RGD:405230581 Rat Genome Database

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Variant: RGD:405230581 -  Homo sapiens

RGD ID: 405230581
ClinVar ID: CV3157237
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUL3  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 225,346,640
GRCh38 2 224,481,923
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.1800A>G
NM_003590.5:c.1998A>G
NM_001257198.2:c.2016A>G
NG_032169.1:g.108475A>G
More... 		02/06/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003865187 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR