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)

63 records found for search term Trim46
Refine Term:
Sort By:
           Export CSV TAB Print

RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598274199CV3935492single nucleotide variantNM_025058.5(TRIM46):c.24G>C (p.Gln8His)not specified [RCV005303805]uncertain significance1155173990155173990Humanname
329395248CV2458238single nucleotide variantNM_025058.5(TRIM46):c.78C>A (p.Asn26Lys)not specified [RCV004265897]uncertain significance1155175400155175400Humanname
401889725CV2763346single nucleotide variantNM_025058.5(TRIM46):c.32C>A (p.Thr11Asn)not specified [RCV004349242]uncertain significance1155173998155173998Humanname
598202835CV3935497single nucleotide variantNM_025058.5(TRIM46):c.28T>C (p.Phe10Leu)not specified [RCV005290440]uncertain significance1155173994155173994Humanname
329357251CV2453501single nucleotide variantNM_025058.5(TRIM46):c.202G>C (p.Gly68Arg)not specified [RCV004269191]uncertain significance1155175524155175524Humanname
401863639CV2770770single nucleotide variantNM_025058.5(TRIM46):c.260G>A (p.Arg87His)not specified [RCV004349809]uncertain significance1155175582155175582Humanname
405796528CV3337029single nucleotide variantNM_025058.5(TRIM46):c.254C>T (p.Ser85Phe)not specified [RCV004475890]uncertain significance1155175576155175576Humanname
407453905CV3490553single nucleotide variantNM_025058.5(TRIM46):c.268C>A (p.Arg90Ser)not specified [RCV004684707]uncertain significance1155175590155175590Humanname
407461463CV3490555single nucleotide variantNM_025058.5(TRIM46):c.1944G>A (p.Ser648=)not specified [RCV004687659]likely benign1155183854155183854Humanname
597801911CV3617809single nucleotide variantNM_025058.5(TRIM46):c.236C>G (p.Ser79Cys)not specified [RCV004880966]uncertain significance1155175558155175558Humanname
15186921CV696138single nucleotide variantNM_025058.5(TRIM46):c.1383C>T (p.His461=)not provided [RCV000953429]benign1155179729155179729Humanname
155973771CV2334474single nucleotide variantNM_025058.5(TRIM46):c.424C>T (p.Arg142Trp)not specified [RCV004188443]uncertain significance1155175986155175986Humanname
156062239CV2392096single nucleotide variantNM_025058.5(TRIM46):c.860C>T (p.Thr287Met)not specified [RCV004237991]uncertain significance1155177241155177241Humanname
329372692CV2451609single nucleotide variantNM_025058.5(TRIM46):c.923A>C (p.Gln308Pro)not specified [RCV004274536]uncertain significance1155178015155178015Humanname
329396839CV2459064single nucleotide variantNM_025058.5(TRIM46):c.341C>T (p.Pro114Leu)not specified [RCV004272532]uncertain significance1155175903155175903Humanname
405796531CV3337030single nucleotide variantNM_025058.5(TRIM46):c.300C>A (p.Asp100Glu)not specified [RCV004475891]uncertain significance1155175622155175622Humanname
405796534CV3337031single nucleotide variantNM_025058.5(TRIM46):c.464G>A (p.Arg155His)not specified [RCV004475892]uncertain significance1155176026155176026Humanname
405796540CV3337033single nucleotide variantNM_025058.5(TRIM46):c.860C>A (p.Thr287Lys)not specified [RCV004475894]uncertain significance1155177241155177241Humanname
407453903CV3490551single nucleotide variantNM_025058.5(TRIM46):c.953G>A (p.Arg318Gln)not specified [RCV004684706]uncertain significance1155178045155178045Humanname
407461459CV3490552single nucleotide variantNM_025058.5(TRIM46):c.368C>T (p.Pro123Leu)not specified [RCV004687658]uncertain significance1155175930155175930Humanname
597801899CV3617803single nucleotide variantNM_025058.5(TRIM46):c.895G>A (p.Val299Met)not specified [RCV004880960]uncertain significance1155177276155177276Humanname
597801901CV3617804single nucleotide variantNM_025058.5(TRIM46):c.425G>A (p.Arg142Gln)not specified [RCV004880961]uncertain significance1155175987155175987Humanname
597801903CV3617805single nucleotide variantNM_025058.5(TRIM46):c.781A>G (p.Thr261Ala)not specified [RCV004880962]uncertain significance1155177043155177043Humanname
597801907CV3617807single nucleotide variantNM_025058.5(TRIM46):c.395C>G (p.Ala132Gly)not specified [RCV004880964]uncertain significance1155175957155175957Humanname
597801913CV3617810single nucleotide variantNM_025058.5(TRIM46):c.794G>A (p.Ser265Asn)not specified [RCV004880967]uncertain significance1155177056155177056Humanname
598202787CV3935486single nucleotide variantNM_025058.5(TRIM46):c.955G>A (p.Gly319Arg)not specified [RCV005290432]uncertain significance1155178047155178047Humanname
598202794CV3935487single nucleotide variantNM_025058.5(TRIM46):c.905C>T (p.Thr302Ile)not specified [RCV005290433]uncertain significance1155177286155177286Humanname
598202817CV3935493single nucleotide variantNM_025058.5(TRIM46):c.476G>A (p.Arg159Gln)not specified [RCV005290437]uncertain significance1155176038155176038Humanname
598274201CV3935496single nucleotide variantNM_025058.5(TRIM46):c.494G>A (p.Ser165Asn)not specified [RCV005303806]uncertain significance1155176056155176056Humanname
598202840CV3935498single nucleotide variantNM_025058.5(TRIM46):c.765C>G (p.His255Gln)not specified [RCV005290441]uncertain significance1155177027155177027Humanname
8624717CV79831single nucleotide variantNM_025058.4(TRIM46):c.385C>T (p.Pro129Ser)Malignant melanoma [RCV000059907]not provided1155175947155175947Humanname
8628966CV84109single nucleotide variantNM_025058.4(TRIM46):c.307G>A (p.Asp103Asn)Malignant melanoma [RCV000064190]not provided1155175629155175629Humanname
156128798CV2238483single nucleotide variantNM_025058.5(TRIM46):c.2141T>G (p.Leu714Trp)not specified [RCV004113535]uncertain significance1155184051155184051Humanname
156167920CV2320052single nucleotide variantNM_025058.5(TRIM46):c.2011G>A (p.Ala671Thr)not specified [RCV004167910]uncertain significance1155183921155183921Humanname
155998749CV2393462single nucleotide variantNM_025058.5(TRIM46):c.1172G>A (p.Arg391Gln)not specified [RCV004228954]uncertain significance1155178500155178500Humanname
329376569CV2428465single nucleotide variantNM_025058.5(TRIM46):c.1033C>T (p.Arg345Cys)not specified [RCV004253257]uncertain significance1155178125155178125Humanname
329359898CV2446465single nucleotide variantNM_025058.5(TRIM46):c.1445G>A (p.Arg482Gln)not specified [RCV004249580]uncertain significance1155179791155179791Humanname
329393717CV2472037single nucleotide variantNM_025058.5(TRIM46):c.1613G>A (p.Arg538His)not specified [RCV004283183]uncertain significance1155181876155181876Humanname
401729535CV2690315single nucleotide variantNM_025058.5(TRIM46):c.2243G>T (p.Arg748Met)not specified [RCV004302310]uncertain significance1155184153155184153Humanname
401731499CV2693835single nucleotide variantNM_025058.5(TRIM46):c.1417G>A (p.Ala473Thr)not specified [RCV004300143]uncertain significance1155179763155179763Humanname
401743763CV2696861single nucleotide variantNM_025058.5(TRIM46):c.1042G>A (p.Ala348Thr)not specified [RCV004290826]uncertain significance1155178134155178134Humanname
401752001CV2703173single nucleotide variantNM_025058.5(TRIM46):c.1183G>A (p.Ala395Thr)not specified [RCV004315241]uncertain significance1155178511155178511Humanname
