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)

97 records found for search term Ccdc157
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156248569CV2222013single nucleotide variantNM_001017437.5(CCDC157):c.26C>G (p.Ala9Gly)not specified [RCV004103002]uncertain significance223036602630366026Humanname
155923443CV2217641single nucleotide variantNM_001017437.5(CCDC157):c.43C>T (p.Arg15Cys)not specified [RCV004090158]uncertain significance223036604330366043Humanname
401912498CV2822120single nucleotide variantNM_001017437.5(CCDC157):c.804G>A (p.Pro268=)not provided [RCV003427220]likely benign223037070930370709Humanname
405768945CV3303099single nucleotide variantNM_001017437.5(CCDC157):c.97G>A (p.Gly33Arg)not specified [RCV004434942]uncertain significance223036609730366097Humanname
597787120CV3647804single nucleotide variantNM_001017437.5(CCDC157):c.92G>A (p.Arg31His)not specified [RCV004901149]uncertain significance223036609230366092Humanname
598178013CV3946850single nucleotide variantNM_001017437.5(CCDC157):c.76G>A (p.Val26Ile)not specified [RCV005310293]uncertain significance223036607630366076Humanname
156180725CV2298482single nucleotide variantNM_001017437.5(CCDC157):c.145G>A (p.Asp49Asn)not specified [RCV004162146]uncertain significance223036614530366145Humanname
156344646CV2381858single nucleotide variantNM_001017437.5(CCDC157):c.188C>T (p.Pro63Leu)not specified [RCV004225804]uncertain significance223036618830366188Humanname
155970709CV2392316single nucleotide variantNM_001017437.5(CCDC157):c.191G>A (p.Gly64Asp)not specified [RCV004243917]uncertain significance223036619130366191Humanname
329360715CV2439632single nucleotide variantNM_001017437.5(CCDC157):c.134G>A (p.Arg45His)not specified [RCV004255649]uncertain significance223036613430366134Humanname
329368589CV2450372single nucleotide variantNM_001017437.5(CCDC157):c.134G>T (p.Arg45Leu)not provided [RCV004696384]|not specified [RCV004271445]uncertain significance223036613430366134Humanname
401724779CV2714969single nucleotide variantNM_001017437.5(CCDC157):c.245A>G (p.Asp82Gly)not specified [RCV004322291]uncertain significance223036624530366245Humanname
401761692CV2726866single nucleotide variantNM_001017437.5(CCDC157):c.199G>A (p.Glu67Lys)not specified [RCV004323161]uncertain significance223036619930366199Humanname
405768860CV3303086single nucleotide variantNM_001017437.5(CCDC157):c.106C>T (p.Arg36Cys)not specified [RCV004434929]uncertain significance223036610630366106Humanname
407484117CV3418367single nucleotide variantNM_001017437.5(CCDC157):c.276G>C (p.Met92Ile)not specified [RCV004602955]uncertain significance223036945930369459Humanname
597787133CV3647807single nucleotide variantNM_001017437.5(CCDC157):c.221C>A (p.Ala74Asp)not specified [RCV004901152]uncertain significance223036622130366221Humanname
597787151CV3647816single nucleotide variantNM_001017437.5(CCDC157):c.196C>T (p.Pro66Ser)not specified [RCV004901157]uncertain significance223036619630366196Humanname
156378977CV2207853single nucleotide variantNM_001017437.5(CCDC157):c.361C>T (p.Arg121Trp)not specified [RCV004084284]uncertain significance223036954430369544Humanname
156306903CV2252788single nucleotide variantNM_001017437.5(CCDC157):c.949G>A (p.Ala317Thr)not specified [RCV004118627]uncertain significance223037085430370854Humanname
156264227CV2282642single nucleotide variantNM_001017437.5(CCDC157):c.410C>T (p.Pro137Leu)not specified [RCV004135199]uncertain significance223036959330369593Humanname
155973524CV2334447single nucleotide variantNM_001017437.5(CCDC157):c.452C>A (p.Ser151Tyr)not specified [RCV004188419]uncertain significance223037035730370357Humanname
156402575CV2361711single nucleotide variantNM_001017437.5(CCDC157):c.853C>T (p.Arg285Cys)not specified [RCV004223191]uncertain significance223037075830370758Humanname
156060281CV2391863single nucleotide variantNM_001017437.5(CCDC157):c.602C>T (p.Thr201Met)not specified [RCV004235736]uncertain significance223037050730370507Humanname
156057461CV2396356single nucleotide variantNM_001017437.5(CCDC157):c.387G>C (p.Arg129Ser)not specified [RCV004242081]uncertain significance223036957030369570Humanname
