rs776990308 Rat Genome Database

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Variant: rs776990308 -  Homo sapiens

RGD ID: 12845619
RS ID: rs776990308
ClinVar ID: CV368838
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP2U1  CYP2U1-AS1  LOC107986298  LOC127401313  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 108,852,778
GRCh38 4 107,931,622
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_183075.2:c.-22C>A
NG_007961.1:g.5062C>A
NC_000004.12:g.107931622C>A
NC_000004.11:g.108852778C>A
More... 		10/06/2016 5 prime utr variant likely benign AllHighlyPenetrant

Gene Symbol:CYP2U1
Accession:NM_183075
Location:5UTRS;EXON

Gene Symbol:CYP2U1
Accession:XM_005262717
Location:5UTRS;EXON

Gene Symbol:CYP2U1
Accession:XM_005262720
Location:5UTRS;EXON

Gene Symbol:CYP2U1-AS1
Accession:NR_125929
Location:INTRON;NON-CODING

Gene Symbol:LOC107986298
Accession:XR_001741784
Location:INTRON;NON-CODING

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Database
Acc Id
Source(s)
ClinVar RCV000440151 CLINVAR
dbSNP (RS) rs776990308 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene 101929595 CLINVAR
  CYP2U1 CLINVAR
OMIM 610670 CLINVAR