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22 records found for search term Capns2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401866250CV2762581single nucleotide variantNM_032330.3(CAPNS2):c.4T>A (p.Phe2Ile)not specified [RCV004338105]uncertain significance165556676055566760Humanname
156309225CV2249617single nucleotide variantNM_032330.3(CAPNS2):c.41G>A (p.Gly14Asp)not specified [RCV004120627]uncertain significance165556679755566797Humanname
405712674CV3299044single nucleotide variantNM_032330.3(CAPNS2):c.28G>A (p.Gly10Arg)not specified [RCV004427043]uncertain significance165556678455566784Humanname
405712681CV3299045single nucleotide variantNM_032330.3(CAPNS2):c.53C>T (p.Ala18Val)not specified [RCV004427044]uncertain significance165556680955566809Humanname
329375143CV2470884single nucleotide variantNM_032330.3(CAPNS2):c.170C>G (p.Thr57Ser)not specified [RCV004276085]uncertain significance165556692655566926Humanname
401857462CV2759242single nucleotide variantNM_032330.3(CAPNS2):c.170C>T (p.Thr57Ile)not specified [RCV004335840]uncertain significance165556692655566926Humanname
405712658CV3299042single nucleotide variantNM_032330.3(CAPNS2):c.178C>T (p.Pro60Ser)not specified [RCV004427041]uncertain significance165556693455566934Humanname
405712664CV3299043single nucleotide variantNM_032330.3(CAPNS2):c.229G>C (p.Glu77Gln)not specified [RCV004427042]uncertain significance165556698555566985Humanname
407476045CV3424703single nucleotide variantNM_032330.3(CAPNS2):c.244C>T (p.Arg82Trp)not specified [RCV004600843]uncertain significance165556700055567000Humanname
407476050CV3424705single nucleotide variantNM_032330.3(CAPNS2):c.197A>G (p.His66Arg)not specified [RCV004600844]uncertain significance165556695355566953Humanname
156178997CV2201628single nucleotide variantNM_032330.3(CAPNS2):c.374G>A (p.Arg125Gln)not specified [RCV004082092]uncertain significance165556713055567130Humanname
156092986CV2216911single nucleotide variantNM_032330.3(CAPNS2):c.453C>G (p.Ile151Met)not specified [RCV004083322]uncertain significance165556720955567209Humanname
156129670CV2279708single nucleotide variantNM_032330.3(CAPNS2):c.692A>T (p.Asp231Val)not specified [RCV004144327]uncertain significance165556744855567448Humanname
401759232CV2690834single nucleotide variantNM_032330.3(CAPNS2):c.397A>G (p.Ser133Gly)not specified [RCV004298541]uncertain significance165556715355567153Humanname
405712690CV3299046single nucleotide variantNM_032330.3(CAPNS2):c.547T>G (p.Phe183Val)not specified [RCV004427045]uncertain significance165556730355567303Humanname
407477369CV3424704single nucleotide variantNM_032330.3(CAPNS2):c.395A>G (p.Asp132Gly)not specified [RCV004607320]uncertain significance165556715155567151Humanname
407476055CV3424707single nucleotide variantNM_032330.3(CAPNS2):c.736A>G (p.Met246Val)not specified [RCV004600846]uncertain significance165556749255567492Humanname
597775457CV3643961single nucleotide variantNM_032330.3(CAPNS2):c.704A>G (p.Gln235Arg)not specified [RCV004898242]uncertain significance165556746055567460Humanname
597775461CV3643962single nucleotide variantNM_032330.3(CAPNS2):c.416T>C (p.Leu139Pro)not specified [RCV004898243]uncertain significance165556717255567172Humanname
598164369CV3939316single nucleotide variantNM_032330.3(CAPNS2):c.586C>T (p.Arg196Trp)not specified [RCV005307532]uncertain significance165556734255567342Humanname
598164377CV3939317single nucleotide variantNM_032330.3(CAPNS2):c.644G>A (p.Arg215His)not specified [RCV005307533]uncertain significance165556740055567400Humanname
598164383CV3939318single nucleotide variantNM_032330.3(CAPNS2):c.331C>T (p.His111Tyr)not specified [RCV005307534]uncertain significance165556708755567087Humanname