RGD:150534969 Rat Genome Database

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Variant: RGD:150534969 -  Homo sapiens

RGD ID: 150534969
RS ID: rs77169716
ClinVar ID: CV1306735
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP7A1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 59,406,884
GRCh38 8 58,494,325
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000780.4:c.1039+181A>G
NC_000008.10:g.59406884T>C
NG_007969.1:g.10838A>G
NC_000008.11:g.58494325T>C
 10/01/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CYP7A1
Accession:NM_000780
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001757733 CLINVAR
dbSNP (RS) rs77169716 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CYP7A1 CLINVAR
OMIM 118455 CLINVAR