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104 records found for search term Wdr27
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405189525CV2968441deletionNM_182552.5(WDR27):c.2524-7_2524-4delnot provided [RCV003677074]benign6169572544169572547Humanname
598257405CV3937033single nucleotide variantNM_182552.5(WDR27):c.19A>G (p.Ile7Val)not specified [RCV005299816]uncertain significance6169688987169688987Humanname
401777312CV2707872single nucleotide variantNM_182552.5(WDR27):c.54A>G (p.Ile18Met)not specified [RCV004309148]uncertain significance6169688952169688952Humanname
156215917CV2257618single nucleotide variantNM_182552.5(WDR27):c.289A>G (p.Ile97Val)not specified [RCV004127443]uncertain significance6169672297169672297Humanname
156254880CV2325689single nucleotide variantNM_182552.5(WDR27):c.271G>A (p.Ala91Thr)not specified [RCV004180093]uncertain significance6169672315169672315Humanname
156216483CV2348011single nucleotide variantNM_182552.5(WDR27):c.104A>T (p.Gln35Leu)not specified [RCV004197694]uncertain significance6169688902169688902Humanname
405802365CV3349211single nucleotide variantNM_182552.5(WDR27):c.178C>T (p.Pro60Ser)not specified [RCV004478286]uncertain significance6169688828169688828Humanname
597739079CV3633519single nucleotide variantNM_182552.5(WDR27):c.283T>C (p.Tyr95His)not specified [RCV004890248]uncertain significance6169672303169672303Humanname
598257394CV3937030single nucleotide variantNM_182552.5(WDR27):c.2656C>T (p.Leu886=)not specified [RCV005299814]likely benign6169457624169457624Humanname
598219567CV3937032single nucleotide variantNM_182552.5(WDR27):c.1482T>C (p.His494=)not specified [RCV005293337]likely benign6169649275169649275Humanname
155926730CV2208280single nucleotide variantNM_182552.5(WDR27):c.629T>G (p.Leu210Arg)not specified [RCV004088723]uncertain significance6169668013169668013Humanname
156116501CV2221720single nucleotide variantNM_182552.5(WDR27):c.911G>A (p.Ser304Asn)not specified [RCV004098480]uncertain significance6169662418169662418Humanname
155931013CV2297178single nucleotide variantNM_182552.5(WDR27):c.935T>C (p.Leu312Pro)not specified [RCV004151069]uncertain significance6169662394169662394Humanname
156259952CV2322267single nucleotide variantNM_182552.5(WDR27):c.509A>G (p.Lys170Arg)not specified [RCV004176035]uncertain significance6169668133169668133Humanname
156344683CV2364317single nucleotide variantNM_182552.5(WDR27):c.820C>T (p.Arg274Cys)not specified [RCV004223539]uncertain significance6169664250169664250Humanname
156100986CV2386760single nucleotide variantNM_182552.5(WDR27):c.560G>T (p.Arg187Leu)not specified [RCV004233429]likely benign6169668082169668082Humanname
155908934CV2387472single nucleotide variantNM_182552.5(WDR27):c.821G>A (p.Arg274His)not specified [RCV004240335]uncertain significance6169664249169664249Humanname
155996545CV2393197single nucleotide variantNM_182552.5(WDR27):c.461G>A (p.Arg154Gln)not specified [RCV004226672]uncertain significance6169668181169668181Humanname
329395355CV2458294single nucleotide variantNM_182552.5(WDR27):c.883T>A (p.Ser295Thr)not specified [RCV004265941]uncertain significance6169664187169664187Humanname
329388230CV2468799single nucleotide variantNM_182552.5(WDR27):c.425C>A (p.Ala142Asp)not specified [RCV004280115]uncertain significance6169670600169670600Humanname
