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45 records found for search term Cdc25c
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405773438CV3300019single nucleotide variantNM_001790.5(CDC25C):c.25A>G (p.Thr9Ala)not specified [RCV004435691]uncertain significance5138331156138331156Humanname
156052137CV2314214single nucleotide variantNM_001790.5(CDC25C):c.77G>T (p.Arg26Met)not specified [RCV004166585]uncertain significance5138331104138331104Humanname
15192142CV764876single nucleotide variantNM_001790.5(CDC25C):c.882C>T (p.Thr294=)not provided [RCV000933001]likely benign5138289546138289546Humanname
156264984CV2198619single nucleotide variantNM_001790.5(CDC25C):c.224C>G (p.Ser75Trp)not specified [RCV004075636]uncertain significance5138329618138329618Humanname
401720479CV2673341single nucleotide variantNM_001790.5(CDC25C):c.100G>C (p.Glu34Gln)not specified [RCV004288326]uncertain significance5138331081138331081Humanname
405773433CV3300018single nucleotide variantNM_001790.5(CDC25C):c.182G>A (p.Ser61Asn)not specified [RCV004435690]uncertain significance5138330999138330999Humanname
597787606CV3644785single nucleotide variantNM_001790.5(CDC25C):c.164G>C (p.Gly55Ala)not specified [RCV004901293]uncertain significance5138331017138331017Humanname
597787623CV3644789single nucleotide variantNM_001790.5(CDC25C):c.170C>G (p.Ser57Cys)not specified [RCV004901297]uncertain significance5138331011138331011Humanname
598167173CV3950947single nucleotide variantNM_001790.5(CDC25C):c.108C>A (p.Asp36Glu)not specified [RCV005308016]uncertain significance5138331073138331073Humanname
156190760CV2226934single nucleotide variantNM_001790.5(CDC25C):c.883G>A (p.Val295Met)not specified [RCV004103905]uncertain significance5138289545138289545Humanname
156072459CV2233371single nucleotide variantNM_001790.5(CDC25C):c.602A>C (p.Asp201Ala)not specified [RCV004105736]uncertain significance5138319232138319232Humanname
155984691CV2247786single nucleotide variantNM_001790.5(CDC25C):c.623G>A (p.Arg208Lys)not specified [RCV004121254]uncertain significance5138292109138292109Humanname
156132556CV2280077single nucleotide variantNM_001790.5(CDC25C):c.698A>G (p.Lys233Arg)not specified [RCV004146433]uncertain significance5138292034138292034Humanname
156249231CV2286589single nucleotide variantNM_001790.5(CDC25C):c.974T>G (p.Phe325Cys)not specified [RCV004142444]uncertain significance5138287221138287221Humanname
156074618CV2291317single nucleotide variantNM_001790.5(CDC25C):c.641C>T (p.Ser214Phe)not specified [RCV004162009]uncertain significance5138292091138292091Humanname
156010298CV2362105single nucleotide variantNM_001790.5(CDC25C):c.346C>G (p.Gln116Glu)not specified [RCV004209910]uncertain significance5138326044138326044Humanname
401771412CV2675593single nucleotide variantNM_001790.5(CDC25C):c.872C>T (p.Ala291Val)not specified [RCV004297254]likely benign5138289556138289556Humanname
401866277CV2762590single nucleotide variantNM_001790.5(CDC25C):c.407G>A (p.Arg136His)not specified [RCV004338114]likely benign5138325867138325867Humanname
405773444CV3300020single nucleotide variantNM_001790.5(CDC25C):c.557A>C (p.Gln186Pro)not specified [RCV004435692]uncertain significance5138319277138319277Humanname
405773451CV3300021single nucleotide variantNM_001790.5(CDC25C):c.644C>T (p.Pro215Leu)not specified [RCV004435693]uncertain significance5138292088138292088Humanname
405773455CV3300022single nucleotide variantNM_001790.5(CDC25C):c.734A>G (p.Tyr245Cys)not specified [RCV004435694]uncertain significance5138291998138291998Humanname
407498547CV3425095single nucleotide variantNM_001790.5(CDC25C):c.908A>C (p.Lys303Thr)not specified [RCV004606667]uncertain significance5138289520138289520Humanname
