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Variants search result for Homo sapiens
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48 records found for search term Ccdc77
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401905793CV2810042single nucleotide variantNM_032358.4(CCDC77):c.102A>G (p.Ala34=)not provided [RCV003396103]likely benign12411810411810Humanname
407491024CV3428386single nucleotide variantNM_032358.4(CCDC77):c.13C>T (p.Pro5Ser)not specified [RCV004604614]uncertain significance12409396409396Humanname
405717687CV3296026single nucleotide variantNM_032358.4(CCDC77):c.74G>A (p.Ser25Asn)not specified [RCV004427745]uncertain significance12411782411782Humanname
156149131CV2265330single nucleotide variantNM_032358.4(CCDC77):c.244C>T (p.Leu82Phe)not specified [RCV004128220]uncertain significance12411952411952Humanname
156356976CV2318218single nucleotide variantNM_032358.4(CCDC77):c.122C>T (p.Pro41Leu)not specified [RCV004179403]uncertain significance12411830411830Humanname
156163789CV2376187single nucleotide variantNM_032358.4(CCDC77):c.255A>C (p.Glu85Asp)not specified [RCV004220413]uncertain significance12411963411963Humanname
401722092CV2680817single nucleotide variantNM_032358.4(CCDC77):c.143G>A (p.Arg48His)not specified [RCV004293465]uncertain significance12411851411851Humanname
405717620CV3296019single nucleotide variantNM_032358.4(CCDC77):c.109C>G (p.Leu37Val)not specified [RCV004427738]likely benign12411817411817Humanname
598191711CV3943416single nucleotide variantNM_032358.4(CCDC77):c.118A>G (p.Thr40Ala)not specified [RCV005312669]uncertain significance12411826411826Humanname
598191737CV3943421single nucleotide variantNM_032358.4(CCDC77):c.239T>C (p.Leu80Pro)not specified [RCV005312673]uncertain significance12411947411947Humanname
598191742CV3943422single nucleotide variantNM_032358.4(CCDC77):c.269A>G (p.Gln90Arg)not specified [RCV005312674]uncertain significance12411977411977Humanname
598191749CV3943423single nucleotide variantNM_032358.4(CCDC77):c.272A>C (p.His91Pro)not specified [RCV005312675]uncertain significance12418495418495Humanname
156314046CV2196587single nucleotide variantNM_032358.4(CCDC77):c.800A>C (p.Lys267Thr)not specified [RCV004073866]uncertain significance12433301433301Humanname
156284048CV2334731single nucleotide variantNM_032358.4(CCDC77):c.752G>A (p.Arg251Gln)not specified [RCV004188710]uncertain significance12433253433253Humanname
155929948CV2389271single nucleotide variantNM_032358.4(CCDC77):c.654A>G (p.Ile218Met)not specified [RCV004235588]uncertain significance12431936431936Humanname
329361893CV2437784single nucleotide variantNM_032358.4(CCDC77):c.493A>G (p.Lys165Glu)not specified [RCV004261084]uncertain significance12428848428848Humanname
401729825CV2686961single nucleotide variantNM_032358.4(CCDC77):c.469G>C (p.Ala157Pro)not specified [RCV004304293]uncertain significance12428824428824Humanname
401772178CV2708180single nucleotide variantNM_032358.4(CCDC77):c.472G>A (p.Gly158Arg)not specified [RCV004311541]uncertain significance12428827428827Humanname
401718397CV2708256single nucleotide variantNM_032358.4(CCDC77):c.736C>T (p.Leu246Phe)not specified [RCV004311601]uncertain significance12433237433237Humanname
401882065CV2774685single nucleotide variantNM_032358.4(CCDC77):c.635A>G (p.Glu212Gly)not specified [RCV004343793]uncertain significance12431917431917Humanname
405717662CV3296023single nucleotide variantNM_032358.4(CCDC77):c.331C>A (p.Leu111Ile)not specified [RCV004427742]uncertain significance12418554418554Humanname
405717672CV3296024single nucleotide variantNM_032358.4(CCDC77):c.341T>C (p.Met114Thr)not specified [RCV004427743]uncertain significance12418564418564Humanname
405717679CV3296025single nucleotide variantNM_032358.4(CCDC77):c.581C>G (p.Ala194Gly)not specified [RCV004427744]uncertain significance12430734430734Humanname
407491018CV3428384single nucleotide variantNM_032358.4(CCDC77):c.710A>G (p.Lys237Arg)not specified [RCV004604612]likely benign12433211433211Humanname
407491022CV3428385single nucleotide variantNM_032358.4(CCDC77):c.716C>T (p.Ser239Phe)not specified [RCV004604613]uncertain significance12433217433217Humanname
407491028CV3428387single nucleotide variantNM_032358.4(CCDC77):c.665T>A (p.Ile222Asn)not specified [RCV004604615]uncertain significance12431947431947Humanname
597764700CV3644686single nucleotide variantNM_032358.4(CCDC77):c.529A>G (p.Thr177Ala)not specified [RCV004895691]uncertain significance12430682430682Humanname
597764704CV3644688single nucleotide variantNM_032358.4(CCDC77):c.845T>G (p.Leu282Arg)not specified [RCV004895692]uncertain significance12438358438358Humanname
597761730CV3644689single nucleotide variantNM_032358.4(CCDC77):c.499C>G (p.Pro167Ala)not specified [RCV004895013]uncertain significance12428854428854Humanname
597764708CV3644690single nucleotide variantNM_032358.4(CCDC77):c.997C>A (p.Pro333Thr)not specified [RCV004895693]uncertain significance12438510438510Humanname
598227987CV3943419single nucleotide variantNM_032358.4(CCDC77):c.541G>A (p.Val181Ile)not specified [RCV005319012]uncertain significance12430694430694Humanname
156253161CV2232483single nucleotide variantNM_032358.4(CCDC77):c.1171C>T (p.Arg391Cys)not specified [RCV004099094]uncertain significance12440847440847Humanname
156306428CV2252731single nucleotide variantNM_032358.4(CCDC77):c.1172G>C (p.Arg391Pro)not specified [RCV004118584]uncertain significance12440848440848Humanname
156274649CV2255569single nucleotide variantNM_032358.4(CCDC77):c.1441C>G (p.Leu481Val)not specified [RCV004119989]uncertain significance12441894441894Humanname
156299381CV2326039single nucleotide variantNM_032358.4(CCDC77):c.1029T>A (p.Ser343Arg)not specified [RCV004176244]uncertain significance12438542438542Humanname
329373904CV2434617single nucleotide variantNM_032358.4(CCDC77):c.1099T>C (p.Cys367Arg)not specified [RCV004248342]uncertain significance12440674440674Humanname
329359220CV2435349single nucleotide variantNM_032358.4(CCDC77):c.1037T>A (p.Ile346Asn)not specified [RCV004253008]uncertain significance12438550438550Humanname
401758078CV2682165single nucleotide variantNM_032358.4(CCDC77):c.1344C>A (p.Asn448Lys)not specified [RCV004290211]uncertain significance12441797441797Humanname
401894814CV2785339single nucleotide variantNM_032358.4(CCDC77):c.1013G>A (p.Ser338Asn)not specified [RCV004357092]uncertain significance12438526438526Humanname
405717632CV3296020single nucleotide variantNM_032358.4(CCDC77):c.1261A>G (p.Lys421Glu)not specified [RCV004427739]uncertain significance12440937440937Humanname
405717640CV3296021single nucleotide variantNM_032358.4(CCDC77):c.1333G>C (p.Ala445Pro)not specified [RCV004427740]uncertain significance12441786441786Humanname
405717650CV3296022single nucleotide variantNM_032358.4(CCDC77):c.1336C>T (p.Arg446Trp)not specified [RCV004427741]uncertain significance12441789441789Humanname
597764694CV3644683single nucleotide variantNM_032358.4(CCDC77):c.1064A>C (p.Gln355Pro)not specified [RCV004895689]uncertain significance12440639440639Humanname
597761718CV3644684single nucleotide variantNM_032358.4(CCDC77):c.1337G>A (p.Arg446Gln)not specified [RCV004895011]likely benign12441790441790Humanname
597764696CV3644685single nucleotide variantNM_032358.4(CCDC77):c.1048A>G (p.Lys350Glu)not specified [RCV004895690]uncertain significance12440623440623Humanname
597761725CV3644687single nucleotide variantNM_032358.4(CCDC77):c.1133G>A (p.Arg378His)not specified [RCV004895012]uncertain significance12440708440708Humanname
598191722CV3943418single nucleotide variantNM_032358.4(CCDC77):c.1214G>A (p.Arg405His)not specified [RCV005312671]uncertain significance12440890440890Humanname
598191731CV3943420single nucleotide variantNM_032358.4(CCDC77):c.1145G>A (p.Gly382Glu)not specified [RCV005312672]uncertain significance12440720440720Humanname