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)

36 records found for search term Cd244
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150498375CV1224127single nucleotide variantNM_016382.4(CD244):c.*578T>Cnot provided [RCV001620239]benign1160830769160830769Humanname
155961925CV2311972single nucleotide variantNM_016382.4(CD244):c.380-4C>Tnot specified [RCV004170789]uncertain significance1160841489160841489Humanname
155961934CV2311973single nucleotide variantNM_016382.4(CD244):c.380-3C>Tnot specified [RCV004170790]uncertain significance1160841488160841488Humanname
8558338CV19934single nucleotide variantNM_016382.4(CD244):c.834+526A>GRheumatoid arthritis [RCV000005173]risk factor1160837925160837925Human2name
15112525CV706805single nucleotide variantNM_016382.4(CD244):c.39C>T (p.Leu13=)CD244-related disorder [RCV003978374]|not provided [RCV000961314]benign1160862639160862639Human1name , trait , alternate_id
8629040CV84183single nucleotide variantNM_016382.3(CD244):c.978G>A (p.Arg326=)Malignant melanoma [RCV000064264]not provided1160832558160832558Humanname
156105692CV2217663single nucleotide variantNM_016382.4(CD244):c.223C>A (p.Pro75Thr)not specified [RCV004090172]likely benign1160841740160841740Humanname
156120988CV2233831single nucleotide variantNM_016382.4(CD244):c.132A>G (p.Ile44Met)not specified [RCV004102049]uncertain significance1160841831160841831Humanname
156336768CV2360807single nucleotide variantNM_016382.4(CD244):c.248T>A (p.Phe83Tyr)not specified [RCV004213583]uncertain significance1160841715160841715Humanname
407497998CV3424919single nucleotide variantNM_016382.4(CD244):c.118C>G (p.Gln40Glu)not specified [RCV004606508]uncertain significance1160841845160841845Humanname
597778132CV3648290single nucleotide variantNM_016382.4(CD244):c.106C>T (p.Pro36Ser)not specified [RCV004898943]uncertain significance1160841857160841857Humanname
9686862CV171304single nucleotide variantNM_016382.4(CD244):c.971G>A (p.Arg324Lys)Prostate cancer [RCV000149080]uncertain significance1160832565160832565Human2name
156235440CV2193394single nucleotide variantNM_016382.4(CD244):c.654G>T (p.Gln218His)not specified [RCV004072894]likely benign1160841211160841211Humanname
155968823CV2312887single nucleotide variantNM_016382.4(CD244):c.417G>T (p.Lys139Asn)not specified [RCV004171376]uncertain significance1160841448160841448Humanname
156291802CV2339919single nucleotide variantNM_016382.4(CD244):c.651T>G (p.His217Gln)not specified [RCV004190024]uncertain significance1160841214160841214Humanname
156391437CV2385354single nucleotide variantNM_016382.4(CD244):c.535T>C (p.Tyr179His)not specified [RCV004230627]likely benign1160841330160841330Humanname
156092571CV2389597single nucleotide variantNM_016382.4(CD244):c.707T>C (p.Phe236Ser)not specified [RCV004243660]uncertain significance1160838998160838998Humanname
329385262CV2451160single nucleotide variantNM_016382.4(CD244):c.793A>G (p.Ile265Val)not specified [RCV004270088]likely benign1160838492160838492Humanname
329357348CV2457503single nucleotide variantNM_016382.4(CD244):c.968C>A (p.Ser323Tyr)not specified [RCV004267314]uncertain significance1160832568160832568Humanname
401754297CV2726955single nucleotide variantNM_016382.4(CD244):c.611G>A (p.Ser204Asn)not specified [RCV004325025]likely benign1160841254160841254Humanname
401894972CV2792638single nucleotide variantNM_016382.4(CD244):c.904C>A (p.Pro302Thr)not specified [RCV004363657]uncertain significance1160834107160834107Humanname
405759589CV3299658single nucleotide variantNM_016382.4(CD244):c.397C>T (p.Arg133Cys)not specified [RCV004433347]uncertain significance1160841468160841468Humanname
405759384CV3299660single nucleotide variantNM_016382.4(CD244):c.617C>A (p.Thr206Asn)not specified [RCV004433349]uncertain significance1160841248160841248Humanname
407497995CV3424918single nucleotide variantNM_016382.4(CD244):c.700G>T (p.Ala234Ser)not specified [RCV004606507]uncertain significance1160839005160839005Humanname
407498000CV3424920single nucleotide variantNM_016382.4(CD244):c.353C>G (p.Thr118Arg)not specified [RCV004606509]likely benign1160841610160841610Humanname
597778136CV3648291single nucleotide variantNM_016382.4(CD244):c.620T>C (p.Leu207Pro)not specified [RCV004898944]uncertain significance1160841245160841245Humanname
597778141CV3648292single nucleotide variantNM_016382.4(CD244):c.461T>A (p.Val154Asp)not specified [RCV004898945]uncertain significance1160841404160841404Humanname
597778145CV3648293single nucleotide variantNM_016382.4(CD244):c.550G>A (p.Val184Ile)not specified [RCV004898946]likely benign1160841315160841315Humanname
597738702CV3648294single nucleotide variantNM_016382.4(CD244):c.658T>C (p.Phe220Leu)not specified [RCV004890174]uncertain significance1160839047160839047Humanname
598206927CV3950662single nucleotide variantNM_016382.4(CD244):c.455G>T (p.Cys152Phe)not specified [RCV005315200]uncertain significance1160841410160841410Humanname
598206933CV3950663single nucleotide variantNM_016382.4(CD244):c.409C>A (p.Gln137Lys)not specified [RCV005315201]uncertain significance1160841456160841456Humanname
15144005CV706804single nucleotide variantNM_016382.4(CD244):c.685A>G (p.Ile229Val)not provided [RCV000966766]benign1160839020160839020Humanname
156288333CV2299176single nucleotide variantNM_016382.4(CD244):c.1080C>A (p.Asn360Lys)not specified [RCV004152518]uncertain significance1160831365160831365Humanname
405272184CV3203123single nucleotide variantNM_016382.4(CD244):c.1063C>T (p.Arg355Cys)CD244-related disorder [RCV003914168]benign1160831382160831382Humanname , trait , alternate_id
405759595CV3299657single nucleotide variantNM_016382.4(CD244):c.1064G>A (p.Arg355His)not specified [RCV004433346]uncertain significance1160831381160831381Humanname
597738698CV3648289single nucleotide variantNM_016382.4(CD244):c.1048C>T (p.Pro350Ser)not specified [RCV004890173]uncertain significance1160831397160831397Humanname