RGD:38463357 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:38463357 -  Homo sapiens

RGD ID: 38463357
RS ID: rs2019733406
ClinVar ID: CV920399
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NACC1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 13,248,957
GRCh38 19 13,138,143
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_052876.3:c.1325-4A>C
NM_052876.4:c.1325-4A>C
NC_000019.10:g.13138143A>C
NC_000019.9:g.13248957A>C
 01/15/2019 intron variant uncertain significance

Variant Details
Variant Transcripts
Gene Symbol:NACC1
Accession:XM_005259721
Location:INTRON

Gene Symbol:NACC1
Accession:XM_047438118
Location:INTRON

Gene Symbol:NACC1
Accession:NM_052876
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001198992 CLINVAR
dbSNP (RS) rs2019733406 CLINVAR
MedGen C4479333 CLINVAR
NCBI Gene NACC1 CLINVAR
OMIM 610672 CLINVAR
  617393 CLINVAR