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)

49 records found for search term Nvl
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401865624CV2778841single nucleotide variantNM_002533.4(NVL):c.16G>A (p.Ala6Thr)not specified [RCV004346733]uncertain significance1224330112224330112Humanname
405681531CV3352654single nucleotide variantNM_002533.4(NVL):c.95T>A (p.Ile32Asn)not specified [RCV004488787]uncertain significance1224326427224326427Humanname
329373489CV2434269single nucleotide variantNM_002533.4(NVL):c.259G>T (p.Ala87Ser)not specified [RCV004251944]uncertain significance1224317719224317719Humanname
401936781CV2816074single nucleotide variantNM_002533.4(NVL):c.2049G>A (p.Val683=)not provided [RCV003414800]likely benign1224275372224275372Humanname
401936782CV2816075single nucleotide variantNM_002533.4(NVL):c.1245G>A (p.Ser415=)not provided [RCV003414801]likely benign1224294347224294347Humanname
597644204CV3570212single nucleotide variantNM_002533.4(NVL):c.101T>C (p.Val34Ala)not specified [RCV004832759]uncertain significance1224326421224326421Humanname
597665339CV3570215single nucleotide variantNM_002533.4(NVL):c.241G>A (p.Glu81Lys)not specified [RCV004835580]uncertain significance1224317737224317737Humanname
597665354CV3570217single nucleotide variantNM_002533.4(NVL):c.119A>C (p.Gln40Pro)not specified [RCV004835582]uncertain significance1224326403224326403Humanname
598266510CV4004955single nucleotide variantNM_002533.4(NVL):c.211G>A (p.Glu71Lys)not specified [RCV005388158]uncertain significance1224317767224317767Humanname
8624904CV80020single nucleotide variantNM_002533.3(NVL):c.2025C>T (p.Pro675=)Malignant melanoma [RCV000060096]not provided1224275396224275396Humanname
156203584CV2234630single nucleotide variantNM_002533.4(NVL):c.844A>G (p.Ile282Val)not specified [RCV004102594]uncertain significance1224303839224303839Humanname
156191931CV2301849single nucleotide variantNM_002533.4(NVL):c.626A>C (p.Asp209Ala)not specified [RCV004156643]uncertain significance1224305156224305156Humanname
155991559CV2384295single nucleotide variantNM_002533.4(NVL):c.380A>G (p.Tyr127Cys)not specified [RCV004227680]uncertain significance1224308226224308226Humanname
329379961CV2444099single nucleotide variantNM_002533.4(NVL):c.616G>A (p.Asp206Asn)not specified [RCV004260842]uncertain significance1224305166224305166Humanname
329382695CV2445404single nucleotide variantNM_002533.4(NVL):c.311A>G (p.Asp104Gly)not specified [RCV004257477]uncertain significance1224311831224311831Humanname
401780726CV2727534single nucleotide variantNM_002533.4(NVL):c.434A>G (p.Glu145Gly)not specified [RCV004329727]uncertain significance1224308172224308172Humanname
405681521CV3352652single nucleotide variantNM_002533.4(NVL):c.324A>C (p.Glu108Asp)not specified [RCV004488785]uncertain significance1224311818224311818Humanname
405681526CV3352653single nucleotide variantNM_002533.4(NVL):c.515G>A (p.Gly172Glu)not specified [RCV004488786]uncertain significance1224308091224308091Humanname
597665307CV3570210single nucleotide variantNM_002533.4(NVL):c.814A>G (p.Met272Val)not specified [RCV004835576]uncertain significance1224304747224304747Humanname
597665317CV3570211single nucleotide variantNM_002533.4(NVL):c.656G>A (p.Arg219Gln)not specified [RCV004835577]uncertain significance1224305126224305126Humanname
597665333CV3570214single nucleotide variantNM_002533.4(NVL):c.319A>T (p.Met107Leu)not specified [RCV004835579]uncertain significance1224311823224311823Humanname
598266502CV4004953single nucleotide variantNM_002533.4(NVL):c.575G>A (p.Cys192Tyr)not specified [RCV005388156]uncertain significance1224308031224308031Humanname
598266513CV4004957single nucleotide variantNM_002533.4(NVL):c.590C>T (p.Pro197Leu)not specified [RCV005388159]uncertain significance1224308016224308016Humanname
8624905CV80021single nucleotide variantNM_002533.3(NVL):c.395C>T (p.Pro132Leu)Malignant melanoma [RCV000060097]not provided1224308211224308211Humanname
