PMID: 38616291

Gene: TNNT2

HGNC ID: 11949

PMID: 42698999

Gene: TNN

HGNC ID:11949

PMID: 40615189

Gene: TNNT2

HGNC ID: HGNC:11949

PMID: 34213952

Gene: TNNT2

HGNC ID: 11949

PMID: 41440877

Gene: TNNT2

HGNC ID: HGNC:11949

Case#: Male, 47

DiseaseAssertion: hypertrophic cardiomyopathy

FamilyInfo: NR

ParentalTesting: NR

CasePresentingHPOs: HP:0025169, HP:0034307, HP:0001712,

CaseHPOFreeText: Severe alterations in inter ventricular septum thickness and left ventricular posterior wall thickness

CaseNotHPOs: NR

CaseNotHPOFreeText: NR

CasePreviousTesting: NR

Genotyping Method: Sanger sequencing

FunctionalAnalysis: NA

Variant: NM_001276345.2:c.423G>A

ClinVar: NR

CAID: CA422532259

gnomAD: NR

AdditionalInfo: IVST, average of 19.2 mm and LVPWT; average of 11.5 mm

PMID: 41440877

Gene: TNNT2

HGNC ID: HGNC:11949

Case#: a 2‐year‐old white girl who was found to have RCM following an evaluation precipitated by the sudden death of her older brother.

DiseaseAssertion: Restrictive cardiomyopathy

FamilyInfo: 4‐year‐old brother presented with a sudden cardiac arrest while running on a soccer field and could not be resuscitated. Her father had restrictive physiology and arrhythmias. The TNNT2 variant was found in the father and two children

ParentalTesting: Father carried the variant. For both paternal grandparents tested negative and the proband inherited the variant from her father.

CasePresentingHPOs: HP:0001723, HP:0001639, HP:0031295, HP:0030718, HP:0001695

CaseHPOFreeText: "Her ECG demonstrated criteria for right and left atrial enlargement with marked repolarization abnormality. Echocardiogram revealed mild right atrial and severe left atrial enlargement (left atrial volume, 61.5 cc/m2; normal, 16–28), with mildly increased left ventricular mass and otherwise normal ventricular dimensions. Right and left ventricular systolic function was preserved. "

CaseNotHPOs: not reported

CaseNotHPOFreeText: Ventricular dimensions and biventricular systolic function were reported as normal.

CasePreviousTesting: Cardiomyopathy‐based panel testing (Familion; Transgenomic, Inc., New Haven, CT) was conducted on the proband, demonstrating a single, heterozygous, variant TNNT2‐R94C (c.280C>T).

Genotyping Method: Clinical genetic testing was performed on family members using the same HCM panel test.

FunctionalAnalysis: Biophysical experiments using recombinant human TNNT2‐R94C demonstrated impaired cardiac regulation at the molecular level attributed to reduced calcium‐dependent blocking of myosin's interaction with the thin filament.

Variant: c.835C>T, p.Gln279Ter

ClinVar: 165549

CAID: CA004288

gnomAD: not reported

AdditionalInfo: not reported

PMID: 32098556

Gene: TNNT2

HGNC ID: 11949

PMID: 37108997

Gene: TNNT2

HGNC ID: 11949

Case#: Male half-brother with mild left ventricular dilation from early childhood and mild left ventricular impairment; latest reported ejection fraction was 51%.

DiseaseAssertion: DCM

FamilyInfo: several of the siblings DCM, two died at age of 12, father had DCM, and heart transplant for an individual who later died

ParentalTesting: father was an obligate carrier

CasePresentingHPOs: HP:0001644

CaseHPOFreeText: Mild left ventricular dilation and mildly increased LV volumes

CaseNotHPOs: not reported

CaseNotHPOFreeText: not reported

CasePreviousTesting: panel-based genetic test was conducted in the index patient.

Genotyping Method: panel-based genetic test was conducted in the index patient. sanger confirmation

FunctionalAnalysis: not reported

Variant: c.659_661del p.(Lys220del)

ClinVar: 43659

CAID: CA006429

gnomAD: not reported

AdditionalInfo: not reported

Case#: A 2-year-old girl with dilated cardiomyopathy (DCM) and left ventricular noncompaction, who received a heart transplant at 26 months.

DiseaseAssertion: DCM with left ventricular noncompaction

FamilyInfo: Family history revealed that three of the father’s (A.II.2) sisters (A.II.4-A.II.6) died in infancy due to cardiac failure.

ParentalTesting: The father and paternal grandmother tested positive for the same TNNT2 variant

CasePresentingHPOs: HP:0001644, HP:0030682, HP:0001635

CaseHPOFreeText: The heart failure signs began at 2 months and got worse. Then got a heart transplant at 26 months.

CaseNotHPOs: not reported

CaseNotHPOFreeText: nothing found

CasePreviousTesting: a genetic panel test, including the genes LDB3, LMNA, MYH7, MYBPC3, and TNNT2, was performed.

Genotyping Method: Variants were confirmed in first-degree family members by Sanger sequencing.

FunctionalAnalysis: not reported

Variant: c.316G>A (p.Glu106Lys)

ClinVar: 224775

CAID: CA088557

gnomAD: not reported

AdditionalInfo: not reported

PMID: 34066613

GENE: TNNT2

HGNC ID: 11949

Case#: 19-year-old boy with coarctation of the aorta who complained of mild exertional dyspnea.

DiseaseAssertion: dilated cardiomyopathy (DCMP). LV systolic dysfunction.

FamilyInfo: The family history was positive to sudden death (his cousin died, aged 3 months) and to DCMP and heart transplant (HT): a maternal aunt and her son who then died at 42 and 24 years old. Cascade family screening revealed a TNNT2 variant in the mother (II.1) and his cousin (IV.3).

ParentalTesting: The 19 year old brother's was tested and carried the TNNT2 variant. She was also affected by DCM. The father’s testing status was not reported.

CasePresentingHPOs: HP:0001680, HP:0002875, HP:0025169, HP:4000141

CaseHPOFreeText: surgically repaired coarctation of the aorta who complained of mild exertional dyspnea repaired at birth (NYHA class II–III). Cardiac MRI showed a moderately dilated, hypokinetic LV with an ejection fraction of 45%; echocardiography showed an ejection fraction around 42%.

CaseNotHPOs: not reported

CaseNotHPOFreeText: Nothing was found that was correlated.

CasePreviousTesting: genetic investigations through next generation sequencing (NGS) with a panel of 325 genes, known to be associated with cardiomyopathies

Genotyping Method: targeted next generation sequencing

FunctionalAnalysis: not reported

Variant: c.518G>A (p. Arg173Gln)

ClinVar: 43649

CAID: CA004727

gnomAD: not reported

AdditionalInfo: not reported

PMID: 21483645

Gene: TNNT2

HGNC ID: 11949

Case#: Female, 6, non-Hispanic white

DiseaseAssertion: Dilated Cardiomyopathy

FamilyInfo: Father and Paternal uncle diagnosed with DCM at age 34.

ParentalTesting: Her father underwent cardiac screening based on family history several years later at age 34

CasePresentingHPOs: HP:0001640

CaseHPOFreeText: NA

CaseNotHPOs: NA

CaseNotHPOFreeText: Acute viral illness and gastroenteritis

CasePreviousTesting: NR

Genotyping Method: Sanger Sequencing

FunctionalAnalysis: NR

Variant: NM_001276345.2:c.149A>G

ClinVar: 2005620

CAID: CA344207232

gnomAD: 1:201337304 T / C

AdditionalInfo: NA

PMID: 19293840

Gene: TNNT2

HGNC ID: 11949

Case#: Male, 65

DiseaseAssertion: Idiopathic dilated cardiomyopathy

FamilyInfo:None of his five siblings were affected

ParentalTesting: NR

CasePresentingHPOs: HP:0005110

CaseHPOFreeText: Slow progression to severe heart failure

CaseNotHPOs: NR

CaseNotHPOFreeText: NR

CasePreviousTesting: NR

Genotyping Method: Bidirectional dna sequencing

FunctionalAnalysis: NR

Variant: NM_001276345.2:c.869A>G

ClinVar: 4881578

CAID: CA344201883

gnomAD: NA

AdditionalInfo: HTX. The index patient carried a known TNNT2 K247R mutation as well as two novel intronic variants in MYH7 (IVS39+7C>A) and MYBPC3 (IVS25+13T>A).

Case5: 65 year-old male

DiseaseAssertion: carried a known TNNT2 K247R mutation as well as two novel intronic variants in MYH7 (IVS39+7C>A) and MYBPC3 (IVS25+13T>A)

FamilyInfo: None of his five siblings were affected, judged by their clinical presentation, nor was there any history of cardiac disease or sudden death in the family.

ParentalTesting:NR

CasePresentingHPOs:HP:0003677, HP:0012828, HP:0001635, HP:0005110, HP:0034307, HP:0012666,

CaseHPOFreeText: had late-onset at age 47 IDC, with a slow progression to severe heart failure and subsequently HTX. He also suffered from atrial fibrillation in the later stages of his disease. Had left ventricular end diastolic diameter (in mm and indexed by body surface area (cm/m2)) with a value of 68mm and 3.4cm/m2. As well with 30% of left ventricular ejection fraction. His ECG is normal, clinical status is heart transplantation from the age of 56. CAG is normal.

CaseNotHPOs:NR

CaseNotHPOFreeText:NR

CasePreviousTesting:NR

Genotyping Method:Genetically screened, also using GenBank with PCR by amplifying the coding region

FunctionalAnalysis: The variant could thus possibly result in the synthesis of a limited amount of the slightly modified β-myosin. The functional significance of this is not easily established, but it suggests that the variant may be a disease modifier.

Variant:NM_001276345.2:c.869A>G

ClinVar:4881578

CAID:CA344201883

gnomAD:NR

AdditionalInfo: MYH7 (IVS39+7C>A) increased the likelihood of a cryptic donor splice site to 70%, possibly resulting in the synthesis of mRNA coding for a β-myosin with a C terminus of –VGLE instead of –GLNEE. As the variant is located in the last exon, the faulty spliced mRNA is probably not degraded but results in the synthesis of a modified protein.

PMID: 20458009

Gene: TNNT2

HGNC ID: 11949

Case#: Female, 20, non-Hispanic white

DiseaseAssertion: Peripartum cardiomyopathy

FamilyInfo: NR

ParentalTesting: NR

CasePresentingHPOs: HP:0034807, HP:0001640

CaseHPOFreeText: NA

CaseNotHPOs: NA

CaseNotHPOFreeText: NA

CasePreviousTesting: NR

Genotyping Method: Sanger sequencing

FunctionalAnalysis: demonstrated decreased calcium sensitivity, which indicated that this mutation was likely to be disease causing

Variant: NM_001276345.2:c.505C>G

ClinVar: 2953222

CAID: CA344204620

gnomAD: NR

AdditionalInfo: PPCM was diagnosed one week postpartum.

PMID: 37626566

Gene: TNNT2

HGNC ID: 11949

Case#: a 20-year-old, female, adopted Indian patient with over 662 Mb regions of homozy-gosity who presented with intellectual disability, ataxia, schizophrenia, retinal dystrophy, moder-ate-to-severe progressive sensorineural hearing loss (SNHL), congenital hypothyroidism, cleft mi-tral valve with mild mitral valve regurgitation, and dysmorphic features.

DiseaseAssertion: a cleft mitral valve with mild regurgitation

FamilyInfo: adopted

ParentalTesting: not reported

CasePresentingHPOs: HP:0001249, HP:0001251, HP:0100753, HP:0000556, HP:0000407, HP:0000851, HP:0001633, HP:0001653

CaseHPOFreeText: cleft mitral valve and dysmorphic features

CaseNotHPOs: HP:0001638

CaseNotHPOFreeText: echocardiograms at 18 were normal

CasePreviousTesting: genetic testing, including targeted panel analysis, exome sequencing on a clinical basis, and a research-based review of her raw clinical exome data, led to identifying at least three causal gene disorders to explain distinct aspects of her complex phenotype.

