NM_172107.4(KCNQ2):c.2094GAA[1] (p.Lys699del) AND Early infantile epileptic encephalopathy with suppression bursts

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 6, 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:: RCV001234749.7

Allele description [Variation Report for NM_172107.4(KCNQ2):c.2094GAA[1] (p.Lys699del)]

NM_172107.4(KCNQ2):c.2094GAA[1] (p.Lys699del)

Gene:

KCNQ2:potassium voltage-gated channel subfamily Q member 2 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

20q13.33

Genomic location:

Preferred name:

NM_172107.4(KCNQ2):c.2094GAA[1] (p.Lys699del)

HGVS:

NC_000020.11:g.63407165TCT[1]
NG_009004.2:g.70472GAA[1]
NM_001382235.1:c.2148GAA[1]
NM_004518.6:c.2010GAA[1]
NM_172106.3:c.2040GAA[1]
NM_172107.4:c.2094GAA[1]MANE SELECT
NM_172108.5:c.2001GAA[1]
NP_001369164.1:p.Lys717del
NP_004509.2:p.Lys671del
NP_742104.1:p.Lys681del
NP_742105.1:p.Lys699del
NP_742106.1:p.Lys668del
NC_000020.10:g.62038517_62038519del
NC_000020.10:g.62038518TCT[1]
NM_172107.2:c.2097_2099del

Protein change:

K668del

Links:

dbSNP: rs777593960

NCBI 1000 Genomes Browser:

rs777593960

Molecular consequence:

NM_001382235.1:c.2148GAA[1] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_004518.6:c.2010GAA[1] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_172106.3:c.2040GAA[1] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_172107.4:c.2094GAA[1] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_172108.5:c.2001GAA[1] - inframe_deletion - [Sequence Ontology: SO:0001822]

Condition(s)

Name:: Early infantile epileptic encephalopathy with suppression bursts (EIEE)
Synonyms:: Early infantile epileptic encephalopathy; Ohtahara syndrome; Developmental and epileptic encephalopathy
Identifiers:: MONDO: MONDO:0100062; MedGen: C0393706; Orphanet: 1934; OMIM: PS308350

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001407407	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Dec 6, 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

SCV001407407

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Dec 6, 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, SCV001407407.5

#	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. ClinVar contains an entry for this variant (Variation ID: 961112). This variant has not been reported in the literature in individuals affected with KCNQ2-related conditions. This variant is not present in population databases (gnomAD no frequency). This variant, c.2097_2099del, results in the deletion of 1 amino acid(s) of the KCNQ2 protein (p.Lys699del), but otherwise preserves the integrity of the reading frame.

#	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

ClinVar

Relating variation to medicine