RGD:405235724 Rat Genome Database

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Variant: RGD:405235724 -  Homo sapiens

RGD ID: 405235724
ClinVar ID: CV3166346
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUL3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 225,367,809
GRCh38 2 224,503,092
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001257197.2:c.1180-20T>C
NM_003590.5:c.1378-20T>C
NM_001257198.2:c.1396-20T>C
NG_032169.1:g.87306T>C
More... 		03/19/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003853795 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR