NM_172107.4(KCNQ2):c.1113del (p.Met371fs) AND Early infantile epileptic encephalopathy with suppression bursts

This record was updated by the submitter. Please see the current version.

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Sep 7, 2020
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:: RCV001390344.5

Allele description

NM_172107.4(KCNQ2):c.1113del (p.Met371fs)

Gene:

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

Variant type:

Deletion

Cytogenetic location:

20q13.33

Genomic location:

Preferred name:

NM_172107.4(KCNQ2):c.1113del (p.Met371fs)

HGVS:

NC_000020.11:g.63433814del
NG_009004.2:g.43827del
NM_001382235.1:c.1113del
NM_004518.6:c.1113del
NM_172106.3:c.1113del
NM_172107.4:c.1113delMANE SELECT
NM_172108.5:c.1113del
NM_172109.3:c.1113del
NP_001369164.1:p.Met371fs
NP_004509.2:p.Met371fs
NP_742104.1:p.Met371fs
NP_742105.1:p.Met371fs
NP_742106.1:p.Met371fs
NP_742107.1:p.Met371fs
NC_000020.10:g.62065167del

Protein change:

M371fs

Links:

dbSNP: rs2145679115

NCBI 1000 Genomes Browser:

rs2145679115

Molecular consequence:

NM_001382235.1:c.1113del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_004518.6:c.1113del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_172106.3:c.1113del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_172107.4:c.1113del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_172108.5:c.1113del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_172109.3:c.1113del - frameshift variant - [Sequence Ontology: SO:0001589]

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

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SKU5 similar 2 [Arabidopsis thaliana]
SKU5 similar 2 [Arabidopsis thaliana]
gi|15242108|ref|NP_199961.1|

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001592030	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Pathogenic (Sep 7, 2020)	germline	clinical testing	PubMed (4) [See all records that cite these PMIDs] 14534157, 23692823, 27779742, 28492532

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001592030

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Pathogenic
(Sep 7, 2020)

germline

clinical testing

PubMed (4)
[See all records that cite these PMIDs]

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

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.

Singh NA, Westenskow P, Charlier C, Pappas C, Leslie J, Dillon J, Anderson VE, Sanguinetti MC, Leppert MF; BFNC Physician Consortium..

Brain. 2003 Dec;126(Pt 12):2726-37. Epub 2003 Oct 8.

PubMed [citation]

PMID:: 14534157

Milh M, Boutry-Kryza N, Sutera-Sardo J, Mignot C, Auvin S, Lacoste C, Villeneuve N, Roubertie A, Heron B, Carneiro M, Kaminska A, Altuzarra C, Blanchard G, Ville D, Barthez MA, Heron D, Gras D, Afenjar A, Dorison N, Doummar D, Billette de Villemeur T, An I, et al.

Orphanet J Rare Dis. 2013 May 22;8:80. doi: 10.1186/1750-1172-8-80.

PubMed [citation]

PMID:: 23692823
PMCID:: PMC3670812

See all PubMed Citations (4)

Details of each submission

From Invitae, SCV001592030.4

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (4)

Description

For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in KCNQ2 are known to be pathogenic (PMID: 14534157, 23692823, 27779742). This variant has not been reported in the literature in individuals with KCNQ2-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Met371Ilefs*18) in the KCNQ2 gene. It is expected to result in an absent or disrupted protein product.

#	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: Feb 28, 2024

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