chr11:2778009:G>A Detail (hg38) (KCNQ1)

Information

Genome

Assembly Position
hg19 chr11:2,799,239-2,799,239 View the variant detail on this assembly version.
hg38 chr11:2,778,009-2,778,009

HGVS

Type Transcript Protein
RefSeq NM_181798.1:c.1385G>A NP_861463.1:p.Gly462Asp
NM_000218.2:c.1766G>A NP_000209.2:p.Gly589Asp
Ensemble ENST00000335475.6:c.1385G>A ENST00000335475.6:p.Gly462Asp
Summary

MGeND

Clinical significance Pathogenic
Variant entry 1
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 Pathogenic
Review star
Show details
Links
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
COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
Pathogenic long qt syndrome germline MGS000001
(TMGS000154) 		Kenjiro Kosaki Keio University
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 2001-02-01 no assertion criteria provided long QT syndrome 1 germline Detail
Pathogenic 2001-02-01 no assertion criteria provided Jervell and Lange-Nielsen syndrome 1 germline Detail
not provided no assertion provided Congenital long QT syndrome germline Detail
Pathogenic 2016-11-22 criteria provided, single submitter not provided germline Detail
Pathogenic 2023-03-03 criteria provided, single submitter germline Detail
Pathogenic 2023-05-25 criteria provided, single submitter long QT syndrome germline Detail
Pathogenic 2019-12-31 criteria provided, single submitter Jervell and Lange-Nielsen syndrome 1,long QT syndrome 1 germline Detail
Pathogenic 2019-12-31 criteria provided, single submitter Jervell and Lange-Nielsen syndrome 1,long QT syndrome 1 germline Detail
Pathogenic 2019-04-28 criteria provided, single submitter Cardiac arrhythmia germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.585 Jervell-Lange Nielsen syndrome NA CLINVAR Detail
<0.001 Acquired long QT syndrome DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G... BeFree 17467628 Detail
0.121 Acquired long QT syndrome DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G... BeFree 17467628 Detail
0.417 long QT syndrome A total of six compound heterozygotes were identified who had the HERG R176W mut... BeFree 16754261 Detail
0.133 Congenital long QT syndrome NA CLINVAR Detail
0.573 Romano-Ward Syndrome NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND Long QT syndrome 1 ClinVar Detail
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND Jervell and Lange-Nielsen syndrome 1 ClinVar Detail
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND Congenital long QT syndrome ClinVar Detail
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND not provided ClinVar Detail
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND Cardiovascular phenotype ClinVar Detail
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND Long QT syndrome ClinVar Detail
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND multiple conditions ClinVar Detail
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND multiple conditions ClinVar Detail
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp) AND Cardiac arrhythmia ClinVar Detail
NA DisGeNET Detail
DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A--&g... DisGeNET Detail
DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A--&g... DisGeNET Detail
A total of six compound heterozygotes were identified who had the HERG R176W mutation in combination... DisGeNET 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
rs120074190 dbSNP
Genome
hg38
Position
chr11:2,778,009-2,778,009
Variant Type
snv
Reference Allele
G
Alternative Allele
A
East Asian Chromosome Counts (ExAC)
8640
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)
120680
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)
8.286377195889957E-6
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