RGD:11663528 Rat Genome Database

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Variant: RGD:11663528 -  Homo sapiens

RGD ID: 11663528
RS ID: rs886056747
ClinVar ID: CV350073
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRNP  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 4,681,663
GRCh38 20 4,701,017
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009087.1:g.19867T>G
NC_000020.11:g.4701017T>G
NC_000020.10:g.4681663T>G
NM_000311.3:c.*1035T>G
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View
prion disease  (IAGP)


Variant Details
Variant Transcripts
Gene Symbol:PRNP
Accession:NM_183079
Location:3UTRS;EXON

Gene Symbol:PRNP
Accession:NM_001080123
Location:3UTRS;EXON

Gene Symbol:PRNP
Accession:NM_001271561
Location:3UTRS;EXON

Gene Symbol:PRNP
Accession:NM_000311
Location:3UTRS;EXON

Gene Symbol:PRNP
Accession:NM_001080121
Location:3UTRS;EXON

Gene Symbol:PRNP
Accession:NM_001080122
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000396906 CLINVAR
dbSNP (RS) rs886056747 CLINVAR
MedGen C5679775 CLINVAR
NCBI Gene PRNP CLINVAR
OMIM 176640 CLINVAR