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Variants search result for Homo sapiens
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49 records found for search term Ccnt1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597766293CV3638267single nucleotide variantNM_001240.4(CCNT1):c.73C>G (p.Arg25Gly)not specified [RCV004896100]uncertain significance124871660348716603Humanname
156196144CV2319063single nucleotide variantNM_001240.4(CCNT1):c.106T>C (p.Ser36Pro)not specified [RCV004178144]uncertain significance124871657048716570Humanname
156151775CV2377578single nucleotide variantNM_001240.4(CCNT1):c.212T>C (p.Met71Thr)not specified [RCV004227771]uncertain significance124871447448714474Humanname
401932072CV2806937single nucleotide variantNM_001240.4(CCNT1):c.1356G>A (p.Leu452=)not provided [RCV003391771]likely benign124869385848693858Humanname
8627289CV82433single nucleotide variantNM_001240.3(CCNT1):c.1998C>T (p.Ser666=)Malignant melanoma [RCV000062512]not provided124869321648693216Humanname
156252211CV2286944single nucleotide variantNM_001240.4(CCNT1):c.800C>G (p.Thr267Arg)not specified [RCV004144548]uncertain significance124869441448694414Humanname
156275292CV2290566single nucleotide variantNM_001240.4(CCNT1):c.988C>G (p.Pro330Ala)not specified [RCV004149113]uncertain significance124869422648694226Humanname
401720909CV2702187single nucleotide variantNM_001240.4(CCNT1):c.843G>C (p.Gln281His)not specified [RCV004314536]uncertain significance124869437148694371Humanname
401897706CV2772843single nucleotide variantNM_001240.4(CCNT1):c.818G>A (p.Gly273Glu)not specified [RCV004357627]uncertain significance124869439648694396Humanname
597766298CV3638268single nucleotide variantNM_001240.4(CCNT1):c.982A>T (p.Met328Leu)not specified [RCV004896101]uncertain significance124869423248694232Humanname
597766307CV3638270single nucleotide variantNM_001240.4(CCNT1):c.831G>T (p.Lys277Asn)not specified [RCV004896103]likely benign124869438348694383Humanname
597766312CV3638271single nucleotide variantNM_001240.4(CCNT1):c.976G>A (p.Val326Met)not specified [RCV004896104]uncertain significance124869423848694238Humanname
598205481CV3939843single nucleotide variantNM_001240.4(CCNT1):c.397C>G (p.Leu133Val)not specified [RCV005314956]uncertain significance124870104948701049Humanname
598205508CV3939848single nucleotide variantNM_001240.4(CCNT1):c.994A>G (p.Lys332Glu)not specified [RCV005314960]likely benign124869422048694220Humanname
156241476CV2203867single nucleotide variantNM_001240.4(CCNT1):c.2125C>T (p.Arg709Trp)not specified [RCV004069924]uncertain significance124869308948693089Humanname
156178926CV2287964single nucleotide variantNM_001240.4(CCNT1):c.1839G>T (p.Met613Ile)not specified [RCV004147738]uncertain significance124869337548693375Humanname
155910378CV2303582single nucleotide variantNM_001240.4(CCNT1):c.1180G>A (p.Ala394Thr)not specified [RCV004161668]uncertain significance124869403448694034Humanname
156270164CV2312123single nucleotide variantNM_001240.4(CCNT1):c.1430C>T (p.Pro477Leu)not specified [RCV004165036]uncertain significance124869378448693784Humanname
156360534CV2329495single nucleotide variantNM_001240.4(CCNT1):c.1067C>A (p.Ala356Glu)not specified [RCV004180632]uncertain significance124869414748694147Humanname
156070992CV2337726single nucleotide variantNM_001240.4(CCNT1):c.1409A>G (p.Asp470Gly)not specified [RCV004183747]uncertain significance124869380548693805Humanname
156071007CV2337727single nucleotide variantNM_001240.4(CCNT1):c.1889G>A (p.Cys630Tyr)not specified [RCV004183748]uncertain significance124869332548693325Humanname
156151720CV2369197single nucleotide variantNM_001240.4(CCNT1):c.1447C>T (p.Arg483Cys)not specified [RCV004208118]uncertain significance124869376748693767Humanname
156043514CV2387992single nucleotide variantNM_001240.4(CCNT1):c.1181C>T (p.Ala394Val)not specified [RCV004236526]uncertain significance124869403348694033Humanname
156202139CV2392548single nucleotide variantNM_001240.4(CCNT1):c.1655G>A (p.Ser552Asn)not specified [RCV004245414]uncertain significance124869355948693559Humanname
329363123CV2464694single nucleotide variantNM_001240.4(CCNT1):c.1994A>C (p.His665Pro)not specified [RCV004284671]uncertain significance124869322048693220Humanname
401731273CV2693702single nucleotide variantNM_001240.4(CCNT1):c.1252T>C (p.Tyr418His)not specified [RCV004298031]uncertain significance124869396248693962Humanname
401864147CV2760823single nucleotide variantNM_001240.4(CCNT1):c.1147C>G (p.Pro383Ala)not specified [RCV004336461]uncertain significance124869406748694067Humanname
401869744CV2772506single nucleotide variantNM_001240.4(CCNT1):c.1898G>A (p.Arg633His)not specified [RCV004355281]uncertain significance124869331648693316Humanname
405741746CV3303212single nucleotide variantNM_001240.4(CCNT1):c.1084C>G (p.His362Asp)not specified [RCV004430833]uncertain significance124869413048694130Humanname
405756414CV3303213single nucleotide variantNM_001240.4(CCNT1):c.1307T>C (p.Ile436Thr)not specified [RCV004432899]uncertain significance124869390748693907Humanname
405756430CV3303215single nucleotide variantNM_001240.4(CCNT1):c.1316T>C (p.Met439Thr)not specified [RCV004432901]uncertain significance124869389848693898Humanname
405756435CV3303216single nucleotide variantNM_001240.4(CCNT1):c.1448G>T (p.Arg483Leu)not specified [RCV004432902]uncertain significance124869376648693766Humanname
405756441CV3303217single nucleotide variantNM_001240.4(CCNT1):c.1691C>T (p.Ser564Phe)not specified [RCV004432903]uncertain significance124869352348693523Humanname
405756447CV3303218single nucleotide variantNM_001240.4(CCNT1):c.1847A>G (p.His616Arg)not specified [RCV004432904]uncertain significance124869336748693367Humanname
407492079CV3428683single nucleotide variantNM_001240.4(CCNT1):c.1480A>G (p.Asn494Asp)not specified [RCV004604876]uncertain significance124869373448693734Humanname
407492083CV3428684single nucleotide variantNM_001240.4(CCNT1):c.1345C>T (p.Arg449Trp)not specified [RCV004604877]uncertain significance124869386948693869Humanname
407492088CV3428685single nucleotide variantNM_001240.4(CCNT1):c.1495A>G (p.Ser499Gly)not specified [RCV004604878]uncertain significance124869371948693719Humanname
407492092CV3428686single nucleotide variantNM_001240.4(CCNT1):c.1596A>T (p.Gln532His)not specified [RCV004604879]uncertain significance124869361848693618Humanname
407492096CV3428687single nucleotide variantNM_001240.4(CCNT1):c.1523A>T (p.Glu508Val)not specified [RCV004604880]uncertain significance124869369148693691Humanname
407492100CV3428688single nucleotide variantNM_001240.4(CCNT1):c.1481A>G (p.Asn494Ser)not specified [RCV004604881]uncertain significance124869373348693733Humanname
407454608CV3428689single nucleotide variantNM_001240.4(CCNT1):c.1303G>A (p.Val435Ile)not specified [RCV004609916]uncertain significance124869391148693911Humanname
597766302CV3638269single nucleotide variantNM_001240.4(CCNT1):c.1190C>T (p.Ala397Val)not specified [RCV004896102]uncertain significance124869402448694024Humanname
597766317CV3638272single nucleotide variantNM_001240.4(CCNT1):c.1325A>T (p.Glu442Val)not specified [RCV004896105]uncertain significance124869388948693889Humanname
597766320CV3638273single nucleotide variantNM_001240.4(CCNT1):c.1744G>C (p.Gly582Arg)not specified [RCV004896106]uncertain significance124869347048693470Humanname
597766325CV3638274single nucleotide variantNM_001240.4(CCNT1):c.1079T>C (p.Val360Ala)not specified [RCV004896107]uncertain significance124869413548694135Humanname
598205473CV3939842single nucleotide variantNM_001240.4(CCNT1):c.1627G>A (p.Gly543Ser)not specified [RCV005314955]uncertain significance124869358748693587Humanname
598205486CV3939845single nucleotide variantNM_001240.4(CCNT1):c.2036C>G (p.Thr679Ser)not specified [RCV005314957]uncertain significance124869317848693178Humanname
598205493CV3939846single nucleotide variantNM_001240.4(CCNT1):c.1643G>A (p.Ser548Asn)not specified [RCV005314958]uncertain significance124869357148693571Humanname
598205501CV3939847single nucleotide variantNM_001240.4(CCNT1):c.1388G>A (p.Arg463Lys)not specified [RCV005314959]uncertain significance124869382648693826Humanname