Kcp Variant Search Result - Rat Genome Database

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172 records found for search term Kcp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405788070	CV3265096	single nucleotide variant	NM_001366122.1(KCP):c.13G>A (p.Gly5Arg)	not specified [RCV004398924]	likely benign	7	128910664	128910664	Human		name
598235845	CV3976373	single nucleotide variant	NM_001366122.1(KCP):c.25C>G (p.Leu9Val)	not specified [RCV005363736]	uncertain significance	7	128910652	128910652	Human		name
405812262	CV3265124	single nucleotide variant	NM_001366122.1(KCP):c.49G>T (p.Ala17Ser)	not specified [RCV004408864]	uncertain significance	7	128910628	128910628	Human		name
598270198	CV3976363	single nucleotide variant	NM_001366122.1(KCP):c.52C>G (p.Leu18Val)	not specified [RCV005350056]	likely benign	7	128910625	128910625	Human		name
597796524	CV3694839	single nucleotide variant	NM_001366122.1(KCP):c.952C>T (p.Arg318Cys)	not specified [RCV004935497]	uncertain significance	7	128894029	128894029	Human		name
597796533	CV3694845	single nucleotide variant	NM_001366122.1(KCP):c.961G>A (p.Glu321Lys)	not specified [RCV004935500]	uncertain significance	7	128894020	128894020	Human		name
597796578	CV3694862	single nucleotide variant	NM_001366122.1(KCP):c.385C>G (p.Gln129Glu)	not specified [RCV004935514]	uncertain significance	7	128907288	128907288	Human		name
598235860	CV3976379	single nucleotide variant	NM_001366122.1(KCP):c.914C>T (p.Pro305Leu)	not specified [RCV005363739]	uncertain significance	7	128894211	128894211	Human		name
156398509	CV2194611	single nucleotide variant	NM_001366122.1(KCP):c.1662C>A (p.Ser554Arg)	not specified [RCV004082019]	likely benign	7	128891779	128891779	Human		name
156069791	CV2203840	single nucleotide variant	NM_001366122.1(KCP):c.2840G>A (p.Arg947Gln)	not specified [RCV004069902]	likely benign	7	128886490	128886490	Human		name
156113336	CV2212692	single nucleotide variant	NM_001366122.1(KCP):c.2518C>T (p.Arg840Cys)	not specified [RCV004085198]	uncertain significance	7	128887295	128887295	Human		name
156227128	CV2216119	single nucleotide variant	NM_001366122.1(KCP):c.2015A>C (p.His672Pro)	not specified [RCV004097126]	likely benign	7	128891054	128891054	Human		name
156401781	CV2217734	single nucleotide variant	NM_001366122.1(KCP):c.2044C>T (p.Pro682Ser)	not specified [RCV004083914]	uncertain significance	7	128891025	128891025	Human		name
156172504	CV2247522	single nucleotide variant	NM_001366122.1(KCP):c.1060C>T (p.Pro354Ser)	not specified [RCV004108836]	uncertain significance	7	128893845	128893845	Human		name
156300059	CV2248754	single nucleotide variant	NM_001366122.1(KCP):c.1532G>C (p.Gly511Ala)	not specified [RCV004121910]	uncertain significance	7	128892603	128892603	Human		name
156300092	CV2248758	single nucleotide variant	NM_001366122.1(KCP):c.2924G>A (p.Ser975Asn)	not specified [RCV004121914]	uncertain significance	7	128885213	128885213	Human		name
156146375	CV2265124	single nucleotide variant	NM_001366122.1(KCP):c.1873T>C (p.Cys625Arg)	not specified [RCV004126259]	uncertain significance	7	128891456	128891456	Human		name
156154509	CV2266080	single nucleotide variant	NM_001366122.1(KCP):c.2531T>C (p.Val844Ala)	not specified [RCV004126890]	uncertain significance	7	128887282	128887282	Human		name
156049172	CV2271779	single nucleotide variant	NM_001366122.1(KCP):c.2273A>G (p.Lys758Arg)	not specified [RCV004130618]	likely benign	7	128890405	128890405	Human		name
156073733	CV2281392	single nucleotide variant	NM_001366122.1(KCP):c.1290G>T (p.Glu430Asp)	not specified [RCV004153731]	uncertain significance	7	128892999	128892999	Human		name
156076513	CV2291521	single nucleotide variant	NM_001366122.1(KCP):c.2635C>T (p.Pro879Ser)	not specified [RCV004155827]	uncertain significance	7	128886930	128886930	Human		name
156292750	CV2296859	single nucleotide variant	NM_001366122.1(KCP):c.2611C>T (p.Arg871Cys)	not specified [RCV004148740]	uncertain significance	7	128886954	128886954	Human		name
156039934	CV2310753	single nucleotide variant	NM_001366122.1(KCP):c.1256A>G (p.Gln419Arg)	not specified [RCV004157682]	uncertain significance	7	128893249	128893249	Human		name
156273496	CV2320190	single nucleotide variant	NM_001366122.1(KCP):c.2395C>T (p.Pro799Ser)	not specified [RCV004169813]	uncertain significance	7	128888980	128888980	Human		name
156163219	CV2323593	single nucleotide variant	NM_001366122.1(KCP):c.2510A>C (p.Gln837Pro)	not specified [RCV004165783]	uncertain significance	7	128888865	128888865	Human		name
156198540	CV2331071	single nucleotide variant	NM_001366122.1(KCP):c.1324C>T (p.Arg442Trp)	not specified [RCV004181685]	uncertain significance	7	128892965	128892965	Human		name
156172323	CV2337589	single nucleotide variant	NM_001366122.1(KCP):c.1325G>A (p.Arg442Gln)	not specified [RCV004181153]	likely benign	7	128892964	128892964	Human		name
155976600	CV2342789	single nucleotide variant	NM_001366122.1(KCP):c.2312G>A (p.Gly771Asp)	not specified [RCV004189831]	uncertain significance	7	128890366	128890366	Human		name
155920142	CV2343297	single nucleotide variant	NM_001366122.1(KCP):c.2740C>T (p.Pro914Ser)	not specified [RCV004194917]	uncertain significance	7	128886687	128886687	Human		name
156123552	CV2350034	single nucleotide variant	NM_001366122.1(KCP):c.1342G>A (p.Val448Ile)	not specified [RCV004199960]	likely benign	7	128892947	128892947	Human		name
156238841	CV2356295	single nucleotide variant	NM_001366122.1(KCP):c.2703G>C (p.Gln901His)	not specified [RCV004206105]	uncertain significance	7	128886724	128886724	Human		name
156015278	CV2360246	single nucleotide variant	NM_001366122.1(KCP):c.1916C>A (p.Pro639Gln)	not specified [RCV004208593]	uncertain significance	7	128891241	128891241	Human		name
156385944	CV2364612	single nucleotide variant	NM_001366122.1(KCP):c.2950G>A (p.Glu984Lys)	not specified [RCV004219506]	uncertain significance	7	128885187	128885187	Human		name
156260916	CV2381249	single nucleotide variant	NM_001366122.1(KCP):c.2972G>A (p.Arg991His)	not specified [RCV004227314]	uncertain significance	7	128885165	128885165	Human		name
156154838	CV2388743	single nucleotide variant	NM_001366122.1(KCP):c.2510A>G (p.Gln837Arg)	not specified [RCV004239608]	uncertain significance	7	128888865	128888865	Human		name
329399730	CV2444119	single nucleotide variant	NM_001366122.1(KCP):c.2128C>T (p.His710Tyr)	not specified [RCV004260860]	uncertain significance	7	128890941	128890941	Human		name
329352447	CV2453037	single nucleotide variant	NM_001366122.1(KCP):c.2314G>A (p.Asp772Asn)	not specified [RCV004277653]	uncertain significance	7	128890364	128890364	Human		name
329402311	CV2454129	single nucleotide variant	NM_001366122.1(KCP):c.2134C>T (p.Arg712Cys)	not specified [RCV004265626]	uncertain significance	7	128890935	128890935	Human		name
401760096	CV2694921	single nucleotide variant	NM_001366122.1(KCP):c.1870C>T (p.Arg624Cys)	not specified [RCV004301310]	uncertain significance	7	128891459	128891459	Human		name
401758096	CV2704169	single nucleotide variant	NM_001366122.1(KCP):c.2708G>A (p.Arg903Gln)	not specified [RCV004311181]	likely benign	7	128886719	128886719	Human		name
401763379	CV2714534	single nucleotide variant	NM_001366122.1(KCP):c.2633C>T (p.Pro878Leu)	not specified [RCV004318051]	uncertain significance	7	128886932	128886932	Human		name
401771795	CV2722949	single nucleotide variant	NM_001366122.1(KCP):c.2428G>A (p.Val810Met)	not specified [RCV004327128]	uncertain significance	7	128888947	128888947	Human		name
401874204	CV2754641	single nucleotide variant	NM_001366122.1(KCP):c.2218A>G (p.Thr740Ala)	not specified [RCV004339314]	uncertain significance	7	128890460	128890460	Human		name
401883299	CV2760891	single nucleotide variant	NM_001366122.1(KCP):c.1340G>A (p.Cys447Tyr)	not specified [RCV004336526]	uncertain significance	7	128892949	128892949	Human		name
401880137	CV2769938	single nucleotide variant	NM_001366122.1(KCP):c.1220C>G (p.Pro407Arg)	not specified [RCV004353776]	uncertain significance	7	128893285	128893285	Human		name
401891247	CV2774921	single nucleotide variant	NM_001366122.1(KCP):c.1157G>A (p.Arg386Gln)	not specified [RCV004346332]	uncertain significance	7	128893419	128893419	Human		name
405788043	CV3265090	single nucleotide variant	NM_001366122.1(KCP):c.1290G>C (p.Glu430Asp)	not specified [RCV004398918]	uncertain significance	7	128892999	128892999	Human		name
405788047	CV3265091	single nucleotide variant	NM_001366122.1(KCP):c.1331G>C (p.Cys444Ser)	not specified [RCV004398919]	uncertain significance	7	128892958	128892958	Human		name
405788052	CV3265092	single nucleotide variant	NM_001366122.1(KCP):c.1346G>A (p.Cys449Tyr)	not specified [RCV004398920]	uncertain significance	7	128892943	128892943	Human		name
405788057	CV3265093	single nucleotide variant	NM_001366122.1(KCP):c.1406C>G (p.Pro469Arg)	not specified [RCV004398921]	uncertain significance	7	128892883	128892883	Human		name
405788060	CV3265094	single nucleotide variant	NM_001366122.1(KCP):c.1409C>T (p.Thr470Ile)	not specified [RCV004398922]	uncertain significance	7	128892880	128892880	Human		name
405788065	CV3265095	single nucleotide variant	NM_001366122.1(KCP):c.1535C>T (p.Thr512Ile)	not specified [RCV004398923]	uncertain significance	7	128892600	128892600	Human		name
405788076	CV3265097	single nucleotide variant	NM_001366122.1(KCP):c.1609C>T (p.Pro537Ser)	not specified [RCV004398925]	uncertain significance	7	128892526	128892526	Human		name
405788082	CV3265098	single nucleotide variant	NM_001366122.1(KCP):c.1616G>A (p.Cys539Tyr)	not specified [RCV004398926]	uncertain significance	7	128892519	128892519	Human		name
405788087	CV3265099	single nucleotide variant	NM_001366122.1(KCP):c.1841C>T (p.Pro614Leu)	not specified [RCV004398927]	uncertain significance	7	128891488	128891488	Human		name
405788091	CV3265100	single nucleotide variant	NM_001366122.1(KCP):c.1874G>A (p.Cys625Tyr)	not specified [RCV004398928]	uncertain significance	7	128891455	128891455	Human		name
405788096	CV3265101	single nucleotide variant	NM_001366122.1(KCP):c.2140G>A (p.Gly714Arg)	not specified [RCV004398929]	uncertain significance	7	128890929	128890929	Human		name
405788101	CV3265102	single nucleotide variant	NM_001366122.1(KCP):c.2152C>A (p.Pro718Thr)	not specified [RCV004398930]	uncertain significance	7	128890917	128890917	Human		name
405788106	CV3265103	single nucleotide variant	NM_001366122.1(KCP):c.2184G>T (p.Lys728Asn)	not specified [RCV004398931]	uncertain significance	7	128890494	128890494	Human		name
405788111	CV3265104	single nucleotide variant	NM_001366122.1(KCP):c.2612G>A (p.Arg871His)	not specified [RCV004398932]	uncertain significance	7	128886953	128886953	Human		name
405788115	CV3265105	single nucleotide variant	NM_001366122.1(KCP):c.2650C>T (p.His884Tyr)	not specified [RCV004398933]	uncertain significance	7	128886915	128886915	Human		name
405788121	CV3265106	single nucleotide variant	NM_001366122.1(KCP):c.2774C>T (p.Ala925Val)	not specified [RCV004398934]	uncertain significance	7	128886556	128886556	Human		name
405788126	CV3265107	single nucleotide variant	NM_001366122.1(KCP):c.2836G>A (p.Glu946Lys)	not specified [RCV004398935]	uncertain significance	7	128886494	128886494	Human		name
405812228	CV3265108	single nucleotide variant	NM_001366122.1(KCP):c.2851T>G (p.Cys951Gly)	not specified [RCV004408848]	uncertain significance	7	128886479	128886479	Human		name
405812230	CV3265109	single nucleotide variant	NM_001366122.1(KCP):c.2995G>A (p.Ala999Thr)	not specified [RCV004408849]	uncertain significance	7	128885142	128885142	Human		name
405812264	CV3265125	single nucleotide variant	NM_001366122.1(KCP):c.1160G>A (p.Gly387Asp)	not specified [RCV004408865]	uncertain significance	7	128893416	128893416	Human		name
407516668	CV3445203	single nucleotide variant	NM_001366122.1(KCP):c.1172G>A (p.Arg391His)	not specified [RCV004628275]	uncertain significance	7	128893404	128893404	Human		name
407516671	CV3445205	single nucleotide variant	NM_001366122.1(KCP):c.2842G>A (p.Gly948Arg)	not specified [RCV004628276]	uncertain significance	7	128886488	128886488	Human		name
407516677	CV3445207	single nucleotide variant	NM_001366122.1(KCP):c.1655G>A (p.Gly552Asp)	not specified [RCV004628278]	uncertain significance	7	128891786	128891786	Human		name
597767280	CV3694836	single nucleotide variant	NM_001366122.1(KCP):c.1886A>C (p.Asn629Thr)	not specified [RCV004927251]	uncertain significance	7	128891271	128891271	Human		name
597796521	CV3694838	single nucleotide variant	NM_001366122.1(KCP):c.1922C>A (p.Pro641His)	not specified [RCV004935496]	uncertain significance	7	128891235	128891235	Human		name
597767285	CV3694841	single nucleotide variant	NM_001366122.1(KCP):c.1912G>C (p.Val638Leu)	not specified [RCV004927252]	uncertain significance	7	128891245	128891245	Human		name
597796530	CV3694844	single nucleotide variant	NM_001366122.1(KCP):c.2870G>T (p.Cys957Phe)	not specified [RCV004935499]	uncertain significance	7	128885267	128885267	Human		name
597796537	CV3694846	single nucleotide variant	NM_001366122.1(KCP):c.1285G>A (p.Glu429Lys)	not specified [RCV004935501]	uncertain significance	7	128893004	128893004	Human		name
597796546	CV3694849	single nucleotide variant	NM_001366122.1(KCP):c.1886A>G (p.Asn629Ser)	not specified [RCV004935504]	uncertain significance	7	128891271	128891271	Human		name
597796549	CV3694850	single nucleotide variant	NM_001366122.1(KCP):c.2603G>A (p.Gly868Asp)	not specified [RCV004935505]	uncertain significance	7	128886962	128886962	Human		name
597796552	CV3694851	single nucleotide variant	NM_001366122.1(KCP):c.2444G>A (p.Arg815Gln)	not specified [RCV004935506]	uncertain significance	7	128888931	128888931	Human		name
597796559	CV3694856	single nucleotide variant	NM_001366122.1(KCP):c.1423G>A (p.Ala475Thr)	not specified [RCV004935508]	uncertain significance	7	128892792	128892792	Human		name
597796565	CV3694858	single nucleotide variant	NM_001366122.1(KCP):c.1658A>T (p.Glu553Val)	not specified [RCV004935510]	uncertain significance	7	128891783	128891783	Human		name
597796575	CV3694861	single nucleotide variant	NM_001366122.1(KCP):c.2639C>T (p.Ala880Val)	not specified [RCV004935513]	uncertain significance	7	128886926	128886926	Human		name
597796582	CV3694863	single nucleotide variant	NM_001366122.1(KCP):c.2500C>T (p.Pro834Ser)	not specified [RCV004935515]	uncertain significance	7	128888875	128888875	Human		name
597767299	CV3694867	single nucleotide variant	NM_001366122.1(KCP):c.2202G>C (p.Glu734Asp)	not specified [RCV004927255]	uncertain significance	7	128890476	128890476	Human		name
597796591	CV3694868	single nucleotide variant	NM_001366122.1(KCP):c.1418C>G (p.Pro473Arg)	not specified [RCV004935518]	uncertain significance	7	128892871	128892871	Human		name
598270194	CV3976362	single nucleotide variant	NM_001366122.1(KCP):c.1490C>T (p.Thr497Met)	not specified [RCV005350055]	uncertain significance	7	128892725	128892725	Human		name
598213211	CV3976367	single nucleotide variant	NM_001366122.1(KCP):c.2437G>A (p.Gly813Ser)	not specified [RCV005358954]	likely benign	7	128888938	128888938	Human		name
598235829	CV3976368	single nucleotide variant	NM_001366122.1(KCP):c.2995G>T (p.Ala999Ser)	not specified [RCV005363733]	uncertain significance	7	128885142	128885142	Human		name
598213216	CV3976372	single nucleotide variant	NM_001366122.1(KCP):c.1171C>T (p.Arg391Cys)	not specified [RCV005358955]	uncertain significance	7	128893405	128893405	Human		name
598270213	CV3976374	single nucleotide variant	NM_001366122.1(KCP):c.1598G>A (p.Gly533Asp)	not specified [RCV005350059]	uncertain significance	7	128892537	128892537	Human		name
598235850	CV3976376	single nucleotide variant	NM_001366122.1(KCP):c.2615G>T (p.Cys872Phe)	not specified [RCV005363737]	uncertain significance	7	128886950	128886950	Human		name
156398729	CV2194754	single nucleotide variant	NM_001366122.1(KCP):c.4589C>T (p.Thr1530Ile)	not specified [RCV004075303]	uncertain significance	7	128877513	128877513	Human		name
156169166	CV2197760	single nucleotide variant	NM_001366122.1(KCP):c.4678C>T (p.Arg1560Cys)	not specified [RCV004074959]	uncertain significance	7	128877252	128877252	Human		name
155921977	CV2207360	single nucleotide variant	NM_001366122.1(KCP):c.3866G>A (p.Arg1289His)	not specified [RCV004088066]	uncertain significance	7	128879979	128879979	Human		name
155942498	CV2225745	single nucleotide variant	NM_001366122.1(KCP):c.3944C>A (p.Thr1315Asn)	not specified [RCV004103159]	uncertain significance	7	128879818	128879818	Human		name
156226493	CV2226449	single nucleotide variant	NM_001366122.1(KCP):c.3732G>T (p.Gln1244His)	not specified [RCV004099657]	uncertain significance	7	128880413	128880413	Human		name
156388808	CV2229674	single nucleotide variant	NM_001366122.1(KCP):c.3733C>T (p.Arg1245Cys)	not specified [RCV004103483]	uncertain significance	7	128880412	128880412	Human		name
155975497	CV2231355	single nucleotide variant	NM_001366122.1(KCP):c.4130C>T (p.Ala1377Val)	not specified [RCV004096450]	uncertain significance	7	128879538	128879538	Human		name
156285345	CV2232816	single nucleotide variant	NM_001366122.1(KCP):c.4219T>G (p.Cys1407Gly)	not specified [RCV004101441]	uncertain significance	7	128878650	128878650	Human		name
156168655	CV2247262	single nucleotide variant	NM_001366122.1(KCP):c.4867G>A (p.Glu1623Lys)	not specified [RCV004115040]	uncertain significance	7	128877063	128877063	Human		name
156237119	CV2265073	single nucleotide variant	NM_001366122.1(KCP):c.4476C>A (p.Phe1492Leu)	not specified [RCV004126222]	uncertain significance	7	128877626	128877626	Human		name
155975935	CV2270126	single nucleotide variant	NM_001366122.1(KCP):c.3208C>G (p.Pro1070Ala)	not specified [RCV004129078]	uncertain significance	7	128884038	128884038	Human		name
156136548	CV2284825	single nucleotide variant	NM_001366122.1(KCP):c.3646C>A (p.Arg1216Ser)	not specified [RCV004143000]	uncertain significance	7	128880499	128880499	Human		name
155978834	CV2318189	single nucleotide variant	NM_001366122.1(KCP):c.4396C>T (p.Arg1466Cys)	not specified [RCV004179375]	uncertain significance	7	128877706	128877706	Human		name
156183958	CV2335482	single nucleotide variant	NM_001366122.1(KCP):c.4292C>T (p.Ala1431Val)	not specified [RCV004191652]	uncertain significance	7	128878577	128878577	Human		name
156305622	CV2338851	single nucleotide variant	NM_001366122.1(KCP):c.4411C>T (p.Arg1471Trp)	not specified [RCV004182406]	uncertain significance	7	128877691	128877691	Human		name
156331248	CV2339609	single nucleotide variant	NM_001366122.1(KCP):c.4367C>T (p.Pro1456Leu)	not specified [RCV004196319]	uncertain significance	7	128877735	128877735	Human		name
156193156	CV2344191	single nucleotide variant	NM_001366122.1(KCP):c.3415G>A (p.Val1139Ile)	not specified [RCV004195786]	uncertain significance	7	128881635	128881635	Human		name
155922676	CV2347361	single nucleotide variant	NM_001366122.1(KCP):c.4801G>A (p.Glu1601Lys)	not specified [RCV004207203]	uncertain significance	7	128877129	128877129	Human		name
156139033	CV2374269	single nucleotide variant	NM_001366122.1(KCP):c.4337G>A (p.Arg1446Gln)	not specified [RCV004229406]	likely benign	7	128877765	128877765	Human		name
156392113	CV2378289	single nucleotide variant	NM_001366122.1(KCP):c.4865G>A (p.Arg1622Gln)	not specified [RCV004226321]	likely benign	7	128877065	128877065	Human		name
155959379	CV2390521	single nucleotide variant	NM_001366122.1(KCP):c.4382G>T (p.Gly1461Val)	not specified [RCV004239057]	uncertain significance	7	128877720	128877720	Human		name
329386292	CV2428242	single nucleotide variant	NM_001366122.1(KCP):c.3851G>A (p.Arg1284His)	not specified [RCV004251273]	uncertain significance	7	128879994	128879994	Human		name
401739603	CV2684117	single nucleotide variant	NM_001366122.1(KCP):c.3907A>G (p.Lys1303Glu)	not specified [RCV004288798]	uncertain significance	7	128879938	128879938	Human		name
401759364	CV2690876	single nucleotide variant	NM_001366122.1(KCP):c.4441A>G (p.Ser1481Gly)	not specified [RCV004298577]	uncertain significance	7	128877661	128877661	Human		name
401759149	CV2694436	single nucleotide variant	NM_001366122.1(KCP):c.4336C>T (p.Arg1446Trp)	not specified [RCV004304609]	uncertain significance	7	128877766	128877766	Human		name
401730504	CV2711359	single nucleotide variant	NM_001366122.1(KCP):c.4289C>T (p.Ala1430Val)	not specified [RCV004313120]	uncertain significance	7	128878580	128878580	Human		name
401774777	CV2728267	single nucleotide variant	NM_001366122.1(KCP):c.3734G>A (p.Arg1245His)	not specified [RCV004326073]	uncertain significance	7	128880411	128880411	Human		name
401779029	CV2733071	single nucleotide variant	NM_001366122.1(KCP):c.4355G>A (p.Arg1452Gln)	not specified [RCV004332005]	uncertain significance	7	128877747	128877747	Human		name
401865240	CV2754146	single nucleotide variant	NM_001366122.1(KCP):c.3058C>T (p.Arg1020Trp)	not specified [RCV004334341]	uncertain significance	7	128884846	128884846	Human		name
401894570	CV2788449	single nucleotide variant	NM_001366122.1(KCP):c.4466C>T (p.Pro1489Leu)	not specified [RCV004354974]	uncertain significance	7	128877636	128877636	Human		name
401884548	CV2789716	single nucleotide variant	NM_001366122.1(KCP):c.3691A>G (p.Ser1231Gly)	not specified [RCV004361837]	uncertain significance	7	128880454	128880454	Human		name
405812233	CV3265110	single nucleotide variant	NM_001366122.1(KCP):c.3190C>A (p.Pro1064Thr)	not specified [RCV004408850]	uncertain significance	7	128884056	128884056	Human		name
405812237	CV3265112	single nucleotide variant	NM_001366122.1(KCP):c.3421C>T (p.Arg1141Trp)	not specified [RCV004408852]	uncertain significance	7	128881629	128881629	Human		name
405812239	CV3265113	single nucleotide variant	NM_001366122.1(KCP):c.3646C>T (p.Arg1216Cys)	not specified [RCV004408853]	uncertain significance	7	128880499	128880499	Human		name
405812241	CV3265114	single nucleotide variant	NM_001366122.1(KCP):c.3707C>T (p.Ala1236Val)	not specified [RCV004408854]	uncertain significance	7	128880438	128880438	Human		name
405812243	CV3265115	single nucleotide variant	NM_001366122.1(KCP):c.3800G>A (p.Arg1267His)	not specified [RCV004408855]	uncertain significance	7	128880045	128880045	Human		name
405812247	CV3265117	single nucleotide variant	NM_001366122.1(KCP):c.3962G>A (p.Arg1321Gln)	not specified [RCV004408857]	uncertain significance	7	128879800	128879800	Human		name
405812249	CV3265118	single nucleotide variant	NM_001366122.1(KCP):c.4010T>C (p.Met1337Thr)	not specified [RCV004408858]	uncertain significance	7	128879752	128879752	Human		name
405812251	CV3265119	single nucleotide variant	NM_001366122.1(KCP):c.4025T>A (p.Leu1342Gln)	not specified [RCV004408859]	uncertain significance	7	128879737	128879737	Human		name
405812253	CV3265120	single nucleotide variant	NM_001366122.1(KCP):c.4064C>T (p.Ala1355Val)	not specified [RCV004408860]	uncertain significance	7	128879604	128879604	Human		name
405812255	CV3265121	single nucleotide variant	NM_001366122.1(KCP):c.4444C>T (p.Arg1482Cys)	not specified [RCV004408861]	uncertain significance	7	128877658	128877658	Human		name
405812258	CV3265122	single nucleotide variant	NM_001366122.1(KCP):c.4483G>A (p.Ala1495Thr)	not specified [RCV004408862]	uncertain significance	7	128877619	128877619	Human		name
405812260	CV3265123	single nucleotide variant	NM_001366122.1(KCP):c.4601G>A (p.Arg1534Gln)	not specified [RCV004408863]	uncertain significance	7	128877501	128877501	Human		name
407516651	CV3445195	single nucleotide variant	NM_001366122.1(KCP):c.4796C>T (p.Pro1599Leu)	not specified [RCV004628269]	uncertain significance	7	128877134	128877134	Human		name
407516654	CV3445196	single nucleotide variant	NM_001366122.1(KCP):c.4609A>G (p.Thr1537Ala)	not specified [RCV004628270]	uncertain significance	7	128877493	128877493	Human		name
407511831	CV3445197	single nucleotide variant	NM_001366122.1(KCP):c.3193C>G (p.Pro1065Ala)	not specified [RCV004626594]	uncertain significance	7	128884053	128884053	Human		name
407516657	CV3445198	single nucleotide variant	NM_001366122.1(KCP):c.3190C>T (p.Pro1064Ser)	not specified [RCV004628271]	uncertain significance	7	128884056	128884056	Human		name
407511834	CV3445199	single nucleotide variant	NM_001366122.1(KCP):c.4472C>G (p.Pro1491Arg)	not specified [RCV004626595]	uncertain significance	7	128877630	128877630	Human		name
407516660	CV3445200	single nucleotide variant	NM_001366122.1(KCP):c.4729G>A (p.Val1577Met)	not specified [RCV004628272]	uncertain significance	7	128877201	128877201	Human		name
407516663	CV3445201	single nucleotide variant	NM_001366122.1(KCP):c.4679G>A (p.Arg1560His)	not specified [RCV004628273]	uncertain significance	7	128877251	128877251	Human		name
407511837	CV3445204	single nucleotide variant	NM_001366122.1(KCP):c.4183G>C (p.Val1395Leu)	not specified [RCV004626596]	uncertain significance	7	128878686	128878686	Human		name
407516674	CV3445206	single nucleotide variant	NM_001366122.1(KCP):c.4283C>T (p.Ser1428Leu)	not specified [RCV004628277]	uncertain significance	7	128878586	128878586	Human		name
407516681	CV3445208	single nucleotide variant	NM_001366122.1(KCP):c.3769C>T (p.Pro1257Ser)	not specified [RCV004628279]	uncertain significance	7	128880076	128880076	Human		name
407516684	CV3445209	single nucleotide variant	NM_001366122.1(KCP):c.3325G>A (p.Asp1109Asn)	not specified [RCV004628280]	uncertain significance	7	128881725	128881725	Human		name
597796517	CV3694837	single nucleotide variant	NM_001366122.1(KCP):c.4241C>T (p.Ala1414Val)	not specified [RCV004935495]	uncertain significance	7	128878628	128878628	Human		name
597796527	CV3694840	single nucleotide variant	NM_001366122.1(KCP):c.4085C>T (p.Pro1362Leu)	not specified [RCV004935498]	uncertain significance	7	128879583	128879583	Human		name
597767289	CV3694843	single nucleotide variant	NM_001366122.1(KCP):c.3194C>G (p.Pro1065Arg)	not specified [RCV004927253]	uncertain significance	7	128884052	128884052	Human		name
597796540	CV3694847	single nucleotide variant	NM_001366122.1(KCP):c.4258G>A (p.Gly1420Ser)	not specified [RCV004935502]	uncertain significance	7	128878611	128878611	Human		name
597796543	CV3694848	single nucleotide variant	NM_001366122.1(KCP):c.3796C>T (p.Pro1266Ser)	not specified [RCV004935503]	uncertain significance	7	128880049	128880049	Human		name
597796556	CV3694852	single nucleotide variant	NM_001366122.1(KCP):c.4728C>G (p.Cys1576Trp)	not specified [RCV004935507]	uncertain significance	7	128877202	128877202	Human		name
597767294	CV3694855	single nucleotide variant	NM_001366122.1(KCP):c.3668G>A (p.Arg1223His)	not specified [RCV004927254]	likely benign	7	128880477	128880477	Human		name
597796562	CV3694857	single nucleotide variant	NM_001366122.1(KCP):c.3961C>T (p.Arg1321Trp)	not specified [RCV004935509]	uncertain significance	7	128879801	128879801	Human		name
597796568	CV3694859	single nucleotide variant	NM_001366122.1(KCP):c.4864C>T (p.Arg1622Trp)	not specified [RCV004935511]	uncertain significance	7	128877066	128877066	Human		name
597796571	CV3694860	single nucleotide variant	NM_001366122.1(KCP):c.4747G>A (p.Gly1583Ser)	not specified [RCV004935512]	uncertain significance	7	128877183	128877183	Human		name
597796584	CV3694864	single nucleotide variant	NM_001366122.1(KCP):c.3992C>T (p.Ala1331Val)	not specified [RCV004935516]	uncertain significance	7	128879770	128879770	Human		name
597796587	CV3694866	single nucleotide variant	NM_001366122.1(KCP):c.3743C>T (p.Pro1248Leu)	not specified [RCV004935517]	uncertain significance	7	128880402	128880402	Human		name
597796593	CV3694869	single nucleotide variant	NM_001366122.1(KCP):c.3020A>C (p.Asp1007Ala)	not specified [RCV004935519]	uncertain significance	7	128885117	128885117	Human		name
598270183	CV3976356	single nucleotide variant	NM_001366122.1(KCP):c.4373G>A (p.Arg1458Gln)	not specified [RCV005350053]	uncertain significance	7	128877729	128877729	Human		name
598213190	CV3976357	single nucleotide variant	NM_001366122.1(KCP):c.4033G>A (p.Gly1345Arg)	not specified [RCV005358950]	likely benign	7	128879729	128879729	Human		name
598213195	CV3976358	single nucleotide variant	NM_001366122.1(KCP):c.3766G>A (p.Ala1256Thr)	not specified [RCV005358951]	uncertain significance	7	128880079	128880079	Human		name
598235820	CV3976359	single nucleotide variant	NM_001366122.1(KCP):c.3955C>T (p.Arg1319Trp)	not specified [RCV005363731]	uncertain significance	7	128879807	128879807	Human		name
598270189	CV3976361	single nucleotide variant	NM_001366122.1(KCP):c.3043T>G (p.Cys1015Gly)	not specified [RCV005350054]	uncertain significance	7	128884861	128884861	Human		name
598213205	CV3976364	single nucleotide variant	NM_001366122.1(KCP):c.3386G>A (p.Arg1129His)	not specified [RCV005358953]	likely benign	7	128881664	128881664	Human		name
598235824	CV3976365	single nucleotide variant	NM_001366122.1(KCP):c.3227G>A (p.Cys1076Tyr)	not specified [RCV005363732]	uncertain significance	7	128884019	128884019	Human		name
598270203	CV3976366	single nucleotide variant	NM_001366122.1(KCP):c.4372C>T (p.Arg1458Trp)	not specified [RCV005350057]	uncertain significance	7	128877730	128877730	Human		name
598270208	CV3976369	single nucleotide variant	NM_001366122.1(KCP):c.4390G>A (p.Ala1464Thr)	not specified [RCV005350058]	uncertain significance	7	128877712	128877712	Human		name
598235833	CV3976370	single nucleotide variant	NM_001366122.1(KCP):c.4334G>T (p.Gly1445Val)	not specified [RCV005363734]	uncertain significance	7	128877768	128877768	Human		name
598270218	CV3976375	single nucleotide variant	NM_001366122.1(KCP):c.4831G>A (p.Asp1611Asn)	not specified [RCV005350060]	uncertain significance	7	128877099	128877099	Human		name
598235856	CV3976377	single nucleotide variant	NM_001366122.1(KCP):c.3985G>C (p.Glu1329Gln)	not specified [RCV005363738]	uncertain significance	7	128879777	128879777	Human		name
598270223	CV3976378	single nucleotide variant	NM_001366122.1(KCP):c.3718C>G (p.Arg1240Gly)	not specified [RCV005350061]	uncertain significance	7	128880427	128880427	Human		name
598270227	CV3976380	single nucleotide variant	NM_001366122.1(KCP):c.3064T>G (p.Tyr1022Asp)	not specified [RCV005350062]	uncertain significance	7	128884840	128884840	Human		name
41405784	CV981590	single nucleotide variant	NM_001366122.1(KCP):c.4120A>T (p.Ile1374Phe)	not provided [RCV001810562]	uncertain significance	7	128879548	128879548	Human		name
41405772	CV981591	single nucleotide variant	NM_001366122.1(KCP):c.3715G>A (p.Val1239Met)	not provided [RCV001810555]	uncertain significance	7	128880430	128880430	Human		name

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