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)

50 records found for search term Dclk2
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407458126CV3430318single nucleotide variantNM_001040260.4(DCLK2):c.961+955A>Gnot specified [RCV004611419]uncertain significance4150199058150199058Humanname
598262297CV3963694single nucleotide variantNM_001040260.4(DCLK2):c.961+967A>Gnot specified [RCV005325355]likely benign4150199070150199070Humanname
8579291CV113689single nucleotide variantNM_001040260.3(DCLK2):c.421+3197G>ALung cancer [RCV000094212]uncertain significance4150082645150082645Humanname
401923530CV2820204single nucleotide variantNM_001040260.4(DCLK2):c.63G>C (p.Pro21=)not provided [RCV003435179]likely benign4150079090150079090Humanname
401730327CV2680103single nucleotide variantNM_001040260.4(DCLK2):c.14G>A (p.Arg5Lys)not specified [RCV004286593]uncertain significance4150079041150079041Humanname
401755961CV2686183single nucleotide variantNM_001040260.4(DCLK2):c.44G>C (p.Arg15Pro)not specified [RCV004297280]uncertain significance4150079071150079071Humanname
156262353CV2201087single nucleotide variantNM_001040260.4(DCLK2):c.136C>A (p.Pro46Thr)not specified [RCV004075210]uncertain significance4150079163150079163Humanname
155987769CV2251154single nucleotide variantNM_001040260.4(DCLK2):c.297C>G (p.Phe99Leu)not specified [RCV004115388]uncertain significance4150079324150079324Humanname
401923532CV2820205single nucleotide variantNM_001040260.4(DCLK2):c.2193T>C (p.Pro731=)not provided [RCV003435180]likely benign4150256139150256139Humanname
401944759CV2840518single nucleotide variantNM_001040260.4(DCLK2):c.1302A>G (p.Glu434=)not provided [RCV003457423]likely benign4150232339150232339Humanname
598262309CV3963696single nucleotide variantNM_001040260.4(DCLK2):c.146C>A (p.Ala49Glu)not specified [RCV005325357]uncertain significance4150079173150079173Humanname
8631044CV86200single nucleotide variantNM_001040260.3(DCLK2):c.1869T>C (p.Ser623=)Malignant melanoma [RCV000066291]not provided4150247693150247693Humanname
156040482CV2261298single nucleotide variantNM_001040260.4(DCLK2):c.988T>C (p.Ser330Pro)not specified [RCV004128161]uncertain significance4150203821150203821Humanname
156150202CV2289629single nucleotide variantNM_001040260.4(DCLK2):c.797T>G (p.Phe266Cys)not specified [RCV004148547]uncertain significance4150193178150193178Humanname
156289153CV2309657single nucleotide variantNM_001040260.4(DCLK2):c.718G>A (p.Gly240Arg)not specified [RCV004160802]uncertain significance4150102774150102774Humanname
155968734CV2337873single nucleotide variantNM_001040260.4(DCLK2):c.350C>T (p.Pro117Leu)not specified [RCV004183883]uncertain significance4150079377150079377Humanname
401863187CV2771966single nucleotide variantNM_001040260.4(DCLK2):c.941G>A (p.Arg314His)not specified [RCV004344656]uncertain significance4150198083150198083Humanname
401888153CV2791293single nucleotide variantNM_001040260.4(DCLK2):c.940C>A (p.Arg314Ser)not specified [RCV004356918]uncertain significance4150198082150198082Humanname
405691093CV3246759single nucleotide variantNM_001040260.4(DCLK2):c.300T>G (p.Asp100Glu)not specified [RCV004373329]uncertain significance4150079327150079327Humanname
405691098CV3246760single nucleotide variantNM_001040260.4(DCLK2):c.724G>A (p.Val242Ile)not specified [RCV004373330]uncertain significance4150102780150102780Humanname
405691102CV3246761single nucleotide variantNM_001040260.4(DCLK2):c.805T>C (p.Cys269Arg)not specified [RCV004373331]uncertain significance4150193186150193186Humanname
405691108CV3246762single nucleotide variantNM_001040260.4(DCLK2):c.833A>G (p.Gln278Arg)not specified [RCV004373332]uncertain significance4150193214150193214Humanname
407458127CV3430319single nucleotide variantNM_001040260.4(DCLK2):c.408C>G (p.Asp136Glu)not specified [RCV004611420]uncertain significance4150079435150079435Humanname
598262319CV3963698single nucleotide variantNM_001040260.4(DCLK2):c.458G>T (p.Arg153Leu)not specified [RCV005325359]uncertain significance4150102514150102514Humanname
156374576CV2194655single nucleotide variantNM_001040260.4(DCLK2):c.1531A>G (p.Ile511Val)not specified [RCV004082058]uncertain significance4150232793150232793Humanname
156314263CV2196618single nucleotide variantNM_001040260.4(DCLK2):c.2203G>A (p.Val735Ile)not specified [RCV004073888]uncertain significance4150256149150256149Humanname
155950476CV2267861single nucleotide variantNM_001040260.4(DCLK2):c.1858A>G (p.Ile620Val)not specified [RCV004136158]uncertain significance4150247682150247682Humanname
156303060CV2308181single nucleotide variantNM_001040260.4(DCLK2):c.2294G>A (p.Arg765Gln)not specified [RCV004164687]uncertain significance4150256240150256240Humanname
156137886CV2354488single nucleotide variantNM_001040260.4(DCLK2):c.1502A>G (p.Asn501Ser)not specified [RCV004202475]uncertain significance4150232764150232764Humanname
401719779CV2675680single nucleotide variantNM_001040260.4(DCLK2):c.2068A>G (p.Ile690Val)not specified [RCV004287931]uncertain significance4150249679150249679Humanname
401776075CV2692592single nucleotide variantNM_001040260.4(DCLK2):c.2284C>T (p.Arg762Cys)not specified [RCV004312329]uncertain significance4150256230150256230Humanname
401731176CV2693650single nucleotide variantNM_001040260.4(DCLK2):c.1236A>G (p.Ile412Met)not specified [RCV004297987]likely benign4150221780150221780Humanname
401759008CV2705321single nucleotide variantNM_001040260.4(DCLK2):c.1243T>G (p.Ser415Ala)not specified [RCV004312004]uncertain significance4150224502150224502Humanname
401856782CV2761779single nucleotide variantNM_001040260.4(DCLK2):c.2207C>T (p.Pro736Leu)not specified [RCV004339430]likely benign4150256153150256153Humanname
401899022CV2785953single nucleotide variantNM_001040260.4(DCLK2):c.1816T>G (p.Leu606Val)not specified [RCV004359797]uncertain significance4150247640150247640Humanname
401870750CV2792493single nucleotide variantNM_001040260.4(DCLK2):c.1577A>T (p.Tyr526Phe)not specified [RCV004363229]uncertain significance4150239752150239752Humanname
405691067CV3246755single nucleotide variantNM_001040260.4(DCLK2):c.1042T>C (p.Phe348Leu)not specified [RCV004373325]uncertain significance4150203875150203875Humanname
405691074CV3246756single nucleotide variantNM_001040260.4(DCLK2):c.1261G>T (p.Ala421Ser)not specified [RCV004373326]uncertain significance4150224520150224520Humanname
405691080CV3246757single nucleotide variantNM_001040260.4(DCLK2):c.1451C>T (p.Ser484Leu)not specified [RCV004373327]uncertain significance4150232713150232713Humanname
405691087CV3246758single nucleotide variantNM_001040260.4(DCLK2):c.1970A>G (p.Gln657Arg)not specified [RCV004373328]uncertain significance4150249581150249581Humanname
407458122CV3430317single nucleotide variantNM_001040260.4(DCLK2):c.1096G>A (p.Gly366Ser)not specified [RCV004611418]uncertain significance4150220742150220742Humanname
407458130CV3430320single nucleotide variantNM_001040260.4(DCLK2):c.2018T>G (p.Phe673Cys)not specified [RCV004611421]uncertain significance4150249629150249629Humanname
597800931CV3652113single nucleotide variantNM_001040260.4(DCLK2):c.2263G>A (p.Gly755Ser)not specified [RCV004905971]uncertain significance4150256209150256209Humanname
598262282CV3963691single nucleotide variantNM_001040260.4(DCLK2):c.2027C>T (p.Ala676Val)not specified [RCV005325352]uncertain significance4150249638150249638Humanname
598262286CV3963692single nucleotide variantNM_001040260.4(DCLK2):c.1360A>T (p.Met454Leu)not specified [RCV005325353]uncertain significance4150232397150232397Humanname
598262293CV3963693single nucleotide variantNM_001040260.4(DCLK2):c.1591A>C (p.Lys531Gln)not specified [RCV005325354]uncertain significance4150239766150239766Humanname
598262303CV3963695single nucleotide variantNM_001040260.4(DCLK2):c.1123A>C (p.Ser375Arg)not specified [RCV005325356]uncertain significance4150220769150220769Humanname
598262314CV3963697single nucleotide variantNM_001040260.4(DCLK2):c.1943A>G (p.His648Arg)not specified [RCV005325358]uncertain significance4150248372150248372Humanname
598262325CV3963699single nucleotide variantNM_001040260.4(DCLK2):c.2285G>A (p.Arg762His)not specified [RCV005325360]uncertain significance4150256231150256231Humanname
598262329CV3963700single nucleotide variantNM_001040260.4(DCLK2):c.1081T>C (p.Ser361Pro)not specified [RCV005325361]uncertain significance4150220727150220727Humanname