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)

50 records found for search term Kif2c
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405652616CV3268963single nucleotide variantNM_006845.4(KIF2C):c.50T>C (p.Ile17Thr)not specified [RCV004414217]uncertain significance14473998244739982Humanname
598248501CV3991025single nucleotide variantNM_006845.4(KIF2C):c.77T>C (p.Ile26Thr)not specified [RCV005366241]uncertain significance14474091944740919Humanname
155993794CV2281366single nucleotide variantNM_006845.4(KIF2C):c.286G>A (p.Val96Ile)not specified [RCV004141165]uncertain significance14474767044747670Humanname
329397107CV2456603single nucleotide variantNM_006845.4(KIF2C):c.278G>A (p.Arg93Gln)not specified [RCV004277795]uncertain significance14474766244747662Humanname
401927926CV2812760single nucleotide variantNM_006845.4(KIF2C):c.1930C>T (p.Leu644=)not provided [RCV003406452]likely benign14476261744762617Humanname
597630868CV3695198single nucleotide variantNM_006845.4(KIF2C):c.253A>T (p.Asn85Tyr)not specified [RCV004939510]uncertain significance14474747144747471Humanname
598248514CV3991029single nucleotide variantNM_006845.4(KIF2C):c.167T>C (p.Ile56Thr)not specified [RCV005366243]uncertain significance14474738544747385Humanname
156334188CV2230886single nucleotide variantNM_006845.4(KIF2C):c.875A>G (p.His292Arg)not specified [RCV004092362]uncertain significance14475613544756135Humanname
156159521CV2322745single nucleotide variantNM_006845.4(KIF2C):c.341T>C (p.Met114Thr)not specified [RCV004182855]uncertain significance14475046644750466Humanname
401736431CV2688788single nucleotide variantNM_006845.4(KIF2C):c.337C>T (p.Arg113Cys)not specified [RCV004303811]uncertain significance14475046244750462Humanname
401748794CV2709603single nucleotide variantNM_006845.4(KIF2C):c.769C>G (p.His257Asp)not specified [RCV004318828]uncertain significance14475593844755938Humanname
405652657CV3268962single nucleotide variantNM_006845.4(KIF2C):c.458C>G (p.Ser153Cys)not specified [RCV004414216]uncertain significance14475315044753150Humanname
405652584CV3268964single nucleotide variantNM_006845.4(KIF2C):c.560C>T (p.Ser187Leu)not specified [RCV004414218]uncertain significance14475325244753252Humanname
405652586CV3268965single nucleotide variantNM_006845.4(KIF2C):c.701G>A (p.Arg234Gln)not specified [RCV004414219]uncertain significance14475478744754787Humanname
405652588CV3268966single nucleotide variantNM_006845.4(KIF2C):c.763G>A (p.Glu255Lys)not specified [RCV004414220]uncertain significance14475593244755932Humanname
597768285CV3695197single nucleotide variantNM_006845.4(KIF2C):c.340A>G (p.Met114Val)not specified [RCV004927451]uncertain significance14475046544750465Humanname
597630863CV3695199single nucleotide variantNM_006845.4(KIF2C):c.355G>C (p.Glu119Gln)not specified [RCV004939511]uncertain significance14475048044750480Humanname
597630852CV3695201single nucleotide variantNM_006845.4(KIF2C):c.838G>A (p.Val280Met)not specified [RCV004939513]uncertain significance14475609844756098Humanname
597630848CV3695202single nucleotide variantNM_006845.4(KIF2C):c.307C>T (p.Pro103Ser)not specified [RCV004939514]uncertain significance14474769144747691Humanname
597630844CV3695205single nucleotide variantNM_006845.4(KIF2C):c.419G>A (p.Arg140His)not specified [RCV004939515]uncertain significance14475054444750544Humanname
598272581CV3991020single nucleotide variantNM_006845.4(KIF2C):c.470T>C (p.Val157Ala)not specified [RCV005350522]uncertain significance14475316244753162Humanname
598220545CV3991021single nucleotide variantNM_006845.4(KIF2C):c.719G>A (p.Arg240Gln)not specified [RCV005360682]uncertain significance14475480544754805Humanname
598248488CV3991022single nucleotide variantNM_006845.4(KIF2C):c.733T>G (p.Cys245Gly)not specified [RCV005366239]uncertain significance14475481944754819Humanname
598272586CV3991024single nucleotide variantNM_006845.4(KIF2C):c.673A>G (p.Ser225Gly)not specified [RCV005350523]uncertain significance14475475944754759Humanname
598272600CV3991030single nucleotide variantNM_006845.4(KIF2C):c.622A>C (p.Lys208Gln)not specified [RCV005350526]uncertain significance14475379244753792Humanname
