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)

33 records found for search term Ccnl1
Refine Term:
Assembly:
    Chr  
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598205373CV3939824single nucleotide variantNM_020307.4(CCNL1):c.11G>C (p.Gly4Ala)not specified [RCV005314940]uncertain significance3157160084157160084Humanname
156365187CV2193146single nucleotide variantNM_020307.4(CCNL1):c.37G>A (p.Ala13Thr)not specified [RCV004071145]uncertain significance3157160058157160058Humanname
156164522CV2270275single nucleotide variantNM_020307.4(CCNL1):c.94A>G (p.Thr32Ala)not specified [RCV004135492]uncertain significance3157160001157160001Humanname
407492032CV3428666single nucleotide variantNM_020307.4(CCNL1):c.37G>T (p.Ala13Ser)not specified [RCV004604861]uncertain significance3157160058157160058Humanname
156023714CV2245505single nucleotide variantNM_020307.4(CCNL1):c.112G>A (p.Gly38Arg)not specified [RCV004109278]uncertain significance3157159983157159983Humanname
407492011CV3428661single nucleotide variantNM_020307.4(CCNL1):c.188G>C (p.Arg63Thr)not specified [RCV004604856]uncertain significance3157159907157159907Humanname
407492024CV3428664single nucleotide variantNM_020307.4(CCNL1):c.211C>G (p.Gln71Glu)not specified [RCV004604859]uncertain significance3157159884157159884Humanname
407492028CV3428665single nucleotide variantNM_020307.4(CCNL1):c.196C>A (p.Pro66Thr)not specified [RCV004604860]uncertain significance3157159899157159899Humanname
597766228CV3638236single nucleotide variantNM_020307.4(CCNL1):c.110C>A (p.Thr37Lys)not specified [RCV004896080]uncertain significance3157159985157159985Humanname
597766237CV3638238single nucleotide variantNM_020307.4(CCNL1):c.1494G>A (p.Arg498=)not specified [RCV004896082]likely benign3157148328157148328Humanname
597766247CV3638240single nucleotide variantNM_020307.4(CCNL1):c.262G>A (p.Glu88Lys)not specified [RCV004896084]uncertain significance3157159833157159833Humanname
156000196CV2296283single nucleotide variantNM_020307.4(CCNL1):c.742G>T (p.Ala248Ser)not specified [RCV004154185]uncertain significance3157150314157150314Humanname
329394394CV2469848single nucleotide variantNM_020307.4(CCNL1):c.436A>G (p.Ile146Val)not specified [RCV004285328]uncertain significance3157158918157158918Humanname
401723575CV2724951single nucleotide variantNM_020307.4(CCNL1):c.491C>T (p.Thr164Ile)not specified [RCV004319715]uncertain significance3157153154157153154Humanname
405741949CV3303175single nucleotide variantNM_020307.4(CCNL1):c.787A>G (p.Thr263Ala)not specified [RCV004430796]uncertain significance3157150157157150157Humanname
405741940CV3303176single nucleotide variantNM_020307.4(CCNL1):c.832A>G (p.Ile278Val)not specified [RCV004430797]uncertain significance3157150112157150112Humanname
598228391CV3939825single nucleotide variantNM_020307.4(CCNL1):c.704A>G (p.Asn235Ser)not specified [RCV005319076]uncertain significance3157150352157150352Humanname
155981675CV2272885single nucleotide variantNM_020307.4(CCNL1):c.1377T>G (p.Ser459Arg)not specified [RCV004135785]uncertain significance3157148445157148445Humanname
156274347CV2320010single nucleotide variantNM_020307.4(CCNL1):c.1438G>T (p.Asp480Tyr)not specified [RCV004167877]uncertain significance3157148384157148384Humanname
329374232CV2434744single nucleotide variantNM_020307.4(CCNL1):c.1174G>C (p.Ala392Pro)not specified [RCV004248448]uncertain significance3157149345157149345Humanname
329380386CV2444361single nucleotide variantNM_020307.4(CCNL1):c.1436G>A (p.Arg479Gln)not specified [RCV004263112]uncertain significance3157148386157148386Humanname
401762965CV2720145single nucleotide variantNM_020307.4(CCNL1):c.1378T>A (p.Ser460Thr)not specified [RCV004323704]uncertain significance3157148444157148444Humanname
405741971CV3303171single nucleotide variantNM_020307.4(CCNL1):c.1042G>A (p.Ala348Thr)not specified [RCV004430792]uncertain significance3157149576157149576Humanname
405741965CV3303172single nucleotide variantNM_020307.4(CCNL1):c.1247G>A (p.Arg416Gln)not specified [RCV004430793]uncertain significance3157148575157148575Humanname
405741954CV3303174single nucleotide variantNM_020307.4(CCNL1):c.1562A>G (p.His521Arg)not specified [RCV004430795]uncertain significance3157148260157148260Humanname
407492015CV3428662single nucleotide variantNM_020307.4(CCNL1):c.1490A>G (p.Asp497Gly)not specified [RCV004604857]uncertain significance3157148332157148332Humanname
407492019CV3428663single nucleotide variantNM_020307.4(CCNL1):c.1556C>T (p.Ser519Leu)not specified [RCV004604858]uncertain significance3157148266157148266Humanname
407454603CV3428667single nucleotide variantNM_020307.4(CCNL1):c.1162A>C (p.Asn388His)not specified [RCV004609914]uncertain significance3157149357157149357Humanname
407492037CV3428668single nucleotide variantNM_020307.4(CCNL1):c.1186A>G (p.Arg396Gly)not specified [RCV004604862]uncertain significance3157149333157149333Humanname
597766233CV3638237single nucleotide variantNM_020307.4(CCNL1):c.1435C>T (p.Arg479Trp)not specified [RCV004896081]uncertain significance3157148387157148387Humanname
597766242CV3638239single nucleotide variantNM_020307.4(CCNL1):c.1217A>G (p.His406Arg)not specified [RCV004896083]uncertain significance3157149302157149302Humanname
598205357CV3939822single nucleotide variantNM_020307.4(CCNL1):c.1358C>A (p.Thr453Asn)not specified [RCV005314938]uncertain significance3157148464157148464Humanname
598205365CV3939823single nucleotide variantNM_020307.4(CCNL1):c.1060A>G (p.Ile354Val)not specified [RCV005314939]likely benign3157149558157149558Humanname