NM_001005242.3(PKP2):c.2001C>T (p.Ala667=) AND Arrhythmogenic right ventricular cardiomyopathy

Germline classification:: Benign (1 submission)
Last evaluated:: Aug 23, 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:: RCV004806094.1

Allele description [Variation Report for NM_001005242.3(PKP2):c.2001C>T (p.Ala667=)]

NM_001005242.3(PKP2):c.2001C>T (p.Ala667=)

Gene:

PKP2:plakophilin 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12p11.21

Genomic location:

Preferred name:

NM_001005242.3(PKP2):c.2001C>T (p.Ala667=)

HGVS:

NC_000012.12:g.32821368G>A
NG_009000.1:g.80479C>T
NM_001005242.3:c.2001C>TMANE SELECT
NM_004572.4:c.2133C>T
NP_001005242.2:p.Ala667=
NP_004563.2:p.Ala711=
NP_004563.2:p.Ala711=
LRG_398t1:c.2133C>T
LRG_398:g.80479C>T
LRG_398p1:p.Ala711=
NC_000012.11:g.32974302G>A
NM_004572.3:c.2133C>T
p.Ala711Ala

Links:

dbSNP: rs529442984

Molecular consequence:

NM_001005242.3:c.2001C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_004572.4:c.2133C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

Condition(s)

Name:: Arrhythmogenic right ventricular cardiomyopathy (ARVD)
Synonyms:: Cardiomyopathy, ARVC; Arrhythmogenic cardiomyopathy; Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC); See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0016587; MeSH: D019571; MedGen: C0349788

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV005429440	All of Us Research Program, National Institutes of Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Aug 23, 2024)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005429440

All of Us Research Program, National Institutes of Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Aug 23, 2024)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	17	not provided	not provided	143475	not provided	clinical 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, SCV005429440.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	17	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	143475	not provided	not provided		17	not provided	not provided	not provided

Last Updated: Jun 27, 2026

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