Cntn6 Variant Search Result - Rat Genome Database

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173 records found for search term Cntn6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8625483	CV80606	single nucleotide variant	NM_014461.3(CNTN6):c.56-1G>A	Malignant melanoma [RCV000060683]	not provided	3	1220686	1220686	Human		name
150535115	CV1293649	single nucleotide variant	NM_001289080.2(CNTN6):c.1213+8G>A	not provided [RCV001757926]	benign	3	1327594	1327594	Human		name
155797636	CV1859437	single nucleotide variant	NM_001289080.2(CNTN6):c.1492+1G>T	Autism spectrum disorder [RCV002465064]	likely pathogenic	3	1352452	1352452	Human	2	name
11525986	CV246936	single nucleotide variant	NM_001289080.2(CNTN6):c.2518-1G>A	not specified [RCV000239164]	uncertain significance	3	1385610	1385610	Human		name
401912416	CV2819818	single nucleotide variant	NM_001289080.2(CNTN6):c.1669-6C>T	not provided [RCV003427282]	uncertain significance	3	1372832	1372832	Human		name
408377547	CV3507537	single nucleotide variant	NM_001289080.2(CNTN6):c.2402-6T>G	CNTN6-related disorder [RCV004750995]	uncertain significance	3	1383287	1383287	Human		name , trait , alternate_id
15198027	CV777379	single nucleotide variant	NM_001289080.2(CNTN6):c.1668+8A>T	CNTN6-related disorder [RCV003926049]\|not provided [RCV000956632]	benign\|likely benign	3	1372482	1372482	Human		name , trait , alternate_id
8577985	CV112363	single nucleotide variant	NM_001289080.1(CNTN6):c.182+710A>T	Lung cancer [RCV000092886]	uncertain significance	3	1221523	1221523	Human		name
8577829	CV112206	single nucleotide variant	NM_001289080.1(CNTN6):c.-83+8540T>A	Lung cancer [RCV000092729]	uncertain significance	3	1101660	1101660	Human		name
8577910	CV112287	single nucleotide variant	NM_001289080.1(CNTN6):c.-82-13287A>T	Lung cancer [RCV000092810]	uncertain significance	3	1134640	1134640	Human		name
8578001	CV112379	single nucleotide variant	NM_001289080.1(CNTN6):c.358+23815T>C	Lung cancer [RCV000092902]	uncertain significance	3	1251808	1251808	Human		name
8578003	CV112381	single nucleotide variant	NM_001289080.1(CNTN6):c.359-21348T>G	Lung cancer [RCV000092904]	uncertain significance	3	1257065	1257065	Human		name
15156506	CV777335	microsatellite	NM_001289080.2(CNTN6):c.761+6GTTTTT[2]	not provided [RCV000946711]	benign	3	1297997	1298002	Human		name
401912797	CV2800827	single nucleotide variant	NM_001289080.2(CNTN6):c.16A>G (p.Lys6Glu)	CNTN6-related disorder [RCV003399970]	uncertain significance	3	1148024	1148024	Human		name , trait , alternate_id
405275737	CV3216003	single nucleotide variant	NM_001289080.2(CNTN6):c.171G>A (p.Ser57=)	CNTN6-related disorder [RCV003952275]	likely benign	3	1220802	1220802	Human		name , trait , alternate_id
15187842	CV697783	single nucleotide variant	NM_001289080.2(CNTN6):c.288C>T (p.Gly96=)	CNTN6-related disorder [RCV003925987]\|not provided [RCV000953707]	benign	3	1227923	1227923	Human		name , trait , alternate_id
8625504	CV80627	single nucleotide variant	NM_014461.3(CNTN6):c.743A>T (p.Glu248Val)	Malignant melanoma [RCV000060704]	not provided	3	1297973	1297973	Human		name
8630594	CV85749	single nucleotide variant	NM_014461.3(CNTN6):c.700C>T (p.Pro234Ser)	Malignant melanoma [RCV000065832]	not provided	3	1297930	1297930	Human		name
156174275	CV2326928	single nucleotide variant	NM_001289080.2(CNTN6):c.64C>A (p.Leu22Ile)	not specified [RCV004176741]	uncertain significance	3	1220695	1220695	Human		name
401781094	CV2681888	single nucleotide variant	NM_001289080.2(CNTN6):c.73C>T (p.Arg25Cys)	not specified [RCV004296880]	uncertain significance	3	1220704	1220704	Human		name
405674954	CV3304795	single nucleotide variant	NM_001289080.2(CNTN6):c.40A>T (p.Ile14Leu)	not specified [RCV004442180]	uncertain significance	3	1148048	1148048	Human		name
405674973	CV3304801	single nucleotide variant	NM_001289080.2(CNTN6):c.89A>T (p.Gln30Leu)	not specified [RCV004442186]	uncertain significance	3	1220720	1220720	Human		name
407470985	CV3425805	single nucleotide variant	NM_001289080.2(CNTN6):c.50C>A (p.Ser17Tyr)	not specified [RCV004615581]	uncertain significance	3	1148058	1148058	Human		name
597771617	CV3650683	single nucleotide variant	NM_001289080.2(CNTN6):c.56G>A (p.Gly19Asp)	not specified [RCV004897169]	uncertain significance	3	1220687	1220687	Human		name
15191829	CV697784	single nucleotide variant	NM_001289080.2(CNTN6):c.339G>A (p.Lys113=)	not provided [RCV000954891]	benign\|likely benign	3	1227974	1227974	Human		name
15186133	CV697826	single nucleotide variant	NM_001289080.2(CNTN6):c.541T>C (p.Leu181=)	not provided [RCV000953192]	benign	3	1295687	1295687	Human		name
8625509	CV80632	single nucleotide variant	NM_014461.3(CNTN6):c.1084G>A (p.Glu362Lys)	Malignant melanoma [RCV000060709]	not provided	3	1327457	1327457	Human		name
8630613	CV85768	single nucleotide variant	NM_014461.3(CNTN6):c.1381G>A (p.Asp461Asn)	Malignant melanoma [RCV000065851]	not provided	3	1352340	1352340	Human		name
401729198	CV2690097	single nucleotide variant	NM_001289080.2(CNTN6):c.119A>T (p.Asp40Val)	not specified [RCV004300332]	uncertain significance	3	1220750	1220750	Human		name
401765794	CV2724486	single nucleotide variant	NM_001289080.2(CNTN6):c.130T>C (p.Ser44Pro)	not specified [RCV004331326]	uncertain significance	3	1220761	1220761	Human		name
401869760	CV2772511	single nucleotide variant	NM_001289080.2(CNTN6):c.139A>G (p.Ile47Val)	not specified [RCV004355284]	uncertain significance	3	1220770	1220770	Human		name
401912419	CV2819820	single nucleotide variant	NM_001289080.2(CNTN6):c.2952C>T (p.Ser984=)	not provided [RCV003427284]	benign	3	1402452	1402452	Human		name
405263255	CV3189434	single nucleotide variant	NM_001289080.2(CNTN6):c.2607G>T (p.Leu869=)	CNTN6-related disorder [RCV003896668]	likely benign	3	1385700	1385700	Human		name , trait , alternate_id
405286090	CV3192036	single nucleotide variant	NM_001289080.2(CNTN6):c.1770C>T (p.Ala590=)	CNTN6-related disorder [RCV003923963]	likely benign	3	1372939	1372939	Human		name , trait , alternate_id
405288379	CV3197389	single nucleotide variant	NM_001289080.2(CNTN6):c.2160G>A (p.Thr720=)	CNTN6-related disorder [RCV003982485]	benign	3	1377069	1377069	Human		name , trait , alternate_id
405293079	CV3207230	single nucleotide variant	NM_001289080.2(CNTN6):c.2187G>A (p.Gln729=)	CNTN6-related disorder [RCV003931628]	likely benign	3	1382962	1382962	Human		name , trait , alternate_id
405283824	CV3213374	single nucleotide variant	NM_001289080.2(CNTN6):c.2523A>G (p.Leu841=)	CNTN6-related disorder [RCV003921962]	likely benign	3	1385616	1385616	Human		name , trait , alternate_id
405293766	CV3214532	single nucleotide variant	NM_001289080.2(CNTN6):c.2664G>A (p.Gly888=)	CNTN6-related disorder [RCV003932205]	benign	3	1385757	1385757	Human		name , trait , alternate_id
405674946	CV3304793	single nucleotide variant	NM_001289080.2(CNTN6):c.295C>A (p.Gln99Lys)	not specified [RCV004442178]	uncertain significance	3	1227930	1227930	Human		name
407470980	CV3425804	single nucleotide variant	NM_001289080.2(CNTN6):c.266C>A (p.Pro89His)	not specified [RCV004615580]	uncertain significance	3	1227901	1227901	Human		name
408378483	CV3513674	single nucleotide variant	NM_001289080.2(CNTN6):c.225T>G (p.Tyr75Ter)	CNTN6-related disorder [RCV004752297]	uncertain significance	3	1227860	1227860	Human		name , trait , alternate_id
597771584	CV3650676	single nucleotide variant	NM_001289080.2(CNTN6):c.279A>T (p.Gln93His)	not specified [RCV004897162]	uncertain significance	3	1227914	1227914	Human		name
597771612	CV3650682	single nucleotide variant	NM_001289080.2(CNTN6):c.155C>G (p.Ala52Gly)	not specified [RCV004897168]	uncertain significance	3	1220786	1220786	Human		name
12896057	CV389529	single nucleotide variant	NM_001289080.2(CNTN6):c.2259G>A (p.Val753=)	not provided [RCV004708885]\|not specified [RCV000454825]	benign	3	1383034	1383034	Human		name
598258442	CV3941420	single nucleotide variant	NM_001289080.2(CNTN6):c.139A>T (p.Ile47Phe)	not specified [RCV005324613]	uncertain significance	3	1220770	1220770	Human		name
598258520	CV3951949	single nucleotide variant	NM_001289080.2(CNTN6):c.160G>T (p.Gly54Cys)	not specified [RCV005324626]	uncertain significance	3	1220791	1220791	Human		name
15112824	CV720200	single nucleotide variant	NM_001289080.2(CNTN6):c.1392C>G (p.Leu464=)	CNTN6-related disorder [RCV003983253]\|not provided [RCV000894543]	benign	3	1352351	1352351	Human		name , trait , alternate_id
15178198	CV733838	single nucleotide variant	NM_001289080.2(CNTN6):c.2979A>G (p.Lys993=)	not provided [RCV000906821]	likely benign	3	1402479	1402479	Human		name
15125882	CV748037	single nucleotide variant	NM_001289080.2(CNTN6):c.2190T>C (p.Asn730=)	not provided [RCV000919233]	likely benign	3	1382965	1382965	Human		name
156265124	CV2198632	single nucleotide variant	NM_001289080.2(CNTN6):c.772G>C (p.Asp258His)	not specified [RCV004075648]	uncertain significance	3	1321660	1321660	Human		name
156140267	CV2247031	single nucleotide variant	NM_001289080.2(CNTN6):c.895G>T (p.Ala299Ser)	not specified [RCV004114591]	uncertain significance	3	1321783	1321783	Human		name
156319515	CV2260850	single nucleotide variant	NM_001289080.2(CNTN6):c.788G>A (p.Arg263Lys)	not specified [RCV004125757]	uncertain significance	3	1321676	1321676	Human		name
156122476	CV2276099	single nucleotide variant	NM_001289080.2(CNTN6):c.816A>C (p.Lys272Asn)	not specified [RCV004141766]	uncertain significance	3	1321704	1321704	Human		name
156176959	CV2296959	single nucleotide variant	NM_001289080.2(CNTN6):c.466G>A (p.Ala156Thr)	not specified [RCV004149102]	uncertain significance	3	1295612	1295612	Human		name
156284599	CV2317556	single nucleotide variant	NM_001289080.2(CNTN6):c.985C>G (p.Leu329Val)	not specified [RCV004172510]	uncertain significance	3	1325853	1325853	Human		name
155928232	CV2346557	single nucleotide variant	NM_001289080.2(CNTN6):c.579C>A (p.Asn193Lys)	not specified [RCV004206472]	uncertain significance	3	1295725	1295725	Human		name
156131128	CV2358197	single nucleotide variant	NM_001289080.2(CNTN6):c.695G>A (p.Arg232His)	not specified [RCV004211997]	uncertain significance	3	1297925	1297925	Human		name
155931955	CV2362684	single nucleotide variant	NM_001289080.2(CNTN6):c.592A>G (p.Ile198Val)	not specified [RCV004215329]	likely benign	3	1295738	1295738	Human		name
156200411	CV2365557	single nucleotide variant	NM_001289080.2(CNTN6):c.839C>G (p.Ala280Gly)	not specified [RCV004211671]	uncertain significance	3	1321727	1321727	Human		name
156055718	CV2370918	single nucleotide variant	NM_001289080.2(CNTN6):c.488C>G (p.Pro163Arg)	CNTN6-related disorder [RCV004750857]\|not specified [RCV004218648]	uncertain significance	3	1295634	1295634	Human		name , trait , alternate_id
156218374	CV2386231	single nucleotide variant	NM_001289080.2(CNTN6):c.496G>A (p.Val166Ile)	not specified [RCV004229266]	uncertain significance	3	1295642	1295642	Human		name
329370169	CV2435497	single nucleotide variant	NM_001289080.2(CNTN6):c.733G>C (p.Val245Leu)	not specified [RCV004253141]	uncertain significance	3	1297963	1297963	Human		name
401779983	CV2725807	single nucleotide variant	NM_001289080.2(CNTN6):c.754C>T (p.Leu252Phe)	not specified [RCV004316279]	uncertain significance	3	1297984	1297984	Human		name
401856955	CV2759886	single nucleotide variant	NM_001289080.2(CNTN6):c.841A>G (p.Ile281Val)	not specified [RCV004345313]	uncertain significance	3	1321729	1321729	Human		name
401897367	CV2786946	single nucleotide variant	NM_001289080.2(CNTN6):c.562C>T (p.Pro188Ser)	not specified [RCV004366081]	uncertain significance	3	1295708	1295708	Human		name
401905268	CV2796173	single nucleotide variant	NM_001289080.2(CNTN6):c.560A>G (p.Glu187Gly)	CNTN6-related disorder [RCV003420803]	uncertain significance	3	1295706	1295706	Human		name , trait , alternate_id
401912413	CV2819816	single nucleotide variant	NM_001289080.2(CNTN6):c.649C>T (p.Arg217Cys)	CNTN6-related disorder [RCV003919179]\|not provided [RCV003427280]	likely benign	3	1295795	1295795	Human		name , trait , alternate_id
405256010	CV3208500	single nucleotide variant	NM_001289080.2(CNTN6):c.383C>T (p.Thr128Ile)	CNTN6-related disorder [RCV003939590]	likely benign	3	1278437	1278437	Human		name , trait , alternate_id
405287259	CV3217258	single nucleotide variant	NM_001289080.2(CNTN6):c.643G>C (p.Val215Leu)	CNTN6-related disorder [RCV003981802]	uncertain significance	3	1295789	1295789	Human		name , trait , alternate_id
405674949	CV3304794	single nucleotide variant	NM_001289080.2(CNTN6):c.408A>T (p.Glu136Asp)	not specified [RCV004442179]	uncertain significance	3	1278462	1278462	Human		name
405674960	CV3304797	single nucleotide variant	NM_001289080.2(CNTN6):c.487C>A (p.Pro163Thr)	not specified [RCV004442182]	uncertain significance	3	1295633	1295633	Human		name
405674963	CV3304798	single nucleotide variant	NM_001289080.2(CNTN6):c.649C>G (p.Arg217Gly)	not specified [RCV004442183]	uncertain significance	3	1295795	1295795	Human		name
405674969	CV3304800	single nucleotide variant	NM_001289080.2(CNTN6):c.817G>A (p.Val273Ile)	not specified [RCV004442185]	uncertain significance	3	1321705	1321705	Human		name
407470976	CV3425803	single nucleotide variant	NM_001289080.2(CNTN6):c.870A>T (p.Glu290Asp)	not specified [RCV004615579]	uncertain significance	3	1321758	1321758	Human		name
407470997	CV3425808	single nucleotide variant	NM_001289080.2(CNTN6):c.610C>G (p.Gln204Glu)	not specified [RCV004615584]	uncertain significance	3	1295756	1295756	Human		name
407471005	CV3425810	single nucleotide variant	NM_001289080.2(CNTN6):c.694C>T (p.Arg232Cys)	not specified [RCV004615586]	uncertain significance	3	1297924	1297924	Human		name
407471013	CV3425812	single nucleotide variant	NM_001289080.2(CNTN6):c.666G>A (p.Met222Ile)	not specified [RCV004615588]	uncertain significance	3	1297896	1297896	Human		name
597771592	CV3650678	single nucleotide variant	NM_001289080.2(CNTN6):c.691G>C (p.Val231Leu)	not specified [RCV004897164]	uncertain significance	3	1297921	1297921	Human		name
597771597	CV3650679	single nucleotide variant	NM_001289080.2(CNTN6):c.827G>C (p.Ser276Thr)	not specified [RCV004897165]	uncertain significance	3	1321715	1321715	Human		name
597771622	CV3650684	single nucleotide variant	NM_001289080.2(CNTN6):c.646C>G (p.Gln216Glu)	not specified [RCV004897170]	uncertain significance	3	1295792	1295792	Human		name
598258413	CV3941415	single nucleotide variant	NM_001289080.2(CNTN6):c.991A>G (p.Ile331Val)	not specified [RCV005324608]	uncertain significance	3	1325859	1325859	Human		name
598258472	CV3941425	single nucleotide variant	NM_001289080.2(CNTN6):c.731C>T (p.Ser244Phe)	not specified [RCV005324618]	uncertain significance	3	1297961	1297961	Human		name
598258498	CV3951945	single nucleotide variant	NM_001289080.2(CNTN6):c.704A>C (p.Glu235Ala)	not specified [RCV005324622]	uncertain significance	3	1297934	1297934	Human		name
13704108	CV539432	single nucleotide variant	NM_001289080.2(CNTN6):c.566C>A (p.Ser189Ter)	Autistic behavior [RCV000663360]	likely pathogenic	3	1295712	1295712	Human	2	name
15098808	CV697813	single nucleotide variant	NM_001289080.2(CNTN6):c.449T>C (p.Phe150Ser)	CNTN6-related disorder [RCV003915979]\|not provided [RCV000958643]	benign	3	1278503	1278503	Human		name , trait , alternate_id
15169608	CV697838	single nucleotide variant	NM_001289080.2(CNTN6):c.908G>A (p.Arg303Gln)	not provided [RCV000949490]	likely benign	3	1321796	1321796	Human		name
15202337	CV763594	single nucleotide variant	NM_001289080.2(CNTN6):c.403C>T (p.Arg135Ter)	not provided [RCV000935917]	benign	3	1278457	1278457	Human		name
15112805	CV781565	single nucleotide variant	NM_001289080.2(CNTN6):c.3003A>G (p.Gly1001=)	not provided [RCV000977901]	benign	3	1403334	1403334	Human		name
152154938	CV1668008	single nucleotide variant	NM_001289080.2(CNTN6):c.2786T>C (p.Met929Thr)	not provided [RCV002221902]	uncertain significance	3	1401514	1401514	Human		name
10449930	CV215272	single nucleotide variant	NM_001289080.2(CNTN6):c.2704C>T (p.Pro902Ser)	not specified [RCV000203131]	uncertain significance	3	1385797	1385797	Human		name
156270702	CV2195179	single nucleotide variant	NM_001289080.2(CNTN6):c.2821C>A (p.Leu941Met)	not specified [RCV004080124]	uncertain significance	3	1402321	1402321	Human		name
156243459	CV2210941	single nucleotide variant	NM_001289080.2(CNTN6):c.2736G>C (p.Trp912Cys)	not specified [RCV004086016]	uncertain significance	3	1401464	1401464	Human		name
155922080	CV2240628	single nucleotide variant	NM_001289080.2(CNTN6):c.1340C>A (p.Thr447Lys)	not specified [RCV004119268]	uncertain significance	3	1329911	1329911	Human		name
155983998	CV2241068	single nucleotide variant	NM_001289080.2(CNTN6):c.1634A>G (p.Lys545Arg)	not specified [RCV004104111]	uncertain significance	3	1372440	1372440	Human		name
156194796	CV2251774	single nucleotide variant	NM_001289080.2(CNTN6):c.2159C>T (p.Thr720Met)	not specified [RCV004119766]	uncertain significance	3	1377068	1377068	Human		name
156095691	CV2253053	single nucleotide variant	NM_001289080.2(CNTN6):c.2870A>G (p.Asn957Ser)	not specified [RCV004120844]	uncertain significance	3	1402370	1402370	Human		name
156148735	CV2265297	single nucleotide variant	NM_001289080.2(CNTN6):c.1499C>T (p.Thr500Ile)	not specified [RCV004128189]	uncertain significance	3	1372305	1372305	Human		name
156235180	CV2271319	single nucleotide variant	NM_001289080.2(CNTN6):c.1325C>T (p.Ser442Phe)	not specified [RCV004136439]	uncertain significance	3	1329896	1329896	Human		name
155902759	CV2274756	single nucleotide variant	NM_001289080.2(CNTN6):c.1390C>T (p.Leu464Phe)	not specified [RCV004139113]	uncertain significance	3	1352349	1352349	Human		name
156274120	CV2279688	single nucleotide variant	NM_001289080.2(CNTN6):c.1160C>T (p.Ala387Val)	not specified [RCV004144310]	uncertain significance	3	1327533	1327533	Human		name
155958066	CV2282152	single nucleotide variant	NM_001289080.2(CNTN6):c.2771A>G (p.Glu924Gly)	not specified [RCV004138884]	uncertain significance	3	1401499	1401499	Human		name
156006009	CV2290433	single nucleotide variant	NM_001289080.2(CNTN6):c.2113G>T (p.Val705Leu)	not specified [RCV004154848]	uncertain significance	3	1377022	1377022	Human		name
156202384	CV2300632	single nucleotide variant	NM_001289080.2(CNTN6):c.2651C>G (p.Thr884Ser)	not specified [RCV004155585]	uncertain significance	3	1385744	1385744	Human		name
156090093	CV2302542	single nucleotide variant	NM_001289080.2(CNTN6):c.1907G>A (p.Arg636Gln)	not specified [RCV004160720]	uncertain significance	3	1373724	1373724	Human		name
156292670	CV2306254	single nucleotide variant	NM_001289080.2(CNTN6):c.2390C>T (p.Ser797Phe)	not specified [RCV004162982]	uncertain significance	3	1383165	1383165	Human		name
155964712	CV2308413	single nucleotide variant	NM_001289080.2(CNTN6):c.2570T>C (p.Val857Ala)	not specified [RCV004166713]	uncertain significance	3	1385663	1385663	Human		name
156011143	CV2362210	single nucleotide variant	NM_001289080.2(CNTN6):c.1114A>G (p.Ile372Val)	not specified [RCV004210007]	uncertain significance	3	1327487	1327487	Human		name
156082404	CV2368909	single nucleotide variant	NM_001289080.2(CNTN6):c.1735G>T (p.Val579Leu)	not specified [RCV004207864]	uncertain significance	3	1372904	1372904	Human		name
155937582	CV2380042	single nucleotide variant	NM_001289080.2(CNTN6):c.1038C>G (p.Asn346Lys)	not specified [RCV004222176]	uncertain significance	3	1325906	1325906	Human		name
156216808	CV2386093	single nucleotide variant	NM_001289080.2(CNTN6):c.2684A>G (p.Asn895Ser)	not specified [RCV004229147]	uncertain significance	3	1385777	1385777	Human		name
329367563	CV2427444	single nucleotide variant	NM_001289080.2(CNTN6):c.1109C>T (p.Thr370Ile)	not specified [RCV004248295]	uncertain significance	3	1327482	1327482	Human		name
329352474	CV2453068	single nucleotide variant	NM_001289080.2(CNTN6):c.2021G>A (p.Arg674His)	not specified [RCV004277678]	uncertain significance	3	1373999	1373999	Human		name
329402382	CV2454225	single nucleotide variant	NM_001289080.2(CNTN6):c.2222G>A (p.Arg741Gln)	not specified [RCV004265704]	uncertain significance	3	1382997	1382997	Human		name
401748004	CV2698906	single nucleotide variant	NM_001289080.2(CNTN6):c.1184T>C (p.Ile395Thr)	not specified [RCV004303449]	uncertain significance	3	1327557	1327557	Human		name
401721141	CV2702283	single nucleotide variant	NM_001289080.2(CNTN6):c.1877G>T (p.Ser626Ile)	not specified [RCV004314614]	uncertain significance	3	1373694	1373694	Human		name
401778730	CV2705590	single nucleotide variant	NM_001289080.2(CNTN6):c.1430A>T (p.Tyr477Phe)	not specified [RCV004318454]	uncertain significance	3	1352389	1352389	Human		name
401752773	CV2720514	single nucleotide variant	NM_001289080.2(CNTN6):c.1552G>C (p.Val518Leu)	not specified [RCV004327919]	uncertain significance	3	1372358	1372358	Human		name
401866919	CV2759041	single nucleotide variant	NM_001289080.2(CNTN6):c.2098C>G (p.Pro700Ala)	not specified [RCV004342348]	uncertain significance	3	1377007	1377007	Human		name
401862653	CV2762305	single nucleotide variant	NM_001289080.2(CNTN6):c.1745C>T (p.Thr582Ile)	not specified [RCV004335421]	uncertain significance	3	1372914	1372914	Human		name
401866368	CV2782782	single nucleotide variant	NM_001289080.2(CNTN6):c.2191G>A (p.Gly731Arg)	not specified [RCV004361601]	uncertain significance	3	1382966	1382966	Human		name
401931707	CV2801406	single nucleotide variant	NM_001289080.2(CNTN6):c.2942G>C (p.Gly981Ala)	CNTN6-related disorder [RCV003408444]	uncertain significance	3	1402442	1402442	Human		name , trait , alternate_id
401934810	CV2803027	single nucleotide variant	NM_001289080.2(CNTN6):c.1833T>A (p.Ser611Arg)	CNTN6-related disorder [RCV003412242]	uncertain significance	3	1373650	1373650	Human		name , trait , alternate_id
401912415	CV2819817	single nucleotide variant	NM_001289080.2(CNTN6):c.1198G>C (p.Glu400Gln)	CNTN6-related disorder [RCV003929124]\|not provided [RCV003427281]	benign	3	1327571	1327571	Human		name , trait , alternate_id
401912417	CV2819819	single nucleotide variant	NM_001289080.2(CNTN6):c.1995G>C (p.Leu665Phe)	not provided [RCV003427283]	uncertain significance	3	1373973	1373973	Human		name
405257019	CV3185446	single nucleotide variant	NM_001289080.2(CNTN6):c.1585A>C (p.Ile529Leu)	CNTN6-related disorder [RCV003931358]\|not provided [RCV003886010]	benign\|likely benign	3	1372391	1372391	Human		name , trait , alternate_id
405275463	CV3196294	single nucleotide variant	NM_001289080.2(CNTN6):c.2957G>C (p.Ser986Thr)	CNTN6-related disorder [RCV003974155]	likely benign	3	1402457	1402457	Human		name , trait , alternate_id
405290459	CV3219951	single nucleotide variant	NM_001289080.2(CNTN6):c.2457G>T (p.Met819Ile)	CNTN6-related disorder [RCV003962283]	likely benign	3	1383348	1383348	Human		name , trait , alternate_id
405674896	CV3304780	single nucleotide variant	NM_001289080.2(CNTN6):c.1051T>C (p.Trp351Arg)	not specified [RCV004442165]	uncertain significance	3	1325919	1325919	Human		name
405674902	CV3304781	single nucleotide variant	NM_001289080.2(CNTN6):c.1124T>A (p.Met375Lys)	not specified [RCV004442166]	uncertain significance	3	1327497	1327497	Human		name
405674906	CV3304782	single nucleotide variant	NM_001289080.2(CNTN6):c.1345A>G (p.Thr449Ala)	not specified [RCV004442167]	uncertain significance	3	1329916	1329916	Human		name
405674915	CV3304785	single nucleotide variant	NM_001289080.2(CNTN6):c.1580C>T (p.Pro527Leu)	not specified [RCV004442170]	uncertain significance	3	1372386	1372386	Human		name
405674919	CV3304786	single nucleotide variant	NM_001289080.2(CNTN6):c.1779T>G (p.Ile593Met)	not specified [RCV004442171]	uncertain significance	3	1372948	1372948	Human		name
405674923	CV3304787	single nucleotide variant	NM_001289080.2(CNTN6):c.1874A>C (p.Asn625Thr)	not specified [RCV004442172]	uncertain significance	3	1373691	1373691	Human		name
405674927	CV3304788	single nucleotide variant	NM_001289080.2(CNTN6):c.2291G>A (p.Arg764Lys)	not specified [RCV004442173]	uncertain significance	3	1383066	1383066	Human		name
405674931	CV3304789	single nucleotide variant	NM_001289080.2(CNTN6):c.2495C>A (p.Thr832Asn)	not specified [RCV004442174]	uncertain significance	3	1383386	1383386	Human		name
405674935	CV3304790	single nucleotide variant	NM_001289080.2(CNTN6):c.2612C>T (p.Ala871Val)	not specified [RCV004442175]	uncertain significance	3	1385705	1385705	Human		name
405674939	CV3304791	single nucleotide variant	NM_001289080.2(CNTN6):c.2627T>C (p.Phe876Ser)	not specified [RCV004442176]	uncertain significance	3	1385720	1385720	Human		name
407470972	CV3425802	single nucleotide variant	NM_001289080.2(CNTN6):c.2249A>G (p.Lys750Arg)	not specified [RCV004615578]	uncertain significance	3	1383024	1383024	Human		name
407470989	CV3425806	single nucleotide variant	NM_001289080.2(CNTN6):c.1358G>A (p.Ser453Asn)	not specified [RCV004615582]	uncertain significance	3	1329929	1329929	Human		name
407471001	CV3425809	single nucleotide variant	NM_001289080.2(CNTN6):c.1613A>G (p.Asn538Ser)	not specified [RCV004615585]	uncertain significance	3	1372419	1372419	Human		name
407471009	CV3425811	single nucleotide variant	NM_001289080.2(CNTN6):c.1396A>G (p.Ile466Val)	not specified [RCV004615587]	uncertain significance	3	1352355	1352355	Human		name
597771549	CV3650669	single nucleotide variant	NM_001289080.2(CNTN6):c.2042T>C (p.Ile681Thr)	not specified [RCV004897155]	uncertain significance	3	1374020	1374020	Human		name
597771559	CV3650671	single nucleotide variant	NM_001289080.2(CNTN6):c.2027T>C (p.Val676Ala)	not specified [RCV004897157]	uncertain significance	3	1374005	1374005	Human		name
597771565	CV3650672	single nucleotide variant	NM_001289080.2(CNTN6):c.1267G>C (p.Val423Leu)	not specified [RCV004897158]	uncertain significance	3	1329838	1329838	Human		name
597771575	CV3650674	single nucleotide variant	NM_001289080.2(CNTN6):c.2840A>G (p.Gln947Arg)	not specified [RCV004897160]	uncertain significance	3	1402340	1402340	Human		name
597771579	CV3650675	single nucleotide variant	NM_001289080.2(CNTN6):c.1711C>A (p.His571Asn)	not specified [RCV004897161]	uncertain significance	3	1372880	1372880	Human		name
597771587	CV3650677	single nucleotide variant	NM_001289080.2(CNTN6):c.1721A>G (p.Lys574Arg)	not specified [RCV004897163]	uncertain significance	3	1372890	1372890	Human		name
597771602	CV3650680	single nucleotide variant	NM_001289080.2(CNTN6):c.1088G>T (p.Arg363Ile)	not specified [RCV004897166]	uncertain significance	3	1327461	1327461	Human		name
597771627	CV3650685	single nucleotide variant	NM_001289080.2(CNTN6):c.2882A>C (p.Glu961Ala)	not specified [RCV004897171]	uncertain significance	3	1402382	1402382	Human		name
597771632	CV3650686	single nucleotide variant	NM_001289080.2(CNTN6):c.2407C>A (p.Gln803Lys)	not specified [RCV004897172]	uncertain significance	3	1383298	1383298	Human		name
597771635	CV3650687	single nucleotide variant	NM_001289080.2(CNTN6):c.2308C>G (p.Pro770Ala)	not specified [RCV004897173]	uncertain significance	3	1383083	1383083	Human		name
597771640	CV3650688	single nucleotide variant	NM_001289080.2(CNTN6):c.1556T>C (p.Leu519Pro)	not specified [RCV004897174]	uncertain significance	3	1372362	1372362	Human		name
597771645	CV3650689	single nucleotide variant	NM_001289080.2(CNTN6):c.1640G>C (p.Gly547Ala)	not specified [RCV004897175]	uncertain significance	3	1372446	1372446	Human		name
597771650	CV3650690	single nucleotide variant	NM_001289080.2(CNTN6):c.1078C>G (p.Pro360Ala)	not specified [RCV004897176]	uncertain significance	3	1325946	1325946	Human		name
598258419	CV3941416	single nucleotide variant	NM_001289080.2(CNTN6):c.1174T>A (p.Tyr392Asn)	not specified [RCV005324609]	uncertain significance	3	1327547	1327547	Human		name
598258436	CV3941419	single nucleotide variant	NM_001289080.2(CNTN6):c.2587A>G (p.Thr863Ala)	not specified [RCV005324612]	uncertain significance	3	1385680	1385680	Human		name
598258448	CV3941421	single nucleotide variant	NM_001289080.2(CNTN6):c.2555T>C (p.Ile852Thr)	not specified [RCV005324614]	uncertain significance	3	1385648	1385648	Human		name
598258454	CV3941422	single nucleotide variant	NM_001289080.2(CNTN6):c.2641G>C (p.Ala881Pro)	not specified [RCV005324615]	uncertain significance	3	1385734	1385734	Human		name
598258460	CV3941423	single nucleotide variant	NM_001289080.2(CNTN6):c.2494A>G (p.Thr832Ala)	not specified [RCV005324616]	uncertain significance	3	1383385	1383385	Human		name
598258467	CV3941424	single nucleotide variant	NM_001289080.2(CNTN6):c.1010G>T (p.Trp337Leu)	not specified [RCV005324617]	uncertain significance	3	1325878	1325878	Human		name
598258486	CV3951943	single nucleotide variant	NM_001289080.2(CNTN6):c.2237C>A (p.Thr746Lys)	not specified [RCV005324620]	uncertain significance	3	1383012	1383012	Human		name
598258503	CV3951946	single nucleotide variant	NM_001289080.2(CNTN6):c.1219G>A (p.Ala407Thr)	not specified [RCV005324623]	uncertain significance	3	1329790	1329790	Human		name
598258510	CV3951947	single nucleotide variant	NM_001289080.2(CNTN6):c.2141G>T (p.Arg714Leu)	not specified [RCV005324624]	uncertain significance	3	1377050	1377050	Human		name
598258515	CV3951948	single nucleotide variant	NM_001289080.2(CNTN6):c.1687A>T (p.Met563Leu)	not specified [RCV005324625]	uncertain significance	3	1372856	1372856	Human		name
15144512	CV708583	single nucleotide variant	NM_001289080.2(CNTN6):c.1318G>T (p.Ala440Ser)	CNTN6-related disorder [RCV003972858]\|not provided [RCV000966845]	benign	3	1329889	1329889	Human		name , trait , alternate_id
15189800	CV720203	single nucleotide variant	NM_001289080.2(CNTN6):c.1637A>G (p.Lys546Arg)	CNTN6-related disorder [RCV003930703]\|not provided [RCV000887923]	benign	3	1372443	1372444	Human	1	name , trait , alternate_id
15189800	CV720203	single nucleotide variant	NM_001289080.2(CNTN6):c.1637A>G (p.Lys546Arg)	CNTN6-related disorder [RCV003930703]\|not provided [RCV000887923]	benign	3	1372443	1372443	Human	1	name , trait , alternate_id
15176854	CV720209	single nucleotide variant	NM_001289080.2(CNTN6):c.2480C>T (p.Ala827Val)	not provided [RCV000884679]	likely benign	3	1383371	1383371	Human		name
401760064	CV2718703	single nucleotide variant	NM_001289080.2(CNTN6):c.3004A>G (p.Ile1002Val)	not specified [RCV004328459]	uncertain significance	3	1403335	1403335	Human		name
597771570	CV3650673	single nucleotide variant	NM_001289080.2(CNTN6):c.3018A>C (p.Glu1006Asp)	not specified [RCV004897159]	uncertain significance	3	1403349	1403349	Human		name
598258431	CV3941418	single nucleotide variant	NM_001289080.2(CNTN6):c.3067G>C (p.Ala1023Pro)	not specified [RCV005324611]	uncertain significance	3	1403398	1403398	Human		name
598258480	CV3951942	single nucleotide variant	NM_001289080.2(CNTN6):c.3055T>A (p.Phe1019Ile)	not specified [RCV005324619]	uncertain significance	3	1403386	1403386	Human		name
15153143	CV720215	single nucleotide variant	NM_001289080.2(CNTN6):c.3070A>C (p.Ile1024Leu)	CNTN6-related disorder [RCV003908399]\|not provided [RCV000879951]	benign	3	1403401	1403401	Human		name , trait , alternate_id

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