401737866CV2703679single nucleotide variantNM_182552.5(WDR27):c.866C>T (p.Ser289Phe)not specified [RCV004315930]likely benign6169664204169664204Humanname
401877937CV2757706single nucleotide variantNM_182552.5(WDR27):c.766G>A (p.Gly256Arg)not specified [RCV004336860]uncertain significance6169665503169665503Humanname
401867401CV2792537single nucleotide variantNM_182552.5(WDR27):c.349A>G (p.Thr117Ala)not specified [RCV004363577]uncertain significance6169670676169670676Humanname
405802388CV3349222single nucleotide variantNM_182552.5(WDR27):c.587C>T (p.Pro196Leu)not specified [RCV004478297]uncertain significance6169668055169668055Humanname
405802390CV3349223single nucleotide variantNM_182552.5(WDR27):c.833G>A (p.Arg278Gln)not specified [RCV004478298]uncertain significance6169664237169664237Humanname
407523797CV3489732single nucleotide variantNM_182552.5(WDR27):c.824G>A (p.Arg275His)not specified [RCV004678187]uncertain significance6169664246169664246Humanname
407523800CV3489733single nucleotide variantNM_182552.5(WDR27):c.314G>A (p.Arg105Lys)not specified [RCV004678188]uncertain significance6169672272169672272Humanname
407523820CV3489740single nucleotide variantNM_182552.5(WDR27):c.737T>A (p.Ile246Asn)not specified [RCV004678195]uncertain significance6169665532169665532Humanname
597739090CV3633525single nucleotide variantNM_182552.5(WDR27):c.502C>T (p.Arg168Cys)not specified [RCV004890250]uncertain significance6169668140169668140Humanname
598257416CV3937035single nucleotide variantNM_182552.5(WDR27):c.691T>G (p.Tyr231Asp)not specified [RCV005299818]uncertain significance6169667157169667157Humanname
598219573CV3937036single nucleotide variantNM_182552.5(WDR27):c.694A>C (p.Ser232Arg)not specified [RCV005293338]uncertain significance6169667154169667154Humanname
156365225CV2193154single nucleotide variantNM_182552.5(WDR27):c.1474G>C (p.Ala492Pro)not specified [RCV004071152]uncertain significance6169651937169651937Humanname
156398824CV2194807single nucleotide variantNM_182552.5(WDR27):c.1217C>T (p.Ser406Phe)not specified [RCV004075349]uncertain significance6169659188169659188Humanname
156036690CV2218416single nucleotide variantNM_182552.5(WDR27):c.2521C>A (p.Gln841Lys)not specified [RCV004090707]uncertain significance6169582838169582838Humanname
156193033CV2223232single nucleotide variantNM_182552.5(WDR27):c.1181G>A (p.Arg394His)not specified [RCV004104064]uncertain significance6169659467169659467Humanname
156160663CV2236373single nucleotide variantNM_182552.5(WDR27):c.1045C>G (p.Arg349Gly)not specified [RCV004108053]uncertain significance6169660747169660747Humanname
156051285CV2237973single nucleotide variantNM_182552.5(WDR27):c.1228G>A (p.Gly410Arg)not specified [RCV004111011]uncertain significance6169659177169659177Humanname
156274909CV2255600single nucleotide variantNM_182552.5(WDR27):c.1070T>G (p.Val357Gly)not specified [RCV004120015]uncertain significance6169660722169660722Humanname
156046137CV2268658single nucleotide variantNM_182552.5(WDR27):c.2437G>C (p.Glu813Gln)not specified [RCV004124063]uncertain significance6169582922169582922Humanname
156200269CV2290449single nucleotide variantNM_182552.5(WDR27):c.1262C>T (p.Ala421Val)not specified [RCV004155156]uncertain significance6169659143169659143Humanname
156294500CV2306420single nucleotide variantNM_182552.5(WDR27):c.1178A>G (p.Asn393Ser)not specified [RCV004156766]likely benign6169659470169659470Humanname
