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NM_001276345.2(TNNT2):c.810+5G>A AND Cardiomyopathy, familial restrictive, 3

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 11, 2023
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV003445595.1

Allele description [Variation Report for NM_001276345.2(TNNT2):c.810+5G>A]

NM_001276345.2(TNNT2):c.810+5G>A

Gene:
TNNT2:troponin T2, cardiac type [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q32.1
Genomic location:
Preferred name:
NM_001276345.2(TNNT2):c.810+5G>A
HGVS:
  • NC_000001.11:g.201361274C>T
  • NG_007556.1:g.21404G>A
  • NM_000364.4:c.801+5G>A
  • NM_001001430.3:c.780+5G>A
  • NM_001001431.3:c.771+5G>A
  • NM_001001432.3:c.762+5G>A
  • NM_001276345.2:c.810+5G>AMANE SELECT
  • NM_001276346.2:c.681+5G>A
  • NM_001276347.2:c.780+5G>A
  • LRG_431t1:c.810+5G>A
  • LRG_431:g.21404G>A
  • NC_000001.10:g.201330402C>T
  • NM_001001430.1:c.780+5G>A
  • NM_001001430.2:c.780+5G>A
  • NM_001276345.2:c.810+5G>A
Links:
dbSNP: rs730881113
NCBI 1000 Genomes Browser:
rs730881113
Molecular consequence:
  • NM_000364.4:c.801+5G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001001430.3:c.780+5G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001001431.3:c.771+5G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001001432.3:c.762+5G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001276345.2:c.810+5G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001276346.2:c.681+5G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001276347.2:c.780+5G>A - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Cardiomyopathy, familial restrictive, 3
Identifiers:
MONDO: MONDO:0012900; MedGen: C2676271; Orphanet: 75249; OMIM: 612422

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004173734Genome-Nilou Lab
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Apr 11, 2023) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Genome-Nilou Lab, SCV004173734.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenonot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024