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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


198 records found for search term Zfpm1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401935723CV2817915single nucleotide variantNM_153813.3(ZFPM1):c.171G>A (p.Pro57=)not provided [RCV003413027]likely benign168848905688489056Humanname
401903551CV2817916single nucleotide variantNM_153813.3(ZFPM1):c.282G>A (p.Pro94=)not provided [RCV003419486]likely benign168851440088514400Humanname
150472913CV1217258single nucleotide variantNM_153813.3(ZFPM1):c.64A>G (p.Arg22Gly)not provided [RCV001615553]benign168848596288485962Humanname
155915318CV2243734single nucleotide variantNM_153813.3(ZFPM1):c.86G>T (p.Gly29Val)not specified [RCV004114433]uncertain significance168848598488485984Humanname
405265381CV3185607single nucleotide variantNM_153813.3(ZFPM1):c.699C>T (p.Thr233=)not provided [RCV003886171]|not specified [RCV004369689]likely benign168852822588528225Humanname
407458084CV3490187single nucleotide variantNM_153813.3(ZFPM1):c.73G>A (p.Val25Met)not specified [RCV004686566]likely benign168848597188485971Humanname
598159042CV3937760single nucleotide variantNM_153813.3(ZFPM1):c.29G>A (p.Arg10Gln)not specified [RCV005306474]uncertain significance168845366788453667Humanname
15152356CV715163single nucleotide variantNM_153813.3(ZFPM1):c.477C>T (p.Ala159=)not provided [RCV000968334]benign168852688888526888Humanname
156253026CV2366110single nucleotide variantNM_153813.3(ZFPM1):c.170C>T (p.Pro57Leu)not specified [RCV004210145]uncertain significance168848905588489055Humanname
329356292CV2430676single nucleotide variantNM_153813.3(ZFPM1):c.247G>A (p.Gly83Ser)not specified [RCV004253865]likely benign168848913288489132Humanname
401903553CV2817917single nucleotide variantNM_153813.3(ZFPM1):c.1005C>T (p.Cys335=)not provided [RCV003419487]likely benign168853267288532672Humanname
401903554CV2817918single nucleotide variantNM_153813.3(ZFPM1):c.1596G>A (p.Gly532=)not provided [RCV003419488]likely benign168853355488533554Humanname
401911924CV2817919single nucleotide variantNM_153813.3(ZFPM1):c.2265G>C (p.Pro755=)not provided [RCV003426889]likely benign168853422388534223Humanname
401911926CV2817920single nucleotide variantNM_153813.3(ZFPM1):c.2274G>C (p.Pro758=)not provided [RCV003426890]likely benign168853423288534232Humanname
405669356CV3360355single nucleotide variantNM_153813.3(ZFPM1):c.112A>C (p.Thr38Pro)not specified [RCV004486162]uncertain significance168848601088486010Humanname
405669370CV3360358single nucleotide variantNM_153813.3(ZFPM1):c.136C>A (p.Pro46Thr)not specified [RCV004486165]uncertain significance168848603488486034Humanname
407459187CV3490195single nucleotide variantNM_153813.3(ZFPM1):c.142G>A (p.Ala48Thr)not specified [RCV004687068]likely benign168848604088486040Humanname
597800250CV3628187single nucleotide variantNM_153813.3(ZFPM1):c.214G>A (p.Glu72Lys)not specified [RCV004880143]uncertain significance168848909988489099Humanname
598259745CV3937753single nucleotide variantNM_153813.3(ZFPM1):c.245C>T (p.Pro82Leu)not specified [RCV005300288]uncertain significance168848913088489130Humanname
15139720CV715162single nucleotide variantNM_153813.3(ZFPM1):c.209G>C (p.Gly70Ala)not provided [RCV000966014]benign168848909488489094Humanname
155901395CV2241995single nucleotide variantNM_153813.3(ZFPM1):c.931A>G (p.Met311Val)not specified [RCV004108942]uncertain significance168853222088532220Humanname
156113682CV2263854single nucleotide variantNM_153813.3(ZFPM1):c.757G>A (p.Glu253Lys)not specified [RCV004137911]uncertain significance168853204688532046Humanname
156156510CV2266222single nucleotide variantNM_153813.3(ZFPM1):c.452C>T (p.Thr151Met)not specified [RCV004128790]uncertain significance168852686388526863Humanname
156103312CV2291598single nucleotide variantNM_153813.3(ZFPM1):c.544G>A (p.Ala182Thr)not specified [RCV004155894]uncertain significance168852807088528070Humanname
156341061CV2348151single nucleotide variantNM_153813.3(ZFPM1):c.884C>A (p.Pro295His)not specified [RCV004197824]uncertain significance168853217388532173Humanname
156281526CV2348783single nucleotide variantNM_153813.3(ZFPM1):c.829G>A (p.Ala277Thr)not specified [RCV004203230]uncertain significance168853211888532118Humanname
156131013CV2358175single nucleotide variantNM_153813.3(ZFPM1):c.898A>G (p.Ser300Gly)not specified [RCV004211975]uncertain significance168853218788532187Humanname
156303844CV2359448single nucleotide variantNM_153813.3(ZFPM1):c.577G>A (p.Glu193Lys)not specified [RCV004214770]uncertain significance168852810388528103Humanname
155965909CV2396010single nucleotide variantNM_153813.3(ZFPM1):c.893G>A (p.Arg298His)not specified [RCV004237557]uncertain significance168853218288532182Humanname
329356247CV2442542single nucleotide variantNM_153813.3(ZFPM1):c.610A>G (p.Lys204Glu)not specified [RCV004266769]uncertain significance168852813688528136Humanname
329391301CV2452224single nucleotide variantNM_153813.3(ZFPM1):c.620C>A (p.Ala207Glu)not specified [RCV004278923]uncertain significance168852814688528146Humanname
401748573CV2712987single nucleotide variantNM_153813.3(ZFPM1):c.562G>A (p.Val188Met)not specified [RCV004314693]uncertain significance168852808888528088Humanname
401878942CV2754892single nucleotide variantNM_153813.3(ZFPM1):c.811G>A (p.Gly271Ser)not specified [RCV004341366]uncertain significance168853210088532100Humanname
405669515CV3360387single nucleotide variantNM_153813.3(ZFPM1):c.511G>A (p.Ala171Thr)not specified [RCV004486194]uncertain significance168852803788528037Humanname
405669520CV3360388single nucleotide variantNM_153813.3(ZFPM1):c.800G>A (p.Arg267His)not specified [RCV004486195]uncertain significance168853208988532089Humanname
405669524CV3360389single nucleotide variantNM_153813.3(ZFPM1):c.827C>T (p.Ala276Val)not specified [RCV004486196]uncertain significance168853211688532116Humanname
407458076CV3490185single nucleotide variantNM_153813.3(ZFPM1):c.572C>T (p.Thr191Met)not specified [RCV004686564]uncertain significance168852809888528098Humanname
407458080CV3490186single nucleotide variantNM_153813.3(ZFPM1):c.706A>G (p.Ile236Val)not specified [RCV004686565]likely benign168852823288528232Humanname
407458096CV3490190single nucleotide variantNM_153813.3(ZFPM1):c.565C>T (p.Leu189Phe)not specified [RCV004686569]uncertain significance168852809188528091Humanname
597726317CV3624750single nucleotide variantNM_153813.3(ZFPM1):c.544G>T (p.Ala182Ser)not specified [RCV004888388]uncertain significance168852807088528070Humanname
598259739CV3937751single nucleotide variantNM_153813.3(ZFPM1):c.625C>T (p.Pro209Ser)not specified [RCV005300287]uncertain significance168852815188528151Humanname
598259778CV3937761single nucleotide variantNM_153813.3(ZFPM1):c.704T>C (p.Val235Ala)not specified [RCV005300294]uncertain significance168852823088528230Humanname
598259790CV3937765single nucleotide variantNM_153813.3(ZFPM1):c.829G>T (p.Ala277Ser)not specified [RCV005300296]uncertain significance168853211888532118Humanname
598259797CV3937766single nucleotide variantNM_153813.3(ZFPM1):c.700G>A (p.Ala234Thr)not specified [RCV005300297]uncertain significance168852822688528226Humanname
598259811CV3937771single nucleotide variantNM_153813.3(ZFPM1):c.376G>A (p.Ala126Thr)not specified [RCV005300300]uncertain significance168851449488514494Humanname
155959712CV2193990single nucleotide variantNM_153813.3(ZFPM1):c.2423C>A (p.Ala808Asp)not specified [RCV004074713]uncertain significance168853438188534381Humanname
156151501CV2209288single nucleotide variantNM_153813.3(ZFPM1):c.1957A>C (p.Thr653Pro)not specified [RCV004091688]uncertain significance168853391588533915Humanname
156045133CV2215985single nucleotide variantNM_153813.3(ZFPM1):c.1039A>T (p.Ser347Cys)not specified [RCV004097040]uncertain significance168853270688532706Humanname
156331120CV2220482single nucleotide variantNM_153813.3(ZFPM1):c.2375A>C (p.Asp792Ala)not specified [RCV004097712]uncertain significance168853433388534333Humanname
