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35 records found for search term Prr15
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401728393CV2686042single nucleotide variantNM_175887.3(PRR15):c.7G>A (p.Asp3Asn)not specified [RCV004297055]uncertain significance72956633629566336Humanname
405796432CV3379741single nucleotide variantNM_175887.3(PRR15):c.16G>A (p.Asp6Asn)not specified [RCV004507714]uncertain significance72956634529566345Humanname
156333344CV2214589single nucleotide variantNM_175887.3(PRR15):c.89G>A (p.Gly30Glu)not specified [RCV004088635]uncertain significance72956641829566418Humanname
401769609CV2731464single nucleotide variantNM_175887.3(PRR15):c.91G>T (p.Val31Leu)not specified [RCV004330819]uncertain significance72956642029566420Humanname
598249175CV3901421single nucleotide variantNM_175887.3(PRR15):c.50T>C (p.Leu17Pro)not specified [RCV005258894]uncertain significance72956637929566379Humanname
156073021CV2251528single nucleotide variantNM_175887.3(PRR15):c.113C>A (p.Ala38Asp)not specified [RCV004117490]uncertain significance72956644229566442Humanname
329394790CV2461468single nucleotide variantNM_175887.3(PRR15):c.286C>T (p.Arg96Cys)not specified [RCV004267610]uncertain significance72956661529566615Humanname
401879871CV2755307single nucleotide variantNM_175887.3(PRR15):c.215C>G (p.Pro72Arg)not specified [RCV004337478]uncertain significance72956654429566544Humanname
401884339CV2765925single nucleotide variantNM_175887.3(PRR15):c.196G>C (p.Gly66Arg)not specified [RCV004337952]uncertain significance72956652529566525Humanname
405796430CV3379740single nucleotide variantNM_175887.3(PRR15):c.149C>T (p.Pro50Leu)not specified [RCV004507713]uncertain significance72956647829566478Humanname
597760137CV3588420single nucleotide variantNM_175887.3(PRR15):c.128C>A (p.Thr43Lys)not specified [RCV004848883]uncertain significance72956645729566457Humanname
597760144CV3588421single nucleotide variantNM_175887.3(PRR15):c.164G>C (p.Ser55Thr)not specified [RCV004848884]uncertain significance72956649329566493Humanname
598249159CV3901419single nucleotide variantNM_175887.3(PRR15):c.212C>A (p.Pro71His)not specified [RCV005258892]uncertain significance72956654129566541Humanname
156147795CV2265230single nucleotide variantNM_175887.3(PRR15):c.375C>G (p.His125Gln)not specified [RCV004126341]likely benign72956670429566704Humanname
401775317CV2710519single nucleotide variantNM_175887.3(PRR15):c.313G>C (p.Ala105Pro)not specified [RCV004319446]uncertain significance72956664229566642Humanname
405796437CV3379742single nucleotide variantNM_175887.3(PRR15):c.374A>G (p.His125Arg)not specified [RCV004507715]uncertain significance72956670329566703Humanname
597760149CV3588422single nucleotide variantNM_175887.3(PRR15):c.325C>T (p.Pro109Ser)not specified [RCV004848885]uncertain significance72956665429566654Humanname
598249168CV3901420single nucleotide variantNM_175887.3(PRR15):c.323T>G (p.Leu108Arg)not specified [RCV005258893]uncertain significance72956665229566652Humanname
407513659CV3461306single nucleotide variantNM_024320.4(PRR15L):c.5C>A (p.Thr2Lys)not specified [RCV004648903]uncertain significance174795323047953230Humanname
8636215CV91439single nucleotide variantNM_024320.3(PRR15L):c.120G>A (p.Pro40=)Malignant melanoma [RCV000071537]not provided174795311547953115Humanname
597760154CV3588423single nucleotide variantNM_024320.4(PRR15L):c.95A>C (p.Gln32Pro)not specified [RCV004848886]uncertain significance174795314047953140Humanname
155923692CV2217696single nucleotide variantNM_024320.4(PRR15L):c.137G>A (p.Gly46Asp)not specified [RCV004083884]uncertain significance174795309847953098Humanname
156146593CV2311099single nucleotide variantNM_024320.4(PRR15L):c.224G>A (p.Arg75His)not specified [RCV004164096]uncertain significance174795301147953011Humanname
156283930CV2334718single nucleotide variantNM_024320.4(PRR15L):c.230A>G (p.Lys77Arg)not specified [RCV004188698]uncertain significance174795300547953005Humanname
156087491CV2336988single nucleotide variantNM_024320.4(PRR15L):c.143A>G (p.Asn48Ser)not specified [RCV004192759]uncertain significance174795309247953092Humanname
156383684CV2361641single nucleotide variantNM_024320.4(PRR15L):c.202G>A (p.Val68Ile)not specified [RCV004221262]uncertain significance174795303347953033Humanname
401742513CV2673802single nucleotide variantNM_024320.4(PRR15L):c.254C>T (p.Thr85Met)not specified [RCV004293186]uncertain significance174795298147952981Humanname
401732205CV2678031single nucleotide variantNM_024320.4(PRR15L):c.119C>T (p.Pro40Leu)not specified [RCV004296555]uncertain significance174795311647953116Humanname
401738099CV2700969single nucleotide variantNM_024320.4(PRR15L):c.285T>G (p.Asp95Glu)not specified [RCV004307228]uncertain significance174795295047952950Humanname
401728871CV2729875single nucleotide variantNM_024320.4(PRR15L):c.295G>A (p.Gly99Arg)not specified [RCV004332880]uncertain significance174795294047952940Humanname
401894832CV2785359single nucleotide variantNM_024320.4(PRR15L):c.200A>G (p.His67Arg)not specified [RCV004357108]uncertain significance174795303547953035Humanname
405796442CV3379743single nucleotide variantNM_024320.4(PRR15L):c.147C>G (p.Ser49Arg)not specified [RCV004507716]uncertain significance174795308847953088Humanname
597760159CV3588424single nucleotide variantNM_024320.4(PRR15L):c.183G>C (p.Lys61Asn)not specified [RCV004848887]uncertain significance174795305247953052Humanname
156175239CV2254645single nucleotide variantNM_024320.4(PRR15L):c.299G>A (p.Arg100Gln)not specified [RCV004115133]likely benign174795293647952936Humanname
598249183CV3901422single nucleotide variantNM_024320.4(PRR15L):c.298C>T (p.Arg100Trp)not specified [RCV005258895]uncertain significance174795293747952937Humanname