329380248CV2466502single nucleotide variantNM_001017437.5(CCDC157):c.898G>A (p.Ala300Thr)not specified [RCV004274047]uncertain significance223037080330370803Humanname
401880372CV2780058single nucleotide variantNM_001017437.5(CCDC157):c.832G>A (p.Glu278Lys)not specified [RCV004355723]uncertain significance223037073730370737Humanname
401897010CV2785496single nucleotide variantNM_001017437.5(CCDC157):c.365G>A (p.Arg122His)not specified [RCV004363024]uncertain significance223036954830369548Humanname
405768927CV3303096single nucleotide variantNM_001017437.5(CCDC157):c.472G>A (p.Glu158Lys)not specified [RCV004434939]uncertain significance223037037730370377Humanname
405768933CV3303097single nucleotide variantNM_001017437.5(CCDC157):c.550T>C (p.Cys184Arg)not specified [RCV004434940]uncertain significance223037045530370455Humanname
407484102CV3418363single nucleotide variantNM_001017437.5(CCDC157):c.391G>A (p.Gly131Ser)not specified [RCV004602953]uncertain significance223036957430369574Humanname
597787113CV3647802single nucleotide variantNM_001017437.5(CCDC157):c.864G>C (p.Lys288Asn)not specified [RCV004901147]uncertain significance223037076930370769Humanname
597787124CV3647805single nucleotide variantNM_001017437.5(CCDC157):c.362G>A (p.Arg121Gln)not specified [RCV004901150]uncertain significance223036954530369545Humanname
597787136CV3647808single nucleotide variantNM_001017437.5(CCDC157):c.317C>T (p.Pro106Leu)not specified [RCV004901153]uncertain significance223036950030369500Humanname
597760931CV3647812single nucleotide variantNM_001017437.5(CCDC157):c.313C>T (p.Pro105Ser)not specified [RCV004894873]uncertain significance223036949630369496Humanname
597787147CV3647815single nucleotide variantNM_001017437.5(CCDC157):c.821G>T (p.Arg274Leu)not specified [RCV004901156]uncertain significance223037072630370726Humanname
597760947CV3647817single nucleotide variantNM_001017437.5(CCDC157):c.875C>T (p.Ala292Val)not specified [RCV004894876]uncertain significance223037078030370780Humanname
597787163CV3647820single nucleotide variantNM_001017437.5(CCDC157):c.728A>G (p.Gln243Arg)not specified [RCV004901160]uncertain significance223037063330370633Humanname
598178046CV3946854single nucleotide variantNM_001017437.5(CCDC157):c.667G>C (p.Ala223Pro)not specified [RCV005310297]uncertain significance223037057230370572Humanname
598178054CV3946857single nucleotide variantNM_001017437.5(CCDC157):c.958C>G (p.Gln320Glu)not specified [RCV005310298]uncertain significance223037086330370863Humanname
155922602CV2207533single nucleotide variantNM_001017437.5(CCDC157):c.1873C>T (p.Arg625Trp)not specified [RCV004089998]uncertain significance223037627430376274Humanname
155919880CV2209754single nucleotide variantNM_001017437.5(CCDC157):c.1588C>T (p.Arg530Trp)not specified [RCV004083070]uncertain significance223037400730374007Humanname
155980644CV2272748single nucleotide variantNM_001017437.5(CCDC157):c.1229A>C (p.Gln410Pro)not specified [RCV004135672]uncertain significance223037218030372180Humanname
155923468CV2280304single nucleotide variantNM_001017437.5(CCDC157):c.2212C>G (p.Arg738Gly)not specified [RCV004140504]uncertain significance223037669830376698Humanname
156172120CV2293266single nucleotide variantNM_001017437.5(CCDC157):c.1449G>C (p.Glu483Asp)not specified [RCV004150763]uncertain significance223037371030373710Humanname
156268423CV2305755single nucleotide variantNM_001017437.5(CCDC157):c.2248C>T (p.Arg750Trp)not specified [RCV004167565]uncertain significance223037673430376734Humanname
156395946CV2326009single nucleotide variantNM_001017437.5(CCDC157):c.1394G>A (p.Arg465His)not specified [RCV004176219]uncertain significance223037365530373655Humanname
155920293CV2343326single nucleotide variantNM_001017437.5(CCDC157):c.1556C>T (p.Thr519Met)not specified [RCV004194942]uncertain significance223037397530373975Humanname
156167208CV2345270single nucleotide variantNM_001017437.5(CCDC157):c.1982C>T (p.Thr661Met)not specified [RCV004196005]uncertain significance223037646830376468Humanname
