U.S. flag

An official website of the United States government

NM_005572.3(LMNA):c.-210T>C AND Hutchinson-Gilford syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 14, 2016
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:
RCV000269044.15

Allele description [Variation Report for NM_005572.3(LMNA):c.-210T>C]

NM_005572.3(LMNA):c.-210T>C

Gene:
LMNA:lamin A/C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q22
Genomic location:
Preferred name:
NM_005572.3(LMNA):c.-210T>C
HGVS:
  • NC_000001.11:g.156114709T>C
  • NG_008692.2:g.37137T>C
  • NG_164639.1:g.336T>C
  • NM_001282625.2:c.-206-4T>C
  • NM_001282626.1:c.-210T>C
  • NM_001406983.1:c.-206-4T>C
  • NM_001406984.1:c.-206-4T>C
  • NM_001406991.1:c.-206-4T>C
  • NM_001406992.1:c.-206-4T>C
  • NM_001406993.1:c.-203+7886T>C
  • NM_001407002.1:c.-611T>C
  • NM_001407003.1:c.-203+7886T>C
  • NM_005572.3:c.-210T>C
  • NM_170707.2:c.-210T>C
  • NM_170707.3:c.-210T>C
  • NM_170708.2:c.-210T>C
  • NM_170708.3:c.-210T>C
  • LRG_254t1:c.-210T>C
  • LRG_254t2:c.-210T>C
  • LRG_254t3:c.-210T>C
  • LRG_254:g.37137T>C
  • NC_000001.10:g.156084500T>C
Links:
dbSNP: rs886045356
NCBI 1000 Genomes Browser:
rs886045356
Molecular consequence:
  • NM_001407002.1:c.-611T>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001282625.2:c.-206-4T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001406983.1:c.-206-4T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001406984.1:c.-206-4T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001406991.1:c.-206-4T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001406992.1:c.-206-4T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001406993.1:c.-203+7886T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407003.1:c.-203+7886T>C - 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

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000348642Illumina Laboratory Services, Illumina
criteria provided, single submitter

(ICSL Variant Classification 20161018)		Uncertain significance
(Jun 14, 2016) 		germlineclinical testing

ICSL_Variant_Classification_20161018.pdf

Citation Link

Help

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, SCV000348642.2

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

Last Updated: Jun 9, 2024