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NM_001165963.4(SCN1A):c.1092C>A (p.Ser364Arg) AND not provided

Germline classification:
Conflicting interpretations of pathogenicity (2 submissions)
Last evaluated:
May 1, 2024
Review status:
criteria provided, conflicting classifications
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:
RCV000728727.5

Allele description [Variation Report for NM_001165963.4(SCN1A):c.1092C>A (p.Ser364Arg)]

NM_001165963.4(SCN1A):c.1092C>A (p.Ser364Arg)

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.1092C>A (p.Ser364Arg)
HGVS:
  • NC_000002.12:g.166047705G>T
  • NG_011906.1:g.30935C>A
  • NM_001165963.1:c.1092C>A
  • NM_001165963.4:c.1092C>AMANE SELECT
  • NM_001165964.3:c.1092C>A
  • NM_001202435.3:c.1092C>A
  • NM_001353948.2:c.1092C>A
  • NM_001353949.2:c.1092C>A
  • NM_001353950.2:c.1092C>A
  • NM_001353951.2:c.1092C>A
  • NM_001353952.2:c.1092C>A
  • NM_001353954.2:c.1092C>A
  • NM_001353955.2:c.1092C>A
  • NM_001353957.2:c.1092C>A
  • NM_001353958.2:c.1092C>A
  • NM_001353960.2:c.1092C>A
  • NM_001353961.2:c.-1334C>A
  • NM_006920.6:c.1092C>A
  • NP_001159435.1:p.Ser364Arg
  • NP_001159436.1:p.Ser364Arg
  • NP_001189364.1:p.Ser364Arg
  • NP_001340877.1:p.Ser364Arg
  • NP_001340878.1:p.Ser364Arg
  • NP_001340879.1:p.Ser364Arg
  • NP_001340880.1:p.Ser364Arg
  • NP_001340881.1:p.Ser364Arg
  • NP_001340883.1:p.Ser364Arg
  • NP_001340884.1:p.Ser364Arg
  • NP_001340886.1:p.Ser364Arg
  • NP_001340887.1:p.Ser364Arg
  • NP_001340889.1:p.Ser364Arg
  • NP_008851.3:p.Ser364Arg
  • LRG_8:g.30935C>A
  • NC_000002.11:g.166904215G>T
  • NR_148667.2:n.1478C>A
Protein change:
S364R
Links:
dbSNP: rs766332635
NCBI 1000 Genomes Browser:
rs766332635
Molecular consequence:
  • NM_001353961.2:c.-1334C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001165963.4:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001165964.3:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001202435.3:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353948.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353949.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353950.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353951.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353952.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353954.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353955.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353957.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353958.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353960.2:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_006920.6:c.1092C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_148667.2:n.1478C>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000856335Eurofins Ntd Llc (ga)
criteria provided, single submitter

(EGL Classification Definitions 2015)		Uncertain significance
(Aug 21, 2017) 		germlineclinical testing

Citation Link,

SCV005078087GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Pathogenic
(May 1, 2024) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Eurofins Ntd Llc (ga), SCV000856335.1

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

From GeneDx, SCV005078087.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Jul 23, 2024