RGD:150428855 Rat Genome Database

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Variant: RGD:150428855 -  Homo sapiens

RGD ID: 150428855
RS ID: rs147205401
ClinVar ID: CV1187281
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP51A1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 91,761,053
GRCh38 7 92,131,739
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001146152.2:c.-25+35A>C
NM_000786.4:c.291+35A>C
NG_007968.1:g.7788A>C
NC_000007.14:g.92131739T>G
More... 		08/26/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CYP51A1
Accession:NM_001146152
Location:5UTRS;INTRON

Gene Symbol:CYP51A1
Accession:NM_000786
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001562815 CLINVAR
dbSNP (RS) rs147205401 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CYP51A1 CLINVAR
OMIM 601637 CLINVAR