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91 records found for search term Dclre1a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156114885CV2268666single nucleotide variantNM_014881.5(DCLRE1A):c.41A>G (p.Lys14Arg)not specified [RCV004124070]uncertain significance10113853142113853142Humanname
405691305CV3243284single nucleotide variantNM_014881.5(DCLRE1A):c.55C>T (p.Pro19Ser)not specified [RCV004373366]uncertain significance10113853128113853128Humanname
597800983CV3652141single nucleotide variantNM_014881.5(DCLRE1A):c.93T>G (p.Ile31Met)not specified [RCV004905999]uncertain significance10113853090113853090Humanname
155950825CV2238655single nucleotide variantNM_014881.5(DCLRE1A):c.284A>G (p.Glu95Gly)not specified [RCV004107557]uncertain significance10113852899113852899Humanname
405691205CV3246779single nucleotide variantNM_014881.5(DCLRE1A):c.163G>A (p.Ala55Thr)not specified [RCV004373349]likely benign10113853020113853020Humanname
405691224CV3246782single nucleotide variantNM_014881.5(DCLRE1A):c.175G>A (p.Glu59Lys)not specified [RCV004373352]uncertain significance10113853008113853008Humanname
597800955CV3652126single nucleotide variantNM_014881.5(DCLRE1A):c.235A>G (p.Ser79Gly)not specified [RCV004905984]uncertain significance10113852948113852948Humanname
597800970CV3652134single nucleotide variantNM_014881.5(DCLRE1A):c.166G>A (p.Glu56Lys)not specified [RCV004905992]uncertain significance10113853017113853017Humanname
156235901CV2224081single nucleotide variantNM_014881.5(DCLRE1A):c.496C>G (p.Pro166Ala)not specified [RCV004095950]uncertain significance10113850609113850609Humanname
156030395CV2238403single nucleotide variantNM_014881.5(DCLRE1A):c.481T>C (p.Cys161Arg)not provided [RCV004695425]|not specified [RCV004113468]uncertain significance10113850624113850624Humanname
155953754CV2274242single nucleotide variantNM_014881.5(DCLRE1A):c.899A>G (p.Tyr300Cys)not specified [RCV004136645]uncertain significance10113850206113850206Humanname
156164267CV2323661single nucleotide variantNM_014881.5(DCLRE1A):c.364T>C (p.Cys122Arg)not specified [RCV004165843]uncertain significance10113852819113852819Humanname
156046716CV2340266single nucleotide variantNM_014881.5(DCLRE1A):c.826C>T (p.Arg276Cys)not specified [RCV004194538]uncertain significance10113850279113850279Humanname
156344077CV2349383single nucleotide variantNM_014881.5(DCLRE1A):c.979G>A (p.Glu327Lys)not specified [RCV004199314]uncertain significance10113850126113850126Humanname
156384136CV2371294single nucleotide variantNM_014881.5(DCLRE1A):c.326A>G (p.His109Arg)not specified [RCV004223308]likely benign10113852857113852857Humanname
329388790CV2469574single nucleotide variantNM_014881.5(DCLRE1A):c.532G>A (p.Ala178Thr)not specified [RCV004283007]uncertain significance10113850573113850573Humanname
401782875CV2707558single nucleotide variantNM_014881.5(DCLRE1A):c.925A>T (p.Thr309Ser)not specified [RCV004312925]uncertain significance10113850180113850180Humanname
401724510CV2714868single nucleotide variantNM_014881.5(DCLRE1A):c.821C>G (p.Ala274Gly)not specified [RCV004320419]likely benign10113850284113850284Humanname
401897162CV2789882single nucleotide variantNM_014881.5(DCLRE1A):c.818T>C (p.Val273Ala)not specified [RCV004362266]uncertain significance10113850287113850287Humanname
405691286CV3243281single nucleotide variantNM_014881.5(DCLRE1A):c.305G>A (p.Cys102Tyr)not specified [RCV004373363]uncertain significance10113852878113852878Humanname
405691293CV3243282single nucleotide variantNM_014881.5(DCLRE1A):c.350T>G (p.Val117Gly)not specified [RCV004373364]uncertain significance10113852833113852833Humanname
405691299CV3243283single nucleotide variantNM_014881.5(DCLRE1A):c.514T>C (p.Tyr172His)not specified [RCV004373365]uncertain significance10113850591113850591Humanname
405691309CV3243285single nucleotide variantNM_014881.5(DCLRE1A):c.578C>T (p.Ala193Val)not specified [RCV004373367]uncertain significance10113850527113850527Humanname
405691315CV3243286single nucleotide variantNM_014881.5(DCLRE1A):c.704T>A (p.Phe235Tyr)not specified [RCV004373368]uncertain significance10113850401113850401Humanname
405691321CV3243287single nucleotide variantNM_014881.5(DCLRE1A):c.812T>C (p.Val271Ala)not specified [RCV004373369]uncertain significance10113850293113850293Humanname
407458150CV3430328single nucleotide variantNM_014881.5(DCLRE1A):c.415T>A (p.Trp139Arg)not specified [RCV004611429]uncertain significance10113852768113852768Humanname
407458155CV3430330single nucleotide variantNM_014881.5(DCLRE1A):c.764C>A (p.Ser255Tyr)not specified [RCV004611431]uncertain significance10113850341113850341Humanname
407458158CV3430331single nucleotide variantNM_014881.5(DCLRE1A):c.634A>G (p.Arg212Gly)not specified [RCV004611432]uncertain significance10113850471113850471Humanname
597800952CV3652124single nucleotide variantNM_014881.5(DCLRE1A):c.817G>A (p.Val273Ile)not specified [RCV004905982]uncertain significance10113850288113850288Humanname
597800959CV3652128single nucleotide variantNM_014881.5(DCLRE1A):c.716C>T (p.Pro239Leu)not specified [RCV004905986]uncertain significance10113850389113850389Humanname
597800962CV3652130single nucleotide variantNM_014881.5(DCLRE1A):c.344G>A (p.Arg115His)not specified [RCV004905988]uncertain significance10113852839113852839Humanname
597800988CV3652144single nucleotide variantNM_014881.5(DCLRE1A):c.389C>T (p.Ser130Phe)not specified [RCV004906002]uncertain significance10113852794113852794Humanname
598262418CV3963718single nucleotide variantNM_014881.5(DCLRE1A):c.448C>T (p.Arg150Cys)not specified [RCV005325379]uncertain significance10113852735113852735Humanname
156322640CV2205171single nucleotide variantNM_014881.5(DCLRE1A):c.1286A>G (p.Lys429Arg)not specified [RCV004077766]uncertain significance10113849819113849819Humanname
155980345CV2223019single nucleotide variantNM_014881.5(DCLRE1A):c.1008A>T (p.Glu336Asp)not specified [RCV004103604]uncertain significance10113850097113850097Humanname
155977961CV2246961single nucleotide variantNM_014881.5(DCLRE1A):c.2261T>C (p.Ile754Thr)not specified [RCV004112751]uncertain significance10113845802113845802Humanname
155987714CV2259494single nucleotide variantNM_014881.5(DCLRE1A):c.1440A>C (p.Gln480His)not specified [RCV004122694]likely benign10113849665113849665Humanname
156075874CV2281549single nucleotide variantNM_014881.5(DCLRE1A):c.2146G>A (p.Ala716Thr)not specified [RCV004153859]uncertain significance10113847315113847315Humanname
156164697CV2315111single nucleotide variantNM_014881.5(DCLRE1A):c.1306C>T (p.His436Tyr)not specified [RCV004165293]uncertain significance10113849799113849799Humanname
156354455CV2324279single nucleotide variantNM_014881.5(DCLRE1A):c.1547G>C (p.Gly516Ala)not specified [RCV004177007]uncertain significance10113849558113849558Humanname
156167019CV2345246single nucleotide variantNM_014881.5(DCLRE1A):c.2249A>T (p.Tyr750Phe)not specified [RCV004195984]uncertain significance10113847212113847212Humanname
155983136CV2371233single nucleotide variantNM_014881.5(DCLRE1A):c.1395G>A (p.Met465Ile)not specified [RCV004220971]uncertain significance10113849710113849710Humanname
155937515CV2373650single nucleotide variantNM_014881.5(DCLRE1A):c.2740C>T (p.Pro914Ser)not specified [RCV004222738]uncertain significance10113841486113841486Humanname
156210363CV2378129single nucleotide variantNM_014881.5(DCLRE1A):c.2918T>C (p.Ile973Thr)not specified [RCV004233046]uncertain significance10113837106113837106Humanname
156110196CV2387607single nucleotide variantNM_014881.5(DCLRE1A):c.2419G>T (p.Gly807Cys)not specified [RCV004234158]uncertain significance10113844204113844204Humanname
156191427CV2388470single nucleotide variantNM_014881.5(DCLRE1A):c.1712A>G (p.Glu571Gly)not specified [RCV004237327]uncertain significance10113849393113849393Humanname
329374887CV2440104single nucleotide variantNM_014881.5(DCLRE1A):c.2455G>T (p.Asp819Tyr)not specified [RCV004260568]uncertain significance10113844168113844168Humanname
329391167CV2447841single nucleotide variantNM_014881.5(DCLRE1A):c.2612A>G (p.His871Arg)not specified [RCV004258614]likely benign10113842396113842396Humanname
329389023CV2448594single nucleotide variantNM_014881.5(DCLRE1A):c.1533G>C (p.Glu511Asp)not specified [RCV004259269]likely benign10113849572113849572Humanname
329382354CV2465157single nucleotide variantNM_014881.5(DCLRE1A):c.1555A>G (p.Thr519Ala)not specified [RCV004287206]uncertain significance10113849550113849550Humanname
401761080CV2689017single nucleotide variantNM_014881.5(DCLRE1A):c.1651A>G (p.Thr551Ala)not specified [RCV004305796]uncertain significance10113849454113849454Humanname
401746003CV2734328single nucleotide variantNM_014881.5(DCLRE1A):c.2581A>G (p.Thr861Ala)not specified [RCV004332530]uncertain significance10113842427113842427Humanname
401874421CV2759203single nucleotide variantNM_014881.5(DCLRE1A):c.1595C>T (p.Pro532Leu)not specified [RCV004342490]uncertain significance10113849510113849510Humanname
401891423CV2769173single nucleotide variantNM_014881.5(DCLRE1A):c.2800A>G (p.Met934Val)not specified [RCV004349016]uncertain significance10113841426113841426Humanname
401865801CV2779102single nucleotide variantNM_014881.5(DCLRE1A):c.2152C>G (p.Gln718Glu)not specified [RCV004348731]uncertain significance10113847309113847309Humanname
401898438CV2787912single nucleotide variantNM_014881.5(DCLRE1A):c.1924A>G (p.Asn642Asp)not specified [RCV004358587]likely benign10113849181113849181Humanname
405691198CV3246778single nucleotide variantNM_014881.5(DCLRE1A):c.1189C>T (p.Pro397Ser)not specified [RCV004373348]uncertain significance10113849916113849916Humanname
405691211CV3246780single nucleotide variantNM_014881.5(DCLRE1A):c.1660A>T (p.Met554Leu)not specified [RCV004373350]uncertain significance10113849445113849445Humanname
405691216CV3246781single nucleotide variantNM_014881.5(DCLRE1A):c.1682T>G (p.Val561Gly)not specified [RCV004373351]uncertain significance10113849423113849423Humanname
405691230CV3246783single nucleotide variantNM_014881.5(DCLRE1A):c.1844G>A (p.Ser615Asn)not specified [RCV004373353]uncertain significance10113849261113849261Humanname
405691236CV3246784single nucleotide variantNM_014881.5(DCLRE1A):c.2111A>G (p.Tyr704Cys)not specified [RCV004373354]uncertain significance10113848994113848994Humanname
405691240CV3246785single nucleotide variantNM_014881.5(DCLRE1A):c.2161G>A (p.Val721Met)not specified [RCV004373355]likely benign10113847300113847300Humanname
405691245CV3246786single nucleotide variantNM_014881.5(DCLRE1A):c.2581A>C (p.Thr861Pro)not specified [RCV004373356]uncertain significance10113842427113842427Humanname
405691251CV3246787single nucleotide variantNM_014881.5(DCLRE1A):c.2669T>C (p.Ile890Thr)not specified [RCV004373357]uncertain significance10113841557113841557Humanname
405691255CV3246788single nucleotide variantNM_014881.5(DCLRE1A):c.2710A>C (p.Lys904Gln)not specified [RCV004373358]uncertain significance10113841516113841516Humanname
405691267CV3246790single nucleotide variantNM_014881.5(DCLRE1A):c.2972A>G (p.Tyr991Cys)not specified [RCV004373360]uncertain significance10113835303113835303Humanname
407458148CV3430327single nucleotide variantNM_014881.5(DCLRE1A):c.1102C>T (p.Arg368Trp)not specified [RCV004611428]uncertain significance10113850003113850003Humanname
407458154CV3430329single nucleotide variantNM_014881.5(DCLRE1A):c.2569T>C (p.Phe857Leu)not specified [RCV004611430]uncertain significance10113842439113842439Humanname
597800950CV3652123single nucleotide variantNM_014881.5(DCLRE1A):c.1727G>A (p.Gly576Glu)not specified [RCV004905981]likely benign10113849378113849378Humanname
597800953CV3652125single nucleotide variantNM_014881.5(DCLRE1A):c.1629G>T (p.Lys543Asn)not specified [RCV004905983]uncertain significance10113849476113849476Humanname
597800961CV3652129single nucleotide variantNM_014881.5(DCLRE1A):c.2939C>T (p.Thr980Ile)not specified [RCV004905987]uncertain significance10113837085113837085Humanname
597800966CV3652132single nucleotide variantNM_014881.5(DCLRE1A):c.1898G>A (p.Arg633His)not specified [RCV004905990]likely benign10113849207113849207Humanname
597800968CV3652133single nucleotide variantNM_014881.5(DCLRE1A):c.1125G>T (p.Leu375Phe)not specified [RCV004905991]uncertain significance10113849980113849980Humanname
597800972CV3652135single nucleotide variantNM_014881.5(DCLRE1A):c.2923G>C (p.Asp975His)not specified [RCV004905993]uncertain significance10113837101113837101Humanname
597800973CV3652136single nucleotide variantNM_014881.5(DCLRE1A):c.1486G>C (p.Ala496Pro)not specified [RCV004905994]uncertain significance10113849619113849619Humanname
597800975CV3652137single nucleotide variantNM_014881.5(DCLRE1A):c.2738T>C (p.Ile913Thr)not specified [RCV004905995]uncertain significance10113841488113841488Humanname
597800977CV3652138single nucleotide variantNM_014881.5(DCLRE1A):c.1662G>T (p.Met554Ile)not specified [RCV004905996]uncertain significance10113849443113849443Humanname
597800979CV3652139single nucleotide variantNM_014881.5(DCLRE1A):c.2279A>G (p.Lys760Arg)not specified [RCV004905997]uncertain significance10113845784113845784Humanname
597800981CV3652140single nucleotide variantNM_014881.5(DCLRE1A):c.2884A>G (p.Thr962Ala)not specified [RCV004905998]uncertain significance10113837140113837140Humanname
597801101CV3652143single nucleotide variantNM_014881.5(DCLRE1A):c.2026G>A (p.Ala676Thr)not specified [RCV004906001]uncertain significance10113849079113849079Humanname
597800990CV3652145single nucleotide variantNM_014881.5(DCLRE1A):c.1652C>T (p.Thr551Ile)not specified [RCV004906003]uncertain significance10113849453113849453Humanname
598262380CV3963710single nucleotide variantNM_014881.5(DCLRE1A):c.1928C>T (p.Ser643Leu)not specified [RCV005325371]uncertain significance10113849177113849177Humanname
598262392CV3963713single nucleotide variantNM_014881.5(DCLRE1A):c.1781A>G (p.Lys594Arg)not specified [RCV005325374]uncertain significance10113849324113849324Humanname
598262398CV3963714single nucleotide variantNM_014881.5(DCLRE1A):c.2881C>T (p.Pro961Ser)not specified [RCV005325375]uncertain significance10113837143113837143Humanname
598262403CV3963715single nucleotide variantNM_014881.5(DCLRE1A):c.1646C>T (p.Pro549Leu)not specified [RCV005325376]uncertain significance10113849459113849459Humanname
598262407CV3963716single nucleotide variantNM_014881.5(DCLRE1A):c.1040G>A (p.Arg347Gln)not specified [RCV005325377]likely benign10113850065113850065Humanname
598262413CV3963717single nucleotide variantNM_014881.5(DCLRE1A):c.1597A>G (p.Lys533Glu)not specified [RCV005325378]uncertain significance10113849508113849508Humanname
405692710CV3243280single nucleotide variantNM_014881.5(DCLRE1A):c.3005G>A (p.Arg1002His)not specified [RCV004373362]uncertain significance10113835270113835270Humanname
405691271CV3246791single nucleotide variantNM_014881.5(DCLRE1A):c.3004C>T (p.Arg1002Cys)not specified [RCV004373361]uncertain significance10113835271113835271Humanname
597800957CV3652127single nucleotide variantNM_014881.5(DCLRE1A):c.3079A>G (p.Met1027Val)not specified [RCV004905985]uncertain significance10113835196113835196Humanname
8626778CV81922single nucleotide variantNM_001271816.1(DCLRE1A):c.1196A>T (p.Asp399Val)Malignant melanoma [RCV000062001]not provided10113849909113849909Humanname