RGD:11591828 Rat Genome Database

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Variant: RGD:11591828 -  Homo sapiens

RGD ID: 11591828
RS ID: rs75661332
ClinVar ID: CV292299
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB33B  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 140,395,683
GRCh38 4 139,474,529
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.139474529C>A
NC_000004.11:g.140395683C>A
NM_031296.1:c.*1403C>A
NG_051587.1:g.26298C>A
More... 		06/14/2016 3 prime utr variant likely benign
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 RCV000332942 CLINVAR
dbSNP (RS) rs75661332 CLINVAR
MedGen C3714896 CLINVAR
NCBI Gene RAB33B CLINVAR
OMIM 605950 CLINVAR
  615222 CLINVAR