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33 records found for search term Ccnl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598205373CV3939824single nucleotide variantNM_020307.4(CCNL1):c.11G>C (p.Gly4Ala)not specified [RCV005314940]uncertain significance3157160084157160084Humanname
156365187CV2193146single nucleotide variantNM_020307.4(CCNL1):c.37G>A (p.Ala13Thr)not specified [RCV004071145]uncertain significance3157160058157160058Humanname
156164522CV2270275single nucleotide variantNM_020307.4(CCNL1):c.94A>G (p.Thr32Ala)not specified [RCV004135492]uncertain significance3157160001157160001Humanname
407492032CV3428666single nucleotide variantNM_020307.4(CCNL1):c.37G>T (p.Ala13Ser)not specified [RCV004604861]uncertain significance3157160058157160058Humanname
156023714CV2245505single nucleotide variantNM_020307.4(CCNL1):c.112G>A (p.Gly38Arg)not specified [RCV004109278]uncertain significance3157159983157159983Humanname
407492011CV3428661single nucleotide variantNM_020307.4(CCNL1):c.188G>C (p.Arg63Thr)not specified [RCV004604856]uncertain significance3157159907157159907Humanname
407492024CV3428664single nucleotide variantNM_020307.4(CCNL1):c.211C>G (p.Gln71Glu)not specified [RCV004604859]uncertain significance3157159884157159884Humanname
407492028CV3428665single nucleotide variantNM_020307.4(CCNL1):c.196C>A (p.Pro66Thr)not specified [RCV004604860]uncertain significance3157159899157159899Humanname
597766228CV3638236single nucleotide variantNM_020307.4(CCNL1):c.110C>A (p.Thr37Lys)not specified [RCV004896080]uncertain significance3157159985157159985Humanname
597766237CV3638238single nucleotide variantNM_020307.4(CCNL1):c.1494G>A (p.Arg498=)not specified [RCV004896082]likely benign3157148328157148328Humanname
597766247CV3638240single nucleotide variantNM_020307.4(CCNL1):c.262G>A (p.Glu88Lys)not specified [RCV004896084]uncertain significance3157159833157159833Humanname
156000196CV2296283single nucleotide variantNM_020307.4(CCNL1):c.742G>T (p.Ala248Ser)not specified [RCV004154185]uncertain significance3157150314157150314Humanname
329394394CV2469848single nucleotide variantNM_020307.4(CCNL1):c.436A>G (p.Ile146Val)not specified [RCV004285328]uncertain significance3157158918157158918Humanname
401723575CV2724951single nucleotide variantNM_020307.4(CCNL1):c.491C>T (p.Thr164Ile)not specified [RCV004319715]uncertain significance3157153154157153154Humanname
405741949CV3303175single nucleotide variantNM_020307.4(CCNL1):c.787A>G (p.Thr263Ala)not specified [RCV004430796]uncertain significance3157150157157150157Humanname
405741940CV3303176single nucleotide variantNM_020307.4(CCNL1):c.832A>G (p.Ile278Val)not specified [RCV004430797]uncertain significance3157150112157150112Humanname
598228391CV3939825single nucleotide variantNM_020307.4(CCNL1):c.704A>G (p.Asn235Ser)not specified [RCV005319076]uncertain significance3157150352157150352Humanname
155981675CV2272885single nucleotide variantNM_020307.4(CCNL1):c.1377T>G (p.Ser459Arg)not specified [RCV004135785]uncertain significance3157148445157148445Humanname
156274347CV2320010single nucleotide variantNM_020307.4(CCNL1):c.1438G>T (p.Asp480Tyr)not specified [RCV004167877]uncertain significance3157148384157148384Humanname
329374232CV2434744single nucleotide variantNM_020307.4(CCNL1):c.1174G>C (p.Ala392Pro)not specified [RCV004248448]uncertain significance3157149345157149345Humanname
329380386CV2444361single nucleotide variantNM_020307.4(CCNL1):c.1436G>A (p.Arg479Gln)not specified [RCV004263112]uncertain significance3157148386157148386Humanname
401762965CV2720145single nucleotide variantNM_020307.4(CCNL1):c.1378T>A (p.Ser460Thr)not specified [RCV004323704]uncertain significance3157148444157148444Humanname
405741971CV3303171single nucleotide variantNM_020307.4(CCNL1):c.1042G>A (p.Ala348Thr)not specified [RCV004430792]uncertain significance3157149576157149576Humanname
405741965CV3303172single nucleotide variantNM_020307.4(CCNL1):c.1247G>A (p.Arg416Gln)not specified [RCV004430793]uncertain significance3157148575157148575Humanname
405741954CV3303174single nucleotide variantNM_020307.4(CCNL1):c.1562A>G (p.His521Arg)not specified [RCV004430795]uncertain significance3157148260157148260Humanname
407492015CV3428662single nucleotide variantNM_020307.4(CCNL1):c.1490A>G (p.Asp497Gly)not specified [RCV004604857]uncertain significance3157148332157148332Humanname
407492019CV3428663single nucleotide variantNM_020307.4(CCNL1):c.1556C>T (p.Ser519Leu)not specified [RCV004604858]uncertain significance3157148266157148266Humanname
407454603CV3428667single nucleotide variantNM_020307.4(CCNL1):c.1162A>C (p.Asn388His)not specified [RCV004609914]uncertain significance3157149357157149357Humanname
407492037CV3428668single nucleotide variantNM_020307.4(CCNL1):c.1186A>G (p.Arg396Gly)not specified [RCV004604862]uncertain significance3157149333157149333Humanname
597766233CV3638237single nucleotide variantNM_020307.4(CCNL1):c.1435C>T (p.Arg479Trp)not specified [RCV004896081]uncertain significance3157148387157148387Humanname
597766242CV3638239single nucleotide variantNM_020307.4(CCNL1):c.1217A>G (p.His406Arg)not specified [RCV004896083]uncertain significance3157149302157149302Humanname
598205357CV3939822single nucleotide variantNM_020307.4(CCNL1):c.1358C>A (p.Thr453Asn)not specified [RCV005314938]uncertain significance3157148464157148464Humanname
598205365CV3939823single nucleotide variantNM_020307.4(CCNL1):c.1060A>G (p.Ile354Val)not specified [RCV005314939]likely benign3157149558157149558Humanname