NM_000527.5(LDLR):c.1130G>C (p.Cys377Ser) 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:: RCV000238163.1

Allele description [Variation Report for NM_000527.5(LDLR):c.1130G>C (p.Cys377Ser)]

NM_000527.5(LDLR):c.1130G>C (p.Cys377Ser)

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.1130G>C (p.Cys377Ser)

HGVS:

NC_000019.10:g.11111583G>C
NG_009060.1:g.27203G>C
NM_000527.5:c.1130G>CMANE SELECT
NM_001195798.2:c.1130G>C
NM_001195799.2:c.1007G>C
NM_001195800.2:c.626G>C
NM_001195803.2:c.749G>C
NP_000518.1:p.Cys377Ser
NP_001182727.1:p.Cys377Ser
NP_001182728.1:p.Cys336Ser
NP_001182729.1:p.Cys209Ser
NP_001182732.1:p.Cys250Ser
LRG_274t1:c.1130G>C
LRG_274:g.27203G>C
NC_000019.9:g.11222259G>C
NM_000527.4:c.1130G>C
c.1130G>C

Protein change:

C209S

Links:

LDLR-LOVD, British Heart Foundation: LDLR_001363; dbSNP: rs879254801

NCBI 1000 Genomes Browser:

rs879254801

Molecular consequence:

NM_000527.5:c.1130G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001195798.2:c.1130G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001195799.2:c.1007G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001195800.2:c.626G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001195803.2:c.749G>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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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000295238	LDLR-LOVD, British Heart Foundation	criteria provided, single submitter (ACGS Guidelines, 2013)	Likely pathogenic (Mar 25, 2016)	germline	literature only	PubMed (1) [See all records that cite this PMID] Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000295238

LDLR-LOVD, British Heart Foundation

criteria provided, single submitter

(ACGS Guidelines, 2013)

Likely pathogenic
(Mar 25, 2016)

germline

literature only

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

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	1	not provided	not provided	1	not provided	literature only

Citations

PubMed

Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy.

Bertolini S, Pisciotta L, Rabacchi C, Cefalù AB, Noto D, Fasano T, Signori A, Fresa R, Averna M, Calandra S.

Atherosclerosis. 2013 Apr;227(2):342-8. doi: 10.1016/j.atherosclerosis.2013.01.007. Epub 2013 Jan 19.

PubMed [citation]

PMID:: 23375686

Details of each submission

From LDLR-LOVD, British Heart Foundation, SCV000295238.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	1	not provided	not provided	literature only	PubMed (1)

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

Last Updated: May 1, 2024

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