156055463CV2243196single nucleotide variantNM_153813.3(ZFPM1):c.1285G>T (p.Asp429Tyr)not specified [RCV004110090]uncertain significance168853324388533243Humanname
156057051CV2243364single nucleotide variantNM_153813.3(ZFPM1):c.2921G>A (p.Arg974Gln)not specified [RCV004112055]uncertain significance168853487988534879Humanname
156202828CV2256271single nucleotide variantNM_153813.3(ZFPM1):c.2645G>A (p.Gly882Asp)not specified [RCV004116520]uncertain significance168853460388534603Humanname
156092638CV2256689single nucleotide variantNM_153813.3(ZFPM1):c.1889C>T (p.Ala630Val)not specified [RCV004118863]uncertain significance168853384788533847Humanname
156240821CV2265603single nucleotide variantNM_153813.3(ZFPM1):c.2660G>C (p.Gly887Ala)not specified [RCV004124338]uncertain significance168853461888534618Humanname
156016246CV2266302single nucleotide variantNM_153813.3(ZFPM1):c.1690G>T (p.Gly564Cys)not specified [RCV004129129]uncertain significance168853364888533648Humanname
156025281CV2273961single nucleotide variantNM_153813.3(ZFPM1):c.2110T>C (p.Tyr704His)not specified [RCV004134361]uncertain significance168853406888534068Humanname
155940787CV2294140single nucleotide variantNM_153813.3(ZFPM1):c.1262C>T (p.Ala421Val)not specified [RCV004149509]uncertain significance168853322088533220Humanname
156087089CV2295392single nucleotide variantNM_153813.3(ZFPM1):c.2966T>A (p.Phe989Tyr)not specified [RCV004158736]uncertain significance168853492488534924Humanname
156176715CV2299910single nucleotide variantNM_153813.3(ZFPM1):c.1538C>A (p.Pro513Gln)not specified [RCV004149047]uncertain significance168853349688533496Humanname
156191694CV2301831single nucleotide variantNM_153813.3(ZFPM1):c.1685C>G (p.Ala562Gly)not specified [RCV004156627]uncertain significance168853364388533643Humanname
155953506CV2303065single nucleotide variantNM_153813.3(ZFPM1):c.1283T>A (p.Leu428Gln)not specified [RCV004156853]uncertain significance168853324188533241Humanname
156265709CV2312252single nucleotide variantNM_153813.3(ZFPM1):c.1243T>C (p.Ser415Pro)not specified [RCV004166967]uncertain significance168853320188533201Humanname
156281843CV2317340single nucleotide variantNM_153813.3(ZFPM1):c.2143C>G (p.Arg715Gly)not specified [RCV004178822]uncertain significance168853410188534101Humanname
156281853CV2317341single nucleotide variantNM_153813.3(ZFPM1):c.2206G>T (p.Ala736Ser)not specified [RCV004178823]uncertain significance168853416488534164Humanname
156044499CV2322399single nucleotide variantNM_153813.3(ZFPM1):c.2449C>G (p.His817Asp)not specified [RCV004176146]uncertain significance168853440788534407Humanname
156069877CV2325026single nucleotide variantNM_153813.3(ZFPM1):c.2582C>G (p.Pro861Arg)not specified [RCV004175573]uncertain significance168853454088534540Humanname
156336293CV2333650single nucleotide variantNM_153813.3(ZFPM1):c.1584G>C (p.Gln528His)not specified [RCV004192490]uncertain significance168853354288533542Humanname
155917331CV2336311single nucleotide variantNM_153813.3(ZFPM1):c.1438G>A (p.Glu480Lys)not specified [RCV004192060]uncertain significance168853339688533396Humanname
156064206CV2352928single nucleotide variantNM_153813.3(ZFPM1):c.2299G>C (p.Glu767Gln)not specified [RCV004200973]uncertain significance168853425788534257Humanname
156236680CV2356131single nucleotide variantNM_153813.3(ZFPM1):c.1101G>C (p.Leu367Phe)not specified [RCV004203939]uncertain significance168853284788532847Humanname
156067810CV2356737single nucleotide variantNM_153813.3(ZFPM1):c.1720C>T (p.Pro574Ser)not specified [RCV004202084]uncertain significance168853367888533678Humanname
155929636CV2356947single nucleotide variantNM_153813.3(ZFPM1):c.1273T>C (p.Ser425Pro)not specified [RCV004204317]uncertain significance168853323188533231Humanname
156136960CV2365082single nucleotide variantNM_153813.3(ZFPM1):c.2143C>T (p.Arg715Cys)not specified [RCV004224238]uncertain significance168853410188534101Humanname
156196812CV2367266single nucleotide variantNM_153813.3(ZFPM1):c.1919G>A (p.Gly640Asp)not specified [RCV004215687]uncertain significance168853387788533877Humanname
