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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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001135428	Mendelics	criteria provided, single submitter (Mendelics Assertion Criteria 2017)	Benign (May 28, 2019)	unknown	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001135428

Mendelics

criteria provided, single submitter

(Mendelics Assertion Criteria 2017)

Benign
(May 28, 2019)

unknown

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Mendelics, SCV001135428.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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