RGD:405161474 Rat Genome Database

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Variant: RGD:405161474 -  Homo sapiens

RGD ID: 405161474
ClinVar ID: CV3125118
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUL3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 225,342,920
GRCh38 2 224,478,203
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.1974G>A
NM_003590.5:c.2172G>A
NM_001257198.2:c.2190G>A
NG_032169.1:g.112195G>A
More... 		01/08/2024 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003818389 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR