ClinVar Miner

Submissions for variant NM_000527.4(LDLR):c.917C>T (p.Ser306Leu) (rs11547917)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 8
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
LDLR-LOVD, British Heart Foundation RCV000211683 SCV000295055 likely pathogenic Familial hypercholesterolemia 1 2016-03-25 criteria provided, single submitter literature only
Robarts Research Institute,Western University RCV000211683 SCV000484690 likely pathogenic Familial hypercholesterolemia 1 criteria provided, single submitter clinical testing
Centre de Génétique Moléculaire et Chromosomique, Unité de génétique de l'Obésité et des Dyslipidémies,APHP, GH Hôpitaux Universitaires Pitié-Salpêtrière / Charles-Foix RCV000211683 SCV000503253 likely pathogenic Familial hypercholesterolemia 1 2016-12-16 criteria provided, single submitter clinical testing subject mutated among 2600 FH index cases screened = 1 , family member = 1 with co-segregation / FH-Amsterdam, 2 to 5% LDLR Activity / Software predictions: Conflicting
Fundacion Hipercolesterolemia Familiar RCV000211683 SCV000607523 likely pathogenic Familial hypercholesterolemia 1 2016-03-01 criteria provided, single submitter research
Cardiovascular Genetics Laboratory,PathWest Laboratory Medicine WA - Fiona Stanley Hospital RCV000211683 SCV000268589 pathogenic Familial hypercholesterolemia 1 2014-11-13 no assertion criteria provided clinical testing
Laboratorium voor Moleculaire Diagnostiek Experimentele Vasculaire Geneeskunde,Academisch Medisch Centrum RCV000211683 SCV000606268 pathogenic Familial hypercholesterolemia 1 no assertion criteria provided research
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000211683 SCV000733816 pathogenic Familial hypercholesterolemia 1 no assertion criteria provided clinical testing
Stanford Center for Inherited Cardiovascular Disease,Stanford University RCV000786353 SCV000925139 pathogenic not provided 2016-09-06 no assertion criteria provided provider interpretation The patient had genetic testing for the familial hypercholesterolemia panel. The test included sequencing of three genes associated with familial hypercholesterolemia: LDLR, APOB and PCSK9. Results showed that the following variant was identified (see report below): p.Ser306Leu (c.917C>T) in the LDLR gene (NM_000527.4) The lab classifies this variant as a pathogenic mutation. Given sufficient case data we consider this variant pathogenic and we do feel it is suitable for assessing risk in healthy relatives ("predictive genetic testing"). The variant has been reported in at least 10 unrelated cases of familial hypercholesterolemia (not including this patient's family). There is strong case data. This variant has been identified in many individuals with familial hypercholesterolemia and one of the most prevalent variants in the Netherlands and has been known as the FH Amsterdam allele in publication (aka p.Ser285Leu). Hobbs, et al 1992 reported this variant in their cohort of Dutch patients. The individual had homozygous FH phenotype but the other variant could no be identified at the time of the study. Schuster, et al 1996 reports a family in which five individuals had the Ser306Leu variant in a heterozygous state and one individual who had p.Ser306Leu in a homozygous state. They had phenotypes of heterozygous and homozygous FH respectively. This study reported on a German cohort. Jensen, et al reported this variant in their Danish cohort in 1999. No individual details were provided other than the patient having the clinical diagnosis of FH. The Rotterdam study (Oosterveer, et al, 2015) identified Ser306Leu in 19 individuals (many unrelated individuals, but clinical information is not proved). Clinvar reports this variant in one individual that was tested at the PathWest Lab Medicine, no additional details are given. In silico analysis with PolyPhen-2 predicts the variant to be probably damaging (HumVar: 0.965). The serine at codon 306 is conserved across species, as are neighboring amino acids. There is no variation at codon 306 listed in the Exome Aggregation Consortium dataset (http://exac.broadinstitute.org/), which currently includes variant calls on ~64,000 individuals of European, African, Latino and Asian descent (as of September 9, 2016). The average coverage at that site in ExAC is 80x.

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.