156194778CV2322186single nucleotide variantNM_182552.5(WDR27):c.1429C>T (p.Arg477Cys)not specified [RCV004175964]uncertain significance6169651982169651982Humanname
156273165CV2333995single nucleotide variantNM_182552.5(WDR27):c.1964T>G (p.Leu655Arg)not specified [RCV004183523]uncertain significance6169636410169636410Humanname
156181145CV2338100single nucleotide variantNM_182552.5(WDR27):c.2195G>A (p.Arg732Gln)not specified [RCV004184135]uncertain significance6169632975169632975Humanname
156045870CV2340211single nucleotide variantNM_182552.5(WDR27):c.2398G>A (p.Ala800Thr)not specified [RCV004192444]uncertain significance6169602245169602245Humanname
156062162CV2351385single nucleotide variantNM_182552.5(WDR27):c.1222T>C (p.Phe408Leu)not specified [RCV004193077]uncertain significance6169659183169659183Humanname
156098412CV2370774single nucleotide variantNM_182552.5(WDR27):c.1048T>C (p.Cys350Arg)not specified [RCV004209171]uncertain significance6169660744169660744Humanname
155994877CV2379603single nucleotide variantNM_182552.5(WDR27):c.1976T>C (p.Ile659Thr)not specified [RCV004217302]uncertain significance6169636398169636398Humanname
156041131CV2384413single nucleotide variantNM_182552.5(WDR27):c.1261G>A (p.Ala421Thr)not specified [RCV004229831]uncertain significance6169659144169659144Humanname
155960153CV2390640single nucleotide variantNM_182552.5(WDR27):c.2420G>A (p.Arg807Lys)not specified [RCV004239161]uncertain significance6169602223169602223Humanname
155961211CV2390843single nucleotide variantNM_182552.5(WDR27):c.2476C>T (p.His826Tyr)not specified [RCV004241116]uncertain significance6169582883169582883Humanname
156202653CV2392592single nucleotide variantNM_182552.5(WDR27):c.1379A>G (p.Lys460Arg)not specified [RCV004245453]uncertain significance6169658299169658299Humanname
156249218CV2394068single nucleotide variantNM_182552.5(WDR27):c.2044T>C (p.Ser682Pro)not specified [RCV004236284]likely benign6169634485169634485Humanname
156148194CV2394472single nucleotide variantNM_182552.5(WDR27):c.1946G>T (p.Gly649Val)not specified [RCV004240837]uncertain significance6169636428169636428Humanname
329374290CV2434764single nucleotide variantNM_182552.5(WDR27):c.1755C>A (p.Asp585Glu)not specified [RCV004248465]uncertain significance6169638653169638653Humanname
329392033CV2445166single nucleotide variantNM_182552.5(WDR27):c.1348T>C (p.Tyr450His)not specified [RCV004263806]uncertain significance6169658330169658330Humanname
329382541CV2449104single nucleotide variantNM_182552.5(WDR27):c.1858G>A (p.Ala620Thr)not specified [RCV004264166]uncertain significance6169638550169638550Humanname
401747102CV2679007single nucleotide variantNM_182552.5(WDR27):c.1801C>G (p.Leu601Val)not specified [RCV004295018]uncertain significance6169638607169638607Humanname
401765725CV2683402single nucleotide variantNM_182552.5(WDR27):c.2374G>A (p.Ala792Thr)not specified [RCV004288171]uncertain significance6169602269169602269Humanname
401758656CV2694211single nucleotide variantNM_182552.5(WDR27):c.2383C>T (p.Pro795Ser)not specified [RCV004302630]uncertain significance6169602260169602260Humanname
401759520CV2701594single nucleotide variantNM_182552.5(WDR27):c.2194C>T (p.Arg732Trp)not specified [RCV004314019]uncertain significance6169632976169632976Humanname
401770005CV2718989single nucleotide variantNM_182552.5(WDR27):c.1368G>C (p.Glu456Asp)not specified [RCV004322579]uncertain significance6169658310169658310Humanname
401883977CV2761199single nucleotide variantNM_182552.5(WDR27):c.2087A>G (p.Asn696Ser)not specified [RCV004341082]uncertain significance6169634442169634442Humanname
401873207CV2779749single nucleotide variantNM_182552.5(WDR27):c.2065A>G (p.Met689Val)not specified [RCV004353388]likely benign6169634464169634464Humanname
401885409CV2783287single nucleotide variantNM_182552.5(WDR27):c.2150T>C (p.Leu717Pro)not specified [RCV004363895]uncertain significance6169633020169633020Humanname
405802353CV3349205single nucleotide variantNM_182552.5(WDR27):c.1036G>A (p.Glu346Lys)not specified [RCV004478280]uncertain significance6169660756169660756Humanname
405802355CV3349206single nucleotide variantNM_182552.5(WDR27):c.1240G>A (p.Val414Met)not specified [RCV004478281]uncertain significance6169659165169659165Humanname
405802357CV3349207single nucleotide variantNM_182552.5(WDR27):c.1241T>C (p.Val414Ala)not specified [RCV004478282]uncertain significance6169659164169659164Humanname
405802359CV3349208single nucleotide variantNM_182552.5(WDR27):c.1414G>A (p.Val472Ile)not specified [RCV004478283]uncertain significance6169651997169651997Humanname
405802361CV3349209single nucleotide variantNM_182552.5(WDR27):c.1444A>G (p.Ser482Gly)not specified [RCV004478284]uncertain significance6169651967169651967Humanname
405802363CV3349210single nucleotide variantNM_182552.5(WDR27):c.1503G>T (p.Lys501Asn)not specified [RCV004478285]uncertain significance6169649254169649254Humanname
405802367CV3349212single nucleotide variantNM_182552.5(WDR27):c.1858G>T (p.Ala620Ser)not specified [RCV004478287]uncertain significance6169638550169638550Humanname
405802369CV3349213single nucleotide variantNM_182552.5(WDR27):c.1929T>A (p.Phe643Leu)not specified [RCV004478288]uncertain significance6169636445169636445Humanname
405802374CV3349215single nucleotide variantNM_182552.5(WDR27):c.2153A>G (p.Asn718Ser)not specified [RCV004478290]uncertain significance6169633017169633017Humanname
405802376CV3349216single nucleotide variantNM_182552.5(WDR27):c.2158G>A (p.Gly720Ser)not specified [RCV004478291]uncertain significance6169633012169633012Humanname
405802378CV3349217single nucleotide variantNM_182552.5(WDR27):c.2158G>T (p.Gly720Cys)not specified [RCV004478292]uncertain significance6169633012169633012Humanname
405802380CV3349218single nucleotide variantNM_182552.5(WDR27):c.2225G>T (p.Gly742Val)not specified [RCV004478293]uncertain significance6169613655169613655Humanname
405802382CV3349219single nucleotide variantNM_182552.5(WDR27):c.2326G>C (p.Glu776Gln)not specified [RCV004478294]uncertain significance6169602317169602317Humanname
405802384CV3349220single nucleotide variantNM_182552.5(WDR27):c.2330G>A (p.Arg777His)not specified [RCV004478295]uncertain significance6169602313169602313Humanname
405802386CV3349221single nucleotide variantNM_182552.5(WDR27):c.2348C>T (p.Pro783Leu)not specified [RCV004478296]uncertain significance6169602295169602295Humanname
407523803CV3489734single nucleotide variantNM_182552.5(WDR27):c.2123G>A (p.Arg708Gln)not specified [RCV004678189]uncertain significance6169633047169633047Humanname
407523806CV3489735single nucleotide variantNM_182552.5(WDR27):c.1558C>T (p.Arg520Trp)not specified [RCV004678190]likely benign6169649199169649199Humanname
407523808CV3489736single nucleotide variantNM_182552.5(WDR27):c.2056G>A (p.Ala686Thr)not specified [RCV004678191]uncertain significance6169634473169634473Humanname
407523811CV3489737single nucleotide variantNM_182552.5(WDR27):c.2189A>G (p.His730Arg)not specified [RCV004678192]uncertain significance6169632981169632981Humanname
407523814CV3489738single nucleotide variantNM_182552.5(WDR27):c.1046G>A (p.Arg349Gln)not specified [RCV004678193]likely benign6169660746169660746Humanname
407523817CV3489739single nucleotide variantNM_182552.5(WDR27):c.1261G>T (p.Ala421Ser)not specified [RCV004678194]uncertain significance6169659144169659144Humanname
407523823CV3489741single nucleotide variantNM_182552.5(WDR27):c.2438A>G (p.Glu813Gly)not specified [RCV004678196]uncertain significance6169582921169582921Humanname
407465273CV3489742single nucleotide variantNM_182552.5(WDR27):c.1932A>G (p.Ile644Met)not specified [RCV004688725]uncertain significance6169636442169636442Humanname
407523827CV3489743single nucleotide variantNM_182552.5(WDR27):c.1986C>G (p.Cys662Trp)not specified [RCV004678197]uncertain significance6169636388169636388Humanname
407523830CV3489744single nucleotide variantNM_182552.5(WDR27):c.1813C>T (p.Arg605Trp)not specified [RCV004678198]uncertain significance6169638595169638595Humanname
597691100CV3633515single nucleotide variantNM_182552.5(WDR27):c.2182G>C (p.Glu728Gln)not specified [RCV004884633]uncertain significance6169632988169632988Humanname
597691114CV3633516single nucleotide variantNM_182552.5(WDR27):c.2078C>T (p.Ser693Leu)not specified [RCV004884634]uncertain significance6169634451169634451Humanname
597739070CV3633517single nucleotide variantNM_182552.5(WDR27):c.1894A>G (p.Ile632Val)not specified [RCV004890246]likely benign6169636480169636480Humanname
597739075CV3633518single nucleotide variantNM_182552.5(WDR27):c.1903G>A (p.Ala635Thr)not specified [RCV004890247]uncertain significance6169636471169636471Humanname
597739085CV3633520single nucleotide variantNM_182552.5(WDR27):c.2365T>A (p.Cys789Ser)not specified [RCV004890249]uncertain significance6169602278169602278Humanname
597691125CV3633521single nucleotide variantNM_182552.5(WDR27):c.2048C>G (p.Thr683Arg)not specified [RCV004884635]uncertain significance6169634481169634481Humanname
597691136CV3633522single nucleotide variantNM_182552.5(WDR27):c.2486C>G (p.Thr829Ser)not specified [RCV004884636]uncertain significance6169582873169582873Humanname
597691145CV3633523single nucleotide variantNM_182552.5(WDR27):c.1744T>C (p.Ser582Pro)not specified [RCV004884637]uncertain significance6169643700169643700Humanname
597691156CV3633524single nucleotide variantNM_182552.5(WDR27):c.1907A>G (p.Gln636Arg)not specified [RCV004884638]uncertain significance6169636467169636467Humanname
597739095CV3633526single nucleotide variantNM_182552.5(WDR27):c.1000C>T (p.Leu334Phe)not specified [RCV004890251]uncertain significance6169662329169662329Humanname
598257399CV3937031single nucleotide variantNM_182552.5(WDR27):c.2516C>T (p.Ala839Val)not specified [RCV005299815]uncertain significance6169582843169582843Humanname
598257411CV3937034single nucleotide variantNM_182552.5(WDR27):c.2081C>T (p.Ala694Val)not specified [RCV005299817]uncertain significance6169634448169634448Humanname
598219581CV3937038single nucleotide variantNM_182552.5(WDR27):c.1326T>G (p.Cys442Trp)not specified [RCV005293339]uncertain significance6169658352169658352Humanname
15157961CV699457single nucleotide variantNM_182552.5(WDR27):c.2533C>T (p.Arg845Cys)not provided [RCV000946983]benign6169572531169572531Humanname