile195Ser)
c.617T>G (p.Ile206Ser)
n.583T>G
c.509T>G (p.Ile170Ser)
n.412T>G
19g.55151883A>GCA407439567TNNI3c.584T>C (p.Ile195Thr)
c.617T>C (p.Ile206Thr)
n.583T>C
c.509T>C (p.Ile170Thr)
n.412T>C
 COSMIC
19g.55151883A>TCA407439570TNNI3c.584T>A (p.Ile195Asn)
c.617T>A (p.Ile206Asn)
n.583T>A
c.509T>A (p.Ile170Asn)
n.412T>A
19g.55151884T>ACA407439576TNNI3c.583A>T (p.Ile195Phe)
c.616A>T (p.Ile206Phe)
n.582A>T
c.508A>T (p.Ile170Phe)
n.411A>T
19g.55151884T>CCA407439577TNNI3c.583A>G (p.Ile195Val)
c.616A>G (p.Ile206Val)
n.582A>G
c.508A>G (p.Ile170Val)
n.411A>G
19g.55151884T>GCA10577114TNNI3c.583A>C (p.Ile195Leu)
c.616A>C (p.Ile206Leu)
n.582A>C
c.508A>C (p.Ile170Leu)
n.411A>C
 ClinVar dbSNP
19g.55151884T=CA2343272581TNNI3c.583A= (p.Ile195=)
c.616A= (p.Ile206=)
n.582A=
c.508A= (p.Ile170=)
n.411A=
19g.55151885G>ACA508989347TNNI3c.582C>T (p.Asn194=)
c.615C>T (p.Asn205=)
n.581C>T
c.507C>T (p.Asn169=)
n.410C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55151885G>CCA022000TNNI3c.582C>G (p.Asn194Lys)
c.615C>G (p.Asn205Lys)
n.581C>G
c.507C>G (p.Asn169Lys)
n.410C>G
 ClinVar dbSNP
19g.55151885G=CA2343272587TNNI3c.582C= (p.Asn194=)
c.615C= (p.Asn205=)
n.581C=
c.507C= (p.Asn169=)
n.410C=
19g.55151885G>TCA407439583TNNI3c.582C>A (p.Asn194Lys)
c.615C>A (p.Asn205Lys)
n.581C>A
c.507C>A (p.Asn169Lys)
n.410C>A
19g.55151886T>ACA407439586TNNI3c.581A>T (p.Asn194Ile)
c.614A>T (p.Asn205Ile)
n.580A>T
c.506A>T (p.Asn169Ile)
n.409A>T
 gnomAD v4
19g.55151886T>CCA021995TNNI3c.581A>G (p.Asn194Ser)
c.614A>G (p.Asn205Ser)
n.580A>G
c.506A>G (p.Asn169Ser)
n.409A>G
 ClinVar dbSNP
19g.55151886T>GCA051878TNNI3c.581A>C (p.Asn194Thr)
c.614A>C (p.Asn205Thr)
n.580A>C
c.506A>C (p.Asn169Thr)
n.409A>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151886T=CA2343272594TNNI3c.581A= (p.Asn194=)
c.614A= (p.Asn205=)
n.580A=
c.506A= (p.Asn169=)
n.409A=
19g.55151887T>ACA407439590TNNI3c.580A>T (p.Asn194Tyr)
c.613A>T (p.Asn205Tyr)
n.579A>T
c.505A>T (p.Asn169Tyr)
n.408A>T
19g.55151887T>CCA407439592TNNI3c.580A>G (p.Asn194Asp)
c.613A>G (p.Asn205Asp)
n.579A>G
c.505A>G (p.Asn169Asp)
n.408A>G
 ClinVar dbSNP
19g.55151887T>GCA407439595TNNI3c.580A>C (p.Asn194His)
c.613A>C (p.Asn205His)
n.579A>C
c.505A>C (p.Asn169His)
n.408A>C
19g.55151888C>ACA021989TNNI3c.579G>T (p.Lys193Asn)
c.612G>T (p.Lys204Asn)
n.578G>T
c.504G>T (p.Lys168Asn)
n.407G>T
 ClinVar dbSNP
19g.55151888C=CA2343272604TNNI3c.579G= (p.Lys193=)
c.612G= (p.Lys204=)
n.578G=
c.504G= (p.Lys168=)
n.407G=
19g.55151888C>GCA021983TNNI3c.579G>C (p.Lys193Asn)
c.612G>C (p.Lys204Asn)
n.578G>C
c.504G>C (p.Lys168Asn)
n.407G>C
 ClinVar dbSNP
19g.55151888C>TCA508989348TNNI3c.579G>A (p.Lys193=)
c.612G>A (p.Lys204=)
n.578G>A
c.504G>A (p.Lys168=)
n.407G>A
19g.55151889T>ACA407439600TNNI3c.578A>T (p.Lys193Met)
c.611A>T (p.Lys204Met)
n.577A>T
c.503A>T (p.Lys168Met)
n.406A>T
19g.55151889T>CCA407439603TNNI3c.578A>G (p.Lys193Arg)
c.611A>G (p.Lys204Arg)