Genotyping Method: Genome-wide single-nucleotide polymorphism (SNP) microarray analysis was clinically performed, with no pathogenic deletions or duplications detected.

FunctionalAnalysis: not reported

Variant: NM_001001430.2:c.68-1592

ClinVar: not reported

CAID: CA032911

gnomAD: total allele frequency: 0.00004522

AdditionalInfo: n/r

Case#: A 50-year-old man diagnosed with HCM at age 41, with asymmetric septal hypertrophy and exertional chest discomfort and pain

DiseaseAssertion: Hypertrophic cardiomyopathy

FamilyInfo: His third elder sister, niece and daughter were also clinically affected by HCM. The proband's mother and eldest sister had suffered from sudden cardiac death. The proband's father, second elder sister (HCM1 in Fig. 1A), nephew (HCM5 in Fig. 1A) and son (HCM7 in Fig. 1A) were 87, 65, 35, and 14 years old, respectively, and had normal echocardiographic measurements.

ParentalTesting: The mother had died suddenly; the 87-year-old father had normal echocardiographic measurements. There was no testing reported.

CasePresentingHPOs: HP:0001639, HP:0005144, HP:0100749, HP:0011712

CaseHPOFreeText: chest distress and chest pain during exercise for 9 years. He presented with an asymmetric hypertrophic interventricular septum and a maximum interventricular septum thickness of 18.04 mm

CaseNotHPOs: not reported

CaseNotHPOFreeText: no findings found in the proband

CasePreviousTesting: nothing reported in the article

Genotyping Method: hole exome sequencing (WES) Exons were captured using Sure Select Human All Exon V5 kit. Sequenced by Illumina HiSeq 4000 sequencer.

FunctionalAnalysis: not reported

Variant: rs796925245 (g.1:201359630G>A, c.835C>T, p.Gln279Ter) (c.835C>T, p.Gln279Ter)

ClinVar: 1175037

CAID: CA088451

gnomAD: not reported

AdditionalInfo: n/r

PMID: 32846832

Gene: TNNT2

HGNC ID: 11949

PMID: 35728000

Gene: TNNT2

HGNC ID: 11949

Case#: 15

DiseaseAssertion: Dilated cardiomyopathy

FamilyInfo: NR

ParentalTesting: NR

CasePresentingHPOs: NA

CaseHPOFreeText: decreased cardiac contractility

CaseNotHPOs: NA

CaseNotHPOFreeText: NA

CasePreviousTesting: NR

Genotyping Method: Sanger sequencing

FunctionalAnalysis: NR

Variant: NM_001276345.2:c.577C>T

ClinVar: 834548

CAID: CA088264

gnomAD: NR

AdditionalInfo: NA

PMID: 21135372

Gene: TNNT2

HGNC ID: 11949

PMID:30565988

Gene:TNNT2

HGNC ID:11949

Case#:A 65-year-old woman with severe hypertrophic cardiomyopathy

DiseaseAssertion:Severe hypertrophic cardiomyopathy

FamilyInfo:no information reported

ParentalTesting:no parental testing reported

CasePresentingHPOs:HP:0001639

CaseHPOFreeText: gene panel testing that identified a single variant

CaseNotHPOs: not found

CaseNotHPOFreeText: not found

CasePreviousTesting: gene panel testing that identified a single variant

Genotyping Method:clinical gene panel testing

FunctionalAnalysis: rapid insertion of TNNT2 gene variants into induced pluripotent stem cell-differentiated cardiomyocytes (iPSC-CMs) for functional annotation of the variants for (E251D)(Figure B)

Variant:c.753G>T (p.Glu251Asp)

ClinVar:not found

CAID:CA090003

gnomAD:not found

AdditionalInfo:not reported

PMID:41969674

Gene:TNNT2

HGNC ID:11949

Case#:male, 41, DCM

DiseaseAssertion:dilated cardiomyopathy

FamilyInfo:The proband reported that his mother died suddenly at approximately 35 years of age (specific cause unknown). Other family members were healthy with no history of cardiac disease. Written informed consent was obtained from all participants.

