NM_145239.3(PRRT2):c.-20_18del (p.Met1fs) AND Episodic kinesigenic dyskinesia

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 9, 2022
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:: RCV002843452.3

Allele description [Variation Report for NM_145239.3(PRRT2):c.-20_18del (p.Met1fs)]

NM_145239.3(PRRT2):c.-20_18del (p.Met1fs)

Genes:

MVP-DT:MVP divergent transcript [Gene - HGNC]
PRRT2:proline rich transmembrane protein 2 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

16p11.2

Genomic location:

Preferred name:

NM_145239.3(PRRT2):c.-20_18del (p.Met1fs)

HGVS:

NC_000016.10:g.29813035_29813072del
NG_032039.1:g.5948_5985del
NG_032039.2:g.5844_5881del
NM_001256442.2:c.-20_18del
NM_001256443.2:c.-20_18del
NM_145239.3:c.-20_18delMANE SELECT
NP_001243371.1:p.Met1fs
NP_001243372.1:p.Met1fs
NP_660282.2:p.Met1fs
NC_000016.9:g.29824351_29824388del
NC_000016.9:g.29824356_29824393del

Protein change:

M1fs

Molecular consequence:

NM_001256442.2:c.-20_18del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001256443.2:c.-20_18del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_145239.3:c.-20_18del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001256442.2:c.-20_18del - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_001256443.2:c.-20_18del - initiator_codon_variant - [Sequence Ontology: SO:0001582]
NM_145239.3:c.-20_18del - initiator_codon_variant - [Sequence Ontology: SO:0001582]

Condition(s)

Name:: Episodic kinesigenic dyskinesia (EKD)
Synonyms:: Familial paroxysmal dystonia; Paroxysmal kinesigenic dyskinesia
Identifiers:: MONDO: MONDO:0044202; MedGen: C1868682; Orphanet: 98809; OMIM: PS128200

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003211779	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Aug 9, 2022)	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

SCV003211779

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Aug 9, 2022)

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	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV003211779.3

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

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. This variant has not been reported in the literature in individuals affected with PRRT2-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change affects the initiator methionine of the PRRT2 mRNA. The next in-frame methionine is located at codon 11.

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

Last Updated: Sep 29, 2024

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