156050779CV2367603single nucleotide variantNM_153813.3(ZFPM1):c.2878C>T (p.Pro960Ser)not specified [RCV004211529]uncertain significance168853483688534836Humanname
156154514CV2369511single nucleotide variantNM_153813.3(ZFPM1):c.2131G>A (p.Asp711Asn)not specified [RCV004210446]uncertain significance168853408988534089Humanname
156307351CV2369686single nucleotide variantNM_153813.3(ZFPM1):c.1495A>G (p.Arg499Gly)not specified [RCV004215086]uncertain significance168853345388533453Humanname
156258506CV2383789single nucleotide variantNM_153813.3(ZFPM1):c.1877C>G (p.Pro626Arg)not specified [RCV004603393]uncertain significance168853383588533835Humanname
156192120CV2388628single nucleotide variantNM_153813.3(ZFPM1):c.1415C>T (p.Ala472Val)not specified [RCV004239509]uncertain significance168853337388533373Humanname
155928879CV2389009single nucleotide variantNM_153813.3(ZFPM1):c.2111A>G (p.Tyr704Cys)not specified [RCV004242002]uncertain significance168853406988534069Humanname
155933289CV2399294single nucleotide variantNM_153813.3(ZFPM1):c.1665G>C (p.Gln555His)not specified [RCV004242588]uncertain significance168853362388533623Humanname
155930768CV2399719single nucleotide variantNM_153813.3(ZFPM1):c.1565G>C (p.Gly522Ala)not specified [RCV004245537]uncertain significance168853352388533523Humanname
329376474CV2428456single nucleotide variantNM_153813.3(ZFPM1):c.1400T>C (p.Val467Ala)not specified [RCV004253249]likely benign168853335888533358Humanname
329375699CV2431613single nucleotide variantNM_153813.3(ZFPM1):c.1874C>T (p.Pro625Leu)not specified [RCV004254759]uncertain significance168853383288533832Humanname
329377964CV2436093single nucleotide variantNM_153813.3(ZFPM1):c.2377G>C (p.Gly793Arg)not specified [RCV004255309]uncertain significance168853433588534335Humanname
329380048CV2444163single nucleotide variantNM_153813.3(ZFPM1):c.1807C>G (p.Arg603Gly)not specified [RCV004260898]uncertain significance168853376588533765Humanname
329358145CV2453909single nucleotide variantNM_153813.3(ZFPM1):c.1481G>A (p.Ser494Asn)not specified [RCV004271297]uncertain significance168853343988533439Humanname
329390679CV2455369single nucleotide variantNM_153813.3(ZFPM1):c.1504G>A (p.Ala502Thr)not specified [RCV004274868]uncertain significance168853346288533462Humanname
329357357CV2456739single nucleotide variantNM_153813.3(ZFPM1):c.2072G>A (p.Arg691His)not specified [RCV004270720]uncertain significance168853403088534030Humanname
329395880CV2463038single nucleotide variantNM_153813.3(ZFPM1):c.1094G>A (p.Ser365Asn)not specified [RCV004272854]uncertain significance168853284088532840Humanname
329397267CV2466004single nucleotide variantNM_153813.3(ZFPM1):c.2293G>A (p.Ala765Thr)not specified [RCV004277905]uncertain significance168853425188534251Humanname
329362101CV2466005single nucleotide variantNM_153813.3(ZFPM1):c.2294C>A (p.Ala765Glu)not specified [RCV004277906]uncertain significance168853425288534252Humanname
329381988CV2467451single nucleotide variantNM_153813.3(ZFPM1):c.2723C>G (p.Ala908Gly)not specified [RCV004287061]uncertain significance168853468188534681Humanname
329392191CV2470461single nucleotide variantNM_153813.3(ZFPM1):c.2408G>A (p.Arg803His)not specified [RCV004273486]uncertain significance168853436688534366Humanname
401739019CV2676420single nucleotide variantNM_153813.3(ZFPM1):c.1835C>T (p.Ala612Val)not specified [RCV004286441]uncertain significance168853379388533793Humanname
401740749CV2680469single nucleotide variantNM_153813.3(ZFPM1):c.2191G>A (p.Ala731Thr)not specified [RCV004291113]uncertain significance168853414988534149Humanname
401759695CV2701676single nucleotide variantNM_153813.3(ZFPM1):c.2326G>A (p.Gly776Arg)not specified [RCV004314088]uncertain significance168853428488534284Humanname
401779163CV2713041single nucleotide variantNM_153813.3(ZFPM1):c.2386G>A (p.Asp796Asn)not specified [RCV004316601]uncertain significance168853434488534344Humanname
401770342CV2715143single nucleotide variantNM_153813.3(ZFPM1):c.1630G>A (p.Ala544Thr)not specified [RCV004322713]uncertain significance168853358888533588Humanname
401879528CV2755183single nucleotide variantNM_153813.3(ZFPM1):c.2261C>G (p.Ala754Gly)not specified [RCV004337375]uncertain significance168853421988534219Humanname
401866889CV2759035single nucleotide variantNM_153813.3(ZFPM1):c.2171C>G (p.Pro724Arg)not specified [RCV004342342]uncertain significance168853412988534129Humanname
401867198CV2759126single nucleotide variantNM_153813.3(ZFPM1):c.1193G>A (p.Ser398Asn)not specified [RCV004342425]uncertain significance168853315188533151Humanname
401889709CV2763338single nucleotide variantNM_153813.3(ZFPM1):c.2848C>T (p.Pro950Ser)not specified [RCV004349234]uncertain significance168853480688534806Humanname
401870763CV2766335single nucleotide variantNM_153813.3(ZFPM1):c.2557G>T (p.Ala853Ser)not specified [RCV004342588]uncertain significance168853451588534515Humanname
401877149CV2769353single nucleotide variantNM_153813.3(ZFPM1):c.2698C>T (p.Pro900Ser)not specified [RCV004357347]uncertain significance168853465688534656Humanname
401887627CV2772056single nucleotide variantNM_153813.3(ZFPM1):c.2257G>C (p.Gly753Arg)not specified [RCV004344726]uncertain significance168853421588534215Humanname
401869515CV2772428single nucleotide variantNM_153813.3(ZFPM1):c.1717G>A (p.Ala573Thr)not specified [RCV004355216]uncertain significance168853367588533675Humanname
401897400CV2786980single nucleotide variantNM_153813.3(ZFPM1):c.2791G>A (p.Gly931Ser)not specified [RCV004366109]uncertain significance168853474988534749Humanname
401868112CV2787770single nucleotide variantNM_153813.3(ZFPM1):c.2179G>C (p.Ala727Pro)not specified [RCV004356676]uncertain significance168853413788534137Humanname
401894514CV2788292single nucleotide variantNM_153813.3(ZFPM1):c.1067T>G (p.Ile356Ser)not specified [RCV004352879]uncertain significance168853281388532813Humanname
401892700CV2791684single nucleotide variantNM_153813.3(ZFPM1):c.2359C>G (p.Pro787Ala)not specified [RCV004353024]uncertain significance168853431788534317Humanname
401870045CV2792260single nucleotide variantNM_153813.3(ZFPM1):c.1310C>T (p.Thr437Ile)not specified [RCV004361451]uncertain significance168853326888533268Humanname
405270047CV3187596single nucleotide variantNM_153813.3(ZFPM1):c.2738G>A (p.Gly913Glu)not provided [RCV003887680]uncertain significance168853469688534696Humanname
405669351CV3360354single nucleotide variantNM_153813.3(ZFPM1):c.1054A>G (p.Ser352Gly)not specified [RCV004486161]uncertain significance168853280088532800Humanname
405669361CV3360356single nucleotide variantNM_153813.3(ZFPM1):c.1162G>A (p.Gly388Arg)not specified [RCV004486163]uncertain significance168853290888532908Humanname
405669365CV3360357single nucleotide variantNM_153813.3(ZFPM1):c.1261G>A (p.Ala421Thr)not specified [RCV004486164]uncertain significance168853321988533219Humanname
405669382CV3360360single nucleotide variantNM_153813.3(ZFPM1):c.1379G>A (p.Arg460Lys)not specified [RCV004486167]uncertain significance168853333788533337Humanname
405669385CV3360361single nucleotide variantNM_153813.3(ZFPM1):c.1651C>T (p.His551Tyr)not specified [RCV004486168]uncertain significance168853360988533609Humanname
405669391CV3360362single nucleotide variantNM_153813.3(ZFPM1):c.1792C>T (p.Leu598Phe)not specified [RCV004486169]uncertain significance168853375088533750Humanname
405669394CV3360363single nucleotide variantNM_153813.3(ZFPM1):c.1852C>T (p.Pro618Ser)not specified [RCV004486170]uncertain significance168853381088533810Humanname
405669401CV3360364single nucleotide variantNM_153813.3(ZFPM1):c.2044C>T (p.Arg682Cys)not specified [RCV004486171]uncertain significance168853400288534002Humanname
405669404CV3360365single nucleotide variantNM_153813.3(ZFPM1):c.2134C>G (p.Pro712Ala)not specified [RCV004486172]uncertain significance168853409288534092Humanname
405669409CV3360366single nucleotide variantNM_153813.3(ZFPM1):c.2155G>A (p.Ala719Thr)not specified [RCV004486173]uncertain significance168853411388534113Humanname
405669414CV3360367single nucleotide variantNM_153813.3(ZFPM1):c.2176C>T (p.Pro726Ser)not specified [RCV004486174]uncertain significance168853413488534134Humanname
405669424CV3360369single nucleotide variantNM_153813.3(ZFPM1):c.2246T>C (p.Leu749Pro)not specified [RCV004486176]uncertain significance168853420488534204Humanname
405669429CV3360370single nucleotide variantNM_153813.3(ZFPM1):c.2260G>A (p.Ala754Thr)not specified [RCV004486177]uncertain significance168853421888534218Humanname
405669434CV3360371single nucleotide variantNM_153813.3(ZFPM1):c.2273C>T (p.Pro758Leu)not specified [RCV004486178]uncertain significance168853423188534231Humanname
405669439CV3360372single nucleotide variantNM_153813.3(ZFPM1):c.2332G>C (p.Gly778Arg)not specified [RCV004486179]uncertain significance168853429088534290Humanname
405669444CV3360373single nucleotide variantNM_153813.3(ZFPM1):c.2357C>G (p.Ser786Trp)not specified [RCV004486180]uncertain significance168853431588534315Humanname
405669449CV3360374single nucleotide variantNM_153813.3(ZFPM1):c.2360C>T (p.Pro787Leu)not specified [RCV004486181]uncertain significance168853431888534318Humanname
405669454CV3360375single nucleotide variantNM_153813.3(ZFPM1):c.2401C>G (p.Pro801Ala)not specified [RCV004486182]uncertain significance168853435988534359Humanname
405669460CV3360376single nucleotide variantNM_153813.3(ZFPM1):c.2441C>T (p.Ala814Val)not specified [RCV004486183]uncertain significance168853439988534399Humanname
405669465CV3360377single nucleotide variantNM_153813.3(ZFPM1):c.2453A>C (p.Glu818Ala)not specified [RCV004486184]uncertain significance168853441188534411Humanname
405669472CV3360378single nucleotide variantNM_153813.3(ZFPM1):c.2479C>T (p.His827Tyr)not specified [RCV004486185]uncertain significance168853443788534437Humanname
405669475CV3360379single nucleotide variantNM_153813.3(ZFPM1):c.2492C>T (p.Ala831Val)not specified [RCV004486186]uncertain significance168853445088534450Humanname
405669481CV3360380single nucleotide variantNM_153813.3(ZFPM1):c.2560G>A (p.Ala854Thr)not specified [RCV004486187]uncertain significance168853451888534518Humanname
405669485CV3360381single nucleotide variantNM_153813.3(ZFPM1):c.2663C>T (p.Pro888Leu)not specified [RCV004486188]uncertain significance168853462188534621Humanname
405669490CV3360382single nucleotide variantNM_153813.3(ZFPM1):c.2704C>T (p.Pro902Ser)not specified [RCV004486189]uncertain significance168853466288534662Humanname
405669495CV3360383single nucleotide variantNM_153813.3(ZFPM1):c.2768C>G (p.Pro923Arg)not specified [RCV004486190]uncertain significance168853472688534726Humanname
405669499CV3360384single nucleotide variantNM_153813.3(ZFPM1):c.2815G>T (p.Ala939Ser)not specified [RCV004486191]uncertain significance168853477388534773Humanname
405669505CV3360385single nucleotide variantNM_153813.3(ZFPM1):c.2836C>T (p.Pro946Ser)not specified [RCV004486192]uncertain significance168853479488534794Humanname
405669510CV3360386single nucleotide variantNM_153813.3(ZFPM1):c.2849C>G (p.Pro950Arg)not specified [RCV004486193]uncertain significance168853480788534807Humanname
407458067CV3490183single nucleotide variantNM_153813.3(ZFPM1):c.2855A>G (p.Tyr952Cys)not specified [RCV004686562]uncertain significance168853481388534813Humanname
407458072CV3490184single nucleotide variantNM_153813.3(ZFPM1):c.1877C>T (p.Pro626Leu)not specified [RCV004686563]uncertain significance168853383588533835Humanname
407458089CV3490188single nucleotide variantNM_153813.3(ZFPM1):c.1551G>C (p.Glu517Asp)not specified [RCV004686567]uncertain significance168853350988533509Humanname
407458093CV3490189single nucleotide variantNM_153813.3(ZFPM1):c.2747G>A (p.Gly916Asp)not specified [RCV004686568]uncertain significance168853470588534705Humanname
407459175CV3490191single nucleotide variantNM_153813.3(ZFPM1):c.2641C>T (p.Leu881Phe)not specified [RCV004687064]uncertain significance168853459988534599Humanname
407459178CV3490192single nucleotide variantNM_153813.3(ZFPM1):c.2005C>T (p.Pro669Ser)not specified [RCV004687065]uncertain significance168853396388533963Humanname
407459181CV3490193single nucleotide variantNM_153813.3(ZFPM1):c.1825G>C (p.Ala609Pro)not specified [RCV004687066]uncertain significance168853378388533783Humanname
407459184CV3490194single nucleotide variantNM_153813.3(ZFPM1):c.2489A>T (p.Glu830Val)not specified [RCV004687067]uncertain significance168853444788534447Humanname
407459189CV3490196single nucleotide variantNM_153813.3(ZFPM1):c.1694C>T (p.Ala565Val)not specified [RCV004687069]uncertain significance168853365288533652Humanname
407459192CV3490197single nucleotide variantNM_153813.3(ZFPM1):c.1202G>C (p.Ser401Thr)not specified [RCV004687070]uncertain significance168853316088533160Humanname
597800267CV3624739single nucleotide variantNM_153813.3(ZFPM1):c.2410C>G (p.Pro804Ala)not specified [RCV004880152]uncertain significance168853436888534368Humanname
597800268CV3624740single nucleotide variantNM_153813.3(ZFPM1):c.2183C>T (p.Ala728Val)not specified [RCV004880153]uncertain significance168853414188534141Humanname
597800271CV3624742single nucleotide variantNM_153813.3(ZFPM1):c.2279C>T (p.Pro760Leu)not specified [RCV004880154]uncertain significance168853423788534237Humanname
597726285CV3624743single nucleotide variantNM_153813.3(ZFPM1):c.1946G>C (p.Gly649Ala)not specified [RCV004888384]uncertain significance168853390488533904Humanname
597726293CV3624744single nucleotide variantNM_153813.3(ZFPM1):c.1949G>A (p.Gly650Asp)not specified [RCV004888385]uncertain significance168853390788533907Humanname
597726300CV3624745single nucleotide variantNM_153813.3(ZFPM1):c.1924G>A (p.Gly642Arg)not specified [RCV004888386]uncertain significance168853388288533882Humanname
597800273CV3624746single nucleotide variantNM_153813.3(ZFPM1):c.1861C>G (p.Pro621Ala)not specified [RCV004880155]uncertain significance168853381988533819Humanname
597726308CV3624747single nucleotide variantNM_153813.3(ZFPM1):c.1420C>A (p.Pro474Thr)not specified [RCV004888387]uncertain significance168853337888533378Humanname
597800275CV3624748single nucleotide variantNM_153813.3(ZFPM1):c.2368G>A (p.Ala790Thr)not specified [RCV004880156]uncertain significance168853432688534326Humanname
597800277CV3624749single nucleotide variantNM_153813.3(ZFPM1):c.2576G>A (p.Cys859Tyr)not specified [RCV004880157]uncertain significance168853453488534534Humanname
597800279CV3624751single nucleotide variantNM_153813.3(ZFPM1):c.1478G>A (p.Arg493His)not specified [RCV004880158]uncertain significance168853343688533436Humanname
597800243CV3628183single nucleotide variantNM_153813.3(ZFPM1):c.2548G>T (p.Gly850Cys)not specified [RCV004880139]uncertain significance168853450688534506Humanname
597800244CV3628184single nucleotide variantNM_153813.3(ZFPM1):c.1635G>C (p.Lys545Asn)not specified [RCV004880140]uncertain significance168853359388533593Humanname
597800246CV3628185single nucleotide variantNM_153813.3(ZFPM1):c.2043C>G (p.Ser681Arg)not specified [RCV004880141]uncertain significance168853400188534001Humanname
597800248CV3628186single nucleotide variantNM_153813.3(ZFPM1):c.1268C>T (p.Thr423Ile)not specified [RCV004880142]uncertain significance168853322688533226Humanname
597800252CV3628188single nucleotide variantNM_153813.3(ZFPM1):c.2521C>T (p.Pro841Ser)not specified [RCV004880144]uncertain significance168853447988534479Humanname
597800254CV3628189single nucleotide variantNM_153813.3(ZFPM1):c.1546G>A (p.Gly516Ser)not specified [RCV004880145]uncertain significance168853350488533504Humanname
597800255CV3628190single nucleotide variantNM_153813.3(ZFPM1):c.1231G>A (p.Gly411Ser)not specified [RCV004880146]uncertain significance168853318988533189Humanname
597800257CV3628192single nucleotide variantNM_153813.3(ZFPM1):c.1348G>A (p.Gly450Arg)not specified [RCV004880147]uncertain significance168853330688533306Humanname
597726270CV3628193single nucleotide variantNM_153813.3(ZFPM1):c.1715G>C (p.Gly572Ala)not specified [RCV004888382]uncertain significance168853367388533673Humanname
597800259CV3628194single nucleotide variantNM_153813.3(ZFPM1):c.1834G>T (p.Ala612Ser)not specified [RCV004880148]uncertain significance168853379288533792Humanname
597800261CV3628195single nucleotide variantNM_153813.3(ZFPM1):c.1702G>A (p.Gly568Arg)not specified [RCV004880149]uncertain significance168853366088533660Humanname
597800263CV3628196single nucleotide variantNM_153813.3(ZFPM1):c.2728C>T (p.Pro910Ser)not specified [RCV004880150]uncertain significance168853468688534686Humanname
597800480CV3628197single nucleotide variantNM_153813.3(ZFPM1):c.2399A>G (p.Lys800Arg)not specified [RCV004880151]uncertain significance168853435788534357Humanname
598259727CV3937748single nucleotide variantNM_153813.3(ZFPM1):c.1597C>A (p.Pro533Thr)not specified [RCV005300285]uncertain significance168853355588533555Humanname
598159028CV3937749single nucleotide variantNM_153813.3(ZFPM1):c.2798C>A (p.Pro933His)not specified [RCV005306471]uncertain significance168853475688534756Humanname
598259733CV3937750single nucleotide variantNM_153813.3(ZFPM1):c.1762A>C (p.Asn588His)not specified [RCV005300286]uncertain significance168853372088533720Humanname
598159033CV3937752single nucleotide variantNM_153813.3(ZFPM1):c.2369C>T (p.Ala790Val)not specified [RCV005306472]uncertain significance168853432788534327Humanname
598259750CV3937754single nucleotide variantNM_153813.3(ZFPM1):c.2261C>T (p.Ala754Val)not specified [RCV005300289]uncertain significance168853421988534219Humanname
598259755CV3937755single nucleotide variantNM_153813.3(ZFPM1):c.1849G>A (p.Ala617Thr)not specified [RCV005300290]uncertain significance168853380788533807Humanname
598259762CV3937756single nucleotide variantNM_153813.3(ZFPM1):c.2149C>A (p.Pro717Thr)not specified [RCV005300291]uncertain significance168853410788534107Humanname
598259767CV3937757single nucleotide variantNM_153813.3(ZFPM1):c.1602C>G (p.Asp534Glu)not specified [RCV005300292]uncertain significance168853356088533560Humanname
598259773CV3937758single nucleotide variantNM_153813.3(ZFPM1):c.2351C>A (p.Ala784Glu)not specified [RCV005300293]uncertain significance168853430988534309Humanname
598159037CV3937759single nucleotide variantNM_153813.3(ZFPM1):c.1952C>T (p.Ala651Val)not specified [RCV005306473]uncertain significance168853391088533910Humanname
598159047CV3937762single nucleotide variantNM_153813.3(ZFPM1):c.2785C>G (p.Pro929Ala)not specified [RCV005306475]uncertain significance168853474388534743Humanname
598159053CV3937763single nucleotide variantNM_153813.3(ZFPM1):c.1721C>G (p.Pro574Arg)not specified [RCV005306476]uncertain significance168853367988533679Humanname
598259783CV3937764single nucleotide variantNM_153813.3(ZFPM1):c.1129G>C (p.Gly377Arg)not specified [RCV005300295]uncertain significance168853287588532875Humanname
598159058CV3937767single nucleotide variantNM_153813.3(ZFPM1):c.2603A>G (p.Asp868Gly)not specified [RCV005306477]uncertain significance168853456188534561Humanname
598259802CV3937768single nucleotide variantNM_153813.3(ZFPM1):c.1880G>A (p.Gly627Asp)not specified [RCV005300298]uncertain significance168853383888533838Humanname
598259807CV3937769single nucleotide variantNM_153813.3(ZFPM1):c.2423C>G (p.Ala808Gly)not specified [RCV005300299]uncertain significance168853438188534381Humanname
598159063CV3937770single nucleotide variantNM_153813.3(ZFPM1):c.2302T>C (p.Ser768Pro)not specified [RCV005306478]uncertain significance168853426088534260Humanname
598259819CV3937772single nucleotide variantNM_153813.3(ZFPM1):c.2803T>C (p.Ser935Pro)not specified [RCV005300301]uncertain significance168853476188534761Humanname
15182489CV715164single nucleotide variantNM_153813.3(ZFPM1):c.1332G>C (p.Glu444Asp)not provided [RCV000974643]benign168853329088533290Humanname
401767673CV2729832single nucleotide variantNM_153813.3(ZFPM1):c.3013G>A (p.Val1005Met)not specified [RCV004332839]uncertain significance168853497188534971Humanname
598129083CV3886887deletionNM_153813.3(ZFPM1):c.2165_2191del (p.Gly722_Pro730del)not provided [RCV005244547]likely benign168853410788534133Humanname
40816190CV969186deletionNM_153813.3(ZFPM1):c.1331_1333del (p.Glu444_Pro445delinsAla)not specified [RCV001260310]uncertain significance168853328988533291Humanname