Mrc2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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114 records found for search term Mrc2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15189401	CV778543	single nucleotide variant	NM_006039.5(MRC2):c.2473+7A>G	not provided [RCV000954164]	benign	17	62680460	62680460	Human		name
597662209	CV3560788	single nucleotide variant	NM_006039.5(MRC2):c.10G>T (p.Gly4Cys)	not specified [RCV004828598]	uncertain significance	17	62627812	62627812	Human		name
598201842	CV3982602	single nucleotide variant	NM_006039.5(MRC2):c.13C>G (p.Arg5Gly)	not specified [RCV005376118]	uncertain significance	17	62627815	62627815	Human		name
329354028	CV2436804	single nucleotide variant	NM_006039.5(MRC2):c.64C>T (p.Leu22Phe)	not specified [RCV004260204]	uncertain significance	17	62627866	62627866	Human		name
597662133	CV3560777	single nucleotide variant	NM_006039.5(MRC2):c.64C>G (p.Leu22Val)	not specified [RCV004828589]	uncertain significance	17	62627866	62627866	Human		name
8636273	CV91496	single nucleotide variant	NM_006039.4(MRC2):c.885C>T (p.Thr295=)	Malignant melanoma [RCV000071594]	not provided	17	62666782	62666782	Human		name
405734734	CV3370156	single nucleotide variant	NM_006039.5(MRC2):c.213C>A (p.Ser71Arg)	not specified [RCV004496751]	uncertain significance	17	62664642	62664642	Human		name
598168679	CV3982600	single nucleotide variant	NM_006039.5(MRC2):c.226C>G (p.Arg76Gly)	not specified [RCV005369747]	uncertain significance	17	62664655	62664655	Human		name
156139953	CV2202940	single nucleotide variant	NM_006039.5(MRC2):c.972T>G (p.Ser324Arg)	not specified [RCV004069206]	uncertain significance	17	62666869	62666869	Human		name
156401313	CV2210901	single nucleotide variant	NM_006039.5(MRC2):c.410G>A (p.Arg137His)	not specified [RCV004085979]	uncertain significance	17	62664839	62664839	Human		name
156045211	CV2215991	single nucleotide variant	NM_006039.5(MRC2):c.830C>T (p.Thr277Met)	not specified [RCV004097045]	uncertain significance	17	62666590	62666590	Human		name
156246465	CV2228302	single nucleotide variant	NM_006039.5(MRC2):c.463A>G (p.Ser155Gly)	not specified [RCV004098303]	uncertain significance	17	62664892	62664892	Human		name
155988679	CV2234239	single nucleotide variant	NM_006039.5(MRC2):c.553A>G (p.Lys185Glu)	not specified [RCV004106315]	uncertain significance	17	62666126	62666126	Human		name
155950190	CV2267803	single nucleotide variant	NM_006039.5(MRC2):c.608G>C (p.Ser203Thr)	not specified [RCV004136113]	uncertain significance	17	62666181	62666181	Human		name
156144370	CV2358656	single nucleotide variant	NM_006039.5(MRC2):c.409C>T (p.Arg137Cys)	not specified [RCV004209577]	uncertain significance	17	62664838	62664838	Human		name
329396535	CV2459697	single nucleotide variant	NM_006039.5(MRC2):c.631C>G (p.Leu211Val)	not specified [RCV004277121]	uncertain significance	17	62666204	62666204	Human		name
401752912	CV2682978	single nucleotide variant	NM_006039.5(MRC2):c.431C>T (p.Pro144Leu)	not specified [RCV004283767]	uncertain significance	17	62664860	62664860	Human		name
401740095	CV2683257	single nucleotide variant	NM_006039.5(MRC2):c.658G>A (p.Gly220Ser)	not specified [RCV004288042]	uncertain significance	17	62666231	62666231	Human		name
