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NM_000384.3(APOB):c.4056_4064dup (p.Gly1354_Leu1356dup) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 29, 2024
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:
RCV004997155.1

Allele description [Variation Report for NM_000384.3(APOB):c.4056_4064dup (p.Gly1354_Leu1356dup)]

NM_000384.3(APOB):c.4056_4064dup (p.Gly1354_Leu1356dup)

Gene:
APOB:apolipoprotein B [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
2p24.1
Genomic location:
Preferred name:
NM_000384.3(APOB):c.4056_4064dup (p.Gly1354_Leu1356dup)
HGVS:
  • NC_000002.12:g.21013313_21013321dup
  • NG_011793.1:g.35754_35762dup
  • NM_000384.3:c.4056_4064dupMANE SELECT
  • NP_000375.3:p.Gly1354_Leu1356dup
  • NC_000002.11:g.21236183_21236184insACACCCAGG
  • NC_000002.11:g.21236185_21236193dup
  • NM_000384.2:c.4056_4064dup
  • NM_000384.2:c.4056_4064dupCCTGGGTGT
Links:
dbSNP: rs777844352
NCBI 1000 Genomes Browser:
rs777844352
Molecular consequence:
  • NM_000384.3:c.4056_4064dup - inframe_insertion - [Sequence Ontology: SO:0001821]

Condition(s)

Synonyms:
none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005624811Quest Diagnostics Nichols Institute San Juan Capistrano
criteria provided, single submitter

(Quest Diagnostics criteria)		Uncertain significance
(Feb 29, 2024) 		unknownclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders.

Karbassi I, Maston GA, Love A, DiVincenzo C, Braastad CD, Elzinga CD, Bright AR, Previte D, Zhang K, Rowland CM, McCarthy M, Lapierre JL, Dubois F, Medeiros KA, Batish SD, Jones J, Liaquat K, Hoffman CA, Jaremko M, Wang Z, Sun W, Buller-Burckle A, et al.

Hum Mutat. 2016 Jan;37(1):127-34. doi: 10.1002/humu.22918. Epub 2015 Oct 29.

PubMed [citation]
PMID:
26467025
PMCID:
PMC4737317

Details of each submission

From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV005624811.1

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

Description

The APOB c.4056_4064dup (p.Gly1354_Leu1356dup) variant does not alter the translational reading frame and has not been reported in individuals with APOB-related conditions in the published literature. The frequency of this variant in the general population, 0.00087 (31/35440 chromosomes in Admixed American subpopulation (Genome Aggregation Database, http://gnomad.broadinstitute.org)), is higher than would generally be expected for pathogenic variants in this gene. Based on the available information, we are unable to determine the clinical significance of this variant.

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

Last Updated: Mar 11, 2025