Cdc42bpg Variant Search Result - Rat Genome Database

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209 records found for search term Cdc42bpg

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156371645	CV2200866	single nucleotide variant	NM_017525.3(CDC42BPG):c.19G>T (p.Ala7Ser)	not specified [RCV004081492]	uncertain significance	11	64844551	64844551	Human		name
401875336	CV2766012	single nucleotide variant	NM_017525.3(CDC42BPG):c.19G>A (p.Ala7Thr)	not specified [RCV004340477]	uncertain significance	11	64844551	64844551	Human		name
597788019	CV3644880	single nucleotide variant	NM_017525.3(CDC42BPG):c.23T>C (p.Leu8Pro)	not specified [RCV004901372]	uncertain significance	11	64844547	64844547	Human		name
15189111	CV738110	single nucleotide variant	NM_017525.3(CDC42BPG):c.231C>T (p.Ile77=)	not provided [RCV000909557]	benign	11	64841834	64841834	Human		name
156078828	CV2300858	single nucleotide variant	NM_017525.3(CDC42BPG):c.98A>C (p.His33Pro)	not specified [RCV004158063]	uncertain significance	11	64844472	64844472	Human		name
15191899	CV738109	single nucleotide variant	NM_017525.3(CDC42BPG):c.510G>A (p.Glu170=)	not provided [RCV000910381]	benign	11	64840191	64840191	Human		name
156248271	CV2276966	single nucleotide variant	NM_017525.3(CDC42BPG):c.208G>T (p.Asp70Tyr)	not specified [RCV004140299]	uncertain significance	11	64841857	64841857	Human		name
401723843	CV2684886	single nucleotide variant	NM_017525.3(CDC42BPG):c.172G>A (p.Val58Ile)	not specified [RCV004296391]	uncertain significance	11	64841893	64841893	Human		name
401890032	CV2758486	single nucleotide variant	NM_017525.3(CDC42BPG):c.194G>A (p.Arg65His)	not specified [RCV004335132]	uncertain significance	11	64841871	64841871	Human		name
401909469	CV2813323	single nucleotide variant	NM_017525.3(CDC42BPG):c.2019G>A (p.Thr673=)	not provided [RCV003397982]	likely benign	11	64835088	64835088	Human		name
598229378	CV3951027	single nucleotide variant	NM_017525.3(CDC42BPG):c.259G>A (p.Val87Met)	not specified [RCV005319213]	uncertain significance	11	64841727	64841727	Human		name
155922364	CV2240676	single nucleotide variant	NM_017525.3(CDC42BPG):c.554C>T (p.Ser185Leu)	not specified [RCV004119307]	uncertain significance	11	64840147	64840147	Human		name
156367219	CV2269843	single nucleotide variant	NM_017525.3(CDC42BPG):c.953G>T (p.Arg318Leu)	not specified [RCV004127076]	uncertain significance	11	64838826	64838826	Human		name
156139642	CV2280762	single nucleotide variant	NM_017525.3(CDC42BPG):c.750G>C (p.Lys250Asn)	not specified [RCV004145027]	uncertain significance	11	64839159	64839159	Human		name
156013406	CV2300431	single nucleotide variant	NM_017525.3(CDC42BPG):c.350G>C (p.Arg117Pro)	not specified [RCV004153631]	uncertain significance	11	64840635	64840635	Human		name
156044882	CV2340136	single nucleotide variant	NM_017525.3(CDC42BPG):c.466C>G (p.Leu156Val)	not specified [RCV004192374]	uncertain significance	11	64840235	64840235	Human		name
156017105	CV2370042	single nucleotide variant	NM_017525.3(CDC42BPG):c.631C>A (p.Leu211Met)	not specified [RCV004210939]	uncertain significance	11	64839522	64839522	Human		name
156062428	CV2380372	single nucleotide variant	NM_017525.3(CDC42BPG):c.958G>A (p.Glu320Lys)	not specified [RCV004217982]	uncertain significance	11	64838821	64838821	Human		name
329401193	CV2442140	single nucleotide variant	NM_017525.3(CDC42BPG):c.514G>A (p.Ala172Thr)	not specified [RCV004264645]	uncertain significance	11	64840187	64840187	Human		name
401754964	CV2682346	single nucleotide variant	NM_017525.3(CDC42BPG):c.595G>A (p.Asp199Asn)	not specified [RCV004290381]	uncertain significance	11	64839558	64839558	Human		name
401732913	CV2705082	single nucleotide variant	NM_017525.3(CDC42BPG):c.910G>A (p.Val304Met)	not specified [RCV004309993]	uncertain significance	11	64838869	64838869	Human		name
401909468	CV2813322	single nucleotide variant	NM_017525.3(CDC42BPG):c.3366C>T (p.Asn1122=)	not provided [RCV003397981]	likely benign	11	64830195	64830195	Human		name
405773907	CV3296204	single nucleotide variant	NM_017525.3(CDC42BPG):c.347T>G (p.Phe116Cys)	not specified [RCV004435769]	uncertain significance	11	64840638	64840638	Human		name
405773968	CV3296214	single nucleotide variant	NM_017525.3(CDC42BPG):c.449A>G (p.Tyr150Cys)	not specified [RCV004435779]	uncertain significance	11	64840252	64840252	Human		name
405773985	CV3296217	single nucleotide variant	NM_017525.3(CDC42BPG):c.830A>G (p.Tyr277Cys)	not specified [RCV004435782]	uncertain significance	11	64839079	64839079	Human		name
405773991	CV3296218	single nucleotide variant	NM_017525.3(CDC42BPG):c.904C>T (p.Pro302Ser)	not specified [RCV004435783]	uncertain significance	11	64838875	64838875	Human		name
405773998	CV3296219	single nucleotide variant	NM_017525.3(CDC42BPG):c.952C>T (p.Arg318Cys)	not specified [RCV004435784]	uncertain significance	11	64838827	64838827	Human		name
405774004	CV3296220	single nucleotide variant	NM_017525.3(CDC42BPG):c.995G>A (p.Arg332Gln)	not specified [RCV004435785]	uncertain significance	11	64838784	64838784	Human		name
407454729	CV3425138	single nucleotide variant	NM_017525.3(CDC42BPG):c.599A>G (p.Asn200Ser)	not specified [RCV004609962]	uncertain significance	11	64839554	64839554	Human		name
407498692	CV3425141	single nucleotide variant	NM_017525.3(CDC42BPG):c.359G>A (p.Arg120Gln)	not specified [RCV004606706]	uncertain significance	11	64840626	64840626	Human		name
597787936	CV3644859	single nucleotide variant	NM_017525.3(CDC42BPG):c.746G>A (p.Gly249Asp)	not specified [RCV004901351]	uncertain significance	11	64839163	64839163	Human		name
597787994	CV3644874	single nucleotide variant	NM_017525.3(CDC42BPG):c.790G>A (p.Val264Ile)	not specified [RCV004901366]	uncertain significance	11	64839119	64839119	Human		name
597788005	CV3644877	single nucleotide variant	NM_017525.3(CDC42BPG):c.490G>A (p.Glu164Lys)	not specified [RCV004901369]	uncertain significance	11	64840211	64840211	Human		name
598167405	CV3951008	single nucleotide variant	NM_017525.3(CDC42BPG):c.416A>G (p.Gln139Arg)	not specified [RCV005308059]	uncertain significance	11	64840569	64840569	Human		name
15199106	CV724574	single nucleotide variant	NM_017525.3(CDC42BPG):c.3771G>A (p.Pro1257=)	not provided [RCV000890542]	benign	11	64829667	64829667	Human		name
156398614	CV2194681	single nucleotide variant	NM_017525.3(CDC42BPG):c.1139C>T (p.Pro380Leu)	not specified [RCV004075241]	uncertain significance	11	64838149	64838149	Human		name
156320038	CV2197211	single nucleotide variant	NM_017525.3(CDC42BPG):c.2969C>T (p.Pro990Leu)	not specified [RCV004078999]	uncertain significance	11	64832640	64832640	Human		name
155916302	CV2197341	single nucleotide variant	NM_017525.3(CDC42BPG):c.2396G>A (p.Arg799Gln)	not specified [RCV004081084]	uncertain significance	11	64834283	64834283	Human		name
156397413	CV2200441	single nucleotide variant	NM_017525.3(CDC42BPG):c.1928G>A (p.Arg643Gln)	not specified [RCV004076756]	likely benign	11	64835372	64835372	Human		name
156323127	CV2201516	single nucleotide variant	NM_017525.3(CDC42BPG):c.1927C>T (p.Arg643Trp)	not specified [RCV004080007]	uncertain significance	11	64835373	64835373	Human		name
156224848	CV2203004	single nucleotide variant	NM_017525.3(CDC42BPG):c.2737G>A (p.Gly913Ser)	not specified [RCV004069258]	uncertain significance	11	64832954	64832954	Human		name
156151885	CV2209313	single nucleotide variant	NM_017525.3(CDC42BPG):c.2044G>A (p.Ala682Thr)	not specified [RCV004091707]	uncertain significance	11	64835063	64835063	Human		name
155927978	CV2218526	single nucleotide variant	NM_017525.3(CDC42BPG):c.1037C>T (p.Ala346Val)	not specified [RCV004090805]	uncertain significance	11	64838742	64838742	Human		name
156232028	CV2227648	single nucleotide variant	NM_017525.3(CDC42BPG):c.1937G>T (p.Ser646Ile)	not specified [RCV004094052]	uncertain significance	11	64835363	64835363	Human		name
155926387	CV2230607	single nucleotide variant	NM_017525.3(CDC42BPG):c.1732C>G (p.Arg578Gly)	not specified [RCV004097567]	uncertain significance	11	64835788	64835788	Human		name
155986874	CV2248025	single nucleotide variant	NM_017525.3(CDC42BPG):c.1450G>A (p.Asp484Asn)	not specified [RCV004121445]	uncertain significance	11	64836465	64836465	Human		name
155995580	CV2250363	single nucleotide variant	NM_017525.3(CDC42BPG):c.2797C>G (p.Leu933Val)	not specified [RCV004127251]	uncertain significance	11	64832894	64832894	Human		name
155995600	CV2250364	single nucleotide variant	NM_017525.3(CDC42BPG):c.2798T>A (p.Leu933His)	not specified [RCV004127252]	uncertain significance	11	64832893	64832893	Human		name
156110173	CV2261585	single nucleotide variant	NM_017525.3(CDC42BPG):c.2374G>A (p.Ala792Thr)	not specified [RCV004125915]	likely benign	11	64834305	64834305	Human		name
155929649	CV2278240	single nucleotide variant	NM_017525.3(CDC42BPG):c.2531T>A (p.Leu844Gln)	not specified [RCV004143469]	uncertain significance	11	64833772	64833772	Human		name
156009686	CV2290920	single nucleotide variant	NM_017525.3(CDC42BPG):c.2553C>G (p.Ser851Arg)	not specified [RCV004151482]	uncertain significance	11	64833750	64833750	Human		name
156076646	CV2291541	single nucleotide variant	NM_017525.3(CDC42BPG):c.1732C>T (p.Arg578Cys)	not specified [RCV004155845]	uncertain significance	11	64835788	64835788	Human		name
155904609	CV2298832	single nucleotide variant	NM_017525.3(CDC42BPG):c.2804G>A (p.Arg935His)	not specified [RCV004156382]	likely benign	11	64832887	64832887	Human		name
156148437	CV2321722	single nucleotide variant	NM_017525.3(CDC42BPG):c.1417A>G (p.Thr473Ala)	not specified [RCV004179720]	uncertain significance	11	64836498	64836498	Human		name
156159299	CV2322727	single nucleotide variant	NM_017525.3(CDC42BPG):c.1850G>A (p.Arg617Gln)	not specified [RCV004182844]	uncertain significance	11	64835530	64835530	Human		name
156072250	CV2335012	single nucleotide variant	NM_017525.3(CDC42BPG):c.1940G>A (p.Arg647Gln)	not specified [RCV004182103]	likely benign	11	64835360	64835360	Human		name
156331989	CV2339717	single nucleotide variant	NM_017525.3(CDC42BPG):c.1706C>T (p.Thr569Met)	not specified [RCV004196419]	likely benign	11	64835814	64835814	Human		name
155922897	CV2347402	single nucleotide variant	NM_017525.3(CDC42BPG):c.1330C>T (p.Arg444Trp)	not specified [RCV004207241]	uncertain significance	11	64836793	64836793	Human		name
156173390	CV2355170	single nucleotide variant	NM_017525.3(CDC42BPG):c.2009G>A (p.Arg670Gln)	not specified [RCV004198556]	uncertain significance	11	64835098	64835098	Human		name
156345416	CV2356209	single nucleotide variant	NM_017525.3(CDC42BPG):c.2011C>T (p.Arg671Trp)	not specified [RCV004206028]	uncertain significance	11	64835096	64835096	Human		name
156189406	CV2356613	single nucleotide variant	NM_017525.3(CDC42BPG):c.2644C>T (p.Arg882Cys)	not specified [RCV004201978]	uncertain significance	11	64833318	64833318	Human		name
156150847	CV2369104	single nucleotide variant	NM_017525.3(CDC42BPG):c.2513A>G (p.His838Arg)	not specified [RCV004214943]	uncertain significance	11	64833790	64833790	Human		name
155988705	CV2371850	single nucleotide variant	NM_017525.3(CDC42BPG):c.1697G>A (p.Arg566Gln)	not specified [RCV004221544]	likely benign	11	64835823	64835823	Human		name
156000387	CV2383197	single nucleotide variant	NM_017525.3(CDC42BPG):c.2537C>T (p.Pro846Leu)	not specified [RCV004220207]	uncertain significance	11	64833766	64833766	Human		name
156108229	CV2390216	single nucleotide variant	NM_017525.3(CDC42BPG):c.2905G>A (p.Val969Met)	not specified [RCV004240597]	uncertain significance	11	64832704	64832704	Human		name
156061526	CV2392006	single nucleotide variant	NM_017525.3(CDC42BPG):c.2960G>C (p.Arg987Thr)	not specified [RCV004235863]	uncertain significance	11	64832649	64832649	Human		name
155970849	CV2392370	single nucleotide variant	NM_017525.3(CDC42BPG):c.1901C>T (p.Ala634Val)	not specified [RCV004243959]	uncertain significance	11	64835399	64835399	Human		name
156167782	CV2399072	single nucleotide variant	NM_017525.3(CDC42BPG):c.1348C>T (p.Arg450Trp)	not specified [RCV004245368]	uncertain significance	11	64836775	64836775	Human		name
329374005	CV2434665	single nucleotide variant	NM_017525.3(CDC42BPG):c.2827G>A (p.Glu943Lys)	not specified [RCV004248385]	uncertain significance	11	64832864	64832864	Human		name
329374399	CV2443882	single nucleotide variant	NM_017525.3(CDC42BPG):c.2728G>C (p.Asp910His)	not specified [RCV004258218]	uncertain significance	11	64833234	64833234	Human		name
329399992	CV2444264	single nucleotide variant	NM_017525.3(CDC42BPG):c.2560A>G (p.Met854Val)	not specified [RCV004263032]	uncertain significance	11	64833743	64833743	Human		name
329364310	CV2447351	single nucleotide variant	NM_017525.3(CDC42BPG):c.1507G>A (p.Ala503Thr)	not specified [RCV004262630]	uncertain significance	11	64836278	64836278	Human		name
329397433	CV2456162	single nucleotide variant	NM_017525.3(CDC42BPG):c.1262G>C (p.Cys421Ser)	not specified [RCV004273355]	uncertain significance	11	64836963	64836963	Human		name
401723202	CV2674743	single nucleotide variant	NM_017525.3(CDC42BPG):c.2651G>A (p.Arg884Gln)	not specified [RCV004294026]	uncertain significance	11	64833311	64833311	Human		name
401781113	CV2681894	single nucleotide variant	NM_017525.3(CDC42BPG):c.1730A>C (p.Gln577Pro)	not specified [RCV004296886]	uncertain significance	11	64835790	64835790	Human		name
401774609	CV2691797	single nucleotide variant	NM_017525.3(CDC42BPG):c.2767C>G (p.Gln923Glu)	not specified [RCV004299248]	uncertain significance	11	64832924	64832924	Human		name
401725267	CV2697339	single nucleotide variant	NM_017525.3(CDC42BPG):c.1250G>A (p.Arg417Gln)	not specified [RCV004304094]	likely benign	11	64836975	64836975	Human		name
401739703	CV2704646	single nucleotide variant	NM_017525.3(CDC42BPG):c.1888G>C (p.Gly630Arg)	not specified [RCV004313677]	uncertain significance	11	64835412	64835412	Human		name
401761680	CV2713847	single nucleotide variant	NM_017525.3(CDC42BPG):c.1220G>T (p.Ser407Ile)	not specified [RCV004315291]	uncertain significance	11	64837005	64837005	Human		name
401738413	CV2714449	single nucleotide variant	NM_017525.3(CDC42BPG):c.2747G>A (p.Cys916Tyr)	not specified [RCV004317976]	uncertain significance	11	64832944	64832944	Human		name
401754510	CV2717415	single nucleotide variant	NM_017525.3(CDC42BPG):c.1291A>G (p.Arg431Gly)	not specified [RCV004330244]	uncertain significance	11	64836934	64836934	Human		name
401773594	CV2727571	single nucleotide variant	NM_017525.3(CDC42BPG):c.1410G>T (p.Leu470Phe)	not specified [RCV004329758]	uncertain significance	11	64836505	64836505	Human		name
401877382	CV2769435	single nucleotide variant	NM_017525.3(CDC42BPG):c.1622G>A (p.Arg541Gln)	not specified [RCV004357418]	likely benign	11	64836163	64836163	Human		name
401876395	CV2770759	single nucleotide variant	NM_017525.3(CDC42BPG):c.2210T>C (p.Met737Thr)	not specified [RCV004349798]	uncertain significance	11	64834543	64834543	Human		name
401897153	CV2789873	single nucleotide variant	NM_017525.3(CDC42BPG):c.2404G>A (p.Gly802Arg)	not specified [RCV004362257]	uncertain significance	11	64834275	64834275	Human		name
405867234	CV2842754	single nucleotide variant	NM_017525.3(CDC42BPG):c.1314C>G (p.His438Gln)	EBV-positive nodal T- and NK-cell lymphoma [RCV004558111]	likely benign	11	64836809	64836809	Human		name
405773799	CV3296186	single nucleotide variant	NM_017525.3(CDC42BPG):c.1162G>A (p.Gly388Ser)	not specified [RCV004435751]	uncertain significance	11	64838126	64838126	Human		name
405773806	CV3296187	single nucleotide variant	NM_017525.3(CDC42BPG):c.1249C>T (p.Arg417Trp)	not specified [RCV004435752]	uncertain significance	11	64836976	64836976	Human		name
405773811	CV3296188	single nucleotide variant	NM_017525.3(CDC42BPG):c.1463G>A (p.Arg488Gln)	not specified [RCV004435753]	likely benign	11	64836452	64836452	Human		name
405773817	CV3296189	single nucleotide variant	NM_017525.3(CDC42BPG):c.1772C>A (p.Ala591Asp)	not specified [RCV004435754]	uncertain significance	11	64835608	64835608	Human		name
405773822	CV3296190	single nucleotide variant	NM_017525.3(CDC42BPG):c.2015A>C (p.Glu672Ala)	not specified [RCV004435755]	uncertain significance	11	64835092	64835092	Human		name
405773826	CV3296191	single nucleotide variant	NM_017525.3(CDC42BPG):c.2047G>T (p.Asp683Tyr)	not specified [RCV004435756]	uncertain significance	11	64835060	64835060	Human		name
405773832	CV3296192	single nucleotide variant	NM_017525.3(CDC42BPG):c.2168G>A (p.Arg723Gln)	not specified [RCV004435757]	uncertain significance	11	64834856	64834856	Human		name
405773835	CV3296193	single nucleotide variant	NM_017525.3(CDC42BPG):c.2423C>G (p.Pro808Arg)	not specified [RCV004435758]	uncertain significance	11	64833968	64833968	Human		name
405773841	CV3296194	single nucleotide variant	NM_017525.3(CDC42BPG):c.2562G>A (p.Met854Ile)	not specified [RCV004435759]	uncertain significance	11	64833741	64833741	Human		name
405773847	CV3296195	single nucleotide variant	NM_017525.3(CDC42BPG):c.2632T>G (p.Ser878Ala)	not specified [RCV004435760]	uncertain significance	11	64833330	64833330	Human		name
405773853	CV3296196	single nucleotide variant	NM_017525.3(CDC42BPG):c.2637C>A (p.His879Gln)	not specified [RCV004435761]	uncertain significance	11	64833325	64833325	Human		name
405773861	CV3296197	single nucleotide variant	NM_017525.3(CDC42BPG):c.2639C>T (p.Thr880Met)	not specified [RCV004435762]	uncertain significance	11	64833323	64833323	Human		name
405773867	CV3296198	single nucleotide variant	NM_017525.3(CDC42BPG):c.2642T>C (p.Leu881Pro)	not specified [RCV004435763]	uncertain significance	11	64833320	64833320	Human		name
405773873	CV3296199	single nucleotide variant	NM_017525.3(CDC42BPG):c.2701G>A (p.Gly901Ser)	not specified [RCV004435764]	uncertain significance	11	64833261	64833261	Human		name
407498648	CV3425128	single nucleotide variant	NM_017525.3(CDC42BPG):c.2459G>A (p.Ser820Asn)	not specified [RCV004606697]	uncertain significance	11	64833932	64833932	Human		name
407454723	CV3425131	single nucleotide variant	NM_017525.3(CDC42BPG):c.1511G>A (p.Gly504Glu)	not specified [RCV004609959]	uncertain significance	11	64836274	64836274	Human		name
407498661	CV3425133	single nucleotide variant	NM_017525.3(CDC42BPG):c.2803C>T (p.Arg935Cys)	not specified [RCV004606700]	uncertain significance	11	64832888	64832888	Human		name
407498671	CV3425135	single nucleotide variant	NM_017525.3(CDC42BPG):c.1495G>A (p.Ala499Thr)	not specified [RCV004606702]	uncertain significance	11	64836290	64836290	Human		name
407498677	CV3425136	single nucleotide variant	NM_017525.3(CDC42BPG):c.2582C>T (p.Ala861Val)	not specified [RCV004606703]	likely benign	11	64833643	64833643	Human		name
407454727	CV3425137	single nucleotide variant	NM_017525.3(CDC42BPG):c.2690C>T (p.Ser897Leu)	not specified [RCV004609961]	uncertain significance	11	64833272	64833272	Human		name
407498702	CV3425143	single nucleotide variant	NM_017525.3(CDC42BPG):c.1597G>C (p.Glu533Gln)	not specified [RCV004606708]	uncertain significance	11	64836188	64836188	Human		name
407498705	CV3425144	single nucleotide variant	NM_017525.3(CDC42BPG):c.2524C>A (p.Pro842Thr)	not specified [RCV004606709]	uncertain significance	11	64833779	64833779	Human		name
407498903	CV3425147	single nucleotide variant	NM_017525.3(CDC42BPG):c.2666C>T (p.Pro889Leu)	not specified [RCV004606712]	uncertain significance	11	64833296	64833296	Human		name
597787940	CV3644860	single nucleotide variant	NM_017525.3(CDC42BPG):c.2167C>T (p.Arg723Trp)	not specified [RCV004901352]	uncertain significance	11	64834857	64834857	Human		name
597787952	CV3644863	single nucleotide variant	NM_017525.3(CDC42BPG):c.1275G>C (p.Glu425Asp)	not specified [RCV004901355]	uncertain significance	11	64836950	64836950	Human		name
597787959	CV3644865	single nucleotide variant	NM_017525.3(CDC42BPG):c.1487G>A (p.Arg496Gln)	not specified [RCV004901357]	likely benign	11	64836428	64836428	Human		name
597787979	CV3644870	single nucleotide variant	NM_017525.3(CDC42BPG):c.2255A>C (p.Glu752Ala)	not specified [RCV004901362]	uncertain significance	11	64834498	64834498	Human		name
597787991	CV3644873	single nucleotide variant	NM_017525.3(CDC42BPG):c.2500G>A (p.Glu834Lys)	not specified [RCV004901365]	uncertain significance	11	64833803	64833803	Human		name
597788011	CV3644878	single nucleotide variant	NM_017525.3(CDC42BPG):c.2294A>G (p.Gln765Arg)	not specified [RCV004901370]	uncertain significance	11	64834459	64834459	Human		name
597788015	CV3644879	single nucleotide variant	NM_017525.3(CDC42BPG):c.2002G>A (p.Gly668Ser)	not specified [RCV004901371]	uncertain significance	11	64835105	64835105	Human		name
597788023	CV3644881	single nucleotide variant	NM_017525.3(CDC42BPG):c.2636A>G (p.His879Arg)	not specified [RCV004901373]	uncertain significance	11	64833326	64833326	Human		name
597788027	CV3644882	single nucleotide variant	NM_017525.3(CDC42BPG):c.1420G>C (p.Asp474His)	not specified [RCV004901374]	uncertain significance	11	64836495	64836495	Human		name
597788030	CV3644883	single nucleotide variant	NM_017525.3(CDC42BPG):c.2156C>T (p.Thr719Met)	not specified [RCV004901375]	uncertain significance	11	64834868	64834868	Human		name
598167400	CV3951007	single nucleotide variant	NM_017525.3(CDC42BPG):c.2423C>T (p.Pro808Leu)	not specified [RCV005308058]	uncertain significance	11	64833968	64833968	Human		name
598229347	CV3951009	single nucleotide variant	NM_017525.3(CDC42BPG):c.1843G>A (p.Ala615Thr)	not specified [RCV005319208]	uncertain significance	11	64835537	64835537	Human		name
598167413	CV3951010	single nucleotide variant	NM_017525.3(CDC42BPG):c.1745C>T (p.Ser582Leu)	not specified [RCV005308060]	uncertain significance	11	64835775	64835775	Human		name
598167443	CV3951015	single nucleotide variant	NM_017525.3(CDC42BPG):c.1300C>G (p.Gln434Glu)	not specified [RCV005308065]	uncertain significance	11	64836925	64836925	Human		name
598167448	CV3951016	single nucleotide variant	NM_017525.3(CDC42BPG):c.2785G>A (p.Val929Met)	not specified [RCV005308066]	uncertain significance	11	64832906	64832906	Human		name
598229353	CV3951017	single nucleotide variant	NM_017525.3(CDC42BPG):c.2859T>G (p.Phe953Leu)	not specified [RCV005319209]	uncertain significance	11	64832832	64832832	Human		name
598167465	CV3951020	single nucleotide variant	NM_017525.3(CDC42BPG):c.2395C>T (p.Arg799Trp)	not specified [RCV005308069]	uncertain significance	11	64834284	64834284	Human		name
598229361	CV3951021	single nucleotide variant	NM_017525.3(CDC42BPG):c.1733G>A (p.Arg578His)	not specified [RCV005319210]	uncertain significance	11	64835787	64835787	Human		name
598167477	CV3951024	single nucleotide variant	NM_017525.3(CDC42BPG):c.2752A>G (p.Thr918Ala)	not specified [RCV005308071]	uncertain significance	11	64832939	64832939	Human		name
598167490	CV3951028	single nucleotide variant	NM_017525.3(CDC42BPG):c.2108C>T (p.Thr703Ile)	not specified [RCV005308073]	uncertain significance	11	64834916	64834916	Human		name
598167495	CV3951029	single nucleotide variant	NM_017525.3(CDC42BPG):c.1237G>A (p.Ala413Thr)	not specified [RCV005308074]	uncertain significance	11	64836988	64836988	Human		name
598167514	CV3951032	single nucleotide variant	NM_017525.3(CDC42BPG):c.2579G>T (p.Arg860Ile)	not specified [RCV005308077]	uncertain significance	11	64833646	64833646	Human		name
598167521	CV3951033	single nucleotide variant	NM_017525.3(CDC42BPG):c.2066A>G (p.Asn689Ser)	not specified [RCV005308078]	uncertain significance	11	64834958	64834958	Human		name
15117253	CV713004	single nucleotide variant	NM_017525.3(CDC42BPG):c.1401G>C (p.Lys467Asn)	not provided [RCV000962173]	benign	11	64836514	64836514	Human		name
8634281	CV89501	single nucleotide variant	NM_017525.2(CDC42BPG):c.1292G>A (p.Arg431Lys)	Malignant melanoma [RCV000069598]	not provided	11	64836933	64836933	Human		name
156080983	CV2195381	single nucleotide variant	NM_017525.3(CDC42BPG):c.4091C>A (p.Ser1364Tyr)	not specified [RCV004080296]	uncertain significance	11	64827586	64827586	Human		name
156085123	CV2205639	single nucleotide variant	NM_017525.3(CDC42BPG):c.4360G>T (p.Gly1454Trp)	not specified [RCV004082549]	uncertain significance	11	64827079	64827079	Human		name
155965074	CV2206316	single nucleotide variant	NM_017525.3(CDC42BPG):c.4334A>G (p.His1445Arg)	not specified [RCV004078656]	uncertain significance	11	64827105	64827105	Human		name
156236996	CV2206758	single nucleotide variant	NM_017525.3(CDC42BPG):c.3167G>A (p.Arg1056His)	not specified [RCV004083446]	uncertain significance	11	64831642	64831642	Human		name
156150355	CV2235007	single nucleotide variant	NM_017525.3(CDC42BPG):c.3653G>A (p.Arg1218His)	not specified [RCV004113197]	uncertain significance	11	64829785	64829785	Human		name
155951185	CV2238744	single nucleotide variant	NM_017525.3(CDC42BPG):c.3086G>A (p.Arg1029Lys)	not specified [RCV004109676]	uncertain significance	11	64832429	64832429	Human		name
155922356	CV2240675	single nucleotide variant	NM_017525.3(CDC42BPG):c.4051G>A (p.Val1351Met)	not specified [RCV004119306]	uncertain significance	11	64827700	64827700	Human		name
155926589	CV2258819	single nucleotide variant	NM_017525.3(CDC42BPG):c.3112C>G (p.Pro1038Ala)	not specified [RCV004118039]	uncertain significance	11	64831697	64831697	Human		name
156256358	CV2264795	single nucleotide variant	NM_017525.3(CDC42BPG):c.3038C>T (p.Ala1013Val)	not specified [RCV004132767]	uncertain significance	11	64832477	64832477	Human		name
156144201	CV2292194	single nucleotide variant	NM_017525.3(CDC42BPG):c.4177C>T (p.Leu1393Phe)	not specified [RCV004148244]	uncertain significance	11	64827372	64827372	Human		name
156000206	CV2296284	single nucleotide variant	NM_017525.3(CDC42BPG):c.3446G>A (p.Cys1149Tyr)	not specified [RCV004154186]	uncertain significance	11	64829992	64829992	Human		name
155905472	CV2303121	single nucleotide variant	NM_017525.3(CDC42BPG):c.3631G>A (p.Gly1211Ser)	not specified [RCV004156897]	uncertain significance	11	64829807	64829807	Human		name
156105149	CV2307304	single nucleotide variant	NM_017525.3(CDC42BPG):c.3045T>A (p.Asp1015Glu)	not specified [RCV004165999]	uncertain significance	11	64832470	64832470	Human		name
155965030	CV2308451	single nucleotide variant	NM_017525.3(CDC42BPG):c.4384T>A (p.Ser1462Thr)	not specified [RCV004166746]	uncertain significance	11	64827055	64827055	Human		name
156277325	CV2316602	single nucleotide variant	NM_017525.3(CDC42BPG):c.3359G>A (p.Arg1120His)	not specified [RCV004171850]	likely benign	11	64830202	64830202	Human		name
156358428	CV2318493	single nucleotide variant	NM_017525.3(CDC42BPG):c.4580C>G (p.Pro1527Arg)	not specified [RCV004173135]	uncertain significance	11	64826489	64826489	Human		name
156331998	CV2339718	single nucleotide variant	NM_017525.3(CDC42BPG):c.3571C>G (p.Arg1191Gly)	not specified [RCV004196420]	uncertain significance	11	64829867	64829867	Human		name
156402080	CV2367951	single nucleotide variant	NM_017525.3(CDC42BPG):c.4465C>G (p.Arg1489Gly)	not specified [RCV004223044]	uncertain significance	11	64826719	64826719	Human		name
156131253	CV2372792	single nucleotide variant	NM_017525.3(CDC42BPG):c.3140T>G (p.Leu1047Arg)	not specified [RCV004221977]	uncertain significance	11	64831669	64831669	Human		name
156094473	CV2377740	single nucleotide variant	NM_017525.3(CDC42BPG):c.3578C>T (p.Pro1193Leu)	not specified [RCV004230327]	uncertain significance	11	64829860	64829860	Human		name
156071023	CV2381358	single nucleotide variant	NM_017525.3(CDC42BPG):c.3011C>T (p.Pro1004Leu)	not specified [RCV004227412]	uncertain significance	11	64832504	64832504	Human		name
156132438	CV2382735	single nucleotide variant	NM_017525.3(CDC42BPG):c.4082C>G (p.Pro1361Arg)	not specified [RCV004224085]	uncertain significance	11	64827595	64827595	Human		name
329356800	CV2431152	single nucleotide variant	NM_017525.3(CDC42BPG):c.4138A>G (p.Asn1380Asp)	not specified [RCV004250504]	uncertain significance	11	64827539	64827539	Human		name
329359977	CV2446504	single nucleotide variant	NM_017525.3(CDC42BPG):c.3650G>A (p.Arg1217His)	not specified [RCV004251406]	uncertain significance	11	64829788	64829788	Human		name
329402107	CV2453980	single nucleotide variant	NM_017525.3(CDC42BPG):c.4228T>G (p.Phe1410Val)	not specified [RCV004271647]	uncertain significance	11	64827321	64827321	Human		name
329371801	CV2454896	single nucleotide variant	NM_017525.3(CDC42BPG):c.4217G>A (p.Ser1406Asn)	not specified [RCV004270392]	uncertain significance	11	64827332	64827332	Human		name
329397828	CV2464057	single nucleotide variant	NM_017525.3(CDC42BPG):c.4510C>G (p.Pro1504Ala)	not specified [RCV004273762]	uncertain significance	11	64826674	64826674	Human		name
329397873	CV2466393	single nucleotide variant	NM_017525.3(CDC42BPG):c.4183G>C (p.Asp1395His)	not specified [RCV004273956]	uncertain significance	11	64827366	64827366	Human		name
401768455	CV2675350	single nucleotide variant	NM_017525.3(CDC42BPG):c.3122C>T (p.Thr1041Met)	not specified [RCV004292158]	uncertain significance	11	64831687	64831687	Human		name
401728060	CV2675934	single nucleotide variant	NM_017525.3(CDC42BPG):c.3232G>A (p.Val1078Met)	not specified [RCV004281931]	uncertain significance	11	64831577	64831577	Human		name
401742021	CV2677490	single nucleotide variant	NM_017525.3(CDC42BPG):c.3595G>A (p.Val1199Ile)	not specified [RCV004289557]	uncertain significance	11	64829843	64829843	Human		name
401743126	CV2684022	single nucleotide variant	NM_017525.3(CDC42BPG):c.4289C>G (p.Pro1430Arg)	not specified [RCV004295627]	uncertain significance	11	64827150	64827150	Human		name
401725253	CV2697333	single nucleotide variant	NM_017525.3(CDC42BPG):c.3226C>T (p.Arg1076Trp)	not specified [RCV004304088]	uncertain significance	11	64831583	64831583	Human		name
401764030	CV2717202	single nucleotide variant	NM_017525.3(CDC42BPG):c.3652C>T (p.Arg1218Cys)	not specified [RCV004324057]	uncertain significance	11	64829786	64829786	Human		name
401779350	CV2718509	single nucleotide variant	NM_017525.3(CDC42BPG):c.3931C>T (p.His1311Tyr)	not specified [RCV004318316]	uncertain significance	11	64829507	64829507	Human		name
401864786	CV2761045	single nucleotide variant	NM_017525.3(CDC42BPG):c.3649C>T (p.Arg1217Cys)	not specified [RCV004338711]	uncertain significance	11	64829789	64829789	Human		name
401879833	CV2788527	single nucleotide variant	NM_017525.3(CDC42BPG):c.4240G>T (p.Val1414Leu)	not specified [RCV004359502]	uncertain significance	11	64827309	64827309	Human		name
405773885	CV3296201	single nucleotide variant	NM_017525.3(CDC42BPG):c.3166C>T (p.Arg1056Cys)	not specified [RCV004435766]	uncertain significance	11	64831643	64831643	Human		name
405773891	CV3296202	single nucleotide variant	NM_017525.3(CDC42BPG):c.3212C>T (p.Ala1071Val)	not specified [RCV004435767]	uncertain significance	11	64831597	64831597	Human		name
405773900	CV3296203	single nucleotide variant	NM_017525.3(CDC42BPG):c.3292G>A (p.Ala1098Thr)	not specified [RCV004435768]	uncertain significance	11	64831517	64831517	Human		name
405773913	CV3296205	single nucleotide variant	NM_017525.3(CDC42BPG):c.3529C>G (p.Arg1177Gly)	not specified [RCV004435770]	uncertain significance	11	64829909	64829909	Human		name
405773918	CV3296206	single nucleotide variant	NM_017525.3(CDC42BPG):c.3536G>A (p.Cys1179Tyr)	not specified [RCV004435771]	uncertain significance	11	64829902	64829902	Human		name
405773924	CV3296207	single nucleotide variant	NM_017525.3(CDC42BPG):c.3643T>C (p.Trp1215Arg)	not specified [RCV004435772]	uncertain significance	11	64829795	64829795	Human		name
405773930	CV3296208	single nucleotide variant	NM_017525.3(CDC42BPG):c.3727G>A (p.Ala1243Thr)	not specified [RCV004435773]	uncertain significance	11	64829711	64829711	Human		name
405773936	CV3296209	single nucleotide variant	NM_017525.3(CDC42BPG):c.3784G>A (p.Ala1262Thr)	not specified [RCV004435774]	uncertain significance	11	64829654	64829654	Human		name
405773945	CV3296210	single nucleotide variant	NM_017525.3(CDC42BPG):c.4057C>T (p.Leu1353Phe)	not specified [RCV004435775]	uncertain significance	11	64827694	64827694	Human		name
405773952	CV3296211	single nucleotide variant	NM_017525.3(CDC42BPG):c.4096T>G (p.Phe1366Val)	not specified [RCV004435776]	uncertain significance	11	64827581	64827581	Human		name
405773962	CV3296213	single nucleotide variant	NM_017525.3(CDC42BPG):c.4322C>G (p.Thr1441Ser)	not specified [RCV004435778]	uncertain significance	11	64827117	64827117	Human		name
407498652	CV3425129	single nucleotide variant	NM_017525.3(CDC42BPG):c.3820G>A (p.Gly1274Arg)	not specified [RCV004606698]	uncertain significance	11	64829618	64829618	Human		name
407498656	CV3425130	single nucleotide variant	NM_017525.3(CDC42BPG):c.3214C>T (p.Arg1072Trp)	not specified [RCV004606699]	uncertain significance	11	64831595	64831595	Human		name
407454725	CV3425132	single nucleotide variant	NM_017525.3(CDC42BPG):c.4453G>A (p.Glu1485Lys)	not specified [RCV004609960]	uncertain significance	11	64826731	64826731	Human		name
407498682	CV3425139	single nucleotide variant	NM_017525.3(CDC42BPG):c.4187A>G (p.Asn1396Ser)	not specified [RCV004606704]	uncertain significance	11	64827362	64827362	Human		name
407498686	CV3425140	single nucleotide variant	NM_017525.3(CDC42BPG):c.4409G>A (p.Arg1470Gln)	not specified [RCV004606705]	uncertain significance	11	64826775	64826775	Human		name
407498696	CV3425142	single nucleotide variant	NM_017525.3(CDC42BPG):c.3857G>A (p.Ser1286Asn)	not specified [RCV004606707]	uncertain significance	11	64829581	64829581	Human		name
597787930	CV3644857	single nucleotide variant	NM_017525.3(CDC42BPG):c.4609C>T (p.Arg1537Trp)	not specified [RCV004901349]	uncertain significance	11	64824520	64824520	Human		name
597787943	CV3644861	single nucleotide variant	NM_017525.3(CDC42BPG):c.3254A>G (p.Tyr1085Cys)	not specified [RCV004901353]	uncertain significance	11	64831555	64831555	Human		name
597787947	CV3644862	single nucleotide variant	NM_017525.3(CDC42BPG):c.3331G>A (p.Glu1111Lys)	not specified [RCV004901354]	uncertain significance	11	64830230	64830230	Human		name
597787955	CV3644864	single nucleotide variant	NM_017525.3(CDC42BPG):c.4462C>T (p.Arg1488Trp)	not specified [RCV004901356]	uncertain significance	11	64826722	64826722	Human		name
597787967	CV3644867	single nucleotide variant	NM_017525.3(CDC42BPG):c.3269C>T (p.Pro1090Leu)	not specified [RCV004901359]	uncertain significance	11	64831540	64831540	Human		name
597787972	CV3644868	single nucleotide variant	NM_017525.3(CDC42BPG):c.3197G>A (p.Arg1066Gln)	not specified [RCV004901360]	uncertain significance	11	64831612	64831612	Human		name
597787975	CV3644869	single nucleotide variant	NM_017525.3(CDC42BPG):c.3466C>T (p.Arg1156Cys)	not specified [RCV004901361]	uncertain significance	11	64829972	64829972	Human		name
597787983	CV3644871	single nucleotide variant	NM_017525.3(CDC42BPG):c.3518T>C (p.Ile1173Thr)	not specified [RCV004901363]	uncertain significance	11	64829920	64829920	Human		name
597787986	CV3644872	single nucleotide variant	NM_017525.3(CDC42BPG):c.3740C>G (p.Ala1247Gly)	not specified [RCV004901364]	uncertain significance	11	64829698	64829698	Human		name
597787999	CV3644875	single nucleotide variant	NM_017525.3(CDC42BPG):c.3215G>A (p.Arg1072Gln)	not specified [RCV004901367]	uncertain significance	11	64831594	64831594	Human		name
598167419	CV3951011	single nucleotide variant	NM_017525.3(CDC42BPG):c.3916C>T (p.Arg1306Cys)	not specified [RCV005308061]	uncertain significance	11	64829522	64829522	Human		name
598167429	CV3951013	single nucleotide variant	NM_017525.3(CDC42BPG):c.3394C>T (p.Arg1132Cys)	not specified [RCV005308063]	uncertain significance	11	64830044	64830044	Human		name
598167436	CV3951014	single nucleotide variant	NM_017525.3(CDC42BPG):c.3617A>G (p.Tyr1206Cys)	not specified [RCV005308064]	uncertain significance	11	64829821	64829821	Human		name
598167455	CV3951018	single nucleotide variant	NM_017525.3(CDC42BPG):c.4165G>A (p.Asp1389Asn)	not specified [RCV005308067]	uncertain significance	11	64827384	64827384	Human		name
598167460	CV3951019	single nucleotide variant	NM_017525.3(CDC42BPG):c.3725C>T (p.Ala1242Val)	not specified [RCV005308068]	uncertain significance	11	64829713	64829713	Human		name
598229366	CV3951022	single nucleotide variant	NM_017525.3(CDC42BPG):c.3626G>T (p.Gly1209Val)	not specified [RCV005319211]	uncertain significance	11	64829812	64829812	Human		name
598167483	CV3951025	single nucleotide variant	NM_017525.3(CDC42BPG):c.3554G>A (p.Gly1185Glu)	not specified [RCV005308072]	uncertain significance	11	64829884	64829884	Human		name
598229372	CV3951026	single nucleotide variant	NM_017525.3(CDC42BPG):c.4448T>G (p.Phe1483Cys)	not specified [RCV005319212]	uncertain significance	11	64826736	64826736	Human		name
598167500	CV3951030	single nucleotide variant	NM_017525.3(CDC42BPG):c.4388C>G (p.Pro1463Arg)	not specified [RCV005308075]	likely benign	11	64827051	64827051	Human		name
598167507	CV3951031	single nucleotide variant	NM_017525.3(CDC42BPG):c.4517A>G (p.Lys1506Arg)	not specified [RCV005308076]	uncertain significance	11	64826552	64826552	Human		name
598167534	CV3951035	single nucleotide variant	NM_017525.3(CDC42BPG):c.4135A>G (p.Arg1379Gly)	not specified [RCV005308080]	uncertain significance	11	64827542	64827542	Human		name

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