RGD:155960890 Rat Genome Database

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Variant: RGD:155960890 -  Homo sapiens

RGD ID: 155960890
ClinVar ID: CV1900464
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: CUL3  
Reference Nucleotide: CA
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 2 225,422,523 - 225,422,525
GRCh38 2 224,557,806 - 224,557,808
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.117_118del
NM_001257198.2:c.135_136del
NM_001257197.2:c.67-22165_67-22164del
NG_032169.1:g.32592_32593del
More... 		07/25/2022 frameshift variant pathogenic none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532   PMID:32341456  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003095838 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR