U.S. flag

An official website of the United States government

NM_016203.4(PRKAG2):c.469_471dup (p.Ser157dup) AND Hypertrophic cardiomyopathy

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 15, 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:
RCV004009148.2

Allele description [Variation Report for NM_016203.4(PRKAG2):c.469_471dup (p.Ser157dup)]

NM_016203.4(PRKAG2):c.469_471dup (p.Ser157dup)

Gene:
PRKAG2:protein kinase AMP-activated non-catalytic subunit gamma 2 [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
7q36.1
Genomic location:
Preferred name:
NM_016203.4(PRKAG2):c.469_471dup (p.Ser157dup)
HGVS:
  • NC_000007.13:g.151372719_151372721dup
  • NC_000007.14:g.151675635_151675637dup
  • NG_007486.2:g.206597_206599dup
  • NM_001040633.2:c.337_339dup
  • NM_001304527.2:c.97_99dup
  • NM_001363698.2:c.97_99dup
  • NM_016203.4:c.469_471dupMANE SELECT
  • NP_001035723.1:p.Ser113dup
  • NP_001291456.1:p.Ser33dup
  • NP_001350627.1:p.Ser33dup
  • NP_057287.2:p.Ser157dup
  • LRG_430t1:c.469_471dup
  • LRG_430:g.206597_206599dup
  • LRG_430p1:p.Ser157dup
  • NC_000007.13:g.151372718_151372719insGGA
  • NC_000007.13:g.151372719_151372721dup
  • NC_000007.13:g.151372721_151372723dup
  • NG_007486.1:g.206596_206598dup
Links:
dbSNP: rs1832797348
NCBI 1000 Genomes Browser:
rs1832797348
Molecular consequence:
  • NM_001040633.2:c.337_339dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001304527.2:c.97_99dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001363698.2:c.97_99dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_016203.4:c.469_471dup - inframe_insertion - [Sequence Ontology: SO:0001821]
Observations:
1

Condition(s)

Name:
Hypertrophic cardiomyopathy
Synonyms:
HYPERTROPHIC MYOCARDIOPATHY
Identifiers:
MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV004842290All of Us Research Program, National Institutes of Health
criteria provided, single submitter

(ACMG Guidelines, 2015)
Uncertain Significance
(Aug 15, 2023)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided108544not providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From All of Us Research Program, National Institutes of Health, SCV004842290.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

This variant causes an in-frame duplication of one amino acid at exon 4 of the PRKAG2 protein.To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with PRKAG2-related disorders in the literature. This variant has not been identified in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown108544not providednot provided1not providednot providednot provided

Last Updated: Sep 29, 2024