NM_001040142.2(SCN2A):c.-51-1733_-51-1732insGAT AND Seizures, benign familial infantile, 3

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 14, 2016
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:: RCV000404921.14

Allele description [Variation Report for NM_001040142.2(SCN2A):c.-51-1733_-51-1732insGAT]

NM_001040142.2(SCN2A):c.-51-1733_-51-1732insGAT

Gene:

SCN2A:sodium voltage-gated channel alpha subunit 2 [Gene - OMIM - HGNC]

Variant type:

Insertion

Cytogenetic location:

2q24.3

Genomic location:

Preferred name:

NM_001040142.2(SCN2A):c.-51-1733_-51-1732insGAT

HGVS:

NC_000002.12:g.165294040_165294041insGAT
NG_008143.1:g.59639_59640insGAT
NG_074009.1:g.402_403insGAT
NM_001040142.2:c.-51-1733_-51-1732insGATMANE SELECT
NM_001040143.2:c.-51-1733_-51-1732insGAT
NM_001371246.1:c.-51-1733_-51-1732insGAT
NM_001371247.1:c.-51-1733_-51-1732insGAT
NM_021007.2:c.-147_-146insGAT
NC_000002.11:g.166150550_166150551insGAT

Links:

dbSNP: rs780674346

NCBI 1000 Genomes Browser:

rs780674346

Molecular consequence:

NM_001040142.2:c.-51-1733_-51-1732insGAT - intron variant - [Sequence Ontology: SO:0001627]
NM_001040143.2:c.-51-1733_-51-1732insGAT - intron variant - [Sequence Ontology: SO:0001627]
NM_001371246.1:c.-51-1733_-51-1732insGAT - intron variant - [Sequence Ontology: SO:0001627]
NM_001371247.1:c.-51-1733_-51-1732insGAT - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Seizures, benign familial infantile, 3 (BFIS3)
Synonyms:: CONVULSIONS, BENIGN FAMILIAL INFANTILE, 3; Familial neonatal seizures
Identifiers:: MONDO: MONDO:0011904; MedGen: C1843140; Orphanet: 140927; Orphanet: 306; OMIM: 607745

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000417372	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification 20161018)	Uncertain significance (Jun 14, 2016)	germline	clinical testing	ICSL_Variant_Classification_20161018.pdf Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000417372

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification 20161018)

Uncertain significance
(Jun 14, 2016)

germline

clinical testing

ICSL_Variant_Classification_20161018.pdf

Citation Link

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

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000417372.2

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

#	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: Apr 15, 2024

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