RGD:13213741 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   new 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

Variant: RGD:13213741 -  Homo sapiens

RGD ID: 13213741
RS ID: rs764128952
ClinVar ID: CV430193
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WDR62  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 36,594,883
GRCh38 19 36,103,981
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NP_775907.4:p.Gly1380Ser
NG_028101.1:g.54101G>A
NC_000019.10:g.36103981G>A
NC_000019.9:g.36594883G>A
More... 		03/14/2016 missense variant uncertain significance AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:WDR62
Accession:XM_005258809
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526841
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438666
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438659
Location:INTRON

Gene Symbol:WDR62
Accession:NM_001411147
Location:INTRON

Gene Symbol:WDR62
Accession:NM_001411145
Location:INTRON

Gene Symbol:WDR62
Accession:NM_173636
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526842
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438657
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526840
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438661
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438663
Location:INTRON

Gene Symbol:WDR62
Accession:NM_001083961
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438662
Location:INTRON

Gene Symbol:WDR62
Accession:NM_001411146
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438660
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526844
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438665
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438658
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:WDR62
Accession:XM_011526843
Location:INTRON

Gene Symbol:WDR62
Accession:XM_017026665
Location:INTRON

Gene Symbol:WDR62
Accession:XM_047438664
Location:INTRON

Gene Symbol:WDR62
Accession:XR_001753671
Location:INTRON;NON-CODING

Gene Symbol:WDR62
Accession:XR_001753672
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000500382 CLINVAR
  RCV001755749 CLINVAR
dbSNP (RS) rs764128952 CLINVAR
MedGen CN169374 CLINVAR
  CN517202 CLINVAR
NCBI Gene WDR62 CLINVAR
OMIM 613583 CLINVAR