ParentalTesting:no parental testing reported. Sanger sequencing of available family members (daughter, half-brother, maternal uncle and maternal aunt) confirmed that none carried the variant, supporting its de novo origin

CasePresentingHPOs:HP:0002875, HP:0001644, HP:4000141, HP:6000313

CaseHPOFreeText: ECG showed sinus bradycardia, occasional atrial premature beats, delayed atrioventricular conduction, left atrial enlargement, left ventricular high voltage, incomplete right bundle branch block, and ST-T changes (Figure 1C). CMR revealed late gadolinium enhancement (LGE) in the basal to mid-septal and anterolateral segments of the left ventricle (Figure 1D).

CaseNotHPOs:HP:0000822, HP:0003077

CaseNotHPOFreeText:He denied a history of hyperlipidemia, hypertension, or substance abuse.

CasePreviousTesting:No reports of previous testing

Genotyping Method:whole-exome sequencing and Sanger sequencing

FunctionalAnalysis:not reported

Variant:c.547C>T p.Arg183Trp

ClinVar:43628

CAID:CA004294

gnomAD:Overall allele frequency: 0.000001239

AdditionalInfo:not reported

Case#:a 40-year-old woman with a history of hypokinetic-dilative cardiomyopathy and heterozygous for TNNT2 gene mutation

DiseaseAssertion:hypokinetic-dilative cardiomyopathy

FamilyInfo: her family appreciated the clear communication, and as her condition improved without further complications, she expressed gratitude for the care provided.

ParentalTesting:n/r

CasePresentingHPOs:HP:0001644, HP:0002094, HP:0002094, HP:0001695,

CaseHPOFreeText:Progressive dyspnea and fatigue began in January 2017. In February 2018, the patient had cardiac arrest due to ventricular fibrillation at 26 weeks’ gestation, followed by emergency caesarean section. She carried a heterozygous TNNT2 variant (c.547C>T, p.Arg183Trp)

CaseNotHPOs: HP:0031972, HP:0031972

CaseNotHPOFreeText:Coronary angiography showed no significant stenosis.

CasePreviousTesting:Testing method and scope

GenotypingMethod:n/a

FunctionalAnalysis:not reported

Variant: c.547C>T p.Arg183Trp)

Clinvar:not known

CAID:CA391630526

gnomAD:n/r

AdditionalInfo:n/r

PMID : 40008267

Gene: TNNT2

HGNC ID: 11949

PMID: 29367541

Gene: TNNT2

HGNC ID: 11949

PMID:39905734

Gene:TNNT2

HGNC ID:11949

Case#: a 50‐year‐old male who was clinically diagnosed with isolated CS and prescribed with prednisolone without much effect, and subsequent genetic analysis revealed pathogenic variants in LMNA and TNNT2, representative genes for cardiomyopathy.

DiseaseAssertion:Dilated cardiomyopathy

FamilyInfo: not reported

ParentalTesting: He had no family history of heart disease or sudden death

CasePresentingHPOs:HP:0002094,HP:0005110,HP:0025169, HP:0005110

CaseHPOFreeText:Progressive cardiac conduction disease: first-degree AV block with left axis deviation on an earlier ECG progressed to high-grade and then complete AV block. At age 50, the patient also had mild dyspnoea on exertion (New York Class ll) and atrial fibrillation. The authors later stated that it was dilated cardiomyopathy.

CaseNotHPOs:HP:0033608,HP:0002716

CaseNotHPOFreeText:CT showed no enlarged lymph nodes, pulmonary nodules, or other organ abnormalities

CasePreviousTesting: whole‐exome sequencing analysis to evaluate the risk of inherited cardiomyopathies and identified two missense variants in TNNT2 (chr1:201364335(hg38), NM_001001430.3, c.422G>A, p.Arg141Gln) and LMNA (chr1:156136096(hg38), NM_170707.4, c.1132A>C, p.Lys378Gln) (Figure 3). Sanger sequencing analysis identified a heterozygous single‐base substitution (c.1132A>C) in the LMNA gene and c.422G>A in the TNNT2 gene (red arrows).

