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)

27 records found for search term Rpp30
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405738570CV3320204single nucleotide variantNM_006413.5(RPP30):c.8T>G (p.Val3Gly)not specified [RCV004452025]uncertain significance109087199490871994Humanname
598220013CV3902967single nucleotide variantNM_006413.5(RPP30):c.25C>A (p.Leu9Met)not specified [RCV005272406]uncertain significance109087201190872011Humanname
156098840CV2378907single nucleotide variantNM_006413.5(RPP30):c.69G>C (p.Glu23Asp)not specified [RCV004233346]uncertain significance109087205590872055Humanname
401907579CV2809458single nucleotide variantNM_006413.5(RPP30):c.32C>T (p.Ala11Val)not provided [RCV003422719]likely benign109087201890872018Humanname
401907581CV2809459single nucleotide variantNM_006413.5(RPP30):c.693T>C (p.His231=)not provided [RCV003422720]likely benign109089638890896388Humanname
329366224CV2438248single nucleotide variantNM_006413.5(RPP30):c.245C>T (p.Ser82Leu)not specified [RCV004257011]uncertain significance109087607390876073Humanname
401860115CV2765476single nucleotide variantNM_006413.5(RPP30):c.241G>A (p.Val81Ile)not specified [RCV004341788]uncertain significance109087606990876069Humanname
598220001CV3902965single nucleotide variantNM_006413.5(RPP30):c.145G>A (p.Glu49Lys)not specified [RCV005272404]uncertain significance109087556490875564Humanname
156312911CV2196435single nucleotide variantNM_006413.5(RPP30):c.683C>T (p.Ala228Val)not specified [RCV004073736]likely benign109089637890896378Humanname
156375236CV2213538single nucleotide variantNM_006413.5(RPP30):c.620G>C (p.Gly207Ala)not specified [RCV004087497]uncertain significance109089631590896315Humanname
156019551CV2272639single nucleotide variantNM_006413.5(RPP30):c.523A>C (p.Asn175His)not specified [RCV004133519]uncertain significance109089486590894865Humanname
155906217CV2357279single nucleotide variantNM_006413.5(RPP30):c.493A>G (p.Met165Val)not specified [RCV004200177]uncertain significance109089483590894835Humanname
155933367CV2399309single nucleotide variantNM_006413.5(RPP30):c.418C>T (p.Pro140Ser)not specified [RCV004242600]uncertain significance109088588790885887Humanname
329363304CV2446130single nucleotide variantNM_006413.5(RPP30):c.400C>T (p.Pro134Ser)not specified [RCV004270680]uncertain significance109088586990885869Humanname
329359476CV2446283single nucleotide variantNM_006413.5(RPP30):c.649G>A (p.Ala217Thr)not specified [RCV004249418]uncertain significance109089634490896344Humanname
329378048CV2461044single nucleotide variantNM_006413.5(RPP30):c.338T>C (p.Phe113Ser)not specified [RCV004265196]uncertain significance109087913090879130Humanname
329393823CV2472146single nucleotide variantNM_006413.5(RPP30):c.620G>A (p.Gly207Asp)not specified [RCV004283273]uncertain significance109089631590896315Humanname
405738537CV3320200single nucleotide variantNM_006413.5(RPP30):c.503A>G (p.Tyr168Cys)not specified [RCV004452021]uncertain significance109089484590894845Humanname
405738544CV3320201single nucleotide variantNM_006413.5(RPP30):c.649G>T (p.Ala217Ser)not specified [RCV004452022]uncertain significance109089634490896344Humanname
405738552CV3320202single nucleotide variantNM_006413.5(RPP30):c.679G>A (p.Ala227Thr)not specified [RCV004452023]uncertain significance109089637490896374Humanname
405738561CV3320203single nucleotide variantNM_006413.5(RPP30):c.717T>G (p.Phe239Leu)not specified [RCV004452024]uncertain significance109090058990900589Humanname
407487813CV3476163single nucleotide variantNM_006413.5(RPP30):c.497G>A (p.Arg166Lys)not specified [RCV004665764]uncertain significance109089483990894839Humanname
407513758CV3476164single nucleotide variantNM_006413.5(RPP30):c.475G>C (p.Ala159Pro)not specified [RCV004674236]uncertain significance109089481790894817Humanname
597785858CV3594282single nucleotide variantNM_006413.5(RPP30):c.436A>G (p.Ile146Val)not specified [RCV004854859]uncertain significance109089477890894778Humanname
597709681CV3594283single nucleotide variantNM_006413.5(RPP30):c.443G>A (p.Arg148Gln)not specified [RCV004860867]uncertain significance109089478590894785Humanname
598219995CV3902964single nucleotide variantNM_006413.5(RPP30):c.460C>T (p.Leu154Phe)not specified [RCV005272403]uncertain significance109089480290894802Humanname
598220008CV3902966single nucleotide variantNM_006413.5(RPP30):c.715T>C (p.Phe239Leu)not specified [RCV005272405]uncertain significance109090058790900587Humanname