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 Behavioral & Substance Use Disorder 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)
Variants search result for All species
(View Results for all Objects and Ontologies)

19 records found for search term Cav2
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156048353CV2271718single nucleotide variantNM_001233.5(CAV2):c.14C>A (p.Thr5Lys)not specified [RCV004130565]uncertain significance7116499795116499795Humanname
156163027CV2319598single nucleotide variantNM_001233.5(CAV2):c.10G>C (p.Glu4Gln)not specified [RCV004185150]uncertain significance7116499791116499791Humanname
401880153CV2769950single nucleotide variantNM_001233.5(CAV2):c.378G>A (p.Leu126=)not specified [RCV004353786]likely benign7116506010116506010Humanname
407482230CV3421910single nucleotide variantNM_001233.5(CAV2):c.77A>C (p.Glu26Ala)not specified [RCV004602617]uncertain significance7116499858116499858Humanname
597785424CV3641094single nucleotide variantNM_001233.5(CAV2):c.363C>G (p.Thr121=)not specified [RCV004900728]likely benign7116505995116505995Humanname
597785428CV3641097single nucleotide variantNM_001233.5(CAV2):c.376C>T (p.Leu126=)not specified [RCV004900729]likely benign7116506008116506008Humanname
15110410CV710723single nucleotide variantNM_001233.5(CAV2):c.441C>T (p.Ser147=)not provided [RCV000960896]benign7116506073116506073Humanname
156162255CV2246500single nucleotide variantNM_001233.5(CAV2):c.167T>A (p.Val56Glu)not specified [RCV004110258]uncertain significance7116500276116500276Humanname
156143096CV2393531single nucleotide variantNM_001233.5(CAV2):c.124C>T (p.Pro42Ser)not specified [RCV004231352]uncertain significance7116499905116499905Humanname
407482610CV3421911single nucleotide variantNM_001233.5(CAV2):c.233A>T (p.Glu78Val)not specified [RCV004602618]uncertain significance7116500342116500342Humanname
597760552CV3641095single nucleotide variantNM_001233.5(CAV2):c.188C>A (p.Thr63Lys)not specified [RCV004894770]uncertain significance7116500297116500297Humanname
597760554CV3641096single nucleotide variantNM_001233.5(CAV2):c.119G>A (p.Arg40Gln)not specified [RCV004894771]uncertain significance7116499900116499900Humanname
155934679CV2225369single nucleotide variantNM_001233.5(CAV2):c.355G>A (p.Val119Ile)not specified [RCV004100786]uncertain significance7116505987116505987Humanname
156101606CV2367671single nucleotide variantNM_001233.5(CAV2):c.442G>A (p.Val148Ile)not specified [RCV004211590]uncertain significance7116506074116506074Humanname
401779974CV2725802single nucleotide variantNM_001233.5(CAV2):c.472C>A (p.Gln158Lys)not specified [RCV004316276]uncertain significance7116506104116506104Humanname
405737351CV3291901single nucleotide variantNM_001233.5(CAV2):c.361A>G (p.Thr121Ala)not specified [RCV004430165]uncertain significance7116505993116505993Humanname
405737358CV3291902single nucleotide variantNM_001233.5(CAV2):c.437C>T (p.Thr146Met)not specified [RCV004430166]uncertain significance7116506069116506069Humanname
405737366CV3291903single nucleotide variantNM_001233.5(CAV2):c.452G>A (p.Cys151Tyr)not specified [RCV004430167]uncertain significance7116506084116506084Humanname
405737374CV3291904single nucleotide variantNM_001233.5(CAV2):c.470T>C (p.Leu157Pro)not specified [RCV004430168]uncertain significance7116506102116506102Humanname