RGD:152055571 Rat Genome Database

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Variant: RGD:152055571 -  Homo sapiens

RGD ID: 152055571
RS ID: rs767016709
ClinVar ID: CV1582150
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACOX2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 58,491,022
GRCh38 3 58,505,295
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003500.4:c.1984-9T>C
NG_052668.1:g.36908T>C
NC_000003.12:g.58505295A>G
NC_000003.11:g.58491022A>G
 08/25/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACOX2
Accession:XM_047449042
Location:INTRON

Gene Symbol:ACOX2
Accession:XM_005265505
Location:INTRON

Gene Symbol:ACOX2
Accession:XM_006713340
Location:INTRON

Gene Symbol:ACOX2
Accession:NM_003500
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002089662 CLINVAR
dbSNP (RS) rs767016709 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACOX2 CLINVAR
OMIM 601641 CLINVAR