597787599CV3644783single nucleotide variantNM_001790.5(CDC25C):c.832A>G (p.Asn278Asp)not specified [RCV004901291]uncertain significance5138290671138290671Humanname
597787611CV3644786single nucleotide variantNM_001790.5(CDC25C):c.977A>G (p.Tyr326Cys)not specified [RCV004901294]uncertain significance5138287218138287218Humanname
597787639CV3644793single nucleotide variantNM_001790.5(CDC25C):c.805A>G (p.Ile269Val)not specified [RCV004901301]uncertain significance5138290698138290698Humanname
598229234CV3950945single nucleotide variantNM_001790.5(CDC25C):c.637C>T (p.Arg213Cys)not specified [RCV005319188]uncertain significance5138292095138292095Humanname
598167178CV3950948single nucleotide variantNM_001790.5(CDC25C):c.382T>C (p.Cys128Arg)not specified [RCV005308017]uncertain significance5138325892138325892Humanname
156133270CV2216738single nucleotide variantNM_001790.5(CDC25C):c.1183G>A (p.Asp395Asn)not specified [RCV004083185]uncertain significance5138286111138286111Humanname
156383714CV2220175single nucleotide variantNM_001790.5(CDC25C):c.1087G>A (p.Val363Ile)not specified [RCV004095652]uncertain significance5138286570138286570Humanname
155974549CV2269969single nucleotide variantNM_001790.5(CDC25C):c.1175G>A (p.Arg392His)not specified [RCV004128964]uncertain significance5138286119138286119Humanname
156244357CV2313101single nucleotide variantNM_001790.5(CDC25C):c.1397T>C (p.Leu466Pro)not specified [RCV004161372]uncertain significance5138285717138285717Humanname
155960717CV2314056single nucleotide variantNM_001790.5(CDC25C):c.1322A>G (p.Lys441Arg)not specified [RCV004164334]uncertain significance5138285792138285792Humanname
156329297CV2342385single nucleotide variantNM_001790.5(CDC25C):c.1261C>A (p.Pro421Thr)not specified [RCV004193998]uncertain significance5138286033138286033Humanname
155997678CV2393335single nucleotide variantNM_001790.5(CDC25C):c.1241G>A (p.Gly414Asp)not specified [RCV004228840]uncertain significance5138286053138286053Humanname
329393531CV2453415single nucleotide variantNM_001790.5(CDC25C):c.1351A>G (p.Ser451Gly)not specified [RCV004267029]uncertain significance5138285763138285763Humanname
401884982CV2766382single nucleotide variantNM_001790.5(CDC25C):c.1303A>G (p.Met435Val)not specified [RCV004342627]uncertain significance5138285811138285811Humanname
401868014CV2767130single nucleotide variantNM_001790.5(CDC25C):c.1145A>G (p.Glu382Gly)not specified [RCV004347529]uncertain significance5138286512138286512Humanname
405773424CV3300016single nucleotide variantNM_001790.5(CDC25C):c.1196A>G (p.Asn399Ser)not specified [RCV004435688]uncertain significance5138286098138286098Humanname
405773429CV3300017single nucleotide variantNM_001790.5(CDC25C):c.1381C>T (p.Arg461Trp)not specified [RCV004435689]uncertain significance5138285733138285733Humanname
597787603CV3644784single nucleotide variantNM_001790.5(CDC25C):c.1147A>G (p.Arg383Gly)not specified [RCV004901292]uncertain significance5138286510138286510Humanname
597787618CV3644788single nucleotide variantNM_001790.5(CDC25C):c.1120G>T (p.Val374Leu)not specified [RCV004901296]uncertain significance5138286537138286537Humanname
597787627CV3644790single nucleotide variantNM_001790.5(CDC25C):c.1252G>T (p.Asp418Tyr)not specified [RCV004901298]uncertain significance5138286042138286042Humanname
597787631CV3644791single nucleotide variantNM_001790.5(CDC25C):c.1217A>C (p.Tyr406Ser)not specified [RCV004901299]uncertain significance5138286077138286077Humanname
597787634CV3644792single nucleotide variantNM_001790.5(CDC25C):c.1042T>C (p.Tyr348His)not specified [RCV004901300]uncertain significance5138286615138286615Humanname
598229240CV3950946single nucleotide variantNM_001790.5(CDC25C):c.1022T>A (p.Ile341Asn)not specified [RCV005319189]uncertain significance5138287173138287173Humanname