156261621CV2204916single nucleotide variantNM_002533.4(NVL):c.1283G>A (p.Arg428Gln)not specified [RCV004075155]uncertain significance1224294309224294309Humanname
156221954CV2208896single nucleotide variantNM_002533.4(NVL):c.1627G>A (p.Glu543Lys)not specified [RCV004085264]uncertain significance1224287942224287942Humanname
156190012CV2301691single nucleotide variantNM_002533.4(NVL):c.1930A>C (p.Ile644Leu)not specified [RCV004156515]uncertain significance1224281155224281155Humanname
156302268CV2311821single nucleotide variantNM_002533.4(NVL):c.1289T>C (p.Ile430Thr)not specified [RCV004170670]uncertain significance1224294303224294303Humanname
156078149CV2331940single nucleotide variantNM_002533.4(NVL):c.1207C>T (p.Arg403Trp)not specified [RCV004186591]uncertain significance1224294385224294385Humanname
329374240CV2443794single nucleotide variantNM_002533.4(NVL):c.1105A>G (p.Ile369Val)not specified [RCV004258135]uncertain significance1224296576224296576Humanname
329373787CV2452665single nucleotide variantNM_002533.4(NVL):c.2410G>T (p.Ala804Ser)not specified [RCV004275228]uncertain significance1224233246224233246Humanname
401884682CV2786545single nucleotide variantNM_002533.4(NVL):c.2546G>A (p.Arg849His)not specified [RCV004363694]uncertain significance1224227651224227651Humanname
405681481CV3352644single nucleotide variantNM_002533.4(NVL):c.1237C>T (p.Pro413Ser)not specified [RCV004488777]uncertain significance1224294355224294355Humanname
405681485CV3352645single nucleotide variantNM_002533.4(NVL):c.1361C>T (p.Pro454Leu)not specified [RCV004488778]uncertain significance1224289698224289698Humanname
405681492CV3352646single nucleotide variantNM_002533.4(NVL):c.1366G>A (p.Ala456Thr)not specified [RCV004488779]likely benign1224289693224289693Humanname
405681497CV3352647single nucleotide variantNM_002533.4(NVL):c.1460A>G (p.Asn487Ser)not specified [RCV004488780]likely benign1224289599224289599Humanname
405681502CV3352648single nucleotide variantNM_002533.4(NVL):c.1612C>G (p.Gln538Glu)not specified [RCV004488781]uncertain significance1224287957224287957Humanname
405681507CV3352649single nucleotide variantNM_002533.4(NVL):c.2125A>T (p.Met709Leu)not specified [RCV004488782]uncertain significance1224268091224268091Humanname
405681512CV3352650single nucleotide variantNM_002533.4(NVL):c.2440A>G (p.Ser814Gly)not specified [RCV004488783]uncertain significance1224233216224233216Humanname
405681517CV3352651single nucleotide variantNM_002533.4(NVL):c.2545C>T (p.Arg849Cys)not specified [RCV004488784]uncertain significance1224227652224227652Humanname
407522200CV3459075single nucleotide variantNM_002533.4(NVL):c.2006G>A (p.Arg669Gln)not specified [RCV004652801]uncertain significance1224275415224275415Humanname
407478148CV3459077single nucleotide variantNM_002533.4(NVL):c.1763A>T (p.Asp588Val)not specified [RCV004638944]uncertain significance1224287806224287806Humanname
597665291CV3570207single nucleotide variantNM_002533.4(NVL):c.2047G>A (p.Val683Met)not specified [RCV004835574]uncertain significance1224275374224275374Humanname
597644196CV3570208single nucleotide variantNM_002533.4(NVL):c.1409T>C (p.Val470Ala)not specified [RCV004832758]uncertain significance1224289650224289650Humanname
597665298CV3570209single nucleotide variantNM_002533.4(NVL):c.2078G>A (p.Arg693Gln)not specified [RCV004835575]uncertain significance1224275343224275343Humanname
597665325CV3570213single nucleotide variantNM_002533.4(NVL):c.1042G>A (p.Glu348Lys)not specified [RCV004835578]uncertain significance1224300582224300582Humanname
597665347CV3570216single nucleotide variantNM_002533.4(NVL):c.2209C>T (p.Pro737Ser)not specified [RCV004835581]uncertain significance1224250292224250292Humanname
598266506CV4004954single nucleotide variantNM_002533.4(NVL):c.1918G>A (p.Gly640Arg)not specified [RCV005388157]uncertain significance1224281167224281167Humanname
598235861CV4004956single nucleotide variantNM_002533.4(NVL):c.1823A>G (p.Lys608Arg)not specified [RCV005382073]likely benign1224286102224286102Humanname