401777119	CV2721613	single nucleotide variant	NM_006039.5(MRC2):c.773C>T (p.Ser258Leu)	not specified [RCV004316117]	uncertain significance	17	62666533	62666533	Human		name
401897672	CV2776606	single nucleotide variant	NM_006039.5(MRC2):c.671G>A (p.Arg224His)	not specified [RCV004357483]	uncertain significance	17	62666244	62666244	Human		name
405734017	CV3370197	single nucleotide variant	NM_006039.5(MRC2):c.341G>A (p.Arg114Gln)	not specified [RCV004496792]	uncertain significance	17	62664770	62664770	Human		name
405749658	CV3370292	single nucleotide variant	NM_006039.5(MRC2):c.659G>A (p.Gly220Asp)	not specified [RCV004498957]	uncertain significance	17	62666232	62666232	Human		name
407496496	CV3454072	single nucleotide variant	NM_006039.5(MRC2):c.649C>A (p.Gln217Lys)	not specified [RCV004643507]	uncertain significance	17	62666222	62666222	Human		name
407496515	CV3454078	single nucleotide variant	NM_006039.5(MRC2):c.808G>C (p.Gly270Arg)	not specified [RCV004643513]	uncertain significance	17	62666568	62666568	Human		name
407496527	CV3454081	single nucleotide variant	NM_006039.5(MRC2):c.766A>G (p.Thr256Ala)	not specified [RCV004643516]	uncertain significance	17	62666526	62666526	Human		name
597662141	CV3560778	single nucleotide variant	NM_006039.5(MRC2):c.311C>T (p.Thr104Met)	not specified [RCV004828590]	uncertain significance	17	62664740	62664740	Human		name
597662182	CV3560783	single nucleotide variant	NM_006039.5(MRC2):c.371G>T (p.Arg124Leu)	not specified [RCV004828595]	uncertain significance	17	62664800	62664800	Human		name
597637540	CV3560785	single nucleotide variant	NM_006039.5(MRC2):c.454C>A (p.Gln152Lys)	not specified [RCV004824743]	uncertain significance	17	62664883	62664883	Human		name
598201837	CV3982601	single nucleotide variant	NM_006039.5(MRC2):c.456G>C (p.Gln152His)	not specified [RCV005376117]	uncertain significance	17	62664885	62664885	Human		name
598168684	CV3982603	single nucleotide variant	NM_006039.5(MRC2):c.460C>T (p.Arg154Cys)	not specified [RCV005369748]	uncertain significance	17	62664889	62664889	Human		name
15103137	CV704273	single nucleotide variant	NM_006039.5(MRC2):c.464G>C (p.Ser155Thr)	not provided [RCV000959421]	benign	17	62664893	62664893	Human		name
156169511	CV2197795	single nucleotide variant	NM_006039.5(MRC2):c.1460C>T (p.Pro487Leu)	not specified [RCV004077036]	uncertain significance	17	62672151	62672151	Human		name
156386519	CV2228238	single nucleotide variant	NM_006039.5(MRC2):c.1934G>A (p.Arg645Gln)	not specified [RCV004097971]	uncertain significance	17	62677368	62677368	Human		name
156294432	CV2243697	single nucleotide variant	NM_006039.5(MRC2):c.1536G>C (p.Gln512His)	not specified [RCV004114400]	uncertain significance	17	62674137	62674137	Human		name
156334720	CV2263403	single nucleotide variant	NM_006039.5(MRC2):c.2068C>T (p.Arg690Trp)	not specified [RCV004133657]	uncertain significance	17	62678519	62678519	Human		name
156024000	CV2273823	single nucleotide variant	NM_006039.5(MRC2):c.1876G>T (p.Ala626Ser)	not specified [RCV004132454]	uncertain significance	17	62677310	62677310	Human		name
155915806	CV2274398	single nucleotide variant	NM_006039.5(MRC2):c.1789A>G (p.Ser597Gly)	not specified [RCV004136772]	uncertain significance	17	62676486	62676486	Human		name
155916978	CV2278475	single nucleotide variant	NM_006039.5(MRC2):c.1859C>T (p.Ala620Val)	not specified [RCV004132919]	uncertain significance	17	62677293	62677293	Human		name
155902645	CV2301479	single nucleotide variant	NM_006039.5(MRC2):c.1656T>G (p.His552Gln)	not specified [RCV004162403]	uncertain significance	17	62675876	62675876	Human		name
156100213	CV2306601	single nucleotide variant	NM_006039.5(MRC2):c.1763A>C (p.Asn588Thr)	not specified [RCV004157203]	uncertain significance	17	62676460	62676460	Human		name
156093171	CV2309910	single nucleotide variant	NM_006039.5(MRC2):c.1921C>T (p.Arg641Cys)	not specified [RCV004161280]	uncertain significance	17	62677355	62677355	Human		name
156402741	CV2371529	single nucleotide variant	NM_006039.5(MRC2):c.2024C>T (p.Ser675Leu)	not specified [RCV004216780]	uncertain significance	17	62677458	62677458	Human		name
155904254	CV2385452	single nucleotide variant	NM_006039.5(MRC2):c.2941A>C (p.Asn981His)	not specified [RCV004233104]	uncertain significance	17	62682372	62682372	Human		name
155952927	CV2393866	single nucleotide variant	NM_006039.5(MRC2):c.2038C>T (p.Arg680Trp)	not specified [RCV004233690]	uncertain significance	17	62677472	62677472	Human		name
155933608	CV2399354	single nucleotide variant	NM_006039.5(MRC2):c.2980C>T (p.Arg994Trp)	not specified [RCV004242642]	uncertain significance	17	62688322	62688322	Human		name
156006210	CV2401174	single nucleotide variant	NM_006039.5(MRC2):c.1639C>T (p.Arg547Cys)	not specified [RCV004245731]	uncertain significance	17	62675859	62675859	Human		name
329366150	CV2438161	single nucleotide variant	NM_006039.5(MRC2):c.1855G>A (p.Val619Met)	not specified [RCV004256938]	uncertain significance	17	62677289	62677289	Human		name
329374876	CV2440100	single nucleotide variant	NM_006039.5(MRC2):c.2446G>A (p.Val816Met)	not specified [RCV004260565]	uncertain significance	17	62680426	62680426	Human		name
329380473	CV2466638	single nucleotide variant	NM_006039.5(MRC2):c.2152G>C (p.Glu718Gln)	not specified [RCV004274160]	uncertain significance	17	62678603	62678603	Human		name
329392343	CV2470631	single nucleotide variant	NM_006039.5(MRC2):c.1985C>T (p.Thr662Met)	not specified [RCV004273624]	uncertain significance	17	62677419	62677419	Human		name
401735117	CV2706672	single nucleotide variant	NM_006039.5(MRC2):c.1961C>T (p.Pro654Leu)	not specified [RCV004319246]	uncertain significance	17	62677395	62677395	Human		name
401855270	CV2757229	single nucleotide variant	NM_006039.5(MRC2):c.1864G>T (p.Ala622Ser)	not specified [RCV004338826]	uncertain significance	17	62677298	62677298	Human		name
405734747	CV3370154	single nucleotide variant	NM_006039.5(MRC2):c.2077G>T (p.Asp693Tyr)	not specified [RCV004496749]	uncertain significance	17	62678528	62678528	Human		name
405734701	CV3370160	single nucleotide variant	NM_006039.5(MRC2):c.2182A>C (p.Asn728His)	not specified [RCV004496755]	uncertain significance	17	62678633	62678633	Human		name
405734671	CV3370163	single nucleotide variant	NM_006039.5(MRC2):c.2222A>G (p.Gln741Arg)	not specified [RCV004496758]	uncertain significance	17	62679826	62679826	Human		name
405734649	CV3370166	single nucleotide variant	NM_006039.5(MRC2):c.2264G>T (p.Gly755Val)	not specified [RCV004496761]	uncertain significance	17	62679868	62679868	Human		name
405733979	CV3370174	single nucleotide variant	NM_006039.5(MRC2):c.2554A>C (p.Ile852Leu)	not specified [RCV004496769]	uncertain significance	17	62680880	62680880	Human		name
