rs200282209 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: rs200282209 -  Homo sapiens

RGD ID: 15169297
RS ID: rs200282209
ClinVar ID: CV743640
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATAD3A  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 1,459,352
GRCh38 1 1,523,972
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001170535.3:c.1089+8C>T
NM_018188.5:c.1233+8C>T
NG_053035.1:g.16830C>T
NC_000001.11:g.1523972C>T
More... 		11/01/2024 intron variant benign|likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:ATAD3A
Accession:NM_018188
Location:INTRON

Gene Symbol:ATAD3A
Accession:XM_047424290
Location:INTRON

Gene Symbol:ATAD3A
Accession:XM_047424289
Location:INTRON

Gene Symbol:ATAD3A
Accession:NM_001170536
Location:INTRON

Gene Symbol:ATAD3A
Accession:NM_001170535
Location:INTRON

Gene Symbol:ATAD3A
Accession:XM_047424288
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV000905029 CLINVAR
dbSNP (RS) rs200282209 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ATAD3A CLINVAR
OMIM 612316 CLINVAR