RGD:152073916 Rat Genome Database

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Variant: RGD:152073916 -  Homo sapiens

RGD ID: 152073916
RS ID: rs904035084
ClinVar ID: CV1599146
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NR2F1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 92,923,604
GRCh38 5 93,587,898
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005654.6:c.464-19C>T
NG_034119.1:g.9562C>T
NC_000005.10:g.93587898C>T
NC_000005.9:g.92923604C>T
 12/12/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NR2F1
Accession:NM_005654
Location:INTRON

Gene Symbol:NR2F1
Accession:NM_001410754
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002148450 CLINVAR
dbSNP (RS) rs904035084 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NR2F1 CLINVAR
OMIM 132890 CLINVAR




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