RGD:11592592 Rat Genome Database

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Variant: RGD:11592592 -  Homo sapiens

RGD ID: 11592592
RS ID: rs36211803
ClinVar ID: CV288871
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DRD3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 113,897,720
GRCh38 3 114,178,873
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001282563.2:c.-155-97C>T
NG_008842.2:g.25535C>T
NC_000003.12:g.114178873G>A
NC_000003.11:g.113897720G>A
More... 		01/12/2018 2kb upstream variant|5 prime utr variant likely benign Familial essential tremor; Tremor familial essential, 1
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DRD3
Accession:NM_033663
Location:5UTRS;EXON

Gene Symbol:DRD3
Accession:NM_000796
Location:5UTRS;EXON

Gene Symbol:DRD3
Accession:NM_001282563
Location:5UTRS;INTRON

Gene Symbol:DRD3
Accession:NM_001290809
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000340085 CLINVAR
dbSNP (RS) rs36211803 CLINVAR
MedGen C1860861 CLINVAR
NCBI Gene DRD3 CLINVAR
OMIM 126451 CLINVAR
  190300 CLINVAR