155921941CV2350748single nucleotide variantNM_001017437.5(CCDC157):c.1283C>T (p.Thr428Met)not specified [RCV004207088]uncertain significance223037223430372234Humanname
156069712CV2355876single nucleotide variantNM_001017437.5(CCDC157):c.1865C>T (p.Pro622Leu)not specified [RCV004201266]uncertain significance223037626630376266Humanname
156157420CV2359954single nucleotide variantNM_001017437.5(CCDC157):c.1621C>A (p.Leu541Met)not specified [RCV004212797]uncertain significance223037404030374040Humanname
156010523CV2362137single nucleotide variantNM_001017437.5(CCDC157):c.1436G>A (p.Arg479Gln)not specified [RCV004209940]uncertain significance223037369730373697Humanname
156099411CV2392862single nucleotide variantNM_001017437.5(CCDC157):c.1253G>C (p.Gly418Ala)not specified [RCV004247216]uncertain significance223037220430372204Humanname
156144542CV2393698single nucleotide variantNM_001017437.5(CCDC157):c.1420G>A (p.Glu474Lys)not specified [RCV004231502]uncertain significance223037368130373681Humanname
329373876CV2434644single nucleotide variantNM_001017437.5(CCDC157):c.2249G>A (p.Arg750Gln)not specified [RCV004248365]uncertain significance223037673530376735Humanname
329400650CV2438613single nucleotide variantNM_001017437.5(CCDC157):c.1564C>T (p.Arg522Trp)not specified [RCV004261784]uncertain significance223037398330373983Humanname
329376874CV2451531single nucleotide variantNM_001017437.5(CCDC157):c.1784T>C (p.Leu595Pro)not specified [RCV004274474]uncertain significance223037559030375590Humanname
329360053CV2462428single nucleotide variantNM_001017437.5(CCDC157):c.2000G>C (p.Gly667Ala)not specified [RCV004268183]uncertain significance223037648630376486Humanname
401757192CV2675157single nucleotide variantNM_001017437.5(CCDC157):c.1777C>T (p.Arg593Trp)not specified [RCV004289933]uncertain significance223037558330375583Humanname
401722421CV2676978single nucleotide variantNM_001017437.5(CCDC157):c.1670A>G (p.His557Arg)not specified [RCV004293580]uncertain significance223037408930374089Humanname
401733545CV2691334single nucleotide variantNM_001017437.5(CCDC157):c.1493G>C (p.Arg498Thr)not specified [RCV004303085]uncertain significance223037375430373754Humanname
401762501CV2696147single nucleotide variantNM_001017437.5(CCDC157):c.2240C>A (p.Pro747His)not specified [RCV004310206]uncertain significance223037672630376726Humanname
401743536CV2696813single nucleotide variantNM_001017437.5(CCDC157):c.2095C>T (p.Arg699Trp)not specified [RCV004290782]uncertain significance223037658130376581Humanname
401759078CV2705368single nucleotide variantNM_001017437.5(CCDC157):c.2195A>G (p.Lys732Arg)not specified [RCV004312041]likely benign223037668130376681Humanname
401731788CV2712156single nucleotide variantNM_001017437.5(CCDC157):c.1654A>G (p.Thr552Ala)not specified [RCV004311879]uncertain significance223037407330374073Humanname
401729348CV2732978single nucleotide variantNM_001017437.5(CCDC157):c.1772G>A (p.Arg591His)not specified [RCV004331154]uncertain significance223037557830375578Humanname
401855796CV2757454single nucleotide variantNM_001017437.5(CCDC157):c.1550C>T (p.Ala517Val)not specified [RCV004340846]likely benign223037396930373969Humanname
401892852CV2758123single nucleotide variantNM_001017437.5(CCDC157):c.1283C>G (p.Thr428Arg)not specified [RCV004341503]uncertain significance223037223430372234Humanname
405768868CV3303087single nucleotide variantNM_001017437.5(CCDC157):c.1154G>C (p.Gly385Ala)not specified [RCV004434930]likely benign223037210530372105Humanname
405768875CV3303088single nucleotide variantNM_001017437.5(CCDC157):c.1160G>A (p.Arg387His)not specified [RCV004434931]uncertain significance223037211130372111Humanname
405768881CV3303089single nucleotide variantNM_001017437.5(CCDC157):c.1343A>G (p.Gln448Arg)not specified [RCV004434932]uncertain significance223037360430373604Humanname
405768887CV3303090single nucleotide variantNM_001017437.5(CCDC157):c.1373T>G (p.Leu458Arg)not specified [RCV004434933]uncertain significance223037363430373634Humanname
