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NM_170707.4(LMNA):c.1149G>A (p.Glu383=) AND Congenital muscular dystrophy due to LMNA mutation

Germline classification:
Likely benign (1 submission)
Last evaluated:
Apr 27, 2017
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:
RCV000327855.5

Allele description [Variation Report for NM_170707.4(LMNA):c.1149G>A (p.Glu383=)]

NM_170707.4(LMNA):c.1149G>A (p.Glu383=)

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.1149G>A (p.Glu383=)
HGVS:
  • NC_000001.11:g.156136113G>A
  • NG_008692.2:g.58541G>A
  • NM_001257374.3:c.813G>A
  • NM_001282624.2:c.906G>A
  • NM_001282625.2:c.1149G>A
  • NM_001282626.2:c.1149G>A
  • NM_005572.4:c.1149G>A
  • NM_170707.4:c.1149G>AMANE SELECT
  • NM_170708.4:c.1149G>A
  • NP_001244303.1:p.Glu271=
  • NP_001269553.1:p.Glu302=
  • NP_001269554.1:p.Glu383=
  • NP_001269555.1:p.Glu383=
  • NP_005563.1:p.Glu383=
  • NP_005563.1:p.Glu383=
  • NP_733821.1:p.Glu383=
  • NP_733822.1:p.Glu383=
  • LRG_254t1:c.1149G>A
  • LRG_254t2:c.1149G>A
  • LRG_254:g.58541G>A
  • LRG_254p1:p.Glu383=
  • NC_000001.10:g.156105904G>A
  • NM_005572.3:c.1149G>A
  • NM_170707.2:c.1149G>A
  • NM_170707.3:c.1149G>A
  • NP_005563.1:p.(=)
Links:
dbSNP: rs267607603
NCBI 1000 Genomes Browser:
rs267607603
Molecular consequence:
  • NM_001257374.3:c.813G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001282624.2:c.906G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001282625.2:c.1149G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001282626.2:c.1149G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_005572.4:c.1149G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_170707.4:c.1149G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_170708.4:c.1149G>A - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Congenital muscular dystrophy due to LMNA mutation
Synonyms:
Congenital muscular dystrophy, LMNA-related; Lamin A-related Congenital Muscular Dystrophy
Identifiers:
MONDO: MONDO:0013178; MedGen: C2750785; Orphanet: 157973; OMIM: 613205

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000348876Illumina Laboratory Services, Illumina
criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)		Likely benign
(Apr 27, 2017) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000348876.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.

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

Last Updated: Jun 29, 2024