RGD:405211802 Rat Genome Database

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Variant: RGD:405211802 -  Homo sapiens

RGD ID: 405211802
ClinVar ID: CV2974349
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUL3  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 225,376,061
GRCh38 2 224,511,344
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.685+10A>C
NM_003590.5:c.883+10A>C
NM_001257198.2:c.901+10A>C
NG_032169.1:g.79054A>C
More... 		11/19/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003679506 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR