RGD:156288027 Rat Genome Database

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Variant: RGD:156288027 -  Homo sapiens

RGD ID: 156288027
ClinVar ID: CV2327375
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUL3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 225,400,358
GRCh38 2 224,535,641
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003590.5:c.265G>A
NM_001257198.2:c.283G>A
NM_001257197.2:c.67G>A
NG_032169.1:g.54757G>A
More... 		12/01/2022 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CUL3
Accession:XM_006712800
Location:INTRON

Gene Symbol:CUL3
Accession:XM_047446024
Location:INTRON

Gene Symbol:CUL3
Accession:NM_001257197
Location:INTRON

Gene Symbol:CUL3
Accession:XM_011511996
Location:INTRON

Gene Symbol:CUL3
Accession:NM_001257198
Location:INTRON

Gene Symbol:CUL3
Accession:NM_003590
Location:INTRON

Gene Symbol:CUL3
Accession:XM_011511995
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002935391 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR