Grin2c Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

129 records found for search term Grin2c

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150494231	CV1256425	duplication	NM_000835.6(GRIN2C):c.400-11dup	not provided [RCV001675390]	benign	17	74852619	74852620	Human		name
408384660	CV3504551	single nucleotide variant	NM_000835.6(GRIN2C):c.2583+4G>C	GRIN2C-related disorder [RCV004731996]	uncertain significance	17	74844272	74844272	Human		name , trait , alternate_id
407463414	CV3433245	single nucleotide variant	NM_000835.6(GRIN2C):c.4G>A (p.Gly2Ser)	not specified [RCV004634820]	uncertain significance	17	74855089	74855089	Human		name
598188213	CV3978135	single nucleotide variant	NM_000835.6(GRIN2C):c.4G>T (p.Gly2Cys)	not specified [RCV005353815]	uncertain significance	17	74855089	74855089	Human		name
15163907	CV706355	single nucleotide variant	NM_000835.6(GRIN2C):c.99C>T (p.Ala33=)	not provided [RCV000948205]	benign	17	74854994	74854994	Human		name
156064270	CV2340747	single nucleotide variant	NM_000835.6(GRIN2C):c.20C>T (p.Pro7Leu)	not specified [RCV004188112]	uncertain significance	17	74855073	74855073	Human		name
15167127	CV717899	single nucleotide variant	NM_000835.6(GRIN2C):c.22G>A (p.Ala8Thr)	not provided [RCV000971334]	likely benign	17	74855071	74855071	Human		name
156357055	CV2253808	single nucleotide variant	NM_000835.6(GRIN2C):c.86G>A (p.Gly29Asp)	not specified [RCV004127507]	uncertain significance	17	74855007	74855007	Human		name
405275449	CV3204844	single nucleotide variant	NM_000835.6(GRIN2C):c.58G>C (p.Gly20Arg)	GRIN2C-related disorder [RCV003952214]	likely benign	17	74855035	74855035	Human		name , trait , alternate_id
405770607	CV3262685	single nucleotide variant	NM_000835.6(GRIN2C):c.65G>A (p.Gly22Asp)	not specified [RCV004395884]	uncertain significance	17	74855028	74855028	Human		name
156238266	CV2285871	single nucleotide variant	NM_000835.6(GRIN2C):c.125C>A (p.Pro42His)	not specified [RCV004143807]	uncertain significance	17	74854968	74854968	Human		name
156170204	CV2380566	single nucleotide variant	NM_000835.6(GRIN2C):c.152C>T (p.Thr51Ile)	not specified [RCV004224888]	uncertain significance	17	74854941	74854941	Human		name
401906552	CV2808345	single nucleotide variant	NM_000835.6(GRIN2C):c.2328G>A (p.Ala776=)	not provided [RCV003421475]	likely benign	17	74846088	74846088	Human		name
401906553	CV2808346	single nucleotide variant	NM_000835.6(GRIN2C):c.2277C>T (p.Tyr759=)	not provided [RCV003421476]	likely benign	17	74846139	74846139	Human		name
405758823	CV3262667	single nucleotide variant	NM_000835.6(GRIN2C):c.145C>T (p.Arg49Cys)	not specified [RCV004393885]	uncertain significance	17	74854948	74854948	Human		name
405758828	CV3262668	single nucleotide variant	NM_000835.6(GRIN2C):c.157C>G (p.Gln53Glu)	not specified [RCV004393886]	uncertain significance	17	74854936	74854936	Human		name
405758839	CV3262670	single nucleotide variant	NM_000835.6(GRIN2C):c.161G>A (p.Ser54Asn)	not specified [RCV004393888]	uncertain significance	17	74854932	74854932	Human		name
407463410	CV3433244	single nucleotide variant	NM_000835.6(GRIN2C):c.199G>A (p.Val67Ile)	not specified [RCV004634819]	uncertain significance	17	74854894	74854894	Human		name
596945631	CV3547970	single nucleotide variant	NM_000835.6(GRIN2C):c.1464C>T (p.Arg488=)	not provided [RCV004809301]	likely benign	17	74850233	74850233	Human		name
598188193	CV3978131	single nucleotide variant	NM_000835.6(GRIN2C):c.205G>A (p.Val69Ile)	not specified [RCV005353812]	uncertain significance	17	74854888	74854888	Human		name
15162455	CV706356	single nucleotide variant	NM_000835.6(GRIN2C):c.140G>A (p.Arg47His)	not provided [RCV000947856]	likely benign	17	74854953	74854953	Human		name
15167221	CV706357	single nucleotide variant	NM_000835.6(GRIN2C):c.2997C>T (p.Ala999=)	not provided [RCV000949012]	likely benign	17	74843140	74843140	Human		name
15111941	CV717897	single nucleotide variant	NM_000835.6(GRIN2C):c.1305G>A (p.Arg435=)	not provided [RCV000961202]	benign	17	74850576	74850576	Human		name
15097963	CV729756	single nucleotide variant	NM_000835.6(GRIN2C):c.193C>T (p.Leu65Phe)	not provided [RCV000891625]	likely benign	17	74854900	74854900	Human		name
15174389	CV743523	single nucleotide variant	NM_000835.6(GRIN2C):c.1557C>T (p.Ile519=)	not provided [RCV000905955]	benign\|likely benign	17	74849868	74849868	Human		name
156229620	CV2209401	single nucleotide variant	NM_000835.6(GRIN2C):c.346C>A (p.His116Asn)	not specified [RCV004093565]	uncertain significance	17	74854747	74854747	Human		name
156376220	CV2210495	single nucleotide variant	NM_000835.6(GRIN2C):c.401A>C (p.Glu134Ala)	not specified [RCV004089625]	uncertain significance	17	74852610	74852610	Human		name
156094954	CV2213510	single nucleotide variant	NM_000835.6(GRIN2C):c.670T>G (p.Phe224Val)	not specified [RCV004087476]	uncertain significance	17	74852341	74852341	Human		name
155919859	CV2279491	single nucleotide variant	NM_000835.6(GRIN2C):c.548G>A (p.Arg183His)	not specified [RCV004142013]	uncertain significance	17	74852463	74852463	Human		name
156139342	CV2280739	single nucleotide variant	NM_000835.6(GRIN2C):c.439G>A (p.Glu147Lys)	not specified [RCV004143191]	uncertain significance	17	74852572	74852572	Human		name
156305812	CV2314746	single nucleotide variant	NM_000835.6(GRIN2C):c.938C>T (p.Pro313Leu)	not specified [RCV004170885]	uncertain significance	17	74852073	74852073	Human		name
156063083	CV2330982	single nucleotide variant	NM_000835.6(GRIN2C):c.785C>T (p.Thr262Ile)	not specified [RCV004188024]	uncertain significance	17	74852226	74852226	Human		name
156148664	CV2358105	single nucleotide variant	NM_000835.6(GRIN2C):c.709T>C (p.Phe237Leu)	not specified [RCV004211914]	uncertain significance	17	74852302	74852302	Human		name
401882761	CV2778498	single nucleotide variant	NM_000835.6(GRIN2C):c.545T>C (p.Val182Ala)	not specified [RCV004344157]	uncertain significance	17	74852466	74852466	Human		name
401888447	CV2784996	single nucleotide variant	NM_000835.6(GRIN2C):c.875G>T (p.Gly292Val)	not specified [RCV004355020]	uncertain significance	17	74852136	74852136	Human		name
405770597	CV3262683	single nucleotide variant	NM_000835.6(GRIN2C):c.437T>C (p.Leu146Pro)	not specified [RCV004395882]	uncertain significance	17	74852574	74852574	Human		name
405770925	CV3262684	single nucleotide variant	NM_000835.6(GRIN2C):c.617G>C (p.Gly206Ala)	not specified [RCV004395883]	uncertain significance	17	74852394	74852394	Human		name
