Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.55154117C>ACA407440432TNNI3c.462G>T (p.Met154Ile)
c.495G>T (p.Met165Ile)
n.461G>T
n.470G>T
c.387G>T (p.Met129Ile)
n.290G>T
19g.55154117C=CA2343273764TNNI3c.462G= (p.Met154=)
c.495G= (p.Met165=)
n.461G=
n.470G=
c.387G= (p.Met129=)
n.290G=
19g.55154117C>GCA407440433TNNI3c.462G>C (p.Met154Ile)
c.495G>C (p.Met165Ile)
n.461G>C
n.470G>C
c.387G>C (p.Met129Ile)
n.290G>C
19g.55154117C>TCA021703TNNI3c.462G>A (p.Met154Ile)
c.495G>A (p.Met165Ile)
n.461G>A
n.470G>A
c.387G>A (p.Met129Ile)
n.290G>A
 ClinVar dbSNP
19g.55154118A>CCA407440439TNNI3c.461T>G (p.Met154Arg)
c.494T>G (p.Met165Arg)
n.460T>G
n.469T>G
c.386T>G (p.Met129Arg)
n.289T>G
19g.55154118A>GCA407440436TNNI3c.461T>C (p.Met154Thr)
c.494T>C (p.Met165Thr)
n.460T>C
n.469T>C
c.386T>C (p.Met129Thr)
n.289T>C
19g.55154118A>TCA407440437TNNI3c.461T>A (p.Met154Lys)
c.494T>A (p.Met165Lys)
n.460T>A
n.469T>A
c.386T>A (p.Met129Lys)
n.289T>A
19g.55154119T>ACA407440440TNNI3c.460A>T (p.Met154Leu)
c.493A>T (p.Met165Leu)
n.459A>T
n.468A>T
c.385A>T (p.Met129Leu)
n.288A>T
19g.55154119T>CCA407440442TNNI3c.460A>G (p.Met154Val)
c.493A>G (p.Met165Val)
n.459A>G
n.468A>G
c.385A>G (p.Met129Val)
n.288A>G
19g.55154119T>GCA407440444TNNI3c.460A>C (p.Met154Leu)
c.493A>C (p.Met165Leu)
n.459A>C
n.468A>C
c.385A>C (p.Met129Leu)
n.288A>C
19g.55154119_55154120insCGGCACACCGGCGGTACCGGCGGGCTCACCATCATCGGAGGAACGCTGAATATCGCGGTCAGCACCAATAATGAACGCCGAACACACGTGGCGCA2814881312TNNI3c.459_460insCGCCACGTGTGTTCGGCGTTCATTATTGGTGCTGACCGCGATATTCAGCGTTCCTCCGATGATGGTGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala153_Met154insArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
c.492_493insCGCCACGTGTGTTCGGCGTTCATTATTGGTGCTGACCGCGATATTCAGCGTTCCTCCGATGATGGTGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala164_Met165insArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
n.458_459insCGCCACGTGTGTTCGGCGTTCATTATTGGTGCTGACCGCGATATTCAGCGTTCCTCCGATGATGGTGAGCCCGCCGGTACCGCCGGTGTGCCG
n.467_468insCGCCACGTGTGTTCGGCGTTCATTATTGGTGCTGACCGCGATATTCAGCGTTCCTCCGATGATGGTGAGCCCGCCGGTACCGCCGGTGTGCCG
c.384_385insCGCCACGTGTGTTCGGCGTTCATTATTGGTGCTGACCGCGATATTCAGCGTTCCTCCGATGATGGTGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala128_Met129insArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
n.287_288insCGCCACGTGTGTTCGGCGTTCATTATTGGTGCTGACCGCGATATTCAGCGTTCCTCCGATGATGGTGAGCCCGCCGGTACCGCCGGTGTGCCG
19g.55154119_55154120insCGGCACACCGGCGGTACCGGCGGGCTCACCGTCATCGGAGGAACGCTGAATATCGCGGTCGGCACCAATAATGAATGCCGAACACACGTGGCGGGCGTCGTGGTAGGTCTTGCGCACCGACTCAATGTACA2540410352TNNI3c.459_460insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGTTCGGCATTCATTATTGGTGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala153_Met154insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
c.492_493insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGTTCGGCATTCATTATTGGTGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala164_Met165insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
n.458_459insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGTTCGGCATTCATTATTGGTGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTGCCG
n.467_468insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGTTCGGCATTCATTATTGGTGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTGCCG
c.384_385insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGTTCGGCATTCATTATTGGTGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala128_Met129insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
n.287_288insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGTTCGGCATTCATTATTGGTGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTGCCG
19g.55154119_55154120insCGGTACACCGGCGGTACCGGCGGGCTCACCGTCATCGGAGGAACGCTGAATATCGCGGTCGGCGCCAATAATGAACGCCGAGCACACGTGGCGGGCGTCGTGGTAGGTCTTGCGCACCGACTCAATGTACA2507690890TNNI3c.459_460insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCATTATTGGCGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTACCG (p.Ala153_Met154insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
c.492_493insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCATTATTGGCGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTACCG (p.Ala164_Met165insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
n.458_459insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCATTATTGGCGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTACCG
n.467_468insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCATTATTGGCGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTACCG
c.384_385insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCATTATTGGCGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTACCG (p.Ala128_Met129insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheIleIleGlyAlaAspArgAspIleGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
n.287_288insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCATTATTGGCGCCGACCGCGATATTCAGCGTTCCTCCGATGACGGTGAGCCCGCCGGTACCGCCGGTGTACCG
19g.55154119_55154120insCGGCACACCGGCGGTACCGGCGGGCTCGCCGTCATCCGAGGAACGCTGCACGTCGCGGTCGGCACCAATCACGAACGCCGAGCACACGTGGCGGGCGTCGTGGTAGGTCTTGCGCACCGACTCAATGTACA2539885688TNNI3c.459_460insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGGATGACGGCGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala153_Met154insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheValIleGlyAlaAspArgAspValGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
c.492_493insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGGATGACGGCGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala164_Met165insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheValIleGlyAlaAspArgAspValGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
n.458_459insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGGATGACGGCGAGCCCGCCGGTACCGCCGGTGTGCCG
n.467_468insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGGATGACGGCGAGCCCGCCGGTACCGCCGGTGTGCCG
c.384_385insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGGATGACGGCGAGCCCGCCGGTACCGCCGGTGTGCCG (p.Ala128_Met129insTyrIleGluSerValArgLysThrTyrHisAspAlaArgHisValCysSerAlaPheValIleGlyAlaAspArgAspValGlnArgSerSerAspAspGlyGluProAlaGlyThrAlaGlyValPro)
n.287_288insTACATTGAGTCGGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGGATGACGGCGAGCCCGCCGGTACCGCCGGTGTGCCG
19g.55154120G>ACA508989422TNNI3c.459C>T (p.Ala153=)
c.492C>T (p.Ala164=)
n.458C>T
n.467C>T
c.384C>T (p.Ala128=)
n.287C>T
19g.55154120G>CCA508989423TNNI3c.459C>G (p.Ala153=)
c.492C>G (p.Ala164=)
n.458C>G
n.467C>G
c.384C>G (p.Ala128=)
n.287C>G
19g.55154120G>TCA508989424TNNI3c.459C>A (p.Ala153=)
c.492C>A (p.Ala164=)
n.458C>A
n.467C>A
c.384C>A (p.Ala128=)
n.287C>A
 gnomAD v4
19g.55154121G>ACA407440446TNNI3c.458C>T (p.Ala153Val)
c.491C>T (p.Ala164Val)
n.457C>T
n.466C>T
c.383C>T (p.Ala128Val)
n.286C>T
 ClinVar dbSNP gnomAD v4
19g.55154121G>CCA407440447TNNI3c.458C>G (p.Ala153Gly)
c.491C>G (p.Ala164Gly)
n.457C>G
n.466C>G
c.383C>G (p.Ala128Gly)
n.286C>G
19g.55154121G=CA2343273765TNNI3c.458C= (p.Ala153=)
c.491C= (p.Ala164=)
n.457C=
n.466C=
c.383C= (p.Ala128=)
n.286C=
19g.55154121G>TCA021698TNNI3c.458C>A (p.Ala153Asp)
c.491C>A (p.Ala164Asp)
n.457C>A
n.466C>A
c.383C>A (p.Ala128Asp)
n.286C>A
 ClinVar dbSNP
19g.55154121_55154122insGCACACCCGCGGTACCGGCGGGCTCGCCGTCA2814881314TNNI3c.457_458insACGGCGAGCCCGCCGGTACCGCGGGTGTGC (p.Ala153delinsAspGlyGluProAlaGlyThrAlaGlyValPro)
c.490_491insACGGCGAGCCCGCCGGTACCGCGGGTGTGC (p.Ala164delinsAspGlyGluProAlaGlyThrAlaGlyValPro)
n.456_457insACGGCGAGCCCGCCGGTACCGCGGGTGTGC
n.465_466insACGGCGAGCCCGCCGGTACCGCGGGTGTGC
c.382_383insACGGCGAGCCCGCCGGTACCGCGGGTGTGC (p.Ala128delinsAspGlyGluProAlaGlyThrAlaGlyValPro)
n.285_286insACGGCGAGCCCGCCGGTACCGCGGGTGTGC
19g.55154122C>ACA407440449TNNI3c.457G>T (p.Ala153Ser)
c.490G>T (p.Ala164Ser)
n.456G>T
n.465G>T
c.382G>T (p.Ala128Ser)
n.285G>T
19g.55154122C>GCA407440451TNNI3c.457G>C (p.Ala153Pro)
c.490G>C (p.Ala164Pro)
n.456G>C
n.465G>C
c.382G>C (p.Ala128Pro)
n.285G>C
19g.55154122C>TCA407440452TNNI3c.457G>A (p.Ala153Thr)
c.490G>A (p.Ala164Thr)
n.456G>A
n.465G>A
c.382G>A (p.Ala128Thr)
n.285G>A
19g.55154123A=CA2343273766TNNI3c.456T= (p.Asp152=)
c.489T= (p.Asp163=)
n.455T=
n.464T=
c.381T= (p.Asp127=)
n.284T=
19g.55154123A>CCA407440454TNNI3c.456T>G (p.Asp152Glu)
c.489T>G (p.Asp163Glu)
n.455T>G
n.464T>G
c.381T>G (p.Asp127Glu)
n.284T>G
19g.55154123A>GCA508989425TNNI3c.456T>C (p.Asp152=)
c.489T>C (p.Asp163=)
n.455T>C
n.464T>C
c.381T>C (p.Asp127=)
n.284T>C
 dbSNP gnomAD v3 gnomAD v4
19g.55154123A>TCA407440455TNNI3c.456T>A (p.Asp152Glu)
c.489T>A (p.Asp163Glu)
n.455T>A
n.464T>A
c.381T>A (p.Asp127Glu)
n.284T>A
19g.55154124T>ACA407440457TNNI3c.455A>T (p.Asp152Val)
c.488A>T (p.Asp163Val)
n.454A>T
n.463A>T
c.380A>T (p.Asp127Val)
n.283A>T
19g.55154124T>CCA407440460TNNI3c.455A>G (p.Asp152Gly)
c.488A>G (p.Asp163Gly)
n.454A>G
n.463A>G
c.380A>G (p.Asp127Gly)
n.283A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.55154124T>GCA407440458TNNI3c.455A>C (p.Asp152Ala)
c.488A>C (p.Asp163Ala)
n.454A>C
n.463A>C
c.380A>C (p.Asp127Ala)
n.283A>C
19g.55154124T=CA2343273767TNNI3c.455A= (p.Asp152=)
c.488A= (p.Asp163=)
n.454A=
n.463A=
c.380A= (p.Asp127=)
n.283A=
19g.55154125C>ACA407440462TNNI3c.454G>T (p.Asp152Tyr)
c.487G>T (p.Asp163Tyr)
n.453G>T
n.462G>T
c.379G>T (p.Asp127Tyr)
n.282G>T
19g.55154125C>GCA407440465TNNI3c.454G>C (p.Asp152His)
c.487G>C (p.Asp163His)
n.453G>C
n.462G>C
c.379G>C (p.Asp127His)
n.282G>C
19g.55154125C>TCA407440464TNNI3c.454G>A (p.Asp152Asn)
c.487G>A (p.Asp163Asn)
n.453G>A
n.462G>A
c.379G>A (p.Asp127Asn)
n.282G>A
 gnomAD v4
19g.55154125_55154126insCGAGGAACGCTGCACGTCGCGGTCGGCACCAATCACGAACGCCGAGCACACGTGGCGGGCGTCGTGGTAGGTCTTGCGCACCCA2814881315TNNI3c.454_455insGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGG (p.Asp152GlyfsTer40)
c.487_488insGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGG (p.Asp163GlyfsTer40)
n.453_454insGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGG
n.462_463insGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGG
c.379_380insGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGG (p.Asp127GlyfsTer40)
n.282_283insGTGCGCAAGACCTACCACGACGCCCGCCACGTGTGCTCGGCGTTCGTGATTGGTGCCGACCGCGACGTGCAGCGTTCCTCGG
19g.55154126T>ACA508989426TNNI3c.453A>T (p.Ala151=)
c.486A>T (p.Ala162=)
n.452A>T
n.461A>T
c.378A>T (p.Ala126=)
n.281A>T
19g.55154126T>CCA508989427TNNI3c.453A>G (p.Ala151=)
c.486A>G (p.Ala162=)
n.452A>G
n.461A>G
c.378A>G (p.Ala126=)
n.281A>G
19g.55154126T>GCA508989428TNNI3c.453A>C (p.Ala151=)
c.486A>C (p.Ala162=)
n.452A>C
n.461A>C
c.378A>C (p.Ala126=)
n.281A>C
19g.55154127G>ACA407440467TNNI3c.452C>T (p.Ala151Val)
c.485C>T (p.Ala162Val)
n.451C>T
n.460C>T
c.377C>T (p.Ala126Val)
n.280C>T
 gnomAD v4
19g.55154127G>CCA407440469TNNI3c.452C>G (p.Ala151Gly)
c.485C>G (p.Ala162Gly)
n.451C>G
n.460C>G
c.377C>G (p.Ala126Gly)
n.280C>G
19g.55154127G>TCA407440470TNNI3c.452C>A (p.Ala151Glu)
c.485C>A (p.Ala162Glu)
n.451C>A
n.460C>A
c.377C>A (p.Ala126Glu)
n.280C>A
 gnomAD v4
19g.55154128C>ACA407440472TNNI3c.451G>T (p.Ala151Ser)
c.484G>T (p.Ala162Ser)
n.450G>T
n.459G>T
c.376G>T (p.Ala126Ser)
n.279G>T
19g.55154128C=CA2343273768TNNI3c.451G= (p.Ala151=)
c.484G= (p.Ala162=)
n.450G=
n.459G=
c.376G= (p.Ala126=)
n.279G=
19g.55154128C>GCA407440473TNNI3c.451G>C (p.Ala151Pro)
c.484G>C (p.Ala162Pro)
n.450G>C
n.459G>C
c.376G>C (p.Ala126Pro)
n.279G>C
19g.55154128C>TCA021690TNNI3c.451G>A (p.Ala151Thr)
c.484G>A (p.Ala162Thr)
n.450G>A
n.459G>A
c.376G>A (p.Ala126Thr)
n.279G>A
 ClinVar dbSNP
19g.55154129A=CA2343273769TNNI3c.450T= (p.Ser150=)
c.483T= (p.Ser161=)
n.449T=
n.458T=
c.375T= (p.Ser125=)
n.278T=
19g.55154129A>CCA508989429TNNI3c.450T>G (p.Ser150=)
c.483T>G (p.Ser161=)
n.449T>G
n.458T>G
c.375T>G (p.Ser125=)
n.278T>G
 dbSNP
19g.55154129A>GCA508989430TNNI3c.450T>C (p.Ser150=)
c.483T>C (p.Ser161=)
n.449T>C
n.458T>C
c.375T>C (p.Ser125=)
n.278T>C
 gnomAD v4
19g.55154129A>TCA508989431TNNI3c.450T>A (p.Ser150=)
c.483T>A (p.Ser161=)
n.449T>A
n.458T>A
c.375T>A (p.Ser125=)
n.278T>A
 dbSNP
19g.55154130G>ACA407440476TNNI3c.449C>T (p.Ser150Phe)
c.482C>T (p.Ser161Phe)
n.448C>T
n.457C>T
c.374C>T (p.Ser125Phe)
n.277C>T
 gnomAD v4
19g.55154130G>CCA407440477TNNI3c.449C>G (p.Ser150Cys)
c.482C>G (p.Ser161Cys)
n.448C>G
n.457C>G
c.374C>G (p.Ser125Cys)
n.277C>G
19g.55154130G>TCA407440478TNNI3c.449C>A (p.Ser150Tyr)
c.482C>A (p.Ser161Tyr)
n.448C>A
n.457C>A
c.374C>A (p.Ser125Tyr)
n.277C>A
 ClinVar
19g.55154131A>CCA407440480TNNI3c.448T>G (p.Ser150Ala)
c.481T>G (p.Ser161Ala)
n.447T>G
n.456T>G
c.373T>G (p.Ser125Ala)
n.276T>G
19g.55154131A>GCA407440482TNNI3c.448T>C (p.Ser150Pro)
c.481T>C (p.Ser161Pro)
n.447T>C
n.456T>C
c.373T>C (p.Ser125Pro)
n.276T>C
19g.55154131A>TCA407440483TNNI3c.448T>A (p.Ser150Thr)
c.481T>A (p.Ser161Thr)
n.447T>A
n.456T>A
c.373T>A (p.Ser125Thr)
n.276T>A
19g.55154132G>ACA508989432TNNI3c.447C>T (p.Ile149=)
c.480C>T (p.Ile160=)
n.446C>T
n.455C>T
c.372C>T (p.Ile124=)
n.275C>T
 ClinVar dbSNP
19g.55154132G>CCA407440485TNNI3c.447C>G (p.Ile149Met)
c.480C>G (p.Ile160Met)
n.446C>G
n.455C>G
c.372C>G (p.Ile124Met)
n.275C>G
19g.55154132G>TCA508989433TNNI3c.447C>A (p.Ile149=)
c.480C>A (p.Ile160=)
n.446C>A
n.455C>A
c.372C>A (p.Ile124=)
n.275C>A
 COSMIC
19g.55154133A>CCA407440486TNNI3c.446T>G (p.Ile149Ser)
c.479T>G (p.Ile160Ser)
n.445T>G
n.454T>G
c.371T>G (p.Ile124Ser)
n.274T>G
19g.55154133A>GCA407440488TNNI3c.446T>C (p.Ile149Thr)
c.479T>C (p.Ile160Thr)
n.445T>C
n.454T>C
c.371T>C (p.Ile124Thr)
n.274T>C
19g.55154133A>TCA407440490TNNI3c.446T>A (p.Ile149Asn)
c.479T>A (p.Ile160Asn)
n.445T>A
n.454T>A
c.371T>A (p.Ile124Asn)
n.274T>A
19g.55154134T>ACA407440491TNNI3c.445A>T (p.Ile149Phe)
c.478A>T (p.Ile160Phe)
n.444A>T
n.453A>T
c.370A>T (p.Ile124Phe)
n.273A>T
 gnomAD v4
19g.55154134T>CCA407440493TNNI3c.445A>G (p.Ile149Val)
c.478A>G (p.Ile160Val)
n.444A>G
n.453A>G
c.370A>G (p.Ile124Val)
n.273A>G
19g.55154134T>GCA407440494TNNI3c.445A>C (p.Ile149Leu)
c.478A>C (p.Ile160Leu)
n.444A>C
n.453A>C
c.370A>C (p.Ile124Leu)
n.273A>C
19g.55154135C>ACA407440496TNNI3c.444G>T (p.Arg148Ser)
c.477G>T (p.Arg159Ser)
n.443G>T
n.452G>T
c.369G>T (p.Arg123Ser)
n.272G>T
19g.55154135C=CA2343273770TNNI3c.444G= (p.Arg148=)
c.477G= (p.Arg159=)
n.443G=
n.452G=
c.369G= (p.Arg123=)
n.272G=
19g.55154135C>GCA407440498TNNI3c.444G>C (p.Arg148Ser)
c.477G>C (p.Arg159Ser)
n.443G>C
n.452G>C
c.369G>C (p.Arg123Ser)
n.272G>C
19g.55154135C>TCA508989434TNNI3c.444G>A (p.Arg148=)
c.477G>A (p.Arg159=)
n.443G>A
n.452G>A
c.369G>A (p.Arg123=)
n.272G>A
 ClinVar dbSNP
19g.55154136C>ACA407440499TNNI3c.443G>T (p.Arg148Met)
c.476G>T (p.Arg159Met)
n.442G>T
n.451G>T
c.368G>T (p.Arg123Met)
n.271G>T
19g.55154136C>GCA407440501TNNI3c.443G>C (p.Arg148Thr)
c.476G>C (p.Arg159Thr)
n.442G>C
n.451G>C
c.368G>C (p.Arg123Thr)
n.271G>C
19g.55154136C>TCA407440503TNNI3c.443G>A (p.Arg148Lys)
c.476G>A (p.Arg159Lys)
n.442G>A
n.451G>A
c.368G>A (p.Arg123Lys)
n.271G>A
19g.55154137T>ACA407440506TNNI3c.442A>T (p.Arg148Trp)
c.475A>T (p.Arg159Trp)
n.441A>T
n.450A>T
c.367A>T (p.Arg123Trp)
n.270A>T
19g.55154137T>CCA407440505TNNI3c.442A>G (p.Arg148Gly)
c.475A>G (p.Arg159Gly)
n.441A>G
n.450A>G
c.367A>G (p.Arg123Gly)
n.270A>G
19g.55154137T>GCA508989435TNNI3c.442A>C (p.Arg148=)
c.475A>C (p.Arg159=)
n.441A>C
n.450A>C
c.367A>C (p.Arg123=)
n.270A>C
19g.55154138C>ACA508989436TNNI3c.441G>T (p.Val147=)
c.474G>T (p.Val158=)
n.440G>T
n.449G>T
c.366G>T (p.Val122=)
n.269G>T
19g.55154138C=CA2343273771TNNI3c.441G= (p.Val147=)
c.474G= (p.Val158=)
n.440G=
n.449G=
c.366G= (p.Val122=)
n.269G=
19g.55154138C>GCA508989437TNNI3c.441G>C (p.Val147=)
c.474G>C (p.Val158=)
n.440G>C
n.449G>C
c.366G>C (p.Val122=)
n.269G>C
 ClinVar dbSNP
19g.55154138C>TCA508989438TNNI3c.441G>A (p.Val147=)
c.474G>A (p.Val158=)
n.440G>A
n.449G>A
c.366G>A (p.Val122=)
n.269G>A
 dbSNP
19g.55154139A=CA2343273772TNNI3c.440T= (p.Val147=)
c.473T= (p.Val158=)
n.439T=
n.448T=
c.365T= (p.Val122=)
n.268T=
19g.55154139A>CCA407440509TNNI3c.440T>G (p.Val147Gly)
c.473T>G (p.Val158Gly)
n.439T>G
n.448T>G
c.365T>G (p.Val122Gly)
n.268T>G
19g.55154139A>GCA407440510TNNI3c.440T>C (p.Val147Ala)
c.473T>C (p.Val158Ala)
n.439T>C
n.448T>C
c.365T>C (p.Val122Ala)
n.268T>C
 ClinVar dbSNP
19g.55154139A>TCA407440512TNNI3c.440T>A (p.Val147Glu)
c.473T>A (p.Val158Glu)
n.439T>A
n.448T>A
c.365T>A (p.Val122Glu)
n.268T>A
19g.55154140C>ACA407440515TNNI3c.439G>T (p.Val147Leu)
c.472G>T (p.Val158Leu)
n.438G>T
n.447G>T
c.364G>T (p.Val122Leu)
n.267G>T
19g.55154140C=CA2343273773TNNI3c.439G= (p.Val147=)
c.472G= (p.Val158=)
n.438G=
n.447G=
c.364G= (p.Val122=)
n.267G=
19g.55154140C>GCA021681TNNI3c.439G>C (p.Val147Leu)
c.472G>C (p.Val158Leu)
n.438G>C
n.447G>C
c.364G>C (p.Val122Leu)
n.267G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154140C>TCA407440518TNNI3c.439G>A (p.Val147Met)
c.472G>A (p.Val158Met)
n.438G>A
n.447G>A
c.364G>A (p.Val122Met)
n.267G>A
19g.55154141T>ACA407440521TNNI3c.438A>T (p.Arg146Ser)
c.471A>T (p.Arg157Ser)
n.437A>T
n.446A>T
c.363A>T (p.Arg121Ser)
n.266A>T
 ClinVar dbSNP gnomAD v4
19g.55154141T>CCA508989439TNNI3c.438A>G (p.Arg146=)
c.471A>G (p.Arg157=)
n.437A>G
n.446A>G
c.363A>G (p.Arg121=)
n.266A>G
19g.55154141T>GCA407440523TNNI3c.438A>C (p.Arg146Ser)
c.471A>C (p.Arg157Ser)
n.437A>C
n.446A>C
c.363A>C (p.Arg121Ser)
n.266A>C
19g.55154141T=CA2343273774TNNI3c.438A= (p.Arg146=)
c.471A= (p.Arg157=)
n.437A=
n.446A=
c.363A= (p.Arg121=)
n.266A=
19g.55154142C>ACA407440525TNNI3c.437G>T (p.Arg146Ile)
c.470G>T (p.Arg157Ile)
n.436G>T
n.445G>T
c.362G>T (p.Arg121Ile)
n.265G>T
19g.55154142C>GCA407440528TNNI3c.437G>C (p.Arg146Thr)
c.470G>C (p.Arg157Thr)
n.436G>C
n.445G>C
c.362G>C (p.Arg121Thr)
n.265G>C
19g.55154142C>TCA407440530TNNI3c.437G>A (p.Arg146Lys)
c.470G>A (p.Arg157Lys)
n.436G>A
n.445G>A
c.362G>A (p.Arg121Lys)
n.265G>A
 dbSNP
19g.55154142_55154147dupCA1139666607TNNI3c.432_437dup (p.Arg146_Val147insArgArg)
c.465_470dup (p.Arg157_Val158insArgArg)
n.431_436dup
n.440_445dup
c.357_362dup (p.Arg121_Val122insArgArg)
n.260_265dup
 ClinVar dbSNP
19g.55154143T>ACA407440532TNNI3c.436A>T (p.Arg146Ter)
c.469A>T (p.Arg157Ter)
n.435A>T
n.444A>T
c.361A>T (p.Arg121Ter)
n.264A>T
19g.55154143T>CCA407440534TNNI3c.436A>G (p.Arg146Gly)
c.469A>G (p.Arg157Gly)
n.435A>G
n.444A>G
c.361A>G (p.Arg121Gly)
n.264A>G
19g.55154143T>GCA508989440TNNI3c.436A>C (p.Arg146=)
c.469A>C (p.Arg157=)
n.435A>C
n.444A>C
c.361A>C (p.Arg121=)
n.264A>C
19g.55154144C>ACA508989441TNNI3c.435G>T (p.Arg145=)
c.468G>T (p.Arg156=)
n.434G>T
n.443G>T
c.360G>T (p.Arg120=)
n.263G>T
19g.55154144C=CA2343273775TNNI3c.435G= (p.Arg145=)
c.468G= (p.Arg156=)
n.434G=
n.443G=
c.360G= (p.Arg120=)
n.263G=
19g.55154144C>GCA508989442TNNI3c.435G>C (p.Arg145=)
c.468G>C (p.Arg156=)
n.434G>C
n.443G>C
c.360G>C (p.Arg120=)
n.263G>C
 ClinVar dbSNP
19g.55154144C>TCA508989443TNNI3c.435G>A (p.Arg145=)
c.468G>A (p.Arg156=)
n.434G>A
n.443G>A
c.360G>A (p.Arg120=)
n.263G>A
 dbSNP gnomAD v4
19g.55154145C>ACA407440540TNNI3c.434G>T (p.Arg145Leu)
c.467G>T (p.Arg156Leu)
n.433G>T
n.442G>T
c.359G>T (p.Arg120Leu)
n.262G>T
 ClinVar dbSNP
19g.55154145C=CA2343273776TNNI3c.434G= (p.Arg145=)
c.467G= (p.Arg156=)
n.433G=
n.442G=
c.359G= (p.Arg120=)
n.262G=
19g.55154145C>GCA407440537TNNI3c.434G>C (p.Arg145Pro)
c.467G>C (p.Arg156Pro)
n.433G>C
n.442G>C
c.359G>C (p.Arg120Pro)
n.262G>C
19g.55154145C>TCA021673TNNI3c.434G>A (p.Arg145Gln)
c.467G>A (p.Arg156Gln)
n.433G>A
n.442G>A
c.359G>A (p.Arg120Gln)
n.262G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154146G>ACA021667TNNI3c.433C>T (p.Arg145Trp)
c.466C>T (p.Arg156Trp)
n.432C>T
n.441C>T
c.358C>T (p.Arg120Trp)
n.261C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.55154146G>CCA021660TNNI3c.433C>G (p.Arg145Gly)
c.466C>G (p.Arg156Gly)
n.432C>G
n.441C>G
c.358C>G (p.Arg120Gly)
n.261C>G
 ClinVar dbSNP gnomAD v4
19g.55154146G=CA2343273777TNNI3c.433C= (p.Arg145=)
c.466C= (p.Arg156=)
n.432C=
n.441C=
c.358C= (p.Arg120=)
n.261C=
19g.55154146G>TCA508989444TNNI3c.433C>A (p.Arg145=)
c.466C>A (p.Arg156=)
n.432C>A
n.441C>A
c.358C>A (p.Arg120=)
n.261C>A
 gnomAD v4
19g.55154147C>ACA051607TNNI3c.432G>T (p.Leu144=)
c.465G>T (p.Leu155=)
n.431G>T
n.440G>T
c.357G>T (p.Leu119=)
n.260G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154147C=CA2343273778TNNI3c.432G= (p.Leu144=)
c.465G= (p.Leu155=)
n.431G=
n.440G=
c.357G= (p.Leu119=)
n.260G=
19g.55154147C>GCA051600TNNI3c.432G>C (p.Leu144=)
c.465G>C (p.Leu155=)
n.431G>C
n.440G>C
c.357G>C (p.Leu119=)
n.260G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154147C>TCA508989445TNNI3c.432G>A (p.Leu144=)
c.465G>A (p.Leu155=)
n.431G>A
n.440G>A
c.357G>A (p.Leu119=)
n.260G>A
19g.55154147_55154148delinsATCA2695229160TNNI3c.431_432delinsAT (p.Leu144His)
c.464_465delinsAT (p.Leu155His)
n.430_431delinsAT
n.439_440delinsAT
c.356_357delinsAT (p.Leu119His)
n.259_260delinsAT
19g.55154148A=CA2343273779TNNI3c.431T= (p.Leu144=)
c.464T= (p.Leu155=)
n.430T=
n.439T=
c.356T= (p.Leu119=)
n.259T=
19g.55154148A>CCA407440545TNNI3c.431T>G (p.Leu144Arg)
c.464T>G (p.Leu155Arg)
n.430T>G
n.439T>G
c.356T>G (p.Leu119Arg)
n.259T>G
19g.55154148A>GCA021654TNNI3c.431T>C (p.Leu144Pro)
c.464T>C (p.Leu155Pro)
n.430T>C
n.439T>C
c.356T>C (p.Leu119Pro)
n.259T>C
 ClinVar dbSNP
19g.55154148A>TCA021648TNNI3c.431T>A (p.Leu144Gln)
c.464T>A (p.Leu155Gln)
n.430T>A
n.439T>A
c.356T>A (p.Leu119Gln)
n.259T>A
 ClinVar dbSNP
19g.55154149G>ACA508989446TNNI3c.430C>T (p.Leu144=)
c.463C>T (p.Leu155=)
n.429C>T
n.438C>T
c.355C>T (p.Leu119=)
n.258C>T
19g.55154149G>CCA407440551TNNI3c.430C>G (p.Leu144Val)
c.463C>G (p.Leu155Val)
n.429C>G
n.438C>G
c.355C>G (p.Leu119Val)
n.258C>G
19g.55154149G>TCA407440552TNNI3c.430C>A (p.Leu144Met)
c.463C>A (p.Leu155Met)
n.429C>A
n.438C>A
c.355C>A (p.Leu119Met)
n.258C>A
19g.55154150G>ACA508989447TNNI3c.429C>T (p.Thr143=)
c.462C>T (p.Thr154=)
n.428C>T
n.437C>T
c.354C>T (p.Thr118=)
n.257C>T
 dbSNP
19g.55154150G>CCA508989448TNNI3c.429C>G (p.Thr143=)
c.462C>G (p.Thr154=)
n.428C>G
n.437C>G
c.354C>G (p.Thr118=)
n.257C>G
 dbSNP gnomAD v3 gnomAD v4
19g.55154150G=CA2343273780TNNI3c.429C= (p.Thr143=)
c.462C= (p.Thr154=)
n.428C=
n.437C=
c.354C= (p.Thr118=)
n.257C=
19g.55154150G>TCA508989449TNNI3c.429C>A (p.Thr143=)
c.462C>A (p.Thr154=)
n.428C>A
n.437C>A
c.354C>A (p.Thr118=)
n.257C>A
19g.55154151G>ACA407440555TNNI3c.428C>T (p.Thr143Ile)
c.461C>T (p.Thr154Ile)
n.427C>T
n.436C>T
c.353C>T (p.Thr118Ile)
n.256C>T
 ClinVar dbSNP gnomAD v4
19g.55154151G>CCA407440556TNNI3c.428C>G (p.Thr143Ser)
c.461C>G (p.Thr154Ser)
n.427C>G
n.436C>G
c.353C>G (p.Thr118Ser)
n.256C>G
19g.55154151G=CA2343273781TNNI3c.428C= (p.Thr143=)
c.461C= (p.Thr154=)
n.427C=
n.436C=
c.353C= (p.Thr118=)
n.256C=
19g.55154151G>TCA021641TNNI3c.428C>A (p.Thr143Asn)
c.461C>A (p.Thr154Asn)
n.427C>A
n.436C>A
c.353C>A (p.Thr118Asn)
n.256C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154152T>ACA407440562TNNI3c.427A>T (p.Thr143Ser)
c.460A>T (p.Thr154Ser)
n.426A>T
n.435A>T
c.352A>T (p.Thr118Ser)
n.255A>T
19g.55154152T>CCA407440565TNNI3c.427A>G (p.Thr143Ala)
c.460A>G (p.Thr154Ala)
n.426A>G
n.435A>G
c.352A>G (p.Thr118Ala)
n.255A>G
 dbSNP gnomAD v3 gnomAD v4
19g.55154152T>GCA407440560TNNI3c.427A>C (p.Thr143Pro)
c.460A>C (p.Thr154Pro)
n.426A>C
n.435A>C
c.352A>C (p.Thr118Pro)
n.255A>C
19g.55154152T=CA2343273782TNNI3c.427A= (p.Thr143=)
c.460A= (p.Thr154=)
n.426A=
n.435A=
c.352A= (p.Thr118=)
n.255A=
19g.55154153G>ACA051576TNNI3c.426C>T (p.Pro142=)
c.459C>T (p.Pro153=)
n.425C>T
n.434C>T
c.351C>T (p.Pro117=)
n.254C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154153G>CCA508989450TNNI3c.426C>G (p.Pro142=)
c.459C>G (p.Pro153=)
n.425C>G
n.434C>G
c.351C>G (p.Pro117=)
n.254C>G
19g.55154153G=CA2343273783TNNI3c.426C= (p.Pro142=)
c.459C= (p.Pro153=)
n.425C=
n.434C=
c.351C= (p.Pro117=)
n.254C=
19g.55154153G>TCA508989451TNNI3c.426C>A (p.Pro142=)
c.459C>A (p.Pro153=)
n.425C>A
n.434C>A
c.351C>A (p.Pro117=)
n.254C>A
19g.55154155delCA2587243155TNNI3c.426del (p.Thr143ProfsTer5)
c.459del (p.Thr154ProfsTer5)
n.425del
n.434del
c.351del (p.Thr118ProfsTer5)
n.254del
 gnomAD v4
19g.55154154G>ACA407440569TNNI3c.425C>T (p.Pro142Leu)
c.458C>T (p.Pro153Leu)
n.424C>T
n.433C>T
c.350C>T (p.Pro117Leu)
n.253C>T
 ClinVar dbSNP
19g.55154154G>CCA407440574TNNI3c.425C>G (p.Pro142Arg)
c.458C>G (p.Pro153Arg)
n.424C>G
n.433C>G
c.350C>G (p.Pro117Arg)
n.253C>G
19g.55154154G>TCA407440571TNNI3c.425C>A (p.Pro142His)
c.458C>A (p.Pro153His)
n.424C>A
n.433C>A
c.350C>A (p.Pro117His)
n.253C>A
 ClinVar
19g.55154155G>ACA407440576TNNI3c.424C>T (p.Pro142Ser)
c.457C>T (p.Pro153Ser)
n.423C>T
n.432C>T
c.349C>T (p.Pro117Ser)
n.252C>T
 gnomAD v4
19g.55154155G>CCA407440577TNNI3c.424C>G (p.Pro142Ala)
c.457C>G (p.Pro153Ala)
n.423C>G
n.432C>G
c.349C>G (p.Pro117Ala)
n.252C>G
19g.55154155G>TCA407440578TNNI3c.424C>A (p.Pro142Thr)
c.457C>A (p.Pro153Thr)
n.423C>A
n.432C>A
c.349C>A (p.Pro117Thr)
n.252C>A
 gnomAD v4
19g.55154156C>ACA508989452TNNI3c.423G>T (p.Arg141=)
c.456G>T (p.Arg152=)
n.422G>T
n.431G>T
c.348G>T (p.Arg116=)
n.251G>T
19g.55154156C>GCA508989453TNNI3c.423G>C (p.Arg141=)
c.456G>C (p.Arg152=)
n.422G>C
n.431G>C
c.348G>C (p.Arg116=)
n.251G>C
19g.55154156C>TCA508989454TNNI3c.423G>A (p.Arg141=)
c.456G>A (p.Arg152=)
n.422G>A
n.431G>A
c.348G>A (p.Arg116=)
n.251G>A
 gnomAD v4
19g.55154157C>ACA407440581TNNI3c.422G>T (p.Arg141Leu)
c.455G>T (p.Arg152Leu)
n.421G>T
n.430G>T
c.347G>T (p.Arg116Leu)
n.250G>T
 ClinVar dbSNP gnomAD v4
19g.55154157C=CA2343273784TNNI3c.422G= (p.Arg141=)
c.455G= (p.Arg152=)
n.421G=
n.430G=
c.347G= (p.Arg116=)
n.250G=
19g.55154157C>GCA407440583TNNI3c.422G>C (p.Arg141Pro)
c.455G>C (p.Arg152Pro)
n.421G>C
n.430G>C
c.347G>C (p.Arg116Pro)
n.250G>C
19g.55154157C>TCA021635TNNI3c.422G>A (p.Arg141Gln)
c.455G>A (p.Arg152Gln)
n.421G>A
n.430G>A
c.347G>A (p.Arg116Gln)
n.250G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.55154158G>ACA021627TNNI3c.421C>T (p.Arg141Trp)
c.454C>T (p.Arg152Trp)
n.420C>T
n.429C>T
c.346C>T (p.Arg116Trp)
n.249C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154158G>CCA407440587TNNI3c.421C>G (p.Arg141Gly)
c.454C>G (p.Arg152Gly)
n.420C>G
n.429C>G
c.346C>G (p.Arg116Gly)
n.249C>G
 ClinVar dbSNP
19g.55154158G=CA2343273785TNNI3c.421C= (p.Arg141=)
c.454C= (p.Arg152=)
n.420C=
n.429C=
c.346C= (p.Arg116=)
n.249C=
19g.55154158G>TCA508989455TNNI3c.421C>A (p.Arg141=)
c.454C>A (p.Arg152=)
n.420C>A
n.429C>A
c.346C>A (p.Arg116=)
n.249C>A
19g.55154159C>ACA407440588TNNI3c.420G>T (p.Lys140Asn)
c.453G>T (p.Lys151Asn)
n.419G>T
n.428G>T
c.345G>T (p.Lys115Asn)
n.248G>T
19g.55154159C=CA2343273786TNNI3c.420G= (p.Lys140=)
c.453G= (p.Lys151=)
n.419G=
n.428G=
c.345G= (p.Lys115=)
n.248G=
19g.55154159C>GCA407440591TNNI3c.420G>C (p.Lys140Asn)
c.453G>C (p.Lys151Asn)
n.419G>C
n.428G>C
c.345G>C (p.Lys115Asn)
n.248G>C
19g.55154159C>TCA051570TNNI3c.420G>A (p.Lys140=)
c.453G>A (p.Lys151=)
n.419G>A
n.428G>A
c.345G>A (p.Lys115=)
