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NM_001330260.2(SCN8A):c.4924T>C (p.Phe1642Leu) AND Developmental and epileptic encephalopathy, 13

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 14, 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:
RCV001089737.1

Allele description [Variation Report for NM_001330260.2(SCN8A):c.4924T>C (p.Phe1642Leu)]

NM_001330260.2(SCN8A):c.4924T>C (p.Phe1642Leu)

Gene:
SCN8A:sodium voltage-gated channel alpha subunit 8 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
12q13.13
Genomic location:
Preferred name:
NM_001330260.2(SCN8A):c.4924T>C (p.Phe1642Leu)
HGVS:
  • NC_000012.12:g.51806410T>C
  • NG_021180.3:g.221453T>C
  • NM_001177984.3:c.4801T>C
  • NM_001330260.2:c.4924T>CMANE SELECT
  • NM_001369788.1:c.4801T>C
  • NM_014191.4:c.4924T>C
  • NP_001171455.1:p.Phe1601Leu
  • NP_001317189.1:p.Phe1642Leu
  • NP_001356717.1:p.Phe1601Leu
  • NP_055006.1:p.Phe1642Leu
  • LRG_1389t1:c.4924T>C
  • LRG_1389t2:c.4924T>C
  • LRG_1389:g.221453T>C
  • LRG_1389p1:p.Phe1642Leu
  • LRG_1389p2:p.Phe1642Leu
  • NC_000012.11:g.52200194T>C
  • NM_014191.3:c.4924T>C
  • p.Phe1642Leu
Protein change:
F1601L
Links:
dbSNP: rs1938703650
NCBI 1000 Genomes Browser:
rs1938703650
Molecular consequence:
  • NM_001177984.3:c.4801T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330260.2:c.4924T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001369788.1:c.4801T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014191.4:c.4924T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Developmental and epileptic encephalopathy, 13 (DEE13)
Synonyms:
Early infantile epileptic encephalopathy 13; SCN8A-Related Epilepsy
Identifiers:
MONDO: MONDO:0013801; MedGen: C3281191; Orphanet: 442835; OMIM: 614558

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001245224Laboratory of Inherited Metabolic Diseases, Research centre for medical genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Feb 14, 2020) 		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 Laboratory of Inherited Metabolic Diseases, Research centre for medical genetics, SCV001245224.1

#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: Aug 5, 2023