Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
19g.55151896A>CCA407439630TNNI3c.571T>G (p.Trp191Gly)
c.604T>G (p.Trp202Gly)
n.570T>G
c.496T>G (p.Trp166Gly)
n.399T>G
19g.55151896A>GCA407439631TNNI3c.571T>C (p.Trp191Arg)
c.604T>C (p.Trp202Arg)
n.570T>C
c.496T>C (p.Trp166Arg)
n.399T>C
19g.55151896A>TCA407439633TNNI3c.571T>A (p.Trp191Arg)
c.604T>A (p.Trp202Arg)
n.570T>A
c.496T>A (p.Trp166Arg)
n.399T>A
19g.55151897G>ACA508989352TNNI3c.570C>T (p.Asp190=)
c.603C>T (p.Asp201=)
n.569C>T
c.495C>T (p.Asp165=)
n.398C>T
 ClinVar dbSNP
19g.55151897G>CCA407439634TNNI3c.570C>G (p.Asp190Glu)
c.603C>G (p.Asp201Glu)
n.569C>G
c.495C>G (p.Asp165Glu)
n.398C>G
 ClinVar dbSNP
19g.55151897G=CA2343272637TNNI3c.570C= (p.Asp190=)
c.603C= (p.Asp201=)
n.569C=
c.495C= (p.Asp165=)
n.398C=
19g.55151897G>TCA407439636TNNI3c.570C>A (p.Asp190Glu)
c.603C>A (p.Asp201Glu)
n.569C>A
c.495C>A (p.Asp165Glu)
n.398C>A
19g.55151897_55151904delinsGTCTCCCACA2343272640TNNI3c.563_570delinsTGGGAGAC (p.Val188=)
c.596_603delinsTGGGAGAC (p.Val199=)
n.562_569delinsTGGGAGAC
c.488_495delinsTGGGAGAC (p.Val163=)
n.391_398delinsTGGGAGAC
19g.55151898T>ACA407439639TNNI3c.569A>T (p.Asp190Val)
c.602A>T (p.Asp201Val)
n.568A>T
c.494A>T (p.Asp165Val)
n.397A>T
19g.55151898T>CCA021945TNNI3c.569A>G (p.Asp190Gly)
c.602A>G (p.Asp201Gly)
n.568A>G
c.494A>G (p.Asp165Gly)
n.397A>G
 ClinVar dbSNP
19g.55151898T>GCA407439642TNNI3c.569A>C (p.Asp190Ala)
c.602A>C (p.Asp201Ala)
n.568A>C
c.494A>C (p.Asp165Ala)
n.397A>C
19g.55151898T=CA2343272645TNNI3c.569A= (p.Asp190=)
c.602A= (p.Asp201=)
n.568A=
c.494A= (p.Asp165=)
n.397A=
19g.55151898_55151904delCA2343272643TNNI3c.563_569del (p.Val188AlafsTer9)
c.596_602del (p.Val199AlafsTer9)
n.562_568del
c.488_494del (p.Val163AlafsTer9)
n.391_397del
 ClinVar dbSNP
19g.55151899C>ACA021939TNNI3c.568G>T (p.Asp190Tyr)
c.601G>T (p.Asp201Tyr)
n.567G>T
c.493G>T (p.Asp165Tyr)
n.396G>T
 ClinVar dbSNP
19g.55151899C=CA2343272647TNNI3c.568G= (p.Asp190=)
c.601G= (p.Asp201=)
n.567G=
c.493G= (p.Asp165=)
n.396G=
19g.55151899C>GCA407439646TNNI3c.568G>C (p.Asp190His)
c.601G>C (p.Asp201His)
n.567G>C
c.493G>C (p.Asp165His)
n.396G>C
19g.55151899C>TCA407439648TNNI3c.568G>A (p.Asp190Asn)
c.601G>A (p.Asp201Asn)
n.567G>A
c.493G>A (p.Asp165Asn)
n.396G>A
19g.55151900T>ACA508989353TNNI3c.567A>T (p.Gly189=)
c.600A>T (p.Gly200=)
n.566A>T
c.492A>T (p.Gly164=)
n.395A>T
19g.55151900T>CCA310144932TNNI3c.567A>G (p.Gly189=)
c.600A>G (p.Gly200=)
n.566A>G
c.492A>G (p.Gly164=)
n.395A>G
 ClinVar dbSNP
19g.55151900T>GCA508989354TNNI3c.567A>C (p.Gly189=)
c.600A>C (p.Gly200=)
n.566A>C
c.492A>C (p.Gly164=)
n.395A>C
19g.55151900T=CA2343272650TNNI3c.567A= (p.Gly189=)
c.600A= (p.Gly200=)
n.566A=
c.492A= (p.Gly164=)
n.395A=
19g.55151901C>ACA407439651TNNI3c.566G>T (p.Gly189Val)
c.599G>T (p.Gly200Val)
n.565G>T
c.491G>T (p.Gly164Val)
n.394G>T
19g.55151901C=CA2343272651TNNI3c.566G= (p.Gly189=)
c.599G= (p.Gly200=)
n.565G=
c.491G= (p.Gly164=)
n.394G=
19g.55151901C>GCA407439652TNNI3c.566G>C (p.Gly189Ala)
c.599G>C (p.Gly200Ala)
n.565G>C
c.491G>C (p.Gly164Ala)
n.394G>C
 ClinVar
19g.55151901C>TCA021932TNNI3c.566G>A (p.Gly189Glu)
c.599G>A (p.Gly200Glu)
n.565G>A
c.491G>A (p.Gly164Glu)
n.394G>A
 ClinVar dbSNP gnomAD v4
19g.55151902C>ACA407439653TNNI3c.565G>T (p.Gly189Ter)
c.598G>T (p.Gly200Ter)
n.564G>T
c.490G>T (p.Gly164Ter)
n.393G>T
19g.55151902C>GCA407439654TNNI3c.565G>C (p.Gly189Arg)
c.598G>C (p.Gly200Arg)
n.564G>C
c.490G>C (p.Gly164Arg)
n.393G>C
19g.55151902C>TCA407439656TNNI3c.565G>A (p.Gly189Arg)
c.598G>A (p.Gly200Arg)
n.564G>A
c.490G>A (p.Gly164Arg)
n.393G>A
 gnomAD v4
19g.55151903C>ACA508989355TNNI3c.564G>T (p.Val188=)
c.597G>T (p.Val199=)
n.563G>T
c.489G>T (p.Val163=)
n.392G>T
 COSMIC
19g.55151903C=CA2343272652TNNI3c.564G= (p.Val188=)
c.597G= (p.Val199=)
n.563G=
c.489G= (p.Val163=)
n.392G=
19g.55151903C>GCA508989356TNNI3c.564G>C (p.Val188=)
c.597G>C (p.Val199=)
n.563G>C
c.489G>C (p.Val163=)
n.392G>C
19g.55151903C>TCA051861TNNI3c.564G>A (p.Val188=)
c.597G>A (p.Val199=)
n.563G>A
c.489G>A (p.Val163=)
n.392G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151904A=CA2343272653TNNI3c.563T= (p.Val188=)
c.596T= (p.Val199=)
n.562T=
c.488T= (p.Val163=)
n.391T=
19g.55151904A>CCA407439660TNNI3c.563T>G (p.Val188Gly)
c.596T>G (p.Val199Gly)
n.562T>G
c.488T>G (p.Val163Gly)
n.391T>G
 dbSNP
19g.55151904A>GCA407439657TNNI3c.563T>C (p.Val188Ala)
c.596T>C (p.Val199Ala)
n.562T>C
c.488T>C (p.Val163Ala)
n.391T>C
19g.55151904A>TCA407439658TNNI3c.563T>A (p.Val188Glu)
c.596T>A (p.Val199Glu)
n.562T>A
c.488T>A (p.Val163Glu)
n.391T>A
19g.55151905C>ACA021928TNNI3c.562G>T (p.Val188Leu)
c.595G>T (p.Val199Leu)
n.561G>T
c.487G>T (p.Val163Leu)
n.390G>T
 ClinVar dbSNP gnomAD v4
19g.55151905C=CA2343272654TNNI3c.562G= (p.Val188=)
c.595G= (p.Val199=)
n.561G=
c.487G= (p.Val163=)
n.390G=
19g.55151905C>GCA407439663TNNI3c.562G>C (p.Val188Leu)
c.595G>C (p.Val199Leu)
n.561G>C
c.487G>C (p.Val163Leu)
n.390G>C
 gnomAD v4
19g.55151905C>TCA021922TNNI3c.562G>A (p.Val188Met)
c.595G>A (p.Val199Met)
n.561G>A
c.487G>A (p.Val163Met)
n.390G>A
 ClinVar dbSNP gnomAD v4
19g.55151906C>ACA051855TNNI3c.561G>T (p.Glu187Asp)
c.594G>T (p.Glu198Asp)
n.560G>T
c.486G>T (p.Glu162Asp)
n.389G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151906C=CA2343272655TNNI3c.561G= (p.Glu187=)
c.594G= (p.Glu198=)
n.560G=
c.486G= (p.Glu162=)
n.389G=
19g.55151906C>GCA407439665TNNI3c.561G>C (p.Glu187Asp)
c.594G>C (p.Glu198Asp)
n.560G>C
c.486G>C (p.Glu162Asp)
n.389G>C
 gnomAD v4
19g.55151906C>TCA508989357TNNI3c.561G>A (p.Glu187=)
c.594G>A (p.Glu198=)
n.560G>A
c.486G>A (p.Glu162=)
n.389G>A
19g.55151907T>ACA407439666TNNI3c.560A>T (p.Glu187Val)
c.593A>T (p.Glu198Val)
n.559A>T
c.485A>T (p.Glu162Val)
n.388A>T
19g.55151907T>CCA407439668TNNI3c.560A>G (p.Glu187Gly)
c.593A>G (p.Glu198Gly)
n.559A>G
c.485A>G (p.Glu162Gly)
n.388A>G
 COSMIC
19g.55151907T>GCA407439669TNNI3c.560A>C (p.Glu187Ala)
c.593A>C (p.Glu198Ala)
n.559A>C
c.485A>C (p.Glu162Ala)
n.388A>C
19g.55151907_55151908delinsCTCA2343272657TNNI3c.559_560delinsAG (p.Glu187Arg)
c.592_593delinsAG (p.Glu198Arg)
n.558_559delinsAG
c.484_485delinsAG (p.Glu162Arg)
n.387_388delinsAG
 ClinVar dbSNP
19g.55151907_55151908delinsTCCA2343272656TNNI3c.559_560delinsGA (p.Glu187=)
c.592_593delinsGA (p.Glu198=)
n.558_559delinsGA
c.484_485delinsGA (p.Glu162=)
n.387_388delinsGA
19g.55151908C>ACA407439670TNNI3c.559G>T (p.Glu187Ter)
c.592G>T (p.Glu198Ter)
n.558G>T
c.484G>T (p.Glu162Ter)
n.387G>T
19g.55151908C=CA2343272658TNNI3c.559G= (p.Glu187=)
c.592G= (p.Glu198=)
n.558G=
c.484G= (p.Glu162=)
n.387G=
19g.55151908C>GCA407439671TNNI3c.559G>C (p.Glu187Gln)
c.592G>C (p.Glu198Gln)
n.558G>C
c.484G>C (p.Glu162Gln)
n.387G>C
19g.55151908C>TCA021916TNNI3c.559G>A (p.Glu187Lys)
c.592G>A (p.Glu198Lys)
n.558G>A
c.484G>A (p.Glu162Lys)
n.387G>A
 ClinVar dbSNP
19g.55151909C>ACA508989358TNNI3c.558G>T (p.Arg186=)
c.591G>T (p.Arg197=)
n.557G>T
c.483G>T (p.Arg161=)
n.386G>T
19g.55151909C>GCA508989359TNNI3c.558G>C (p.Arg186=)
c.591G>C (p.Arg197=)
n.557G>C
c.483G>C (p.Arg161=)
n.386G>C
19g.55151909C>TCA508989360TNNI3c.558G>A (p.Arg186=)
c.591G>A (p.Arg197=)
n.557G>A
c.483G>A (p.Arg161=)
n.386G>A
 COSMIC
19g.55151910C>ACA407439673TNNI3c.557G>T (p.Arg186Leu)
c.590G>T (p.Arg197Leu)
n.556G>T
c.482G>T (p.Arg161Leu)
n.385G>T
19g.55151910C=CA2343272659TNNI3c.557G= (p.Arg186=)
c.590G= (p.Arg197=)
n.556G=
c.482G= (p.Arg161=)
n.385G=
19g.55151910C>GCA407439675TNNI3c.557G>C (p.Arg186Pro)
c.590G>C (p.Arg197Pro)
n.556G>C
c.482G>C (p.Arg161Pro)
n.385G>C
19g.55151910C>TCA021907TNNI3c.557G>A (p.Arg186Gln)
c.590G>A (p.Arg197Gln)
n.556G>A
c.482G>A (p.Arg161Gln)
n.385G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.55151911G>ACA051839TNNI3c.556C>T (p.Arg186Trp)
c.589C>T (p.Arg197Trp)
n.555C>T
c.481C>T (p.Arg161Trp)
n.384C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.55151911G>CCA407439677TNNI3c.556C>G (p.Arg186Gly)
c.589C>G (p.Arg197Gly)
n.555C>G
c.481C>G (p.Arg161Gly)
n.384C>G
19g.55151911G=CA2343272660TNNI3c.556C= (p.Arg186=)
c.589C= (p.Arg197=)
n.555C=
c.481C= (p.Arg161=)
n.384C=
19g.55151911G>TCA508989361TNNI3c.556C>A (p.Arg186=)
c.589C>A (p.Arg197=)
n.555C>A
c.481C>A (p.Arg161=)
n.384C>A
 gnomAD v4
19g.55151912G>ACA508989362TNNI3c.555C>T (p.Asn185=)
c.588C>T (p.Asn196=)
n.554C>T
c.480C>T (p.Asn160=)
n.383C>T
19g.55151912G>CCA021902TNNI3c.555C>G (p.Asn185Lys)
c.588C>G (p.Asn196Lys)
n.554C>G
c.480C>G (p.Asn160Lys)
n.383C>G
 ClinVar dbSNP
19g.55151912G=CA2343272661TNNI3c.555C= (p.Asn185=)
c.588C= (p.Asn196=)
n.554C=
c.480C= (p.Asn160=)
n.383C=
19g.55151912G>TCA407439680TNNI3c.555C>A (p.Asn185Lys)
c.588C>A (p.Asn196Lys)
n.554C>A
c.480C>A (p.Asn160Lys)
n.383C>A
19g.55151913T>ACA407439681TNNI3c.554A>T (p.Asn185Ile)
c.587A>T (p.Asn196Ile)
n.553A>T
c.479A>T (p.Asn160Ile)
n.382A>T
19g.55151913T>CCA021896TNNI3c.554A>G (p.Asn185Ser)
c.587A>G (p.Asn196Ser)
n.553A>G
c.479A>G (p.Asn160Ser)
n.382A>G
 ClinVar dbSNP
19g.55151913T>GCA407439684TNNI3c.554A>C (p.Asn185Thr)
c.587A>C (p.Asn196Thr)
n.553A>C
c.479A>C (p.Asn160Thr)
n.382A>C
19g.55151913T=CA2343272662TNNI3c.554A= (p.Asn185=)
c.587A= (p.Asn196=)
n.553A=
c.479A= (p.Asn160=)
n.382A=
19g.55151916delCA2695229155TNNI3c.554del (p.Asn185ThrfsTer14)
c.587del (p.Asn196ThrfsTer14)
n.553del
c.479del (p.Asn160ThrfsTer14)
n.382del
19g.55151914T>ACA021890TNNI3c.553A>T (p.Asn185Tyr)
c.586A>T (p.Asn196Tyr)
n.552A>T
c.478A>T (p.Asn160Tyr)
n.381A>T
 ClinVar dbSNP
19g.55151914T>CCA407439686TNNI3c.553A>G (p.Asn185Asp)
c.586A>G (p.Asn196Asp)
n.552A>G
c.478A>G (p.Asn160Asp)
n.381A>G
19g.55151914T>GCA407439687TNNI3c.553A>C (p.Asn185His)
c.586A>C (p.Asn196His)
n.552A>C
c.478A>C (p.Asn160His)
n.381A>C
19g.55151914T=CA2343272663TNNI3c.553A= (p.Asn185=)
c.586A= (p.Asn196=)
n.552A=
c.478A= (p.Asn160=)
n.381A=
19g.55151915T>ACA407439689TNNI3c.552A>T (p.Glu184Asp)
c.585A>T (p.Glu195Asp)
n.551A>T
c.477A>T (p.Glu159Asp)
n.380A>T
19g.55151915T>CCA508989363TNNI3c.552A>G (p.Glu184=)
c.585A>G (p.Glu195=)
n.551A>G
c.477A>G (p.Glu159=)
n.380A>G
19g.55151915T>GCA407439690TNNI3c.552A>C (p.Glu184Asp)
c.585A>C (p.Glu195Asp)
n.551A>C
c.477A>C (p.Glu159Asp)
n.380A>C
19g.55151916T>ACA407439692TNNI3c.551A>T (p.Glu184Val)
c.584A>T (p.Glu195Val)
n.550A>T
c.476A>T (p.Glu159Val)
n.379A>T
19g.55151916T>CCA407439694TNNI3c.551A>G (p.Glu184Gly)
c.584A>G (p.Glu195Gly)
n.550A>G
c.476A>G (p.Glu159Gly)
n.379A>G
19g.55151916T>GCA407439695TNNI3c.551A>C (p.Glu184Ala)
c.584A>C (p.Glu195Ala)
n.550A>C
c.476A>C (p.Glu159Ala)
n.379A>C
19g.55151917C>ACA407439697TNNI3c.550G>T (p.Glu184Ter)
c.583G>T (p.Glu195Ter)
n.549G>T
c.475G>T (p.Glu159Ter)
n.378G>T
19g.55151917C=CA2343272664TNNI3c.550G= (p.Glu184=)
c.583G= (p.Glu195=)
n.549G=
c.475G= (p.Glu159=)
n.378G=
19g.55151917C>GCA407439699TNNI3c.550G>C (p.Glu184Gln)
c.583G>C (p.Glu195Gln)
n.549G>C
c.475G>C (p.Glu159Gln)
n.378G>C
 ClinVar dbSNP
19g.55151917C>TCA021885TNNI3c.550G>A (p.Glu184Lys)
c.583G>A (p.Glu195Lys)
n.549G>A
c.475G>A (p.Glu159Lys)
n.378G>A
 ClinVar dbSNP
19g.55151918C>ACA407439701TNNI3c.550-1G>T (n.550-1G>T)
c.583-1G>T (n.583-1G>T)
n.549-1G>T
c.475-1G>T (n.475-1G>T)
n.378-1G>T
19g.55151918C=CA2343272665TNNI3c.550-1G= (n.550-1G=)
c.583-1G= (n.583-1G=)
n.549-1G=
c.475-1G= (n.475-1G=)
n.378-1G=
19g.55151918C>GCA407439704TNNI3c.550-1G>C (n.550-1G>C)
c.583-1G>C (n.583-1G>C)
n.549-1G>C
c.475-1G>C (n.475-1G>C)
n.378-1G>C
19g.55151918C>TCA407439702TNNI3c.550-1G>A (n.550-1G>A)
c.583-1G>A (n.583-1G>A)
n.549-1G>A
c.475-1G>A (n.475-1G>A)
n.378-1G>A
 ClinVar dbSNP COSMIC
19g.55151919T>ACA407439706TNNI3c.550-2A>T (n.550-2A>T)
c.583-2A>T (n.583-2A>T)
n.549-2A>T
c.475-2A>T (n.475-2A>T)
n.378-2A>T
 ClinVar dbSNP
19g.55151919T>CCA407439707TNNI3c.550-2A>G (n.550-2A>G)
c.583-2A>G (n.583-2A>G)
n.549-2A>G
c.475-2A>G (n.475-2A>G)
n.378-2A>G
19g.55151919T>GCA407439709TNNI3c.550-2A>C (n.550-2A>C)
c.583-2A>C (n.583-2A>C)
n.549-2A>C
c.475-2A>C (n.475-2A>C)
n.378-2A>C
 gnomAD v4
19g.55151920G>CCA310144959TNNI3c.550-3C>G (n.550-3C>G)
c.583-3C>G (n.583-3C>G)
n.549-3C>G
c.475-3C>G (n.475-3C>G)
n.378-3C>G
 dbSNP
19g.55151920G=CA2343272666TNNI3c.550-3C= (n.550-3C=)
c.583-3C= (n.583-3C=)
n.549-3C=
c.475-3C= (n.475-3C=)
n.378-3C=
19g.55151920G>TCA310144962TNNI3c.550-3C>A (n.550-3C>A)
c.583-3C>A (n.583-3C>A)
n.549-3C>A
c.475-3C>A (n.475-3C>A)
n.378-3C>A
 dbSNP
19g.55151923G>ACA2587243161TNNI3c.550-6C>T (n.550-6C>T)
c.583-6C>T (n.583-6C>T)
n.549-6C>T
c.475-6C>T (n.475-6C>T)
n.378-6C>T
 ClinVar gnomAD v4
19g.55151924G>ACA2587243162TNNI3c.550-7C>T (n.550-7C>T)
c.583-7C>T (n.583-7C>T)
n.549-7C>T
c.475-7C>T (n.475-7C>T)
n.378-7C>T
 gnomAD v4
19g.55151925A=CA2343272667TNNI3c.550-8T= (n.550-8T=)
c.583-8T= (n.583-8T=)
n.549-8T=
c.475-8T= (n.475-8T=)
n.378-8T=
19g.55151925A>GCA2587243163TNNI3c.550-8T>C (n.550-8T>C)
c.583-8T>C (n.583-8T>C)
n.549-8T>C
c.475-8T>C (n.475-8T>C)
n.378-8T>C
 gnomAD v4
19g.55151925A>TCA051830TNNI3c.550-8T>A (n.550-8T>A)
c.583-8T>A (n.583-8T>A)
n.549-8T>A
c.475-8T>A (n.475-8T>A)
n.378-8T>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151925_55151930delinsATGGCGCA2343272668TNNI3c.550-13_550-8delinsCGCCAT (n.550-13_550-8delinsCGCCAT)
c.583-13_583-8delinsCGCCAT (n.583-13_583-8delinsCGCCAT)
n.549-13_549-8delinsCGCCAT
c.475-13_475-8delinsCGCCAT (n.475-13_475-8delinsCGCCAT)
n.378-13_378-8delinsCGCCAT
19g.55151926_55151930delCA2343272669TNNI3c.550-13_550-9del (n.550-13_550-9del)
c.583-13_583-9del (n.583-13_583-9del)
n.549-13_549-9del
c.475-13_475-9del (n.475-13_475-9del)
n.378-13_378-9del
 dbSNP
19g.55151927G>ACA021879TNNI3c.550-10C>T (n.550-10C>T)
c.583-10C>T (n.583-10C>T)
n.549-10C>T
c.475-10C>T (n.475-10C>T)
n.378-10C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151927G=CA2343272670TNNI3c.550-10C= (n.550-10C=)
c.583-10C= (n.583-10C=)
n.549-10C=
c.475-10C= (n.475-10C=)
n.378-10C=
19g.55151928G>ACA10649138TNNI3c.550-11C>T (n.550-11C>T)
c.583-11C>T (n.583-11C>T)
n.549-11C>T
c.475-11C>T (n.475-11C>T)
n.378-11C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.55151928G=CA2343272671TNNI3c.550-11C= (n.550-11C=)
c.583-11C= (n.583-11C=)
n.549-11C=
c.475-11C= (n.475-11C=)
n.378-11C=
19g.55151929C>ACA633870498TNNI3c.550-12G>T (n.550-12G>T)
c.583-12G>T (n.583-12G>T)
n.549-12G>T
c.475-12G>T (n.475-12G>T)
n.378-12G>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55151929C=CA2343272672TNNI3c.550-12G= (n.550-12G=)
c.583-12G= (n.583-12G=)
n.549-12G=
c.475-12G= (n.475-12G=)
n.378-12G=
19g.55151929C>TCA051748TNNI3c.550-12G>A (n.550-12G>A)
c.583-12G>A (n.583-12G>A)
n.549-12G>A
c.475-12G>A (n.475-12G>A)
n.378-12G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151930G>ACA051759TNNI3c.550-13C>T (n.550-13C>T)
c.583-13C>T (n.583-13C>T)
n.549-13C>T
c.475-13C>T (n.475-13C>T)
n.378-13C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
19g.55151930G>CCA051751TNNI3c.550-13C>G (n.550-13C>G)
c.583-13C>G (n.583-13C>G)
n.549-13C>G
c.475-13C>G (n.475-13C>G)
n.378-13C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55151930G=CA2343272673TNNI3c.550-13C= (n.550-13C=)
c.583-13C= (n.583-13C=)
n.549-13C=
c.475-13C= (n.475-13C=)
n.378-13C=
19g.55151931A=CA2343272674TNNI3c.550-14T= (n.550-14T=)
c.583-14T= (n.583-14T=)
n.549-14T=
c.475-14T= (n.475-14T=)
n.378-14T=
19g.55151931A>GCA051770TNNI3c.550-14T>C (n.550-14T>C)
c.583-14T>C (n.583-14T>C)
n.549-14T>C
c.475-14T>C (n.475-14T>C)
n.378-14T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151931A>TCA2576892607TNNI3c.550-14T>A (n.550-14T>A)
c.583-14T>A (n.583-14T>A)
n.549-14T>A
c.475-14T>A (n.475-14T>A)
n.378-14T>A
19g.55151932T>GCA2343272676TNNI3c.550-15A>C (n.550-15A>C)
c.583-15A>C (n.583-15A>C)
n.549-15A>C
c.475-15A>C (n.475-15A>C)
n.378-15A>C
 dbSNP
19g.55151932T=CA2343272675TNNI3c.550-15A= (n.550-15A=)
c.583-15A= (n.583-15A=)
n.549-15A=
c.475-15A= (n.475-15A=)
n.378-15A=
19g.55151933G>ACA2343272678TNNI3c.550-16C>T (n.550-16C>T)
c.583-16C>T (n.583-16C>T)
n.549-16C>T
c.475-16C>T (n.475-16C>T)
n.378-16C>T
 dbSNP
19g.55151933G=CA2343272677TNNI3c.550-16C= (n.550-16C=)
c.583-16C= (n.583-16C=)
n.549-16C=
c.475-16C= (n.475-16C=)
n.378-16C=
19g.55151935G>ACA2587243175TNNI3c.550-18C>T (n.550-18C>T)
c.583-18C>T (n.583-18C>T)
n.549-18C>T
c.475-18C>T (n.475-18C>T)
n.378-18C>T
 gnomAD v4
19g.55151935G>TCA2587243176TNNI3c.550-18C>A (n.550-18C>A)
c.583-18C>A (n.583-18C>A)
n.549-18C>A
c.475-18C>A (n.475-18C>A)
n.378-18C>A
 gnomAD v4
19g.55151936T>CCA2587243177TNNI3c.550-19A>G (n.550-19A>G)
c.583-19A>G (n.583-19A>G)
n.549-19A>G
c.475-19A>G (n.475-19A>G)
n.378-19A>G
 gnomAD v4
19g.55151937C=CA2343272679TNNI3c.550-20G= (n.550-20G=)
c.583-20G= (n.583-20G=)
n.549-20G=
c.475-20G= (n.475-20G=)
n.378-20G=
19g.55151938A>GCA2587243179TNNI3c.550-21T>C (n.550-21T>C)
c.583-21T>C (n.583-21T>C)
n.549-21T>C
c.475-21T>C (n.475-21T>C)
n.378-21T>C
 gnomAD v4
19g.55151938dupCA997245871TNNI3c.550-21dup (n.550-21dup)
c.583-21dup (n.583-21dup)
n.549-21dup
c.475-21dup (n.475-21dup)
n.378-21dup
 dbSNP gnomAD v3 gnomAD v4
19g.55151940_55151941delCA2576892608TNNI3c.550-22_550-21del (n.550-22_550-21del)
c.583-22_583-21del (n.583-22_583-21del)
n.549-22_549-21del
c.475-22_475-21del (n.475-22_475-21del)
n.378-22_378-21del
19g.55151939G>CCA2587243180TNNI3c.550-22C>G (n.550-22C>G)
c.583-22C>G (n.583-22C>G)
n.549-22C>G
c.475-22C>G (n.475-22C>G)
n.378-22C>G
 gnomAD v4
19g.55151940A=CA2343272680TNNI3c.550-23T= (n.550-23T=)
c.583-23T= (n.583-23T=)
n.549-23T=
c.475-23T= (n.475-23T=)
n.378-23T=
19g.55151940A>CCA051773TNNI3c.550-23T>G (n.550-23T>G)
c.583-23T>G (n.583-23T>G)
n.549-23T>G
c.475-23T>G (n.475-23T>G)
n.378-23T>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151942G>ACA2587243184TNNI3c.550-25C>T (n.550-25C>T)
c.583-25C>T (n.583-25C>T)
n.549-25C>T
c.475-25C>T (n.475-25C>T)
n.378-25C>T
 gnomAD v4
19g.55151942G>TCA2576892609TNNI3c.550-25C>A (n.550-25C>A)
c.583-25C>A (n.583-25C>A)
n.549-25C>A
c.475-25C>A (n.475-25C>A)
n.378-25C>A
 gnomAD v4
19g.55151943T>CCA2587243187TNNI3c.550-26A>G (n.550-26A>G)
c.583-26A>G (n.583-26A>G)
n.549-26A>G
c.475-26A>G (n.475-26A>G)
n.378-26A>G
 gnomAD v4
19g.55151943T=CA2343272681TNNI3c.550-26A= (n.550-26A=)
c.583-26A= (n.583-26A=)
n.549-26A=
c.475-26A= (n.475-26A=)
n.378-26A=
19g.55151944delCA2587243186TNNI3c.550-26del (n.550-26del)
c.583-26del (n.583-26del)
n.549-26del
c.475-26del (n.475-26del)
n.378-26del
 gnomAD v4
19g.55151944_55151947dupCA633870510TNNI3c.550-30_550-27dup (n.550-30_550-27dup)
c.583-30_583-27dup (n.583-30_583-27dup)
n.549-30_549-27dup
c.475-30_475-27dup (n.475-30_475-27dup)
n.378-30_378-27dup
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55151946G>TCA2814880944TNNI3c.550-29C>A (n.550-29C>A)
c.583-29C>A (n.583-29C>A)
n.549-29C>A
c.475-29C>A (n.475-29C>A)
n.378-29C>A
19g.55151947G>ACA051781TNNI3c.550-30C>T (n.550-30C>T)
c.583-30C>T (n.583-30C>T)
n.549-30C>T
c.475-30C>T (n.475-30C>T)
n.378-30C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151947G=CA2343272682TNNI3c.550-30C= (n.550-30C=)
c.583-30C= (n.583-30C=)
n.549-30C=
c.475-30C= (n.475-30C=)
n.378-30C=
19g.55151947G>TCA883720544TNNI3c.550-30C>A (n.550-30C>A)
c.583-30C>A (n.583-30C>A)
n.549-30C>A
c.475-30C>A (n.475-30C>A)
n.378-30C>A
 dbSNP gnomAD v3 gnomAD v4
19g.55151948G=CA2343272683TNNI3c.550-31C= (n.550-31C=)
c.583-31C= (n.583-31C=)
n.549-31C=
c.475-31C= (n.475-31C=)
n.378-31C=
19g.55151948G>TCA633870511TNNI3c.550-31C>A (n.550-31C>A)
c.583-31C>A (n.583-31C>A)
n.549-31C>A
c.475-31C>A (n.475-31C>A)
n.378-31C>A
 dbSNP gnomAD v2 gnomAD v4
19g.55151949T>CCA051789TNNI3c.550-32A>G (n.550-32A>G)
c.583-32A>G (n.583-32A>G)
n.549-32A>G
c.475-32A>G (n.475-32A>G)
n.378-32A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151949T>GCA2343272685TNNI3c.550-32A>C (n.550-32A>C)
c.583-32A>C (n.583-32A>C)
n.549-32A>C
c.475-32A>C (n.475-32A>C)
n.378-32A>C
 dbSNP
19g.55151949T=CA2343272684TNNI3c.550-32A= (n.550-32A=)
c.583-32A= (n.583-32A=)
n.549-32A=
c.475-32A= (n.475-32A=)
n.378-32A=
19g.55151950C>ACA2587243192TNNI3c.550-33G>T (n.550-33G>T)
c.583-33G>T (n.583-33G>T)
n.549-33G>T
c.475-33G>T (n.475-33G>T)
n.378-33G>T
 gnomAD v4
19g.55151951T>ACA883720549TNNI3c.550-34A>T (n.550-34A>T)
c.583-34A>T (n.583-34A>T)
n.549-34A>T
c.475-34A>T (n.475-34A>T)
n.378-34A>T
 dbSNP gnomAD v3 gnomAD v4
19g.55151951T=CA2343272686TNNI3c.550-34A= (n.550-34A=)
c.583-34A= (n.583-34A=)
n.549-34A=
c.475-34A= (n.475-34A=)
n.378-34A=
19g.55151952C=CA2343272687TNNI3c.550-35G= (n.550-35G=)
c.583-35G= (n.583-35G=)
n.549-35G=
c.475-35G= (n.475-35G=)
n.378-35G=
19g.55151952C>TCA997245889TNNI3c.550-35G>A (n.550-35G>A)
c.583-35G>A (n.583-35G>A)
n.549-35G>A
c.475-35G>A (n.475-35G>A)
n.378-35G>A
 dbSNP gnomAD v3 gnomAD v4
19g.55151953T>CCA2576892610TNNI3c.550-36A>G (n.550-36A>G)
c.583-36A>G (n.583-36A>G)
n.549-36A>G
c.475-36A>G (n.475-36A>G)
n.378-36A>G
19g.55151953T>GCA051797TNNI3c.550-36A>C (n.550-36A>C)
c.583-36A>C (n.583-36A>C)
n.549-36A>C
c.475-36A>C (n.475-36A>C)
n.378-36A>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55151953T=CA2343272688TNNI3c.550-36A= (n.550-36A=)
c.583-36A= (n.583-36A=)
n.549-36A=
c.475-36A= (n.475-36A=)
n.378-36A=
19g.55151955C>ACA2343272690TNNI3c.550-38G>T (n.550-38G>T)
c.583-38G>T (n.583-38G>T)
n.549-38G>T
c.475-38G>T (n.475-38G>T)
n.378-38G>T
 dbSNP
19g.55151955C=CA2343272689TNNI3c.550-38G= (n.550-38G=)
c.583-38G= (n.583-38G=)
n.549-38G=
c.475-38G= (n.475-38G=)
n.378-38G=
19g.55151955C>GCA2814880948TNNI3c.550-38G>C (n.550-38G>C)
c.583-38G>C (n.583-38G>C)
n.549-38G>C
c.475-38G>C (n.475-38G>C)
n.378-38G>C
19g.55151955C>TCA2576892611TNNI3c.550-38G>A (n.550-38G>A)
c.583-38G>A (n.583-38G>A)
n.549-38G>A
c.475-38G>A (n.475-38G>A)
n.378-38G>A
19g.55151956T>CCA2736113300TNNI3c.550-39A>G (n.550-39A>G)
c.583-39A>G (n.583-39A>G)
n.549-39A>G
c.475-39A>G (n.475-39A>G)
n.378-39A>G
 dbSNP
19g.55151958G>ACA2576892612TNNI3c.550-41C>T (n.550-41C>T)
c.583-41C>T (n.583-41C>T)
n.549-41C>T
c.475-41C>T (n.475-41C>T)
n.378-41C>T
19g.55151958G>CCA633870513TNNI3c.550-41C>G (n.550-41C>G)
c.583-41C>G (n.583-41C>G)
n.549-41C>G
c.475-41C>G (n.475-41C>G)
n.378-41C>G
 dbSNP gnomAD v2 gnomAD v4
19g.55151958G=CA2343272691TNNI3c.550-41C= (n.550-41C=)
c.583-41C= (n.583-41C=)
n.549-41C=
c.475-41C= (n.475-41C=)
n.378-41C=
19g.55151958G>TCA2576892613TNNI3c.550-41C>A (n.550-41C>A)
c.583-41C>A (n.583-41C>A)
n.549-41C>A
c.475-41C>A (n.475-41C>A)
n.378-41C>A

Number of alleles fetched