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Variants search result for Homo sapiens
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84 records found for search term Otud7b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15137128CV706667single nucleotide variantNM_020205.4(OTUD7B):c.177G>A (p.Gly59=)not provided [RCV000965564]benign1149971160149971160Humanname
155902253CV2274656single nucleotide variantNM_020205.4(OTUD7B):c.31G>C (p.Asp11His)not specified [RCV004139036]uncertain significance1149977480149977480Humanname
156115240CV2273296single nucleotide variantNM_020205.4(OTUD7B):c.115A>C (p.Ser39Arg)not specified [RCV004132088]uncertain significance1149971222149971222Humanname
155936149CV2380303single nucleotide variantNM_020205.4(OTUD7B):c.230G>A (p.Arg77His)not specified [RCV004224652]uncertain significance1149971107149971107Humanname
401770258CV2711028single nucleotide variantNM_020205.4(OTUD7B):c.216C>G (p.Asp72Glu)not specified [RCV004310727]uncertain significance1149971121149971121Humanname
405785866CV3374582single nucleotide variantNM_020205.4(OTUD7B):c.295A>G (p.Ile99Val)not specified [RCV004504795]uncertain significance1149967501149967501Humanname
597656266CV3567965single nucleotide variantNM_020205.4(OTUD7B):c.232C>T (p.Pro78Ser)not specified [RCV004827496]uncertain significance1149971105149971105Humanname
597691466CV3567967single nucleotide variantNM_020205.4(OTUD7B):c.112C>T (p.Leu38Phe)not specified [RCV004838745]uncertain significance1149971225149971225Humanname
597691538CV3567976single nucleotide variantNM_020205.4(OTUD7B):c.197C>G (p.Pro66Arg)not specified [RCV004838752]uncertain significance1149971140149971140Humanname
598162682CV3995706single nucleotide variantNM_020205.4(OTUD7B):c.1305A>G (p.Pro435=)not specified [RCV005390859]likely benign1149947269149947269Humanname
15182292CV706665single nucleotide variantNM_020205.4(OTUD7B):c.2103G>T (p.Pro701=)not provided [RCV000974596]benign1149944286149944286Humanname
15182296CV706666single nucleotide variantNM_020205.4(OTUD7B):c.1221C>T (p.Asp407=)not provided [RCV000974597]benign1149948986149948986Humanname
8624678CV79792single nucleotide variantNM_020205.3(OTUD7B):c.235C>T (p.Pro79Ser)Malignant melanoma [RCV000059868]not provided1149971102149971102Humanname
155923669CV2217687single nucleotide variantNM_020205.4(OTUD7B):c.506G>A (p.Arg169His)not specified [RCV004083877]uncertain significance1149965875149965875Humanname
156045439CV2268599single nucleotide variantNM_020205.4(OTUD7B):c.836A>G (p.Asn279Ser)not specified [RCV004124013]uncertain significance1149959693149959693Humanname
155963930CV2282787single nucleotide variantNM_020205.4(OTUD7B):c.442C>T (p.Arg148Cys)not specified [RCV004141640]uncertain significance1149967354149967354Humanname
155963051CV2308230single nucleotide variantNM_020205.4(OTUD7B):c.805C>A (p.Pro269Thr)not specified [RCV004164730]uncertain significance1149959724149959724Humanname
156040219CV2384338single nucleotide variantNM_020205.4(OTUD7B):c.338A>G (p.His113Arg)not specified [RCV004227717]uncertain significance1149967458149967458Humanname
155963918CV2395779single nucleotide variantNM_020205.4(OTUD7B):c.398G>A (p.Cys133Tyr)not specified [RCV004235307]uncertain significance1149967398149967398Humanname
401862775CV2779005single nucleotide variantNM_020205.4(OTUD7B):c.476C>G (p.Ser159Cys)not specified [RCV004348658]uncertain significance1149967320149967320Humanname
405785876CV3371026single nucleotide variantNM_020205.4(OTUD7B):c.832G>A (p.Ala278Thr)not specified [RCV004504797]uncertain significance1149959697149959697Humanname
405785881CV3371027single nucleotide variantNM_020205.4(OTUD7B):c.911A>T (p.His304Leu)not specified [RCV004504798]uncertain significance1149950156149950156Humanname
405785871CV3374583single nucleotide variantNM_020205.4(OTUD7B):c.478A>G (p.Met160Val)not specified [RCV004504796]uncertain significance1149967318149967318Humanname
407517183CV3459812single nucleotide variantNM_020205.4(OTUD7B):c.332G>A (p.Arg111Gln)not specified [RCV004650573]uncertain significance1149967464149967464Humanname
407470082CV3459818single nucleotide variantNM_020205.4(OTUD7B):c.452T>C (p.Ile151Thr)not specified [RCV004661936]uncertain significance1149967344149967344Humanname
407470088CV3459820single nucleotide variantNM_020205.4(OTUD7B):c.907G>A (p.Ala303Thr)not specified [RCV004661937]uncertain significance1149950160149950160Humanname
597656256CV3567963single nucleotide variantNM_020205.4(OTUD7B):c.865C>G (p.Pro289Ala)not specified [RCV004827495]uncertain significance1149950202149950202Humanname
597656740CV3567973single nucleotide variantNM_020205.4(OTUD7B):c.421A>G (p.Thr141Ala)not specified [RCV004827499]uncertain significance1149967375149967375Humanname
597656299CV3567977single nucleotide variantNM_020205.4(OTUD7B):c.454G>C (p.Glu152Gln)not specified [RCV004827500]uncertain significance1149967342149967342Humanname
598162662CV3995703single nucleotide variantNM_020205.4(OTUD7B):c.565A>G (p.Thr189Ala)not specified [RCV005390856]uncertain significance1149965816149965816Humanname
598162668CV3995704single nucleotide variantNM_020205.4(OTUD7B):c.665A>C (p.Glu222Ala)not specified [RCV005390857]uncertain significance1149964289149964289Humanname
598184227CV3995712single nucleotide variantNM_020205.4(OTUD7B):c.964G>A (p.Gly322Arg)not specified [RCV005395420]uncertain significance1149950103149950103Humanname
155968866CV2213235single nucleotide variantNM_020205.4(OTUD7B):c.2380G>A (p.Gly794Ser)not specified [RCV004085457]uncertain significance1149944009149944009Humanname
156292545CV2233462single nucleotide variantNM_020205.4(OTUD7B):c.1888C>T (p.Arg630Cys)not specified [RCV004106086]uncertain significance1149944501149944501Humanname
156267372CV2243973single nucleotide variantNM_020205.4(OTUD7B):c.1514A>C (p.Lys505Thr)not specified [RCV004108471]uncertain significance1149944875149944875Humanname
156211924CV2259916single nucleotide variantNM_020205.4(OTUD7B):c.1375C>T (p.Arg459Trp)not specified [RCV004118948]uncertain significance1149945014149945014Humanname
156147672CV2265222single nucleotide variantNM_020205.4(OTUD7B):c.1475G>A (p.Arg492Gln)not specified [RCV004126336]uncertain significance1149944914149944914Humanname
156020088CV2270187single nucleotide variantNM_020205.4(OTUD7B):c.1354G>A (p.Ala452Thr)not specified [RCV004135413]uncertain significance1149945035149945035Humanname
156176543CV2317491single nucleotide variantNM_020205.4(OTUD7B):c.1563G>C (p.Met521Ile)not specified [RCV004172453]uncertain significance1149944826149944826Humanname
156151792CV2318835single nucleotide variantNM_020205.4(OTUD7B):c.2030C>T (p.Thr677Ile)not specified [RCV004175744]uncertain significance1149944359149944359Humanname
156307807CV2332118single nucleotide variantNM_020205.4(OTUD7B):c.2378G>A (p.Arg793Gln)not specified [RCV004189158]uncertain significance1149944011149944011Humanname
156332060CV2339726single nucleotide variantNM_020205.4(OTUD7B):c.1285A>G (p.Met429Val)not specified [RCV004196428]uncertain significance1149947289149947289Humanname
156345827CV2372988single nucleotide variantNM_020205.4(OTUD7B):c.2161G>T (p.Val721Phe)not specified [RCV004224021]uncertain significance1149944228149944228Humanname
156000592CV2378718single nucleotide variantNM_020205.4(OTUD7B):c.1874A>G (p.Glu625Gly)not specified [RCV004231178]uncertain significance1149944515149944515Humanname
401758961CV2694363single nucleotide variantNM_020205.4(OTUD7B):c.1485C>A (p.Asp495Glu)not specified [RCV004304553]likely benign1149944904149944904Humanname
401718388CV2708251single nucleotide variantNM_020205.4(OTUD7B):c.2092A>G (p.Ile698Val)not specified [RCV004311597]uncertain significance1149944297149944297Humanname
401889437CV2756573single nucleotide variantNM_020205.4(OTUD7B):c.1025C>T (p.Ala342Val)not specified [RCV004345098]uncertain significance1149949727149949727Humanname
401863999CV2767459single nucleotide variantNM_020205.4(OTUD7B):c.1858C>T (p.Arg620Cys)not specified [RCV004343625]uncertain significance1149944531149944531Humanname
405785822CV3374573single nucleotide variantNM_020205.4(OTUD7B):c.1081G>T (p.Ala361Ser)not specified [RCV004504786]uncertain significance1149949671149949671Humanname
405785832CV3374575single nucleotide variantNM_020205.4(OTUD7B):c.1565G>A (p.Gly522Glu)not specified [RCV004504788]uncertain significance1149944824149944824Humanname
405785837CV3374576single nucleotide variantNM_020205.4(OTUD7B):c.1595C>G (p.Pro532Arg)not specified [RCV004504789]uncertain significance1149944794149944794Humanname
405785842CV3374577single nucleotide variantNM_020205.4(OTUD7B):c.2066C>G (p.Ser689Cys)not specified [RCV004504790]uncertain significance1149944323149944323Humanname
405785848CV3374578single nucleotide variantNM_020205.4(OTUD7B):c.2111G>A (p.Gly704Asp)not specified [RCV004504791]uncertain significance1149944278149944278Humanname
405785850CV3374579single nucleotide variantNM_020205.4(OTUD7B):c.2299C>A (p.Pro767Thr)not specified [RCV004504792]uncertain significance1149944090149944090Humanname
405785855CV3374580single nucleotide variantNM_020205.4(OTUD7B):c.2333G>T (p.Gly778Val)not specified [RCV004504793]uncertain significance1149944056149944056Humanname
405785861CV3374581single nucleotide variantNM_020205.4(OTUD7B):c.2377C>T (p.Arg793Trp)not specified [RCV004504794]uncertain significance1149944012149944012Humanname
407517178CV3459811single nucleotide variantNM_020205.4(OTUD7B):c.1039C>T (p.Arg347Cys)not specified [RCV004650572]uncertain significance1149949713149949713Humanname
407517186CV3459813single nucleotide variantNM_020205.4(OTUD7B):c.2098C>G (p.Arg700Gly)not specified [RCV004650574]uncertain significance1149944291149944291Humanname
407470077CV3459814single nucleotide variantNM_020205.4(OTUD7B):c.2302C>G (p.Pro768Ala)not specified [RCV004661935]uncertain significance1149944087149944087Humanname
407517189CV3459815single nucleotide variantNM_020205.4(OTUD7B):c.2424C>A (p.Ser808Arg)not specified [RCV004650575]uncertain significance1149943965149943965Humanname
407517192CV3459816single nucleotide variantNM_020205.4(OTUD7B):c.2300C>G (p.Pro767Arg)not specified [RCV004650576]uncertain significance1149944089149944089Humanname
407517197CV3459817single nucleotide variantNM_020205.4(OTUD7B):c.1451G>A (p.Arg484Gln)not specified [RCV004650577]uncertain significance1149944938149944938Humanname
407517200CV3459819single nucleotide variantNM_020205.4(OTUD7B):c.1691A>G (p.Glu564Gly)not specified [RCV004650578]uncertain significance1149944698149944698Humanname
597692571CV3567962single nucleotide variantNM_020205.4(OTUD7B):c.1286T>C (p.Met429Thr)not specified [RCV004838743]uncertain significance1149947288149947288Humanname
597692581CV3567964single nucleotide variantNM_020205.4(OTUD7B):c.2168G>T (p.Gly723Val)not specified [RCV004838744]uncertain significance1149944221149944221Humanname
597656275CV3567966single nucleotide variantNM_020205.4(OTUD7B):c.2078C>G (p.Pro693Arg)not specified [RCV004827497]uncertain significance1149944311149944311Humanname
597691476CV3567968single nucleotide variantNM_020205.4(OTUD7B):c.2224C>G (p.His742Asp)not specified [RCV004838746]uncertain significance1149944165149944165Humanname
597656283CV3567969single nucleotide variantNM_020205.4(OTUD7B):c.1277A>T (p.His426Leu)not specified [RCV004827498]uncertain significance1149947297149947297Humanname
597691486CV3567970single nucleotide variantNM_020205.4(OTUD7B):c.2390C>G (p.Pro797Arg)not specified [RCV004838747]uncertain significance1149943999149943999Humanname
597691497CV3567971single nucleotide variantNM_020205.4(OTUD7B):c.2153G>T (p.Gly718Val)not specified [RCV004838748]uncertain significance1149944236149944236Humanname
597691505CV3567972single nucleotide variantNM_020205.4(OTUD7B):c.1153A>G (p.Lys385Glu)not specified [RCV004838749]uncertain significance1149949054149949054Humanname
597691526CV3567975single nucleotide variantNM_020205.4(OTUD7B):c.1182C>G (p.Asp394Glu)not specified [RCV004838751]uncertain significance1149949025149949025Humanname
597691547CV3567978single nucleotide variantNM_020205.4(OTUD7B):c.1584G>T (p.Lys528Asn)not specified [RCV004838753]uncertain significance1149944805149944805Humanname
598162640CV3995699single nucleotide variantNM_020205.4(OTUD7B):c.1759A>G (p.Lys587Glu)not specified [RCV005390852]uncertain significance1149944630149944630Humanname
598162644CV3995700single nucleotide variantNM_020205.4(OTUD7B):c.2462G>A (p.Cys821Tyr)not specified [RCV005390853]uncertain significance1149943927149943927Humanname
598162651CV3995701single nucleotide variantNM_020205.4(OTUD7B):c.2501C>T (p.Pro834Leu)not specified [RCV005390854]uncertain significance1149943888149943888Humanname
598162656CV3995702single nucleotide variantNM_020205.4(OTUD7B):c.2005C>T (p.Pro669Ser)not specified [RCV005390855]uncertain significance1149944384149944384Humanname
598162676CV3995705single nucleotide variantNM_020205.4(OTUD7B):c.1610C>T (p.Thr537Ile)not specified [RCV005390858]uncertain significance1149944779149944779Humanname
598162687CV3995707single nucleotide variantNM_020205.4(OTUD7B):c.1138A>G (p.Thr380Ala)not specified [RCV005390860]uncertain significance1149949069149949069Humanname
598162693CV3995708single nucleotide variantNM_020205.4(OTUD7B):c.2114G>T (p.Gly705Val)not specified [RCV005390861]uncertain significance1149944275149944275Humanname
598162699CV3995709single nucleotide variantNM_020205.4(OTUD7B):c.2027C>G (p.Pro676Arg)not specified [RCV005390862]uncertain significance1149944362149944362Humanname
598162705CV3995710single nucleotide variantNM_020205.4(OTUD7B):c.1277A>G (p.His426Arg)not specified [RCV005390863]uncertain significance1149947297149947297Humanname
598162713CV3995711single nucleotide variantNM_020205.4(OTUD7B):c.2515C>G (p.Leu839Val)not specified [RCV005390864]uncertain significance1149943874149943874Humanname
8628898CV84042single nucleotide variantNM_020205.3(OTUD7B):c.2414C>T (p.Pro805Leu)Malignant melanoma [RCV000064123]not provided1149943975149943975Humanname