Genotyping Method:Whole-exome sequencing (WES) identified the variants; Sanger sequencing of the TNNT2 and LMNA variants is shown in Figure 3.

FunctionalAnalysis:Not reported

Variant:TNNT2: NM_001001430.3:c.422G>A (p.Arg141Gln),LMNA: NM_170707.4:c.1132A>C (p.Lys378Gln)

ClinVar:43637

CAID:CA004540

gnomAD:not reported

AdditionalInfo:not reported

PMID: 28815794

Gene: TNNT2

HGNC ID: 11949

PMID:20973921

Gene:TNNT2

HGNC ID:11949

Case#:A 70‐year‐old woman, previously healthy with a left ventricular ejection fraction presented with DCM

DiseaseAssertion:dilated cardiomyopathy and a 4-month history of progressive heart failure

FamilyInfo:"Family history was negative for IDC or heart failure (Figure 3), although an uncle (II‐3) reportedly had an enlarged heart, and three other relatives (II‐1, II‐2, and III‐4) had cardiac related deaths confirmed by death certificate. The proband’s father (II‐1) died of myocardial failure and pulmonary edema; her mother (II‐2) died of pulmonary embolism; and her sister (III‐4) died suddenly of coronary artery disease in her 60s. Her daughter, the proband’s niece (IV‐3), had a history of palpitations and lower extremity swelling, intermittent numbness, and blanching of the fingers at age 49. Her echocardiogram was normal. Her ECG showed nonspecific ST‐T wave changes and left anterior hemiblock."

ParentalTesting:no parental testing reported because both parents were deceased. The two offsprings that were reported were tested and carried both variants.

CasePresentingHPOs:HP:0001644, HP:0001635, HP:0002875, HP:0012378

CaseHPOFreeText:symptoms of progressive dyspnea on exertion and fatigue that began 2–3 months prior to her presentation. Also, she had an unrelenting progression of symptoms and was hospitalized with advanced NYHA Class IV heart failure 6 weeks later. Lastly, she received a heart transplant.

CaseNotHPOs:not reported

CaseNotHPOFreeText:no myocarditis or infiltrative process and no histological evidence of hemochromatosis,

CasePreviousTesting:Oligonucleotide hybridization‐based DNA sequencing was conducted in the proband for a panel of 19 DCM genes ( Table 1 )

Genotyping Method:Oligonucleotide hybridization‐based DNA sequencing and genomic DNA was extracted from whole blood and was sequenced in our laboratory in both directions to detect and/or confirm nucleotide variants in TNNT2 in the proband and the proband’s relatives using an Applied Biosystems 3130XL capillary sequencer

FunctionalAnalysis:R139H (Figure 4): Functional studies in porcine cardiac skinned fibers reconstituted with the mutant R139H troponin T protein showed decreased Ca2+ sensitivity at pH 7, characteristic of DCM.

Variant:416G>A (R139H) in exon 10 and 690–6G>A in intron 13.

ClinVar:not found

CAID:CA004513

gnomAD:not found

AdditionalInfo:not reported

Case#: Female, Hispanic, 4

DiseaseAssertion:Dilated cardiomyopathy

FamilyInfo: Uncle who died at a young age of sudden cardiac death.

ParentalTesting:

CasePresentingHPOs: HP:0001638

"severe decompensated cardiomyopathy at age 4."

CaseHPOFreeText: NR

CaseNotHPOs: NR

CaseNotHPOFreeText:NR

CasePreviousTesting: NR

Genotyping Method: commercial genetic testing and Sanger sequencing

FunctionalAnalysis:

Variant: NM_001276345.2:c.*187C>T

ClinVar: NR

CAID:CA2649785730

gnomAD:NR

AdditionalInfo:

PMID: 26498512

Gene: TNNT2

HGNC ID: 11949

PMID: 28538763

Gene: TNNT2

HGNC ID: 11949

Case#: Male, 17

DiseaseAssertion: hypertrophic cardiomyopathy

FamilyInfo: All family members were asymptomatic, with normal TTE and ECG, with no evidence of VH.

