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Variants search result for Homo sapiens
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27 records found for search term Cdadc1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405772956CV3299939single nucleotide variantNM_030911.4(CDADC1):c.88A>G (p.Ile30Val)not specified [RCV004435611]uncertain significance134924887649248876Humanname
598166900CV3950879single nucleotide variantNM_030911.4(CDADC1):c.197A>G (p.His66Arg)not specified [RCV005307960]uncertain significance134925585849255858Humanname
156287319CV2229612single nucleotide variantNM_030911.4(CDADC1):c.356G>A (p.Gly119Glu)not provided [RCV004695415]|not specified [RCV004103428]uncertain significance134925944949259449Humanname
156147880CV2307302single nucleotide variantNM_030911.4(CDADC1):c.716A>G (p.Tyr239Cys)not specified [RCV004165997]uncertain significance134926777549267775Humanname
156246427CV2310603single nucleotide variantNM_030911.4(CDADC1):c.674C>A (p.Thr225Asn)not specified [RCV004157270]uncertain significance134926773349267733Humanname
401720509CV2673353single nucleotide variantNM_030911.4(CDADC1):c.766A>G (p.Met256Val)not specified [RCV004288336]uncertain significance134926782549267825Humanname
401718979CV2704896single nucleotide variantNM_030911.4(CDADC1):c.899G>A (p.Arg300His)not specified [RCV004307471]uncertain significance134926795849267958Humanname
401738459CV2711896single nucleotide variantNM_030911.4(CDADC1):c.938G>A (p.Ser313Asn)not specified [RCV004309518]uncertain significance134926799749267997Humanname
401860541CV2758518single nucleotide variantNM_030911.4(CDADC1):c.334C>A (p.Gln112Lys)not specified [RCV004335566]likely benign134925942749259427Humanname
401891735CV2780713single nucleotide variantNM_030911.4(CDADC1):c.995G>A (p.Arg332Gln)not specified [RCV004352052]uncertain significance134926805449268054Humanname
405772944CV3299937single nucleotide variantNM_030911.4(CDADC1):c.512A>G (p.Lys171Arg)not specified [RCV004435609]uncertain significance134926757149267571Humanname
405772951CV3299938single nucleotide variantNM_030911.4(CDADC1):c.747A>C (p.Glu249Asp)not specified [RCV004435610]uncertain significance134926780649267806Humanname
407498395CV3425054single nucleotide variantNM_030911.4(CDADC1):c.819G>T (p.Arg273Ser)not specified [RCV004606629]uncertain significance134926787849267878Humanname
597787418CV3648569single nucleotide variantNM_030911.4(CDADC1):c.422T>G (p.Ile141Ser)not specified [RCV004901224]uncertain significance134925951549259515Humanname
597787429CV3648571single nucleotide variantNM_030911.4(CDADC1):c.691T>C (p.Cys231Arg)not specified [RCV004901226]uncertain significance134926775049267750Humanname
597787433CV3648572single nucleotide variantNM_030911.4(CDADC1):c.595A>G (p.Met199Val)not specified [RCV004901227]uncertain significance134926765449267654Humanname
598166884CV3950876single nucleotide variantNM_030911.4(CDADC1):c.316G>A (p.Glu106Lys)not specified [RCV005307957]uncertain significance134925940949259409Humanname
598166890CV3950877single nucleotide variantNM_030911.4(CDADC1):c.485C>T (p.Thr162Met)not specified [RCV005307958]uncertain significance134926754449267544Humanname
598166895CV3950878single nucleotide variantNM_030911.4(CDADC1):c.686A>T (p.Tyr229Phe)not specified [RCV005307959]uncertain significance134926774549267745Humanname
155960505CV2204244single nucleotide variantNM_030911.4(CDADC1):c.1043G>C (p.Gly348Ala)not specified [RCV004079082]uncertain significance134927433349274333Humanname
156377685CV2211407single nucleotide variantNM_030911.4(CDADC1):c.1529G>A (p.Arg510His)not specified [RCV004090320]uncertain significance134929174149291741Humanname
156188691CV2226785single nucleotide variantNM_030911.4(CDADC1):c.1320A>C (p.Gln440His)not specified [RCV004101999]uncertain significance134928060849280608Humanname
155911987CV2312468single nucleotide variantNM_030911.4(CDADC1):c.1367C>T (p.Ser456Phe)not specified [RCV004167144]uncertain significance134928065549280655Humanname
405772927CV3299934single nucleotide variantNM_030911.4(CDADC1):c.1226A>G (p.Gln409Arg)not specified [RCV004435606]uncertain significance134928051449280514Humanname
405772932CV3299935single nucleotide variantNM_030911.4(CDADC1):c.1510C>T (p.His504Tyr)not specified [RCV004435607]uncertain significance134929172249291722Humanname
405772938CV3299936single nucleotide variantNM_030911.4(CDADC1):c.1534G>A (p.Gly512Arg)not specified [RCV004435608]uncertain significance134929174649291746Humanname
598166910CV3950881single nucleotide variantNM_030911.4(CDADC1):c.1158A>T (p.Lys386Asn)not specified [RCV005307962]uncertain significance134927845749278457Humanname