Incenp Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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218 records found for search term Incenp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150453902	CV1219899	single nucleotide variant	NM_001040694.2(INCENP):c.*30G>A	not provided [RCV001612280]	benign	11	62152006	62152006	Human		name
150431979	CV1236607	single nucleotide variant	NM_001040694.2(INCENP):c.*67C>G	not provided [RCV001642011]	benign	11	62152043	62152043	Human		name
150490380	CV1239105	single nucleotide variant	NM_001040694.2(INCENP):c.*121G>C	not provided [RCV001654673]	benign	11	62152097	62152097	Human		name
150330877	CV1172275	single nucleotide variant	NM_001040694.2(INCENP):c.255-57C>T	not provided [RCV001538339]	benign	11	62129725	62129725	Human		name
150332519	CV1172276	single nucleotide variant	NM_001040694.2(INCENP):c.2391+5C>A	not provided [RCV001539077]	benign	11	62148851	62148851	Human		name
150513893	CV1210754	single nucleotide variant	NM_001040694.2(INCENP):c.-11-82A>G	not provided [RCV001598795]	benign	11	62128069	62128069	Human		name
150434834	CV1231191	single nucleotide variant	NM_001040694.2(INCENP):c.141-27G>A	not provided [RCV001643835]	benign	11	62128743	62128743	Human		name
150490631	CV1251061	single nucleotide variant	NM_001040694.2(INCENP):c.1593+8G>T	not provided [RCV001674728]	benign	11	62141052	62141052	Human		name
150501805	CV1256404	single nucleotide variant	NM_001040694.2(INCENP):c.2391+6A>G	not provided [RCV001677028]	benign	11	62148852	62148852	Human		name
150453087	CV1260472	single nucleotide variant	NM_001040694.2(INCENP):c.1960-8T>C	not provided [RCV001680963]	benign	11	62146650	62146650	Human		name
150448344	CV1270447	single nucleotide variant	NM_001040694.2(INCENP):c.1959+9A>G	not provided [RCV001691585]	benign	11	62145760	62145760	Human		name
401905258	CV2816686	single nucleotide variant	NM_001040694.2(INCENP):c.1064-5C>G	not provided [RCV003395838]	uncertain significance	11	62137827	62137827	Human		name
150332920	CV1169463	single nucleotide variant	NM_001040694.2(INCENP):c.-11-147G>A	not provided [RCV001537074]	benign	11	62128004	62128004	Human		name
150453820	CV1219888	single nucleotide variant	NM_001040694.2(INCENP):c.2283+64C>T	not provided [RCV001612269]	benign	11	62148618	62148618	Human		name
150484275	CV1222456	single nucleotide variant	NM_001040694.2(INCENP):c.2205-41C>G	not provided [RCV001617459]	benign	11	62148435	62148435	Human		name
150508583	CV1229680	deletion	NM_001040694.2(INCENP):c.-11-179del	not provided [RCV001636258]	benign	11	62127972	62127972	Human		name
150459287	CV1236075	single nucleotide variant	NM_001040694.2(INCENP):c.1606-54G>A	not provided [RCV001649046]	benign	11	62144928	62144928	Human		name
150494025	CV1238785	single nucleotide variant	NM_001040694.2(INCENP):c.2392-89A>G	not provided [RCV001655329]	benign	11	62149968	62149968	Human		name
150510924	CV1242547	single nucleotide variant	NM_001040694.2(INCENP):c.1292-75T>A	not provided [RCV001660899]	benign	11	62140159	62140159	Human		name
150439668	CV1247751	single nucleotide variant	NM_001040694.2(INCENP):c.255-181C>T	not provided [RCV001666118]	benign	11	62129601	62129601	Human		name
150510278	CV1248599	single nucleotide variant	NM_001040694.2(INCENP):c.2392-16A>G	not provided [RCV001659669]	benign	11	62150041	62150041	Human		name
150446485	CV1250672	single nucleotide variant	NM_001040694.2(INCENP):c.1837-10G>C	not provided [RCV001667177]	benign	11	62145619	62145619	Human		name
150444226	CV1258487	single nucleotide variant	NM_001040694.2(INCENP):c.2283+20G>A	not provided [RCV001679685]	benign	11	62148574	62148574	Human		name
150457628	CV1260167	single nucleotide variant	NM_001040694.2(INCENP):c.1291+61G>A	not provided [RCV001681647]	benign	11	62139066	62139066	Human		name
150438136	CV1264781	deletion	NM_001040694.2(INCENP):c.-11-175del	not provided [RCV001678774]	benign	11	62127973	62127973	Human		name
150488784	CV1265303	single nucleotide variant	NM_001040694.2(INCENP):c.1173+57A>G	not provided [RCV001687339]	benign	11	62138827	62138827	Human		name
150474971	CV1271126	single nucleotide variant	NM_001040694.2(INCENP):c.254+234T>G	not provided [RCV001695949]	benign	11	62129117	62129117	Human		name
150460442	CV1275822	single nucleotide variant	NM_001040694.2(INCENP):c.2204+89T>C	not provided [RCV001709760]	benign	11	62146991	62146991	Human		name
150445252	CV1278121	single nucleotide variant	NM_001040694.2(INCENP):c.1837-22C>T	not provided [RCV001707264]	benign	11	62145607	62145607	Human		name
150478068	CV1281825	single nucleotide variant	NM_001040694.2(INCENP):c.1960-74G>A	not provided [RCV001714231]	benign	11	62146584	62146584	Human		name
150509553	CV1284569	single nucleotide variant	NM_001040694.2(INCENP):c.1343+64C>A	not provided [RCV001720677]	benign	11	62140349	62140349	Human		name
150340178	CV1168243	single nucleotide variant	NM_001040694.2(INCENP):c.2543-186G>A	not provided [RCV001535076]	benign	11	62151576	62151576	Human		name
150333944	CV1169465	single nucleotide variant	NM_001040694.2(INCENP):c.2391+237C>G	not provided [RCV001537545]	benign	11	62149083	62149083	Human		name
150503041	CV1212386	single nucleotide variant	NM_001040694.2(INCENP):c.1959+173T>C	not provided [RCV001595261]	benign	11	62145924	62145924	Human		name
150433720	CV1216996	single nucleotide variant	NM_001040694.2(INCENP):c.2391+201C>G	not provided [RCV001608898]	benign	11	62149047	62149047	Human		name
150472884	CV1217253	single nucleotide variant	NM_001040694.2(INCENP):c.1063+112T>C	not provided [RCV001615548]	benign	11	62130702	62130702	Human		name
150516737	CV1227215	single nucleotide variant	NM_001040694.2(INCENP):c.1343+152A>G	not provided [RCV001639313]	benign	11	62140437	62140437	Human		name
150472770	CV1235114	single nucleotide variant	NM_001040694.2(INCENP):c.1344-207C>T	not provided [RCV001651483]	benign	11	62140497	62140497	Human		name
150431321	CV1235408	single nucleotide variant	NM_001040694.2(INCENP):c.2205-198C>A	not provided [RCV001641778]	benign	11	62148278	62148278	Human		name
150478697	CV1240542	single nucleotide variant	NM_001040694.2(INCENP):c.2542+163T>C	not provided [RCV001652417]	benign	11	62150370	62150370	Human		name
150481399	CV1243303	single nucleotide variant	NM_001040694.2(INCENP):c.1116-200G>A	not provided [RCV001652939]	benign	11	62138513	62138513	Human		name
150475897	CV1251782	single nucleotide variant	NM_001040694.2(INCENP):c.1606-244C>T	not provided [RCV001671980]	benign	11	62144738	62144738	Human		name
150474773	CV1252912	single nucleotide variant	NM_001040694.2(INCENP):c.1960-174C>T	not provided [RCV001671820]	benign	11	62146484	62146484	Human		name
150502422	CV1254525	single nucleotide variant	NM_001040694.2(INCENP):c.1960-127G>A	not provided [RCV001677227]	benign	11	62146531	62146531	Human		name
150474009	CV1262997	single nucleotide variant	NM_001040694.2(INCENP):c.2391+135T>A	not provided [RCV001684813]	benign	11	62148981	62148981	Human		name
150454502	CV1266018	single nucleotide variant	NM_001040694.2(INCENP):c.2204+178A>G	not provided [RCV001692595]	benign	11	62147080	62147080	Human		name
150491373	CV1267766	single nucleotide variant	NM_001040694.2(INCENP):c.1959+134G>T	not provided [RCV001687791]	benign	11	62145885	62145885	Human		name
150469562	CV1268119	single nucleotide variant	NM_001040694.2(INCENP):c.2205-125A>G	not provided [RCV001694982]	benign	11	62148351	62148351	Human	1	name
150469562	CV1268119	single nucleotide variant	NM_001040694.2(INCENP):c.2205-125A>G	not provided [RCV001694982]	benign	11	62148351	62148352	Human	1	name
150495656	CV1272686	single nucleotide variant	NM_001040694.2(INCENP):c.1063+130G>A	not provided [RCV001688609]	benign	11	62130720	62130720	Human		name
150477693	CV1279498	single nucleotide variant	NM_001040694.2(INCENP):c.1593+156G>A	not provided [RCV001714168]	benign	11	62141200	62141200	Human		name
150509556	CV1284570	single nucleotide variant	NM_001040694.2(INCENP):c.1344-154G>A	not provided [RCV001720678]	benign	11	62140550	62140550	Human		name
150509575	CV1284577	single nucleotide variant	NM_001040694.2(INCENP):c.1959+139C>G	not provided [RCV001720685]	benign	11	62145890	62145890	Human		name
150444268	CV1266506	single nucleotide variant	NM_001040694.2(INCENP):c.108A>G (p.Glu36=)	not provided [RCV001690942]	benign	11	62128269	62128269	Human		name
405782919	CV3267584	single nucleotide variant	NM_001040694.2(INCENP):c.11C>T (p.Thr4Met)	not specified [RCV004397958]	uncertain significance	11	62128172	62128172	Human		name
405782960	CV3267591	single nucleotide variant	NM_001040694.2(INCENP):c.16C>T (p.Pro6Ser)	not specified [RCV004397965]	uncertain significance	11	62128177	62128177	Human		name
150435380	CV1233844	single nucleotide variant	NM_001040694.2(INCENP):c.360C>T (p.Val120=)	not provided [RCV001643971]	benign	11	62129887	62129887	Human		name
156026476	CV2271069	single nucleotide variant	NM_001040694.2(INCENP):c.85A>G (p.Lys29Glu)	not specified [RCV004134460]	uncertain significance	11	62128246	62128246	Human		name
329368872	CV2450445	single nucleotide variant	NM_001040694.2(INCENP):c.37G>A (p.Glu13Lys)	not specified [RCV004265371]	uncertain significance	11	62128198	62128198	Human		name
401905257	CV2816685	single nucleotide variant	NM_001040694.2(INCENP):c.876G>A (p.Thr292=)	not provided [RCV003395837]	likely benign	11	62130403	62130403	Human		name
597775677	CV3686747	single nucleotide variant	NM_001040694.2(INCENP):c.29A>G (p.His10Arg)	not specified [RCV004929418]	uncertain significance	11	62128190	62128190	Human		name
15191250	CV701832	single nucleotide variant	NM_001040694.2(INCENP):c.405C>T (p.Thr135=)	not provided [RCV000954720]	benign	11	62129932	62129932	Human		name
150449817	CV1215160	single nucleotide variant	NM_001040694.2(INCENP):c.2385C>T (p.Asp795=)	not provided [RCV001611750]	benign	11	62148840	62148840	Human		name
150486831	CV1225807	single nucleotide variant	NM_001040694.2(INCENP):c.1302G>A (p.Thr434=)	not provided [RCV001617968]	benign	11	62140244	62140244	Human		name
150486859	CV1251426	single nucleotide variant	NM_001040694.2(INCENP):c.1188T>C (p.Asn396=)	not provided [RCV001674097]	benign	11	62138902	62138902	Human		name
150500339	CV1256079	single nucleotide variant	NM_001040694.2(INCENP):c.2112G>A (p.Glu704=)	not provided [RCV001676703]	benign	11	62146810	62146810	Human		name
150446673	CV1271902	single nucleotide variant	NM_001040694.2(INCENP):c.2199C>T (p.Ala733=)	not provided [RCV001691316]	benign	11	62146897	62146897	Human		name
156380590	CV2208278	single nucleotide variant	NM_001040694.2(INCENP):c.255G>T (p.Arg85Ser)	not specified [RCV004088721]	uncertain significance	11	62129782	62129782	Human		name
156360032	CV2254177	single nucleotide variant	NM_001040694.2(INCENP):c.287T>C (p.Leu96Pro)	not specified [RCV004129859]	uncertain significance	11	62129814	62129814	Human		name
156055954	CV2326625	single nucleotide variant	NM_001040694.2(INCENP):c.176C>T (p.Thr59Ile)	not specified [RCV004183163]	uncertain significance	11	62128805	62128805	Human		name
156001069	CV2378773	single nucleotide variant	NM_001040694.2(INCENP):c.128G>A (p.Arg43His)	not specified [RCV004231224]	uncertain significance	11	62128289	62128289	Human		name
155964070	CV2395793	single nucleotide variant	NM_001040694.2(INCENP):c.275G>A (p.Arg92Gln)	not specified [RCV004235318]	uncertain significance	11	62129802	62129802	Human		name
329389048	CV2469753	single nucleotide variant	NM_001040694.2(INCENP):c.293C>T (p.Ser98Phe)	not specified [RCV004284948]	uncertain significance	11	62129820	62129820	Human		name
401739172	CV2673236	single nucleotide variant	NM_001040694.2(INCENP):c.296G>A (p.Arg99Gln)	not specified [RCV004286042]	uncertain significance	11	62129823	62129823	Human		name
401738396	CV2676270	single nucleotide variant	NM_001040694.2(INCENP):c.194G>A (p.Arg65Gln)	not specified [RCV004286308]	uncertain significance	11	62128823	62128823	Human		name
401877229	CV2764548	single nucleotide variant	NM_001040694.2(INCENP):c.121G>T (p.Ala41Ser)	not specified [RCV004339103]	uncertain significance	11	62128282	62128282	Human		name
401905261	CV2816687	single nucleotide variant	NM_001040694.2(INCENP):c.2094C>G (p.Arg698=)	not provided [RCV003395839]	likely benign	11	62146792	62146792	Human		name
401905262	CV2816688	single nucleotide variant	NM_001040694.2(INCENP):c.2124G>C (p.Arg708=)	not provided [RCV003395840]	likely benign	11	62146822	62146822	Human		name
401905263	CV2816689	single nucleotide variant	NM_001040694.2(INCENP):c.2139C>G (p.Arg713=)	not provided [RCV003395841]\|not specified [RCV004364495]	likely benign	11	62146837	62146837	Human		name
405782952	CV3267590	single nucleotide variant	NM_001040694.2(INCENP):c.158C>T (p.Pro53Leu)	not specified [RCV004397964]	uncertain significance	11	62128787	62128787	Human		name
405783035	CV3267604	single nucleotide variant	NM_001040694.2(INCENP):c.274C>T (p.Arg92Trp)	not specified [RCV004397978]	uncertain significance	11	62129801	62129801	Human		name
597775633	CV3686737	single nucleotide variant	NM_001040694.2(INCENP):c.249G>T (p.Arg83Ser)	not specified [RCV004929408]	uncertain significance	11	62128878	62128878	Human		name
597775714	CV3686756	single nucleotide variant	NM_001040694.2(INCENP):c.127C>A (p.Arg43Ser)	not specified [RCV004929427]	uncertain significance	11	62128288	62128288	Human		name
15191253	CV701835	single nucleotide variant	NM_001040694.2(INCENP):c.2700G>A (p.Pro900=)	not provided [RCV000954721]	benign	11	62151919	62151919	Human		name
150453593	CV1276868	single nucleotide variant	NM_001040694.2(INCENP):c.410C>T (p.Ala137Val)	not provided [RCV001708658]	benign	11	62129937	62129937	Human		name
156153838	CV2209475	single nucleotide variant	NM_001040694.2(INCENP):c.925G>A (p.Ala309Thr)	not specified [RCV004093618]	uncertain significance	11	62130452	62130452	Human		name
156078342	CV2230351	single nucleotide variant	NM_001040694.2(INCENP):c.619A>G (p.Thr207Ala)	not specified [RCV004099951]	likely benign	11	62130146	62130146	Human		name
156165352	CV2243477	single nucleotide variant	NM_001040694.2(INCENP):c.377G>A (p.Arg126His)	not specified [RCV004112439]	uncertain significance	11	62129904	62129904	Human		name
156299441	CV2326059	single nucleotide variant	NM_001040694.2(INCENP):c.812C>G (p.Ala271Gly)	not specified [RCV004176262]	likely benign	11	62130339	62130339	Human		name
155917265	CV2336302	single nucleotide variant	NM_001040694.2(INCENP):c.527G>A (p.Arg176His)	not specified [RCV004192051]	uncertain significance	11	62130054	62130054	Human		name
156284040	CV2348987	single nucleotide variant	NM_001040694.2(INCENP):c.839G>A (p.Arg280Gln)	not specified [RCV004203417]	uncertain significance	11	62130366	62130366	Human		name
156238153	CV2356231	single nucleotide variant	NM_001040694.2(INCENP):c.397G>A (p.Ala133Thr)	not specified [RCV004206046]	uncertain significance	11	62129924	62129924	Human		name
156208520	CV2382515	single nucleotide variant	NM_001040694.2(INCENP):c.740G>T (p.Gly247Val)	not specified [RCV004232850]	uncertain significance	11	62130267	62130267	Human		name
156224736	CV2395234	single nucleotide variant	NM_001040694.2(INCENP):c.841G>T (p.Val281Leu)	not specified [RCV004236896]	uncertain significance	11	62130368	62130368	Human		name
156057339	CV2396339	single nucleotide variant	NM_001040694.2(INCENP):c.716C>T (p.Thr239Ile)	not specified [RCV004242066]	uncertain significance	11	62130243	62130243	Human		name
329359725	CV2462244	single nucleotide variant	NM_001040694.2(INCENP):c.496G>T (p.Val166Leu)	not specified [RCV004266245]	uncertain significance	11	62130023	62130023	Human		name
329397980	CV2467132	single nucleotide variant	NM_001040694.2(INCENP):c.841G>A (p.Val281Met)	not specified [RCV004282859]	uncertain significance	11	62130368	62130368	Human		name
401737184	CV2679247	single nucleotide variant	NM_001040694.2(INCENP):c.568G>A (p.Glu190Lys)	not specified [RCV004285798]	uncertain significance	11	62130095	62130095	Human		name
401731457	CV2701375	single nucleotide variant	NM_001040694.2(INCENP):c.874A>G (p.Thr292Ala)	not specified [RCV004311743]	uncertain significance	11	62130401	62130401	Human		name
401861470	CV2779771	single nucleotide variant	NM_001040694.2(INCENP):c.327G>T (p.Lys109Asn)	not specified [RCV004353407]	uncertain significance	11	62129854	62129854	Human		name
401905254	CV2816684	single nucleotide variant	NM_001040694.2(INCENP):c.754C>T (p.Arg252Trp)	not provided [RCV003395836]	uncertain significance	11	62130281	62130281	Human		name
405783040	CV3267605	single nucleotide variant	NM_001040694.2(INCENP):c.383C>T (p.Ala128Val)	not specified [RCV004397979]	uncertain significance	11	62129910	62129910	Human		name
405783046	CV3267606	single nucleotide variant	NM_001040694.2(INCENP):c.416C>T (p.Ala139Val)	not specified [RCV004397980]	uncertain significance	11	62129943	62129943	Human		name
405783052	CV3267607	single nucleotide variant	NM_001040694.2(INCENP):c.622T>C (p.Ser208Pro)	not specified [RCV004397981]	uncertain significance	11	62130149	62130149	Human		name
405783058	CV3267608	single nucleotide variant	NM_001040694.2(INCENP):c.908T>G (p.Val303Gly)	not specified [RCV004397982]	uncertain significance	11	62130435	62130435	Human		name
405783064	CV3267609	single nucleotide variant	NM_001040694.2(INCENP):c.938C>T (p.Pro313Leu)	not specified [RCV004397983]	likely benign	11	62130465	62130465	Human		name
405783070	CV3267610	single nucleotide variant	NM_001040694.2(INCENP):c.949G>A (p.Val317Ile)	not specified [RCV004397984]	uncertain significance	11	62130476	62130476	Human		name
407511243	CV3444731	single nucleotide variant	NM_001040694.2(INCENP):c.998G>T (p.Arg333Leu)	not specified [RCV004626398]	uncertain significance	11	62130525	62130525	Human		name
407522296	CV3444733	single nucleotide variant	NM_001040694.2(INCENP):c.560T>C (p.Met187Thr)	not specified [RCV004630648]	uncertain significance	11	62130087	62130087	Human		name
597775655	CV3686742	single nucleotide variant	NM_001040694.2(INCENP):c.514G>A (p.Gly172Ser)	not specified [RCV004929413]	likely benign	11	62130041	62130041	Human		name
597775669	CV3686745	single nucleotide variant	NM_001040694.2(INCENP):c.651A>C (p.Glu217Asp)	not specified [RCV004929416]	uncertain significance	11	62130178	62130178	Human		name
597775681	CV3686748	single nucleotide variant	NM_001040694.2(INCENP):c.305G>A (p.Arg102His)	not specified [RCV004929419]	uncertain significance	11	62129832	62129832	Human		name
597775693	CV3686751	single nucleotide variant	NM_001040694.2(INCENP):c.734G>A (p.Gly245Asp)	not specified [RCV004929422]	uncertain significance	11	62130261	62130261	Human		name
597775697	CV3686752	single nucleotide variant	NM_001040694.2(INCENP):c.666G>T (p.Lys222Asn)	not specified [RCV004929423]	uncertain significance	11	62130193	62130193	Human		name
597775707	CV3686754	single nucleotide variant	NM_001040694.2(INCENP):c.713C>T (p.Ala238Val)	not specified [RCV004929425]	uncertain significance	11	62130240	62130240	Human		name
597775972	CV3686759	single nucleotide variant	NM_001040694.2(INCENP):c.449C>T (p.Thr150Met)	not specified [RCV004929430]	uncertain significance	11	62129976	62129976	Human		name
597775969	CV3686760	single nucleotide variant	NM_001040694.2(INCENP):c.983A>G (p.Gln328Arg)	not specified [RCV004929431]	uncertain significance	11	62130510	62130510	Human		name
597775950	CV3686765	single nucleotide variant	NM_001040694.2(INCENP):c.953T>C (p.Leu318Ser)	not specified [RCV004929436]	uncertain significance	11	62130480	62130480	Human		name
598207911	CV3972475	single nucleotide variant	NM_001040694.2(INCENP):c.491A>C (p.Gln164Pro)	not specified [RCV005338047]	uncertain significance	11	62130018	62130018	Human		name
15199122	CV701833	single nucleotide variant	NM_001040694.2(INCENP):c.469G>A (p.Glu157Lys)	not provided [RCV000956951]	benign	11	62129996	62129996	Human		name
15105934	CV712928	single nucleotide variant	NM_001040694.2(INCENP):c.299G>A (p.Arg100His)	not provided [RCV000959980]	benign	11	62129826	62129826	Human		name
150339644	CV1167531	single nucleotide variant	NM_001040694.2(INCENP):c.1932G>T (p.Glu644Asp)	not provided [RCV001534409]	benign	11	62145724	62145724	Human		name
150330836	CV1169464	single nucleotide variant	NM_001040694.2(INCENP):c.2090G>A (p.Arg697Gln)	not provided [RCV001536162]	benign	11	62146788	62146788	Human		name
150480788	CV1279578	single nucleotide variant	NM_001040694.2(INCENP):c.1517T>C (p.Met506Thr)	not provided [RCV001714716]	benign	11	62140968	62140968	Human	12	name
155915068	CV2203957	single nucleotide variant	NM_001040694.2(INCENP):c.2150G>A (p.Arg717Gln)	not specified [RCV004070002]	uncertain significance	11	62146848	62146848	Human		name
156029743	CV2206098	single nucleotide variant	NM_001040694.2(INCENP):c.1022A>G (p.Lys341Arg)	not specified [RCV004078507]	uncertain significance	11	62130549	62130549	Human		name
156130054	CV2209924	single nucleotide variant	NM_001040694.2(INCENP):c.1543G>A (p.Val515Ile)	not specified [RCV004076372]	uncertain significance	11	62140994	62140994	Human		name
155920606	CV2211881	single nucleotide variant	NM_001040694.2(INCENP):c.2074C>T (p.Arg692Trp)	not specified [RCV004087015]	uncertain significance	11	62146772	62146772	Human		name
155917838	CV2236669	single nucleotide variant	NM_001040694.2(INCENP):c.1783A>C (p.Lys595Gln)	not specified [RCV004110632]	uncertain significance	11	62145236	62145236	Human		name
156136796	CV2239728	single nucleotide variant	NM_001040694.2(INCENP):c.2242A>G (p.Lys748Glu)	not specified [RCV004108265]	uncertain significance	11	62148513	62148513	Human		name
156292955	CV2246763	single nucleotide variant	NM_001040694.2(INCENP):c.2524A>G (p.Ile842Val)	not specified [RCV004112298]	uncertain significance	11	62150189	62150189	Human		name
155967360	CV2261151	single nucleotide variant	NM_001040694.2(INCENP):c.2386G>A (p.Val796Met)	not specified [RCV004128046]	uncertain significance	11	62148841	62148841	Human		name
156022662	CV2273677	single nucleotide variant	NM_001040694.2(INCENP):c.1732C>G (p.Leu578Val)	not specified [RCV004132336]	uncertain significance	11	62145185	62145185	Human		name
155918455	CV2279232	single nucleotide variant	NM_001040694.2(INCENP):c.2308C>T (p.Arg770Trp)	not specified [RCV004139759]	uncertain significance	11	62148763	62148763	Human		name
155956603	CV2281948	single nucleotide variant	NM_001040694.2(INCENP):c.2223G>T (p.Glu741Asp)	not specified [RCV004138717]	uncertain significance	11	62148494	62148494	Human		name
155905100	CV2285831	single nucleotide variant	NM_001040694.2(INCENP):c.1225G>A (p.Ala409Thr)	not specified [RCV004143778]	uncertain significance	11	62138939	62138939	Human		name
155998168	CV2287115	single nucleotide variant	NM_001040694.2(INCENP):c.2718G>C (p.Arg906Ser)	not specified [RCV004144984]	uncertain significance	11	62151937	62151937	Human		name
156281939	CV2288783	single nucleotide variant	NM_001040694.2(INCENP):c.1670A>T (p.Gln557Leu)	not specified [RCV004147997]	uncertain significance	11	62145046	62145046	Human		name
156000399	CV2296306	single nucleotide variant	NM_001040694.2(INCENP):c.2134C>T (p.Arg712Trp)	not specified [RCV004154205]	uncertain significance	11	62146832	62146832	Human		name
156257669	CV2322084	single nucleotide variant	NM_001040694.2(INCENP):c.2191C>G (p.Leu731Val)	not specified [RCV004173827]	uncertain significance	11	62146889	62146889	Human		name
156061798	CV2323197	single nucleotide variant	NM_001040694.2(INCENP):c.1518G>A (p.Met506Ile)	not specified [RCV004187596]	uncertain significance	11	62140969	62140969	Human		name
156362592	CV2330260	single nucleotide variant	NM_001040694.2(INCENP):c.1352G>A (p.Arg451His)	not specified [RCV004187709]	uncertain significance	11	62140712	62140712	Human		name
156080028	CV2337419	single nucleotide variant	NM_001040694.2(INCENP):c.1217C>T (p.Thr406Met)	not specified [RCV004187859]	uncertain significance	11	62138931	62138931	Human		name
156274099	CV2344190	single nucleotide variant	NM_001040694.2(INCENP):c.1973G>A (p.Arg658Gln)	not specified [RCV004195785]	uncertain significance	11	62146671	62146671	Human		name
156274511	CV2344245	single nucleotide variant	NM_001040694.2(INCENP):c.1616G>A (p.Arg539Gln)	not specified [RCV004197878]	uncertain significance	11	62144992	62144992	Human		name
155902915	CV2356551	single nucleotide variant	NM_001040694.2(INCENP):c.2188C>T (p.Arg730Trp)	not specified [RCV004199460]	uncertain significance	11	62146886	62146886	Human		name
156212019	CV2366903	single nucleotide variant	NM_001040694.2(INCENP):c.1435C>G (p.Pro479Ala)	not specified [RCV004213316]	uncertain significance	11	62140795	62140795	Human		name
156263304	CV2377193	single nucleotide variant	NM_001040694.2(INCENP):c.1448G>T (p.Cys483Phe)	not specified [RCV004231868]	uncertain significance	11	62140808	62140808	Human		name
156346935	CV2382816	single nucleotide variant	NM_001040694.2(INCENP):c.1615C>T (p.Arg539Trp)	not specified [RCV004224152]	uncertain significance	11	62144991	62144991	Human		name
156134027	CV2383079	single nucleotide variant	NM_001040694.2(INCENP):c.2093G>A (p.Arg698His)	not specified [RCV004217653]	uncertain significance	11	62146791	62146791	Human		name
156040827	CV2384390	single nucleotide variant	NM_001040694.2(INCENP):c.1936C>T (p.Arg646Cys)	not specified [RCV004229811]	uncertain significance	11	62145728	62145728	Human		name
155908642	CV2387397	single nucleotide variant	NM_001040694.2(INCENP):c.1690C>T (p.Arg564Trp)	not specified [RCV004240266]	uncertain significance	11	62145066	62145066	Human		name
156091158	CV2389422	single nucleotide variant	NM_001040694.2(INCENP):c.1828A>G (p.Thr610Ala)	not specified [RCV004238150]	uncertain significance	11	62145281	62145281	Human		name
156062752	CV2392152	single nucleotide variant	NM_001040694.2(INCENP):c.2140G>A (p.Glu714Lys)	not specified [RCV004238044]	uncertain significance	11	62146838	62146838	Human		name
155965062	CV2395916	single nucleotide variant	NM_001040694.2(INCENP):c.2048G>A (p.Arg683Gln)	not specified [RCV004237474]	uncertain significance	11	62146746	62146746	Human		name
156270589	CV2398698	single nucleotide variant	NM_001040694.2(INCENP):c.1387G>C (p.Glu463Gln)	not specified [RCV004240042]	uncertain significance	11	62140747	62140747	Human		name
329367688	CV2427508	single nucleotide variant	NM_001040694.2(INCENP):c.2588C>T (p.Pro863Leu)	not specified [RCV004250146]	uncertain significance	11	62151807	62151807	Human		name
329400563	CV2438494	single nucleotide variant	NM_001040694.2(INCENP):c.2488G>A (p.Asp830Asn)	not specified [RCV004259641]	uncertain significance	11	62150153	62150153	Human		name
329400049	CV2440443	single nucleotide variant	NM_001040694.2(INCENP):c.2104C>T (p.Arg702Trp)	not specified [RCV004256377]	uncertain significance	11	62146802	62146802	Human		name
401781792	CV2678283	single nucleotide variant	NM_001040694.2(INCENP):c.2189G>A (p.Arg730Gln)	not specified [RCV004290279]	uncertain significance	11	62146887	62146887	Human		name
401744030	CV2688082	single nucleotide variant	NM_001040694.2(INCENP):c.1111G>T (p.Val371Phe)	not specified [RCV004305145]	uncertain significance	11	62137879	62137879	Human		name
401744485	CV2688172	single nucleotide variant	NM_001040694.2(INCENP):c.1748A>G (p.Gln583Arg)	not specified [RCV004305215]	uncertain significance	11	62145201	62145201	Human		name
401749929	CV2695880	single nucleotide variant	NM_001040694.2(INCENP):c.1154T>G (p.Val385Gly)	not specified [RCV004308159]	uncertain significance	11	62138751	62138751	Human		name
401889806	CV2755009	single nucleotide variant	NM_001040694.2(INCENP):c.2105G>A (p.Arg702Gln)	not specified [RCV004335166]	uncertain significance	11	62146803	62146803	Human		name
401873414	CV2761456	single nucleotide variant	NM_001040694.2(INCENP):c.1913G>A (p.Arg638His)	not specified [RCV004334631]	uncertain significance	11	62145705	62145705	Human		name
401856118	CV2764375	single nucleotide variant	NM_001040694.2(INCENP):c.2120G>A (p.Arg707Gln)	not specified [RCV004338947]	uncertain significance	11	62146818	62146818	Human		name
401886144	CV2774860	single nucleotide variant	NM_001040694.2(INCENP):c.1045G>C (p.Ala349Pro)	not specified [RCV004343944]	uncertain significance	11	62130572	62130572	Human		name
401863225	CV2776830	single nucleotide variant	NM_001040694.2(INCENP):c.2170C>T (p.Arg724Cys)	not specified [RCV004357973]	uncertain significance	11	62146868	62146868	Human		name
405782925	CV3267585	single nucleotide variant	NM_001040694.2(INCENP):c.1345A>G (p.Arg449Gly)	not specified [RCV004397959]	uncertain significance	11	62140705	62140705	Human		name
405782941	CV3267588	single nucleotide variant	NM_001040694.2(INCENP):c.1477C>T (p.Arg493Trp)	not specified [RCV004397962]	uncertain significance	11	62140928	62140928	Human		name
405782945	CV3267589	single nucleotide variant	NM_001040694.2(INCENP):c.1486C>G (p.Leu496Val)	not specified [RCV004397963]	uncertain significance	11	62140937	62140937	Human		name
405782968	CV3267592	single nucleotide variant	NM_001040694.2(INCENP):c.1849C>T (p.Arg617Trp)	not specified [RCV004397966]	uncertain significance	11	62145641	62145641	Human		name
405782974	CV3267593	single nucleotide variant	NM_001040694.2(INCENP):c.2027G>A (p.Arg676Gln)	not specified [RCV004397967]	uncertain significance	11	62146725	62146725	Human		name
405782977	CV3267594	single nucleotide variant	NM_001040694.2(INCENP):c.2075G>A (p.Arg692Gln)	not specified [RCV004397968]	uncertain significance	11	62146773	62146773	Human		name
405782989	CV3267596	single nucleotide variant	NM_001040694.2(INCENP):c.2120G>T (p.Arg707Leu)	not specified [RCV004397970]	uncertain significance	11	62146818	62146818	Human		name
405782994	CV3267597	single nucleotide variant	NM_001040694.2(INCENP):c.2138G>A (p.Arg713His)	not specified [RCV004397971]	uncertain significance	11	62146836	62146836	Human		name
405782998	CV3267598	single nucleotide variant	NM_001040694.2(INCENP):c.2200G>A (p.Glu734Lys)	not specified [RCV004397972]	uncertain significance	11	62146898	62146898	Human		name
405783010	CV3267600	single nucleotide variant	NM_001040694.2(INCENP):c.2660G>A (p.Arg887His)	not specified [RCV004397974]	uncertain significance	11	62151879	62151879	Human		name
405783016	CV3267601	single nucleotide variant	NM_001040694.2(INCENP):c.2711G>T (p.Gly904Val)	not specified [RCV004397975]	uncertain significance	11	62151930	62151930	Human		name
405783022	CV3267602	single nucleotide variant	NM_001040694.2(INCENP):c.2713G>A (p.Ala905Thr)	not specified [RCV004397976]	likely benign	11	62151932	62151932	Human		name
405783026	CV3267603	single nucleotide variant	NM_001040694.2(INCENP):c.2732T>G (p.Leu911Arg)	not specified [RCV004397977]	uncertain significance	11	62151951	62151951	Human		name
407522284	CV3444728	single nucleotide variant	NM_001040694.2(INCENP):c.2245G>A (p.Glu749Lys)	not specified [RCV004630644]	uncertain significance	11	62148516	62148516	Human		name
407522287	CV3444729	single nucleotide variant	NM_001040694.2(INCENP):c.2173C>T (p.Arg725Trp)	not specified [RCV004630645]	uncertain significance	11	62146871	62146871	Human		name
407522291	CV3444730	single nucleotide variant	NM_001040694.2(INCENP):c.1301C>T (p.Thr434Met)	not specified [RCV004630646]	likely benign	11	62140243	62140243	Human		name
407522293	CV3444732	single nucleotide variant	NM_001040694.2(INCENP):c.1735C>T (p.Arg579Cys)	not specified [RCV004630647]	uncertain significance	11	62145188	62145188	Human		name
407522301	CV3444734	single nucleotide variant	NM_001040694.2(INCENP):c.2089C>T (p.Arg697Trp)	not specified [RCV004630649]	uncertain significance	11	62146787	62146787	Human		name
407522304	CV3444735	single nucleotide variant	NM_001040694.2(INCENP):c.2020C>T (p.Arg674Trp)	not specified [RCV004630650]	uncertain significance	11	62146718	62146718	Human		name
407511248	CV3444736	single nucleotide variant	NM_001040694.2(INCENP):c.2540G>A (p.Arg847Gln)	not specified [RCV004626399]	uncertain significance	11	62150205	62150205	Human		name
407522307	CV3444737	single nucleotide variant	NM_001040694.2(INCENP):c.2449A>G (p.Ile817Val)	not specified [RCV004630651]	uncertain significance	11	62150114	62150114	Human		name
407522312	CV3444739	single nucleotide variant	NM_001040694.2(INCENP):c.2537C>A (p.Ala846Asp)	not specified [RCV004630653]	uncertain significance	11	62150202	62150202	Human		name
597775639	CV3686738	single nucleotide variant	NM_001040694.2(INCENP):c.1564C>T (p.Arg522Cys)	not specified [RCV004929409]	uncertain significance	11	62141015	62141015	Human		name
597775643	CV3686739	single nucleotide variant	NM_001040694.2(INCENP):c.2116G>A (p.Glu706Lys)	not specified [RCV004929410]	uncertain significance	11	62146814	62146814	Human		name
597775647	CV3686740	single nucleotide variant	NM_001040694.2(INCENP):c.1640G>A (p.Arg547Gln)	not specified [RCV004929411]	uncertain significance	11	62145016	62145016	Human		name
597775651	CV3686741	single nucleotide variant	NM_001040694.2(INCENP):c.2708A>G (p.Gln903Arg)	not specified [RCV004929412]	uncertain significance	11	62151927	62151927	Human		name
597775659	CV3686743	single nucleotide variant	NM_001040694.2(INCENP):c.2659C>T (p.Arg887Cys)	not specified [RCV004929414]	uncertain significance	11	62151878	62151878	Human		name
597775664	CV3686744	single nucleotide variant	NM_001040694.2(INCENP):c.2563A>G (p.Ile855Val)	not specified [RCV004929415]	uncertain significance	11	62151782	62151782	Human		name
597775673	CV3686746	single nucleotide variant	NM_001040694.2(INCENP):c.2135G>A (p.Arg712Gln)	not specified [RCV004929417]	uncertain significance	11	62146833	62146833	Human		name
597775685	CV3686749	single nucleotide variant	NM_001040694.2(INCENP):c.2110G>A (p.Glu704Lys)	not specified [RCV004929420]	uncertain significance	11	62146808	62146808	Human		name
597775689	CV3686750	single nucleotide variant	NM_001040694.2(INCENP):c.1142A>T (p.Glu381Val)	not specified [RCV004929421]	uncertain significance	11	62138739	62138739	Human		name
597775702	CV3686753	single nucleotide variant	NM_001040694.2(INCENP):c.2657C>T (p.Pro886Leu)	not specified [RCV004929424]	uncertain significance	11	62151876	62151876	Human		name
597775711	CV3686755	single nucleotide variant	NM_001040694.2(INCENP):c.2060A>G (p.Gln687Arg)	not specified [RCV004929426]	uncertain significance	11	62146758	62146758	Human		name
597775718	CV3686757	single nucleotide variant	NM_001040694.2(INCENP):c.1943T>C (p.Leu648Pro)	not specified [RCV004929428]	uncertain significance	11	62145735	62145735	Human		name
597775975	CV3686758	single nucleotide variant	NM_001040694.2(INCENP):c.1975C>T (p.Arg659Trp)	not specified [RCV004929429]	uncertain significance	11	62146673	62146673	Human		name
597775966	CV3686761	single nucleotide variant	NM_001040694.2(INCENP):c.1579C>T (p.Arg527Cys)	not specified [RCV004929432]	uncertain significance	11	62141030	62141030	Human		name
597775962	CV3686762	single nucleotide variant	NM_001040694.2(INCENP):c.1684G>A (p.Asp562Asn)	not specified [RCV004929433]	uncertain significance	11	62145060	62145060	Human		name
597775957	CV3686763	single nucleotide variant	NM_001040694.2(INCENP):c.1051G>A (p.Gly351Ser)	not specified [RCV004929434]	uncertain significance	11	62130578	62130578	Human		name
597775954	CV3686764	single nucleotide variant	NM_001040694.2(INCENP):c.1636C>T (p.Arg546Trp)	not specified [RCV004929435]	uncertain significance	11	62145012	62145012	Human		name
598181077	CV3972472	single nucleotide variant	NM_001040694.2(INCENP):c.1244C>T (p.Pro415Leu)	not specified [RCV005352434]	uncertain significance	11	62138958	62138958	Human		name
598181082	CV3972473	single nucleotide variant	NM_001040694.2(INCENP):c.1696C>T (p.Arg566Trp)	not specified [RCV005352435]	uncertain significance	11	62145072	62145072	Human		name
598181087	CV3972474	single nucleotide variant	NM_001040694.2(INCENP):c.2177G>A (p.Arg726Gln)	not specified [RCV005352436]	uncertain significance	11	62146875	62146875	Human		name
598181098	CV3972477	single nucleotide variant	NM_001040694.2(INCENP):c.2297G>A (p.Arg766His)	not specified [RCV005352438]	uncertain significance	11	62148752	62148752	Human		name
598207918	CV3972478	single nucleotide variant	NM_001040694.2(INCENP):c.1697G>A (p.Arg566Gln)	not specified [RCV005338048]	uncertain significance	11	62145073	62145073	Human		name
598207923	CV3972479	single nucleotide variant	NM_001040694.2(INCENP):c.1372A>C (p.Ser458Arg)	not specified [RCV005338049]	uncertain significance	11	62140732	62140732	Human		name
598181104	CV3972480	single nucleotide variant	NM_001040694.2(INCENP):c.2722C>A (p.Pro908Thr)	not specified [RCV005352439]	uncertain significance	11	62151941	62151941	Human		name
598181108	CV3972481	single nucleotide variant	NM_001040694.2(INCENP):c.1741G>A (p.Val581Met)	not specified [RCV005352440]	uncertain significance	11	62145194	62145194	Human		name
13704942	CV539148	single nucleotide variant	NM_001040694.2(INCENP):c.2415G>C (p.Gln805His)	Nephronophthisis [RCV000662273]	likely pathogenic	11	62150080	62150080	Human	2	name
15159814	CV701834	single nucleotide variant	NM_001040694.2(INCENP):c.1880C>T (p.Ala627Val)	not provided [RCV000947353]	benign	11	62145672	62145672	Human		name
15117105	CV712929	single nucleotide variant	NM_001040694.2(INCENP):c.1147G>A (p.Glu383Lys)	not provided [RCV000962146]	benign	11	62138744	62138744	Human		name

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