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NM_170707.4(LMNA):c.357-739T>G AND Hutchinson-Gilford syndrome

Germline classification:
Benign (1 submission)
Last evaluated:
May 28, 2019
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:
RCV000986428.1

Allele description [Variation Report for NM_170707.4(LMNA):c.357-739T>G]

NM_170707.4(LMNA):c.357-739T>G

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.357-739T>G
HGVS:
  • NC_000001.11:g.156129878T>G
  • NG_008692.2:g.52306T>G
  • NM_001257374.3:c.21-739T>G
  • NM_001282624.2:c.114-739T>G
  • NM_001282625.2:c.357-739T>G
  • NM_001282626.2:c.357-739T>G
  • NM_005572.4:c.357-739T>G
  • NM_170707.4:c.357-739T>GMANE SELECT
  • NM_170708.4:c.357-739T>G
  • LRG_254t1:c.357-739T>G
  • LRG_254:g.52306T>G
  • NC_000001.10:g.156099669T>G
  • NM_005572.3:c.357-739T>G
Links:
dbSNP: rs513043
NCBI 1000 Genomes Browser:
rs513043
Molecular consequence:
  • NM_001257374.3:c.21-739T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001282624.2:c.114-739T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001282625.2:c.357-739T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001282626.2:c.357-739T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_005572.4:c.357-739T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_170707.4:c.357-739T>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_170708.4:c.357-739T>G - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Hutchinson-Gilford syndrome (HGPS)
Synonyms:
Progerin-producing progeroid laminopathy
Identifiers:
MONDO: MONDO:0008310; MedGen: C0033300; Orphanet: 740; OMIM: 176670

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001135428Mendelics
criteria provided, single submitter

(Mendelics Assertion Criteria 2017)		Benign
(May 28, 2019) 		unknownclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Mendelics, SCV001135428.1

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

Last Updated: Sep 29, 2024