RGD:11618445 Rat Genome Database

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Variant: RGD:11618445 -  Homo sapiens

RGD ID: 11618445
RS ID: rs45510192
ClinVar ID: CV326212
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNQ1  KCNQ1-AS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 2,869,715
GRCh38 11 2,848,485
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_287t1:c.*482G>A
LRG_287t2:c.*482G>A
LRG_287:g.408495G>A
NG_008935.1:g.408495G>A
More... 		05/13/2021 3 prime utr variant benign|likely benign Cardioauditory syndrome of Jervell and Lange-Nielsen; Deafness, congenital, and functional heart disease; Familial long QT syndrome; none provided; Prolonged QT interval in EKG and sudden death; Romano-Ward syndrome; Surdo-cardiac syndrome; Ventricular fibrillation with prolonged QT interval
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:KCNQ1
Accession:NM_001406837
Location:3UTRS;EXON

Gene Symbol:KCNQ1
Accession:NM_000218
Location:3UTRS;EXON

Gene Symbol:KCNQ1
Accession:NM_181798
Location:3UTRS;EXON

Gene Symbol:KCNQ1
Accession:NM_001406836
Location:3UTRS;EXON

Gene Symbol:KCNQ1
Accession:NM_001406839
Location:3UTRS;EXON

Gene Symbol:KCNQ1
Accession:NM_001406838
Location:3UTRS;EXON

Gene Symbol:KCNQ1-AS1
Accession:NR_130721
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000308155 CLINVAR
  RCV000313831 CLINVAR
  RCV000352333 CLINVAR
  RCV000390839 CLINVAR
  RCV000403746 CLINVAR
  RCV001683225 CLINVAR
dbSNP (RS) rs45510192 CLINVAR
MedGen C1141890 CLINVAR
  C1837014 CLINVAR
  C1865019 CLINVAR
  C3661900 CLINVAR
  C4551509 CLINVAR
  C4551647 CLINVAR
NCBI Gene KCNQ1 CLINVAR
  KCNQ1-AS1 CLINVAR
OMIM 192500 CLINVAR
  220400 CLINVAR
  607542 CLINVAR
  607554 CLINVAR
  609621 CLINVAR
SNOMED CT 442917000 CLINVAR