RGD:14727825 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:14727825 -  Homo sapiens

RGD ID: 14727825
RS ID: rs73198184
ClinVar ID: CV660525
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EVC2  LOC126806961  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 5,642,612
GRCh38 4 5,640,885
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001166136.2:c.906-47G>C
NM_147127.5:c.1146-47G>C
NG_015821.1:g.73664G>C
NC_000004.12:g.5640885C>G
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:EVC2
Accession:XM_047449610
Location:INTRON

Gene Symbol:EVC2
Accession:XM_047449611
Location:INTRON

Gene Symbol:EVC2
Accession:XM_047449612
Location:INTRON

Gene Symbol:EVC2
Accession:XM_017007736
Location:INTRON

Gene Symbol:EVC2
Accession:NM_147127
Location:INTRON

Gene Symbol:EVC2
Accession:NM_001166136
Location:INTRON

Gene Symbol:EVC2
Accession:XM_017007738
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000834498 CLINVAR
dbSNP (RS) rs73198184 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EVC2 CLINVAR
  LOC126806961 CLINVAR
OMIM 607261 CLINVAR