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NM_001330260.2(SCN8A):c.2549G>A (p.Arg850Gln) AND Complex neurodevelopmental disorder

Germline classification:
not provided (1 submission)
Review status:
no classification 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:
RCV003992189.1

Allele description [Variation Report for NM_001330260.2(SCN8A):c.2549G>A (p.Arg850Gln)]

NM_001330260.2(SCN8A):c.2549G>A (p.Arg850Gln)

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.2549G>A (p.Arg850Gln)
Other names:
NM_001177984.2(SCN8A):c.2549G>A(p.Arg850Gln); NM_014191.3(SCN8A):c.2549G>A(p.Arg850Gln); NP_055006.1:p.(Arg850Gln)
HGVS:
  • NC_000012.12:g.51765675G>A
  • NG_021180.3:g.180718G>A
  • NM_001177984.3:c.2549G>A
  • NM_001330260.2:c.2549G>AMANE SELECT
  • NM_001369788.1:c.2549G>A
  • NM_014191.4:c.2549G>A
  • NP_001171455.1:p.Arg850Gln
  • NP_001317189.1:p.Arg850Gln
  • NP_001356717.1:p.Arg850Gln
  • NP_055006.1:p.Arg850Gln
  • NP_055006.1:p.Arg850Gln
  • LRG_1389t1:c.2549G>A
  • LRG_1389t2:c.2549G>A
  • LRG_1389:g.180718G>A
  • LRG_1389p1:p.Arg850Gln
  • LRG_1389p2:p.Arg850Gln
  • NC_000012.11:g.52159459G>A
  • NM_014191.2:c.2549G>A
  • NM_014191.3:c.2549G>A
  • NM_014191.4:c.2549G>A
  • Q9UQD0:p.Arg850Gln
  • p.R850Q
Protein change:
R850Q
Links:
UniProtKB: Q9UQD0#VAR_076604
Molecular consequence:
  • NM_001177984.3:c.2549G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330260.2:c.2549G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001369788.1:c.2549G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014191.4:c.2549G>A - missense variant - [Sequence Ontology: SO:0001583]
Functional consequence:
  • Increase in resurgent current [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0099]
  • Increase in slope of activation [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0035]
  • Increase in slope of fast inactivation [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0073]
  • Mild hyperpolarizing shift of voltage dependence of activation [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0029]
  • Moderate increase in persistent current [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0042]
  • Normal peak current [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0096]
  • Normal rate of recovery from fast inactivation [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0054]
  • Normal voltage dependence of fast inactivation [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0070]
  • Overall gain-of-function effect with respect to biophysical channel activity [Functional Epilepsy Nomenclature for Ion Channels: FENICS-0140]

Condition(s)

Name:
Complex neurodevelopmental disorder
Identifiers:
MONDO: MONDO:0100038; MedGen: C5568766

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV004809232Channelopathy-Associated Epilepsy Research Center
no classification provided
not providednot applicableliterature only

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providednot applicablenot applicablenot providednot providednot providednot providednot providedliterature only

Citations

PubMed

Distinct functional alterations in SCN8A epilepsy mutant channels.

Pan Y, Cummins TR.

J Physiol. 2020 Jan;598(2):381-401. doi: 10.1113/JP278952. Epub 2019 Dec 31.

PubMed [citation]
PMID:
31715021
PMCID:
PMC7216308

Details of each submission

From Channelopathy-Associated Epilepsy Research Center, SCV004809232.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedliterature only PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1not applicablenot applicablenot providednot providednot providednot providednot providednot providednot provided

Last Updated: May 19, 2024