Kank4 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

328 records found for search term Kank4

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150484693	CV1222548	single nucleotide variant	NM_181712.5(KANK4):c.*263C>T	not provided [RCV001617551]	benign	1	62238014	62238014	Human		name
405071797	CV3140263	single nucleotide variant	NM_181712.5(KANK4):c.16+9G>A	not provided [RCV003833418]	likely benign	1	62281540	62281540	Human		name
150539313	CV1308647	duplication	NM_181712.5(KANK4):c.17-22dup	not provided [RCV001766151]	likely benign	1	62275108	62275109	Human		name
405079078	CV2945370	single nucleotide variant	NM_181712.5(KANK4):c.16+13C>A	not provided [RCV003664417]	likely benign	1	62281536	62281536	Human		name
150339594	CV1167203	single nucleotide variant	NM_181712.5(KANK4):c.17-290G>T	not provided [RCV001534347]	benign	1	62275377	62275377	Human		name
150340049	CV1167908	single nucleotide variant	NM_181712.5(KANK4):c.17-171T>C	not provided [RCV001534909]	benign	1	62275258	62275258	Human		name
150543374	CV1308957	single nucleotide variant	NM_181712.5(KANK4):c.16+234T>C	not provided [RCV001769870]	likely benign	1	62281315	62281315	Human		name
405240572	CV2893074	single nucleotide variant	NM_181712.5(KANK4):c.2231+3G>A	not provided [RCV003557320]	uncertain significance	1	62268284	62268284	Human		name
405269277	CV3201507	single nucleotide variant	NM_181712.5(KANK4):c.1901-5C>T	KANK4-related disorder [RCV003899423]	likely benign	1	62271594	62271594	Human		name , trait , alternate_id
407467434	CV3448266	single nucleotide variant	NM_181712.5(KANK4):c.2013-2A>G	not specified [RCV004635891]	uncertain significance	1	62268507	62268507	Human		name
597884099	CV3834861	single nucleotide variant	NM_181712.5(KANK4):c.2320-7G>T	not provided [RCV005178585]	likely benign	1	62263318	62263318	Human		name
15186010	CV777143	deletion	NM_181712.5(KANK4):c.2231+1del	not provided [RCV000953153]	likely benign	1	62268286	62268286	Human		name
150464499	CV1241305	single nucleotide variant	NM_181712.5(KANK4):c.2884-81T>C	not provided [RCV001649816]	benign	1	62238462	62238462	Human		name
150470278	CV1243298	single nucleotide variant	NM_181712.5(KANK4):c.2012+25A>G	not provided [RCV001650820]	benign	1	62271453	62271453	Human		name
150451061	CV1261029	single nucleotide variant	NM_181712.5(KANK4):c.2231+20C>T	not provided [RCV001680698]	benign	1	62268267	62268267	Human		name
150452097	CV1276683	single nucleotide variant	NM_181712.5(KANK4):c.2319+47G>T	not provided [RCV001708472]	benign	1	62266685	62266685	Human		name
150514634	CV1285269	single nucleotide variant	NM_181712.5(KANK4):c.2320-32C>T	not provided [RCV001722722]	benign	1	62263343	62263343	Human		name
150532764	CV1308106	single nucleotide variant	NM_181712.5(KANK4):c.2540-73T>C	not provided [RCV001753096]	likely benign	1	62253282	62253282	Human		name
155913510	CV2153541	single nucleotide variant	NM_181712.5(KANK4):c.2539+16A>G	not provided [RCV003012427]	likely benign	1	62263076	62263076	Human		name
405100519	CV2947885	single nucleotide variant	NM_181712.5(KANK4):c.2320-19G>A	not provided [RCV003665966]	likely benign	1	62263330	62263330	Human		name
150333114	CV1168843	single nucleotide variant	NM_181712.5(KANK4):c.2884-272C>A	not provided [RCV001537167]	benign	1	62238653	62238653	Human		name
150333506	CV1168844	single nucleotide variant	NM_181712.5(KANK4):c.2540-260T>C	not provided [RCV001537370]	benign	1	62253469	62253469	Human		name
150335483	CV1170752	single nucleotide variant	NM_181712.5(KANK4):c.2539+168A>G	not provided [RCV001540585]	benign	1	62262924	62262924	Human		name
150335099	CV1170753	single nucleotide variant	NM_181712.5(KANK4):c.2539+136G>A	not provided [RCV001540402]	benign	1	62262956	62262956	Human		name
150515811	CV1216338	single nucleotide variant	NM_181712.5(KANK4):c.1901-111T>G	not provided [RCV001608529]	benign	1	62271700	62271700	Human		name
150436553	CV1220565	duplication	NM_181712.5(KANK4):c.2884-266dup	not provided [RCV001609549]	benign	1	62238632	62238633	Human		name
150451393	CV1220856	single nucleotide variant	NM_181712.5(KANK4):c.1900+216C>T	not provided [RCV001611950]	benign	1	62272988	62272988	Human		name
150438946	CV1221239	deletion	NM_181712.5(KANK4):c.2883+167del	not provided [RCV001609933]	benign	1	62247305	62247305	Human		name
150481791	CV1222224	single nucleotide variant	NM_181712.5(KANK4):c.2884-247A>C	not provided [RCV001617022]	benign	1	62238628	62238628	Human		name
150435535	CV1233880	single nucleotide variant	NM_181712.5(KANK4):c.2683-125A>G	not provided [RCV001644007]	benign	1	62247797	62247797	Human		name
150510647	CV1242458	single nucleotide variant	NM_181712.5(KANK4):c.2683-126C>T	not provided [RCV001660808]	benign	1	62247798	62247798	Human		name
150443325	CV1249265	single nucleotide variant	NM_181712.5(KANK4):c.2012+309T>C	not provided [RCV001666697]	benign	1	62271169	62271169	Human		name
150445153	CV1249528	single nucleotide variant	NM_181712.5(KANK4):c.2231+133A>G	not provided [RCV001666961]	benign	1	62268154	62268154	Human		name
150455609	CV1259892	duplication	NM_181712.5(KANK4):c.2540-218dup	not provided [RCV001681371]	benign	1	62253409	62253410	Human		name
150437603	CV1262334	single nucleotide variant	NM_181712.5(KANK4):c.2319+234T>A	not provided [RCV001678692]	benign	1	62266498	62266498	Human		name
150445236	CV1269402	deletion	NM_181712.5(KANK4):c.2883+144del	not provided [RCV001691090]	benign	1	62247328	62247328	Human		name
150459062	CV1269739	single nucleotide variant	NM_181712.5(KANK4):c.2884-273C>T	not provided [RCV001693279]	benign	1	62238654	62238654	Human		name
150456229	CV1278471	single nucleotide variant	NM_181712.5(KANK4):c.2884-128C>T	not provided [RCV001709086]	benign	1	62238509	62238509	Human		name
150543060	CV1306701	single nucleotide variant	NM_181712.5(KANK4):c.2232-170C>T	not provided [RCV001769765]	likely benign	1	62266989	62266989	Human		name
150542684	CV1307859	deletion	NM_181712.5(KANK4):c.2884-252del	not provided [RCV001769634]	likely benign	1	62238633	62238633	Human		name
150539312	CV1308646	duplication	NM_181712.5(KANK4):c.2883+167dup	not provided [RCV001766150]	likely benign	1	62247304	62247305	Human		name
150541391	CV1308848	single nucleotide variant	NM_181712.5(KANK4):c.2231+274A>G	not provided [RCV001767936]	likely benign	1	62268013	62268013	Human		name
150441140	CV1233496	single nucleotide variant	NM_181712.5(KANK4):c.24C>T (p.Asp8=)	not provided [RCV001645184]	benign	1	62275080	62275080	Human		name
597940098	CV3836605	single nucleotide variant	NM_181712.5(KANK4):c.57T>C (p.Pro19=)	not provided [RCV005187626]	likely benign	1	62275047	62275047	Human		name
152130421	CV1523387	single nucleotide variant	NM_181712.5(KANK4):c.150C>T (p.Asn50=)	not provided [RCV002136851]	benign	1	62274954	62274954	Human		name
156201847	CV1916824	single nucleotide variant	NM_181712.5(KANK4):c.138C>T (p.Ile46=)	not provided [RCV002595733]	likely benign	1	62274966	62274966	Human		name
156116177	CV2093193	single nucleotide variant	NM_181712.5(KANK4):c.207G>A (p.Leu69=)	KANK4-related disorder [RCV003963412]\|not provided [RCV002913978]	likely benign	1	62274897	62274897	Human		name , trait , alternate_id
