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42 records found for search term Cxadr
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156389175CV2373614single nucleotide variantNM_001338.5(CXADR):c.25C>T (p.Leu9Phe)not specified [RCV004222705]uncertain significance211751315417513154Humanname
405665489CV3243202single nucleotide variantNM_001338.5(CXADR):c.870T>A (p.Thr290=)not specified [RCV004367555]likely benign211756546417565464Humanname
405665493CV3243203single nucleotide variantNM_001338.5(CXADR):c.885C>T (p.Ile295=)not specified [RCV004367556]likely benign211756547917565479Humanname
597783056CV3661766single nucleotide variantNM_001338.5(CXADR):c.933A>G (p.Glu311=)not specified [RCV004900149]likely benign211756552717565527Humanname
597655083CV3661769single nucleotide variantNM_001338.5(CXADR):c.62G>A (p.Ser21Asn)not specified [RCV004911010]uncertain significance211754704517547045Humanname
598236526CV3956150single nucleotide variantNM_001338.5(CXADR):c.864G>C (p.Thr288=)not specified [RCV005320451]likely benign211756545817565458Humanname
598236540CV3956153single nucleotide variantNM_001338.5(CXADR):c.64A>C (p.Ile22Leu)not specified [RCV005320454]uncertain significance211754704717547047Humanname
15169879CV742570single nucleotide variantNM_001338.5(CXADR):c.579T>A (p.Thr193=)not provided [RCV000905156]benign211756070917560709Humanname
329398829CV2471736single nucleotide variantNM_001338.5(CXADR):c.137G>A (p.Ser46Asn)not specified [RCV004280785]uncertain significance211754712017547120Humanname
401774979CV2713722single nucleotide variantNM_001338.5(CXADR):c.230A>G (p.Asp77Gly)not specified [RCV004321075]uncertain significance211755176817551768Humanname
405665453CV3243194single nucleotide variantNM_001338.5(CXADR):c.1002T>G (p.Thr334=)not specified [RCV004367547]likely benign211756559617565596Humanname
405665462CV3243196single nucleotide variantNM_001338.5(CXADR):c.142G>A (p.Glu48Lys)not specified [RCV004367549]uncertain significance211754712517547125Humanname
405665466CV3243197single nucleotide variantNM_001338.5(CXADR):c.155C>T (p.Pro52Leu)not specified [RCV004367550]uncertain significance211754713817547138Humanname
407473281CV3419956single nucleotide variantNM_001338.5(CXADR):c.220T>C (p.Tyr74His)not specified [RCV004616179]uncertain significance211755175817551758Humanname
407473286CV3419957single nucleotide variantNM_001338.5(CXADR):c.295A>G (p.Lys99Glu)not specified [RCV004616180]uncertain significance211755183317551833Humanname
597655030CV3661762single nucleotide variantNM_001338.5(CXADR):c.125A>G (p.Lys42Arg)not specified [RCV004911004]uncertain significance211754710817547108Humanname
597655074CV3661768single nucleotide variantNM_001338.5(CXADR):c.166G>A (p.Glu56Lys)not specified [RCV004911009]uncertain significance211754714917547149Humanname
598236534CV3956152single nucleotide variantNM_001338.5(CXADR):c.269G>A (p.Arg90Gln)not specified [RCV005320453]uncertain significance211755180717551807Humanname
8637467CV92693single nucleotide variantNM_001338.4(CXADR):c.1074G>A (p.Gln358=)Malignant melanoma [RCV000072791]not provided211756566817565668Humanname
155959049CV2193724single nucleotide variantNM_001338.5(CXADR):c.495A>C (p.Lys165Asn)not specified [RCV004074488]uncertain significance211755905517559055Humanname
156377425CV2207080single nucleotide variantNM_001338.5(CXADR):c.782G>A (p.Arg261His)not specified [RCV004085684]likely benign211756142517561425Humanname
156186260CV2232624single nucleotide variantNM_001338.5(CXADR):c.349A>T (p.Thr117Ser)not specified [RCV004101299]uncertain significance211755188717551887Humanname
156159337CV2322731single nucleotide variantNM_001338.5(CXADR):c.323C>T (p.Thr108Met)not specified [RCV004182846]uncertain significance211755186117551861Humanname
155905404CV2349758single nucleotide variantNM_001338.5(CXADR):c.886G>A (p.Gly296Ser)not specified [RCV004204172]uncertain significance211756548017565480Humanname
329358963CV2450772single nucleotide variantNM_001338.5(CXADR):c.790C>T (p.Arg264Cys)not specified [RCV004267699]uncertain significance211756143317561433Humanname
401717995CV2704123single nucleotide variantNM_001338.5(CXADR):c.869C>T (p.Thr290Ile)not specified [RCV004308987]uncertain significance211756546317565463Humanname
405665470CV3243198single nucleotide variantNM_001338.5(CXADR):c.357G>T (p.Gln119His)not specified [RCV004367551]uncertain significance211755189517551895Humanname
405665475CV3243199single nucleotide variantNM_001338.5(CXADR):c.677G>C (p.Arg226Pro)not specified [RCV004367552]uncertain significance211756080717560807Humanname
405665479CV3243200single nucleotide variantNM_001338.5(CXADR):c.748C>G (p.Leu250Val)not specified [RCV004367553]uncertain significance211756139117561391Humanname
405665484CV3243201single nucleotide variantNM_001338.5(CXADR):c.763C>T (p.Leu255Phe)not specified [RCV004367554]uncertain significance211756140617561406Humanname
405665498CV3243204single nucleotide variantNM_001338.5(CXADR):c.964C>T (p.Pro322Ser)not specified [RCV004367557]uncertain significance211756555817565558Humanname
405665503CV3243205single nucleotide variantNM_001338.5(CXADR):c.983G>A (p.Arg328His)not specified [RCV004367558]uncertain significance211756557717565577Humanname
597655039CV3661763single nucleotide variantNM_001338.5(CXADR):c.650G>A (p.Arg217Lys)not specified [RCV004911005]uncertain significance211756078017560780Humanname
597655051CV3661764single nucleotide variantNM_001338.5(CXADR):c.736A>G (p.Thr246Ala)not specified [RCV004911006]uncertain significance211756137917561379Humanname
597655058CV3661765single nucleotide variantNM_001338.5(CXADR):c.431C>T (p.Ala144Val)not specified [RCV004911007]uncertain significance211755899117558991Humanname
598236522CV3956149single nucleotide variantNM_001338.5(CXADR):c.859C>T (p.Arg287Cys)not specified [RCV005320450]uncertain significance211756545317565453Humanname
598236531CV3956151single nucleotide variantNM_001338.5(CXADR):c.805T>A (p.Tyr269Asn)not specified [RCV005320452]uncertain significance211756144817561448Humanname
156355826CV2324557single nucleotide variantNM_001338.5(CXADR):c.1083T>G (p.Asp361Glu)not specified [RCV004179030]uncertain significance211756567717565677Humanname
156355832CV2324558single nucleotide variantNM_001338.5(CXADR):c.1088C>T (p.Ser363Phe)not specified [RCV004179031]uncertain significance211756568217565682Humanname
401865057CV2768653single nucleotide variantNM_001338.5(CXADR):c.1061T>C (p.Met354Thr)not specified [RCV004344502]uncertain significance211756565517565655Humanname
405665457CV3243195single nucleotide variantNM_001338.5(CXADR):c.1081G>A (p.Asp361Asn)not specified [RCV004367548]uncertain significance211756567517565675Humanname
597655066CV3661767single nucleotide variantNM_001338.5(CXADR):c.1090A>G (p.Ile364Val)not specified [RCV004911008]uncertain significance211756568417565684Humanname