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)

42 records found for search term Upp2
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401766230CV2714368single nucleotide variantNM_173355.4(UPP2):c.-11T>Cnot specified [RCV004317903]uncertain significance2158102053158102053Humanname
8576703CV111071single nucleotide variantNM_001135098.1(UPP2):c.148-35343G>TLung cancer [RCV000091594]uncertain significance2158066697158066697Humanname
405810389CV3345262single nucleotide variantNM_173355.4(UPP2):c.5C>G (p.Ala2Gly)not specified [RCV004482222]uncertain significance2158102068158102068Humanname
405810391CV3345263single nucleotide variantNM_173355.4(UPP2):c.8C>T (p.Ser3Leu)not specified [RCV004482223]uncertain significance2158102071158102071Humanname
405810393CV3345264single nucleotide variantNM_173355.4(UPP2):c.29G>A (p.Arg10Lys)not specified [RCV004482224]likely benign2158102092158102092Humanname
405810395CV3345265single nucleotide variantNM_173355.4(UPP2):c.79G>A (p.Val27Ile)not specified [RCV004482225]uncertain significance2158106115158106115Humanname
597790983CV3629219single nucleotide variantNM_173355.4(UPP2):c.68G>T (p.Arg23Met)not specified [RCV004876511]uncertain significance2158106104158106104Humanname
15133018CV707785single nucleotide variantNM_173355.4(UPP2):c.462A>C (p.Ala154=)not provided [RCV000964877]benign2158121416158121416Humanname
156347901CV2383002single nucleotide variantNM_173355.4(UPP2):c.247G>A (p.Gly83Arg)not specified [RCV004217587]likely benign2158115167158115167Humanname
329362016CV2456649single nucleotide variantNM_173355.4(UPP2):c.241G>A (p.Glu81Lys)not specified [RCV004277834]uncertain significance2158115161158115161Humanname
401752433CV2682818single nucleotide variantNM_173355.4(UPP2):c.193G>A (p.Gly65Ser)not specified [RCV004281789]uncertain significance2158115113158115113Humanname
401895312CV2786353single nucleotide variantNM_173355.4(UPP2):c.242A>G (p.Glu81Gly)not specified [RCV004361956]uncertain significance2158115162158115162Humanname
405810397CV3345266single nucleotide variantNM_173355.4(UPP2):c.253G>C (p.Glu85Gln)not specified [RCV004482226]uncertain significance2158115173158115173Humanname
597721730CV3629220single nucleotide variantNM_173355.4(UPP2):c.146C>A (p.Thr49Lys)not specified [RCV004887940]uncertain significance2158106182158106182Humanname
598191680CV3925795single nucleotide variantNM_173355.4(UPP2):c.194G>A (p.Gly65Asp)not specified [RCV005288397]uncertain significance2158115114158115114Humanname
15098552CV697094single nucleotide variantNM_173355.4(UPP2):c.232A>C (p.Met78Leu)not provided [RCV000958586]benign2158115152158115152Humanname
156238562CV2221182single nucleotide variantNM_173355.4(UPP2):c.643T>C (p.Cys215Arg)not specified [RCV004094628]uncertain significance2158121597158121597Humanname
155984749CV2241153single nucleotide variantNM_173355.4(UPP2):c.916T>C (p.Ser306Pro)not specified [RCV004104179]uncertain significance2158134852158134852Humanname
155923492CV2251974single nucleotide variantNM_173355.4(UPP2):c.594C>A (p.Asn198Lys)not specified [RCV004121726]uncertain significance2158121548158121548Humanname
156132283CV2280045single nucleotide variantNM_173355.4(UPP2):c.758T>C (p.Ile253Thr)not specified [RCV004146403]uncertain significance2158123842158123842Humanname
156135309CV2284726single nucleotide variantNM_173355.4(UPP2):c.809A>G (p.Lys270Arg)not specified [RCV004140873]uncertain significance2158123893158123893Humanname
