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86 records found for search term Fcrl3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156171725CV2198035single nucleotide variantNM_052939.4(FCRL3):c.4C>G (p.Leu2Val)not specified [RCV004077238]uncertain significance1157700486157700486Humanname
597740072CV3676092single nucleotide variantNM_052939.4(FCRL3):c.27C>G (p.Ile9Met)not specified [RCV004921387]uncertain significance1157700463157700463Humanname
329360146CV2446612single nucleotide variantNM_052939.4(FCRL3):c.53G>T (p.Gly18Val)not specified [RCV004251503]uncertain significance1157698629157698629Humanname
405742531CV3256938single nucleotide variantNM_052939.4(FCRL3):c.47A>G (p.Gln16Arg)not specified [RCV004391554]uncertain significance1157699697157699697Humanname
405742575CV3256944single nucleotide variantNM_052939.4(FCRL3):c.94T>A (p.Ser32Thr)not specified [RCV004391560]uncertain significance1157698588157698588Humanname
407483200CV3438883single nucleotide variantNM_052939.4(FCRL3):c.73C>T (p.Leu25Phe)not specified [RCV004618526]uncertain significance1157698609157698609Humanname
156084567CV2289721single nucleotide variantNM_052939.4(FCRL3):c.118G>C (p.Val40Leu)not specified [RCV004150416]uncertain significance1157698564157698564Humanname
156176965CV2374486single nucleotide variantNM_052939.4(FCRL3):c.158A>G (p.Gln53Arg)not specified [RCV004231992]likely benign1157698524157698524Humanname
401743820CV2696873single nucleotide variantNM_052939.4(FCRL3):c.209A>G (p.Asp70Gly)not specified [RCV004290837]uncertain significance1157698473157698473Humanname
407483192CV3438882single nucleotide variantNM_052939.4(FCRL3):c.125T>C (p.Leu42Pro)not specified [RCV004618525]uncertain significance1157698557157698557Humanname
597740077CV3676093single nucleotide variantNM_052939.4(FCRL3):c.268A>C (p.Ser90Arg)not specified [RCV004921388]uncertain significance1157698414157698414Humanname
15193690CV718288single nucleotide variantNM_052939.4(FCRL3):c.1854G>A (p.Glu618=)not provided [RCV000889016]benign1157681084157681084Humanname
8628993CV84136single nucleotide variantNM_052939.3(FCRL3):c.127A>C (p.Ile43Leu)Malignant melanoma [RCV000064217]not provided1157698555157698555Humanname
156230051CV2235022single nucleotide variantNM_052939.4(FCRL3):c.394G>A (p.Val132Ile)not specified [RCV004113209]uncertain significance1157697824157697824Humanname
156155849CV2238302single nucleotide variantNM_052939.4(FCRL3):c.992T>C (p.Leu331Pro)not specified [RCV004113380]uncertain significance1157696180157696180Humanname
156294903CV2239509single nucleotide variantNM_052939.4(FCRL3):c.762C>A (p.Asp254Glu)not specified [RCV004114510]uncertain significance1157697222157697222Humanname
156255607CV2264741single nucleotide variantNM_052939.4(FCRL3):c.617C>T (p.Pro206Leu)not specified [RCV004132724]uncertain significance1157697367157697367Humanname
155959698CV2285306single nucleotide variantNM_052939.4(FCRL3):c.958T>C (p.Phe320Leu)not specified [RCV004139186]uncertain significance1157696214157696214Humanname
156152163CV2307609single nucleotide variantNM_052939.4(FCRL3):c.446T>A (p.Ile149Asn)not specified [RCV004168032]uncertain significance1157697772157697772Humanname
156080432CV2337516single nucleotide variantNM_052939.4(FCRL3):c.315G>C (p.Gln105His)not specified [RCV004187946]uncertain significance1157697903157697903Humanname
156170303CV2354853single nucleotide variantNM_052939.4(FCRL3):c.836G>A (p.Arg279His)not specified [RCV004191351]likely benign1157697148157697148Humanname
155992602CV2381529single nucleotide variantNM_052939.4(FCRL3):c.437T>C (p.Leu146Ser)not specified [RCV004230006]likely benign1157697781157697781Humanname
156051693CV2386405single nucleotide variantNM_052939.4(FCRL3):c.584G>A (p.Arg195Lys)not specified [RCV004228734]uncertain significance1157697400157697400Humanname
329402050CV2453952single nucleotide variantNM_052939.4(FCRL3):c.599C>T (p.Thr200Met)not specified [RCV004271624]uncertain significance1157697385157697385Humanname
401889286CV2759761single nucleotide variantNM_052939.4(FCRL3):c.915G>C (p.Met305Ile)not specified [RCV004342806]uncertain significance1157696257157696257Humanname
401864964CV2791432single nucleotide variantNM_052939.4(FCRL3):c.599C>A (p.Thr200Lys)not specified [RCV004358823]uncertain significance1157697385157697385Humanname
405262823CV3185040single nucleotide variantNM_052939.4(FCRL3):c.935C>A (p.Ala312Asp)not provided [RCV003885604]likely benign1157696237157696237Human1name
405262823CV3185040single nucleotide variantNM_052939.4(FCRL3):c.935C>A (p.Ala312Asp)not provided [RCV003885604]likely benign1157696237157696238Human1name
405742542CV3256939single nucleotide variantNM_052939.4(FCRL3):c.548T>C (p.Ile183Thr)not specified [RCV004391555]uncertain significance1157697670157697670Humanname
405742556CV3256941single nucleotide variantNM_052939.4(FCRL3):c.722G>A (p.Arg241Lys)not specified [RCV004391557]uncertain significance1157697262157697262Humanname
405742562CV3256942single nucleotide variantNM_052939.4(FCRL3):c.791C>G (p.Thr264Arg)not specified [RCV004391558]uncertain significance1157697193157697193Humanname
405742569CV3256943single nucleotide variantNM_052939.4(FCRL3):c.834A>G (p.Ile278Met)not specified [RCV004391559]uncertain significance1157697150157697150Humanname
407483186CV3438881single nucleotide variantNM_052939.4(FCRL3):c.328G>T (p.Val110Phe)not specified [RCV004618524]uncertain significance1157697890157697890Humanname
407483218CV3438886single nucleotide variantNM_052939.4(FCRL3):c.926G>T (p.Cys309Phe)not specified [RCV004618529]uncertain significance1157696246157696246Humanname
597740035CV3676084single nucleotide variantNM_052939.4(FCRL3):c.926G>A (p.Cys309Tyr)not specified [RCV004921379]uncertain significance1157696246157696246Humanname
597740050CV3676087single nucleotide variantNM_052939.4(FCRL3):c.889G>C (p.Gly297Arg)not specified [RCV004921382]uncertain significance1157696283157696283Humanname
597740055CV3676088single nucleotide variantNM_052939.4(FCRL3):c.431A>G (p.Tyr144Cys)not specified [RCV004921383]uncertain significance1157697787157697787Humanname
597740060CV3676089single nucleotide variantNM_052939.4(FCRL3):c.941G>A (p.Gly314Asp)not specified [RCV004921384]uncertain significance1157696231157696231Humanname
597740087CV3676095single nucleotide variantNM_052939.4(FCRL3):c.629C>A (p.Thr210Asn)not specified [RCV004921390]uncertain significance1157697355157697355Humanname
598239861CV3959160single nucleotide variantNM_052939.4(FCRL3):c.548T>A (p.Ile183Asn)not specified [RCV005344095]uncertain significance1157697670157697670Humanname
598239873CV3959162single nucleotide variantNM_052939.4(FCRL3):c.499A>T (p.Arg167Trp)not specified [RCV005344097]uncertain significance1157697719157697719Humanname
598239881CV3959163single nucleotide variantNM_052939.4(FCRL3):c.839T>C (p.Val280Ala)not specified [RCV005344098]uncertain significance1157697145157697145Humanname
598239887CV3959164single nucleotide variantNM_052939.4(FCRL3):c.403A>G (p.Lys135Glu)not specified [RCV005344099]uncertain significance1157697815157697815Humanname
15193031CV696184single nucleotide variantNM_052939.4(FCRL3):c.878G>T (p.Arg293Leu)not provided [RCV000955251]benign1157696294157696294Humanname
15178980CV731787single nucleotide variantNM_052939.4(FCRL3):c.919C>T (p.Leu307Phe)not provided [RCV000907001]benign1157696253157696253Humanname
150492884CV1281484single nucleotide variantNM_052939.4(FCRL3):c.2162A>G (p.Asn721Ser)not provided [RCV001716897]benign1157678753157678753Humanname
156134588CV2213188single nucleotide variantNM_052939.4(FCRL3):c.1966G>A (p.Gly656Arg)not specified [RCV004085417]uncertain significance1157680762157680762Humanname
155978583CV2215062single nucleotide variantNM_052939.4(FCRL3):c.1120G>A (p.Val374Ile)not specified [RCV004084832]uncertain significance1157696052157696052Humanname
156284964CV2334804single nucleotide variantNM_052939.4(FCRL3):c.1031A>T (p.His344Leu)not specified [RCV004181918]uncertain significance1157696141157696141Humanname
156331116CV2339590single nucleotide variantNM_052939.4(FCRL3):c.1811G>A (p.Gly604Glu)not specified [RCV004603314]uncertain significance1157683244157683244Humanname
156345411CV2382192single nucleotide variantNM_052939.4(FCRL3):c.1537G>A (p.Glu513Lys)not specified [RCV004228144]uncertain significance1157690408157690408Humanname
156345423CV2382193single nucleotide variantNM_052939.4(FCRL3):c.1799G>A (p.Arg600Gln)not specified [RCV004228145]likely benign1157689809157689809Humanname
156059709CV2383563single nucleotide variantNM_052939.4(FCRL3):c.1507T>G (p.Ser503Ala)not specified [RCV004224434]uncertain significance1157690438157690438Humanname
156082105CV2384823single nucleotide variantNM_052939.4(FCRL3):c.1956T>A (p.Asn652Lys)not specified [RCV004225712]uncertain significance1157680982157680982Humanname
329368729CV2428118single nucleotide variantNM_052939.4(FCRL3):c.1930A>G (p.Met644Val)not specified [RCV004254490]likely benign1157681008157681008Humanname
401743623CV2687994single nucleotide variantNM_052939.4(FCRL3):c.1417G>A (p.Val473Met)not specified [RCV004305069]uncertain significance1157690528157690528Humanname
401734666CV2690647single nucleotide variantNM_052939.4(FCRL3):c.1363A>G (p.Asn455Asp)not specified [RCV004298384]uncertain significance1157695377157695377Humanname
401759916CV2698673single nucleotide variantNM_052939.4(FCRL3):c.1679T>C (p.Leu560Pro)not specified [RCV004299139]uncertain significance1157690266157690266Humanname
401749156CV2708483single nucleotide variantNM_052939.4(FCRL3):c.2075A>G (p.Tyr692Cys)not specified [RCV004313576]uncertain significance1157678840157678840Humanname
401761870CV2713928single nucleotide variantNM_052939.4(FCRL3):c.1871C>T (p.Ser624Leu)not specified [RCV004315354]likely benign1157681067157681067Humanname
401861839CV2766427single nucleotide variantNM_052939.4(FCRL3):c.1676C>T (p.Thr559Ile)not specified [RCV004345270]uncertain significance1157690269157690269Humanname
401862845CV2779040single nucleotide variantNM_052939.4(FCRL3):c.1514C>T (p.Pro505Leu)not specified [RCV004348685]uncertain significance1157690431157690431Humanname
405867566CV2842325single nucleotide variantNM_052939.4(FCRL3):c.1087G>A (p.Val363Ile)EBV-positive nodal T- and NK-cell lymphoma [RCV004560274]likely benign1157696085157696085Humanname
405742460CV3256927single nucleotide variantNM_052939.4(FCRL3):c.1328C>T (p.Ala443Val)not specified [RCV004391543]uncertain significance1157695412157695412Humanname
405742468CV3256928single nucleotide variantNM_052939.4(FCRL3):c.1382A>G (p.His461Arg)not specified [RCV004391544]likely benign1157695358157695358Humanname