ParentalTesting:

CasePresentingHPOs: HP:0001639, HP:0001279, HP:0001670, HP:0032092, HP:0031295

CaseHPOFreeText: diastolic type II dysfunction,

CaseNotHPOs: NR

CaseNotHPOFreeText: NR

CasePreviousTesting: genetic analysis of the proband was performed through direct sequencing of the three sarcomere genes: MYH7, MYBPC3 and TNNT2

Genotyping Method: Sanger Sequencing

FunctionalAnalysis: NR

Variant: NR

ClinVar:NR

CAID: NR

gnomAD: NR

AdditionalInfo: underwent clinical and cardiovascular examination, including a 12-lead electrocardiogram (ECG), transthoracic echocardiography (TTE) and 24-hour Holter monitoring. TNNT2 sequenced, but not reported.

Case#: Female, 4 months, Swedish

DiseaseAssertion: dilated cardiomyopathy

FamilyInfo: Strong family history of DCM and faily history of SCD due to DCM. Maternal grandfather had enlarged left ventricle.

ParentalTesting:

CasePresentingHPOs: HP:0005162, HP:0031295, HP:0001653,

CaseHPOFreeText: enlarged left ventricle,

CaseNotHPOs:HP:0011947

CaseNotHPOFreeText: circulatory collapse

CasePreviousTesting: NR

Genotyping Method: Sanger sequencing

FunctionalAnalysis: NR

Variant: NM_001276345.2:c.548G>A

ClinVar:43649

CAID: CA004727

gnomAD:NR

AdditionalInfo: During cardiac catheterization, cardiac resuscitation due to circulatory collapse was needed.

PMID: 28669108

Gene: TNNT2

HGNC ID: 11949

PMID: 27141495

Gene: TNNT2

HGNC ID: 11949

PMID: 27199119

Gene: TNNT2

HGNC ID: 11949

PMID: 31770195

Gene: TNNT2

HGNC ID: 11949

Case#: Female, 6 months

DiseaseAssertion: Dilated cardiomyopathy

FamilyInfo: Mother was age 40 at time of birth, which is a high-risk factor for birth defects

ParentalTesting:

CasePresentingHPOs: HP:0031664, HP:0010438, HP:0005162

CaseHPOFreeText: blood pressure of the four limbs was "92/44 mmHg at the right upper limb, 96/58 mmHg at the left upper limb, 101/60 mmHg at the right lower limb, and 103/54 mmHg at the left lower limb." Enlarged heart boundaries. Shifted apex.

CaseNotHPOs: HP:0000975

CaseNotHPOFreeText: decreased milk consumption

CasePreviousTesting: NR

Genotyping Method: genomic sequencing.

FunctionalAnalysis: NR

Variant: NM_001276345.2:c.548G>A

ClinVar:43649

CAID:CA004727

gnomAD: NR

AdditionalInfo:

Case#: Japanese female

DiseaseAssertion: Mild cardiac hypertrophy and asymmetric septal hypertrophy with myocardial hypertrophy increasing.

FamilyInfo: mother and grandmother showed phenotype. Probands mother has the Arg92Trp mutation of TNNT2.

ParentalTesting:not reported

CasePresentingHPOs: HP:0001670

CaseHPOFreeText: not reported

CaseNotHPOs:not reported

CaseNotHPOFreeText:not reported

CasePreviousTesting: DNA analysis

Genotyping Method: Patients with familial HCM

FunctionalAnalysis:not reported

Variant:NM_001276345.2:c.107A>T

ClinVar:not reported

CAID:CA344207376

gnomAD:not reported

AdditionalInfo: pedigree and phenotype associated with Family C.

PMID: 27082122

Gene: TNNT2

HGNC ID: 11949

PMID: 35861968

Gene: TNNT2

HGNC ID: HGNC:11949

PMID: 19087273

Gene: TNNT2

HGNC ID: 11849

PMID: 18651846

Gene: TNNT2

HGNC ID: 11949

PMID: 24992688

Gene: TNNT2

HGNC ID: 11949

PMID: 23494605

Gene: TNNT2

HGNC ID: 11949