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172 records found for search term Radil
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401757756CV2707953single nucleotide variantNM_018059.5(RADIL):c.4T>C (p.Phe2Leu)not specified [RCV004309217]uncertain significance748781364878136Humanname
156148651CV2394506single nucleotide variantNM_018059.5(RADIL):c.14C>T (p.Thr5Met)not specified [RCV004240864]uncertain significance748781264878126Humanname
329362080CV2448278single nucleotide variantNM_018059.5(RADIL):c.17A>G (p.His6Arg)not specified [RCV004263477]uncertain significance748781234878123Humanname
405692066CV3315201single nucleotide variantNM_018059.5(RADIL):c.23T>G (p.Ile8Ser)not specified [RCV004445531]uncertain significance748781174878117Humanname
8632593CV87808single nucleotide variantNM_018059.4(RADIL):c.279G>A (p.Val93=)Malignant melanoma [RCV000067900]not provided748778614877861Humanname
401908704CV2828260single nucleotide variantNM_018059.5(RADIL):c.897C>T (p.Thr299=)not provided [RCV003423534]likely benign748351264835126Humanname
401908708CV2828263single nucleotide variantNM_018059.5(RADIL):c.345G>C (p.Val115=)not provided [RCV003423537]likely benign748777954877795Humanname
597753389CV3582447single nucleotide variantNM_018059.5(RADIL):c.74C>G (p.Ser25Cys)not specified [RCV004847069]uncertain significance748780664878066Humanname
156061567CV2323180single nucleotide variantNM_018059.5(RADIL):c.143C>T (p.Ala48Val)not specified [RCV004187581]uncertain significance748779974877997Humanname
156081230CV2368782single nucleotide variantNM_018059.5(RADIL):c.190G>C (p.Val64Leu)not specified [RCV004214658]uncertain significance748779504877950Humanname
407485480CV3472126single nucleotide variantNM_018059.5(RADIL):c.271G>A (p.Glu91Lys)not specified [RCV004665305]uncertain significance748778694877869Humanname
407485484CV3472127single nucleotide variantNM_018059.5(RADIL):c.1542C>T (p.Ile514=)not specified [RCV004665306]likely benign748224674822467Humanname
597753392CV3582448single nucleotide variantNM_018059.5(RADIL):c.260C>G (p.Ser87Cys)not specified [RCV004847070]uncertain significance748778804877880Humanname
598174128CV3905119single nucleotide variantNM_018059.5(RADIL):c.253G>A (p.Gly85Ser)not specified [RCV005263805]uncertain significance748778874877887Humanname
15197413CV700122single nucleotide variantNM_018059.5(RADIL):c.2013C>T (p.Cys671=)not provided [RCV000956458]likely benign748154044815404Humanname
15127323CV711031single nucleotide variantNM_018059.5(RADIL):c.1749G>A (p.Pro583=)not provided [RCV000963882]benign748164454816445Humanname
15101413CV750674single nucleotide variantNM_018059.5(RADIL):c.2100C>T (p.Thr700=)not provided [RCV000914777]likely benign748153174815317Humanname
156282480CV2295197single nucleotide variantNM_018059.5(RADIL):c.905G>T (p.Arg302Leu)not specified [RCV004158288]uncertain significance748351184835118Humanname
156291115CV2296599single nucleotide variantNM_018059.5(RADIL):c.619C>T (p.Pro207Ser)not specified [RCV004154661]uncertain significance748365224836522Humanname
156092168CV2302488single nucleotide variantNM_018059.5(RADIL):c.365C>T (p.Ala122Val)not specified [RCV004161214]uncertain significance748777754877775Humanname
156063705CV2315970single nucleotide variantNM_018059.5(RADIL):c.979G>A (p.Val327Ile)not specified [RCV004172036]uncertain significance748350444835044Humanname
155904610CV2353919single nucleotide variantNM_018059.5(RADIL):c.587C>T (p.Pro196Leu)not specified [RCV004201914]uncertain significance748365544836554Humanname
156149096CV2377378single nucleotide variantNM_018059.5(RADIL):c.961C>G (p.Pro321Ala)not specified [RCV004225557]uncertain significance748350624835062Humanname
401739845CV2684191single nucleotide variantNM_018059.5(RADIL):c.571C>T (p.Arg191Cys)not specified [RCV004288861]uncertain significance748365704836570Humanname
401732999CV2691172single nucleotide variantNM_018059.5(RADIL):c.682G>A (p.Ala228Thr)not specified [RCV004302949]uncertain significance748364594836459Humanname
401749793CV2694752single nucleotide variantNM_018059.5(RADIL):c.319G>C (p.Ala107Pro)not specified [RCV004298838]uncertain significance748778214877821Humanname
401758239CV2729610single nucleotide variantNM_018059.5(RADIL):c.725G>A (p.Arg242Gln)not specified [RCV004331874]uncertain significance748364164836416Humanname
401888457CV2761420single nucleotide variantNM_018059.5(RADIL):c.493G>A (p.Val165Met)not specified [RCV004334599]uncertain significance748776474877647Humanname
401908705CV2828261single nucleotide variantNM_018059.5(RADIL):c.709G>C (p.Gly237Arg)not provided [RCV003423535]likely benign748364324836432Humanname
405692132CV3315210single nucleotide variantNM_018059.5(RADIL):c.429C>G (p.Ile143Met)not specified [RCV004445540]uncertain significance748777114877711Humanname
405692138CV3315211single nucleotide variantNM_018059.5(RADIL):c.474G>T (p.Glu158Asp)not specified [RCV004445541]uncertain significance748776664877666Humanname
405692142CV3315212single nucleotide variantNM_018059.5(RADIL):c.620C>A (p.Pro207His)not specified [RCV004445542]uncertain significance748365214836521Humanname
405692150CV3315213single nucleotide variantNM_018059.5(RADIL):c.688G>T (p.Ala230Ser)not specified [RCV004445543]uncertain significance748364534836453Humanname
405692157CV3315214single nucleotide variantNM_018059.5(RADIL):c.904C>T (p.Arg302Trp)not specified [RCV004445544]uncertain significance748351194835119Humanname
405692162CV3315215single nucleotide variantNM_018059.5(RADIL):c.956C>T (p.Pro319Leu)not specified [RCV004445545]uncertain significance748350674835067Humanname
405692168CV3315216single nucleotide variantNM_018059.5(RADIL):c.970C>A (p.His324Asn)not specified [RCV004445546]uncertain significance748350534835053Humanname
407485457CV3472120single nucleotide variantNM_018059.5(RADIL):c.395G>A (p.Arg132Gln)not specified [RCV004665301]uncertain significance748777454877745Humanname
597753353CV3582427single nucleotide variantNM_018059.5(RADIL):c.629G>A (p.Arg210Gln)not specified [RCV004847060]uncertain significance748365124836512Humanname
597684531CV3582429single nucleotide variantNM_018059.5(RADIL):c.809G>A (p.Arg270Gln)not specified [RCV004858183]uncertain significance748352144835214Humanname
597684565CV3582435single nucleotide variantNM_018059.5(RADIL):c.610C>T (p.Arg204Trp)not specified [RCV004858187]uncertain significance748365314836531Humanname
597684585CV3582437single nucleotide variantNM_018059.5(RADIL):c.488C>T (p.Ser163Leu)not specified [RCV004858189]uncertain significance748776524877652Humanname
597753396CV3582449single nucleotide variantNM_018059.5(RADIL):c.547C>G (p.Gln183Glu)not specified [RCV004847071]uncertain significance748365944836594Humanname
597684645CV3582452single nucleotide variantNM_018059.5(RADIL):c.760C>G (p.Leu254Val)not specified [RCV004858195]uncertain significance748363814836381Humanname
597684661CV3582454single nucleotide variantNM_018059.5(RADIL):c.968C>T (p.Ala323Val)not specified [RCV004858197]uncertain significance748350554835055Humanname
597753407CV3582456single nucleotide variantNM_018059.5(RADIL):c.635G>A (p.Arg212His)not specified [RCV004847074]uncertain significance748365064836506Humanname
598174025CV3905103single nucleotide variantNM_018059.5(RADIL):c.700G>A (p.Glu234Lys)not specified [RCV005263789]uncertain significance748364414836441Humanname
598174056CV3905108single nucleotide variantNM_018059.5(RADIL):c.374G>A (p.Arg125Gln)not specified [RCV005263794]likely benign748777664877766Humanname
598174107CV3905116single nucleotide variantNM_018059.5(RADIL):c.553C>T (p.Arg185Trp)not specified [RCV005263802]uncertain significance748365884836588Humanname
598174112CV3905117single nucleotide variantNM_018059.5(RADIL):c.449G>A (p.Arg150Gln)not specified [RCV005263803]uncertain significance748776914877691Humanname
598174119CV3905118single nucleotide variantNM_018059.5(RADIL):c.911C>G (p.Pro304Arg)not specified [RCV005263804]uncertain significance748351124835112Humanname
15197410CV700120single nucleotide variantNM_018059.5(RADIL):c.3072C>T (p.Asp1024=)not provided [RCV000956457]benign747996804799680Humanname
156320829CV2197415single nucleotide variantNM_018059.5(RADIL):c.1937C>T (p.Thr646Ile)not specified [RCV004081153]uncertain significance748162574816257Humanname
156264871CV2198609single nucleotide variantNM_018059.5(RADIL):c.1448C>T (p.Ala483Val)not specified [RCV004075627]uncertain significance748321474832147Humanname
156377096CV2206961single nucleotide variantNM_018059.5(RADIL):c.2896T>G (p.Ser966Ala)not specified [RCV004085583]uncertain significance748002574800257Humanname
156125241CV2223544single nucleotide variantNM_018059.5(RADIL):c.2432G>A (p.Arg811Gln)not specified [RCV004091921]uncertain significance748036134803613Humanname
156383028CV2223750single nucleotide variantNM_018059.5(RADIL):c.2600G>A (p.Arg867His)not specified [RCV004093835]likely benign748018954801895Humanname
155914227CV2242649single nucleotide variantNM_018059.5(RADIL):c.2267A>G (p.Asp756Gly)not specified [RCV004113704]uncertain significance748055894805589Humanname
156275034CV2287561single nucleotide variantNM_018059.5(RADIL):c.2659C>T (p.Arg887Cys)not specified [RCV004141011]uncertain significance748018364801836Humanname
156346324CV2305268single nucleotide variantNM_018059.5(RADIL):c.2158C>T (p.Arg720Trp)not specified [RCV004171189]uncertain significance748056984805698Humanname
156246737CV2310676single nucleotide variantNM_018059.5(RADIL):c.2413C>T (p.His805Tyr)not specified [RCV004157335]uncertain significance748036324803632Humanname
155967382CV2312718single nucleotide variantNM_018059.5(RADIL):c.2225C>T (p.Ser742Leu)not specified [RCV004169442]uncertain significance748056314805631Humanname
155974393CV2317910single nucleotide variantNM_018059.5(RADIL):c.1217T>C (p.Leu406Pro)not specified [RCV004175134]uncertain significance748348064834806Humanname
156360397CV2329396single nucleotide variantNM_018059.5(RADIL):c.1335G>T (p.Gln445His)not specified [RCV004187408]uncertain significance748346884834688Humanname
156303674CV2359411single nucleotide variantNM_018059.5(RADIL):c.2660G>A (p.Arg887His)not specified [RCV004214735]uncertain significance748018354801835Humanname
156337356CV2360944single nucleotide variantNM_018059.5(RADIL):c.2684C>T (p.Pro895Leu)not specified [RCV004215757]likely benign748018114801811Humanname
156133338CV2361838single nucleotide variantNM_018059.5(RADIL):c.2596G>C (p.Glu866Gln)not specified [RCV004207617]uncertain significance748018994801899Humanname
156152898CV2367166single nucleotide variantNM_018059.5(RADIL):c.1649C>T (p.Thr550Met)not specified [RCV004215599]uncertain significance748173184817318Humanname
156384420CV2371424single nucleotide variantNM_018059.5(RADIL):c.1804G>A (p.Ala602Thr)not specified [RCV004216687]uncertain significance748163904816390Humanname
156093012CV2382016single nucleotide variantNM_018059.5(RADIL):c.2431C>T (p.Arg811Trp)not specified [RCV004225943]uncertain significance748036144803614Humanname
156206616CV2385344single nucleotide variantNM_018059.5(RADIL):c.1831C>T (p.Arg611Cys)not specified [RCV004230618]uncertain significance748163634816363Humanname
156155135CV2388762single nucleotide variantNM_018059.5(RADIL):c.1441A>G (p.Lys481Glu)not specified [RCV004239623]uncertain significance748321544832154Humanname
156248807CV2394013single nucleotide variantNM_018059.5(RADIL):c.2053G>A (p.Gly685Ser)not specified [RCV004236233]uncertain significance748153644815364Humanname
156267853CV2398378single nucleotide variantNM_018059.5(RADIL):c.2216A>G (p.Gln739Arg)not specified [RCV004237716]uncertain significance748056404805640Humanname
329390774CV2437254single nucleotide variantNM_018059.5(RADIL):c.2711C>T (p.Thr904Met)not specified [RCV004256142]uncertain significance748017844801784Humanname
329400415CV2441642single nucleotide variantNM_018059.5(RADIL):c.2641C>A (p.Pro881Thr)not specified [RCV004259466]uncertain significance748018544801854Humanname
329395916CV2451775single nucleotide variantNM_018059.5(RADIL):c.2681C>T (p.Pro894Leu)not specified [RCV004276462]uncertain significance748018144801814Humanname
329352489CV2453088single nucleotide variantNM_018059.5(RADIL):c.2983C>A (p.His995Asn)not specified [RCV004277695]uncertain significance747997694799769Humanname
329401897CV2457494single nucleotide variantNM_018059.5(RADIL):c.1063T>C (p.Phe355Leu)not specified [RCV004267308]uncertain significance748349604834960Humanname
329394400CV2460743single nucleotide variantNM_018059.5(RADIL):c.1886A>T (p.His629Leu)not specified [RCV004271076]uncertain significance748163084816308Humanname
401731464CV2674382single nucleotide variantNM_018059.5(RADIL):c.1778C>G (p.Thr593Arg)not specified [RCV004289252]uncertain significance748164164816416Humanname
401743325CV2684675single nucleotide variantNM_018059.5(RADIL):c.2582G>A (p.Arg861Gln)not specified [RCV004293771]uncertain significance748019134801913Humanname
401758844CV2694309single nucleotide variantNM_018059.5(RADIL):c.2642C>A (p.Pro881His)not specified [RCV004304506]uncertain significance748018534801853Humanname
401721732CV2710132single nucleotide variantNM_018059.5(RADIL):c.2996G>A (p.Gly999Asp)not specified [RCV004315183]uncertain significance747997564799756Humanname
401855990CV2754196single nucleotide variantNM_018059.5(RADIL):c.2410C>T (p.Arg804Cys)not specified [RCV004334386]uncertain significance748036354803635Humanname
401876512CV2761087single nucleotide variantNM_018059.5(RADIL):c.2018G>A (p.Arg673His)not specified [RCV004338746]uncertain significance748153994815399Humanname
401889835CV2763442single nucleotide variantNM_018059.5(RADIL):c.2371T>C (p.Cys791Arg)not specified [RCV004349330]uncertain significance748036744803674Humanname
401856152CV2764415single nucleotide variantNM_018059.5(RADIL):c.2947C>T (p.Pro983Ser)not specified [RCV004338985]uncertain significance748002064800206Humanname
401886486CV2771297single nucleotide variantNM_018059.5(RADIL):c.1834G>A (p.Val612Met)not specified [RCV004346270]uncertain significance748163604816360Humanname
401899061CV2785992single nucleotide variantNM_018059.5(RADIL):c.2905G>A (p.Glu969Lys)not specified [RCV004359829]uncertain significance748002484800248Humanname
401908703CV2828258single nucleotide variantNM_018059.5(RADIL):c.2743G>T (p.Gly915Trp)not provided [RCV003423533]likely benign748017524801752Humanname
401922368CV2828259single nucleotide variantNM_018059.5(RADIL):c.2605C>G (p.Leu869Val)not provided [RCV003433735]likely benign748018904801890Humanname
405692009CV3315192single nucleotide variantNM_018059.5(RADIL):c.1757T>C (p.Leu586Pro)not specified [RCV004445522]uncertain significance748164374816437Humanname
405692015CV3315193single nucleotide variantNM_018059.5(RADIL):c.1802C>T (p.Ser601Leu)not specified [RCV004445523]uncertain significance748163924816392Humanname
405692020CV3315194single nucleotide variantNM_018059.5(RADIL):c.1832G>A (p.Arg611His)not specified [RCV004445524]uncertain significance748163624816362Humanname
405692029CV3315196single nucleotide variantNM_018059.5(RADIL):c.2006A>G (p.Gln669Arg)not specified [RCV004445526]uncertain significance748154114815411Humanname
405692034CV3315197single nucleotide variantNM_018059.5(RADIL):c.2014G>A (p.Ala672Thr)not specified [RCV004445527]uncertain significance748154034815403Humanname
405692044CV3315198single nucleotide variantNM_018059.5(RADIL):c.2152G>A (p.Ala718Thr)not specified [RCV004445528]likely benign748057044805704Humanname
405692050CV3315199single nucleotide variantNM_018059.5(RADIL):c.2197C>G (p.Arg733Gly)not specified [RCV004445529]uncertain significance748056594805659Humanname
405692056CV3315200single nucleotide variantNM_018059.5(RADIL):c.2356G>A (p.Asp786Asn)not specified [RCV004445530]uncertain significance748036894803689Humanname
405692077CV3315202single nucleotide variantNM_018059.5(RADIL):c.2411G>A (p.Arg804His)not specified [RCV004445532]uncertain significance748036344803634Humanname
405692084CV3315203single nucleotide variantNM_018059.5(RADIL):c.2449G>A (p.Gly817Ser)not specified [RCV004445533]uncertain significance748035964803596Humanname
405692092CV3315204single nucleotide variantNM_018059.5(RADIL):c.2485C>G (p.Pro829Ala)not specified [RCV004445534]uncertain significance748035604803560Humanname
405692099CV3315205single nucleotide variantNM_018059.5(RADIL):c.2798G>C (p.Arg933Thr)not specified [RCV004445535]uncertain significance748016974801697Humanname
405692105CV3315206single nucleotide variantNM_018059.5(RADIL):c.2900G>T (p.Ser967Ile)not specified [RCV004445536]uncertain significance748002534800253Humanname
405691973CV3319075single nucleotide variantNM_018059.5(RADIL):c.1051T>C (p.Tyr351His)not specified [RCV004445516]uncertain significance748349724834972Humanname
405691980CV3319076single nucleotide variantNM_018059.5(RADIL):c.1117C>T (p.Arg373Trp)not specified [RCV004445517]uncertain significance748349064834906Humanname
405691985CV3319077single nucleotide variantNM_018059.5(RADIL):c.1175C>T (p.Ala392Val)not specified [RCV004445518]uncertain significance748348484834848Humanname
405691992CV3319078single nucleotide variantNM_018059.5(RADIL):c.1204C>T (p.Arg402Cys)not specified [RCV004445519]uncertain significance748348194834819Humanname
405692004CV3319080single nucleotide variantNM_018059.5(RADIL):c.1670C>T (p.Ala557Val)not specified [RCV004445521]uncertain significance748172974817297Humanname
407500246CV3472117single nucleotide variantNM_018059.5(RADIL):c.2045G>A (p.Arg682Gln)not specified [RCV004669511]uncertain significance748153724815372Humanname
407485448CV3472118single nucleotide variantNM_018059.5(RADIL):c.2540C>T (p.Pro847Leu)not specified [RCV004665299]uncertain significance748019554801955Humanname
407485453CV3472119single nucleotide variantNM_018059.5(RADIL):c.1403G>A (p.Arg468His)not specified [RCV004665300]uncertain significance748346204834620Humanname
407500250CV3472121single nucleotide variantNM_018059.5(RADIL):c.1139G>A (p.Arg380Gln)not specified [RCV004669512]uncertain significance748348844834884Humanname
407485463CV3472122single nucleotide variantNM_018059.5(RADIL):c.2497G>A (p.Glu833Lys)not specified [RCV004665302]uncertain significance748035484803548Humanname
407485473CV3472124single nucleotide variantNM_018059.5(RADIL):c.1465A>G (p.Ile489Val)not specified [RCV004665304]uncertain significance748225444822544Humanname
407500254CV3472125single nucleotide variantNM_018059.5(RADIL):c.2725C>T (p.Pro909Ser)not specified [RCV004669513]uncertain significance748017704801770Humanname
407485489CV3472128single nucleotide variantNM_018059.5(RADIL):c.1700T>C (p.Phe567Ser)not specified [RCV004665307]uncertain significance748172674817267Humanname
407500259CV3472129single nucleotide variantNM_018059.5(RADIL):c.1702C>A (p.Gln568Lys)not specified [RCV004669514]uncertain significance748172654817265Humanname
407500263CV3472130single nucleotide variantNM_018059.5(RADIL):c.1715A>T (p.Tyr572Phe)not specified [RCV004669515]uncertain significance748172524817252Humanname
597753358CV3582428single nucleotide variantNM_018059.5(RADIL):c.2544C>G (p.Ser848Arg)not specified [RCV004847061]uncertain significance748019514801951Humanname
597753363CV3582430single nucleotide variantNM_018059.5(RADIL):c.2989C>T (p.His997Tyr)not specified [RCV004847062]uncertain significance747997634799763Humanname
597684536CV3582431single nucleotide variantNM_018059.5(RADIL):c.2770G>A (p.Gly924Ser)not specified [RCV004858184]uncertain significance748017254801725Humanname
597753366CV3582432single nucleotide variantNM_018059.5(RADIL):c.1805C>T (p.Ala602Val)not specified [RCV004847063]uncertain significance748163894816389Humanname
597684557CV3582434single nucleotide variantNM_018059.5(RADIL):c.2977G>A (p.Gly993Arg)not specified [RCV004858186]uncertain significance748001764800176Humanname
597684575CV3582436single nucleotide variantNM_018059.5(RADIL):c.2971A>G (p.Ile991Val)not specified [RCV004858188]uncertain significance748001824800182Humanname
597684596CV3582438single nucleotide variantNM_018059.5(RADIL):c.1793G>A (p.Ser598Asn)not specified [RCV004858190]uncertain significance748164014816401Humanname
597753369CV3582439single nucleotide variantNM_018059.5(RADIL):c.1651G>C (p.Ala551Pro)not specified [RCV004847064]uncertain significance748173164817316Humanname
597753374CV3582440single nucleotide variantNM_018059.5(RADIL):c.1336C>T (p.His446Tyr)not specified [RCV004847065]uncertain significance748346874834687Humanname
597753377CV3582441single nucleotide variantNM_018059.5(RADIL):c.1970C>T (p.Pro657Leu)not specified [RCV004847066]uncertain significance748154474815447Humanname
597753381CV3582443single nucleotide variantNM_018059.5(RADIL):c.2379C>A (p.Asp793Glu)not specified [RCV004847067]uncertain significance748036664803666Humanname
597684617CV3582444single nucleotide variantNM_018059.5(RADIL):c.2066C>T (p.Ala689Val)not specified [RCV004858192]uncertain significance748153514815351Humanname
597753385CV3582445single nucleotide variantNM_018059.5(RADIL):c.1969C>G (p.Pro657Ala)not specified [RCV004847068]uncertain significance748154484815448Humanname
597684628CV3582446single nucleotide variantNM_018059.5(RADIL):c.1766C>T (p.Pro589Leu)not specified [RCV004858193]uncertain significance748164284816428Humanname
597684637CV3582450single nucleotide variantNM_018059.5(RADIL):c.2435G>A (p.Ser812Asn)not specified [RCV004858194]uncertain significance748036104803610Humanname
597753399CV3582451single nucleotide variantNM_018059.5(RADIL):c.2809G>C (p.Gly937Arg)not specified [RCV004847072]uncertain significance748016864801686Humanname
597753403CV3582455single nucleotide variantNM_018059.5(RADIL):c.2024A>G (p.Gln675Arg)not specified [RCV004847073]uncertain significance748153934815393Humanname
597753411CV3582457single nucleotide variantNM_018059.5(RADIL):c.2536G>T (p.Ala846Ser)not specified [RCV004847075]uncertain significance748019594801959Humanname
597753415CV3582458single nucleotide variantNM_018059.5(RADIL):c.2537C>T (p.Ala846Val)not specified [RCV004847076]uncertain significance748019584801958Humanname
598174017CV3905102single nucleotide variantNM_018059.5(RADIL):c.2243G>T (p.Ser748Ile)not specified [RCV005263788]uncertain significance748056134805613Humanname
598174040CV3905105single nucleotide variantNM_018059.5(RADIL):c.1657G>A (p.Glu553Lys)not specified [RCV005263791]uncertain significance748173104817310Humanname
598174046CV3905106single nucleotide variantNM_018059.5(RADIL):c.2690C>T (p.Thr897Met)not specified [RCV005263792]uncertain significance748018054801805Humanname
598174052CV3905107single nucleotide variantNM_018059.5(RADIL):c.2723C>T (p.Thr908Ile)not specified [RCV005263793]uncertain significance748017724801772Humanname
598174062CV3905109single nucleotide variantNM_018059.5(RADIL):c.1112G>A (p.Arg371His)not specified [RCV005263795]uncertain significance748349114834911Humanname
598174068CV3905110single nucleotide variantNM_018059.5(RADIL):c.2044C>T (p.Arg682Trp)not specified [RCV005263796]uncertain significance748153734815373Humanname
598174082CV3905112single nucleotide variantNM_018059.5(RADIL):c.2765C>T (p.Ser922Phe)not specified [RCV005263798]uncertain significance748017304801730Humanname
598174100CV3905115single nucleotide variantNM_018059.5(RADIL):c.2973C>G (p.Ile991Met)not specified [RCV005263801]uncertain significance748001804800180Humanname
598174134CV3905120single nucleotide variantNM_018059.5(RADIL):c.1224G>T (p.Glu408Asp)not specified [RCV005263806]uncertain significance748347994834799Humanname
598174141CV3905121single nucleotide variantNM_018059.5(RADIL):c.2680C>T (p.Pro894Ser)not specified [RCV005263807]uncertain significance748018154801815Humanname
598174158CV3905124single nucleotide variantNM_018059.5(RADIL):c.2176C>G (p.Leu726Val)not specified [RCV005263810]uncertain significance748056804805680Humanname
598174165CV3905125single nucleotide variantNM_018059.5(RADIL):c.2786C>A (p.Ala929Glu)not specified [RCV005263811]uncertain significance748017094801709Humanname
598174171CV3905126single nucleotide variantNM_018059.5(RADIL):c.2483A>G (p.Gln828Arg)not specified [RCV005263812]uncertain significance748035624803562Humanname
598174179CV3905127single nucleotide variantNM_018059.5(RADIL):c.2953G>A (p.Gly985Arg)not specified [RCV005263813]uncertain significance748002004800200Humanname
598174185CV3905128single nucleotide variantNM_018059.5(RADIL):c.2462G>A (p.Arg821Lys)not specified [RCV005263814]uncertain significance748035834803583Humanname
598174193CV3905129single nucleotide variantNM_018059.5(RADIL):c.2768G>T (p.Gly923Val)not specified [RCV005263815]uncertain significance748017274801727Humanname
598174201CV3905130single nucleotide variantNM_018059.5(RADIL):c.2113G>A (p.Ala705Thr)not specified [RCV005263816]uncertain significance748153044815304Humanname
156027182CV2199295single nucleotide variantNM_018059.5(RADIL):c.3038C>T (p.Pro1013Leu)not specified [RCV004082645]uncertain significance747997144799714Humanname
155925061CV2220427single nucleotide variantNM_018059.5(RADIL):c.3043G>A (p.Ala1015Thr)not specified [RCV004095829]uncertain significance747997094799709Humanname
156389305CV2226188single nucleotide variantNM_018059.5(RADIL):c.3107G>A (p.Gly1036Asp)not specified [RCV004105587]uncertain significance747996454799645Humanname
156359471CV2328209single nucleotide variantNM_018059.5(RADIL):c.3018G>C (p.Gln1006His)not specified [RCV004173302]uncertain significance747997344799734Humanname
156079669CV2341269single nucleotide variantNM_018059.5(RADIL):c.3212G>A (p.Arg1071His)not specified [RCV004186680]uncertain significance747993944799394Humanname
156063981CV2375928single nucleotide variantNM_018059.5(RADIL):c.3217C>T (p.Pro1073Ser)not specified [RCV004218138]uncertain significance747993894799389Humanname
156269317CV2379250single nucleotide variantNM_018059.5(RADIL):c.3145G>A (p.Gly1049Ser)not specified [RCV004223726]uncertain significance747994614799461Humanname
329369747CV2424901single nucleotide variantNM_018059.5(RADIL):c.3056G>A (p.Arg1019His)not specified [RCV004248782]uncertain significance747996964799696Humanname
329361244CV2436819single nucleotide variantNM_018059.5(RADIL):c.3220C>T (p.Pro1074Ser)not specified [RCV004260218]uncertain significance747993864799386Humanname
329400658CV2438621single nucleotide variantNM_018059.5(RADIL):c.3160C>T (p.Arg1054Trp)not specified [RCV004261792]uncertain significance747994464799446Humanname
329360581CV2439513single nucleotide variantNM_018059.5(RADIL):c.3218C>T (p.Pro1073Leu)not specified [RCV004262451]uncertain significance747993884799388Humanname
405692110CV3315207single nucleotide variantNM_018059.5(RADIL):c.2998G>A (p.Ala1000Thr)not specified [RCV004445537]likely benign747997544799754Humanname
405692118CV3315208single nucleotide variantNM_018059.5(RADIL):c.3008T>C (p.Leu1003Pro)not specified [RCV004445538]uncertain significance747997444799744Humanname
405692123CV3315209single nucleotide variantNM_018059.5(RADIL):c.3190A>G (p.Thr1064Ala)not specified [RCV004445539]uncertain significance747994164799416Humanname
598174075CV3905111single nucleotide variantNM_018059.5(RADIL):c.3161G>A (p.Arg1054Gln)not specified [RCV005263797]uncertain significance747994454799445Humanname
598174090CV3905113single nucleotide variantNM_018059.5(RADIL):c.3181G>A (p.Asp1061Asn)not specified [RCV005263799]uncertain significance747994254799425Humanname
598174147CV3905122single nucleotide variantNM_018059.5(RADIL):c.3127G>A (p.Val1043Met)not specified [RCV005263808]uncertain significance747994794799479Humanname