chr3:38592996:G>T Detail (hg19) (SCN5A)

Go to:

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

Information

Genome

Assembly	Position
hg19	chr3:38,592,996-38,592,996
hg38	chr3:38,551,505-38,551,505 View the variant detail on this assembly version.

HGVS

SCN5A

Type	Transcript	Protein
RefSeq	NM_000335.4:c.4867C>A	NP_000326.2:p.Arg1623=
	NM_198056.2:c.4867C>A	NP_932173.1:p.Arg1623=
	NM_001099404.1:c.4867C>A	NP_001092874.1:p.Arg1623=
	NM_001160160.1:c.4867C>A	NP_001153632.1:p.Arg1623=
Ensemble	ENST00000333535.9:c.4867C>A	ENST00000333535.9:p.Arg1623=
	ENST00000413689.6:c.4867C>A	ENST00000413689.6:p.Arg1623=
	ENST00000414099.6:c.4813C>A	ENST00000414099.6:p.Arg1605=
	ENST00000423572.7:c.4864C>A	ENST00000423572.7:p.Arg1622=
	ENST00000449557.6:c.4705C>A	ENST00000449557.6:p.Arg1569=
	ENST00000450102.6:c.4705C>A	ENST00000450102.6:p.Arg1569=
	ENST00000455624.6:c.4768C>A	ENST00000455624.6:p.Arg1590=

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

JP	HGVD:[No Data.]
	ToMMo:[No Data.]
	NCBN:[No Data.]
	NCBN(Hondo):[No Data.]
	NCBN(Ryukyu):[No Data.]
East asia	ExAC:<0.001

Prediction

ClinVar

Clinical Significance	Likely benign
Review star
Show details

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
Likely benign	2023-09-08	criteria provided, multiple submitters, no conflicts	not provided	germline	Detail
Likely benign	2023-08-08	criteria provided, multiple submitters, no conflicts	Cardiac arrhythmia	germline	Detail
Likely benign	2020-10-08	criteria provided, single submitter		germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.360	SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000335.5(SCN5A):c.4864C>A (p.Arg1622=) AND not provided	ClinVar	Detail
NM_000335.5(SCN5A):c.4864C>A (p.Arg1622=) AND Cardiac arrhythmia	ClinVar	Detail
NM_000335.5(SCN5A):c.4864C>A (p.Arg1622=) AND Cardiovascular phenotype	ClinVar	Detail
NA	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: rs137854613 dbSNP
Genome: hg19
Position: chr3:38,592,996-38,592,996
Variant Type: snv
Reference Allele: G
Alternative Allele: T
East Asian Chromosome Counts (ExAC): 8644
East Asian Allele Counts (ExAC): 0
East Asian Heterozygous Counts (ExAC): 0
East Asian Homozygous Counts (ExAC): 0
East Asian Allele Frequency (ExAC): 0.0
Chromosome Counts in All Race (ExAC): 121156
Allele Counts in All Race (ExAC): 1
Heterozygous Counts in All Race (ExAC): 1
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 8.253821519363466E-6

Genome browser