rs460267 Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

Variant: rs460267 -  Homo sapiens

RGD ID: 11609312
RS ID: rs460267
ClinVar ID: CV304550
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDE8B  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 76,722,891
GRCh38 5 77,427,066
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000005.10:g.77427066T>C
NC_000005.9:g.76722891T>C
NG_023364.2:g.251815T>C
NM_001349752.3:c.*512T>C
More... 		01/13/2018 3 prime utr variant benign none provided; Striatal degeneration, autosomal dominant 1
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:PDE8B
Accession:NM_001376068
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001029851
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376071
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376066
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_003719
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001349748
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376062
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376064
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376072
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376075
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376063
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001414623
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001414622
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376074
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001349750
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001029854
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001349753
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001349749
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376065
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001029853
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376069
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376067
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001349752
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376073
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001029852
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001349751
Location:3UTRS;EXON

Gene Symbol:PDE8B
Accession:NM_001376070
Location:3UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000366496 CLINVAR
  RCV004716398 CLINVAR
dbSNP (RS) rs460267 CLINVAR
MedGen C3661900 CLINVAR
  C4310808 CLINVAR
NCBI Gene PDE8B CLINVAR
OMIM 603390 CLINVAR
  609161 CLINVAR