chr3:38566426:C>A Detail (hg38) (SCN5A)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr3:38,607,917-38,607,917 View the variant detail on this assembly version.
hg38	chr3:38,566,426-38,566,426

HGVS

SCN5A

Type	Transcript	Protein
RefSeq	NM_000335.4:c.3823G>T	NP_000326.2:p.Asp1275Tyr
	NM_198056.2:c.3823G>T	NP_932173.1:p.Asp1275Tyr
	NM_001099404.1:c.3823G>T	NP_001092874.1:p.Asp1275Tyr
	NM_001160160.1:c.3823G>T	NP_001153632.1:p.Asp1275Tyr
Ensemble	ENST00000333535.9:c.3823G>T	ENST00000333535.9:p.Asp1275Tyr
	ENST00000413689.6:c.3823G>T	ENST00000413689.6:p.Asp1275Tyr
	ENST00000414099.6:c.3823G>T	ENST00000414099.6:p.Asp1275Tyr
	ENST00000423572.7:c.3820G>T	ENST00000423572.7:p.Asp1274Tyr
	ENST00000449557.6:c.3661G>T	ENST00000449557.6:p.Asp1221Tyr
	ENST00000450102.6:c.3661G>T	ENST00000450102.6:p.Asp1221Tyr
	ENST00000455624.6:c.3820G>T	ENST00000455624.6:p.Asp1274Tyr

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
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Links

SCN5A

Type	Database	ID	Link
Gene	MIM	600163	OMIM
	HGNC	10593	HGNC
	Ensembl	ENSG00000183873	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2014-01-15	criteria provided, single submitter	not provided	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.837	Brugada Syndrome (disorder)	NA	CLINVAR		Detail
0.360	CARDIOMYOPATHY, DILATED, 1E	NA	CLINVAR		Detail
0.240	Atrial fibrillation, familial, 10	NA	CLINVAR		Detail
0.133	Cardiomyopathy, Dilated	The D1275N SCN5A mutation has been associated with a range of unusual phenotypes...	BeFree	21824921	Detail
0.133	Cardiomyopathy, Dilated	The aim of this study was to generate and characterize a transgenic zebrafish ar...	BeFree	23791817	Detail

Annotation

Annotations

Descrption	Source	Links
NM_000335.5(SCN5A):c.3820G>T (p.Asp1274Tyr) AND not provided	ClinVar	Detail
NA	DisGeNET	Detail
NA	DisGeNET	Detail
NA	DisGeNET	Detail
The D1275N SCN5A mutation has been associated with a range of unusual phenotypes, including conducti...	DisGeNET	Detail
The aim of this study was to generate and characterize a transgenic zebrafish arrhythmia model harbo...	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs137854618 dbSNP
Genome: hg38
Position: chr3:38,566,426-38,566,426
Variant Type: snv
Reference Allele: C
Alternative Allele: A

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