156292175CV2340023single nucleotide variantNM_173355.4(UPP2):c.406C>T (p.Arg136Trp)not specified [RCV004192271]uncertain significance2158117890158117890Humanname
155928884CV2369604single nucleotide variantNM_173355.4(UPP2):c.932G>A (p.Arg311Gln)not specified [RCV004215016]likely benign2158134868158134868Humanname
156039209CV2390293single nucleotide variantNM_173355.4(UPP2):c.935G>A (p.Arg312Gln)not specified [RCV004240659]likely benign2158134871158134871Humanname
401732353CV2678077single nucleotide variantNM_173355.4(UPP2):c.515G>A (p.Arg172Gln)not specified [RCV004296594]likely benign2158121469158121469Humanname
401732299CV2698275single nucleotide variantNM_173355.4(UPP2):c.436G>A (p.Gly146Ser)not specified [RCV004304826]uncertain significance2158117920158117920Humanname
405810382CV3345259single nucleotide variantNM_173355.4(UPP2):c.830C>T (p.Thr277Ile)not specified [RCV004482219]uncertain significance2158134766158134766Humanname
405810385CV3345260single nucleotide variantNM_173355.4(UPP2):c.869C>T (p.Pro290Leu)not specified [RCV004482220]uncertain significance2158134805158134805Humanname
405810399CV3345267single nucleotide variantNM_173355.4(UPP2):c.437G>C (p.Gly146Ala)not specified [RCV004482227]uncertain significance2158117921158117921Humanname
405810401CV3345268single nucleotide variantNM_173355.4(UPP2):c.540C>G (p.Asn180Lys)not specified [RCV004482228]uncertain significance2158121494158121494Humanname
405810403CV3345269single nucleotide variantNM_173355.4(UPP2):c.674G>T (p.Arg225Leu)not specified [RCV004482229]uncertain significance2158123758158123758Humanname
407454882CV3489442single nucleotide variantNM_173355.4(UPP2):c.308T>C (p.Met103Thr)not specified [RCV004685281]uncertain significance2158115228158115228Humanname
407454885CV3489443single nucleotide variantNM_173355.4(UPP2):c.921C>A (p.Asn307Lys)not specified [RCV004685282]uncertain significance2158134857158134857Humanname
407462547CV3489444single nucleotide variantNM_173355.4(UPP2):c.925A>G (p.Ile309Val)not specified [RCV004687997]uncertain significance2158134861158134861Humanname
597721717CV3629217single nucleotide variantNM_173355.4(UPP2):c.899G>A (p.Arg300Gln)not specified [RCV004887939]uncertain significance2158134835158134835Humanname
597790981CV3629218single nucleotide variantNM_173355.4(UPP2):c.415G>A (p.Asp139Asn)not specified [RCV004876510]uncertain significance2158117899158117899Humanname
597790986CV3629221single nucleotide variantNM_173355.4(UPP2):c.484G>T (p.Asp162Tyr)not specified [RCV004876512]uncertain significance2158121438158121438Humanname
597790989CV3629222single nucleotide variantNM_173355.4(UPP2):c.790T>C (p.Cys264Arg)not specified [RCV004876513]uncertain significance2158123874158123874Humanname
598191674CV3925794single nucleotide variantNM_173355.4(UPP2):c.838G>A (p.Asp280Asn)not specified [RCV005288396]likely benign2158134774158134774Humanname
598274790CV3925796single nucleotide variantNM_173355.4(UPP2):c.721T>G (p.Tyr241Asp)not specified [RCV005304119]uncertain significance2158123805158123805Humanname
598274792CV3925797single nucleotide variantNM_173355.4(UPP2):c.461C>T (p.Ala154Val)not specified [RCV005304120]uncertain significance2158121415158121415Humanname
598274794CV3925798single nucleotide variantNM_173355.4(UPP2):c.382C>G (p.Leu128Val)not specified [RCV005304121]uncertain significance2158117866158117866Humanname