chr3:38609803:C>T Detail (hg38) (SCN5A)

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

Information

Genome

Assembly	Position
hg19	chr3:38,651,294-38,651,294 View the variant detail on this assembly version.
hg38	chr3:38,609,803-38,609,803

HGVS

SCN5A

Type	Transcript	Protein
RefSeq	NM_000335.4:c.865G>A	NP_000326.2:p.Gly289Ser
	NM_198056.2:c.865G>A	NP_932173.1:p.Gly289Ser
	NM_001099404.1:c.865G>A	NP_001092874.1:p.Gly289Ser
	NM_001160160.1:c.865G>A	NP_001153632.1:p.Gly289Ser
Ensemble	ENST00000333535.9:c.865G>A	ENST00000333535.9:p.Gly289Ser
	ENST00000413689.6:c.865G>A	ENST00000413689.6:p.Gly289Ser
	ENST00000414099.6:c.865G>A	ENST00000414099.6:p.Gly289Ser
	ENST00000423572.7:c.865G>A	ENST00000423572.7:p.Gly289Ser
	ENST00000449557.6:c.865G>A	ENST00000449557.6:p.Gly289Ser
	ENST00000450102.6:c.865G>A	ENST00000450102.6:p.Gly289Ser
	ENST00000455624.6:c.865G>A	ENST00000455624.6:p.Gly289Ser

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	Uncertain significance
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	tgv249577031	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
not provided		no assertion provided	Congenital long QT syndrome	germline	Detail
Uncertain significance	2014-06-01	no assertion criteria provided	long QT syndrome	germline	Detail
Uncertain significance	2021-09-07	criteria provided, single submitter	not provided	germline	Detail
Uncertain significance	2022-08-31	criteria provided, single submitter	Brugada syndrome	germline	Detail
Uncertain significance	2023-08-15	criteria provided, multiple submitters, no conflicts	Cardiac arrhythmia	germline	Detail
Uncertain significance	2021-02-21	criteria provided, single submitter		germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.130	Congenital long QT syndrome	NA	CLINVAR		Detail
0.335	long QT syndrome	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000335.5(SCN5A):c.865G>A (p.Gly289Ser) AND Congenital long QT syndrome	ClinVar	Detail
NM_000335.5(SCN5A):c.865G>A (p.Gly289Ser) AND Long QT syndrome	ClinVar	Detail
NM_000335.5(SCN5A):c.865G>A (p.Gly289Ser) AND not provided	ClinVar	Detail
NM_000335.5(SCN5A):c.865G>A (p.Gly289Ser) AND Brugada syndrome	ClinVar	Detail
NM_000335.5(SCN5A):c.865G>A (p.Gly289Ser) AND Cardiac arrhythmia	ClinVar	Detail
NM_000335.5(SCN5A):c.865G>A (p.Gly289Ser) AND Cardiovascular phenotype	ClinVar	Detail
NA	DisGeNET	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: rs199473084 dbSNP
Genome: hg38
Position: chr3:38,609,803-38,609,803
Variant Type: snv
Reference Allele: C
Alternative Allele: T
East Asian Chromosome Counts (ExAC): 8620
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): 120598
Allele Counts in All Race (ExAC): 3
Heterozygous Counts in All Race (ExAC): 3
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 2.487603442843165E-5

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