U.S. flag

An official website of the United States government

NM_170707.4(LMNA):c.141C>A (p.Asp47Glu) AND Cardiomyopathy

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 1, 2018
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:
RCV001182106.3

Allele description [Variation Report for NM_170707.4(LMNA):c.141C>A (p.Asp47Glu)]

NM_170707.4(LMNA):c.141C>A (p.Asp47Glu)

Gene:
LMNA:lamin A/C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q22
Genomic location:
Preferred name:
NM_170707.4(LMNA):c.141C>A (p.Asp47Glu)
HGVS:
  • NC_000001.11:g.156115059C>A
  • NG_008692.2:g.37487C>A
  • NM_001282625.2:c.141C>A
  • NM_001282626.2:c.141C>A
  • NM_005572.4:c.141C>A
  • NM_170707.4:c.141C>AMANE SELECT
  • NM_170708.4:c.141C>A
  • NP_001269554.1:p.Asp47Glu
  • NP_001269555.1:p.Asp47Glu
  • NP_005563.1:p.Asp47Glu
  • NP_733821.1:p.Asp47Glu
  • NP_733822.1:p.Asp47Glu
  • LRG_254t2:c.141C>A
  • LRG_254:g.37487C>A
  • NC_000001.10:g.156084850C>A
  • NM_170707.2:c.141C>A
Protein change:
D47E
Links:
dbSNP: rs1649715628
NCBI 1000 Genomes Browser:
rs1649715628
Molecular consequence:
  • NM_001282625.2:c.141C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001282626.2:c.141C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_005572.4:c.141C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_170707.4:c.141C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_170708.4:c.141C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cardiomyopathy (CMYO)
Synonyms:
Cardiomyopathies
Identifiers:
MONDO: MONDO:0004994; MedGen: C0878544; Human Phenotype Ontology: HP:0001638

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001347458Color Diagnostics, LLC DBA Color Health
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Dec 1, 2018) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot 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 Color Diagnostics, LLC DBA Color Health, SCV001347458.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

Variant of Uncertain Significance due to insufficient evidence: This missense variant is located in the intermediate filament rod domain of the lamin A/C protein. Computational prediction tools and conservation analyses are inconclusive regarding the impact of this variant on the protein function. Computational splicing tools suggest that this variant may not impact RNA splicing. To our knowledge, functional assays have not been performed for this variant nor has this variant been reported in individuals affected with cardiovascular disorders in the literature. This variant is rare in the general population and has been identified in 0/277264 chromosomes by the Genome Aggregation Database (gnomAD). Available evidence is insufficient to determine the pathogenicity of this variant conclusively.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 5, 2022