U.S. flag

An official website of the United States government

NM_000335.5(SCN5A):c.206G>A (p.Gly69Asp) AND Cardiac arrhythmia

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Aug 28, 2023
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV001840998.13

Allele description [Variation Report for NM_000335.5(SCN5A):c.206G>A (p.Gly69Asp)]

NM_000335.5(SCN5A):c.206G>A (p.Gly69Asp)

Gene:
SCN5A:sodium voltage-gated channel alpha subunit 5 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3p22.2
Genomic location:
Preferred name:
NM_000335.5(SCN5A):c.206G>A (p.Gly69Asp)
Other names:
p.Gly69Asp
HGVS:
  • NC_000003.12:g.38633102C>T
  • NG_008934.1:g.21571G>A
  • NM_000335.5:c.206G>AMANE SELECT
  • NM_001099404.2:c.206G>A
  • NM_001099405.2:c.206G>A
  • NM_001160160.2:c.206G>A
  • NM_001160161.2:c.206G>A
  • NM_001354701.2:c.206G>A
  • NM_198056.3:c.206G>A
  • NP_000326.2:p.Gly69Asp
  • NP_001092874.1:p.Gly69Asp
  • NP_001092875.1:p.Gly69Asp
  • NP_001153632.1:p.Gly69Asp
  • NP_001153633.1:p.Gly69Asp
  • NP_001341630.1:p.Gly69Asp
  • NP_932173.1:p.Gly69Asp
  • LRG_289t1:c.206G>A
  • LRG_289:g.21571G>A
  • NC_000003.11:g.38674593C>T
  • NM_198056.2:c.206G>A
Protein change:
G69D
Links:
dbSNP: rs758404546
NCBI 1000 Genomes Browser:
rs758404546
Molecular consequence:
  • NM_000335.5:c.206G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001099404.2:c.206G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001099405.2:c.206G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001160160.2:c.206G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001160161.2:c.206G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354701.2:c.206G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198056.3:c.206G>A - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Cardiac arrhythmia
Synonyms:
Cardiac rhythm disease
Identifiers:
EFO: EFO_0004269; MONDO: MONDO:0007263; MedGen: C0003811; Human Phenotype Ontology: HP:0011675

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
SCV001354290Color Diagnostics, LLC DBA Color Health
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Aug 17, 2023) 		germlineclinical testing

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

SCV004827871All of Us Research Program, National Institutes of Health
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain Significance
(Aug 28, 2023) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided108544not 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 Color Diagnostics, LLC DBA Color Health, SCV001354290.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This missense variant replaces glycine with aspartic acid at codon 69 of the SCN5A protein. Computational prediction suggests that this variant may have deleterious impact on protein structure and function (internally defined REVEL score threshold >= 0.7, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with SCN5A-related disorders in the literature. This variant has been identified in 5/247674 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

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

From All of Us Research Program, National Institutes of Health, SCV004827871.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

This missense variant replaces glycine with aspartic acid at codon 69 of the SCN5A protein. Computational prediction suggests that this variant may have deleterious impact on protein structure and function (internally defined REVEL score threshold >= 0.7, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with SCN5A-related disorders in the literature. This variant has been identified in 5/247674 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown108544not providednot provided1not providednot providednot provided

Last Updated: Nov 30, 2024