405770612	CV3262686	single nucleotide variant	NM_000835.6(GRIN2C):c.667G>C (p.Val223Leu)	not specified [RCV004395885]	uncertain significance	17	74852344	74852344	Human		name
405770617	CV3262687	single nucleotide variant	NM_000835.6(GRIN2C):c.731G>C (p.Gly244Ala)	not specified [RCV004395886]	uncertain significance	17	74852280	74852280	Human		name
405770622	CV3262688	single nucleotide variant	NM_000835.6(GRIN2C):c.860A>G (p.Gln287Arg)	not specified [RCV004395887]	uncertain significance	17	74852151	74852151	Human		name
405770628	CV3262689	single nucleotide variant	NM_000835.6(GRIN2C):c.935C>T (p.Ala312Val)	not specified [RCV004395888]	uncertain significance	17	74852076	74852076	Human		name
407463389	CV3433237	single nucleotide variant	NM_000835.6(GRIN2C):c.869G>A (p.Arg290His)	not specified [RCV004634814]	uncertain significance	17	74852142	74852142	Human		name
407463418	CV3433246	single nucleotide variant	NM_000835.6(GRIN2C):c.545T>G (p.Val182Gly)	not specified [RCV004634821]	uncertain significance	17	74852466	74852466	Human		name
597770764	CV3678685	single nucleotide variant	NM_000835.6(GRIN2C):c.982C>T (p.Arg328Trp)	not specified [RCV004928344]	uncertain significance	17	74852029	74852029	Human		name
597770770	CV3678686	single nucleotide variant	NM_000835.6(GRIN2C):c.686C>T (p.Ser229Leu)	not specified [RCV004928345]	uncertain significance	17	74852325	74852325	Human		name
597755812	CV3678687	single nucleotide variant	NM_000835.6(GRIN2C):c.721G>A (p.Ala241Thr)	not specified [RCV004924714]	uncertain significance	17	74852290	74852290	Human		name
597755818	CV3678690	single nucleotide variant	NM_000835.6(GRIN2C):c.569A>G (p.His190Arg)	not specified [RCV004924716]	uncertain significance	17	74852442	74852442	Human		name
597770785	CV3678692	single nucleotide variant	NM_000835.6(GRIN2C):c.845G>A (p.Arg282His)	not specified [RCV004928348]	uncertain significance	17	74852166	74852166	Human		name
598188200	CV3978133	single nucleotide variant	NM_000835.6(GRIN2C):c.691G>A (p.Glu231Lys)	not specified [RCV005353813]	uncertain significance	17	74852320	74852320	Human		name
598188206	CV3978134	single nucleotide variant	NM_000835.6(GRIN2C):c.970G>A (p.Val324Ile)	not specified [RCV005353814]	uncertain significance	17	74852041	74852041	Human		name
598188218	CV3978136	single nucleotide variant	NM_000835.6(GRIN2C):c.964G>A (p.Gly322Arg)	not specified [RCV005353816]	uncertain significance	17	74852047	74852047	Human		name
598188238	CV3978140	single nucleotide variant	NM_000835.6(GRIN2C):c.584T>C (p.Leu195Pro)	not specified [RCV005353819]	uncertain significance	17	74852427	74852427	Human		name
598234780	CV3978144	single nucleotide variant	NM_000835.6(GRIN2C):c.967C>T (p.Pro323Ser)	not specified [RCV005342960]	uncertain significance	17	74852044	74852044	Human		name
15101945	CV706358	single nucleotide variant	NM_000835.6(GRIN2C):c.572T>C (p.Val191Ala)	not provided [RCV000959193]	likely benign	17	74852439	74852439	Human		name
156108815	CV2211066	single nucleotide variant	NM_000835.6(GRIN2C):c.1252A>G (p.Ser418Gly)	not specified [RCV004088247]	uncertain significance	17	74850629	74850629	Human		name
156181980	CV2246367	single nucleotide variant	NM_000835.6(GRIN2C):c.2911G>C (p.Val971Leu)	not specified [RCV004107806]	uncertain significance	17	74843226	74843226	Human		name
155961616	CV2254228	single nucleotide variant	NM_000835.6(GRIN2C):c.2530C>T (p.Arg844Cys)	not specified [RCV004129907]	uncertain significance	17	74844329	74844329	Human		name
156177218	CV2258154	single nucleotide variant	NM_000835.6(GRIN2C):c.2255A>G (p.Lys752Arg)	not specified [RCV004121541]	uncertain significance	17	74846161	74846161	Human		name
156212288	CV2259941	single nucleotide variant	NM_000835.6(GRIN2C):c.1030G>A (p.Asp344Asn)	not specified [RCV004118965]	uncertain significance	17	74851660	74851660	Human		name
156015413	CV2298805	single nucleotide variant	NM_000835.6(GRIN2C):c.2020C>G (p.Gln674Glu)	not specified [RCV004156357]	uncertain significance	17	74846902	74846902	Human		name
156288436	CV2299188	single nucleotide variant	NM_000835.6(GRIN2C):c.1300C>T (p.Arg434Cys)	not specified [RCV004152527]	uncertain significance	17	74850581	74850581	Human		name
156051066	CV2328930	single nucleotide variant	NM_000835.6(GRIN2C):c.1465G>A (p.Gly489Ser)	not specified [RCV004180232]	uncertain significance	17	74850232	74850232	Human		name
156344696	CV2346177	single nucleotide variant	NM_000835.6(GRIN2C):c.2093A>G (p.Asp698Gly)	not specified [RCV004201635]	uncertain significance	17	74846829	74846829	Human		name
156174040	CV2355225	single nucleotide variant	NM_000835.6(GRIN2C):c.2858C>A (p.Pro953Gln)	not specified [RCV004198597]	uncertain significance	17	74843279	74843279	Human		name
156050710	CV2367582	single nucleotide variant	NM_000835.6(GRIN2C):c.2647G>A (p.Asp883Asn)	not specified [RCV004211510]	uncertain significance	17	74843490	74843490	Human		name
155995112	CV2374881	single nucleotide variant	NM_000835.6(GRIN2C):c.2531G>A (p.Arg844His)	not specified [RCV004227906]	uncertain significance	17	74844328	74844328	Human		name
156165129	CV2376320	single nucleotide variant	NM_000835.6(GRIN2C):c.1231C>T (p.Arg411Trp)	not specified [RCV004222581]	uncertain significance	17	74850650	74850650	Human		name
156153471	CV2394976	single nucleotide variant	NM_000835.6(GRIN2C):c.1201C>T (p.Arg401Trp)	not specified [RCV004236672]	uncertain significance	17	74850680	74850680	Human		name
156254529	CV2397556	single nucleotide variant	NM_000835.6(GRIN2C):c.1093C>T (p.Arg365Trp)	not specified [RCV004237018]	uncertain significance	17	74851597	74851597	Human		name
329373291	CV2456002	single nucleotide variant	NM_000835.6(GRIN2C):c.2288T>C (p.Met763Thr)	not specified [RCV004272909]	uncertain significance	17	74846128	74846128	Human		name
329371296	CV2458067	single nucleotide variant	NM_000835.6(GRIN2C):c.1786G>A (p.Ala596Thr)	not specified [RCV004271898]	uncertain significance	17	74847523	74847523	Human		name
329362322	CV2463813	single nucleotide variant	NM_000835.6(GRIN2C):c.2858C>G (p.Pro953Arg)	not specified [RCV004279902]	uncertain significance	17	74843279	74843279	Human		name
401780381	CV2673999	single nucleotide variant	NM_000835.6(GRIN2C):c.2009G>A (p.Arg670Gln)	not specified [RCV004293366]	uncertain significance	17	74846913	74846913	Human		name
401771266	CV2675523	single nucleotide variant	NM_000835.6(GRIN2C):c.1037C>T (p.Ser346Phe)	not specified [RCV004295139]	uncertain significance	17	74851653	74851653	Human		name
401749744	CV2694733	single nucleotide variant	NM_000835.6(GRIN2C):c.2890G>C (p.Asp964His)	not specified [RCV004298820]	uncertain significance	17	74843247	74843247	Human		name
401719158	CV2704985	single nucleotide variant	NM_000835.6(GRIN2C):c.2197C>G (p.Leu733Val)	not specified [RCV004309591]	uncertain significance	17	74846219	74846219	Human		name
401722359	CV2706484	single nucleotide variant	NM_000835.6(GRIN2C):c.1966T>A (p.Tyr656Asn)	not specified [RCV004317300]	uncertain significance	17	74847343	74847343	Human		name
401770001	CV2718987	single nucleotide variant	NM_000835.6(GRIN2C):c.1349C>A (p.Thr450Asn)	not specified [RCV004322577]	uncertain significance	17	74850348	74850348	Human		name
401780572	CV2727451	single nucleotide variant	NM_000835.6(GRIN2C):c.2885C>T (p.Pro962Leu)	not specified [RCV004329657]	uncertain significance	17	74843252	74843252	Human		name
401887561	CV2772014	single nucleotide variant	NM_000835.6(GRIN2C):c.1211C>T (p.Thr404Met)	not specified [RCV004344692]	uncertain significance	17	74850670	74850670	Human		name
401898807	CV2782714	single nucleotide variant	NM_000835.6(GRIN2C):c.2069G>A (p.Arg690Gln)	not specified [RCV004359722]	uncertain significance	17	74846853	74846853	Human		name
401866730	CV2782927	single nucleotide variant	NM_000835.6(GRIN2C):c.2234T>C (p.Leu745Pro)	not specified [RCV004361726]	uncertain significance	17	74846182	74846182	Human		name
401937619	CV2798829	single nucleotide variant	NM_000835.6(GRIN2C):c.1295C>G (p.Pro432Arg)	GRIN2C-related disorder [RCV003416683]	uncertain significance	17	74850586	74850586	Human		name , trait , alternate_id
405758800	CV3262664	single nucleotide variant	NM_000835.6(GRIN2C):c.1072A>G (p.Met358Val)	not specified [RCV004393882]	uncertain significance	17	74851618	74851618	Human		name
405758808	CV3262665	single nucleotide variant	NM_000835.6(GRIN2C):c.1121G>T (p.Arg374Leu)	not specified [RCV004393883]	uncertain significance	17	74850760	74850760	Human		name
405758817	CV3262666	single nucleotide variant	NM_000835.6(GRIN2C):c.1397C>G (p.Ala466Gly)	not specified [RCV004393884]	uncertain significance	17	74850300	74850300	Human		name
405758834	CV3262669	single nucleotide variant	NM_000835.6(GRIN2C):c.1618G>A (p.Gly540Ser)	not specified [RCV004393887]	uncertain significance	17	74849807	74849807	Human		name
405758845	CV3262671	single nucleotide variant	NM_000835.6(GRIN2C):c.1711G>A (p.Val571Ile)	not specified [RCV004393889]	uncertain significance	17	74847912	74847912	Human		name
405758853	CV3262672	single nucleotide variant	NM_000835.6(GRIN2C):c.1969A>G (p.Ile657Val)	not specified [RCV004393890]	uncertain significance	17	74847340	74847340	Human		name
405758858	CV3262673	single nucleotide variant	NM_000835.6(GRIN2C):c.2029C>T (p.Pro677Ser)	not specified [RCV004393891]	uncertain significance	17	74846893	74846893	Human		name
405758865	CV3262674	single nucleotide variant	NM_000835.6(GRIN2C):c.2311C>T (p.Arg771Trp)	not specified [RCV004393892]	uncertain significance	17	74846105	74846105	Human		name
405770554	CV3262675	single nucleotide variant	NM_000835.6(GRIN2C):c.2434A>G (p.Ile812Val)	not specified [RCV004395874]	uncertain significance	17	74844425	74844425	Human		name
405770559	CV3262676	single nucleotide variant	NM_000835.6(GRIN2C):c.2456T>A (p.Phe819Tyr)	not specified [RCV004395875]	uncertain significance	17	74844403	74844403	Human		name
405770565	CV3262677	single nucleotide variant	NM_000835.6(GRIN2C):c.2573C>G (p.Ala858Gly)	not specified [RCV004395876]	uncertain significance	17	74844286	74844286	Human		name
405770571	CV3262678	single nucleotide variant	NM_000835.6(GRIN2C):c.2624G>C (p.Ser875Thr)	not specified [RCV004395877]	uncertain significance	17	74843513	74843513	Human		name
405770577	CV3262679	single nucleotide variant	NM_000835.6(GRIN2C):c.2625C>G (p.Ser875Arg)	not specified [RCV004395878]	uncertain significance	17	74843512	74843512	Human		name
405770580	CV3262680	single nucleotide variant	NM_000835.6(GRIN2C):c.2659A>G (p.Ser887Gly)	not specified [RCV004395879]	likely benign	17	74843478	74843478	Human		name
405770585	CV3262681	single nucleotide variant	NM_000835.6(GRIN2C):c.2815C>T (p.Arg939Trp)	not specified [RCV004395880]	uncertain significance	17	74843322	74843322	Human		name
407463399	CV3433239	single nucleotide variant	NM_000835.6(GRIN2C):c.2786C>T (p.Ala929Val)	not specified [RCV004634816]	uncertain significance	17	74843351	74843351	Human		name
407463402	CV3433240	single nucleotide variant	NM_000835.6(GRIN2C):c.2816G>A (p.Arg939Gln)	not specified [RCV004634817]	uncertain significance	17	74843321	74843321	Human		name
407504313	CV3433241	single nucleotide variant	NM_000835.6(GRIN2C):c.1195G>C (p.Asp399His)	not specified [RCV004624041]	uncertain significance	17	74850686	74850686	Human		name
407463406	CV3433242	single nucleotide variant	NM_000835.6(GRIN2C):c.2645C>T (p.Pro882Leu)	not specified [RCV004634818]	uncertain significance	17	74843492	74843492	Human		name
407504317	CV3433243	single nucleotide variant	NM_000835.6(GRIN2C):c.1301G>A (p.Arg434His)	not specified [RCV004624042]	uncertain significance	17	74850580	74850580	Human		name
597755802	CV3678682	single nucleotide variant	NM_000835.6(GRIN2C):c.2125C>T (p.Arg709Cys)	not specified [RCV004924712]	uncertain significance	17	74846797	74846797	Human		name
597755808	CV3678683	single nucleotide variant	NM_000835.6(GRIN2C):c.2735C>T (p.Ser912Phe)	not specified [RCV004924713]	uncertain significance	17	74843402	74843402	Human		name
597770759	CV3678684	single nucleotide variant	NM_000835.6(GRIN2C):c.1750C>A (p.Gln584Lys)	not specified [RCV004928343]	uncertain significance	17	74847873	74847873	Human		name
597770775	CV3678688	single nucleotide variant	NM_000835.6(GRIN2C):c.1274G>A (p.Gly425Asp)	not specified [RCV004928346]	uncertain significance	17	74850607	74850607	Human		name
597755815	CV3678689	single nucleotide variant	NM_000835.6(GRIN2C):c.1744T>C (p.Tyr582His)	not specified [RCV004924715]	uncertain significance	17	74847879	74847879	Human		name
597770780	CV3678691	single nucleotide variant	NM_000835.6(GRIN2C):c.1049G>A (p.Gly350Asp)	not specified [RCV004928347]	uncertain significance	17	74851641	74851641	Human		name
597770790	CV3678693	single nucleotide variant	NM_000835.6(GRIN2C):c.2045C>T (p.Thr682Met)	not specified [RCV004928349]	uncertain significance	17	74846877	74846877	Human		name
597755822	CV3678694	single nucleotide variant	NM_000835.6(GRIN2C):c.2812C>G (p.Pro938Ala)	not specified [RCV004924717]	uncertain significance	17	74843325	74843325	Human		name
597755826	CV3678695	single nucleotide variant	NM_000835.6(GRIN2C):c.1736C>T (p.Pro579Leu)	not specified [RCV004924718]	uncertain significance	17	74847887	74847887	Human		name
597770796	CV3678696	single nucleotide variant	NM_000835.6(GRIN2C):c.1972G>A (p.Asp658Asn)	not specified [RCV004928350]	uncertain significance	17	74847337	74847337	Human		name
598188183	CV3978129	single nucleotide variant	NM_000835.6(GRIN2C):c.1931C>T (p.Thr644Met)	not specified [RCV005353810]	uncertain significance	17	74847378	74847378	Human		name
598188189	CV3978130	single nucleotide variant	NM_000835.6(GRIN2C):c.2701C>T (p.Arg901Cys)	not specified [RCV005353811]	uncertain significance	17	74843436	74843436	Human		name
598234755	CV3978132	single nucleotide variant	NM_000835.6(GRIN2C):c.2863C>T (p.Pro955Ser)	not specified [RCV005342957]	uncertain significance	17	74843274	74843274	Human		name
598188232	CV3978138	single nucleotide variant	NM_000835.6(GRIN2C):c.1601T>C (p.Met534Thr)	not specified [RCV005353818]	uncertain significance	17	74849824	74849824	Human		name
598234764	CV3978139	single nucleotide variant	NM_000835.6(GRIN2C):c.1777G>C (p.Gly593Arg)	not specified [RCV005342958]	uncertain significance	17	74847532	74847532	Human		name
598234772	CV3978141	single nucleotide variant	NM_000835.6(GRIN2C):c.2297A>T (p.Asp766Val)	not specified [RCV005342959]	uncertain significance	17	74846119	74846119	Human		name
598188243	CV3978142	single nucleotide variant	NM_000835.6(GRIN2C):c.1606G>A (p.Ala536Thr)	not specified [RCV005353820]	uncertain significance	17	74849819	74849819	Human		name
598188250	CV3978143	single nucleotide variant	NM_000835.6(GRIN2C):c.1508C>A (p.Ala503Glu)	not specified [RCV005353821]	uncertain significance	17	74849917	74849917	Human		name
15171092	CV717898	single nucleotide variant	NM_000835.6(GRIN2C):c.1468G>A (p.Val490Ile)	not provided [RCV000972132]	benign	17	74850229	74850229	Human		name
15162467	CV743522	single nucleotide variant	NM_000835.6(GRIN2C):c.1202G>A (p.Arg401Gln)	not provided [RCV000903557]	benign	17	74850679	74850679	Human		name
405275156	CV3204671	single nucleotide variant	NM_000835.6(GRIN2C):c.3333C>G (p.His1111Gln)	GRIN2C-related disorder [RCV003952069]	likely benign	17	74842804	74842804	Human		name , trait , alternate_id
405275712	CV3215988	single nucleotide variant	NM_000835.6(GRIN2C):c.3329G>C (p.Gly1110Ala)	GRIN2C-related disorder [RCV003952264]	likely benign	17	74842808	74842808	Human		name , trait , alternate_id
15162704	CV717900	single nucleotide variant	NM_000835.6(GRIN2C):c.3587C>T (p.Thr1196Ile)	not provided [RCV000970324]	benign	17	74842550	74842550	Human		name
405270527	CV3213306	deletion	NM_000835.6(GRIN2C):c.3560_3580del (p.His1187_Gly1193del)	GRIN2C-related disorder [RCV003971401]	benign	17	74842557	74842577	Human		name , trait , alternate_id
405260925	CV3204342	deletion	NM_000835.6(GRIN2C):c.3594_3595del (p.Tyr1198_Arg1199delinsTer)	GRIN2C-related disorder [RCV003944176]	uncertain significance	17	74842542	74842543	Human		name , trait , alternate_id
405266560	CV3211835	duplication	NM_000835.6(GRIN2C):c.3547_3567dup (p.Gly1189_Arg1190insGlyProLeuGlyHisArgGly)	GRIN2C-related disorder [RCV003947119]	likely benign	17	74842569	74842570	Human		name , trait , alternate_id

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