405768894CV3303091single nucleotide variantNM_001017437.5(CCDC157):c.1469G>A (p.Arg490Gln)not specified [RCV004434934]uncertain significance223037373030373730Humanname
405768909CV3303093single nucleotide variantNM_001017437.5(CCDC157):c.1801C>T (p.Arg601Trp)not specified [RCV004434936]uncertain significance223037560730375607Humanname
405768916CV3303094single nucleotide variantNM_001017437.5(CCDC157):c.1849G>A (p.Gly617Ser)not specified [RCV004434937]uncertain significance223037565530375655Humanname
407484109CV3418364single nucleotide variantNM_001017437.5(CCDC157):c.1704A>G (p.Ile568Met)not specified [RCV004602954]uncertain significance223037551030375510Humanname
407454370CV3418365single nucleotide variantNM_001017437.5(CCDC157):c.1046A>G (p.Glu349Gly)not specified [RCV004609833]uncertain significance223037165030371650Humanname
407454372CV3418366single nucleotide variantNM_001017437.5(CCDC157):c.2072G>C (p.Arg691Pro)not specified [RCV004609834]uncertain significance223037655830376558Humanname
407484124CV3418368single nucleotide variantNM_001017437.5(CCDC157):c.1457T>G (p.Leu486Arg)not specified [RCV004602956]uncertain significance223037371830373718Humanname
597787116CV3647803single nucleotide variantNM_001017437.5(CCDC157):c.1244G>A (p.Arg415Gln)not specified [RCV004901148]uncertain significance223037219530372195Humanname
597787128CV3647806single nucleotide variantNM_001017437.5(CCDC157):c.1312G>A (p.Asp438Asn)not specified [RCV004901151]uncertain significance223037226330372263Humanname
597787140CV3647809single nucleotide variantNM_001017437.5(CCDC157):c.1997T>C (p.Leu666Pro)not specified [RCV004901154]likely benign223037648330376483Humanname
597760926CV3647810single nucleotide variantNM_001017437.5(CCDC157):c.2072G>A (p.Arg691Gln)not specified [RCV004894872]uncertain significance223037655830376558Humanname
597760937CV3647813single nucleotide variantNM_001017437.5(CCDC157):c.1406G>A (p.Arg469Gln)not specified [RCV004894874]likely benign223037366730373667Humanname
597760942CV3647814single nucleotide variantNM_001017437.5(CCDC157):c.1729G>A (p.Val577Ile)not specified [RCV004894875]uncertain significance223037553530375535Humanname
597787155CV3647818single nucleotide variantNM_001017437.5(CCDC157):c.1103G>A (p.Arg368Gln)not specified [RCV004901158]likely benign223037170730371707Humanname
597787159CV3647819single nucleotide variantNM_001017437.5(CCDC157):c.1675G>A (p.Gly559Ser)not specified [RCV004901159]uncertain significance223037548130375481Humanname
597787167CV3647821single nucleotide variantNM_001017437.5(CCDC157):c.1177A>G (p.Arg393Gly)not specified [RCV004901161]uncertain significance223037212830372128Humanname
597787175CV3647823single nucleotide variantNM_001017437.5(CCDC157):c.1178G>A (p.Arg393Lys)not specified [RCV004901163]uncertain significance223037212930372129Humanname
598178005CV3946849single nucleotide variantNM_001017437.5(CCDC157):c.1115A>G (p.Gln372Arg)not specified [RCV005310292]uncertain significance223037171930371719Humanname
598178021CV3946851single nucleotide variantNM_001017437.5(CCDC157):c.1166C>T (p.Ala389Val)not specified [RCV005310294]uncertain significance223037211730372117Humanname
598178030CV3946852single nucleotide variantNM_001017437.5(CCDC157):c.1324C>T (p.Arg442Cys)not specified [RCV005310295]uncertain significance223037227530372275Humanname
598178038CV3946853single nucleotide variantNM_001017437.5(CCDC157):c.1220C>T (p.Ala407Val)not specified [RCV005310296]uncertain significance223037217130372171Humanname
598227292CV3946855single nucleotide variantNM_001017437.5(CCDC157):c.2078C>G (p.Pro693Arg)not specified [RCV005318901]uncertain significance223037656430376564Humanname
598227298CV3946856single nucleotide variantNM_001017437.5(CCDC157):c.1172C>T (p.Ala391Val)not specified [RCV005318902]uncertain significance223037212330372123Humanname
598178062CV3946858single nucleotide variantNM_001017437.5(CCDC157):c.2245G>A (p.Glu749Lys)not specified [RCV005310299]uncertain significance223037673130376731Humanname
598178070CV3946859single nucleotide variantNM_001017437.5(CCDC157):c.1258G>A (p.Gly420Ser)not specified [RCV005310300]likely benign223037220930372209Humanname