RGD:14705902 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:14705902 -  Homo sapiens

RGD ID: 14705902
RS ID: rs11897687
ClinVar ID: CV658194
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TTC21B  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 166,764,598
GRCh38 2 165,908,088
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_024753.5:c.2462-304A>G
NG_030345.1:g.50751A>G
NC_000002.12:g.165908088T>C
NC_000002.11:g.166764598T>C
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TTC21B
Accession:XM_047445870
Location:INTRON

Gene Symbol:TTC21B
Accession:XM_017004967
Location:INTRON

Gene Symbol:TTC21B
Accession:XM_006712761
Location:INTRON

Gene Symbol:TTC21B
Accession:XM_011511871
Location:INTRON

Gene Symbol:TTC21B
Accession:NM_024753
Location:INTRON

Gene Symbol:TTC21B
Accession:XM_011511872
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000826349 CLINVAR
dbSNP (RS) rs11897687 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TTC21B CLINVAR
OMIM 612014 CLINVAR