NM_000335.5(SCN5A):c.568C>G (p.Arg190Gly) AND Cardiac arrhythmia

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Nov 30, 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:: RCV001842390.12

Allele description [Variation Report for NM_000335.5(SCN5A):c.568C>G (p.Arg190Gly)]

NM_000335.5(SCN5A):c.568C>G (p.Arg190Gly)

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.568C>G (p.Arg190Gly)

Other names:

p.R190G:CGG>GGG

HGVS:

NC_000003.12:g.38620886G>C
NG_008934.1:g.33787C>G
NM_000335.5:c.568C>GMANE SELECT
NM_001099404.2:c.568C>G
NM_001099405.2:c.568C>G
NM_001160160.2:c.568C>G
NM_001160161.2:c.568C>G
NM_001354701.2:c.568C>G
NM_198056.3:c.568C>G
NP_000326.2:p.Arg190Gly
NP_001092874.1:p.Arg190Gly
NP_001092875.1:p.Arg190Gly
NP_001153632.1:p.Arg190Gly
NP_001153633.1:p.Arg190Gly
NP_001341630.1:p.Arg190Gly
NP_932173.1:p.Arg190Gly
NP_932173.1:p.Arg190Gly
LRG_289t1:c.568C>G
LRG_289:g.33787C>G
LRG_289p1:p.Arg190Gly
NC_000003.11:g.38662377G>C
NM_198056.2:c.568C>G

Protein change:

R190G

Links:

dbSNP: rs199473068

NCBI 1000 Genomes Browser:

rs199473068

Molecular consequence:

NM_000335.5:c.568C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001099404.2:c.568C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001099405.2:c.568C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001160160.2:c.568C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001160161.2:c.568C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001354701.2:c.568C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_198056.3:c.568C>G - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

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

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001346736	Color Diagnostics, LLC DBA Color Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Feb 25, 2019)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV004827153	All of Us Research Program, National Institutes of Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely Benign (Nov 30, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001346736

Color Diagnostics, LLC DBA Color Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(Feb 25, 2019)

germline

clinical testing

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

SCV004827153

All of Us Research Program, National Institutes of Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely Benign
(Nov 30, 2023)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	3	not provided	not provided	108544	not provided	clinical 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, SCV001346736.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From All of Us Research Program, National Institutes of Health, SCV004827153.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	3	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	108544	not provided	not provided		3	not provided	not provided	not provided

Last Updated: Oct 26, 2024

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