RGD:150459295 Rat Genome Database

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Variant: RGD:150459295 -  Homo sapiens

RGD ID: 150459295
RS ID: rs16825685
ClinVar ID: CV1236076
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUL3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 225,434,256
GRCh38 2 224,569,539
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.66+15405G>C
NM_003590.5:c.67-11683G>C
NM_001257198.2:c.84+150G>C
NG_032169.1:g.20859G>C
More... 		11/11/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CUL3
Accession:XM_011511996
Location:INTRON

Gene Symbol:CUL3
Accession:XM_011511995
Location:INTRON

Gene Symbol:CUL3
Accession:NM_003590
Location:INTRON

Gene Symbol:CUL3
Accession:NM_001257198
Location:INTRON

Gene Symbol:CUL3
Accession:XM_047446024
Location:INTRON

Gene Symbol:CUL3
Accession:NM_001257197
Location:INTRON

Gene Symbol:CUL3
Accession:XM_006712800
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001649047 CLINVAR
dbSNP (RS) rs16825685 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR