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41 records found for search term Ric3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8634403CV89623single nucleotide variantNM_024557.4(RIC3):c.606C>T (p.Phe202=)Malignant melanoma [RCV000069720]not provided1181267208126720Humanname
8634405CV89625single nucleotide variantNM_024557.4(RIC3):c.318G>A (p.Gly106=)Malignant melanoma [RCV000069722]not provided1181400008140000Humanname
156351319CV2323740single nucleotide variantNM_001206671.4(RIC3):c.17T>C (p.Val6Ala)not specified [RCV004176294]uncertain significance1181689738168973Humanname
597788671CV3586698single nucleotide variantNM_001206671.4(RIC3):c.25G>A (p.Val9Ile)not specified [RCV004855556]uncertain significance1181689658168965Humanname
8634404CV89624single nucleotide variantNM_024557.4(RIC3):c.326T>C (p.Leu109Ser)Malignant melanoma [RCV000069721]not provided1181399928139992Humanname
401898134CV2780985single nucleotide variantNM_001206671.4(RIC3):c.83T>G (p.Leu28Arg)not specified [RCV004354516]uncertain significance1181689078168907Humanname
401961839CV2844161duplicationNM_001206671.4(RIC3):c.245dup (p.Gly83fs)not provided [RCV003482002]uncertain significance1181400728140073Humanname
405294242CV3214743single nucleotide variantNM_001206671.4(RIC3):c.74A>G (p.Lys25Arg)RIC3-related disorder [RCV003934169]likely benign1181689168168916Humanname , trait , alternate_id
405735312CV3319547single nucleotide variantNM_001206671.4(RIC3):c.29C>T (p.Ala10Val)not specified [RCV004451558]uncertain significance1181689618168961Humanname
405735347CV3319551single nucleotide variantNM_001206671.4(RIC3):c.76G>T (p.Ala26Ser)not specified [RCV004451562]uncertain significance1181689148168914Humanname
597788656CV3586692single nucleotide variantNM_001206671.4(RIC3):c.52G>A (p.Ala18Thr)not specified [RCV004855552]uncertain significance1181689388168938Humanname
156238041CV2265326single nucleotide variantNM_001206671.4(RIC3):c.269G>A (p.Gly90Asp)not specified [RCV004128217]uncertain significance1181400498140049Humanname
329393352CV2466873single nucleotide variantNM_001206671.4(RIC3):c.196C>T (p.Arg66Cys)not specified [RCV004282645]uncertain significance1181401228140122Humanname
11545093CV249263single nucleotide variantNM_001206671.4(RIC3):c.169C>A (p.Pro57Thr)not provided [RCV000244674]uncertain significance1181401498140149Humanname
401882540CV2778409single nucleotide variantNM_001206671.4(RIC3):c.162C>A (p.His54Gln)not specified [RCV004344088]uncertain significance1181401568140156Humanname
596932564CV3539186single nucleotide variantNM_001206671.4(RIC3):c.136C>T (p.Arg46Ter)not provided [RCV004793312]uncertain significance1181401828140182Humanname
597788659CV3586693single nucleotide variantNM_001206671.4(RIC3):c.154C>A (p.His52Asn)not specified [RCV004855553]uncertain significance1181401648140164Humanname
597776441CV3586694single nucleotide variantNM_001206671.4(RIC3):c.187C>G (p.Pro63Ala)not specified [RCV004852513]uncertain significance1181401318140131Humanname
597788663CV3586695single nucleotide variantNM_001206671.4(RIC3):c.289G>C (p.Gly97Arg)not specified [RCV004855554]uncertain significance1181400298140029Humanname
598190869CV3902814single nucleotide variantNM_001206671.4(RIC3):c.230C>T (p.Ala77Val)not specified [RCV005266909]uncertain significance1181400888140088Humanname
598190874CV3902815single nucleotide variantNM_001206671.4(RIC3):c.280G>A (p.Gly94Ser)not specified [RCV005266910]uncertain significance1181400388140038Humanname
598190882CV3902816single nucleotide variantNM_001206671.4(RIC3):c.109C>T (p.Pro37Ser)not specified [RCV005266911]uncertain significance1181688818168881Humanname
156035955CV2243439single nucleotide variantNM_001206671.4(RIC3):c.727C>A (p.Gln243Lys)not specified [RCV004112410]uncertain significance1181110818111081Humanname
156036276CV2303673single nucleotide variantNM_001206671.4(RIC3):c.746A>G (p.Asp249Gly)not specified [RCV004161746]uncertain significance1181110628111062Humanname
156345003CV2372853single nucleotide variantNM_001206671.4(RIC3):c.760A>G (p.Lys254Glu)not specified [RCV004222035]uncertain significance1181110488111048Humanname
329396945CV2463684single nucleotide variantNM_001206671.4(RIC3):c.565C>T (p.His189Tyr)not specified [RCV004279259]uncertain significance1181267648126764Humanname
401752545CV2682856single nucleotide variantNM_001206671.4(RIC3):c.977G>T (p.Ser326Ile)not specified [RCV004283656]uncertain significance1181108318110831Humanname
401749909CV2704814single nucleotide variantNM_001206671.4(RIC3):c.832T>A (p.Trp278Arg)not specified [RCV004307400]uncertain significance1181109768110976Humanname
401721887CV2710218single nucleotide variantNM_001206671.4(RIC3):c.299T>C (p.Ile100Thr)not specified [RCV004317117]uncertain significance1181400198140019Humanname
401896863CV2788884single nucleotide variantNM_001206671.4(RIC3):c.610A>G (p.Ile204Val)not specified [RCV004362924]uncertain significance1181267198126719Humanname
405735322CV3319548single nucleotide variantNM_001206671.4(RIC3):c.335T>C (p.Leu112Pro)not specified [RCV004451559]uncertain significance1181399838139983Humanname
405735328CV3319549single nucleotide variantNM_001206671.4(RIC3):c.358A>G (p.Lys120Glu)not specified [RCV004451560]uncertain significance1181383418138341Humanname
405735337CV3319550single nucleotide variantNM_001206671.4(RIC3):c.416A>C (p.His139Pro)not specified [RCV004451561]uncertain significance1181382838138283Humanname
405735353CV3319552single nucleotide variantNM_001206671.4(RIC3):c.845C>T (p.Pro282Leu)not specified [RCV004451563]uncertain significance1181109638110963Humanname
407474699CV3483068single nucleotide variantNM_001206671.4(RIC3):c.775G>A (p.Glu259Lys)not specified [RCV004663089]uncertain significance1181110338111033Humanname
596932563CV3539185single nucleotide variantNM_001206671.4(RIC3):c.301C>T (p.Pro101Ser)not provided [RCV004793311]uncertain significance1181400178140017Humanname
597776435CV3586690single nucleotide variantNM_001206671.4(RIC3):c.428C>A (p.Thr143Asn)not specified [RCV004852512]uncertain significance1181374718137471Humanname
597788652CV3586691single nucleotide variantNM_001206671.4(RIC3):c.893C>T (p.Pro298Leu)not specified [RCV004855551]uncertain significance1181109158110915Humanname
598190853CV3902812single nucleotide variantNM_001206671.4(RIC3):c.733A>G (p.Thr245Ala)not specified [RCV005266907]uncertain significance1181110758111075Humanname
598190860CV3902813single nucleotide variantNM_001206671.4(RIC3):c.722G>A (p.Arg241His)not specified [RCV005266908]likely benign1181110868111086Humanname
15164721CV713217single nucleotide variantNM_001206671.4(RIC3):c.589G>T (p.Val197Phe)not provided [RCV000970789]benign1181267408126740Humanname