RGD:405162343 Rat Genome Database

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Variant: RGD:405162343 -  Homo sapiens

RGD ID: 405162343
ClinVar ID: CV2895413
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUL3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 225,379,454
GRCh38 2 224,514,737
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NP_003581.1:p.Asn138=
NP_001244127.1:p.Asn144=
NP_001244126.1:p.Asn72=
NM_001257197.2:c.216C>T
More... 		09/15/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003562484 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR