chr11:2570733:C>T Detail (hg38) (KCNQ1)

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

Information

Genome

Assembly	Position
hg19	chr11:2,591,963-2,591,963 View the variant detail on this assembly version.
hg38	chr11:2,570,733-2,570,733

HGVS

KCNQ1

Type	Transcript	Protein
RefSeq	NM_000218.2:c.583C>T	NP_000209.2:p.Arg195Trp
	NM_181798.1:c.202C>T	NP_861463.1:p.Arg68Trp
Ensemble	ENST00000155840.12:c.583C>T	ENST00000155840.12:p.Arg195Trp
	ENST00000335475.6:c.202C>T	ENST00000335475.6:p.Arg68Trp
	ENST00000496887.7:c.322C>T	ENST00000496887.7:p.Arg108Trp
	ENST00000646564.2:c.478-12702C>T
	ENST00000713725.1:c.583C>T	ENST00000713725.1:p.Arg195Trp

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

KCNQ1

Type	Database	ID	Link
Gene	MIM	607542	OMIM
	HGNC	6294	HGNC
	Ensembl	ENSG00000053918	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar	tgv216120082	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	2023-12-13	criteria provided, multiple submitters, no conflicts	long QT syndrome	germline	Detail
Uncertain significance	2022-12-19	criteria provided, single submitter	Cardiac arrhythmia	germline	Detail
Uncertain significance	2021-12-23	criteria provided, single submitter	Atrial fibrillation, familial, 3,Beckwith-Wiedemann syndrome,Jervell and Lange-Nielsen syndrome 1,long QT syndrome 1,Short QT syndrome type 2	unknown	Detail
Uncertain significance	2021-12-23	criteria provided, single submitter	Atrial fibrillation, familial, 3,Beckwith-Wiedemann syndrome,Jervell and Lange-Nielsen syndrome 1,long QT syndrome 1,Short QT syndrome type 2	unknown	Detail
Uncertain significance	2021-12-23	criteria provided, single submitter	Atrial fibrillation, familial, 3,Beckwith-Wiedemann syndrome,Jervell and Lange-Nielsen syndrome 1,long QT syndrome 1,Short QT syndrome type 2	unknown	Detail
Uncertain significance	2021-12-23	criteria provided, single submitter	Atrial fibrillation, familial, 3,Beckwith-Wiedemann syndrome,Jervell and Lange-Nielsen syndrome 1,long QT syndrome 1,Short QT syndrome type 2	unknown	Detail
Uncertain significance	2021-12-23	criteria provided, single submitter	Atrial fibrillation, familial, 3,Beckwith-Wiedemann syndrome,Jervell and Lange-Nielsen syndrome 1,long QT syndrome 1,Short QT syndrome type 2	unknown	Detail
Uncertain significance	2023-03-02	criteria provided, single submitter		germline	Detail
Uncertain significance	2024-02-15	criteria provided, single submitter	not specified	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.417	long QT syndrome	NA	CLINVAR		Detail
0.133	Congenital long QT syndrome	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND Congenital long QT syndrome	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND Long QT syndrome	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND Cardiac arrhythmia	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND multiple conditions	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND multiple conditions	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND multiple conditions	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND multiple conditions	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND multiple conditions	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND Cardiovascular phenotype	ClinVar	Detail
NM_000218.3(KCNQ1):c.583C>T (p.Arg195Trp) AND not specified	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: rs150172393 dbSNP
Genome: hg38
Position: chr11:2,570,733-2,570,733
Variant Type: snv
Reference Allele: C
Alternative Allele: T
East Asian Chromosome Counts (ExAC): 8580
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): 119800
Allele Counts in All Race (ExAC): 2
Heterozygous Counts in All Race (ExAC): 2
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 1.669449081803005E-5

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