n.248G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154160T>ACA407440604TNNI3c.419A>T (p.Lys140Met)
c.452A>T (p.Lys151Met)
n.418A>T
n.427A>T
c.344A>T (p.Lys115Met)
n.247A>T
19g.55154160T>CCA407440600TNNI3c.419A>G (p.Lys140Arg)
c.452A>G (p.Lys151Arg)
n.418A>G
n.427A>G
c.344A>G (p.Lys115Arg)
n.247A>G
19g.55154160T>GCA407440602TNNI3c.419A>C (p.Lys140Thr)
c.452A>C (p.Lys151Thr)
n.418A>C
n.427A>C
c.344A>C (p.Lys115Thr)
n.247A>C
19g.55154161T>ACA407440607TNNI3c.418A>T (p.Lys140Ter)
c.451A>T (p.Lys151Ter)
n.417A>T
n.426A>T
c.343A>T (p.Lys115Ter)
n.246A>T
19g.55154161T>CCA407440609TNNI3c.418A>G (p.Lys140Glu)
c.451A>G (p.Lys151Glu)
n.417A>G
n.426A>G
c.343A>G (p.Lys115Glu)
n.246A>G
19g.55154161T>GCA407440610TNNI3c.418A>C (p.Lys140Gln)
c.451A>C (p.Lys151Gln)
n.417A>C
n.426A>C
c.343A>C (p.Lys115Gln)
n.246A>C
 ClinVar
19g.55154162A=CA2343273787TNNI3c.417T= (p.Phe139=)
c.450T= (p.Phe150=)
n.416T=
n.425T=
c.342T= (p.Phe114=)
n.245T=
19g.55154162A>CCA407440612TNNI3c.417T>G (p.Phe139Leu)
c.450T>G (p.Phe150Leu)
n.416T>G
n.425T>G
c.342T>G (p.Phe114Leu)
n.245T>G
19g.55154162A>GCA508989456TNNI3c.417T>C (p.Phe139=)
c.450T>C (p.Phe150=)
n.416T>C
n.425T>C
c.342T>C (p.Phe114=)
n.245T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154162A>TCA407440614TNNI3c.417T>A (p.Phe139Leu)
c.450T>A (p.Phe150Leu)
n.416T>A
n.425T>A
c.342T>A (p.Phe114Leu)
n.245T>A
19g.55154163A=CA2343273788TNNI3c.416T= (p.Phe139=)
c.449T= (p.Phe150=)
n.415T=
n.424T=
c.341T= (p.Phe114=)
n.244T=
19g.55154163A>CCA407440617TNNI3c.416T>G (p.Phe139Cys)
c.449T>G (p.Phe150Cys)
n.415T>G
n.424T>G
c.341T>G (p.Phe114Cys)
n.244T>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154163A>GCA407440619TNNI3c.416T>C (p.Phe139Ser)
c.449T>C (p.Phe150Ser)
n.415T>C
n.424T>C
c.341T>C (p.Phe114Ser)
n.244T>C
19g.55154163A>TCA407440621TNNI3c.416T>A (p.Phe139Tyr)
c.449T>A (p.Phe150Tyr)
n.415T>A
n.424T>A
c.341T>A (p.Phe114Tyr)
n.244T>A
19g.55154164A>CCA407440623TNNI3c.415T>G (p.Phe139Val)
c.448T>G (p.Phe150Val)
n.414T>G
n.423T>G
c.340T>G (p.Phe114Val)
n.243T>G
19g.55154164A>GCA407440625TNNI3c.415T>C (p.Phe139Leu)
c.448T>C (p.Phe150Leu)
n.414T>C
n.423T>C
c.340T>C (p.Phe114Leu)
n.243T>C
19g.55154164A>TCA407440628TNNI3c.415T>A (p.Phe139Ile)
c.448T>A (p.Phe150Ile)
n.414T>A
n.423T>A
c.340T>A (p.Phe114Ile)
n.243T>A
19g.55154165C>ACA407440634TNNI3c.414G>T (p.Lys138Asn)
c.447G>T (p.Lys149Asn)
n.413G>T
n.422G>T
c.339G>T (p.Lys113Asn)
n.242G>T
19g.55154165C>GCA407440632TNNI3c.414G>C (p.Lys138Asn)
c.447G>C (p.Lys149Asn)
n.413G>C
n.422G>C
c.339G>C (p.Lys113Asn)
n.242G>C
19g.55154165C>TCA508989457TNNI3c.414G>A (p.Lys138=)
c.447G>A (p.Lys149=)
n.413G>A
n.422G>A
c.339G>A (p.Lys113=)
n.242G>A
19g.55154166T>ACA407440637TNNI3c.413A>T (p.Lys138Met)
c.446A>T (p.Lys149Met)
n.412A>T
n.421A>T
c.338A>T (p.Lys113Met)
n.241A>T
19g.55154166T>CCA407440639TNNI3c.413A>G (p.Lys138Arg)
c.446A>G (p.Lys149Arg)
n.412A>G
n.421A>G
c.338A>G (p.Lys113Arg)
n.241A>G
19g.55154166T>GCA407440642TNNI3c.413A>C (p.Lys138Thr)
c.446A>C (p.Lys149Thr)
n.412A>C
n.421A>C
c.338A>C (p.Lys113Thr)
n.241A>C
19g.55154167T>ACA407440644TNNI3c.412A>T (p.Lys138Ter)
c.445A>T (p.Lys149Ter)
n.411A>T
n.420A>T
c.337A>T (p.Lys113Ter)
n.240A>T
 dbSNP
19g.55154167T>CCA407440645TNNI3c.412A>G (p.Lys138Glu)
c.445A>G (p.Lys149Glu)
n.411A>G
n.420A>G
c.337A>G (p.Lys113Glu)
n.240A>G
19g.55154167T>GCA407440648TNNI3c.412A>C (p.Lys138Gln)
c.445A>C (p.Lys149Gln)
n.411A>C
n.420A>C
c.337A>C (p.Lys113Gln)
n.240A>C
19g.55154167T=CA2343273789TNNI3c.412A= (p.Lys138=)
c.445A= (p.Lys149=)
n.411A=
n.420A=
c.337A= (p.Lys113=)
n.240A=
19g.55154168G>ACA508989458TNNI3c.411C>T (p.Gly137=)
c.444C>T (p.Gly148=)
n.410C>T
n.419C>T
c.336C>T (p.Gly112=)
n.239C>T
 gnomAD v4
19g.55154168G>CCA508989459TNNI3c.411C>G (p.Gly137=)
c.444C>G (p.Gly148=)
n.410C>G
n.419C>G
c.336C>G (p.Gly112=)
n.239C>G
19g.55154168G>TCA508989460TNNI3c.411C>A (p.Gly137=)
c.444C>A (p.Gly148=)
n.410C>A
n.419C>A
c.336C>A (p.Gly112=)
n.239C>A
 gnomAD v4
19g.55154169C>ACA407440650TNNI3c.410G>T (p.Gly137Val)
c.443G>T (p.Gly148Val)
n.409G>T
n.418G>T
c.335G>T (p.Gly112Val)
n.238G>T
19g.55154169C>GCA407440652TNNI3c.410G>C (p.Gly137Ala)
c.443G>C (p.Gly148Ala)
n.409G>C
n.418G>C
c.335G>C (p.Gly112Ala)
n.238G>C
19g.55154169C>TCA407440660TNNI3c.410G>A (p.Gly137Asp)
c.443G>A (p.Gly148Asp)
n.409G>A
n.418G>A
c.335G>A (p.Gly112Asp)
n.238G>A
 ClinVar
19g.55154170C>ACA407440663TNNI3c.409G>T (p.Gly137Cys)
c.442G>T (p.Gly148Cys)
n.408G>T
n.417G>T
c.334G>T (p.Gly112Cys)
n.237G>T
19g.55154170C>GCA407440665TNNI3c.409G>C (p.Gly137Arg)
c.442G>C (p.Gly148Arg)
n.408G>C
n.417G>C
c.334G>C (p.Gly112Arg)
n.237G>C
19g.55154170C>TCA407440668TNNI3c.409G>A (p.Gly137Ser)
c.442G>A (p.Gly148Ser)
n.408G>A
n.417G>A
c.334G>A (p.Gly112Ser)
n.237G>A
 ClinVar
19g.55154171T>ACA508989461TNNI3c.408A>T (p.Arg136=)
c.441A>T (p.Arg147=)
n.407A>T
n.416A>T
c.333A>T (p.Arg111=)
n.236A>T
 dbSNP
19g.55154171T>CCA508989462TNNI3c.408A>G (p.Arg136=)
c.441A>G (p.Arg147=)
n.407A>G
n.416A>G
c.333A>G (p.Arg111=)
n.236A>G
19g.55154171T>GCA508989463TNNI3c.408A>C (p.Arg136=)
c.441A>C (p.Arg147=)
n.407A>C
n.416A>C
c.333A>C (p.Arg111=)
n.236A>C
19g.55154171T=CA2343273790TNNI3c.408A= (p.Arg136=)
c.441A= (p.Arg147=)
n.407A=
n.416A=
c.333A= (p.Arg111=)
n.236A=
19g.55154172C>ACA407440674TNNI3c.407G>T (p.Arg136Leu)
c.440G>T (p.Arg147Leu)
n.406G>T
n.415G>T
c.332G>T (p.Arg111Leu)
n.235G>T
 gnomAD v4
19g.55154172C=CA2343273791TNNI3c.407G= (p.Arg136=)
c.440G= (p.Arg147=)
n.406G=
n.415G=
c.332G= (p.Arg111=)
n.235G=
19g.55154172C>GCA407440672TNNI3c.407G>C (p.Arg136Pro)
c.440G>C (p.Arg147Pro)
n.406G>C
n.415G>C
c.332G>C (p.Arg111Pro)
n.235G>C
 ClinVar
19g.55154172C>TCA021615TNNI3c.407G>A (p.Arg136Gln)
c.440G>A (p.Arg147Gln)
n.406G>A
n.415G>A
c.332G>A (p.Arg111Gln)
n.235G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.55154173G>ACA407440677TNNI3c.406C>T (p.Arg136Ter)
c.439C>T (p.Arg147Ter)
n.405C>T
n.414C>T
c.331C>T (p.Arg111Ter)
n.234C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154173G>CCA407440680TNNI3c.406C>G (p.Arg136Gly)
c.439C>G (p.Arg147Gly)
n.405C>G
n.414C>G
c.331C>G (p.Arg111Gly)
n.234C>G
 ClinVar gnomAD v4
19g.55154173G=CA2343273792TNNI3c.406C= (p.Arg136=)
c.439C= (p.Arg147=)
n.405C=
n.414C=
c.331C= (p.Arg111=)
n.234C=
19g.55154173G>TCA508989464TNNI3c.406C>A (p.Arg136=)
c.439C>A (p.Arg147=)
n.405C>A
n.414C>A
c.331C>A (p.Arg111=)
n.234C>A
19g.55154174A=CA2343273793TNNI3c.405T= (p.Leu135=)
c.438T= (p.Leu146=)
n.404T=
n.413T=
c.330T= (p.Leu110=)
n.233T=
19g.55154174A>CCA508989465TNNI3c.405T>G (p.Leu135=)
c.438T>G (p.Leu146=)
n.404T>G
n.413T>G
c.330T>G (p.Leu110=)
n.233T>G
 dbSNP
19g.55154174A>GCA508989466TNNI3c.405T>C (p.Leu135=)
c.438T>C (p.Leu146=)
n.404T>C
n.413T>C
c.330T>C (p.Leu110=)
n.233T>C
19g.55154174A>TCA508989467TNNI3c.405T>A (p.Leu135=)
c.438T>A (p.Leu146=)
n.404T>A
n.413T>A
c.330T>A (p.Leu110=)
n.233T>A
19g.55154175A=CA2343273794TNNI3c.404T= (p.Leu135=)
c.437T= (p.Leu146=)
n.403T=
n.412T=
c.329T= (p.Leu110=)
n.232T=
19g.55154175A>CCA407440681TNNI3c.404T>G (p.Leu135Arg)
c.437T>G (p.Leu146Arg)
n.403T>G
n.412T>G
c.329T>G (p.Leu110Arg)
n.232T>G
19g.55154175A>GCA407440682TNNI3c.404T>C (p.Leu135Pro)
c.437T>C (p.Leu146Pro)
n.403T>C
n.412T>C
c.329T>C (p.Leu110Pro)
n.232T>C
 ClinVar dbSNP
19g.55154175A>TCA407440684TNNI3c.404T>A (p.Leu135His)
c.437T>A (p.Leu146His)
n.403T>A
n.412T>A
c.329T>A (p.Leu110His)
n.232T>A
19g.55154176G>ACA407440686TNNI3c.403C>T (p.Leu135Phe)
c.436C>T (p.Leu146Phe)
n.402C>T
n.411C>T
c.328C>T (p.Leu110Phe)
n.231C>T
 ClinVar dbSNP
19g.55154176G>CCA407440687TNNI3c.403C>G (p.Leu135Val)
c.436C>G (p.Leu146Val)
n.402C>G
n.411C>G
c.328C>G (p.Leu110Val)
n.231C>G
19g.55154176G=CA2343273795TNNI3c.403C= (p.Leu135=)
c.436C= (p.Leu146=)
n.402C=
n.411C=
c.328C= (p.Leu110=)
n.231C=
19g.55154176G>TCA407440688TNNI3c.403C>A (p.Leu135Ile)
c.436C>A (p.Leu146Ile)
n.402C>A
n.411C>A
c.328C>A (p.Leu110Ile)
n.231C>A
 ClinVar
19g.55154177G>ACA508989468TNNI3c.402C>T (p.Asp134=)
c.435C>T (p.Asp145=)
n.401C>T
n.410C>T
c.327C>T (p.Asp109=)
n.230C>T
 ClinVar dbSNP
19g.55154177G>CCA407440691TNNI3c.402C>G (p.Asp134Glu)
c.435C>G (p.Asp145Glu)
n.401C>G
n.410C>G
c.327C>G (p.Asp109Glu)
n.230C>G
19g.55154177G=CA2343273796TNNI3c.402C= (p.Asp134=)
c.435C= (p.Asp145=)
n.401C=
n.410C=
c.327C= (p.Asp109=)
n.230C=
19g.55154177G>TCA407440693TNNI3c.402C>A (p.Asp134Glu)
c.435C>A (p.Asp145Glu)
n.401C>A
n.410C>A
c.327C>A (p.Asp109Glu)
n.230C>A
 gnomAD v4
19g.55154178T>ACA407440696TNNI3c.401A>T (p.Asp134Val)
c.434A>T (p.Asp145Val)
n.400A>T
n.409A>T
c.326A>T (p.Asp109Val)
n.229A>T
19g.55154178T>CCA021608TNNI3c.401A>G (p.Asp134Gly)
c.434A>G (p.Asp145Gly)
n.400A>G
n.409A>G
c.326A>G (p.Asp109Gly)
n.229A>G
 ClinVar dbSNP
19g.55154178T>GCA407440699TNNI3c.401A>C (p.Asp134Ala)
c.434A>C (p.Asp145Ala)
n.400A>C
n.409A>C
c.326A>C (p.Asp109Ala)
n.229A>C
19g.55154178T=CA2343273797TNNI3c.401A= (p.Asp134=)
c.434A= (p.Asp145=)
n.400A=
n.409A=
c.326A= (p.Asp109=)
n.229A=
19g.55154179C>ACA407440703TNNI3c.400G>T (p.Asp134Tyr)
c.433G>T (p.Asp145Tyr)
n.399G>T
n.408G>T
c.325G>T (p.Asp109Tyr)
n.228G>T
19g.55154179C>GCA407440704TNNI3c.400G>C (p.Asp134His)
c.433G>C (p.Asp145His)
n.399G>C
n.408G>C
c.325G>C (p.Asp109His)
n.228G>C
19g.55154179C>TCA407440701TNNI3c.400G>A (p.Asp134Asn)
c.433G>A (p.Asp145Asn)
n.399G>A
n.408G>A
c.325G>A (p.Asp109Asn)
n.228G>A
19g.55154180A>CCA407440707TNNI3c.399T>G (p.Phe133Leu)
c.432T>G (p.Phe144Leu)
n.398T>G
n.407T>G
c.324T>G (p.Phe108Leu)
n.227T>G
19g.55154180A>GCA508989469TNNI3c.399T>C (p.Phe133=)
c.432T>C (p.Phe144=)
n.398T>C
n.407T>C
c.324T>C (p.Phe108=)
n.227T>C
19g.55154180A>TCA407440705TNNI3c.399T>A (p.Phe133Leu)
c.432T>A (p.Phe144Leu)
n.398T>A
n.407T>A
c.324T>A (p.Phe108Leu)
n.227T>A
19g.55154181A=CA2343273798TNNI3c.398T= (p.Phe133=)
c.431T= (p.Phe144=)
n.397T=
n.406T=
c.323T= (p.Phe108=)
n.226T=
19g.55154181A>CCA407440710TNNI3c.398T>G (p.Phe133Cys)
c.431T>G (p.Phe144Cys)
n.397T>G
n.406T>G
c.323T>G (p.Phe108Cys)
n.226T>G
19g.55154181A>GCA407440712TNNI3c.398T>C (p.Phe133Ser)
c.431T>C (p.Phe144Ser)
n.397T>C
n.406T>C
c.323T>C (p.Phe108Ser)
n.226T>C
19g.55154181A>TCA407440714TNNI3c.398T>A (p.Phe133Tyr)
c.431T>A (p.Phe144Tyr)
n.397T>A
n.406T>A
c.323T>A (p.Phe108Tyr)
n.226T>A
 dbSNP
19g.55154182A>CCA407440716TNNI3c.397T>G (p.Phe133Val)
c.430T>G (p.Phe144Val)
n.396T>G
n.405T>G
c.322T>G (p.Phe108Val)
n.225T>G
19g.55154182A>GCA407440719TNNI3c.397T>C (p.Phe133Leu)
c.430T>C (p.Phe144Leu)
n.396T>C
n.405T>C
c.322T>C (p.Phe108Leu)
n.225T>C
 ClinVar
19g.55154182A>TCA407440720TNNI3c.397T>A (p.Phe133Ile)
c.430T>A (p.Phe144Ile)
n.396T>A
n.405T>A
c.322T>A (p.Phe108Ile)
n.225T>A
19g.55154183G>ACA508989470TNNI3c.396C>T (p.Ile132=)
c.429C>T (p.Ile143=)
n.395C>T
n.404C>T
c.321C>T (p.Ile107=)
n.224C>T
19g.55154183G>CCA407440722TNNI3c.396C>G (p.Ile132Met)
c.429C>G (p.Ile143Met)
n.395C>G
n.404C>G
c.321C>G (p.Ile107Met)
n.224C>G
19g.55154183G>TCA508989471TNNI3c.396C>A (p.Ile132=)
c.429C>A (p.Ile143=)
n.395C>A
n.404C>A
c.321C>A (p.Ile107=)
n.224C>A
 gnomAD v4 COSMIC
19g.55154184A>CCA407440724TNNI3c.395T>G (p.Ile132Ser)
c.428T>G (p.Ile143Ser)
n.394T>G
n.403T>G
c.320T>G (p.Ile107Ser)
n.223T>G
19g.55154184A>GCA407440726TNNI3c.395T>C (p.Ile132Thr)
c.428T>C (p.Ile143Thr)
n.394T>C
n.403T>C
c.320T>C (p.Ile107Thr)
n.223T>C
19g.55154184A>TCA407440727TNNI3c.395T>A (p.Ile132Asn)
c.428T>A (p.Ile143Asn)
n.394T>A
n.403T>A
c.320T>A (p.Ile107Asn)
n.223T>A
19g.55154184_55154187delinsATCTCA2343273799TNNI3c.392_395delinsAGAT (p.Lys131=)
c.425_428delinsAGAT (p.Lys142=)
n.391_394delinsAGAT
n.400_403delinsAGAT
c.317_320delinsAGAT (p.Lys106=)
n.220_223delinsAGAT
19g.55154185T>ACA407440734TNNI3c.394A>T (p.Ile132Phe)
c.427A>T (p.Ile143Phe)
n.393A>T
n.402A>T
c.319A>T (p.Ile107Phe)
n.222A>T
19g.55154185T>CCA407440732TNNI3c.394A>G (p.Ile132Val)
c.427A>G (p.Ile143Val)
n.393A>G
n.402A>G
c.319A>G (p.Ile107Val)
n.222A>G
19g.55154185T>GCA407440729TNNI3c.394A>C (p.Ile132Leu)
c.427A>C (p.Ile143Leu)
n.393A>C
n.402A>C
c.319A>C (p.Ile107Leu)
n.222A>C
19g.55154188_55154190delCA883722514TNNI3c.392_394del (p.Lys131del)
c.425_427del (p.Lys142del)
n.391_393del
n.400_402del
c.317_319del (p.Lys106del)
n.220_222del
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.55154186C>ACA407440737TNNI3c.393G>T (p.Lys131Asn)
c.426G>T (p.Lys142Asn)
n.392G>T
n.401G>T
c.318G>T (p.Lys106Asn)
n.221G>T
19g.55154186C>GCA407440738TNNI3c.393G>C (p.Lys131Asn)
c.426G>C (p.Lys142Asn)
n.392G>C
n.401G>C
c.318G>C (p.Lys106Asn)
n.221G>C
19g.55154186C>TCA508989472TNNI3c.393G>A (p.Lys131=)
c.426G>A (p.Lys142=)
n.392G>A
n.401G>A
c.318G>A (p.Lys106=)
n.221G>A
 ClinVar gnomAD v4
19g.55154187T>ACA407440740TNNI3c.392A>T (p.Lys131Met)
c.425A>T (p.Lys142Met)
n.391A>T
n.400A>T
c.317A>T (p.Lys106Met)
n.220A>T
19g.55154187T>CCA407440741TNNI3c.392A>G (p.Lys131Arg)
c.425A>G (p.Lys142Arg)
n.391A>G
n.400A>G
c.317A>G (p.Lys106Arg)
n.220A>G
19g.55154187T>GCA407440743TNNI3c.392A>C (p.Lys131Thr)
c.425A>C (p.Lys142Thr)
n.391A>C
n.400A>C
c.317A>C (p.Lys106Thr)
n.220A>C
19g.55154188T>ACA407440747TNNI3c.391A>T (p.Lys131Ter)
c.424A>T (p.Lys142Ter)
n.390A>T
n.399A>T
c.316A>T (p.Lys106Ter)
n.219A>T
19g.55154188T>CCA407440748TNNI3c.391A>G (p.Lys131Glu)
c.424A>G (p.Lys142Glu)
n.390A>G
n.399A>G
c.316A>G (p.Lys106Glu)
n.219A>G
 ClinVar dbSNP
19g.55154188T>GCA407440750TNNI3c.391A>C (p.Lys131Gln)
c.424A>C (p.Lys142Gln)
n.390A>C
n.399A>C
c.316A>C (p.Lys106Gln)
n.219A>C
19g.55154188T=CA2343273800TNNI3c.391A= (p.Lys131=)
c.424A= (p.Lys142=)
n.390A=
n.399A=
c.316A= (p.Lys106=)
n.219A=
19g.55154189C>ACA407440752TNNI3c.390G>T (p.Gln130His)
c.423G>T (p.Gln141His)
n.389G>T
n.398G>T
c.315G>T (p.Gln105His)
n.218G>T
19g.55154189C=CA2343273801TNNI3c.390G= (p.Gln130=)
c.423G= (p.Gln141=)
n.389G=
n.398G=
c.315G= (p.Gln105=)
n.218G=
19g.55154189C>GCA407440754TNNI3c.390G>C (p.Gln130His)
c.423G>C (p.Gln141His)
n.389G>C
n.398G>C
c.315G>C (p.Gln105His)
n.218G>C
19g.55154189C>TCA508989473TNNI3c.390G>A (p.Gln130=)
c.423G>A (p.Gln141=)
n.389G>A
n.398G>A
c.315G>A (p.Gln105=)
n.218G>A
 dbSNP
19g.55154190T>ACA407440756TNNI3c.389A>T (p.Gln130Leu)
c.422A>T (p.Gln141Leu)
n.388A>T
n.397A>T
c.314A>T (p.Gln105Leu)
n.217A>T
19g.55154190T>CCA407440757TNNI3c.389A>G (p.Gln130Arg)
c.422A>G (p.Gln141Arg)
n.388A>G
n.397A>G
c.314A>G (p.Gln105Arg)
n.217A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154190T>GCA407440760TNNI3c.389A>C (p.Gln130Pro)
c.422A>C (p.Gln141Pro)
n.388A>C
n.397A>C
c.314A>C (p.Gln105Pro)
n.217A>C
19g.55154190T=CA2343273802TNNI3c.389A= (p.Gln130=)
c.422A= (p.Gln141=)
n.388A=
n.397A=
c.314A= (p.Gln105=)
n.217A=
19g.55154191G>ACA407440763TNNI3c.388C>T (p.Gln130Ter)
c.421C>T (p.Gln141Ter)
n.387C>T
n.396C>T
c.313C>T (p.Gln105Ter)
n.216C>T
 dbSNP gnomAD v3 gnomAD v4 COSMIC
19g.55154191G>CCA407440766TNNI3c.388C>G (p.Gln130Glu)
c.421C>G (p.Gln141Glu)
n.387C>G
n.396C>G
c.313C>G (p.Gln105Glu)
n.216C>G
19g.55154191G=CA2343273803TNNI3c.388C= (p.Gln130=)
c.421C= (p.Gln141=)
n.387C=
n.396C=
c.313C= (p.Gln105=)
n.216C=
19g.55154191G>TCA407440761TNNI3c.388C>A (p.Gln130Lys)
c.421C>A (p.Gln141Lys)
n.387C>A
n.396C>A
c.313C>A (p.Gln105Lys)
n.216C>A
19g.55154192A=CA2343273804TNNI3c.387T= (p.Thr129=)
c.420T= (p.Thr140=)
n.386T=
n.395T=
c.312T= (p.Thr104=)
n.215T=
19g.55154192A>CCA508989476TNNI3c.387T>G (p.Thr129=)
c.420T>G (p.Thr140=)
n.386T>G
n.395T>G
c.312T>G (p.Thr104=)
n.215T>G
19g.55154192A>GCA508989474TNNI3c.387T>C (p.Thr129=)
c.420T>C (p.Thr140=)
n.386T>C
n.395T>C
c.312T>C (p.Thr104=)
n.215T>C
 dbSNP
19g.55154192A>TCA508989475TNNI3c.387T>A (p.Thr129=)
c.420T>A (p.Thr140=)
n.386T>A
n.395T>A
c.312T>A (p.Thr104=)
n.215T>A
19g.55154193G>ACA407440769TNNI3c.386C>T (p.Thr129Ile)
c.419C>T (p.Thr140Ile)
n.385C>T
n.394C>T
c.311C>T (p.Thr104Ile)
n.214C>T
 ClinVar dbSNP
19g.55154193G>CCA407440771TNNI3c.386C>G (p.Thr129Ser)
c.419C>G (p.Thr140Ser)
n.385C>G
n.394C>G
c.311C>G (p.Thr104Ser)
n.214C>G
19g.55154193G>TCA407440773TNNI3c.386C>A (p.Thr129Asn)
c.419C>A (p.Thr140Asn)
n.385C>A
n.394C>A
c.311C>A (p.Thr104Asn)
n.214C>A
19g.55154194T>ACA407440776TNNI3c.385A>T (p.Thr129Ser)
c.418A>T (p.Thr140Ser)
n.384A>T
n.393A>T
c.310A>T (p.Thr104Ser)
n.213A>T
19g.55154194T>CCA407440777TNNI3c.385A>G (p.Thr129Ala)
c.418A>G (p.Thr140Ala)
n.384A>G
n.393A>G
c.310A>G (p.Thr104Ala)
n.213A>G
19g.55154194T>GCA407440779TNNI3c.385A>C (p.Thr129Pro)
c.418A>C (p.Thr140Pro)
n.384A>C
n.393A>C
c.310A>C (p.Thr104Pro)
n.213A>C
19g.55154195C>ACA051551TNNI3c.384G>T (p.Leu128=)
c.417G>T (p.Leu139=)
n.383G>T
n.392G>T
c.309G>T (p.Leu103=)
n.212G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154195C=CA2343273805TNNI3c.384G= (p.Leu128=)
c.417G= (p.Leu139=)
n.383G=
n.392G=
c.309G= (p.Leu103=)
n.212G=
19g.55154195C>GCA508989477TNNI3c.384G>C (p.Leu128=)
c.417G>C (p.Leu139=)
n.383G>C
n.392G>C
c.309G>C (p.Leu103=)
n.212G>C
19g.55154195C>TCA021596TNNI3c.384G>A (p.Leu128=)
c.417G>A (p.Leu139=)
n.383G>A
n.392G>A
c.309G>A (p.Leu103=)
n.212G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154196A>CCA407440784TNNI3c.383T>G (p.Leu128Arg)
c.416T>G (p.Leu139Arg)
n.382T>G
n.391T>G
c.308T>G (p.Leu103Arg)
n.211T>G
19g.55154196A>GCA407440785TNNI3c.383T>C (p.Leu128Pro)
c.416T>C (p.Leu139Pro)
n.382T>C
n.391T>C
c.308T>C (p.Leu103Pro)
n.211T>C
 gnomAD v4
19g.55154196A>TCA407440786TNNI3c.383T>A (p.Leu128Gln)
c.416T>A (p.Leu139Gln)
n.382T>A
n.391T>A
c.308T>A (p.Leu103Gln)
n.211T>A
 gnomAD v4
19g.55154197G>ACA508989478TNNI3c.382C>T (p.Leu128=)
c.415C>T (p.Leu139=)
n.381C>T
n.390C>T
c.307C>T (p.Leu103=)
n.210C>T
19g.55154197G>CCA407440787TNNI3c.382C>G (p.Leu128Val)
c.415C>G (p.Leu139Val)
n.381C>G
n.390C>G
c.307C>G (p.Leu103Val)
n.210C>G
 ClinVar
19g.55154197G>TCA407440789TNNI3c.382C>A (p.Leu128Met)
c.415C>A (p.Leu139Met)
n.381C>A
n.390C>A
c.307C>A (p.Leu103Met)
n.210C>A
19g.55154198A>CCA407440791TNNI3c.381T>G (p.Asp127Glu)
c.414T>G (p.Asp138Glu)
n.380T>G
n.389T>G
c.306T>G (p.Asp102Glu)
n.209T>G
19g.55154198A>GCA508989479TNNI3c.381T>C (p.Asp127=)
c.414T>C (p.Asp138=)
n.380T>C
n.389T>C
c.306T>C (p.Asp102=)
n.209T>C
 ClinVar dbSNP
19g.55154198A>TCA407440792TNNI3c.381T>A (p.Asp127Glu)
c.414T>A (p.Asp138Glu)
n.380T>A
n.389T>A
c.306T>A (p.Asp102Glu)
n.209T>A
19g.55154199T>ACA407440794TNNI3c.380A>T (p.Asp127Val)
c.413A>T (p.Asp138Val)
n.379A>T
n.388A>T
c.305A>T (p.Asp102Val)
n.208A>T
19g.55154199T>CCA407440797TNNI3c.380A>G (p.Asp127Gly)
c.413A>G (p.Asp138Gly)
n.379A>G
n.388A>G
c.305A>G (p.Asp102Gly)
n.208A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154199T>GCA407440795TNNI3c.380A>C (p.Asp127Ala)
c.413A>C (p.Asp138Ala)
n.379A>C
n.388A>C
c.305A>C (p.Asp102Ala)
n.208A>C
19g.55154199T=CA2343273806TNNI3c.380A= (p.Asp127=)
c.413A= (p.Asp138=)
n.379A=
n.388A=
c.305A= (p.Asp102=)
n.208A=
19g.55154200C>ACA407440799TNNI3c.379G>T (p.Asp127Tyr)
c.412G>T (p.Asp138Tyr)
n.378G>T
n.387G>T
c.304G>T (p.Asp102Tyr)
n.207G>T
 ClinVar dbSNP
19g.55154200C=CA2343273807TNNI3c.379G= (p.Asp127=)
c.412G= (p.Asp138=)
n.378G=
n.387G=
c.304G= (p.Asp102=)
n.207G=
19g.55154200C>GCA407440800TNNI3c.379G>C (p.Asp127His)
c.412G>C (p.Asp138His)
n.378G>C
n.387G>C
c.304G>C (p.Asp102His)
n.207G>C
 dbSNP
19g.55154200C>TCA407440801TNNI3c.379G>A (p.Asp127Asn)
c.412G>A (p.Asp138Asn)
n.378G>A
n.387G>A
c.304G>A (p.Asp102Asn)
n.207G>A
19g.55154201T>ACA508989482TNNI3c.378A>T (p.Ala126=)
c.411A>T (p.Ala137=)
n.377A>T
n.386A>T
c.303A>T (p.Ala101=)
n.206A>T
19g.55154201T>CCA508989480TNNI3c.378A>G (p.Ala126=)
c.411A>G (p.Ala137=)
n.377A>G
n.386A>G
c.303A>G (p.Ala101=)
n.206A>G
19g.55154201T>GCA508989481TNNI3c.378A>C (p.Ala126=)
c.411A>C (p.Ala137=)
n.377A>C
n.386A>C
c.303A>C (p.Ala101=)
n.206A>C
19g.55154202G>ACA407440802TNNI3c.377C>T (p.Ala126Val)
c.410C>T (p.Ala137Val)
n.376C>T
n.385C>T
c.302C>T (p.Ala101Val)
n.205C>T
 gnomAD v4
19g.55154202G>CCA407440803TNNI3c.377C>G (p.Ala126Gly)
c.410C>G (p.Ala137Gly)
n.376C>G
n.385C>G
c.302C>G (p.Ala101Gly)
n.205C>G
19g.55154202G>TCA407440804TNNI3c.377C>A (p.Ala126Glu)
c.410C>A (p.Ala137Glu)
n.376C>A
n.385C>A
c.302C>A (p.Ala101Glu)
n.205C>A
19g.55154203C>ACA407440805TNNI3c.376G>T (p.Ala126Ser)
c.409G>T (p.Ala137Ser)
n.375G>T
n.384G>T
c.301G>T (p.Ala101Ser)
n.204G>T