405070356	CV2923999	single nucleotide variant	NM_181712.5(KANK4):c.228T>C (p.Pro76=)	not provided [RCV003580951]	likely benign	1	62274876	62274876	Human		name
150334804	CV1170755	single nucleotide variant	NM_181712.5(KANK4):c.327A>G (p.Ser109=)	not provided [RCV001540248]	benign	1	62274777	62274777	Human		name
150463756	CV1252568	single nucleotide variant	NM_181712.5(KANK4):c.330A>G (p.Pro110=)	not provided [RCV001669891]	benign	1	62274774	62274774	Human		name
150504963	CV1255349	single nucleotide variant	NM_181712.5(KANK4):c.711T>C (p.Gly237=)	not provided [RCV001677796]	benign	1	62274393	62274393	Human		name
150532517	CV1309247	deletion	NM_181712.5(KANK4):c.1900+45_1900+47del	not provided [RCV001752928]	likely benign	1	62273157	62273159	Human		name
150548469	CV1316360	duplication	NM_181712.5(KANK4):c.2683-12_2683-10dup	not provided [RCV001786162]	benign\|likely benign	1	62247681	62247682	Human		name
152116917	CV1569798	single nucleotide variant	NM_181712.5(KANK4):c.858G>A (p.Pro286=)	not provided [RCV002117315]	likely benign	1	62274246	62274246	Human		name
156322785	CV1978988	single nucleotide variant	NM_181712.5(KANK4):c.546G>T (p.Leu182=)	not provided [RCV002630460]	likely benign	1	62274558	62274558	Human		name
156050479	CV2006723	single nucleotide variant	NM_181712.5(KANK4):c.504G>A (p.Thr168=)	not provided [RCV002659350]	likely benign	1	62274600	62274600	Human		name
156367932	CV2007463	deletion	NM_181712.5(KANK4):c.269del (p.Asn90fs)	not provided [RCV002676695]	uncertain significance	1	62274835	62274835	Human		name
156115852	CV2104627	single nucleotide variant	NM_181712.5(KANK4):c.618T>A (p.Pro206=)	KANK4-related disorder [RCV003906327]\|not provided [RCV002927619]	benign\|likely benign	1	62274486	62274486	Human		name , trait , alternate_id
156214779	CV2127931	single nucleotide variant	NM_181712.5(KANK4):c.912G>A (p.Glu304=)	not provided [RCV002957898]	likely benign	1	62274192	62274192	Human		name
402488275	CV2941567	single nucleotide variant	NM_181712.5(KANK4):c.537C>T (p.Gly179=)	not provided [RCV003660295]	likely benign	1	62274567	62274567	Human		name
405080574	CV3050489	single nucleotide variant	NM_181712.5(KANK4):c.657A>C (p.Arg219=)	not provided [RCV003717103]	likely benign	1	62274447	62274447	Human		name
405292407	CV3192415	single nucleotide variant	NM_181712.5(KANK4):c.939G>A (p.Pro313=)	KANK4-related disorder [RCV003929682]	likely benign	1	62274165	62274165	Human		name , trait , alternate_id
405801718	CV3271866	single nucleotide variant	NM_181712.5(KANK4):c.40G>C (p.Asp14His)	not specified [RCV004403564]	uncertain significance	1	62275064	62275064	Human		name
597911552	CV3850539	single nucleotide variant	NM_181712.5(KANK4):c.783A>G (p.Leu261=)	not provided [RCV005203688]	likely benign	1	62274321	62274321	Human		name
150333997	CV1168845	single nucleotide variant	NM_181712.5(KANK4):c.1281G>A (p.Ser427=)	not provided [RCV001537572]	benign	1	62273823	62273823	Human		name
150482902	CV1245021	single nucleotide variant	NM_181712.5(KANK4):c.1815C>T (p.Ser605=)	not provided [RCV001653198]	benign	1	62273289	62273289	Human		name
150447685	CV1253439	single nucleotide variant	NM_181712.5(KANK4):c.2385C>T (p.Pro795=)	not provided [RCV001667367]	benign	1	62263246	62263246	Human		name
150504918	CV1255338	single nucleotide variant	NM_181712.5(KANK4):c.1872A>G (p.Pro624=)	not provided [RCV001677785]	benign	1	62273232	62273232	Human		name
150447804	CV1261870	single nucleotide variant	NM_181712.5(KANK4):c.1578C>T (p.Ser526=)	not provided [RCV001680255]	benign	1	62273526	62273526	Human		name
150486000	CV1262209	single nucleotide variant	NM_181712.5(KANK4):c.2781C>T (p.His927=)	not provided [RCV001686900]	benign	1	62247574	62247574	Human		name
150514711	CV1285295	single nucleotide variant	NM_181712.5(KANK4):c.2442A>G (p.Lys814=)	not provided [RCV001722748]	benign	1	62263189	62263189	Human		name
150556946	CV1307715	single nucleotide variant	NM_181712.5(KANK4):c.2157C>A (p.Gly719=)	KANK4-related disorder [RCV003931322]\|not provided [RCV001774993]	benign\|likely benign	1	62268361	62268361	Human		name , trait , alternate_id
151821614	CV1453623	single nucleotide variant	NM_181712.5(KANK4):c.212G>A (p.Arg71Gln)	not provided [RCV001879266]	uncertain significance	1	62274892	62274892	Human		name
152082508	CV1526203	single nucleotide variant	NM_181712.5(KANK4):c.2958C>T (p.His986=)	KANK4-related disorder [RCV003950897]\|not provided [RCV002170724]	likely benign	1	62238307	62238307	Human		name , trait , alternate_id
152172143	CV1575740	single nucleotide variant	NM_181712.5(KANK4):c.2775G>A (p.Gln925=)	not provided [RCV002183744]	benign	1	62247580	62247580	Human		name
152122398	CV1613533	single nucleotide variant	NM_181712.5(KANK4):c.1440A>G (p.Pro480=)	not provided [RCV002081732]	likely benign	1	62273664	62273664	Human		name
152082835	CV1647749	single nucleotide variant	NM_181712.5(KANK4):c.2266C>A (p.Arg756=)	not provided [RCV002076598]	likely benign	1	62266785	62266785	Human		name
156109206	CV1903775	single nucleotide variant	NM_181712.5(KANK4):c.2472G>A (p.Gly824=)	not provided [RCV003080900]	likely benign	1	62263159	62263159	Human		name
155943333	CV1920899	single nucleotide variant	NM_181712.5(KANK4):c.1668G>A (p.Thr556=)	not provided [RCV002615782]	likely benign	1	62273436	62273436	Human		name
156390186	CV1955274	single nucleotide variant	NM_181712.5(KANK4):c.1701C>T (p.Ile567=)	not provided [RCV002583799]	likely benign	1	62273403	62273403	Human		name
156413427	CV1969067	single nucleotide variant	NM_181712.5(KANK4):c.2091G>A (p.Lys697=)	not provided [RCV002608833]	likely benign	1	62268427	62268427	Human		name
156308227	CV1999939	single nucleotide variant	NM_181712.5(KANK4):c.1435C>T (p.Leu479=)	not provided [RCV002671489]	likely benign	1	62273669	62273669	Human		name
155987863	CV2105324	single nucleotide variant	NM_181712.5(KANK4):c.2907C>T (p.Ile969=)	not provided [RCV002947187]	benign	1	62238358	62238358	Human		name
156310270	CV2111254	single nucleotide variant	NM_181712.5(KANK4):c.1761C>T (p.Ser587=)	not provided [RCV002937122]	benign	1	62273343	62273343	Human		name
156327962	CV2116194	single nucleotide variant	NM_181712.5(KANK4):c.1080C>T (p.Thr360=)	KANK4-related disorder [RCV003916636]\|not provided [RCV002938197]	likely benign	1	62274024	62274024	Human		name , trait , alternate_id
156140347	CV2116690	single nucleotide variant	NM_181712.5(KANK4):c.2541C>A (p.Gly847=)	not provided [RCV002914884]	likely benign	1	62253208	62253208	Human		name
156265433	CV2125227	single nucleotide variant	NM_181712.5(KANK4):c.154A>C (p.Ile52Leu)	not provided [RCV002934036]	uncertain significance	1	62274950	62274950	Human		name
156122617	CV2128601	single nucleotide variant	NM_181712.5(KANK4):c.1749G>A (p.Pro583=)	not provided [RCV002953557]	benign\|likely benign	1	62273355	62273355	Human		name
156034729	CV2132820	single nucleotide variant	NM_181712.5(KANK4):c.1911A>G (p.Pro637=)	not provided [RCV002999287]	benign	1	62271579	62271579	Human		name
155970311	CV2158014	single nucleotide variant	NM_181712.5(KANK4):c.2289A>G (p.Pro763=)	not provided [RCV003033403]	likely benign	1	62266762	62266762	Human		name
329391253	CV2452189	single nucleotide variant	NM_181712.5(KANK4):c.201C>A (p.Ser67Arg)	not specified [RCV004278897]	uncertain significance	1	62274903	62274903	Human		name
401730248	CV2680063	single nucleotide variant	NM_181712.5(KANK4):c.242G>A (p.Arg81His)	not specified [RCV004286559]	uncertain significance	1	62274862	62274862	Human		name
401776021	CV2706853	single nucleotide variant	NM_181712.5(KANK4):c.177A>C (p.Arg59Ser)	not specified [RCV004321482]	uncertain significance	1	62274927	62274927	Human		name
401927800	CV2808939	single nucleotide variant	NM_181712.5(KANK4):c.1449C>T (p.Pro483=)	not provided [RCV003406536]	likely benign	1	62273655	62273655	Human		name
405089265	CV2859225	single nucleotide variant	NM_181712.5(KANK4):c.170T>A (p.Ile57Asn)	not provided [RCV003549786]	benign	1	62274934	62274934	Human		name
405238187	CV2881436	single nucleotide variant	NM_181712.5(KANK4):c.2667C>T (p.Asn889=)	not provided [RCV003556820]	likely benign	1	62253082	62253082	Human		name
405121205	CV2888082	single nucleotide variant	NM_181712.5(KANK4):c.2619T>C (p.Asn873=)	not provided [RCV003559111]	likely benign	1	62253130	62253130	Human		name
405068120	CV2924000	single nucleotide variant	NM_181712.5(KANK4):c.209C>T (p.Pro70Leu)	not provided [RCV003580952]	uncertain significance	1	62274895	62274895	Human		name
402514117	CV2943075	single nucleotide variant	NM_181712.5(KANK4):c.2697G>A (p.Ala899=)	not provided [RCV003662805]	likely benign	1	62247658	62247658	Human		name
405173191	CV2955322	single nucleotide variant	NM_181712.5(KANK4):c.2706G>A (p.Leu902=)	not provided [RCV003675563]	likely benign	1	62247649	62247649	Human		name
405252615	CV3047388	single nucleotide variant	NM_181712.5(KANK4):c.1674C>T (p.Ala558=)	not provided [RCV003722278]	likely benign	1	62273430	62273430	Human		name
405244511	CV3050646	deletion	NM_181712.5(KANK4):c.918del (p.Asn306fs)	not provided [RCV003720004]	uncertain significance	1	62274186	62274186	Human		name
405134513	CV3115583	single nucleotide variant	NM_181712.5(KANK4):c.2742G>A (p.Ala914=)	not provided [RCV003816240]	likely benign	1	62247613	62247613	Human		name
405260099	CV3190165	single nucleotide variant	NM_181712.5(KANK4):c.2460C>G (p.Ala820=)	KANK4-related disorder [RCV003894568]	likely benign	1	62263171	62263171	Human		name , trait , alternate_id
405289022	CV3204870	single nucleotide variant	NM_181712.5(KANK4):c.2874G>A (p.Leu958=)	KANK4-related disorder [RCV003961526]	likely benign	1	62247481	62247481	Human		name , trait , alternate_id
405279617	CV3217550	single nucleotide variant	NM_181712.5(KANK4):c.1893G>A (p.Pro631=)	KANK4-related disorder [RCV003976938]\|not specified [RCV005353332]	likely benign	1	62273211	62273211	Human		name , trait , alternate_id
405289604	CV3218306	single nucleotide variant	NM_181712.5(KANK4):c.2745G>A (p.Leu915=)	KANK4-related disorder [RCV003983708]	likely benign	1	62247610	62247610	Human		name , trait , alternate_id
405278256	CV3221831	single nucleotide variant	NM_181712.5(KANK4):c.2079C>T (p.Ser693=)	KANK4-related disorder [RCV003976397]	likely benign	1	62268439	62268439	Human		name , trait , alternate_id
405801712	CV3271863	single nucleotide variant	NM_181712.5(KANK4):c.280G>A (p.Val94Met)	not specified [RCV004403561]	uncertain significance	1	62274824	62274824	Human		name
407511664	CV3448262	single nucleotide variant	NM_181712.5(KANK4):c.179G>A (p.Arg60Lys)	not specified [RCV004626538]	uncertain significance	1	62274925	62274925	Human		name
408379249	CV3516610	single nucleotide variant	NM_181712.5(KANK4):c.2256T>C (p.Leu752=)	KANK4-related disorder [RCV004752612]	likely benign	1	62266795	62266795	Human		name , trait , alternate_id
597786273	CV3690722	single nucleotide variant	NM_181712.5(KANK4):c.223C>A (p.Leu75Ile)	not specified [RCV004932190]	uncertain significance	1	62274881	62274881	Human		name
597942080	CV3785939	single nucleotide variant	NM_181712.5(KANK4):c.1080C>G (p.Thr360=)	not provided [RCV005133832]	likely benign	1	62274024	62274024	Human		name
597973597	CV3801472	single nucleotide variant	NM_181712.5(KANK4):c.2979G>T (p.Leu993=)	not provided [RCV005143461]	likely benign	1	62238286	62238286	Human		name
597929460	CV3837435	single nucleotide variant	NM_181712.5(KANK4):c.2547C>T (p.Cys849=)	not provided [RCV005185593]	likely benign	1	62253202	62253202	Human		name
597953875	CV3844287	single nucleotide variant	NM_181712.5(KANK4):c.1800G>A (p.Gln600=)	not provided [RCV005190960]	likely benign	1	62273304	62273304	Human		name
597949631	CV3852994	single nucleotide variant	NM_181712.5(KANK4):c.2184C>T (p.Ala728=)	not provided [RCV005189875]	likely benign	1	62268334	62268334	Human		name
150330878	CV1170754	single nucleotide variant	NM_181712.5(KANK4):c.512A>G (p.His171Arg)	not provided [RCV001538340]	benign	1	62274592	62274592	Human		name
150465791	CV1218080	duplication	NM_181712.5(KANK4):c.2540-218_2540-216dup	not provided [RCV001614206]	benign	1	62253409	62253410	Human		name
150441546	CV1233560	duplication	NM_181712.5(KANK4):c.2884-266_2884-265dup	not provided [RCV001645248]	benign	1	62238632	62238633	Human		name
150500038	CV1256020	duplication	NM_181712.5(KANK4):c.2540-218_2540-217dup	not provided [RCV001676643]	benign	1	62253409	62253410	Human		name
151738792	CV1358752	single nucleotide variant	NM_181712.5(KANK4):c.394C>G (p.Leu132Val)	not provided [RCV001967931]\|not specified [RCV004043154]	uncertain significance	1	62274710	62274710	Human		name
151819998	CV1416085	single nucleotide variant	NM_181712.5(KANK4):c.647C>T (p.Ser216Phe)	not provided [RCV001919472]\|not specified [RCV004044151]	uncertain significance	1	62274457	62274457	Human		name
152110530	CV1665495	single nucleotide variant	NM_181712.5(KANK4):c.848C>T (p.Thr283Met)	not provided [RCV002080182]	benign	1	62274256	62274256	Human		name
156410671	CV1882676	single nucleotide variant	NM_181712.5(KANK4):c.344C>T (p.Ala115Val)	not provided [RCV003072166]\|not specified [RCV004632179]	uncertain significance	1	62274760	62274760	Human		name
155931183	CV1909106	single nucleotide variant	NM_181712.5(KANK4):c.503C>T (p.Thr168Met)	not provided [RCV002615001]	uncertain significance	1	62274601	62274601	Human		name
156092487	CV1963427	single nucleotide variant	NM_181712.5(KANK4):c.328C>T (p.Pro110Ser)	not provided [RCV002570275]\|not specified [RCV004927820]	uncertain significance	1	62274776	62274776	Human		name
156149232	CV1967379	single nucleotide variant	NM_181712.5(KANK4):c.856C>T (p.Pro286Ser)	not provided [RCV002594091]	uncertain significance	1	62274248	62274248	Human		name
156023206	CV2019482	single nucleotide variant	NM_181712.5(KANK4):c.586G>A (p.Glu196Lys)	not provided [RCV002691101]	uncertain significance	1	62274518	62274518	Human		name
156202742	CV2021302	single nucleotide variant	NM_181712.5(KANK4):c.437A>T (p.Glu146Val)	not provided [RCV002711459]	uncertain significance	1	62274667	62274667	Human		name
156206140	CV2110283	single nucleotide variant	NM_181712.5(KANK4):c.332C>T (p.Pro111Leu)	KANK4-related disorder [RCV004753594]\|not provided [RCV002957562]\|not specified [RCV004067215]	uncertain significance	1	62274772	62274772	Human		name , trait , alternate_id
156360721	CV2126431	single nucleotide variant	NM_181712.5(KANK4):c.749C>T (p.Pro250Leu)	KANK4-related disorder [RCV003916677]\|not provided [RCV002966963]	benign\|likely benign	1	62274355	62274355	Human		name , trait , alternate_id
156263760	CV2289725	single nucleotide variant	NM_181712.5(KANK4):c.881C>T (p.Pro294Leu)	not provided [RCV005059332]\|not specified [RCV004150419]	uncertain significance	1	62274223	62274223	Human		name
155974022	CV2334503	single nucleotide variant	NM_181712.5(KANK4):c.797A>G (p.Asp266Gly)	not specified [RCV004188467]	uncertain significance	1	62274307	62274307	Human		name
155939913	CV2378898	single nucleotide variant	NM_181712.5(KANK4):c.721G>A (p.Val241Ile)	not provided [RCV005099148]\|not specified [RCV004233338]	uncertain significance	1	62274383	62274383	Human		name
156142814	CV2383802	single nucleotide variant	NM_181712.5(KANK4):c.975C>G (p.Ile325Met)	not provided [RCV003720741]\|not specified [RCV004231672]	uncertain significance	1	62274129	62274129	Human		name
329371471	CV2431892	single nucleotide variant	NM_181712.5(KANK4):c.464G>A (p.Gly155Glu)	not specified [RCV004255026]	uncertain significance	1	62274640	62274640	Human		name
329398027	CV2464707	single nucleotide variant	NM_181712.5(KANK4):c.910G>A (p.Glu304Lys)	not specified [RCV004284681]	uncertain significance	1	62274194	62274194	Human		name
329387946	CV2468499	single nucleotide variant	NM_181712.5(KANK4):c.956A>C (p.Asp319Ala)	not specified [RCV004278078]	uncertain significance	1	62274148	62274148	Human		name
329375416	CV2468581	single nucleotide variant	NM_181712.5(KANK4):c.694G>A (p.Ala232Thr)	not specified [RCV004278146]	uncertain significance	1	62274410	62274410	Human		name
329398683	CV2471650	single nucleotide variant	NM_181712.5(KANK4):c.664A>G (p.Thr222Ala)	not provided [RCV003779739]\|not specified [RCV004286939]	uncertain significance	1	62274440	62274440	Human		name
401741046	CV2690361	single nucleotide variant	NM_181712.5(KANK4):c.938C>T (p.Pro313Leu)	not specified [RCV004302355]	uncertain significance	1	62274166	62274166	Human		name
401757355	CV2692952	single nucleotide variant	NM_181712.5(KANK4):c.869C>T (p.Pro290Leu)	not specified [RCV004306469]	uncertain significance	1	62274235	62274235	Human		name
401872756	CV2779991	single nucleotide variant	NM_181712.5(KANK4):c.592A>G (p.Ser198Gly)	not specified [RCV004353582]	uncertain significance	1	62274512	62274512	Human		name
401932098	CV2799107	single nucleotide variant	NM_181712.5(KANK4):c.545T>A (p.Leu182Gln)	KANK4-related disorder [RCV003408612]	uncertain significance	1	62274559	62274559	Human		name , trait , alternate_id
401931239	CV2800644	single nucleotide variant	NM_181712.5(KANK4):c.364A>G (p.Arg122Gly)	KANK4-related disorder [RCV003391266]	uncertain significance	1	62274740	62274740	Human		name , trait , alternate_id
402475178	CV2863724	single nucleotide variant	NM_181712.5(KANK4):c.638T>C (p.Phe213Ser)	not provided [RCV003543250]	uncertain significance	1	62274466	62274466	Human		name
405217931	CV2873593	single nucleotide variant	NM_181712.5(KANK4):c.676G>C (p.Glu226Gln)	not provided [RCV003553463]\|not specified [RCV005353199]	uncertain significance	1	62274428	62274428	Human		name
402504195	CV2879759	single nucleotide variant	NM_181712.5(KANK4):c.445G>A (p.Glu149Lys)	not provided [RCV003546105]	uncertain significance	1	62274659	62274659	Human		name
405240379	CV2892971	single nucleotide variant	NM_181712.5(KANK4):c.781C>A (p.Leu261Ile)	not provided [RCV003557280]	uncertain significance	1	62274323	62274323	Human		name
402507690	CV2944507	deletion	NM_181712.5(KANK4):c.2856del (p.Ala953fs)	not provided [RCV003662233]	uncertain significance	1	62247499	62247499	Human		name
405041132	CV3007480	single nucleotide variant	NM_181712.5(KANK4):c.947T>C (p.Val316Ala)	not provided [RCV003696331]	uncertain significance	1	62274157	62274157	Human		name
405170968	CV3151668	single nucleotide variant	NM_181712.5(KANK4):c.488C>G (p.Ser163Cys)	not provided [RCV003857819]	uncertain significance	1	62274616	62274616	Human		name
405206016	CV3154593	single nucleotide variant	NM_181712.5(KANK4):c.467G>A (p.Arg156Gln)	not provided [RCV003845103]	uncertain significance	1	62274637	62274637	Human		name
405165112	CV3160474	single nucleotide variant	NM_181712.5(KANK4):c.806A>G (p.Asn269Ser)	not provided [RCV003857354]	uncertain significance	1	62274298	62274298	Human		name
402507019	CV3181721	single nucleotide variant	NM_181712.5(KANK4):c.761T>C (p.Phe254Ser)	not provided [RCV003878555]	uncertain significance	1	62274343	62274343	Human		name
405801716	CV3271865	single nucleotide variant	NM_181712.5(KANK4):c.314A>T (p.Glu105Val)	not specified [RCV004403563]	likely benign\|uncertain significance	1	62274790	62274790	Human		name
405801720	CV3271867	single nucleotide variant	NM_181712.5(KANK4):c.543C>G (p.Ser181Arg)	not specified [RCV004403565]	uncertain significance	1	62274561	62274561	Human		name
405801722	CV3271868	single nucleotide variant	NM_181712.5(KANK4):c.829T>C (p.Phe277Leu)	not specified [RCV004403566]	uncertain significance	1	62274275	62274275	Human		name
407467431	CV3448264	single nucleotide variant	NM_181712.5(KANK4):c.986A>C (p.Glu329Ala)	not specified [RCV004635890]	uncertain significance	1	62274118	62274118	Human		name
407467438	CV3448267	single nucleotide variant	NM_181712.5(KANK4):c.495G>A (p.Met165Ile)	not specified [RCV004635892]	uncertain significance	1	62274609	62274609	Human		name
408380407	CV3514348	single nucleotide variant	NM_181712.5(KANK4):c.506T>G (p.Leu169Arg)	KANK4-related disorder [RCV004754115]	uncertain significance	1	62274598	62274598	Human		name , trait , alternate_id
597786199	CV3690705	single nucleotide variant	NM_181712.5(KANK4):c.487T>C (p.Ser163Pro)	not provided [RCV005110391]\|not specified [RCV004932173]	uncertain significance	1	62274617	62274617	Human		name
597786203	CV3690706	single nucleotide variant	NM_181712.5(KANK4):c.739C>G (p.Leu247Val)	not specified [RCV004932174]	uncertain significance	1	62274365	62274365	Human		name
597786213	CV3690708	single nucleotide variant	NM_181712.5(KANK4):c.550C>T (p.Pro184Ser)	not specified [RCV004932176]	uncertain significance	1	62274554	62274554	Human		name
597786217	CV3690709	single nucleotide variant	NM_181712.5(KANK4):c.765G>C (p.Gln255His)	not specified [RCV004932177]	uncertain significance	1	62274339	62274339	Human		name
597786234	CV3690713	single nucleotide variant	NM_181712.5(KANK4):c.625G>A (p.Gly209Arg)	not specified [RCV004932181]	uncertain significance	1	62274479	62274479	Human		name
597786243	CV3690715	single nucleotide variant	NM_181712.5(KANK4):c.543C>A (p.Ser181Arg)	not specified [RCV004932183]	uncertain significance	1	62274561	62274561	Human		name
597786252	CV3690717	single nucleotide variant	NM_181712.5(KANK4):c.798T>A (p.Asp266Glu)	not specified [RCV004932185]	uncertain significance	1	62274306	62274306	Human		name
597786260	CV3690719	single nucleotide variant	NM_181712.5(KANK4):c.826T>A (p.Leu276Met)	not provided [RCV005110392]\|not specified [RCV004932187]	uncertain significance	1	62274278	62274278	Human		name
597875388	CV3766279	single nucleotide variant	NM_181712.5(KANK4):c.376A>T (p.Ser126Cys)	not provided [RCV005108411]	likely benign	1	62274728	62274728	Human		name
597903661	CV3846015	single nucleotide variant	NM_181712.5(KANK4):c.745G>T (p.Gly249Cys)	not provided [RCV005181637]	uncertain significance	1	62274359	62274359	Human		name
597966580	CV3859151	single nucleotide variant	NM_181712.5(KANK4):c.518G>A (p.Arg173Lys)	not provided [RCV005194546]	uncertain significance	1	62274586	62274586	Human		name
597888336	CV3859481	single nucleotide variant	NM_181712.5(KANK4):c.779T>C (p.Val260Ala)	not provided [RCV005200137]	uncertain significance	1	62274325	62274325	Human		name
598258984	CV3979902	single nucleotide variant	NM_181712.5(KANK4):c.884A>G (p.Glu295Gly)	not specified [RCV005347322]	uncertain significance	1	62274220	62274220	Human		name
598258989	CV3979904	single nucleotide variant	NM_181712.5(KANK4):c.901G>A (p.Glu301Lys)	not specified [RCV005347323]	uncertain significance	1	62274203	62274203	Human		name
598233970	CV3979908	single nucleotide variant	NM_181712.5(KANK4):c.430G>C (p.Glu144Gln)	not specified [RCV005363441]	uncertain significance	1	62274674	62274674	Human		name
598258999	CV3979909	single nucleotide variant	NM_181712.5(KANK4):c.431A>G (p.Glu144Gly)	not specified [RCV005347325]	uncertain significance	1	62274673	62274673	Human		name
13831935	CV582432	single nucleotide variant	NM_181712.5(KANK4):c.676G>T (p.Glu226Ter)	not provided [RCV000722620]	uncertain significance	1	62274428	62274428	Human		name
15168160	CV719043	single nucleotide variant	NM_181712.5(KANK4):c.857C>T (p.Pro286Leu)	not provided [RCV000883005]	benign\|likely benign	1	62274247	62274247	Human		name
15119575	CV732537	deletion	NM_181712.5(KANK4):c.2095del (p.Cys699fs)	not provided [RCV000895751]	likely benign\|conflicting interpretations of pathogenicity	1	62268423	62268423	Human		name
150508786	CV1229731	single nucleotide variant	NM_181712.5(KANK4):c.2519T>C (p.Val840Ala)	not provided [RCV001636309]	benign	1	62263112	62263112	Human		name
150468942	CV1243077	single nucleotide variant	NM_181712.5(KANK4):c.2960C>T (p.Ala987Val)	not provided [RCV001650595]	benign	1	62238305	62238305	Human		name
150437441	CV1249869	single nucleotide variant	NM_181712.5(KANK4):c.2803G>C (p.Val935Leu)	not provided [RCV001665783]	benign	1	62247552	62247552	Human		name
150448390	CV1260678	single nucleotide variant	NM_181712.5(KANK4):c.2101G>A (p.Gly701Ser)	not provided [RCV001680346]	benign	1	62268417	62268417	Human		name
150482765	CV1261673	single nucleotide variant	NM_181712.5(KANK4):c.2465A>G (p.His822Arg)	not provided [RCV001686276]	benign	1	62263166	62263166	Human		name
150514753	CV1285309	single nucleotide variant	NM_181712.5(KANK4):c.2302A>G (p.Thr768Ala)	not provided [RCV001722762]	benign	1	62266749	62266749	Human		name
151749637	CV1338414	single nucleotide variant	NM_181712.5(KANK4):c.2098G>A (p.Asp700Asn)	not provided [RCV001927390]\|not specified [RCV004041521]	uncertain significance	1	62268420	62268420	Human		name
151870942	CV1340421	single nucleotide variant	NM_181712.5(KANK4):c.1579G>A (p.Asp527Asn)	not provided [RCV001939792]	uncertain significance	1	62273525	62273525	Human		name
151782077	CV1381332	single nucleotide variant	NM_181712.5(KANK4):c.1670A>T (p.Asp557Val)	not provided [RCV001875452]	uncertain significance	1	62273434	62273434	Human		name
151839081	CV1382846	single nucleotide variant	NM_181712.5(KANK4):c.2930T>A (p.Met977Lys)	KANK4-related disorder [RCV003408103]\|not provided [RCV002031602]\|not specified [RCV004044848]	uncertain significance	1	62238335	62238335	Human		name , trait , alternate_id
151842148	CV1436094	single nucleotide variant	NM_181712.5(KANK4):c.2057C>T (p.Thr686Ile)	not provided [RCV001956886]	uncertain significance	1	62268461	62268461	Human		name
151735848	CV1506938	single nucleotide variant	NM_181712.5(KANK4):c.1739A>G (p.His580Arg)	not provided [RCV001984706]	uncertain significance	1	62273365	62273365	Human		name
152134797	CV1528188	single nucleotide variant	NM_181712.5(KANK4):c.2891G>A (p.Arg964His)	KANK4-related disorder [RCV003951024]\|not provided [RCV002099968]	likely benign	1	62238374	62238374	Human		name , trait , alternate_id
156307144	CV1877847	single nucleotide variant	NM_181712.5(KANK4):c.2908G>A (p.Ala970Thr)	KANK4-related disorder [RCV003936511]\|not provided [RCV003062245]	likely benign	1	62238357	62238357	Human		name , trait , alternate_id
156413080	CV1887640	single nucleotide variant	NM_181712.5(KANK4):c.2584G>A (p.Val862Ile)	not provided [RCV003073150]\|not specified [RCV005356275]	uncertain significance	1	62253165	62253165	Human		name
156296871	CV1900908	single nucleotide variant	NM_181712.5(KANK4):c.1666A>G (p.Thr556Ala)	not provided [RCV002598986]	uncertain significance	1	62273438	62273438	Human		name
156216873	CV1903397	single nucleotide variant	NM_181712.5(KANK4):c.2074G>A (p.Asp692Asn)	KANK4-related disorder [RCV003420340]\|not provided [RCV003093165]\|not specified [RCV004073249]	uncertain significance	1	62268444	62268444	Human		name , trait , alternate_id
156279237	CV1912067	single nucleotide variant	NM_181712.5(KANK4):c.2068T>G (p.Leu690Val)	not provided [RCV002628371]\|not specified [RCV005353122]	uncertain significance	1	62268450	62268450	Human		name
156274569	CV1915548	single nucleotide variant	NM_181712.5(KANK4):c.2932G>C (p.Glu978Gln)	not provided [RCV002628220]	uncertain significance	1	62238333	62238333	Human		name
156405176	CV1919223	single nucleotide variant	NM_181712.5(KANK4):c.2470G>A (p.Gly824Arg)	not provided [RCV002585590]	uncertain significance	1	62263161	62263161	Human		name
156291853	CV1926557	single nucleotide variant	NM_181712.5(KANK4):c.1057G>A (p.Glu353Lys)	not provided [RCV002628847]	uncertain significance	1	62274047	62274047	Human		name
156436986	CV1936810	single nucleotide variant	NM_181712.5(KANK4):c.2147C>A (p.Ala716Asp)	not provided [RCV003106513]	uncertain significance	1	62268371	62268371	Human		name
156434538	CV1940078	single nucleotide variant	NM_181712.5(KANK4):c.1408G>T (p.Glu470Ter)	not provided [RCV003104494]	uncertain significance	1	62273696	62273696	Human		name
156101615	CV1960346	single nucleotide variant	NM_181712.5(KANK4):c.1240G>A (p.Val414Met)	not provided [RCV002570868]\|not specified [RCV004631999]	uncertain significance	1	62273864	62273864	Human		name
156189165	CV1961538	single nucleotide variant	NM_181712.5(KANK4):c.1769A>G (p.Lys590Arg)	not provided [RCV002574356]	uncertain significance	1	62273335	62273335	Human		name
156345146	CV1970475	single nucleotide variant	NM_181712.5(KANK4):c.1814G>A (p.Ser605Asn)	KANK4-related disorder [RCV004753567]\|not provided [RCV002601488]	uncertain significance	1	62273290	62273290	Human		name , trait , alternate_id
156196914	CV1995822	single nucleotide variant	NM_181712.5(KANK4):c.2267G>A (p.Arg756Gln)	not provided [RCV002643497]	uncertain significance	1	62266784	62266784	Human		name
156123715	CV2021076	single nucleotide variant	NM_181712.5(KANK4):c.2368C>T (p.Arg790Trp)	not provided [RCV002740298]	uncertain significance	1	62263263	62263263	Human		name
156037577	CV2047720	single nucleotide variant	NM_181712.5(KANK4):c.2119G>A (p.Val707Ile)	not provided [RCV002781368]	uncertain significance	1	62268399	62268399	Human		name
156010101	CV2079538	single nucleotide variant	NM_181712.5(KANK4):c.1145A>G (p.Gln382Arg)	not provided [RCV002866058]	uncertain significance	1	62273959	62273959	Human		name
156268405	CV2102724	single nucleotide variant	NM_181712.5(KANK4):c.2594C>T (p.Thr865Ile)	KANK4-related disorder [RCV003926478]\|not provided [RCV002895842]	benign	1	62253155	62253155	Human		name , trait , alternate_id
156103645	CV2107880	single nucleotide variant	NM_181712.5(KANK4):c.1957C>T (p.Arg653Cys)	not provided [RCV002927142]\|not specified [RCV004066304]	uncertain significance	1	62271533	62271533	Human		name
156090998	CV2109997	single nucleotide variant	NM_181712.5(KANK4):c.1343G>A (p.Arg448Gln)	KANK4-related disorder [RCV003926557]\|not provided [RCV002952358]	likely benign	1	62273761	62273761	Human		name , trait , alternate_id
155939304	CV2110581	single nucleotide variant	NM_181712.5(KANK4):c.2618A>G (p.Asn873Ser)	not provided [RCV002904358]\|not specified [RCV005362912]	likely benign\|uncertain significance	1	62253131	62253131	Human		name
156118988	CV2115860	single nucleotide variant	NM_181712.5(KANK4):c.1154G>A (p.Arg385Gln)	not provided [RCV002927736]\|not specified [RCV004067025]	likely benign\|uncertain significance	1	62273950	62273950	Human		name
156157036	CV2118271	single nucleotide variant	NM_181712.5(KANK4):c.2011G>A (p.Gly671Arg)	KANK4-related disorder [RCV003936451]\|not provided [RCV002929105]	likely benign	1	62271479	62271479	Human		name , trait , alternate_id
156252065	CV2130242	single nucleotide variant	NM_181712.5(KANK4):c.1180C>G (p.Leu394Val)	not provided [RCV002959244]\|not specified [RCV004068255]	uncertain significance	1	62273924	62273924	Human		name
156369683	CV2194053	single nucleotide variant	NM_181712.5(KANK4):c.1874C>T (p.Pro625Leu)	KANK4-related disorder [RCV003410145]\|not specified [RCV004076815]	uncertain significance	1	62273230	62273230	Human		name , trait , alternate_id
156264554	CV2198585	single nucleotide variant	NM_181712.5(KANK4):c.1643C>T (p.Pro548Leu)	not provided [RCV005099483]\|not specified [RCV004075605]	uncertain significance	1	62273461	62273461	Human		name
155920866	CV2210912	single nucleotide variant	NM_181712.5(KANK4):c.2369G>A (p.Arg790Gln)	not provided [RCV003561075]\|not specified [RCV004085990]	uncertain significance	1	62263262	62263262	Human		name
156379666	CV2217935	single nucleotide variant	NM_181712.5(KANK4):c.2227G>A (p.Glu743Lys)	not specified [RCV004086391]	uncertain significance	1	62268291	62268291	Human		name
156245398	CV2218970	single nucleotide variant	NM_181712.5(KANK4):c.2716C>T (p.His906Tyr)	not specified [RCV004087152]	uncertain significance	1	62247639	62247639	Human		name
156237428	CV2235679	single nucleotide variant	NM_181712.5(KANK4):c.2686G>A (p.Gly896Ser)	not specified [RCV004111821]	uncertain significance	1	62247669	62247669	Human		name
155914642	CV2242782	single nucleotide variant	NM_181712.5(KANK4):c.1985A>G (p.Asn662Ser)	not specified [RCV004107382]	uncertain significance	1	62271505	62271505	Human		name
155914925	CV2242871	single nucleotide variant	NM_181712.5(KANK4):c.1603A>T (p.Arg535Trp)	not specified [RCV004107462]	uncertain significance	1	62273501	62273501	Human		name
156119714	CV2275844	single nucleotide variant	NM_181712.5(KANK4):c.2045G>T (p.Gly682Val)	not specified [RCV004139509]	uncertain significance	1	62268473	62268473	Human		name
156099601	CV2294649	single nucleotide variant	NM_181712.5(KANK4):c.2143G>A (p.Glu715Lys)	not specified [RCV004161902]	likely benign	1	62268375	62268375	Human		name
156282556	CV2317396	single nucleotide variant	NM_181712.5(KANK4):c.1406C>G (p.Ala469Gly)	not specified [RCV004172370]	uncertain significance	1	62273698	62273698	Human		name
156186137	CV2324710	single nucleotide variant	NM_181712.5(KANK4):c.2696C>T (p.Ala899Val)	not specified [RCV004172949]	uncertain significance	1	62247659	62247659	Human		name
156039202	CV2332699	single nucleotide variant	NM_181712.5(KANK4):c.1007G>T (p.Arg336Met)	KANK4-related disorder [RCV003396839]\|not provided [RCV005099910]\|not specified [RCV004189375]	uncertain significance	1	62274097	62274097	Human		name , trait , alternate_id
156187135	CV2332700	single nucleotide variant	NM_181712.5(KANK4):c.1049C>T (p.Ser350Leu)	KANK4-related disorder [RCV003420485]\|not provided [RCV005099911]\|not specified [RCV004189376]	uncertain significance	1	62274055	62274055	Human		name , trait , alternate_id
156202893	CV2334807	single nucleotide variant	NM_181712.5(KANK4):c.2617A>G (p.Asn873Asp)	not specified [RCV004181920]	likely benign	1	62253132	62253132	Human		name
156079588	CV2351199	single nucleotide variant	NM_181712.5(KANK4):c.2824G>A (p.Val942Met)	not specified [RCV004214047]	uncertain significance	1	62247531	62247531	Human		name
156387781	CV2383359	single nucleotide variant	NM_181712.5(KANK4):c.1450G>A (p.Glu484Lys)	not specified [RCV004222391]	uncertain significance	1	62273654	62273654	Human		name
401767544	CV2681698	single nucleotide variant	NM_181712.5(KANK4):c.2357G>A (p.Arg786His)	not specified [RCV004294249]	uncertain significance	1	62263274	62263274	Human		name
401724043	CV2684945	single nucleotide variant	NM_181712.5(KANK4):c.2741C>G (p.Ala914Gly)	not specified [RCV004296446]	uncertain significance	1	62247614	62247614	Human		name
401717666	CV2703957	single nucleotide variant	NM_181712.5(KANK4):c.1816T>A (p.Ser606Thr)	not specified [RCV004308853]	uncertain significance	1	62273288	62273288	Human		name
401717670	CV2703958	single nucleotide variant	NM_181712.5(KANK4):c.1817C>T (p.Ser606Phe)	not specified [RCV004308854]	uncertain significance	1	62273287	62273287	Human		name
401733133	CV2712984	single nucleotide variant	NM_181712.5(KANK4):c.2389G>A (p.Val797Met)	not specified [RCV004314691]	uncertain significance	1	62263242	62263242	Human		name
401769460	CV2735067	single nucleotide variant	NM_181712.5(KANK4):c.1517C>T (p.Thr506Ile)	not specified [RCV004333764]	uncertain significance	1	62273587	62273587	Human		name
401902821	CV2799643	single nucleotide variant	NM_181712.5(KANK4):c.1411C>T (p.Arg471Cys)	KANK4-related disorder [RCV003419075]\|not provided [RCV003720903]	uncertain significance	1	62273693	62273693	Human		name , trait , alternate_id
401936256	CV2803022	single nucleotide variant	NM_181712.5(KANK4):c.1259A>G (p.His420Arg)	KANK4-related disorder [RCV003414259]	uncertain significance	1	62273845	62273845	Human		name , trait , alternate_id
402485922	CV2865233	single nucleotide variant	NM_181712.5(KANK4):c.2114A>G (p.Lys705Arg)	not provided [RCV003544469]\|not specified [RCV004366473]	likely benign\|uncertain significance	1	62268404	62268404	Human		name
405208557	CV2870301	single nucleotide variant	NM_181712.5(KANK4):c.1522C>T (p.Gln508Ter)	not provided [RCV003552131]	uncertain significance	1	62273582	62273582	Human		name
405066916	CV2875472	single nucleotide variant	NM_181712.5(KANK4):c.2608G>A (p.Ala870Thr)	not provided [RCV003548293]	uncertain significance	1	62253141	62253141	Human		name
405146334	CV2885305	single nucleotide variant	NM_181712.5(KANK4):c.2000G>A (p.Gly667Glu)	not provided [RCV003561367]	uncertain significance	1	62271490	62271490	Human		name
405053520	CV2893847	single nucleotide variant	NM_181712.5(KANK4):c.1376A>T (p.Asp459Val)	not provided [RCV003579962]	uncertain significance	1	62273728	62273728	Human		name
405163650	CV2895467	single nucleotide variant	NM_181712.5(KANK4):c.2266C>T (p.Arg756Trp)	not provided [RCV003562518]	likely benign	1	62266785	62266785	Human		name
405110700	CV2948259	single nucleotide variant	NM_181712.5(KANK4):c.1223G>C (p.Gly408Ala)	not provided [RCV003666194]	uncertain significance	1	62273881	62273881	Human		name
405116397	CV2953321	single nucleotide variant	NM_181712.5(KANK4):c.1502T>A (p.Ile501Asn)	not provided [RCV003666965]	uncertain significance	1	62273602	62273602	Human		name
405245421	CV3051497	single nucleotide variant	NM_181712.5(KANK4):c.2018A>G (p.Glu673Gly)	not provided [RCV003720294]\|not specified [RCV004374042]	uncertain significance	1	62268500	62268500	Human		name
405199629	CV3056606	single nucleotide variant	NM_181712.5(KANK4):c.1409A>G (p.Glu470Gly)	not provided [RCV003730589]\|not specified [RCV005363233]	uncertain significance	1	62273695	62273695	Human		name
405221458	CV3060209	single nucleotide variant	NM_181712.5(KANK4):c.1778C>T (p.Ala593Val)	not provided [RCV003733377]	uncertain significance	1	62273326	62273326	Human		name
405026674	CV3075983	single nucleotide variant	NM_181712.5(KANK4):c.2044G>A (p.Gly682Ser)	KANK4-related disorder [RCV004753718]\|not provided [RCV003738837]	uncertain significance	1	62268474	62268474	Human		name , trait , alternate_id
405115910	CV3119202	single nucleotide variant	NM_181712.5(KANK4):c.2732T>C (p.Met911Thr)	not provided [RCV003814238]\|not specified [RCV004366718]	uncertain significance	1	62247623	62247623	Human		name
405086790	CV3122116	single nucleotide variant	NM_181712.5(KANK4):c.2920C>T (p.Pro974Ser)	not provided [RCV003810871]	uncertain significance	1	62238345	62238345	Human		name
405148214	CV3123156	single nucleotide variant	NM_181712.5(KANK4):c.2959G>A (p.Ala987Thr)	not provided [RCV003817389]	uncertain significance	1	62238306	62238306	Human		name
404979923	CV3127892	single nucleotide variant	NM_181712.5(KANK4):c.2045G>A (p.Gly682Asp)	not provided [RCV003825924]	uncertain significance	1	62268473	62268473	Human		name
405202160	CV3129286	single nucleotide variant	NM_181712.5(KANK4):c.1477A>G (p.Ser493Gly)	not provided [RCV003822139]	uncertain significance	1	62273627	62273627	Human		name
405178143	CV3146986	single nucleotide variant	NM_181712.5(KANK4):c.1475A>G (p.His492Arg)	not provided [RCV003842082]	uncertain significance	1	62273629	62273629	Human		name
405064142	CV3148547	single nucleotide variant	NM_181712.5(KANK4):c.2410G>A (p.Glu804Lys)	not provided [RCV003850503]	uncertain significance	1	62263221	62263221	Human		name
405171299	CV3151633	single nucleotide variant	NM_181712.5(KANK4):c.2132A>G (p.His711Arg)	not provided [RCV003857784]	uncertain significance	1	62268386	62268386	Human		name
405218239	CV3161271	single nucleotide variant	NM_181712.5(KANK4):c.2234A>G (p.Tyr745Cys)	not provided [RCV003863140]	uncertain significance	1	62266817	62266817	Human		name
405000744	CV3183971	single nucleotide variant	NM_181712.5(KANK4):c.2626A>G (p.Met876Val)	not provided [RCV003882554]	uncertain significance	1	62253123	62253123	Human		name
405000993	CV3183997	single nucleotide variant	NM_181712.5(KANK4):c.2741C>T (p.Ala914Val)	not provided [RCV003882580]	uncertain significance	1	62247614	62247614	Human		name
405263528	CV3189763	single nucleotide variant	NM_181712.5(KANK4):c.2314C>T (p.Leu772Phe)	KANK4-related disorder [RCV003896812]	likely benign	1	62266737	62266737	Human		name , trait , alternate_id
405285358	CV3212349	single nucleotide variant	NM_181712.5(KANK4):c.1591C>T (p.Pro531Ser)	KANK4-related disorder [RCV003958963]	likely benign	1	62273513	62273513	Human		name , trait , alternate_id
405270994	CV3218808	single nucleotide variant	NM_181712.5(KANK4):c.2557C>T (p.His853Tyr)	KANK4-related disorder [RCV003971571]	likely benign	1	62253192	62253192	Human		name , trait , alternate_id
405801685	CV3271850	single nucleotide variant	NM_181712.5(KANK4):c.1181T>G (p.Leu394Arg)	not specified [RCV004403548]	uncertain significance	1	62273923	62273923	Human		name
405801687	CV3271851	single nucleotide variant	NM_181712.5(KANK4):c.1313G>A (p.Gly438Asp)	not specified [RCV004403549]	uncertain significance	1	62273791	62273791	Human		name
405801689	CV3271852	single nucleotide variant	NM_181712.5(KANK4):c.1317C>A (p.Ser439Arg)	not specified [RCV004403550]	uncertain significance	1	62273787	62273787	Human		name
405801691	CV3271853	single nucleotide variant	NM_181712.5(KANK4):c.1537C>G (p.Gln513Glu)	not specified [RCV004403551]	uncertain significance	1	62273567	62273567	Human		name
405801693	CV3271854	single nucleotide variant	NM_181712.5(KANK4):c.1600G>A (p.Gly534Arg)	not specified [RCV004403552]	uncertain significance	1	62273504	62273504	Human		name
405801695	CV3271855	single nucleotide variant	NM_181712.5(KANK4):c.1736A>G (p.Glu579Gly)	not specified [RCV004403553]	uncertain significance	1	62273368	62273368	Human		name
405801697	CV3271856	single nucleotide variant	NM_181712.5(KANK4):c.1862C>A (p.Pro621His)	not specified [RCV004403554]	uncertain significance	1	62273242	62273242	Human		name
405801699	CV3271857	single nucleotide variant	NM_181712.5(KANK4):c.2216A>T (p.His739Leu)	not specified [RCV004403555]	uncertain significance	1	62268302	62268302	Human		name
405801706	CV3271860	single nucleotide variant	NM_181712.5(KANK4):c.2436C>A (p.Phe812Leu)	not specified [RCV004403558]	likely benign	1	62263195	62263195	Human		name
405801708	CV3271861	single nucleotide variant	NM_181712.5(KANK4):c.2461G>T (p.Asp821Tyr)	not specified [RCV004403559]	uncertain significance	1	62263170	62263170	Human		name
405801710	CV3271862	single nucleotide variant	NM_181712.5(KANK4):c.2647T>G (p.Leu883Val)	not specified [RCV004403560]	uncertain significance	1	62253102	62253102	Human		name
407467414	CV3448258	single nucleotide variant	NM_181712.5(KANK4):c.1234G>T (p.Val412Leu)	not provided [RCV005059675]\|not specified [RCV004635886]	uncertain significance	1	62273870	62273870	Human		name
407467418	CV3448259	single nucleotide variant	NM_181712.5(KANK4):c.2764G>A (p.Val922Ile)	not specified [RCV004635887]	uncertain significance	1	62247591	62247591	Human		name
407467422	CV3448260	single nucleotide variant	NM_181712.5(KANK4):c.1379G>A (p.Gly460Asp)	not specified [RCV004635888]	uncertain significance	1	62273725	62273725	Human		name
407467426	CV3448261	single nucleotide variant	NM_181712.5(KANK4):c.2359G>A (p.Val787Ile)	not specified [RCV004635889]	likely benign	1	62263272	62263272	Human		name
407511667	CV3448263	single nucleotide variant	NM_181712.5(KANK4):c.2701A>T (p.Met901Leu)	not specified [RCV004626539]	uncertain significance	1	62247654	62247654	Human		name
407511670	CV3448265	single nucleotide variant	NM_181712.5(KANK4):c.2228A>T (p.Glu743Val)	not specified [RCV004626540]	uncertain significance	1	62268290	62268290	Human		name
407467441	CV3448268	single nucleotide variant	NM_181712.5(KANK4):c.1594C>G (p.Pro532Ala)	not specified [RCV004635893]	uncertain significance	1	62273510	62273510	Human		name
408384605	CV3504399	single nucleotide variant	NM_181712.5(KANK4):c.1340A>G (p.His447Arg)	KANK4-related disorder [RCV004731949]	uncertain significance	1	62273764	62273764	Human		name , trait , alternate_id
408380045	CV3509514	single nucleotide variant	NM_181712.5(KANK4):c.1474C>T (p.His492Tyr)	KANK4-related disorder [RCV004753879]\|not provided [RCV005059813]\|not specified [RCV004927979]	uncertain significance	1	62273630	62273630	Human		name , trait , alternate_id
597786191	CV3690703	single nucleotide variant	NM_181712.5(KANK4):c.2021C>T (p.Thr674Ile)	not specified [RCV004932171]	uncertain significance	1	62268497	62268497	Human		name
597786195	CV3690704	single nucleotide variant	NM_181712.5(KANK4):c.2593A>G (p.Thr865Ala)	not specified [RCV004932172]	uncertain significance	1	62253156	62253156	Human		name
597786207	CV3690707	single nucleotide variant	NM_181712.5(KANK4):c.2890C>T (p.Arg964Cys)	not specified [RCV004932175]	uncertain significance	1	62238375	62238375	Human		name
597786225	CV3690711	single nucleotide variant	NM_181712.5(KANK4):c.1304A>G (p.Asn435Ser)	not specified [RCV004932179]	uncertain significance	1	62273800	62273800	Human		name
597786230	CV3690712	single nucleotide variant	NM_181712.5(KANK4):c.1292G>A (p.Gly431Asp)	not specified [RCV004932180]	uncertain significance	1	62273812	62273812	Human		name
597786238	CV3690714	single nucleotide variant	NM_181712.5(KANK4):c.2758G>A (p.Ala920Thr)	not specified [RCV004932182]	uncertain significance	1	62247597	62247597	Human		name
597786247	CV3690716	single nucleotide variant	NM_181712.5(KANK4):c.2951G>A (p.Arg984Lys)	not specified [RCV004932184]	uncertain significance	1	62238314	62238314	Human		name
597786256	CV3690718	single nucleotide variant	NM_181712.5(KANK4):c.2082G>C (p.Glu694Asp)	not specified [RCV004932186]	uncertain significance	1	62268436	62268436	Human		name
597786268	CV3690721	single nucleotide variant	NM_181712.5(KANK4):c.1897G>A (p.Val633Met)	not specified [RCV004932189]	likely benign	1	62273207	62273207	Human		name
597853221	CV3737723	single nucleotide variant	NM_181712.5(KANK4):c.1172T>C (p.Val391Ala)	not provided [RCV005066496]	uncertain significance	1	62273932	62273932	Human		name
597970884	CV3750559	single nucleotide variant	NM_181712.5(KANK4):c.2578A>G (p.Thr860Ala)	not provided [RCV005084303]	uncertain significance	1	62253171	62253171	Human		name
597939443	CV3788541	single nucleotide variant	NM_181712.5(KANK4):c.2350T>G (p.Trp784Gly)	not provided [RCV005133216]	uncertain significance	1	62263281	62263281	Human		name
597917929	CV3789650	single nucleotide variant	NM_181712.5(KANK4):c.1840T>C (p.Tyr614His)	not provided [RCV005129745]	uncertain significance	1	62273264	62273264	Human		name
597848954	CV3793031	single nucleotide variant	NM_181712.5(KANK4):c.1958G>A (p.Arg653His)	not provided [RCV005145167]	uncertain significance	1	62271532	62271532	Human		name
597884188	CV3799570	single nucleotide variant	NM_181712.5(KANK4):c.1844C>T (p.Ser615Leu)	not provided [RCV005150237]	uncertain significance	1	62273260	62273260	Human		name
597888196	CV3804442	single nucleotide variant	NM_181712.5(KANK4):c.2461G>A (p.Asp821Asn)	not provided [RCV005150893]	uncertain significance	1	62263170	62263170	Human		name
597898734	CV3806992	single nucleotide variant	NM_181712.5(KANK4):c.2543T>C (p.Val848Ala)	not provided [RCV005152379]	uncertain significance	1	62253206	62253206	Human		name
597917502	CV3811178	single nucleotide variant	NM_181712.5(KANK4):c.1019G>A (p.Gly340Asp)	not provided [RCV005155213]	uncertain significance	1	62274085	62274085	Human		name
597856138	CV3816493	single nucleotide variant	NM_181712.5(KANK4):c.1996G>T (p.Val666Phe)	not provided [RCV005146065]	uncertain significance	1	62271494	62271494	Human		name
597875650	CV3816829	single nucleotide variant	NM_181712.5(KANK4):c.1973G>A (p.Gly658Glu)	not provided [RCV005148882]	uncertain significance	1	62271517	62271517	Human		name
597872036	CV3849426	single nucleotide variant	NM_181712.5(KANK4):c.2587A>G (p.Met863Val)	not provided [RCV005197607]	uncertain significance	1	62253162	62253162	Human		name
597889443	CV3856090	single nucleotide variant	NM_181712.5(KANK4):c.1412G>A (p.Arg471His)	not provided [RCV005200335]	uncertain significance	1	62273692	62273692	Human		name
598233955	CV3979903	single nucleotide variant	NM_181712.5(KANK4):c.1519G>C (p.Glu507Gln)	not specified [RCV005363439]	uncertain significance	1	62273585	62273585	Human		name
598212403	CV3979905	single nucleotide variant	NM_181712.5(KANK4):c.2131C>T (p.His711Tyr)	not specified [RCV005358820]	uncertain significance	1	62268387	62268387	Human		name
598233963	CV3979906	single nucleotide variant	NM_181712.5(KANK4):c.2672A>G (p.Gln891Arg)	not specified [RCV005363440]	uncertain significance	1	62253077	62253077	Human		name
598259004	CV3979910	single nucleotide variant	NM_181712.5(KANK4):c.2338A>G (p.Ile780Val)	not specified [RCV005347326]	uncertain significance	1	62263293	62263293	Human		name
598233978	CV3979911	single nucleotide variant	NM_181712.5(KANK4):c.2651G>T (p.Arg884Ile)	not specified [RCV005363442]	uncertain significance	1	62253098	62253098	Human		name
13462483	CV439844	single nucleotide variant	NM_181712.5(KANK4):c.2401T>C (p.Tyr801His)	KANK4-related disorder [RCV003962424]\|Nephrotic syndrome [RCV001849394]\|not provided [RCV000515633]	likely pathogenic\|likely benign\|uncertain significance	1	62263230	62263230	Human	2	name , trait , alternate_id
14696521	CV622096	single nucleotide variant	NM_181712.5(KANK4):c.1342C>T (p.Arg448Ter)	not provided [RCV000782239]	uncertain significance	1	62273762	62273762	Human		name
15130073	CV707485	single nucleotide variant	NM_181712.5(KANK4):c.1550G>A (p.Arg517Lys)	not provided [RCV000964371]	benign\|likely benign	1	62273554	62273554	Human		name
15159161	CV719042	single nucleotide variant	NM_181712.5(KANK4):c.1229C>T (p.Thr410Met)	not provided [RCV000881143]	benign\|likely benign	1	62273875	62273875	Human		name
15191759	CV732538	single nucleotide variant	NM_181712.5(KANK4):c.1234G>A (p.Val412Met)	not provided [RCV000910341]	likely benign	1	62273870	62273870	Human		name
8625037	CV80156	single nucleotide variant	NM_181712.4(KANK4):c.2375C>T (p.Ser792Leu)	Malignant melanoma [RCV000060232]	not provided	1	62263256	62263256	Human		name
8625038	CV80157	single nucleotide variant	NM_181712.5(KANK4):c.1126G>A (p.Glu376Lys)	not provided [RCV002579401]	uncertain significance\|not provided	1	62273978	62273978	Human		name
156404688	CV1898366	inversion	NM_181712.5(KANK4):c.711_712inv (p.Val238Met)	not provided [RCV002585465]	uncertain significance	1	62274392	62274393	Human		name
405220481	CV3032049	microsatellite	NM_181712.5(KANK4):c.2089AAG[1] (p.Lys698del)	not provided [RCV003709834]	uncertain significance	1	62268424	62268426	Human		name
405801702	CV3271858	deletion	NM_181712.5(KANK4):c.2295_2296del (p.Gly766fs)	not specified [RCV004403556]	uncertain significance	1	62266755	62266756	Human		name
405213088	CV3078149	inversion	NM_181712.5(KANK4):c.2301_2302inv (p.Thr768Ala)	not provided [RCV003732279]	likely benign	1	62266749	62266750	Human		name
597872638	CV3849531	inversion	NM_181712.5(KANK4):c.1871_1872inv (p.Pro624Leu)	not provided [RCV005197712]	uncertain significance	1	62273232	62273233	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message