n.577A>G
c.503A>G (p.Lys168Arg)
n.406A>G
 ClinVar gnomAD v4
19g.55151889T>GCA407439605TNNI3c.578A>C (p.Lys193Thr)
c.611A>C (p.Lys204Thr)
n.577A>C
c.503A>C (p.Lys168Thr)
n.406A>C
19g.55151890T>ACA407439611TNNI3c.577A>T (p.Lys193Ter)
c.610A>T (p.Lys204Ter)
n.576A>T
c.502A>T (p.Lys168Ter)
n.405A>T
19g.55151890T>CCA021977TNNI3c.577A>G (p.Lys193Glu)
c.610A>G (p.Lys204Glu)
n.576A>G
c.502A>G (p.Lys168Glu)
n.405A>G
 ClinVar dbSNP
19g.55151890T>GCA407439608TNNI3c.577A>C (p.Lys193Gln)
c.610A>C (p.Lys204Gln)
n.576A>C
c.502A>C (p.Lys168Gln)
n.405A>C
 dbSNP
19g.55151890T=CA2343272611TNNI3c.577A= (p.Lys193=)
c.610A= (p.Lys204=)
n.576A=
c.502A= (p.Lys168=)
n.405A=
19g.55151891G>ACA508989349TNNI3c.576C>T (p.Arg192=)
c.609C>T (p.Arg203=)
n.575C>T
c.501C>T (p.Arg167=)
n.404C>T
 gnomAD v4
19g.55151891G>CCA508989350TNNI3c.576C>G (p.Arg192=)
c.609C>G (p.Arg203=)
n.575C>G
c.501C>G (p.Arg167=)
n.404C>G
19g.55151891G>TCA508989351TNNI3c.576C>A (p.Arg192=)
c.609C>A (p.Arg203=)
n.575C>A
c.501C>A (p.Arg167=)
n.404C>A
19g.55151892C>ACA021971TNNI3c.575G>T (p.Arg192Leu)
c.608G>T (p.Arg203Leu)
n.574G>T
c.500G>T (p.Arg167Leu)
n.403G>T
 ClinVar dbSNP
19g.55151892C=CA2343272621TNNI3c.575G= (p.Arg192=)
c.608G= (p.Arg203=)
n.574G=
c.500G= (p.Arg167=)
n.403G=
19g.55151892C>GCA021964TNNI3c.575G>C (p.Arg192Pro)
c.608G>C (p.Arg203Pro)
n.574G>C
c.500G>C (p.Arg167Pro)
n.403G>C
 ClinVar dbSNP
19g.55151892C>TCA021957TNNI3c.575G>A (p.Arg192His)
c.608G>A (p.Arg203His)
n.574G>A
c.500G>A (p.Arg167His)
n.403G>A
 ClinVar dbSNP gnomAD v4 COSMIC
19g.55151893G>ACA021951TNNI3c.574C>T (p.Arg192Cys)
c.607C>T (p.Arg203Cys)
n.573C>T
c.499C>T (p.Arg167Cys)
n.402C>T
 ClinVar dbSNP COSMIC
19g.55151893G>CCA407439617TNNI3c.574C>G (p.Arg192Gly)
c.607C>G (p.Arg203Gly)
n.573C>G
c.499C>G (p.Arg167Gly)
n.402C>G
19g.55151893G=CA2343272629TNNI3c.574C= (p.Arg192=)
c.607C= (p.Arg203=)
n.573C=
c.499C= (p.Arg167=)
n.402C=
19g.55151893G>TCA407439618TNNI3c.574C>A (p.Arg192Ser)
c.607C>A (p.Arg203Ser)
n.573C>A
c.499C>A (p.Arg167Ser)
n.402C>A
19g.55151894C>ACA407439620TNNI3c.573G>T (p.Trp191Cys)
c.606G>T (p.Trp202Cys)
n.572G>T
c.498G>T (p.Trp166Cys)
n.401G>T
 dbSNP
19g.55151894C>GCA407439622TNNI3c.573G>C (p.Trp191Cys)
c.606G>C (p.Trp202Cys)
n.572G>C
c.498G>C (p.Trp166Cys)
n.401G>C
19g.55151894C>TCA407439623TNNI3c.573G>A (p.Trp191Ter)
c.606G>A (p.Trp202Ter)
n.572G>A
c.498G>A (p.Trp166Ter)
n.401G>A
19g.55151895C>ACA407439626TNNI3c.572G>T (p.Trp191Leu)
c.605G>T (p.Trp202Leu)
n.571G>T
c.497G>T (p.Trp166Leu)
n.400G>T
19g.55151895C=CA2343272634TNNI3c.572G= (p.Trp191=)
c.605G= (p.Trp202=)
n.571G=
c.497G= (p.Trp166=)
n.400G=
19g.55151895C>GCA407439627TNNI3c.572G>C (p.Trp191Ser)
c.605G>C (p.Trp202Ser)
n.571G>C
c.497G>C (p.Trp166Ser)
n.400G>C
19g.55151895C>TCA310144922TNNI3c.572G>A (p.Trp191Ter)
c.605G>A (p.Trp202Ter)
n.571G>A
c.497G>A (p.Trp166Ter)
n.400G>A
 dbSNP

Number of alleles fetched