405733858	CV3370177	single nucleotide variant	NM_006039.5(MRC2):c.2812G>A (p.Gly938Arg)	not specified [RCV004496772]	uncertain significance	17	62682243	62682243	Human		name
405733535	CV3373671	single nucleotide variant	NM_006039.5(MRC2):c.1135A>C (p.Lys379Gln)	not specified [RCV004496707]	uncertain significance	17	62671666	62671666	Human		name
405733549	CV3373673	single nucleotide variant	NM_006039.5(MRC2):c.1201C>T (p.Arg401Cys)	not specified [RCV004496709]	uncertain significance	17	62671732	62671732	Human		name
405733557	CV3373674	single nucleotide variant	NM_006039.5(MRC2):c.1285A>C (p.Ile429Leu)	not specified [RCV004496710]	uncertain significance	17	62671816	62671816	Human		name
405733582	CV3373677	single nucleotide variant	NM_006039.5(MRC2):c.1509C>G (p.Ile503Met)	not specified [RCV004496713]	uncertain significance	17	62674110	62674110	Human		name
405733598	CV3373679	single nucleotide variant	NM_006039.5(MRC2):c.1577C>A (p.Thr526Lys)	not specified [RCV004496715]	uncertain significance	17	62675797	62675797	Human		name
405733631	CV3373684	single nucleotide variant	NM_006039.5(MRC2):c.1822C>T (p.Arg608Trp)	not specified [RCV004496720]	uncertain significance	17	62676519	62676519	Human		name
405733689	CV3373691	single nucleotide variant	NM_006039.5(MRC2):c.1915C>T (p.Arg639Trp)	not specified [RCV004496727]	uncertain significance	17	62677349	62677349	Human		name
405733741	CV3373698	single nucleotide variant	NM_006039.5(MRC2):c.1958C>T (p.Thr653Met)	not specified [RCV004496734]	uncertain significance	17	62677392	62677392	Human		name
407496506	CV3454075	single nucleotide variant	NM_006039.5(MRC2):c.2572G>T (p.Ala858Ser)	not specified [RCV004643510]	uncertain significance	17	62680898	62680898	Human		name
597662107	CV3560774	single nucleotide variant	NM_006039.5(MRC2):c.1723T>G (p.Trp575Gly)	not specified [RCV004828586]	uncertain significance	17	62676420	62676420	Human		name
597662115	CV3560775	single nucleotide variant	NM_006039.5(MRC2):c.2863G>A (p.Val955Ile)	not specified [RCV004828587]	uncertain significance	17	62682294	62682294	Human		name
597662124	CV3560776	single nucleotide variant	NM_006039.5(MRC2):c.1543G>A (p.Ala515Thr)	not specified [RCV004828588]	uncertain significance	17	62674144	62674144	Human		name
597662158	CV3560780	single nucleotide variant	NM_006039.5(MRC2):c.1269G>A (p.Met423Ile)	not specified [RCV004828592]	uncertain significance	17	62671800	62671800	Human		name
597662166	CV3560781	single nucleotide variant	NM_006039.5(MRC2):c.2350G>T (p.Gly784Cys)	not specified [RCV004828593]	uncertain significance	17	62680221	62680221	Human		name
597637546	CV3560786	single nucleotide variant	NM_006039.5(MRC2):c.2297G>A (p.Gly766Glu)	not specified [RCV004824744]	uncertain significance	17	62679901	62679901	Human		name
597662201	CV3560787	single nucleotide variant	NM_006039.5(MRC2):c.1993C>G (p.Leu665Val)	not specified [RCV004828597]	uncertain significance	17	62677427	62677427	Human		name
597662219	CV3560790	single nucleotide variant	NM_006039.5(MRC2):c.2353T>A (p.Cys785Ser)	not specified [RCV004828600]	uncertain significance	17	62680224	62680224	Human		name
598168661	CV3982596	single nucleotide variant	NM_006039.5(MRC2):c.1546G>A (p.Glu516Lys)	not specified [RCV005369744]	uncertain significance	17	62674147	62674147	Human		name