598248519CV3991031single nucleotide variantNM_006845.4(KIF2C):c.542C>T (p.Ser181Phe)not specified [RCV005366244]uncertain significance14475323444753234Humanname
598248527CV3991032single nucleotide variantNM_006845.4(KIF2C):c.390G>C (p.Glu130Asp)not specified [RCV005366245]uncertain significance14475051544750515Humanname
155988648CV2259593single nucleotide variantNM_006845.4(KIF2C):c.1826C>T (p.Ala609Val)not specified [RCV004116638]uncertain significance14476242044762420Humanname
156142650CV2296105single nucleotide variantNM_006845.4(KIF2C):c.1259G>A (p.Arg420His)not specified [RCV004154039]uncertain significance14475924044759240Humanname
156294192CV2306394single nucleotide variantNM_006845.4(KIF2C):c.1333G>A (p.Val445Ile)not specified [RCV004163089]uncertain significance14475931444759314Humanname
156156850CV2322523single nucleotide variantNM_006845.4(KIF2C):c.1219G>A (p.Gly407Arg)not specified [RCV004182684]uncertain significance14475813544758135Humanname
156141508CV2358411single nucleotide variantNM_006845.4(KIF2C):c.1519C>G (p.Arg507Gly)not specified [RCV004207305]uncertain significance14476043144760431Humanname
156163225CV2389547single nucleotide variantNM_006845.4(KIF2C):c.1849C>T (p.Pro617Ser)not specified [RCV004243617]uncertain significance14476244344762443Humanname
401730346CV2711227single nucleotide variantNM_006845.4(KIF2C):c.1519C>T (p.Arg507Trp)not specified [RCV004313018]uncertain significance14476043144760431Humanname
401872298CV2779450single nucleotide variantNM_006845.4(KIF2C):c.1769C>T (p.Pro590Leu)not specified [RCV004351087]uncertain significance14476236344762363Humanname
401927923CV2812761single nucleotide variantNM_006845.4(KIF2C):c.2093G>A (p.Arg698Gln)not provided [RCV003406453]likely benign14476694744766947Humanname
405653002CV3268954single nucleotide variantNM_006845.4(KIF2C):c.1171C>T (p.Arg391Trp)not specified [RCV004414208]uncertain significance14475808744758087Humanname
405653000CV3268955single nucleotide variantNM_006845.4(KIF2C):c.1217A>G (p.Asn406Ser)not specified [RCV004414209]uncertain significance14475813344758133Humanname
405652947CV3268957single nucleotide variantNM_006845.4(KIF2C):c.1667A>T (p.Asn556Ile)not specified [RCV004414211]uncertain significance14476068644760686Humanname
405652872CV3268958single nucleotide variantNM_006845.4(KIF2C):c.1850C>T (p.Pro617Leu)not specified [RCV004414212]uncertain significance14476244444762444Humanname
405652812CV3268959single nucleotide variantNM_006845.4(KIF2C):c.1858T>A (p.Leu620Ile)not specified [RCV004414213]uncertain significance14476254544762545Humanname
405652749CV3268960single nucleotide variantNM_006845.4(KIF2C):c.2021A>G (p.Tyr674Cys)not specified [RCV004414214]uncertain significance14476687544766875Humanname
405652703CV3268961single nucleotide variantNM_006845.4(KIF2C):c.2167C>T (p.Arg723Trp)not specified [RCV004414215]uncertain significance14476716844767168Humanname
407524718CV3452165single nucleotide variantNM_006845.4(KIF2C):c.1658T>C (p.Ile553Thr)not specified [RCV004631476]uncertain significance14476067744760677Humanname
407469622CV3452166single nucleotide variantNM_006845.4(KIF2C):c.1372T>A (p.Ser458Thr)not specified [RCV004636898]uncertain significance14476028444760284Humanname
597630858CV3695200single nucleotide variantNM_006845.4(KIF2C):c.1120T>A (p.Tyr374Asn)not specified [RCV004939512]uncertain significance14475795944757959Humanname
597768288CV3695203single nucleotide variantNM_006845.4(KIF2C):c.1155G>C (p.Lys385Asn)not specified [RCV004927452]uncertain significance14475807144758071Humanname
597768293CV3695204single nucleotide variantNM_006845.4(KIF2C):c.1556G>C (p.Ser519Thr)not specified [RCV004927453]uncertain significance14476046844760468Humanname
598248495CV3991023single nucleotide variantNM_006845.4(KIF2C):c.1728A>C (p.Leu576Phe)not specified [RCV005366240]uncertain significance14476196044761960Humanname
598272593CV3991026single nucleotide variantNM_006845.4(KIF2C):c.1832C>G (p.Ser611Cys)not specified [RCV005350524]uncertain significance14476242644762426Humanname