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Variants search result for Homo sapiens
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51 records found for search term Cdyl2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15141991CV715096single nucleotide variantNM_152342.4(CDYL2):c.783G>A (p.Thr261=)not provided [RCV000966401]benign168063307080633070Humanname
155996123CV2375899single nucleotide variantNM_152342.4(CDYL2):c.122C>T (p.Pro41Leu)not specified [RCV004217741]uncertain significance168068503280685032Humanname
329378363CV2463653single nucleotide variantNM_152342.4(CDYL2):c.217A>G (p.Ser73Gly)not specified [RCV004277447]likely benign168068493780684937Humanname
405744128CV3303669single nucleotide variantNM_152342.4(CDYL2):c.251C>T (p.Pro84Leu)not specified [RCV004431119]uncertain significance168068490380684903Humanname
405743952CV3303670single nucleotide variantNM_152342.4(CDYL2):c.287C>T (p.Pro96Leu)not specified [RCV004431120]uncertain significance168068486780684867Humanname
407460802CV3418724single nucleotide variantNM_152342.4(CDYL2):c.184A>G (p.Lys62Glu)not specified [RCV004612425]uncertain significance168068497080684970Humanname
597767573CV3648837single nucleotide variantNM_152342.4(CDYL2):c.167A>G (p.Asn56Ser)not specified [RCV004896383]uncertain significance168068498780684987Humanname
598193813CV3940471single nucleotide variantNM_152342.4(CDYL2):c.245G>A (p.Arg82Gln)not specified [RCV005313056]uncertain significance168068490980684909Humanname
15119513CV715095single nucleotide variantNM_152342.4(CDYL2):c.1065G>T (p.Gly355=)not provided [RCV000962563]benign168061277980612779Humanname
156142384CV2208524single nucleotide variantNM_152342.4(CDYL2):c.598C>G (p.Leu200Val)not specified [RCV004091055]uncertain significance168068455680684556Humanname
156301541CV2245095single nucleotide variantNM_152342.4(CDYL2):c.931C>G (p.Leu311Val)not specified [RCV004104808]uncertain significance168062083980620839Humanname
156362520CV2265550single nucleotide variantNM_152342.4(CDYL2):c.806C>T (p.Thr269Ile)not specified [RCV004124293]uncertain significance168063304780633047Humanname
156004436CV2295937single nucleotide variantNM_152342.4(CDYL2):c.359A>G (p.Tyr120Cys)not specified [RCV004151836]uncertain significance168068479580684795Humanname
156058867CV2316927single nucleotide variantNM_152342.4(CDYL2):c.341C>G (p.Ala114Gly)not specified [RCV004174438]uncertain significance168068481380684813Humanname
155982234CV2337139single nucleotide variantNM_152342.4(CDYL2):c.680A>G (p.Glu227Gly)not specified [RCV004192899]uncertain significance168063317380633173Humanname
155994421CV2377511single nucleotide variantNM_152342.4(CDYL2):c.988C>T (p.Arg330Trp)not specified [RCV004225672]uncertain significance168062078280620782Humanname
401757359CV2675258single nucleotide variantNM_152342.4(CDYL2):c.488C>T (p.Ser163Phe)not specified [RCV004290025]uncertain significance168068466680684666Humanname
401769648CV2689871single nucleotide variantNM_152342.4(CDYL2):c.549T>A (p.Asp183Glu)not specified [RCV004297768]uncertain significance168068460580684605Humanname
401757179CV2692846single nucleotide variantNM_152342.4(CDYL2):c.850C>T (p.Arg284Trp)not specified [RCV004306385]uncertain significance168062092080620920Humanname
401724657CV2714915single nucleotide variantNM_152342.4(CDYL2):c.620C>A (p.Ser207Tyr)not specified [RCV004322247]uncertain significance168063323380633233Humanname
401867162CV2776674single nucleotide variantNM_152342.4(CDYL2):c.701A>G (p.Lys234Arg)not specified [RCV004357839]uncertain significance168063315280633152Humanname
401879574CV2785303single nucleotide variantNM_152342.4(CDYL2):c.659T>C (p.Val220Ala)not specified [RCV004357061]uncertain significance168063319480633194Humanname
405743797CV3303671single nucleotide variantNM_152342.4(CDYL2):c.353A>G (p.Lys118Arg)not specified [RCV004431121]uncertain significance168068480180684801Humanname
405743694CV3303672single nucleotide variantNM_152342.4(CDYL2):c.399G>C (p.Lys133Asn)not specified [RCV004431122]uncertain significance168068475580684755Humanname
405743700CV3303673single nucleotide variantNM_152342.4(CDYL2):c.804G>T (p.Gln268His)not specified [RCV004431123]uncertain significance168063304980633049Humanname
405743705CV3303674single nucleotide variantNM_152342.4(CDYL2):c.857C>T (p.Ala286Val)not specified [RCV004431124]uncertain significance168062091380620913Humanname
405743721CV3303676single nucleotide variantNM_152342.4(CDYL2):c.952G>A (p.Gly318Ser)not specified [RCV004431126]uncertain significance168062081880620818Humanname
597767537CV3648830single nucleotide variantNM_152342.4(CDYL2):c.301G>T (p.Gly101Trp)not specified [RCV004896376]uncertain significance168068485380684853Humanname
597767552CV3648833single nucleotide variantNM_152342.4(CDYL2):c.511G>A (p.Gly171Arg)not specified [RCV004896379]uncertain significance168068464380684643Humanname
597767558CV3648834single nucleotide variantNM_152342.4(CDYL2):c.989G>A (p.Arg330Gln)not specified [RCV004896380]uncertain significance168062078180620781Humanname
597767563CV3648835single nucleotide variantNM_152342.4(CDYL2):c.784C>T (p.His262Tyr)not specified [RCV004896381]uncertain significance168063306980633069Humanname
597767584CV3648839single nucleotide variantNM_152342.4(CDYL2):c.715A>C (p.Ser239Arg)not specified [RCV004896385]uncertain significance168063313880633138Humanname
598193763CV3940462single nucleotide variantNM_152342.4(CDYL2):c.484G>A (p.Gly162Ser)not specified [RCV005313047]uncertain significance168068467080684670Humanname
598193774CV3940464single nucleotide variantNM_152342.4(CDYL2):c.424A>C (p.Ser142Arg)not specified [RCV005313049]uncertain significance168068473080684730Humanname
598193786CV3940466single nucleotide variantNM_152342.4(CDYL2):c.498T>A (p.Asp166Glu)not specified [RCV005313051]uncertain significance168068465680684656Humanname
598193792CV3940467single nucleotide variantNM_152342.4(CDYL2):c.866A>G (p.Asn289Ser)not specified [RCV005313052]uncertain significance168062090480620904Humanname
155939180CV2225372single nucleotide variantNM_152342.4(CDYL2):c.1210G>T (p.Val404Phe)not specified [RCV004100789]uncertain significance168061263480612634Humanname
156053297CV2320372single nucleotide variantNM_152342.4(CDYL2):c.1243C>T (p.Arg415Trp)not specified [RCV004178533]uncertain significance168060821180608211Humanname
156291865CV2339949single nucleotide variantNM_152342.4(CDYL2):c.1391G>A (p.Arg464Gln)not specified [RCV004192212]uncertain significance168060451880604518Humanname
405744357CV3303667single nucleotide variantNM_152342.4(CDYL2):c.1051G>C (p.Val351Leu)not specified [RCV004431117]uncertain significance168061279380612793Humanname
405744350CV3303668single nucleotide variantNM_152342.4(CDYL2):c.1372G>A (p.Glu458Lys)not specified [RCV004431118]uncertain significance168060453780604537Humanname
407460805CV3418725single nucleotide variantNM_152342.4(CDYL2):c.1160G>A (p.Arg387His)not specified [RCV004612426]uncertain significance168061268480612684Humanname
597767532CV3648828single nucleotide variantNM_152342.4(CDYL2):c.1210G>A (p.Val404Ile)not specified [RCV004896375]uncertain significance168061263480612634Humanname
597767543CV3648831single nucleotide variantNM_152342.4(CDYL2):c.1159C>T (p.Arg387Cys)not specified [RCV004896377]uncertain significance168061268580612685Humanname
597767547CV3648832single nucleotide variantNM_152342.4(CDYL2):c.1198C>A (p.Gln400Lys)not specified [RCV004896378]uncertain significance168061264680612646Humanname
597767567CV3648836single nucleotide variantNM_152342.4(CDYL2):c.1452G>C (p.Gln484His)not specified [RCV004896382]uncertain significance168060445780604457Humanname
597767580CV3648838single nucleotide variantNM_152342.4(CDYL2):c.1024T>C (p.Phe342Leu)not specified [RCV004896384]uncertain significance168061282080612820Humanname
598193768CV3940463single nucleotide variantNM_152342.4(CDYL2):c.1022C>G (p.Ala341Gly)not specified [RCV005313048]uncertain significance168061282280612822Humanname
598193779CV3940465single nucleotide variantNM_152342.4(CDYL2):c.1108A>G (p.Ile370Val)not specified [RCV005313050]uncertain significance168061273680612736Humanname
598193797CV3940468single nucleotide variantNM_152342.4(CDYL2):c.1259A>G (p.Gln420Arg)not specified [RCV005313053]uncertain significance168060819580608195Humanname
598193808CV3940470single nucleotide variantNM_152342.4(CDYL2):c.1408G>T (p.Val470Leu)not specified [RCV005313055]uncertain significance168060450180604501Humanname