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NM_000527.5(LDLR):c.2482T>C (p.Tyr828His) AND Hypercholesterolemia, familial, 1

Germline classification:
Likely pathogenic (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:
RCV000237960.1

Allele description [Variation Report for NM_000527.5(LDLR):c.2482T>C (p.Tyr828His)]

NM_000527.5(LDLR):c.2482T>C (p.Tyr828His)

Gene:
LDLR:low density lipoprotein receptor [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
19p13.2
Genomic location:
Preferred name:
NM_000527.5(LDLR):c.2482T>C (p.Tyr828His)
HGVS:
  • NC_000019.10:g.11129605T>C
  • NG_009060.1:g.45225T>C
  • NM_000527.5:c.2482T>CMANE SELECT
  • NM_001195798.2:c.2482T>C
  • NM_001195799.2:c.2359T>C
  • NM_001195800.2:c.1978T>C
  • NM_001195803.2:c.1948T>C
  • NP_000518.1:p.Tyr828His
  • NP_001182727.1:p.Tyr828His
  • NP_001182728.1:p.Tyr787His
  • NP_001182729.1:p.Tyr660His
  • NP_001182732.1:p.Tyr650His
  • LRG_274:g.45225T>C
  • NC_000019.9:g.11240281T>C
  • c.2482T>C
Protein change:
Y650H
Links:
LDLR-LOVD, British Heart Foundation: LDLR_001658; dbSNP: rs879255218
NCBI 1000 Genomes Browser:
rs879255218
Molecular consequence:
  • NM_000527.5:c.2482T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001195798.2:c.2482T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001195799.2:c.2359T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001195800.2:c.1978T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001195803.2:c.1948T>C - missense variant - [Sequence Ontology: SO:0001583]

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
SCV000296020LDLR-LOVD, British Heart Foundation
criteria provided, single submitter

(ACGS Guidelines, 2013)		Likely pathogenic
(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 providedgermlineyes1not providednot provided1not providedliterature only

Citations

PubMed

Molecular spectrum of autosomal dominant hypercholesterolemia in France.

Marduel M, Carrié A, Sassolas A, Devillers M, Carreau V, Di Filippo M, Erlich D, Abifadel M, Marques-Pinheiro A, Munnich A, Junien C; French ADH Research Network., Boileau C, Varret M, Rabès JP.

Hum Mutat. 2010 Nov;31(11):E1811-24. doi: 10.1002/humu.21348.

PubMed [citation]
PMID:
20809525
PMCID:
PMC3152176

Details of each submission

From LDLR-LOVD, British Heart Foundation, SCV000296020.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedliterature only PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyes1not providednot provided1not providednot providednot provided

Last Updated: Aug 5, 2023