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59 records found for search term Vwc2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8590859CV125568single nucleotide variantNM_198570.3(VWC2):c.697-1663C>TLung cancer [RCV000106087]uncertain significance74980104849801048Humanname
8590860CV125569single nucleotide variantNM_198570.3(VWC2):c.826+33511G>TLung cancer [RCV000106088]uncertain significance74983635149836351Humanname
405664805CV3338718single nucleotide variantNM_198570.5(VWC2):c.26T>G (p.Val9Gly)not specified [RCV004485248]uncertain significance74977546149775461Humanname
407450818CV3491650single nucleotide variantNM_198570.5(VWC2):c.41G>A (p.Ser14Asn)not specified [RCV004683436]uncertain significance74977547649775476Humanname
597688635CV3623536single nucleotide variantNM_198570.5(VWC2):c.38C>G (p.Ser13Cys)not specified [RCV004884412]uncertain significance74977547349775473Humanname
156138500CV2236700single nucleotide variantNM_198570.5(VWC2):c.150C>A (p.His50Gln)not specified [RCV004110655]uncertain significance74977558549775585Humanname
155945863CV2238041single nucleotide variantNM_198570.5(VWC2):c.197C>A (p.Ala66Glu)not specified [RCV004111068]uncertain significance74977563249775632Humanname
156244486CV2243115single nucleotide variantNM_198570.5(VWC2):c.205G>C (p.Glu69Gln)not specified [RCV004110024]uncertain significance74977564049775640Humanname
329392067CV2445281single nucleotide variantNM_198570.5(VWC2):c.218G>C (p.Gly73Ala)not specified [RCV004263909]uncertain significance74977565349775653Humanname
401877544CV2769493single nucleotide variantNM_198570.5(VWC2):c.273C>A (p.Ser91Arg)not specified [RCV004357465]uncertain significance74977570849775708Humanname
405664798CV3338717single nucleotide variantNM_198570.5(VWC2):c.163G>T (p.Gly55Cys)not specified [RCV004485247]uncertain significance74977559849775598Humanname
407450805CV3491645single nucleotide variantNM_198570.5(VWC2):c.205G>A (p.Glu69Lys)not specified [RCV004683431]uncertain significance74977564049775640Humanname
407450815CV3491649single nucleotide variantNM_198570.5(VWC2):c.167C>A (p.Pro56Gln)not specified [RCV004683435]uncertain significance74977560249775602Humanname
597700252CV3623538single nucleotide variantNM_198570.5(VWC2):c.217G>A (p.Gly73Ser)not specified [RCV004885591]uncertain significance74977565249775652Humanname
597700260CV3623539single nucleotide variantNM_198570.5(VWC2):c.194C>A (p.Pro65Gln)not specified [RCV004885592]uncertain significance74977562949775629Humanname
597688643CV3623540single nucleotide variantNM_198570.5(VWC2):c.109G>T (p.Ala37Ser)not specified [RCV004884413]uncertain significance74977554449775544Humanname
597700267CV3623541single nucleotide variantNM_198570.5(VWC2):c.250C>A (p.Leu84Ile)not specified [RCV004885593]uncertain significance74977568549775685Humanname
597700277CV3623542single nucleotide variantNM_198570.5(VWC2):c.295T>G (p.Ser99Ala)not specified [RCV004885594]likely benign74977573049775730Humanname
597700284CV3623543single nucleotide variantNM_198570.5(VWC2):c.296C>A (p.Ser99Tyr)not specified [RCV004885595]uncertain significance74977573149775731Humanname
598256517CV3936699single nucleotide variantNM_198570.5(VWC2):c.214A>C (p.Ser72Arg)not specified [RCV005299639]uncertain significance74977564949775649Humanname
155925308CV2211802single nucleotide variantNM_198570.5(VWC2):c.319G>A (p.Gly107Arg)not specified [RCV004086635]uncertain significance74977575449775754Humanname
156150199CV2318628single nucleotide variantNM_198570.5(VWC2):c.595T>A (p.Cys199Ser)not specified [RCV004173527]uncertain significance74977603049776030Humanname
155917879CV2332899single nucleotide variantNM_198570.5(VWC2):c.383A>G (p.Gln128Arg)not specified [RCV004192158]uncertain significance74977581849775818Humanname
156000859CV2378748single nucleotide variantNM_198570.5(VWC2):c.938G>A (p.Arg313Gln)not specified [RCV004231203]uncertain significance74991214549912145Humanname
155932347CV2400005single nucleotide variantNM_198570.5(VWC2):c.350C>T (p.Thr117Ile)not specified [RCV004246929]uncertain significance74977578549775785Humanname
329354144CV2447189single nucleotide variantNM_198570.5(VWC2):c.665G>A (p.Gly222Asp)not specified [RCV004262492]uncertain significance74977610049776100Humanname
329362892CV2464822single nucleotide variantNM_198570.5(VWC2):c.691T>C (p.Phe231Leu)not specified [RCV004284771]uncertain significance74977612649776126Humanname
329394020CV2472273single nucleotide variantNM_198570.5(VWC2):c.578C>A (p.Pro193Gln)not specified [RCV004283378]uncertain significance74977601349776013Humanname
401779330CV2680243single nucleotide variantNM_198570.5(VWC2):c.680C>T (p.Thr227Ile)not specified [RCV004286715]uncertain significance74977611549776115Humanname
401884715CV2761839single nucleotide variantNM_198570.5(VWC2):c.850G>A (p.Ala284Thr)not specified [RCV004339482]uncertain significance74991205749912057Humanname
405664809CV3338719single nucleotide variantNM_198570.5(VWC2):c.310G>A (p.Ala104Thr)not specified [RCV004485249]uncertain significance74977574549775745Humanname
405664814CV3338720single nucleotide variantNM_198570.5(VWC2):c.410C>G (p.Pro137Arg)not specified [RCV004485250]uncertain significance74977584549775845Humanname
405664819CV3338721single nucleotide variantNM_198570.5(VWC2):c.619T>G (p.Cys207Gly)not specified [RCV004485251]uncertain significance74977605449776054Humanname
405664824CV3338722single nucleotide variantNM_198570.5(VWC2):c.656A>G (p.Glu219Gly)not specified [RCV004485252]uncertain significance74977609149776091Humanname
405664827CV3338723single nucleotide variantNM_198570.5(VWC2):c.697G>A (p.Val233Met)not specified [RCV004485253]uncertain significance74980271149802711Humanname
407450807CV3491646single nucleotide variantNM_198570.5(VWC2):c.305G>T (p.Gly102Val)not specified [RCV004683432]uncertain significance74977574049775740Humanname
407450810CV3491647single nucleotide variantNM_198570.5(VWC2):c.386A>T (p.Asp129Val)not specified [RCV004683433]uncertain significance74977582149775821Humanname
597688623CV3623534single nucleotide variantNM_198570.5(VWC2):c.770C>T (p.Thr257Met)not specified [RCV004884411]uncertain significance74980278449802784Humanname
597700232CV3623535single nucleotide variantNM_198570.5(VWC2):c.662G>A (p.Arg221Gln)not specified [RCV004885589]uncertain significance74977609749776097Humanname
597700242CV3623537single nucleotide variantNM_198570.5(VWC2):c.629A>G (p.Gln210Arg)not specified [RCV004885590]uncertain significance74977606449776064Humanname
597688654CV3623544single nucleotide variantNM_198570.5(VWC2):c.427G>A (p.Glu143Lys)not specified [RCV004884414]uncertain significance74977586249775862Humanname
598256513CV3936698single nucleotide variantNM_198570.5(VWC2):c.968G>A (p.Arg323Lys)not specified [RCV005299638]uncertain significance74991217549912175Humanname
598218514CV3936700single nucleotide variantNM_198570.5(VWC2):c.617A>G (p.Gln206Arg)not specified [RCV005293181]uncertain significance74977605249776052Humanname
405664837CV3338725single nucleotide variantNM_001080500.4(VWC2L):c.23C>T (p.Ala8Val)not specified [RCV004485255]uncertain significance2214414216214414216Humanname
401732854CV2691130single nucleotide variantNM_001080500.4(VWC2L):c.59C>T (p.Thr20Ile)not specified [RCV004301125]uncertain significance2214414252214414252Humanname
597700293CV3623545single nucleotide variantNM_001080500.4(VWC2L):c.55G>T (p.Val19Phe)not specified [RCV004885596]uncertain significance2214414248214414248Humanname
8630174CV85321single nucleotide variantNM_001080500.2(VWC2L):c.360G>A (p.Gly120=)Malignant melanoma [RCV000065403]not provided2214414553214414553Humanname
156185829CV2324690single nucleotide variantNM_001080500.4(VWC2L):c.197G>T (p.Arg66Leu)not specified [RCV004172934]uncertain significance2214414390214414390Humanname
329401523CV2461007single nucleotide variantNM_001080500.4(VWC2L):c.119A>G (p.Asn40Ser)not specified [RCV004265162]uncertain significance2214414312214414312Humanname
405664832CV3338724single nucleotide variantNM_001080500.4(VWC2L):c.154G>T (p.Gly52Trp)not specified [RCV004485254]uncertain significance2214414347214414347Humanname
598218522CV3936701single nucleotide variantNM_001080500.4(VWC2L):c.168C>G (p.Asp56Glu)not specified [RCV005293182]uncertain significance2214414361214414361Humanname
156074479CV2365531single nucleotide variantNM_001080500.4(VWC2L):c.563T>C (p.Ile188Thr)not specified [RCV004211647]uncertain significance2214575714214575714Humanname
155996195CV2393154single nucleotide variantNM_001080500.4(VWC2L):c.536C>T (p.Ala179Val)not specified [RCV004226631]uncertain significance2214575687214575687Humanname
329382482CV2465136single nucleotide variantNM_001080500.4(VWC2L):c.662C>G (p.Thr221Ser)not specified [RCV004287190]uncertain significance2214575813214575813Humanname
401862739CV2758879single nucleotide variantNM_001080500.4(VWC2L):c.545C>T (p.Thr182Met)not specified [RCV004339967]uncertain significance2214575696214575696Humanname
405664842CV3338726single nucleotide variantNM_001080500.4(VWC2L):c.482T>C (p.Val161Ala)not specified [RCV004485256]uncertain significance2214436720214436720Humanname
407450822CV3491651single nucleotide variantNM_001080500.4(VWC2L):c.542C>T (p.Thr181Met)not specified [RCV004683437]uncertain significance2214575693214575693Humanname
597688664CV3623546single nucleotide variantNM_001080500.4(VWC2L):c.458C>G (p.Ala153Gly)not specified [RCV004884415]uncertain significance2214436696214436696Humanname
8630175CV85322single nucleotide variantNM_001080500.2(VWC2L):c.382G>A (p.Glu128Lys)Malignant melanoma [RCV000065404]not provided2214414575214414575Humanname