405742474CV3256929single nucleotide variantNM_052939.4(FCRL3):c.1450G>A (p.Gly484Arg)not specified [RCV004391545]uncertain significance1157690495157690495Humanname
405742480CV3256930single nucleotide variantNM_052939.4(FCRL3):c.1484T>C (p.Leu495Pro)not specified [RCV004391546]uncertain significance1157690461157690461Humanname
405742486CV3256931single nucleotide variantNM_052939.4(FCRL3):c.1580G>A (p.Gly527Glu)not specified [RCV004391547]uncertain significance1157690365157690365Humanname
405742492CV3256932single nucleotide variantNM_052939.4(FCRL3):c.1720G>A (p.Ala574Thr)not specified [RCV004391548]likely benign1157689888157689888Humanname
405742497CV3256933single nucleotide variantNM_052939.4(FCRL3):c.1720G>T (p.Ala574Ser)not specified [RCV004391549]uncertain significance1157689888157689888Humanname
405742503CV3256934single nucleotide variantNM_052939.4(FCRL3):c.1756G>A (p.Val586Ile)not specified [RCV004391550]uncertain significance1157689852157689852Humanname
405742510CV3256935single nucleotide variantNM_052939.4(FCRL3):c.2021A>G (p.Asn674Ser)not specified [RCV004391551]uncertain significance1157680707157680707Humanname
405742519CV3256936single nucleotide variantNM_052939.4(FCRL3):c.2104G>A (p.Asp702Asn)not specified [RCV004391552]uncertain significance1157678811157678811Humanname
407483213CV3438885single nucleotide variantNM_052939.4(FCRL3):c.1298G>A (p.Gly433Glu)not specified [RCV004618528]uncertain significance1157695442157695442Humanname
407483224CV3438887single nucleotide variantNM_052939.4(FCRL3):c.1108A>G (p.Thr370Ala)not specified [RCV004618530]uncertain significance1157696064157696064Humanname
407483230CV3438888single nucleotide variantNM_052939.4(FCRL3):c.1102C>T (p.Leu368Phe)not specified [RCV004618531]uncertain significance1157696070157696070Humanname
597740020CV3676081single nucleotide variantNM_052939.4(FCRL3):c.1513C>A (p.Pro505Thr)not specified [RCV004921376]uncertain significance1157690432157690432Humanname
597740025CV3676082single nucleotide variantNM_052939.4(FCRL3):c.1691G>C (p.Gly564Ala)not specified [RCV004921377]uncertain significance1157689917157689917Humanname
597740040CV3676085single nucleotide variantNM_052939.4(FCRL3):c.2179C>A (p.Arg727Ser)not specified [RCV004921380]uncertain significance1157678736157678736Humanname
597740045CV3676086single nucleotide variantNM_052939.4(FCRL3):c.1597T>C (p.Ser533Pro)not specified [RCV004921381]uncertain significance1157690348157690348Humanname
597740062CV3676090single nucleotide variantNM_052939.4(FCRL3):c.1775C>T (p.Ala592Val)not specified [RCV004921385]uncertain significance1157689833157689833Humanname
597740067CV3676091single nucleotide variantNM_052939.4(FCRL3):c.1643A>G (p.Asn548Ser)not specified [RCV004921386]uncertain significance1157690302157690302Humanname
597740082CV3676094single nucleotide variantNM_052939.4(FCRL3):c.2114G>A (p.Gly705Glu)not specified [RCV004921389]uncertain significance1157678801157678801Humanname
597740090CV3676096single nucleotide variantNM_052939.4(FCRL3):c.1735G>C (p.Gly579Arg)not specified [RCV004921391]uncertain significance1157689873157689873Humanname
598239867CV3959161single nucleotide variantNM_052939.4(FCRL3):c.1958T>C (p.Val653Ala)not specified [RCV005344096]uncertain significance1157680770157680770Humanname
15198002CV696183single nucleotide variantNM_052939.4(FCRL3):c.1132A>G (p.Ile378Val)not provided [RCV000956624]benign|likely benign1157696040157696040Humanname