RGD:11652444 Rat Genome Database

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Variant: RGD:11652444 -  Homo sapiens

RGD ID: 11652444
RS ID: rs886059085
ClinVar ID: CV292307
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB33B  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 140,396,879
GRCh38 4 139,475,725
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.139475725A>G
NC_000004.11:g.140396879A>G
NM_031296.1:c.*2599A>G
NM_031296.3:c.*2599A>G
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RAB33B
Accession:XM_011532299
Location:3UTRS;EXON

Gene Symbol:RAB33B
Accession:NM_031296
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000304838 CLINVAR
dbSNP (RS) rs886059085 CLINVAR
MedGen C3714896 CLINVAR
NCBI Gene RAB33B CLINVAR
OMIM 605950 CLINVAR
  615222 CLINVAR