Kirrel3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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157 records found for search term Kirrel3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150474207	CV1217761	single nucleotide variant	NM_032531.4(KIRREL3):c.*11C>T	not provided [RCV001615772]	benign	11	126424569	126424569	Human		name
405271744	CV3209511	single nucleotide variant	NM_032531.4(KIRREL3):c.434-4G>A	KIRREL3-related disorder [RCV003949821]	likely benign	11	126473470	126473470	Human		name , trait , alternate_id
12895611	CV408304	single nucleotide variant	NM_032531.4(KIRREL3):c.997+1G>A	not provided [RCV000487122]	likely pathogenic	11	126449008	126449008	Human		name
15193671	CV759948	single nucleotide variant	NM_032531.4(KIRREL3):c.998-4G>A	not provided [RCV000910907]	benign	11	126446890	126446890	Human		name
8657592	CV134869	single nucleotide variant	NM_032531.4(KIRREL3):c.1354-6G>C	not provided [RCV000117430]	uncertain significance	11	126437015	126437015	Human		name
401920952	CV2802073	single nucleotide variant	NM_032531.4(KIRREL3):c.1807-8G>A	KIRREL3-related disorder [RCV003402793]	uncertain significance	11	126425732	126425732	Human		name , trait , alternate_id
405284862	CV3190918	single nucleotide variant	NM_032531.4(KIRREL3):c.1588+4C>T	KIRREL3-related disorder [RCV003909479]	likely benign	11	126435264	126435264	Human		name , trait , alternate_id
405286022	CV3191941	single nucleotide variant	NM_032531.4(KIRREL3):c.1589-5C>T	KIRREL3-related disorder [RCV003923880]	likely benign	11	126431531	126431531	Human		name , trait , alternate_id
13509740	CV481979	single nucleotide variant	NM_032531.4(KIRREL3):c.1696+5G>A	not provided [RCV000578817]	uncertain significance	11	126431414	126431414	Human		name
405262188	CV3194361	single nucleotide variant	NM_032531.4(KIRREL3):c.1696+93G>T	KIRREL3-related disorder [RCV003896393]	uncertain significance	11	126431326	126431326	Human		name , trait , alternate_id
13612133	CV514007	single nucleotide variant	NM_032531.4(KIRREL3):c.1696+19G>C	Global developmental delay [RCV000626770]	uncertain significance	11	126431400	126431400	Human	2	name
8652670	CV129245	single nucleotide variant	NM_032531.3(KIRREL3):c.1589-270T>A	Lung cancer [RCV000109732]	uncertain significance	11	126431796	126431796	Human		name
8652671	CV129246	single nucleotide variant	NM_032531.3(KIRREL3):c.434-1845G>A	Lung cancer [RCV000109733]	uncertain significance	11	126475311	126475311	Human		name
8652672	CV129247	single nucleotide variant	NM_032531.3(KIRREL3):c.434-2917G>T	Lung cancer [RCV000109734]	uncertain significance	11	126476383	126476383	Human		name
8652674	CV129249	single nucleotide variant	NM_032531.3(KIRREL3):c.56-32114C>T	Lung cancer [RCV000109736]	uncertain significance	11	126595026	126595026	Human		name
8652675	CV129250	single nucleotide variant	NM_032531.3(KIRREL3):c.56-37651G>T	Lung cancer [RCV000109737]	uncertain significance	11	126600563	126600563	Human		name
8652676	CV129251	single nucleotide variant	NM_032531.3(KIRREL3):c.56-49830G>C	Lung cancer [RCV000109738]	uncertain significance	11	126612742	126612742	Human		name
8652677	CV129252	single nucleotide variant	NM_032531.3(KIRREL3):c.56-63867C>T	Lung cancer [RCV000109739]	uncertain significance	11	126626779	126626779	Human		name
8652678	CV129253	single nucleotide variant	NM_032531.3(KIRREL3):c.56-80292G>A	Lung cancer [RCV000109740]	uncertain significance	11	126643204	126643204	Human		name
8652683	CV129258	single nucleotide variant	NM_032531.3(KIRREL3):c.55+94750G>C	Lung cancer [RCV000109745]	uncertain significance	11	126905705	126905705	Human		name
8652684	CV129259	single nucleotide variant	NM_032531.3(KIRREL3):c.55+15312A>T	Lung cancer [RCV000109746]	uncertain significance	11	126985143	126985143	Human		name
401910294	CV2810017	single nucleotide variant	NM_032531.4(KIRREL3):c.848+1222T>C	not provided [RCV003424923]	benign	11	126455127	126455127	Human		name
8652673	CV129248	single nucleotide variant	NM_032531.3(KIRREL3):c.434-11989G>C	Lung cancer [RCV000109735]	uncertain significance	11	126485455	126485455	Human		name
8652679	CV129254	single nucleotide variant	NM_032531.3(KIRREL3):c.56-121009G>T	Lung cancer [RCV000109741]	uncertain significance	11	126683921	126683921	Human		name
8652680	CV129255	single nucleotide variant	NM_032531.3(KIRREL3):c.56-158613C>G	Lung cancer [RCV000109742]	uncertain significance	11	126721525	126721525	Human		name
8652681	CV129256	single nucleotide variant	NM_032531.3(KIRREL3):c.55+152356C>T	Lung cancer [RCV000109743]	uncertain significance	11	126848100	126848100	Human		name
8652682	CV129257	single nucleotide variant	NM_032531.3(KIRREL3):c.55+106672T>A	Lung cancer [RCV000109744]	uncertain significance	11	126893783	126893783	Human		name
151355939	CV1327122	single nucleotide variant	NM_032531.4(KIRREL3):c.174G>A (p.Val58=)	KIRREL3-related disorder [RCV003913396]\|not specified [RCV001822292]	benign\|likely benign	11	126526647	126526647	Human		name , trait , alternate_id
155743405	CV1839403	single nucleotide variant	NM_032531.4(KIRREL3):c.183G>C (p.Ser61=)	not specified [RCV004059974]	likely benign	11	126526638	126526638	Human		name
10403458	CV207825	single nucleotide variant	NM_032531.4(KIRREL3):c.207C>T (p.Cys69=)	not specified [RCV000192579]	uncertain significance	11	126526614	126526614	Human		name
10403378	CV207826	single nucleotide variant	NM_032531.4(KIRREL3):c.183G>A (p.Ser61=)	not specified [RCV000192377]	likely benign\|uncertain significance	11	126526638	126526638	Human		name
405273426	CV3191969	single nucleotide variant	NM_032531.4(KIRREL3):c.198G>A (p.Thr66=)	KIRREL3-related disorder [RCV003914692]	likely benign	11	126526623	126526623	Human		name , trait , alternate_id
15181761	CV712704	single nucleotide variant	NM_032531.4(KIRREL3):c.249C>T (p.Asp83=)	not provided [RCV000974471]	likely benign	11	126526572	126526572	Human		name
15149302	CV724297	single nucleotide variant	NM_032531.4(KIRREL3):c.222C>T (p.Tyr74=)	not provided [RCV000879137]	likely benign	11	126526599	126526599	Human		name
151353970	CV1327522	single nucleotide variant	NM_032531.4(KIRREL3):c.669G>A (p.Gln223=)	not specified [RCV001817466]	uncertain significance	11	126463230	126463230	Human		name
151354890	CV1327957	single nucleotide variant	NM_032531.4(KIRREL3):c.327G>A (p.Glu109=)	not specified [RCV001819433]	uncertain significance	11	126521421	126521421	Human		name
8659893	CV134873	single nucleotide variant	NM_032531.4(KIRREL3):c.346A>C (p.Arg116=)	not provided [RCV001709488]\|not specified [RCV000117434]	benign\|likely benign	11	126521402	126521402	Human		name
10404267	CV207823	single nucleotide variant	NM_032531.4(KIRREL3):c.870C>A (p.Ile290=)	not provided [RCV003422096]\|not specified [RCV000194665]	benign\|likely benign\|uncertain significance	11	126449136	126449136	Human		name
10403793	CV207824	single nucleotide variant	NM_032531.4(KIRREL3):c.396C>T (p.Ala132=)	not provided [RCV000899522]\|not specified [RCV000193418]	likely benign\|uncertain significance	11	126521352	126521352	Human		name
10403580	CV207827	single nucleotide variant	NM_032531.4(KIRREL3):c.88G>A (p.Val30Met)	KIRREL3-related disorder [RCV003937695]\|not specified [RCV000192881]	benign\|likely benign\|uncertain significance	11	126562880	126562880	Human		name , trait , alternate_id
401910293	CV2810016	single nucleotide variant	NM_032531.4(KIRREL3):c.954C>T (p.Asn318=)	not provided [RCV003424922]	likely benign	11	126449052	126449052	Human		name
401910295	CV2810018	single nucleotide variant	NM_032531.4(KIRREL3):c.375C>T (p.Tyr125=)	KIRREL3-related disorder [RCV003946524]\|not provided [RCV003424924]	likely benign	11	126521373	126521373	Human		name , trait , alternate_id
407469745	CV3452281	single nucleotide variant	NM_032531.4(KIRREL3):c.95G>A (p.Gly32Asp)	not specified [RCV004636977]	uncertain significance	11	126562873	126562873	Human		name
597638543	CV3695446	single nucleotide variant	NM_032531.4(KIRREL3):c.849G>A (p.Arg283=)	not specified [RCV004941185]	likely benign	11	126449157	126449157	Human		name
15140141	CV737857	single nucleotide variant	NM_032531.4(KIRREL3):c.756C>T (p.Val252=)	not provided [RCV000899266]	likely benign	11	126456441	126456441	Human		name
15146773	CV752533	single nucleotide variant	NM_032531.4(KIRREL3):c.885T>C (p.Ser295=)	not provided [RCV000922777]	likely benign	11	126449121	126449121	Human		name
8657588	CV134865	single nucleotide variant	NM_032531.4(KIRREL3):c.103G>A (p.Ala35Thr)	not provided [RCV000117426]\|not specified [RCV004019640]	uncertain significance	11	126562865	126562865	Human		name
8657589	CV134866	single nucleotide variant	NM_032531.4(KIRREL3):c.116T>A (p.Phe39Tyr)	not provided [RCV001719864]\|not specified [RCV000442575]	benign\|likely benign\|uncertain significance	11	126562852	126562852	Human		name
8659891	CV134871	single nucleotide variant	NM_032531.4(KIRREL3):c.1995C>T (p.Gly665=)	not provided [RCV001610414]\|not specified [RCV000117432]	benign\|likely benign	11	126424922	126424922	Human		name
8659892	CV134872	single nucleotide variant	NM_032531.4(KIRREL3):c.2151C>T (p.Ser717=)	not provided [RCV000957030]\|not specified [RCV000117433]	benign\|likely benign	11	126424766	126424766	Human		name
8595947	CV17925	single nucleotide variant	NM_032531.4(KIRREL3):c.118C>T (p.Arg40Trp)	Intellectual disability, autosomal dominant 4 [RCV000003020]	pathogenic\|uncertain significance	11	126562850	126562850	Human	1	name
155719241	CV1835592	single nucleotide variant	NM_032531.4(KIRREL3):c.1293C>G (p.Leu431=)	not specified [RCV004058207]	likely benign	11	126440509	126440509	Human		name
155739088	CV1842893	single nucleotide variant	NM_032531.4(KIRREL3):c.1911C>T (p.Tyr637=)	KIRREL3-related disorder [RCV003926390]\|not specified [RCV004060821]	likely benign	11	126425006	126425006	Human		name , trait , alternate_id
155739939	CV1846134	single nucleotide variant	NM_032531.4(KIRREL3):c.1926C>T (p.Thr642=)	not specified [RCV004060885]	likely benign	11	126424991	126424991	Human		name
155748183	CV1846880	single nucleotide variant	NM_032531.4(KIRREL3):c.2112C>T (p.Ile704=)	not specified [RCV004060372]	likely benign	11	126424805	126424805	Human		name
155699257	CV1847483	single nucleotide variant	NM_032531.4(KIRREL3):c.2229C>T (p.Phe743=)	not specified [RCV004061823]	likely benign	11	126424688	126424688	Human		name
10403867	CV207821	single nucleotide variant	NM_032531.4(KIRREL3):c.1983G>A (p.Leu661=)	not provided [RCV000964426]\|not specified [RCV000193594]	benign\|likely benign	11	126424934	126424934	Human		name
10404220	CV207822	single nucleotide variant	NM_032531.4(KIRREL3):c.1395G>A (p.Ser465=)	not provided [RCV000882838]\|not specified [RCV000194528]	likely benign\|uncertain significance	11	126436968	126436968	Human		name
155904589	CV2276029	single nucleotide variant	NM_032531.4(KIRREL3):c.101T>C (p.Met34Thr)	not specified [RCV004141706]	uncertain significance	11	126562867	126562867	Human		name
156337429	CV2370422	single nucleotide variant	NM_032531.4(KIRREL3):c.119G>A (p.Arg40Gln)	not specified [RCV004215775]	uncertain significance	11	126562849	126562849	Human		name
156170617	CV2400595	single nucleotide variant	NM_032531.4(KIRREL3):c.217G>A (p.Glu73Lys)	not provided [RCV005412511]\|not specified [RCV004246775]	uncertain significance	11	126526604	126526604	Human		name
401889763	CV2763376	single nucleotide variant	NM_032531.4(KIRREL3):c.223G>A (p.Asp75Asn)	not specified [RCV004349266]	uncertain significance	11	126526598	126526598	Human		name
401910291	CV2810014	single nucleotide variant	NM_032531.4(KIRREL3):c.1464C>T (p.Ile488=)	not provided [RCV003424920]	likely benign	11	126436899	126436899	Human		name
401910292	CV2810015	single nucleotide variant	NM_032531.4(KIRREL3):c.1068C>T (p.Cys356=)	not provided [RCV003424921]	likely benign	11	126446816	126446816	Human		name
405286182	CV3192715	single nucleotide variant	NM_032531.4(KIRREL3):c.1977C>T (p.Pro659=)	KIRREL3-related disorder [RCV003981470]	likely benign	11	126424940	126424940	Human		name , trait , alternate_id
405277602	CV3195964	single nucleotide variant	NM_032531.4(KIRREL3):c.1407G>A (p.Thr469=)	KIRREL3-related disorder [RCV003904487]	likely benign	11	126436956	126436956	Human		name , trait , alternate_id
405284080	CV3213571	single nucleotide variant	NM_032531.4(KIRREL3):c.2073C>T (p.Tyr691=)	KIRREL3-related disorder [RCV003922144]	likely benign	11	126424844	126424844	Human		name , trait , alternate_id
405261176	CV3216254	single nucleotide variant	NM_032531.4(KIRREL3):c.2202C>T (p.Ser734=)	KIRREL3-related disorder [RCV003944358]	likely benign	11	126424715	126424715	Human		name , trait , alternate_id
405279189	CV3217407	single nucleotide variant	NM_032531.4(KIRREL3):c.1176C>T (p.Asp392=)	KIRREL3-related disorder [RCV003976831]	likely benign	11	126445055	126445055	Human		name , trait , alternate_id
13215740	CV429181	single nucleotide variant	NM_032531.4(KIRREL3):c.1917C>T (p.Ser639=)	not specified [RCV000502883]	likely benign	11	126425000	126425000	Human		name
13213277	CV429182	single nucleotide variant	NM_032531.4(KIRREL3):c.1500G>C (p.Thr500=)	not provided [RCV003424058]\|not specified [RCV000499827]	likely benign	11	126436863	126436863	Human		name
13215002	CV429183	single nucleotide variant	NM_032531.4(KIRREL3):c.1473C>T (p.Ala491=)	not provided [RCV001726202]\|not specified [RCV000501956]	likely benign	11	126436890	126436890	Human		name
15178620	CV712703	single nucleotide variant	NM_032531.4(KIRREL3):c.1791C>T (p.Thr597=)	not provided [RCV000973709]	benign	11	126429194	126429194	Human		name
15176369	CV737854	single nucleotide variant	NM_032531.4(KIRREL3):c.2280G>A (p.Ser760=)	not provided [RCV000906415]	likely benign	11	126424637	126424637	Human		name
15144200	CV737855	single nucleotide variant	NM_032531.4(KIRREL3):c.2118T>G (p.Leu706=)	KIRREL3-related disorder [RCV003922948]\|not provided [RCV000899963]	benign\|likely benign	11	126424799	126424799	Human		name , trait , alternate_id
15177403	CV737856	single nucleotide variant	NM_032531.4(KIRREL3):c.1386G>A (p.Ser462=)	not provided [RCV000906643]\|not specified [RCV001818795]	benign	11	126436977	126436977	Human		name
15134633	CV752532	single nucleotide variant	NM_032531.4(KIRREL3):c.1098C>T (p.Ile366=)	not provided [RCV000920720]	likely benign	11	126446786	126446786	Human		name
15118086	CV768298	single nucleotide variant	NM_032531.4(KIRREL3):c.1470G>A (p.Arg490=)	not provided [RCV000939944]	benign	11	126436893	126436893	Human		name
38460987	CV919339	single nucleotide variant	NM_032531.4(KIRREL3):c.232G>A (p.Val78Ile)	not provided [RCV001197125]\|not specified [RCV004935190]	uncertain significance	11	126526589	126526589	Human		name
126733593	CV1020836	single nucleotide variant	NM_032531.4(KIRREL3):c.742C>T (p.His248Tyr)	Intellectual disability, autosomal dominant 4 [RCV001334367]	uncertain significance	11	126463157	126463157	Human	1	name
150411101	CV1196064	single nucleotide variant	NM_032531.4(KIRREL3):c.955G>A (p.Ala319Thr)	not provided [RCV001573491]	uncertain significance	11	126449051	126449051	Human		name
8657591	CV134868	single nucleotide variant	NM_032531.4(KIRREL3):c.655G>A (p.Val219Met)	not provided [RCV000117429]	uncertain significance	11	126463244	126463244	Human		name
8659894	CV134874	single nucleotide variant	NM_032531.4(KIRREL3):c.568A>G (p.Ile190Val)	KIRREL3-related disorder [RCV003975024]\|not provided [RCV004707968]\|not specified [RCV000117435]	benign\|likely benign	11	126473332	126473332	Human		name , trait , alternate_id
8659895	CV134875	single nucleotide variant	NM_032531.4(KIRREL3):c.908T>C (p.Val303Ala)	not provided [RCV001729393]\|not specified [RCV000117436]	likely benign\|uncertain significance	11	126449098	126449098	Human		name
155932060	CV2293861	single nucleotide variant	NM_032531.4(KIRREL3):c.580A>G (p.Thr194Ala)	not specified [RCV004155122]	uncertain significance	11	126473320	126473320	Human		name
243062670	CV2405096	single nucleotide variant	NM_032531.4(KIRREL3):c.613C>T (p.Arg205Trp)	Autism spectrum disorder [RCV003225263]	uncertain significance	11	126463286	126463286	Human	2	name
401781314	CV2726490	single nucleotide variant	NM_032531.4(KIRREL3):c.796G>T (p.Val266Phe)	not specified [RCV004328676]	uncertain significance	11	126456401	126456401	Human		name
407469739	CV3452278	single nucleotide variant	NM_032531.4(KIRREL3):c.980G>T (p.Arg327Leu)	not specified [RCV004636975]	uncertain significance	11	126449026	126449026	Human		name
407469751	CV3452282	single nucleotide variant	NM_032531.4(KIRREL3):c.875A>C (p.Lys292Thr)	not specified [RCV004636978]	uncertain significance	11	126449131	126449131	Human		name
597638502	CV3695438	single nucleotide variant	NM_032531.4(KIRREL3):c.554G>A (p.Arg185Gln)	not specified [RCV004941178]	uncertain significance	11	126473346	126473346	Human		name
12834811	CV372071	single nucleotide variant	NM_032531.4(KIRREL3):c.622A>G (p.Ile208Val)	not provided [RCV000420590]	uncertain significance	11	126463277	126463277	Human		name
598249106	CV3991194	single nucleotide variant	NM_032531.4(KIRREL3):c.985G>C (p.Val329Leu)	not specified [RCV005366320]	uncertain significance	11	126449021	126449021	Human		name
598249121	CV3991202	single nucleotide variant	NM_032531.4(KIRREL3):c.767T>C (p.Val256Ala)	not specified [RCV005366322]	uncertain significance	11	126456430	126456430	Human		name
598220825	CV3991204	single nucleotide variant	NM_032531.4(KIRREL3):c.419G>A (p.Arg140His)	not specified [RCV005360721]	uncertain significance	11	126521329	126521329	Human		name
12905602	CV413332	single nucleotide variant	NM_032531.4(KIRREL3):c.404G>A (p.Arg135His)	not provided [RCV000487723]	uncertain significance	11	126521344	126521344	Human		name
41408129	CV980793	single nucleotide variant	NM_032531.4(KIRREL3):c.941G>T (p.Cys314Phe)	not provided [RCV001281609]	likely pathogenic	11	126449065	126449065	Human		name
151353783	CV1327335	single nucleotide variant	NM_032531.4(KIRREL3):c.1786T>C (p.Ser596Pro)	not specified [RCV001817279]	benign	11	126429199	126429199	Human		name
151354063	CV1327615	single nucleotide variant	NM_032531.4(KIRREL3):c.1217G>A (p.Gly406Glu)	not specified [RCV001817559]	uncertain significance	11	126445014	126445014	Human		name
151354146	CV1329279	single nucleotide variant	NM_032531.4(KIRREL3):c.1039G>A (p.Asp347Asn)	not specified [RCV001817642]	likely benign	11	126446845	126446845	Human		name
151716824	CV1334768	single nucleotide variant	NM_032531.4(KIRREL3):c.2302C>T (p.Arg768Ter)	Developmental disorder [RCV001843724]	likely benign	11	126424615	126424615	Human	1	name
8657590	CV134867	single nucleotide variant	NM_032531.4(KIRREL3):c.1177G>A (p.Ala393Thr)	not specified [RCV000117428]	likely benign	11	126445054	126445054	Human		name
8657593	CV134870	single nucleotide variant	NM_032531.4(KIRREL3):c.1537C>T (p.Arg513Trp)	not specified [RCV000117431]	likely benign\|uncertain significance	11	126436826	126436826	Human		name
153301310	CV1689158	single nucleotide variant	NM_032531.4(KIRREL3):c.1565A>T (p.Lys522Met)	not provided [RCV002266886]	uncertain significance	11	126435291	126435291	Human		name
8595948	CV17926	single nucleotide variant	NM_032531.4(KIRREL3):c.1007G>A (p.Arg336Gln)	Intellectual disability, autosomal dominant 4 [RCV000003021]\|KIRREL3-related disorder [RCV003944793]\|not provided [RCV003421898]	pathogenic\|likely benign\|uncertain significance	11	126446877	126446877	Human	1	name , trait , alternate_id
8595949	CV17927	single nucleotide variant	NM_032531.4(KIRREL3):c.2191G>T (p.Val731Phe)	Intellectual disability, autosomal dominant 4 [RCV000003022]\|not provided [RCV000782039]	pathogenic\|uncertain significance	11	126424726	126424726	Human	1	name
10404337	CV207820	single nucleotide variant	NM_032531.4(KIRREL3):c.1991C>T (p.Ala664Val)	not specified [RCV000194828]	uncertain significance	11	126424926	126424926	Human		name
155970520	CV2262245	single nucleotide variant	NM_032531.4(KIRREL3):c.1712T>C (p.Val571Ala)	not specified [RCV004128455]	uncertain significance	11	126429273	126429273	Human		name
156028237	CV2278510	single nucleotide variant	NM_032531.4(KIRREL3):c.2074G>A (p.Gly692Arg)	not specified [RCV004132950]	uncertain significance	11	126424843	126424843	Human		name
156285550	CV2317643	single nucleotide variant	NM_032531.4(KIRREL3):c.1375G>A (p.Val459Ile)	not specified [RCV004172579]	uncertain significance	11	126436988	126436988	Human		name
156111833	CV2353371	single nucleotide variant	NM_032531.4(KIRREL3):c.1036G>A (p.Val346Met)	not specified [RCV004205832]	uncertain significance	11	126446848	126446848	Human		name
155939989	CV2378967	single nucleotide variant	NM_032531.4(KIRREL3):c.1742T>C (p.Ile581Thr)	not specified [RCV004233387]	uncertain significance	11	126429243	126429243	Human		name
329359324	CV2435425	single nucleotide variant	NM_032531.4(KIRREL3):c.1406C>T (p.Thr469Met)	not specified [RCV004253077]	uncertain significance	11	126436957	126436957	Human		name
329358420	CV2450313	single nucleotide variant	NM_032531.4(KIRREL3):c.2060G>A (p.Arg687His)	not specified [RCV004271402]	uncertain significance	11	126424857	126424857	Human		name
329394262	CV2460681	single nucleotide variant	NM_032531.4(KIRREL3):c.1297G>T (p.Gly433Cys)	not specified [RCV004271029]	uncertain significance	11	126440505	126440505	Human		name
401731887	CV2674509	single nucleotide variant	NM_032531.4(KIRREL3):c.1106T>G (p.Met369Arg)	not specified [RCV004291389]	uncertain significance	11	126446778	126446778	Human		name
11639269	CV269142	single nucleotide variant	NM_032531.4(KIRREL3):c.2191G>A (p.Val731Ile)	not provided [RCV000317943]	uncertain significance	11	126424726	126424726	Human		name
401778997	CV2702003	single nucleotide variant	NM_032531.4(KIRREL3):c.1967G>A (p.Ser656Asn)	not specified [RCV004320593]	uncertain significance	11	126424950	126424950	Human		name
401776333	CV2707203	single nucleotide variant	NM_032531.4(KIRREL3):c.1987C>G (p.Pro663Ala)	not specified [RCV004315561]	uncertain significance	11	126424930	126424930	Human		name
401894937	CV2782176	single nucleotide variant	NM_032531.4(KIRREL3):c.1532T>C (p.Ile511Thr)	not specified [RCV004359154]	uncertain significance	11	126436831	126436831	Human		name
401913811	CV2799128	single nucleotide variant	NM_032531.4(KIRREL3):c.1006C>T (p.Arg336Trp)	KIRREL3-related disorder [RCV003400271]	uncertain significance	11	126446878	126446878	Human		name , trait , alternate_id
405266392	CV3186628	single nucleotide variant	NM_032531.4(KIRREL3):c.1280C>G (p.Thr427Ser)	not provided [RCV003886709]	uncertain significance	11	126440522	126440522	Human		name
405807302	CV3265412	single nucleotide variant	NM_032531.4(KIRREL3):c.1015A>G (p.Thr339Ala)	not specified [RCV004406483]	uncertain significance	11	126446869	126446869	Human		name
405807304	CV3265413	single nucleotide variant	NM_032531.4(KIRREL3):c.1156A>G (p.Lys386Glu)	not specified [RCV004406484]	uncertain significance	11	126445075	126445075	Human		name
405807306	CV3265414	single nucleotide variant	NM_032531.4(KIRREL3):c.1229G>C (p.Arg410Thr)	not specified [RCV004406485]	uncertain significance	11	126445002	126445002	Human		name
405807308	CV3265415	single nucleotide variant	NM_032531.4(KIRREL3):c.1289C>T (p.Ala430Val)	not specified [RCV004406486]	uncertain significance	11	126440513	126440513	Human		name
405807310	CV3265416	single nucleotide variant	NM_032531.4(KIRREL3):c.1465G>A (p.Val489Met)	not specified [RCV004406487]	uncertain significance	11	126436898	126436898	Human		name
405807312	CV3265417	single nucleotide variant	NM_032531.4(KIRREL3):c.1484C>G (p.Thr495Ser)	not specified [RCV004406488]	uncertain significance	11	126436879	126436879	Human		name
405807314	CV3265418	single nucleotide variant	NM_032531.4(KIRREL3):c.1768C>T (p.Arg590Trp)	not specified [RCV004406489]	uncertain significance	11	126429217	126429217	Human		name
405807315	CV3265419	single nucleotide variant	NM_032531.4(KIRREL3):c.1939C>T (p.His647Tyr)	not specified [RCV004406490]	uncertain significance	11	126424978	126424978	Human		name
405807317	CV3265420	single nucleotide variant	NM_032531.4(KIRREL3):c.2174C>T (p.Thr725Met)	not specified [RCV004406491]	uncertain significance	11	126424743	126424743	Human		name
407469742	CV3452279	single nucleotide variant	NM_032531.4(KIRREL3):c.1522G>A (p.Asp508Asn)	not specified [RCV004636976]	uncertain significance	11	126436841	126436841	Human		name
407524834	CV3452280	single nucleotide variant	NM_032531.4(KIRREL3):c.1009A>G (p.Met337Val)	not specified [RCV004631512]	uncertain significance	11	126446875	126446875	Human		name
407524837	CV3452283	single nucleotide variant	NM_032531.4(KIRREL3):c.2230G>T (p.Asp744Tyr)	not specified [RCV004631513]	uncertain significance	11	126424687	126424687	Human		name
408383734	CV3525822	single nucleotide variant	NM_032531.4(KIRREL3):c.1732C>T (p.Arg578Ter)	not specified [RCV004766732]	uncertain significance	11	126429253	126429253	Human		name
12791932	CV362444	single nucleotide variant	NM_032531.4(KIRREL3):c.2019G>A (p.Met673Ile)	Intellectual disability, autosomal dominant 4 [RCV000417096]	likely pathogenic	11	126424898	126424898	Human	1	name
597638507	CV3695439	single nucleotide variant	NM_032531.4(KIRREL3):c.1339C>T (p.Pro447Ser)	not specified [RCV004941179]	uncertain significance	11	126440463	126440463	Human		name
597638513	CV3695440	single nucleotide variant	NM_032531.4(KIRREL3):c.1978G>A (p.Asp660Asn)	not specified [RCV004941180]	uncertain significance	11	126424939	126424939	Human		name
597638518	CV3695441	single nucleotide variant	NM_032531.4(KIRREL3):c.1918G>A (p.Val640Ile)	not specified [RCV004941181]	uncertain significance	11	126424999	126424999	Human		name
597768403	CV3695442	single nucleotide variant	NM_032531.4(KIRREL3):c.2267A>G (p.His756Arg)	not specified [RCV004927479]	uncertain significance	11	126424650	126424650	Human		name
597638524	CV3695443	single nucleotide variant	NM_032531.4(KIRREL3):c.1165C>T (p.Arg389Cys)	not specified [RCV004941182]	uncertain significance	11	126445066	126445066	Human		name
597638530	CV3695444	single nucleotide variant	NM_032531.4(KIRREL3):c.2171A>G (p.Asp724Gly)	not specified [RCV004941183]	uncertain significance	11	126424746	126424746	Human		name
597638537	CV3695445	single nucleotide variant	NM_032531.4(KIRREL3):c.1573G>T (p.Ala525Ser)	not specified [RCV004941184]	uncertain significance	11	126435283	126435283	Human		name
597638552	CV3695448	single nucleotide variant	NM_032531.4(KIRREL3):c.1274C>A (p.Thr425Asn)	not specified [RCV004941187]	uncertain significance	11	126440528	126440528	Human		name
12834065	CV373950	single nucleotide variant	NM_032531.4(KIRREL3):c.1166G>A (p.Arg389His)	not provided [RCV000927330]\|not specified [RCV000419692]	likely benign	11	126445065	126445065	Human		name
598220795	CV3991195	single nucleotide variant	NM_032531.4(KIRREL3):c.1057A>G (p.Ile353Val)	not specified [RCV005360717]	likely benign	11	126446827	126446827	Human		name
598249113	CV3991196	single nucleotide variant	NM_032531.4(KIRREL3):c.2314C>T (p.Arg772Trp)	not specified [RCV005366321]	uncertain significance	11	126424603	126424603	Human		name
598220803	CV3991197	single nucleotide variant	NM_032531.4(KIRREL3):c.1904A>G (p.Asn635Ser)	not specified [RCV005360718]	uncertain significance	11	126425013	126425013	Human		name
598220811	CV3991198	single nucleotide variant	NM_032531.4(KIRREL3):c.1975C>T (p.Pro659Ser)	not specified [RCV005360719]	uncertain significance	11	126424942	126424942	Human		name
598182028	CV3991199	single nucleotide variant	NM_032531.4(KIRREL3):c.2185A>G (p.Ser729Gly)	not specified [RCV005352648]	uncertain significance	11	126424732	126424732	Human		name
598182032	CV3991200	single nucleotide variant	NM_032531.4(KIRREL3):c.1648G>A (p.Val550Ile)	not specified [RCV005352649]	uncertain significance	11	126431467	126431467	Human		name
598182036	CV3991201	single nucleotide variant	NM_032531.4(KIRREL3):c.1771G>A (p.Glu591Lys)	not specified [RCV005352650]	uncertain significance	11	126429214	126429214	Human		name
598220817	CV3991203	single nucleotide variant	NM_032531.4(KIRREL3):c.1234G>T (p.Val412Leu)	not specified [RCV005360720]	uncertain significance	11	126444997	126444997	Human		name
13216162	CV429184	single nucleotide variant	NM_032531.4(KIRREL3):c.1195C>T (p.Arg399Trp)	not specified [RCV000503420]	uncertain significance	11	126445036	126445036	Human		name
13820871	CV576139	single nucleotide variant	NM_032531.4(KIRREL3):c.1238C>T (p.Thr413Ile)	Intellectual disability, autosomal dominant 4 [RCV000709965]	not provided	11	126444993	126444993	Human		name
13834173	CV585415	single nucleotide variant	NM_032531.4(KIRREL3):c.1669G>A (p.Ala557Thr)	not provided [RCV000729615]	uncertain significance	11	126431446	126431446	Human		name
38597785	CV964357	single nucleotide variant	NM_032531.4(KIRREL3):c.1952C>T (p.Thr651Ile)	Intellectual disability [RCV001253130]	uncertain significance	11	126424965	126424965	Human	2	name
42723484	CV984371	single nucleotide variant	NM_032531.4(KIRREL3):c.1985G>A (p.Arg662His)	Autism spectrum disorder [RCV001291392]	association	11	126424932	126424932	Human	2	name

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