RGD:15124869 Rat Genome Database

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Variant: RGD:15124869 -  Homo sapiens

RGD ID: 15124869
RS ID: rs1219646022
ClinVar ID: CV695396
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP7B1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 65,528,842
GRCh38 8 64,616,285
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001324112.2:c.260-4C>T
NM_004820.5:c.260-4C>T
NG_008338.2:g.187507C>T
NC_000008.11:g.64616285G>A
More... 		06/28/2017 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CYP7B1
Accession:NM_001324112
Location:INTRON

Gene Symbol:CYP7B1
Accession:NM_004820
Location:INTRON

Gene Symbol:CYP7B1
Accession:XM_017014002
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000874851 CLINVAR
dbSNP (RS) rs1219646022 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene CYP7B1 CLINVAR
OMIM 603711 CLINVAR