RGD:11585585 Rat Genome Database

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Variant: RGD:11585585 -  Homo sapiens

RGD ID: 11585585
RS ID: rs654561
ClinVar ID: CV282901
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DHCR24  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 55,316,082
GRCh38 1 54,850,409
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_008839.1:g.41840T>G
NC_000001.11:g.54850409A>C
NC_000001.10:g.55316082A>C
NM_014762.4:c.*1824T>G
More... 		06/14/2016 3 prime utr variant benign antenatal <1 / 1 000 000
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:DHCR24
Accession:NM_014762
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000281973 CLINVAR
dbSNP (RS) rs654561 CLINVAR
MedGen C1865596 CLINVAR
NCBI Gene DHCR24 CLINVAR
OMIM 602398 CLINVAR
  606418 CLINVAR