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Variants search result for Homo sapiens
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46 records found for search term Ctsw
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405700869CV3246354single nucleotide variantNM_001335.4(CTSW):c.22T>C (p.Ser8Pro)not specified [RCV004375090]uncertain significance116587987665879876Humanname
156032199CV2274995single nucleotide variantNM_001335.4(CTSW):c.194T>A (p.Ile65Asn)not specified [RCV004135039]uncertain significance116588142865881428Humanname
155958102CV2395106single nucleotide variantNM_001335.4(CTSW):c.193A>T (p.Ile65Phe)not specified [RCV004236785]uncertain significance116588142765881427Humanname
405700156CV3246350single nucleotide variantNM_001335.4(CTSW):c.121G>A (p.Ala41Thr)not specified [RCV004375086]uncertain significance116588023565880235Humanname
405700163CV3246351single nucleotide variantNM_001335.4(CTSW):c.122C>A (p.Ala41Asp)not specified [RCV004375087]uncertain significance116588023665880236Humanname
405700169CV3246352single nucleotide variantNM_001335.4(CTSW):c.190G>C (p.Asp64His)not specified [RCV004375088]uncertain significance116588142465881424Humanname
405700174CV3246353single nucleotide variantNM_001335.4(CTSW):c.211G>A (p.Ala71Thr)not specified [RCV004375089]uncertain significance116588144565881445Humanname
597653240CV3661429single nucleotide variantNM_001335.4(CTSW):c.296T>C (p.Phe99Ser)not specified [RCV004910786]uncertain significance116588218465882184Humanname
598221796CV3955928single nucleotide variantNM_001335.4(CTSW):c.151C>T (p.Arg51Trp)not specified [RCV005317763]uncertain significance116588026565880265Humanname
598221801CV3955929single nucleotide variantNM_001335.4(CTSW):c.231G>T (p.Gln77His)not specified [RCV005317764]uncertain significance116588146565881465Humanname
156256009CV2219721single nucleotide variantNM_001335.4(CTSW):c.341G>A (p.Ser114Asn)not specified [RCV004095425]uncertain significance116588222965882229Humanname
156249953CV2273227single nucleotide variantNM_001335.4(CTSW):c.418G>A (p.Ala140Thr)not specified [RCV004132024]uncertain significance116588230665882306Humanname
156170621CV2273568single nucleotide variantNM_001335.4(CTSW):c.526G>A (p.Val176Ile)not specified [RCV004134095]uncertain significance116588251465882514Humanname
156010409CV2291016single nucleotide variantNM_001335.4(CTSW):c.795C>G (p.Asn265Lys)not specified [RCV004151559]uncertain significance116588311865883118Humanname
156055444CV2308784single nucleotide variantNM_001335.4(CTSW):c.485T>G (p.Ile162Arg)not specified [RCV004169098]uncertain significance116588247365882473Humanname
155973846CV2317739single nucleotide variantNM_001335.4(CTSW):c.499C>T (p.Arg167Cys)not specified [RCV004174995]uncertain significance116588248765882487Humanname
156175207CV2327087single nucleotide variantNM_001335.4(CTSW):c.326C>G (p.Ala109Gly)not specified [RCV004178669]uncertain significance116588221465882214Humanname
156105129CV2352508single nucleotide variantNM_001335.4(CTSW):c.494T>C (p.Leu165Pro)not specified [RCV004203011]uncertain significance116588248265882482Humanname
156153943CV2369439single nucleotide variantNM_001335.4(CTSW):c.532G>A (p.Val178Met)not specified [RCV004210382]uncertain significance116588252065882520Humanname
329399022CV2428721single nucleotide variantNM_001335.4(CTSW):c.549C>A (p.Asp183Glu)not specified [RCV004255511]uncertain significance116588261965882619Humanname
329374939CV2430987single nucleotide variantNM_001335.4(CTSW):c.782C>T (p.Thr261Ile)not specified [RCV004250366]uncertain significance116588310565883105Humanname
329376866CV2460589single nucleotide variantNM_001335.4(CTSW):c.731A>C (p.Gln244Pro)not specified [RCV004268866]likely benign116588289065882890Humanname
