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Variants search result for Homo sapiens
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30 records found for search term Ccne1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407491910CV3428629single nucleotide variantNM_001238.4(CCNE1):c.14G>T (p.Arg5Leu)not specified [RCV004604827]uncertain significance192981256929812569Humanname
407491914CV3428630single nucleotide variantNM_001238.4(CCNE1):c.22C>T (p.Arg8Trp)not specified [RCV004604828]uncertain significance192981257729812577Humanname
598205103CV3939780single nucleotide variantNM_001238.4(CCNE1):c.37C>T (p.Arg13Trp)not specified [RCV005314901]uncertain significance192981270229812702Humanname
155943280CV2244968single nucleotide variantNM_001238.4(CCNE1):c.112T>C (p.Phe38Leu)not specified [RCV004104704]uncertain significance192981296929812969Humanname
156189549CV2289189single nucleotide variantNM_001238.4(CCNE1):c.109G>C (p.Val37Leu)not specified [RCV004152193]uncertain significance192981277429812774Humanname
156263863CV2329406single nucleotide variantNM_001238.4(CCNE1):c.232C>A (p.Pro78Thr)not specified [RCV004187416]uncertain significance192981718829817188Humanname
156293456CV2336477single nucleotide variantNM_001238.4(CCNE1):c.125C>A (p.Pro42Gln)not specified [RCV004194689]uncertain significance192981298229812982Humanname
405741275CV3292651single nucleotide variantNM_001238.4(CCNE1):c.245A>G (p.Asp82Gly)not specified [RCV004430740]uncertain significance192981720129817201Humanname
405741281CV3292652single nucleotide variantNM_001238.4(CCNE1):c.247G>C (p.Asp83His)not specified [RCV004430741]uncertain significance192981720329817203Humanname
597762126CV3641672single nucleotide variantNM_001238.4(CCNE1):c.194A>G (p.Asn65Ser)not specified [RCV004895087]uncertain significance192981715029817150Humanname
598205092CV3939778single nucleotide variantNM_001238.4(CCNE1):c.129T>A (p.Asp43Glu)not specified [RCV005314899]uncertain significance192981298629812986Humanname
598205098CV3939779single nucleotide variantNM_001238.4(CCNE1):c.248A>G (p.Asp83Gly)not specified [RCV005314900]uncertain significance192981720429817204Humanname
598205119CV3939783single nucleotide variantNM_001238.4(CCNE1):c.227C>T (p.Pro76Leu)not specified [RCV005314904]uncertain significance192981718329817183Humanname
156131579CV2235249single nucleotide variantNM_001238.4(CCNE1):c.319G>A (p.Val107Ile)not specified [RCV004107296]uncertain significance192981727529817275Humanname
156203242CV2300710single nucleotide variantNM_001238.4(CCNE1):c.787C>T (p.His263Tyr)not specified [RCV004155648]likely benign192982207729822077Humanname
401886805CV2776749single nucleotide variantNM_001238.4(CCNE1):c.700A>G (p.Met234Val)not specified [RCV004357903]uncertain significance192982181229821812Humanname
401877303CV2790122single nucleotide variantNM_001238.4(CCNE1):c.892A>G (p.Ile298Val)not specified [RCV004364062]likely benign192982229129822291Humanname
405741286CV3292653single nucleotide variantNM_001238.4(CCNE1):c.332C>G (p.Ala111Gly)not specified [RCV004430742]uncertain significance192981741129817411Humanname
405741294CV3292654single nucleotide variantNM_001238.4(CCNE1):c.533C>T (p.Ala178Val)not specified [RCV004430743]uncertain significance192982077229820772Humanname
405741298CV3292655single nucleotide variantNM_001238.4(CCNE1):c.803C>T (p.Pro268Leu)not specified [RCV004430744]uncertain significance192982209329822093Humanname
407454595CV3428631single nucleotide variantNM_001238.4(CCNE1):c.972A>G (p.Ile324Met)not specified [RCV004609911]uncertain significance192982246529822465Humanname
597765983CV3641673single nucleotide variantNM_001238.4(CCNE1):c.883C>T (p.Pro295Ser)not specified [RCV004896035]likely benign192982228229822282Humanname
597765987CV3641674single nucleotide variantNM_001238.4(CCNE1):c.569T>C (p.Leu190Pro)not specified [RCV004896036]uncertain significance192982080829820808Humanname
598205113CV3939782single nucleotide variantNM_001238.4(CCNE1):c.680T>G (p.Leu227Arg)not specified [RCV005314903]uncertain significance192982179229821792Humanname
156400569CV2199269single nucleotide variantNM_001238.4(CCNE1):c.1078A>G (p.Ile360Val)not specified [RCV004082624]uncertain significance192982257129822571Humanname
156286390CV2334928single nucleotide variantNM_001238.4(CCNE1):c.1048A>G (p.Arg350Gly)not specified [RCV004182031]uncertain significance192982254129822541Humanname
401767855CV2677839single nucleotide variantNM_001238.4(CCNE1):c.1198G>A (p.Gly400Ser)not specified [RCV004294336]likely benign192982374229823742Humanname
401877485CV2790186single nucleotide variantNM_001238.4(CCNE1):c.1216G>A (p.Gly406Arg)not specified [RCV004364108]uncertain significance192982376029823760Humanname
598228340CV3939776single nucleotide variantNM_001238.4(CCNE1):c.1104T>A (p.Asp368Glu)not specified [RCV005319070]uncertain significance192982259729822597Humanname
598205109CV3939781single nucleotide variantNM_001238.4(CCNE1):c.1006A>G (p.Met336Val)not specified [RCV005314902]uncertain significance192982249929822499Humanname