NM_000527.5(LDLR):c.1447T>C (p.Trp483Arg) AND Familial hypercholesterolemia

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Oct 18, 2023
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:: RCV001210317.7

Allele description [Variation Report for NM_000527.5(LDLR):c.1447T>C (p.Trp483Arg)]

NM_000527.5(LDLR):c.1447T>C (p.Trp483Arg)

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.1447T>C (p.Trp483Arg)

Other names:

NM_000527.5(LDLR):c.1447T>C

HGVS:

NC_000019.10:g.11113623T>C
NG_009060.1:g.29243T>C
NM_000527.5:c.1447T>CMANE SELECT
NM_001195798.2:c.1447T>C
NM_001195799.2:c.1324T>C
NM_001195800.2:c.943T>C
NM_001195803.2:c.1066T>C
NP_000518.1:p.Trp483Arg
NP_000518.1:p.Trp483Arg
NP_001182727.1:p.Trp483Arg
NP_001182728.1:p.Trp442Arg
NP_001182729.1:p.Trp315Arg
NP_001182732.1:p.Trp356Arg
LRG_274t1:c.1447T>C
LRG_274:g.29243T>C
LRG_274p1:p.Trp483Arg
NC_000019.9:g.11224299T>C
NM_000527.4:c.1447T>C
P01130:p.Trp483Arg
c.1447T>C

Protein change:

W315R

Links:

LDLR-LOVD, British Heart Foundation: LDLR_001430; UniProtKB: P01130#VAR_005392; dbSNP: rs879254905

NCBI 1000 Genomes Browser:

rs879254905

Molecular consequence:

NM_000527.5:c.1447T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001195798.2:c.1447T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001195799.2:c.1324T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001195800.2:c.943T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001195803.2:c.1066T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Familial hypercholesterolemia
Identifiers:: MONDO: MONDO:0005439; MedGen: C0020445; OMIM: PS143890

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001381800	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Pathogenic (Oct 18, 2023)	germline	clinical testing	PubMed (7) [See all records that cite these PMIDs] 8535447, 17539906, 19837725, 21382890, 27680772, 26892515, 28492532

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001381800

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Pathogenic
(Oct 18, 2023)

germline

clinical testing

PubMed (7)
[See all records that cite these PMIDs]

Help

Summary from all submissions

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

Citations

PubMed

Three novel mutations in the EGF precursor homology domain of the low-density lipoprotein receptor gene in Northern Irish patients with familial hypercholesterolemia.

Ward AJ, O'Kane M, Young I, Nicholls DP, Nevin NC, Graham CA.

Hum Mutat. 1995;6(3):254-6. No abstract available.

PubMed [citation]

PMID:: 8535447

Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia.

Taylor A, Tabrah S, Wang D, Sozen M, Duxbury N, Whittall R, Humphries SE, Norbury G.

Clin Genet. 2007 Jun;71(6):561-8.

PubMed [citation]

PMID:: 17539906

See all PubMed Citations (7)

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001381800.5

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (7)

Description

This sequence change replaces tryptophan, which is neutral and slightly polar, with arginine, which is basic and polar, at codon 483 of the LDLR protein (p.Trp483Arg). This variant is not present in population databases (gnomAD no frequency). This missense change has been observed in individuals with familial hypercholesterolemia (PMID: 8535447, 17539906, 19837725, 21382890, 27680772). This variant is also known as p.W462R. ClinVar contains an entry for this variant (Variation ID: 251847). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt LDLR protein function. This variant disrupts the p.Trp483 amino acid residue in LDLR. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 26892515). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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

Last Updated: Sep 29, 2024

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