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16 records found for search term Marveld1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156068407CV2280664single nucleotide variantNM_031484.4(MARVELD1):c.13C>T (p.Pro5Ser)not specified [RCV004143129]uncertain significance109771388997713889Humanname
156106270CV2387068single nucleotide variantNM_031484.4(MARVELD1):c.17C>G (p.Pro6Arg)not specified [RCV004226812]uncertain significance109771389397713893Humanname
401886115CV2771083single nucleotide variantNM_031484.4(MARVELD1):c.62G>C (p.Arg21Pro)not specified [RCV004346089]uncertain significance109771393897713938Humanname
405658539CV3281686single nucleotide variantNM_031484.4(MARVELD1):c.94G>A (p.Gly32Ser)not specified [RCV004416507]uncertain significance109771397097713970Humanname
155957200CV2282031single nucleotide variantNM_031484.4(MARVELD1):c.277C>T (p.Arg93Cys)not specified [RCV004138785]uncertain significance109771415397714153Humanname
405658531CV3281683single nucleotide variantNM_031484.4(MARVELD1):c.220G>A (p.Gly74Ser)not specified [RCV004416504]uncertain significance109771409697714096Humanname
405658534CV3281684single nucleotide variantNM_031484.4(MARVELD1):c.232C>T (p.Leu78Phe)not specified [RCV004416505]uncertain significance109771410897714108Humanname
597636758CV3697649single nucleotide variantNM_031484.4(MARVELD1):c.107T>G (p.Leu36Arg)not specified [RCV004940844]uncertain significance109771398397713983Humanname
598177016CV3985534single nucleotide variantNM_031484.4(MARVELD1):c.272G>A (p.Gly91Asp)not specified [RCV005371522]uncertain significance109771414897714148Humanname
329383894CV2434908single nucleotide variantNM_031484.4(MARVELD1):c.427G>A (p.Ala143Thr)not specified [RCV004250782]uncertain significance109771430397714303Humanname
401742321CV2677559single nucleotide variantNM_031484.4(MARVELD1):c.485G>T (p.Cys162Phe)not specified [RCV004291663]uncertain significance109771436197714361Humanname
401770203CV2710980single nucleotide variantNM_031484.4(MARVELD1):c.428C>G (p.Ala143Gly)not specified [RCV004310690]uncertain significance109771430497714304Humanname
405658536CV3281685single nucleotide variantNM_031484.4(MARVELD1):c.380A>G (p.Asn127Ser)not specified [RCV004416506]uncertain significance109771425697714256Humanname
407494894CV3456911single nucleotide variantNM_031484.4(MARVELD1):c.340G>A (p.Gly114Ser)not specified [RCV004643094]uncertain significance109771421697714216Humanname
597636762CV3697650single nucleotide variantNM_031484.4(MARVELD1):c.457C>G (p.Leu153Val)not specified [RCV004940845]uncertain significance109771433397714333Humanname
597636768CV3697651single nucleotide variantNM_031484.4(MARVELD1):c.395C>A (p.Pro132Gln)not specified [RCV004940846]likely benign109771427197714271Humanname