156294791	CV2243796	single nucleotide variant	NM_006039.5(MRC2):c.3332C>T (p.Thr1111Met)	not specified [RCV004114484]	uncertain significance	17	62688958	62688958	Human		name
156273041	CV2283759	single nucleotide variant	NM_006039.5(MRC2):c.3205G>C (p.Ala1069Pro)	not specified [RCV004142280]	uncertain significance	17	62688644	62688644	Human		name
156171463	CV2293139	single nucleotide variant	NM_006039.5(MRC2):c.3649C>T (p.Pro1217Ser)	not specified [RCV004150661]	uncertain significance	17	62689969	62689969	Human		name
156188445	CV2302872	single nucleotide variant	NM_006039.5(MRC2):c.3752C>T (p.Pro1251Leu)	not specified [RCV004162768]	uncertain significance	17	62690165	62690165	Human		name
156039084	CV2332683	single nucleotide variant	NM_006039.5(MRC2):c.3875G>A (p.Arg1292Gln)	not specified [RCV004189360]	uncertain significance	17	62690288	62690288	Human		name
156154590	CV2369521	single nucleotide variant	NM_006039.5(MRC2):c.3434G>A (p.Arg1145His)	not specified [RCV004210455]	uncertain significance	17	62689621	62689621	Human		name
156388841	CV2376135	single nucleotide variant	NM_006039.5(MRC2):c.3530G>A (p.Arg1177Gln)	not specified [RCV004220366]	uncertain significance	17	62689717	62689717	Human		name
329371640	CV2454823	single nucleotide variant	NM_006039.5(MRC2):c.4364G>A (p.Ser1455Asn)	not specified [RCV004270334]	uncertain significance	17	62692375	62692375	Human		name
329390793	CV2455474	single nucleotide variant	NM_006039.5(MRC2):c.3607C>G (p.Pro1203Ala)	not specified [RCV004276744]	uncertain significance	17	62689927	62689927	Human		name
401755018	CV2682358	single nucleotide variant	NM_006039.5(MRC2):c.3641C>T (p.Pro1214Leu)	not specified [RCV004290392]	uncertain significance	17	62689961	62689961	Human		name
401772173	CV2687437	single nucleotide variant	NM_006039.5(MRC2):c.3773A>C (p.His1258Pro)	not specified [RCV004300682]	uncertain significance	17	62690186	62690186	Human		name
401725451	CV2697417	single nucleotide variant	NM_006039.5(MRC2):c.3706A>G (p.Thr1236Ala)	not specified [RCV004304166]	uncertain significance	17	62690026	62690026	Human		name
401754335	CV2717343	single nucleotide variant	NM_006039.5(MRC2):c.3305C>T (p.Thr1102Ile)	not specified [RCV004330208]	uncertain significance	17	62688931	62688931	Human		name
401778946	CV2733004	single nucleotide variant	NM_006039.5(MRC2):c.3466C>T (p.Arg1156Cys)	not specified [RCV004331178]	uncertain significance	17	62689653	62689653	Human		name
401886103	CV2771616	single nucleotide variant	NM_006039.5(MRC2):c.3205G>T (p.Ala1069Ser)	not specified [RCV004350423]	uncertain significance	17	62688644	62688644	Human		name
405733943	CV3370188	single nucleotide variant	NM_006039.5(MRC2):c.3223C>A (p.Pro1075Thr)	not specified [RCV004496783]	uncertain significance	17	62688662	62688662	Human		name
405734010	CV3370196	single nucleotide variant	NM_006039.5(MRC2):c.3379G>A (p.Gly1127Ser)	not specified [RCV004496791]	uncertain significance	17	62689566	62689566	Human		name
405734071	CV3370205	single nucleotide variant	NM_006039.5(MRC2):c.3472G>A (p.Ala1158Thr)	not specified [RCV004496800]	likely benign	17	62689659	62689659	Human		name
405734088	CV3370208	single nucleotide variant	NM_006039.5(MRC2):c.3530G>T (p.Arg1177Leu)	not specified [RCV004496803]	uncertain significance	17	62689717	62689717	Human		name
405734250	CV3370229	single nucleotide variant	NM_006039.5(MRC2):c.3767G>A (p.Ser1256Asn)	not specified [RCV004496824]	uncertain significance	17	62690180	62690180	Human		name
405734390	CV3370246	single nucleotide variant	NM_006039.5(MRC2):c.3844A>G (p.Met1282Val)	not specified [RCV004496841]	uncertain significance	17	62690257	62690257	Human		name
405734526	CV3370263	single nucleotide variant	NM_006039.5(MRC2):c.4330C>T (p.Arg1444Cys)	not specified [RCV004496858]	uncertain significance	17	62692341	62692341	Human		name
405734560	CV3370267	single nucleotide variant	NM_006039.5(MRC2):c.4331G>A (p.Arg1444His)	not specified [RCV004496862]	uncertain significance	17	62692342	62692342	Human		name
407496492	CV3454071	single nucleotide variant	NM_006039.5(MRC2):c.3806C>T (p.Ala1269Val)	not specified [RCV004643506]	uncertain significance	17	62690219	62690219	Human		name
407496499	CV3454073	single nucleotide variant	NM_006039.5(MRC2):c.3050C>T (p.Pro1017Leu)	not specified [RCV004643508]	uncertain significance	17	62688392	62688392	Human		name
407496502	CV3454074	single nucleotide variant	NM_006039.5(MRC2):c.4064G>A (p.Gly1355Glu)	not specified [RCV004643509]	uncertain significance	17	62691000	62691000	Human		name
407496508	CV3454076	single nucleotide variant	NM_006039.5(MRC2):c.3095T>C (p.Phe1032Ser)	not specified [RCV004643511]	uncertain significance	17	62688534	62688534	Human		name
407496512	CV3454077	single nucleotide variant	NM_006039.5(MRC2):c.3067A>G (p.Ile1023Val)	not specified [RCV004643512]	uncertain significance	17	62688506	62688506	Human		name
407496520	CV3454079	single nucleotide variant	NM_006039.5(MRC2):c.3155C>G (p.Pro1052Arg)	not specified [RCV004643514]	uncertain significance	17	62688594	62688594	Human		name
597662150	CV3560779	single nucleotide variant	NM_006039.5(MRC2):c.3673G>A (p.Val1225Met)	not specified [RCV004828591]	uncertain significance	17	62689993	62689993	Human		name
597662174	CV3560782	single nucleotide variant	NM_006039.5(MRC2):c.3608C>T (p.Pro1203Leu)	not specified [RCV004828594]	uncertain significance	17	62689928	62689928	Human		name
597662192	CV3560784	single nucleotide variant	NM_006039.5(MRC2):c.4049A>G (p.Asn1350Ser)	not specified [RCV004828596]	uncertain significance	17	62690985	62690985	Human		name
598201832	CV3982597	single nucleotide variant	NM_006039.5(MRC2):c.4360C>T (p.Arg1454Cys)	not specified [RCV005376116]	uncertain significance	17	62692371	62692371	Human		name
598168673	CV3982599	single nucleotide variant	NM_006039.5(MRC2):c.3226A>T (p.Thr1076Ser)	not specified [RCV005369746]	uncertain significance	17	62688852	62688852	Human		name
598201847	CV3982604	single nucleotide variant	NM_006039.5(MRC2):c.4105T>C (p.Cys1369Arg)	not specified [RCV005376119]	uncertain significance	17	62691041	62691041	Human		name
598168689	CV3982605	single nucleotide variant	NM_006039.5(MRC2):c.3640C>T (p.Pro1214Ser)	not specified [RCV005369749]	uncertain significance	17	62689960	62689960	Human		name
15139834	CV715609	single nucleotide variant	NM_006039.5(MRC2):c.4291G>A (p.Ala1431Thr)	not provided [RCV000966033]	benign	17	62692302	62692302	Human		name
8628047	CV83191	single nucleotide variant	NM_006039.4(MRC2):c.3635G>A (p.Gly1212Glu)	Malignant melanoma [RCV000063271]	not provided	17	62689955	62689955	Human		name

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