RGD:11659344 Rat Genome Database

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Variant: RGD:11659344 -  Homo sapiens

RGD ID: 11659344
RS ID: rs886059076
ClinVar ID: CV297056
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB33B  RAB33B-AS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 140,375,187
GRCh38 4 139,454,033
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.139454033C>T
NM_031296.1:c.-163C>T
NG_051587.1:g.5802C>T
NR_159963.1:n.9G>A
More... 		06/14/2016 5 prime utr variant|non-coding transcript variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RAB33B-AS1
Accession:NR_159964
Location:EXON;NON-CODING

Gene Symbol:RAB33B-AS1
Accession:NR_159963
Location:EXON;NON-CODING

Gene Symbol:RAB33B
Accession:XM_011532299
Location:INTRON

Gene Symbol:RAB33B
Accession:NM_031296
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000356865 CLINVAR
dbSNP (RS) rs886059076 CLINVAR
MedGen C1846431 CLINVAR
NCBI Gene 107984036 CLINVAR
  LOC129993109 CLINVAR
  RAB33B CLINVAR
OMIM 605950 CLINVAR
  607326 CLINVAR