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Variants search result for Homo sapiens
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29 records found for search term Sdcbp2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407462025CV3480328single nucleotide variantNM_080489.5(SDCBP2):c.82C>T (p.Pro28Ser)not specified [RCV004658921]uncertain significance2013196321319632Humanname
407462028CV3480329single nucleotide variantNM_080489.5(SDCBP2):c.43C>G (p.Gln15Glu)not specified [RCV004658922]uncertain significance2013203741320374Humanname
8628462CV83606single nucleotide variantNM_080489.4(SDCBP2):c.666C>T (p.Ala222=)Malignant melanoma [RCV000063687]not provided2013124031312403Humanname
8586272CV120871single nucleotide variantNR_037661.1(FKBP1A-SDCBP2):n.259+31082T>CLung cancer [RCV000101391]uncertain significance2013617521361752Humanname
155904692CV2298847single nucleotide variantNM_080489.5(SDCBP2):c.119C>T (p.Pro40Leu)not specified [RCV004156394]uncertain significance2013195951319595Humanname
401891168CV2769112single nucleotide variantNM_080489.5(SDCBP2):c.161T>C (p.Met54Thr)not specified [RCV004348965]uncertain significance2013183821318382Humanname
405760716CV3314243single nucleotide variantNM_080489.5(SDCBP2):c.274G>C (p.Gly92Arg)not specified [RCV004455258]uncertain significance2013134501313450Humanname
597694381CV3595070single nucleotide variantNM_080489.5(SDCBP2):c.238G>A (p.Gly80Ser)not specified [RCV004859196]uncertain significance2013134861313486Humanname
597694393CV3595071single nucleotide variantNM_080489.5(SDCBP2):c.143C>T (p.Ala48Val)not specified [RCV004859197]uncertain significance2013184001318400Humanname
156249389CV2215550single nucleotide variantNM_080489.5(SDCBP2):c.494C>T (p.Ser165Leu)not specified [RCV004089323]uncertain significance2013126531312653Humanname
156334661CV2230954single nucleotide variantNM_080489.5(SDCBP2):c.709G>C (p.Gly237Arg)not specified [RCV004092415]uncertain significance2013123601312360Humanname
156318660CV2260724single nucleotide variantNM_080489.5(SDCBP2):c.812A>C (p.His271Pro)not specified [RCV004125652]uncertain significance2013108121310812Humanname
156280348CV2348441single nucleotide variantNM_080489.5(SDCBP2):c.674G>T (p.Gly225Val)not specified [RCV004193631]uncertain significance2013123951312395Humanname
156052682CV2363491single nucleotide variantNM_080489.5(SDCBP2):c.862T>C (p.Ser288Pro)not specified [RCV004216064]uncertain significance2013104581310458Humanname
329388324CV2437305single nucleotide variantNM_080489.5(SDCBP2):c.571C>T (p.Arg191Trp)not specified [RCV004256186]uncertain significance2013124981312498Humanname
401722365CV2676956single nucleotide variantNM_080489.5(SDCBP2):c.772G>A (p.Val258Ile)not specified [RCV004293558]uncertain significance2013108521310852Humanname
401750205CV2695979single nucleotide variantNM_080489.5(SDCBP2):c.647T>G (p.Val216Gly)not specified [RCV004308245]uncertain significance2013124221312422Humanname
401783199CV2703871single nucleotide variantNM_080489.5(SDCBP2):c.563C>T (p.Pro188Leu)not specified [RCV004306733]uncertain significance2013125061312506Humanname
401855967CV2754173single nucleotide variantNM_080489.5(SDCBP2):c.844C>T (p.His282Tyr)not specified [RCV004334365]uncertain significance2013104761310476Humanname
401892690CV2791665single nucleotide variantNM_080489.5(SDCBP2):c.493T>G (p.Ser165Ala)not specified [RCV004353007]uncertain significance2013126541312654Humanname
405760723CV3314244single nucleotide variantNM_080489.5(SDCBP2):c.415A>C (p.Thr139Pro)not specified [RCV004455259]uncertain significance2013127321312732Humanname
405760727CV3314245single nucleotide variantNM_080489.5(SDCBP2):c.452A>G (p.Gln151Arg)not specified [RCV004455260]uncertain significance2013126951312695Humanname
405760733CV3314246single nucleotide variantNM_080489.5(SDCBP2):c.583A>G (p.Met195Val)not specified [RCV004455261]uncertain significance2013124861312486Humanname
407462021CV3480327single nucleotide variantNM_080489.5(SDCBP2):c.391T>C (p.Phe131Leu)not specified [RCV004658920]uncertain significance2013127561312756Humanname
597694346CV3595067single nucleotide variantNM_080489.5(SDCBP2):c.473G>A (p.Arg158His)not specified [RCV004859193]uncertain significance2013126741312674Humanname
597694359CV3595068single nucleotide variantNM_080489.5(SDCBP2):c.554G>A (p.Arg185Gln)not specified [RCV004859194]uncertain significance2013125931312593Humanname
597694370CV3595069single nucleotide variantNM_080489.5(SDCBP2):c.746T>C (p.Met249Thr)not specified [RCV004859195]likely benign2013108781310878Humanname
598236450CV3906848single nucleotide variantNM_080489.5(SDCBP2):c.414C>G (p.Asn138Lys)not specified [RCV005275428]uncertain significance2013127331312733Humanname
598236455CV3906849single nucleotide variantNM_080489.5(SDCBP2):c.476A>T (p.Asp159Val)not specified [RCV005275429]uncertain significance2013126711312671Humanname