401883906CV2785800single nucleotide variantNM_001335.4(CTSW):c.334G>A (p.Val112Ile)not specified [RCV004365046]uncertain significance116588222265882222Humanname
401933232CV2813362deletionNM_001335.4(CTSW):c.29_36del (p.Leu10fs)not provided [RCV003409302]likely benign116587988065879887Humanname
405700834CV3242848single nucleotide variantNM_001335.4(CTSW):c.800A>C (p.Lys267Thr)not specified [RCV004375096]uncertain significance116588312365883123Humanname
405700830CV3242849single nucleotide variantNM_001335.4(CTSW):c.818G>A (p.Arg273Gln)not specified [RCV004375097]likely benign116588322265883222Humanname
405700863CV3246355single nucleotide variantNM_001335.4(CTSW):c.421A>G (p.Ile141Val)not specified [RCV004375091]uncertain significance116588230965882309Humanname
405700856CV3246356single nucleotide variantNM_001335.4(CTSW):c.521T>C (p.Val174Ala)not specified [RCV004375092]uncertain significance116588250965882509Humanname
405700849CV3246357single nucleotide variantNM_001335.4(CTSW):c.557G>A (p.Arg186His)not specified [RCV004375093]uncertain significance116588262765882627Humanname
405700843CV3246358single nucleotide variantNM_001335.4(CTSW):c.617A>G (p.Asn206Ser)not specified [RCV004375094]uncertain significance116588268765882687Humanname
405700839CV3246359single nucleotide variantNM_001335.4(CTSW):c.797T>C (p.Met266Thr)not specified [RCV004375095]uncertain significance116588312065883120Humanname
407472795CV3426419single nucleotide variantNM_001335.4(CTSW):c.532G>T (p.Val178Leu)not specified [RCV004616027]uncertain significance116588252065882520Humanname
407472800CV3426420single nucleotide variantNM_001335.4(CTSW):c.790A>G (p.Ile264Val)not specified [RCV004616028]uncertain significance116588311365883113Humanname
407472805CV3426421single nucleotide variantNM_001335.4(CTSW):c.320G>A (p.Arg107Lys)not specified [RCV004616029]uncertain significance116588220865882208Humanname
407472810CV3426422single nucleotide variantNM_001335.4(CTSW):c.916G>A (p.Gly306Arg)not specified [RCV004616030]uncertain significance116588332065883320Humanname
597653231CV3661428single nucleotide variantNM_001335.4(CTSW):c.404G>A (p.Arg135Gln)not specified [RCV004910785]uncertain significance116588229265882292Humanname
597653247CV3661430single nucleotide variantNM_001335.4(CTSW):c.491C>A (p.Thr164Asn)not specified [RCV004910787]uncertain significance116588247965882479Humanname
597653255CV3661431single nucleotide variantNM_001335.4(CTSW):c.791T>G (p.Ile264Ser)not specified [RCV004910788]uncertain significance116588311465883114Humanname
597653262CV3661433single nucleotide variantNM_001335.4(CTSW):c.453C>G (p.Asn151Lys)not specified [RCV004910789]uncertain significance116588244165882441Humanname
598221791CV3955927single nucleotide variantNM_001335.4(CTSW):c.556C>T (p.Arg186Cys)not specified [RCV005317762]uncertain significance116588262665882626Humanname
598221805CV3955930single nucleotide variantNM_001335.4(CTSW):c.450C>G (p.Cys150Trp)not specified [RCV005317765]uncertain significance116588243865882438Humanname
155927156CV2396039single nucleotide variantNM_001335.4(CTSW):c.1030C>T (p.Arg344Trp)not specified [RCV004237579]uncertain significance116588351765883517Humanname
329402281CV2454019single nucleotide variantNM_001335.4(CTSW):c.1108C>T (p.Pro370Ser)not specified [RCV004271673]uncertain significance116588359565883595Humanname
405700143CV3246348single nucleotide variantNM_001335.4(CTSW):c.1073C>T (p.Pro358Leu)not specified [RCV004375084]uncertain significance116588356065883560Humanname
405700149CV3246349single nucleotide variantNM_001335.4(CTSW):c.1085G>A (p.Arg362His)not specified [RCV004375085]uncertain significance116588357265883572Humanname
597653270CV3661434single nucleotide variantNM_001335.4(CTSW):c.1043G>T (p.Gly348Val)not specified [RCV004910790]uncertain significance116588353065883530Humanname