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 Homo sapiens
(View Results for all Objects and Ontologies)

28 records found for search term Gipr
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407456509CV3415910single nucleotide variantNM_000164.4(GIPR):c.280+273A>Cnot provided [RCV004598787]benign194567166545671665Humanname
156224601CV2229827single nucleotide variantNM_000164.4(GIPR):c.22C>G (p.Gln8Glu)not specified [RCV004105398]uncertain significance194566954245669542Humanname
156257771CV2219921single nucleotide variantNM_000164.4(GIPR):c.92C>A (p.Thr31Lys)not specified [RCV004095548]uncertain significance194567065445670654Humanname
156302869CV2319789single nucleotide variantNM_000164.4(GIPR):c.68C>G (p.Ala23Gly)not specified [RCV004187317]uncertain significance194566958845669588Humanname
329357214CV2431282single nucleotide variantNM_000164.4(GIPR):c.47G>A (p.Cys16Tyr)not specified [RCV004250615]uncertain significance194566956745669567Humanname
329398539CV2471165single nucleotide variantNM_000164.4(GIPR):c.49G>A (p.Gly17Arg)not specified [RCV004278413]uncertain significance194566956945669569Humanname
405736842CV3254908single nucleotide variantNM_000164.4(GIPR):c.34C>G (p.Arg12Gly)not specified [RCV004390726]uncertain significance194566955445669554Humanname
597706969CV3684535single nucleotide variantNM_000164.4(GIPR):c.324A>G (p.Gln108=)not specified [RCV004917042]likely benign194567289445672894Humanname
156235019CV2245395single nucleotide variantNM_000164.4(GIPR):c.101A>G (p.Glu34Gly)not specified [RCV004109186]uncertain significance194567066345670663Humanname
405736821CV3254905single nucleotide variantNM_000164.4(GIPR):c.107A>C (p.Tyr36Ser)not specified [RCV004390723]uncertain significance194567066945670669Humanname
405736834CV3254907single nucleotide variantNM_000164.4(GIPR):c.197A>T (p.Asp66Val)not specified [RCV004390725]uncertain significance194567130945671309Humanname
156118100CV2209226single nucleotide variantNM_000164.4(GIPR):c.387C>A (p.Asp129Glu)not specified [RCV004093418]uncertain significance194567407645674076Humanname
156250359CV2232165single nucleotide variantNM_000164.4(GIPR):c.856T>C (p.Cys286Arg)not specified [RCV004104970]uncertain significance194567771145677711Humanname
155916290CV2282012single nucleotide variantNM_000164.4(GIPR):c.898C>T (p.Arg300Trp)not specified [RCV004138769]uncertain significance194567775345677753Humanname
155908630CV2302475single nucleotide variantNM_000164.4(GIPR):c.782T>A (p.Leu261His)not specified [RCV004161202]uncertain significance194567709745677097Humanname
156065423CV2323708single nucleotide variantNM_000164.4(GIPR):c.331C>G (p.Leu111Val)not specified [RCV004174370]uncertain significance194567290145672901Humanname
156274706CV2334134single nucleotide variantNM_000164.4(GIPR):c.419T>C (p.Met140Thr)not specified [RCV004183647]uncertain significance194567410845674108Humanname
156308351CV2369912single nucleotide variantNM_000164.4(GIPR):c.911T>G (p.Leu304Arg)not specified [RCV004208380]uncertain significance194567776645677766Humanname
405736851CV3254909single nucleotide variantNM_000164.4(GIPR):c.913A>G (p.Met305Val)not specified [RCV004390727]uncertain significance194567776845677768Humanname
597706978CV3684536single nucleotide variantNM_000164.4(GIPR):c.754G>A (p.Glu252Lys)not specified [RCV004917043]uncertain significance194567706945677069Humanname
8628351CV83495single nucleotide variantNM_000164.2(GIPR):c.616C>T (p.Leu206Phe)Malignant melanoma [RCV000063576]not provided194567480945674809Humanname
155902579CV2274711single nucleotide variantNM_000164.4(GIPR):c.1243A>G (p.Ser415Gly)not specified [RCV004139079]uncertain significance194568177745681777Humanname
156027363CV2278426single nucleotide variantNM_000164.4(GIPR):c.1067T>C (p.Val356Ala)not specified [RCV004132880]uncertain significance194567814145678141Humanname
156201954CV2313184single nucleotide variantNM_000164.4(GIPR):c.1339T>A (p.Ser447Thr)not specified [RCV004161443]uncertain significance194568187345681873Humanname
156210451CV2378143single nucleotide variantNM_000164.4(GIPR):c.1244G>T (p.Ser415Ile)not specified [RCV004233060]uncertain significance194568177845681778Humanname
156153892CV2395029single nucleotide variantNM_000164.4(GIPR):c.1108C>A (p.Arg370Ser)not specified [RCV004236719]uncertain significance194567818245678182Humanname
401729814CV2731753single nucleotide variantNM_000164.4(GIPR):c.1210C>A (p.Arg404Ser)not specified [RCV004332242]uncertain significance194568174445681744Humanname
405736829CV3254906single nucleotide variantNM_000164.4(GIPR):c.1231C>T (p.Arg411Cys)not specified [RCV004390724]uncertain significance194568176545681765Humanname