RGD:156364336 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: RGD:156364336 -  Homo sapiens

RGD ID: 156364336
ClinVar ID: CV1897194
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: USP8  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 50,784,878
GRCh38 15 50,492,681
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001283049.2:c.1917-20G>T
NM_001128610.3:c.2235-20G>T
NM_005154.5:c.2235-20G>T
NG_047101.2:g.73278G>T
More... 		05/22/2022 intron variant likely benign Familial spastic paraparesis
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV1897194Humanhereditary spastic paraplegia  IAGP 8554872ClinVar Annotator: match by term: Hereditary spastic paraplegiaClinVarPMID:28492532
Gene Symbol:USP8
Accession:NM_001128610
Location:INTRON

Gene Symbol:USP8
Accession:NM_005154
Location:INTRON

Gene Symbol:USP8
Accession:NM_001283049
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002581951 CLINVAR
MedGen C0037773 CLINVAR
NCBI Gene USP8 CLINVAR
OMIM 603158 CLINVAR
SNOMED CT 39912006 CLINVAR