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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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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000417372Illumina Laboratory Services, Illumina
criteria provided, single submitter

(ICSL Variant Classification 20161018)		Uncertain significance
(Jun 14, 2016) 		germlineclinical testing

ICSL_Variant_Classification_20161018.pdf

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000417372.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 10, 2024