U.S. flag

An official website of the United States government

NM_001165963.4(SCN1A):c.472G>C (p.Glu158Gln) AND Severe myoclonic epilepsy in infancy

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Jan 1, 2019
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
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:
RCV001252613.3

Allele description [Variation Report for NM_001165963.4(SCN1A):c.472G>C (p.Glu158Gln)]

NM_001165963.4(SCN1A):c.472G>C (p.Glu158Gln)

Gene:
SCN1A:sodium voltage-gated channel alpha subunit 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q24.3
Genomic location:
Preferred name:
NM_001165963.4(SCN1A):c.472G>C (p.Glu158Gln)
Other names:
p.E158Q:GAA>CAA
HGVS:
  • NC_000002.12:g.166056412C>G
  • NG_011906.1:g.22228G>C
  • NM_001165963.4:c.472G>CMANE SELECT
  • NM_001165964.3:c.472G>C
  • NM_001202435.3:c.472G>C
  • NM_001353948.2:c.472G>C
  • NM_001353949.2:c.472G>C
  • NM_001353950.2:c.472G>C
  • NM_001353951.2:c.472G>C
  • NM_001353952.2:c.472G>C
  • NM_001353954.2:c.472G>C
  • NM_001353955.2:c.472G>C
  • NM_001353957.2:c.472G>C
  • NM_001353958.2:c.472G>C
  • NM_001353960.2:c.472G>C
  • NM_001353961.2:c.-1954G>C
  • NM_006920.6:c.472G>C
  • NP_001159435.1:p.Glu158Gln
  • NP_001159436.1:p.Glu158Gln
  • NP_001189364.1:p.Glu158Gln
  • NP_001340877.1:p.Glu158Gln
  • NP_001340878.1:p.Glu158Gln
  • NP_001340879.1:p.Glu158Gln
  • NP_001340880.1:p.Glu158Gln
  • NP_001340881.1:p.Glu158Gln
  • NP_001340883.1:p.Glu158Gln
  • NP_001340884.1:p.Glu158Gln
  • NP_001340886.1:p.Glu158Gln
  • NP_001340887.1:p.Glu158Gln
  • NP_001340889.1:p.Glu158Gln
  • NP_008851.3:p.Glu158Gln
  • LRG_8:g.22228G>C
  • NC_000002.11:g.166912922C>G
  • NM_001165963.1:c.472G>C
  • NR_148667.2:n.858G>C
Protein change:
E158Q
Links:
dbSNP: rs796053090
NCBI 1000 Genomes Browser:
rs796053090
Molecular consequence:
  • NM_001353961.2:c.-1954G>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001165963.4:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001165964.3:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001202435.3:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353948.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353949.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353950.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353951.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353952.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353954.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353955.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353957.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353958.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353960.2:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_006920.6:c.472G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NR_148667.2:n.858G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Severe myoclonic epilepsy in infancy (DRVT)
Synonyms:
Epilepsy, Myoclonic, Infantile, Severe; Dravet syndrome; Epileptic encephalopathy, early infantile, 6 (Dravet syndrome); See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0100135; MedGen: C0751122; Orphanet: 33069; OMIM: 607208

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001428372Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille
no assertion criteria provided
Likely pathogenic
(Jan 1, 2019) 		unknownclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille, SCV001428372.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 15, 2024