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NM_000527.5(LDLR):c.941-14dup AND Hypercholesterolemia, familial, 1

Germline classification:
Likely benign (1 submission)
Last evaluated:
Mar 25, 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:
RCV000237968.1

Allele description [Variation Report for NM_000527.5(LDLR):c.941-14dup]

NM_000527.5(LDLR):c.941-14dup

Gene:
LDLR:low density lipoprotein receptor [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
19p13.2
Genomic location:
Preferred name:
NM_000527.5(LDLR):c.941-14dup
HGVS:
  • NC_000019.10:g.11110638dup
  • NG_009060.1:g.26258dup
  • NM_000527.5:c.941-14dupMANE SELECT
  • NM_001195798.2:c.941-14dup
  • NM_001195799.2:c.818-14dup
  • NM_001195800.2:c.437-14dup
  • NM_001195803.2:c.560-14dup
  • LRG_274:g.26258dup
  • NC_000019.9:g.11221314dup
  • c.941-14_941-13insC
Links:
LDLR-LOVD, British Heart Foundation: LDLR_001197; dbSNP: rs879254732
NCBI 1000 Genomes Browser:
rs879254732
Molecular consequence:
  • NM_000527.5:c.941-14dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001195798.2:c.941-14dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001195799.2:c.818-14dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001195800.2:c.437-14dup - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001195803.2:c.560-14dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Hypercholesterolemia, familial, 1
Synonyms:
LDL RECEPTOR DISORDER; Hyperlipoproteinemia Type IIa; HYPER-LOW-DENSITY-LIPOPROTEINEMIA; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0007750; MedGen: C0745103; Orphanet: 391665; OMIM: 143890

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000295086LDLR-LOVD, British Heart Foundation
criteria provided, single submitter

(ACGS Guidelines, 2013)		Likely benign
(Mar 25, 2016) 		germlineliterature only

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

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineno1not providednot provided1not providedliterature only

Citations

PubMed

Genetic characterization of Swedish patients with familial hypercholesterolemia: a heterogeneous pattern of mutations in the LDL receptor gene.

Lind S, Rystedt E, Eriksson M, Wiklund O, Angelin B, Eggertsen G.

Atherosclerosis. 2002 Aug;163(2):399-407.

PubMed [citation]
PMID:
12052488

Details of each submission

From LDLR-LOVD, British Heart Foundation, SCV000295086.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedliterature only PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineno1not providednot provided1not providednot providednot provided

Last Updated: Aug 5, 2023