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NM_174936.4(PCSK9):c.835C>A (p.Pro279Thr) AND Cardiovascular phenotype

Germline classification:
Likely benign (1 submission)
Last evaluated:
Mar 19, 2020
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:
RCV002436242.2

Allele description [Variation Report for NM_174936.4(PCSK9):c.835C>A (p.Pro279Thr)]

NM_174936.4(PCSK9):c.835C>A (p.Pro279Thr)

Gene:
PCSK9:proprotein convertase subtilisin/kexin type 9 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p32.3
Genomic location:
Preferred name:
NM_174936.4(PCSK9):c.835C>A (p.Pro279Thr)
HGVS:
  • NC_000001.11:g.55056028C>A
  • NG_009061.1:g.21482C>A
  • NM_001407240.1:c.958C>A
  • NM_001407241.1:c.835C>A
  • NM_001407242.1:c.838C>A
  • NM_001407243.1:c.778C>A
  • NM_001407244.1:c.835C>A
  • NM_001407245.1:c.643C>A
  • NM_001407246.1:c.460C>A
  • NM_001407247.1:c.835C>A
  • NM_174936.4:c.835C>AMANE SELECT
  • NP_001394169.1:p.Pro320Thr
  • NP_001394170.1:p.Pro279Thr
  • NP_001394171.1:p.Pro280Thr
  • NP_001394172.1:p.Pro260Thr
  • NP_001394173.1:p.Pro279Thr
  • NP_001394174.1:p.Pro215Thr
  • NP_001394175.1:p.Pro154Thr
  • NP_001394176.1:p.Pro279Thr
  • NP_777596.2:p.Pro279Thr
  • NP_777596.2:p.Pro279Thr
  • LRG_275t1:c.835C>A
  • LRG_275:g.21482C>A
  • LRG_275p1:p.Pro279Thr
  • NC_000001.10:g.55521701C>A
  • NM_174936.3:c.835C>A
  • NR_110451.2:n.494C>A
  • NR_110451.3:n.1168C>A
  • NR_176318.1:n.809C>A
  • NR_176319.1:n.1125C>A
  • NR_176320.1:n.1248C>A
  • NR_176321.1:n.1125C>A
  • NR_176322.1:n.1125C>A
  • NR_176323.1:n.1125C>A
  • NR_176324.1:n.1387C>A
Protein change:
P154T
Links:
dbSNP: rs72646509
NCBI 1000 Genomes Browser:
rs72646509
Molecular consequence:
  • NM_001407240.1:c.958C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407241.1:c.835C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407242.1:c.838C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407243.1:c.778C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407244.1:c.835C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407245.1:c.643C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407246.1:c.460C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407247.1:c.835C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_174936.4:c.835C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002681508Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Mar 19, 2020) 		germlineclinical testing

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

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.

Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang ZZ, Bizon C, Lange EM, Smith JD, Turner EH, Jun G, Kang HM, Peloso G, Auer P, Li KP, Flannick J, Zhang J, Fuchsberger C, Gaulton K, Lindgren C, Locke A, Manning A, et al.

Am J Hum Genet. 2014 Feb 6;94(2):233-45. doi: 10.1016/j.ajhg.2014.01.010.

PubMed [citation]
PMID:
24507775
PMCID:
PMC3928660

Details of each submission

From Ambry Genetics, SCV002681508.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024