401879309CV2791383single nucleotide variantNM_025058.5(TRIM46):c.1363C>G (p.His455Asp)not specified [RCV004358785]uncertain significance1155179709155179709Humanname
405796500CV3337021single nucleotide variantNM_025058.5(TRIM46):c.1198C>T (p.Arg400Trp)not specified [RCV004475882]uncertain significance1155178526155178526Humanname
405796508CV3337023single nucleotide variantNM_025058.5(TRIM46):c.1592T>G (p.Leu531Arg)not specified [RCV004475884]uncertain significance1155181855155181855Humanname
405796511CV3337024single nucleotide variantNM_025058.5(TRIM46):c.1606G>A (p.Asp536Asn)not specified [RCV004475885]uncertain significance1155181869155181869Humanname
405796514CV3337025single nucleotide variantNM_025058.5(TRIM46):c.1621G>A (p.Ala541Thr)not specified [RCV004475886]likely benign1155181884155181884Humanname
405796517CV3337026single nucleotide variantNM_025058.5(TRIM46):c.1628G>A (p.Arg543Gln)not specified [RCV004475887]uncertain significance1155181891155181891Humanname
405796520CV3337027single nucleotide variantNM_025058.5(TRIM46):c.2102G>T (p.Arg701Leu)not specified [RCV004475888]uncertain significance1155184012155184012Humanname
405796525CV3337028single nucleotide variantNM_025058.5(TRIM46):c.2191A>G (p.Ile731Val)not specified [RCV004475889]uncertain significance1155184101155184101Humanname
407453892CV3490547single nucleotide variantNM_025058.5(TRIM46):c.1403G>A (p.Arg468His)not specified [RCV004684702]uncertain significance1155179749155179749Humanname
407453895CV3490548single nucleotide variantNM_025058.5(TRIM46):c.1171C>G (p.Arg391Gly)not specified [RCV004684703]uncertain significance1155178499155178499Humanname
407453897CV3490549single nucleotide variantNM_025058.5(TRIM46):c.2044G>A (p.Gly682Ser)not specified [RCV004684704]likely benign1155183954155183954Humanname
407453900CV3490550single nucleotide variantNM_025058.5(TRIM46):c.1789G>A (p.Ala597Thr)not specified [RCV004684705]uncertain significance1155182052155182052Humanname
407453908CV3490554single nucleotide variantNM_025058.5(TRIM46):c.1705C>T (p.Arg569Trp)not specified [RCV004684708]uncertain significance1155181968155181968Humanname
597801905CV3617806single nucleotide variantNM_025058.5(TRIM46):c.1202C>T (p.Pro401Leu)not specified [RCV004880963]uncertain significance1155178530155178530Humanname
597801909CV3617808single nucleotide variantNM_025058.5(TRIM46):c.1234C>T (p.Leu412Phe)not specified [RCV004880965]uncertain significance1155178562155178562Humanname
598274196CV3935488single nucleotide variantNM_025058.5(TRIM46):c.2255T>C (p.Ile752Thr)not specified [RCV005303804]uncertain significance1155184165155184165Humanname
598202799CV3935489single nucleotide variantNM_025058.5(TRIM46):c.1609A>G (p.Ser537Gly)not specified [RCV005290434]likely benign1155181872155181872Humanname
598202805CV3935490single nucleotide variantNM_025058.5(TRIM46):c.1999G>T (p.Ala667Ser)not specified [RCV005290435]uncertain significance1155183909155183909Humanname
598202823CV3935494single nucleotide variantNM_025058.5(TRIM46):c.1966A>G (p.Ile656Val)not specified [RCV005290438]uncertain significance1155183876155183876Humanname
598202829CV3935495single nucleotide variantNM_025058.5(TRIM46):c.1406C>T (p.Thr469Met)not specified [RCV005290439]uncertain significance1155179752155179752Humanname
8574916CV109255single nucleotide variantNM_001256599.1(TRIM46):c.1999C>T (p.Arg667Cys)Lung cancer [RCV000089780]uncertain significance1155183978155183978Humanname