RGD:28898150 Rat Genome Database

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Variant: RGD:28898150 -  Homo sapiens

RGD ID: 28898150
RS ID: rs1691077506
ClinVar ID: CV883894
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CUL3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 225,335,004
GRCh38 2 224,470,287
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003590.5:c.*3958C>T
NC_000002.12:g.224470287G>A
NM_003590.4:c.*3958C>T
NM_001257197.2:c.*3958C>T
More... 		01/13/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CUL3
Accession:XM_011511995
Location:3UTRS;EXON

Gene Symbol:CUL3
Accession:XM_047446024
Location:3UTRS;EXON

Gene Symbol:CUL3
Accession:NM_001257197
Location:3UTRS;EXON

Gene Symbol:CUL3
Accession:XM_011511996
Location:3UTRS;EXON

Gene Symbol:CUL3
Accession:NM_003590
Location:3UTRS;EXON

Gene Symbol:CUL3
Accession:NM_001257198
Location:3UTRS;EXON

Gene Symbol:CUL3
Accession:XM_006712800
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001141856 CLINVAR
dbSNP (RS) rs1691077506 CLINVAR
MedGen C3469606 CLINVAR
NCBI Gene CUL3 CLINVAR
OMIM 603136 CLINVAR
  614496 CLINVAR