rs28499367 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: rs28499367 -  Homo sapiens

RGD ID: 150495069
RS ID: rs28499367
ClinVar ID: CV1282855
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP2U1  LOC107986298  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 108,868,411
GRCh38 4 107,947,255
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_183075.3:c.1127-121A>G
NG_007961.1:g.20695A>G
NC_000004.12:g.107947255A>G
NC_000004.11:g.108868411A>G
 06/26/2018 intron variant benign none provided

Gene Symbol:CYP2U1
Accession:NM_183075
Location:INTRON

Gene Symbol:CYP2U1
Accession:XM_005262717
Location:INTRON

Gene Symbol:CYP2U1
Accession:XM_005262720
Location:INTRON

Gene Symbol:LOC107986298
Accession:XR_001741784
Location:INTRON;NON-CODING

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001717309 CLINVAR
dbSNP (RS) rs28499367 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CYP2U1 CLINVAR
OMIM 610670 CLINVAR