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)

24 records found for search term Wnt6
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155939907CV2293997single nucleotide variantNM_006522.4(WNT6):c.25C>G (p.Leu9Val)not specified [RCV004149392]uncertain significance2218860062218860062Humanname
10046767CV187236single nucleotide variantNM_006522.4(WNT6):c.570G>A (p.Arg190=)Bladder exstrophy-epispadias-cloacal extrophy complex [RCV000172900]likely benign2218871753218871753Human1name
401930115CV2818934single nucleotide variantNM_006522.4(WNT6):c.627G>A (p.Ala209=)not provided [RCV003440170]likely benign2218871810218871810Humanname
405812172CV3352950single nucleotide variantNM_006522.4(WNT6):c.522C>T (p.Asp174=)not specified [RCV004483150]likely benign2218871705218871705Humanname
401770524CV2707263single nucleotide variantNM_006522.4(WNT6):c.181G>A (p.Val61Met)not specified [RCV004310882]uncertain significance2218871127218871127Humanname
405812167CV3352947single nucleotide variantNM_006522.4(WNT6):c.149G>A (p.Arg50Gln)not specified [RCV004483147]uncertain significance2218871095218871095Humanname
405812169CV3352948single nucleotide variantNM_006522.4(WNT6):c.209G>A (p.Arg70Gln)not specified [RCV004483148]uncertain significance2218871155218871155Humanname
597741040CV3624242single nucleotide variantNM_006522.4(WNT6):c.133C>T (p.Arg45Trp)not specified [RCV004890673]uncertain significance2218871079218871079Humanname
156281662CV2220590single nucleotide variantNM_006522.4(WNT6):c.448G>A (p.Gly150Ser)not specified [RCV004097784]uncertain significance2218871631218871631Humanname
156032690CV2239480single nucleotide variantNM_006522.4(WNT6):c.591C>A (p.Asp197Glu)not specified [RCV004114194]uncertain significance2218871774218871774Humanname
156285771CV2360837single nucleotide variantNM_006522.4(WNT6):c.754G>C (p.Glu252Gln)not specified [RCV004213609]uncertain significance2218873501218873501Humanname
329368369CV2442734single nucleotide variantNM_006522.4(WNT6):c.865G>C (p.Asp289His)not specified [RCV004266865]uncertain significance2218873612218873612Humanname
401729701CV2683770single nucleotide variantNM_006522.4(WNT6):c.412C>T (p.Arg138Cys)not specified [RCV004284506]uncertain significance2218871595218871595Humanname
405812171CV3352949single nucleotide variantNM_006522.4(WNT6):c.427C>G (p.Pro143Ala)not specified [RCV004483149]uncertain significance2218871610218871610Humanname
405812174CV3352951single nucleotide variantNM_006522.4(WNT6):c.638C>T (p.Ala213Val)not specified [RCV004483151]uncertain significance2218873385218873385Humanname
405812176CV3352952single nucleotide variantNM_006522.4(WNT6):c.817G>T (p.Val273Phe)not specified [RCV004483152]uncertain significance2218873564218873564Humanname
405812178CV3352953single nucleotide variantNM_006522.4(WNT6):c.999C>G (p.Ser333Arg)not specified [RCV004483153]uncertain significance2218873746218873746Humanname
597800133CV3624243single nucleotide variantNM_006522.4(WNT6):c.923G>A (p.Arg308His)not specified [RCV004879985]uncertain significance2218873670218873670Humanname
598192290CV3937185single nucleotide variantNM_006522.4(WNT6):c.839G>A (p.Gly280Asp)not specified [RCV005288496]uncertain significance2218873586218873586Humanname
598192295CV3937186single nucleotide variantNM_006522.4(WNT6):c.382G>A (p.Glu128Lys)not specified [RCV005288497]uncertain significance2218871565218871565Humanname
598275522CV3937187single nucleotide variantNM_006522.4(WNT6):c.983G>A (p.Gly328Glu)not specified [RCV005304656]uncertain significance2218873730218873730Humanname
598275524CV3937189single nucleotide variantNM_006522.4(WNT6):c.860C>T (p.Ala287Val)not specified [RCV005304658]uncertain significance2218873607218873607Humanname
598275525CV3937190single nucleotide variantNM_006522.4(WNT6):c.371G>A (p.Cys124Tyr)not specified [RCV005304659]uncertain significance2218871554218871554Humanname
156051595CV2238042single nucleotide variantNM_006522.4(WNT6):c.1000G>A (p.Val334Met)not specified [RCV004111069]uncertain significance2218873747218873747Humanname