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NM_001267550.2(TTN):c.84370_84373del (p.Glu28124fs) AND Dilated cardiomyopathy 1G

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Jan 6, 2024
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV004764955.1

Allele description [Variation Report for NM_001267550.2(TTN):c.84370_84373del (p.Glu28124fs)]

NM_001267550.2(TTN):c.84370_84373del (p.Glu28124fs)

Genes:
TTN-AS1:TTN antisense RNA 1 [Gene - HGNC]
TTN:titin [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
2q31.2
Genomic location:
Preferred name:
NM_001267550.2(TTN):c.84370_84373del (p.Glu28124fs)
HGVS:
  • NC_000002.12:g.178561762_178561765del
  • NG_011618.3:g.274041_274044del
  • NG_051363.1:g.43936_43939del
  • NM_001256850.1:c.79447_79450del
  • NM_001267550.2:c.84370_84373delMANE SELECT
  • NM_003319.4:c.57175_57178del
  • NM_133378.4:c.76666_76669del
  • NM_133432.3:c.57550_57553del
  • NM_133437.4:c.57751_57754del
  • NP_001243779.1:p.Glu26483fs
  • NP_001254479.2:p.Glu28124fs
  • NP_003310.4:p.Glu19059fs
  • NP_596869.4:p.Glu25556fs
  • NP_597676.3:p.Glu19184fs
  • NP_597681.4:p.Glu19251fs
  • LRG_391:g.274041_274044del
  • NC_000002.11:g.179426486_179426489del
  • NC_000002.11:g.179426489_179426492del
Protein change:
E19059fs
Links:
dbSNP: rs1559301344
NCBI 1000 Genomes Browser:
rs1559301344
Molecular consequence:
  • NM_001256850.1:c.79447_79450del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001267550.2:c.84370_84373del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_003319.4:c.57175_57178del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_133378.4:c.76666_76669del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_133432.3:c.57550_57553del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_133437.4:c.57751_57754del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Dilated cardiomyopathy 1G (CMD1G)
Identifiers:
MONDO: MONDO:0011400; MedGen: C1858763; Orphanet: 154; OMIM: 604145

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005375023Cardiogenetics and Myogenetics Molecular and Cellular Functional Unit, Aphp Sorbonne University-Hopital Pitie Salpetriere
no assertion criteria provided
Likely pathogenic
(Jan 6, 2024) 		germlineclinical testing

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Cardiogenetics and Myogenetics Molecular and Cellular Functional Unit, Aphp Sorbonne University-Hopital Pitie Salpetriere, SCV005375023.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Mar 11, 2025