19g.55154203C>GCA407440806TNNI3c.376G>C (p.Ala126Pro)
c.409G>C (p.Ala137Pro)
n.375G>C
n.384G>C
c.301G>C (p.Ala101Pro)
n.204G>C
19g.55154203C>TCA407440808TNNI3c.376G>A (p.Ala126Thr)
c.409G>A (p.Ala137Thr)
n.375G>A
n.384G>A
c.301G>A (p.Ala101Thr)
n.204G>A
19g.55154204A>CCA407440809TNNI3c.375T>G (p.Ile125Met)
c.408T>G (p.Ile136Met)
n.374T>G
n.383T>G
c.300T>G (p.Ile100Met)
n.203T>G
 gnomAD v4
19g.55154204A>GCA508989483TNNI3c.375T>C (p.Ile125=)
c.408T>C (p.Ile136=)
n.374T>C
n.383T>C
c.300T>C (p.Ile100=)
n.203T>C
19g.55154204A>TCA508989484TNNI3c.375T>A (p.Ile125=)
c.408T>A (p.Ile136=)
n.374T>A
n.383T>A
c.300T>A (p.Ile100=)
n.203T>A
19g.55154205A=CA2343273808TNNI3c.374T= (p.Ile125=)
c.407T= (p.Ile136=)
n.373T=
n.382T=
c.299T= (p.Ile100=)
n.202T=
19g.55154205A>CCA407440813TNNI3c.374T>G (p.Ile125Ser)
c.407T>G (p.Ile136Ser)
n.373T>G
n.382T>G
c.299T>G (p.Ile100Ser)
n.202T>G
 dbSNP
19g.55154205A>GCA10583863TNNI3c.374T>C (p.Ile125Thr)
c.407T>C (p.Ile136Thr)
n.373T>C
n.382T>C
c.299T>C (p.Ile100Thr)
n.202T>C
 ClinVar dbSNP gnomAD v4
19g.55154205A>TCA407440815TNNI3c.374T>A (p.Ile125Asn)
c.407T>A (p.Ile136Asn)
n.373T>A
n.382T>A
c.299T>A (p.Ile100Asn)
n.202T>A
19g.55154206T>ACA407440819TNNI3c.373A>T (p.Ile125Phe)
c.406A>T (p.Ile136Phe)
n.372A>T
n.381A>T
c.298A>T (p.Ile100Phe)
n.201A>T
 ClinVar dbSNP
19g.55154206T>CCA407440822TNNI3c.373A>G (p.Ile125Val)
c.406A>G (p.Ile136Val)
n.372A>G
n.381A>G
c.298A>G (p.Ile100Val)
n.201A>G
19g.55154206T>GCA407440818TNNI3c.373A>C (p.Ile125Leu)
c.406A>C (p.Ile136Leu)
n.372A>C
n.381A>C
c.298A>C (p.Ile100Leu)
n.201A>C
 gnomAD v4
19g.55154206T=CA2343273809TNNI3c.373A= (p.Ile125=)
c.406A= (p.Ile136=)
n.372A=
n.381A=
c.298A= (p.Ile100=)
n.201A=
19g.55154207C>ACA051468TNNI3c.373-1G>T (n.373-1G>T)
c.406-1G>T (n.406-1G>T)
n.372-1G>T
n.381-1G>T
c.298-1G>T (n.298-1G>T)
n.200G>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154207C=CA2343273810TNNI3c.373-1G= (n.373-1G=)
c.406-1G= (n.406-1G=)
n.372-1G=
n.381-1G=
c.298-1G= (n.298-1G=)
n.200G=
19g.55154207C>GCA407440823TNNI3c.373-1G>C (n.373-1G>C)
c.406-1G>C (n.406-1G>C)
n.372-1G>C
n.381-1G>C
c.298-1G>C (n.298-1G>C)
n.200G>C
 ClinVar gnomAD v4
19g.55154207C>TCA407440832TNNI3c.373-1G>A (n.373-1G>A)
c.406-1G>A (n.406-1G>A)
n.372-1G>A
n.381-1G>A
c.298-1G>A (n.298-1G>A)
n.200G>A
19g.55154208T>ACA407440835TNNI3c.373-2A>T (n.373-2A>T)
c.406-2A>T (n.406-2A>T)
n.372-2A>T
n.381-2A>T
c.298-2A>T (n.298-2A>T)
n.199A>T
19g.55154208T>CCA407440841TNNI3c.373-2A>G (n.373-2A>G)
c.406-2A>G (n.406-2A>G)
n.372-2A>G
n.381-2A>G
c.298-2A>G (n.298-2A>G)
n.199A>G
19g.55154208T>GCA407440839TNNI3c.373-2A>C (n.373-2A>C)
c.406-2A>C (n.406-2A>C)
n.372-2A>C
n.381-2A>C
c.298-2A>C (n.298-2A>C)
n.199A>C
19g.55154209G>ACA051512TNNI3c.373-3C>T (n.373-3C>T)
c.406-3C>T (n.406-3C>T)
n.372-3C>T
n.381-3C>T
c.298-3C>T (n.298-3C>T)
n.198C>T
 dbSNP ExAC gnomAD v2
19g.55154209G=CA2343273811TNNI3c.373-3C= (n.373-3C=)
c.406-3C= (n.406-3C=)
n.372-3C=
n.381-3C=
c.298-3C= (n.298-3C=)
n.198C=
19g.55154209G>TCA051510TNNI3c.373-3C>A (n.373-3C>A)
c.406-3C>A (n.406-3C>A)
n.372-3C>A
n.381-3C>A
c.298-3C>A (n.298-3C>A)
n.198C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154213dupCA2814881323TNNI3c.373-3dup (n.373-3dup)
c.406-3dup (n.406-3dup)
n.372-3dup
n.381-3dup
c.298-3dup (n.298-3dup)
n.198dup
19g.55154210G>ACA997261411TNNI3c.373-4C>T (n.373-4C>T)
c.406-4C>T (n.406-4C>T)
n.372-4C>T
n.381-4C>T
c.298-4C>T (n.298-4C>T)
n.197C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.55154210G>CCA021587TNNI3c.373-4C>G (n.373-4C>G)
c.406-4C>G (n.406-4C>G)
n.372-4C>G
n.381-4C>G
c.298-4C>G (n.298-4C>G)
n.197C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154210G=CA2343273812TNNI3c.373-4C= (n.373-4C=)
c.406-4C= (n.406-4C=)
n.372-4C=
n.381-4C=
c.298-4C= (n.298-4C=)
n.197C=
19g.55154210G>TCA2587243156TNNI3c.373-4C>A (n.373-4C>A)
c.406-4C>A (n.406-4C>A)
n.372-4C>A
n.381-4C>A
c.298-4C>A (n.298-4C>A)
n.197C>A
 gnomAD v4
19g.55154211G>TCA2587243157TNNI3c.373-5C>A (n.373-5C>A)
c.406-5C>A (n.406-5C>A)
n.372-5C>A
n.381-5C>A
c.298-5C>A (n.298-5C>A)
n.196C>A
 gnomAD v4
19g.55154212G>TCA2587243158TNNI3c.373-6C>A (n.373-6C>A)
c.406-6C>A (n.406-6C>A)
n.372-6C>A
n.381-6C>A
c.298-6C>A (n.298-6C>A)
n.195C>A
 gnomAD v4
19g.55154213G>ACA051540TNNI3c.373-7C>T (n.373-7C>T)
c.406-7C>T (n.406-7C>T)
n.372-7C>T
n.381-7C>T
c.298-7C>T (n.298-7C>T)
n.194C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154213G=CA2343273813TNNI3c.373-7C= (n.373-7C=)
c.406-7C= (n.406-7C=)
n.372-7C=
n.381-7C=
c.298-7C= (n.298-7C=)
n.194C=
19g.55154213G>TCA2587243159TNNI3c.373-7C>A (n.373-7C>A)
c.406-7C>A (n.406-7C>A)
n.372-7C>A
n.381-7C>A
c.298-7C>A (n.298-7C>A)
n.194C>A
 gnomAD v4
19g.55154214C=CA2343273814TNNI3c.373-8G= (n.373-8G=)
c.406-8G= (n.406-8G=)
n.372-8G=
n.381-8G=
c.298-8G= (n.298-8G=)
n.193G=
19g.55154214C>GCA658658864TNNI3c.373-8G>C (n.373-8G>C)
c.406-8G>C (n.406-8G>C)
n.372-8G>C
n.381-8G>C
c.298-8G>C (n.298-8G>C)
n.193G>C
 ClinVar dbSNP
19g.55154214C>TCA310148435TNNI3c.373-8G>A (n.373-8G>A)
c.406-8G>A (n.406-8G>A)
n.372-8G>A
n.381-8G>A
c.298-8G>A (n.298-8G>A)
n.193G>A
 ClinVar dbSNP gnomAD v4
19g.55154215A=CA2343273815TNNI3c.373-9T= (n.373-9T=)
c.406-9T= (n.406-9T=)
n.372-9T=
n.381-9T=
c.298-9T= (n.298-9T=)
n.192T=
19g.55154215A>CCA2343273816TNNI3c.373-9T>G (n.373-9T>G)
c.406-9T>G (n.406-9T>G)
n.372-9T>G
n.381-9T>G
c.298-9T>G (n.298-9T>G)
n.192T>G
 dbSNP
19g.55154215A>GCA633906547TNNI3c.373-9T>C (n.373-9T>C)
c.406-9T>C (n.406-9T>C)
n.372-9T>C
n.381-9T>C
c.298-9T>C (n.298-9T>C)
n.192T>C
 dbSNP gnomAD v2 gnomAD v4
19g.55154216C>ACA310148442TNNI3c.373-10G>T (n.373-10G>T)
c.406-10G>T (n.406-10G>T)
n.372-10G>T
n.381-10G>T
c.298-10G>T (n.298-10G>T)
n.191G>T
 dbSNP gnomAD v3 gnomAD v4
19g.55154216C=CA021572TNNI3c.373-10G= (n.373-10G=)
c.406-10G= (n.406-10G=)
n.372-10G=
n.381-10G=
c.298-10G= (n.298-10G=)
n.191G=
19g.55154216C>GCA2343273817TNNI3c.373-10G>C (n.373-10G>C)
c.406-10G>C (n.406-10G>C)
n.372-10G>C
n.381-10G>C
c.298-10G>C (n.298-10G>C)
n.191G>C
 dbSNP
19g.55154216C>TCA2343273818TNNI3c.373-10G>A (n.373-10G>A)
c.406-10G>A (n.406-10G>A)
n.372-10G>A
n.381-10G>A
c.298-10G>A (n.298-10G>A)
n.191G>A
 dbSNP gnomAD v4
19g.55154217A=CA2343273819TNNI3c.373-11T= (n.373-11T=)
c.406-11T= (n.406-11T=)
n.372-11T=
n.381-11T=
c.298-11T= (n.298-11T=)
n.190T=
19g.55154217A>GCA633906548TNNI3c.373-11T>C (n.373-11T>C)
c.406-11T>C (n.406-11T>C)
n.372-11T>C
n.381-11T>C
c.298-11T>C (n.298-11T>C)
n.190T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154217A>TCA051446TNNI3c.373-11T>A (n.373-11T>A)
c.406-11T>A (n.406-11T>A)
n.372-11T>A
n.381-11T>A
c.298-11T>A (n.298-11T>A)
n.190T>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched