Lilrb3 Variant Search Result - Rat Genome Database

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77 records found for search term Lilrb3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156152726	CV2307654	single nucleotide variant	NM_006864.4(LILRB3):c.4A>C (p.Thr2Pro)	not specified [RCV004168071]	uncertain significance	19	54222973	54222973	Human		name
598129704	CV3887124	variation	NM_006864.4(LILRB3):c.870= (p.Tyr290=)	not provided [RCV005245184]	likely benign	19	54221168	54221168	Human		name
329386381	CV2428278	variation	NM_006864.4(LILRB3):c.1042= (p.Arg348=)	not specified [RCV004251306]	uncertain significance	19	54220744	54220744	Human		name
598129575	CV3886992	single nucleotide variant	NM_006864.4(LILRB3):c.411G>A (p.Gly137=)	not provided [RCV005245052]	likely benign	19	54222075	54222075	Human		name
617153131	CV4021103	single nucleotide variant	NM_006864.4(LILRB3):c.330C>T (p.Ser110=)	not provided [RCV005428856]	likely benign	19	54222303	54222303	Human		name
329381874	CV2424249	single nucleotide variant	NM_006864.4(LILRB3):c.290G>A (p.Arg97His)	not specified [RCV004252160]	uncertain significance	19	54222343	54222343	Human		name
401748397	CV2700344	single nucleotide variant	NM_006864.4(LILRB3):c.188A>G (p.Glu63Gly)	not specified [RCV004311002]	uncertain significance	19	54222445	54222445	Human		name
401937406	CV2818754	single nucleotide variant	NM_006864.4(LILRB3):c.1096C>T (p.Leu366=)	not provided [RCV003415416]	likely benign	19	54220690	54220690	Human		name
401929185	CV2818755	single nucleotide variant	NM_006864.4(LILRB3):c.1095A>G (p.Pro365=)	not provided [RCV003407106]	likely benign	19	54220691	54220691	Human		name
405655032	CV3276823	single nucleotide variant	NM_006864.4(LILRB3):c.193A>G (p.Ser65Gly)	not specified [RCV004415168]	uncertain significance	19	54222440	54222440	Human		name
405655035	CV3276824	single nucleotide variant	NM_006864.4(LILRB3):c.202C>T (p.Pro68Ser)	not specified [RCV004415169]	uncertain significance	19	54222431	54222431	Human		name
407492597	CV3449005	single nucleotide variant	NM_006864.4(LILRB3):c.194G>A (p.Ser65Asn)	not specified [RCV004642541]	uncertain significance	19	54222439	54222439	Human		name
156028349	CV2238219	single nucleotide variant	NM_006864.4(LILRB3):c.400G>T (p.Val134Leu)	not specified [RCV004113311]	uncertain significance	19	54222086	54222086	Human		name
156179031	CV2258292	single nucleotide variant	NM_006864.4(LILRB3):c.644A>G (p.Glu215Gly)	not specified [RCV004121654]	uncertain significance	19	54221842	54221842	Human		name
155959053	CV2275723	single nucleotide variant	NM_006864.4(LILRB3):c.527G>C (p.Gly176Ala)	not specified [RCV004137332]	uncertain significance	19	54221959	54221959	Human		name
156078477	CV2289475	single nucleotide variant	NM_006864.4(LILRB3):c.334C>G (p.Pro112Ala)	not specified [RCV004152417]	uncertain significance	19	54222299	54222299	Human		name
156284703	CV2360685	single nucleotide variant	NM_006864.4(LILRB3):c.333C>A (p.Asp111Glu)	not specified [RCV004213479]	uncertain significance	19	54222300	54222300	Human		name
156053003	CV2363569	single nucleotide variant	NM_006864.4(LILRB3):c.417T>A (p.Asn139Lys)	not specified [RCV004216132]	uncertain significance	19	54222069	54222069	Human		name
155937958	CV2364943	single nucleotide variant	NM_006864.4(LILRB3):c.988C>G (p.Gln330Glu)	not specified [RCV004222238]	uncertain significance	19	54220798	54220798	Human		name
401740153	CV2684280	single nucleotide variant	NM_006864.4(LILRB3):c.343C>G (p.Leu115Val)	not specified [RCV004288937]	uncertain significance	19	54222290	54222290	Human		name
401746691	CV2690949	single nucleotide variant	NM_006864.4(LILRB3):c.643G>C (p.Glu215Gln)	not specified [RCV004300974]	uncertain significance	19	54221843	54221843	Human		name
401775536	CV2692408	single nucleotide variant	NM_006864.4(LILRB3):c.547G>A (p.Val183Met)	not specified [RCV004312171]	uncertain significance	19	54221939	54221939	Human		name
401721846	CV2710193	single nucleotide variant	NM_006864.4(LILRB3):c.884G>C (p.Arg295Thr)	not specified [RCV004315233]	uncertain significance	19	54221154	54221154	Human		name
401862857	CV2779046	single nucleotide variant	NM_006864.4(LILRB3):c.527G>T (p.Gly176Val)	not specified [RCV004348690]	uncertain significance	19	54221959	54221959	Human		name
405655038	CV3276825	single nucleotide variant	NM_006864.4(LILRB3):c.377T>G (p.Leu126Arg)	not specified [RCV004415170]	uncertain significance	19	54222109	54222109	Human		name
405655041	CV3276826	single nucleotide variant	NM_006864.4(LILRB3):c.418A>G (p.Met140Val)	not specified [RCV004415171]	likely benign	19	54222068	54222068	Human		name
405655044	CV3276827	single nucleotide variant	NM_006864.4(LILRB3):c.422C>T (p.Thr141Ile)	not specified [RCV004415172]	uncertain significance	19	54222064	54222064	Human		name
597795854	CV3696415	single nucleotide variant	NM_006864.4(LILRB3):c.968A>G (p.Asp323Gly)	not specified [RCV004934993]	uncertain significance	19	54220818	54220818	Human		name
597642558	CV3696416	single nucleotide variant	NM_006864.4(LILRB3):c.478G>A (p.Glu160Lys)	not specified [RCV004941885]	uncertain significance	19	54222008	54222008	Human		name
597642586	CV3696421	single nucleotide variant	NM_006864.4(LILRB3):c.556G>A (p.Val186Met)	not specified [RCV004941890]	uncertain significance	19	54221930	54221930	Human		name
597642604	CV3696426	single nucleotide variant	NM_006864.4(LILRB3):c.368A>G (p.Lys123Arg)	not specified [RCV004941893]	uncertain significance	19	54222118	54222118	Human		name
598237217	CV3980750	single nucleotide variant	NM_006864.4(LILRB3):c.330C>A (p.Ser110Arg)	not specified [RCV005364036]	uncertain significance	19	54222303	54222303	Human		name
598237234	CV3980753	single nucleotide variant	NM_006864.4(LILRB3):c.514C>T (p.Leu172Phe)	not specified [RCV005364039]	uncertain significance	19	54221972	54221972	Human		name
156372792	CV2204569	single nucleotide variant	NM_006864.4(LILRB3):c.1582C>A (p.Leu528Met)	not specified [RCV004081680]	uncertain significance	19	54218372	54218372	Human		name
156372796	CV2204570	single nucleotide variant	NM_006864.4(LILRB3):c.1589G>C (p.Ser530Thr)	not specified [RCV004081681]	uncertain significance	19	54218365	54218365	Human		name
156257331	CV2204571	single nucleotide variant	NM_006864.4(LILRB3):c.1592A>G (p.Gln531Arg)	not specified [RCV004081682]	uncertain significance	19	54218362	54218362	Human		name
155931415	CV2221029	single nucleotide variant	NM_006864.4(LILRB3):c.1060T>G (p.Phe354Val)	not specified [RCV004092708]	uncertain significance	19	54220726	54220726	Human		name
156338578	CV2271292	single nucleotide variant	NM_006864.4(LILRB3):c.1522G>A (p.Val508Ile)	not specified [RCV004136416]	likely benign	19	54218663	54218663	Human		name
155904491	CV2298814	single nucleotide variant	NM_006864.4(LILRB3):c.1436A>C (p.Lys479Thr)	not specified [RCV004156366]	uncertain significance	19	54218829	54218829	Human		name
156326316	CV2335445	single nucleotide variant	NM_006864.4(LILRB3):c.1346C>T (p.Ser449Leu)	not specified [RCV004186992]	uncertain significance	19	54219209	54219209	Human		name
155981169	CV2337007	single nucleotide variant	NM_006864.4(LILRB3):c.1222T>A (p.Ser408Thr)	not specified [RCV004192776]	uncertain significance	19	54220564	54220564	Human		name
155976731	CV2342813	single nucleotide variant	NM_006864.4(LILRB3):c.1203C>A (p.Ser401Arg)	not specified [RCV004189853]	uncertain significance	19	54220583	54220583	Human		name
155976744	CV2342814	single nucleotide variant	NM_006864.4(LILRB3):c.1205C>T (p.Ser402Phe)	not specified [RCV004189854]	uncertain significance	19	54220581	54220581	Human		name
155976754	CV2342815	single nucleotide variant	NM_006864.4(LILRB3):c.1207A>T (p.Asn403Tyr)	not specified [RCV004189855]	uncertain significance	19	54220579	54220579	Human		name
156291109	CV2342816	single nucleotide variant	NM_006864.4(LILRB3):c.1208A>T (p.Asn403Ile)	not specified [RCV004189856]	uncertain significance	19	54220578	54220578	Human		name
156090234	CV2344634	single nucleotide variant	NM_006864.4(LILRB3):c.1744A>G (p.Thr582Ala)	not specified [RCV004197403]	uncertain significance	19	54217324	54217324	Human		name
155904224	CV2353794	single nucleotide variant	NM_006864.4(LILRB3):c.1450C>T (p.Arg484Cys)	not specified [RCV004201799]	uncertain significance	19	54218815	54218815	Human		name
155928473	CV2388884	single nucleotide variant	NM_006864.4(LILRB3):c.1202G>A (p.Ser401Asn)	not specified [RCV004241891]	uncertain significance	19	54220584	54220584	Human		name
155928482	CV2388885	single nucleotide variant	NM_006864.4(LILRB3):c.1207A>G (p.Asn403Asp)	not specified [RCV004241892]	uncertain significance	19	54220579	54220579	Human		name
401766178	CV2679597	single nucleotide variant	NM_006864.4(LILRB3):c.1814G>C (p.Arg605Pro)	not specified [RCV004282078]	uncertain significance	19	54217175	54217175	Human		name
401781600	CV2682053	single nucleotide variant	NM_006864.4(LILRB3):c.1394T>A (p.Leu465His)	not specified [RCV004290118]	uncertain significance	19	54219161	54219161	Human		name
401756082	CV2686281	single nucleotide variant	NM_006864.4(LILRB3):c.1020C>A (p.Asn340Lys)	not specified [RCV004297365]	uncertain significance	19	54220766	54220766	Human		name
401896012	CV2776335	single nucleotide variant	NM_006864.4(LILRB3):c.1181A>T (p.Tyr394Phe)	not specified [RCV004355475]	uncertain significance	19	54220605	54220605	Human		name
401879380	CV2791548	single nucleotide variant	NM_006864.4(LILRB3):c.1745C>G (p.Thr582Ser)	not specified [RCV004358921]	uncertain significance	19	54217323	54217323	Human		name
405655009	CV3276814	single nucleotide variant	NM_006864.4(LILRB3):c.1124A>C (p.His375Pro)	not specified [RCV004415159]	uncertain significance	19	54220662	54220662	Human		name
405655011	CV3276815	single nucleotide variant	NM_006864.4(LILRB3):c.1134G>C (p.Gln378His)	not specified [RCV004415160]	uncertain significance	19	54220652	54220652	Human		name
405655016	CV3276817	single nucleotide variant	NM_006864.4(LILRB3):c.1192G>A (p.Gly398Ser)	not specified [RCV004415162]	likely benign	19	54220594	54220594	Human		name
405655019	CV3276818	single nucleotide variant	NM_006864.4(LILRB3):c.1357G>A (p.Val453Ile)	not specified [RCV004415163]	likely benign	19	54219198	54219198	Human		name
405655022	CV3276819	single nucleotide variant	NM_006864.4(LILRB3):c.1516G>C (p.Ala506Pro)	not specified [RCV004415164]	uncertain significance	19	54218669	54218669	Human		name
405655024	CV3276820	single nucleotide variant	NM_006864.4(LILRB3):c.1572C>G (p.Asp524Glu)	not specified [RCV004415165]	likely benign	19	54218382	54218382	Human		name
405655027	CV3276821	single nucleotide variant	NM_006864.4(LILRB3):c.1846G>A (p.Gly616Arg)	not specified [RCV004415166]	uncertain significance	19	54217143	54217143	Human		name
405655029	CV3276822	single nucleotide variant	NM_006864.4(LILRB3):c.1888A>G (p.Ile630Val)	not specified [RCV004415167]	uncertain significance	19	54217101	54217101	Human		name
407460911	CV3449002	single nucleotide variant	NM_006864.4(LILRB3):c.1133A>G (p.Gln378Arg)	not specified [RCV004633989]	uncertain significance	19	54220653	54220653	Human		name
407492589	CV3449003	single nucleotide variant	NM_006864.4(LILRB3):c.1057A>G (p.Thr353Ala)	not specified [RCV004642539]	uncertain significance	19	54220729	54220729	Human		name
407492593	CV3449004	single nucleotide variant	NM_006864.4(LILRB3):c.1112T>A (p.Met371Lys)	not specified [RCV004642540]	likely benign	19	54220674	54220674	Human		name
597642563	CV3696417	single nucleotide variant	NM_006864.4(LILRB3):c.1790A>G (p.Gln597Arg)	not specified [RCV004941886]	uncertain significance	19	54217199	54217199	Human		name
597642568	CV3696418	single nucleotide variant	NM_006864.4(LILRB3):c.1803G>T (p.Leu601Phe)	not specified [RCV004941887]	uncertain significance	19	54217186	54217186	Human		name
597642574	CV3696419	single nucleotide variant	NM_006864.4(LILRB3):c.1733G>A (p.Arg578Lys)	not specified [RCV004941888]	uncertain significance	19	54217335	54217335	Human		name
597642580	CV3696420	single nucleotide variant	NM_006864.4(LILRB3):c.1504T>C (p.Ser502Pro)	not specified [RCV004941889]	uncertain significance	19	54218681	54218681	Human		name
597642592	CV3696423	single nucleotide variant	NM_006864.4(LILRB3):c.1375C>G (p.Leu459Val)	not specified [RCV004941891]	uncertain significance	19	54219180	54219180	Human		name
597795858	CV3696424	single nucleotide variant	NM_006864.4(LILRB3):c.1710G>C (p.Lys570Asn)	not specified [RCV004934994]	uncertain significance	19	54217358	54217358	Human		name
597642599	CV3696425	single nucleotide variant	NM_006864.4(LILRB3):c.1295C>T (p.Pro432Leu)	not specified [RCV004941892]	uncertain significance	19	54220169	54220169	Human		name
598237223	CV3980751	single nucleotide variant	NM_006864.4(LILRB3):c.1880C>T (p.Thr627Ile)	not specified [RCV005364037]	uncertain significance	19	54217109	54217109	Human		name
598237228	CV3980752	single nucleotide variant	NM_006864.4(LILRB3):c.1375C>T (p.Leu459Phe)	not specified [RCV005364038]	uncertain significance	19	54219180	54219180	Human		name
598260625	CV3980754	single nucleotide variant	NM_006864.4(LILRB3):c.1070C>A (p.Thr357Asn)	not specified [RCV005347663]	uncertain significance	19	54220716	54220716	Human		name
8628397	CV83541	single nucleotide variant	NM_001081450.2(LILRB3):c.1158G>A (p.Val386=)	Malignant melanoma [RCV000063622]	not provided	19	54220628	54220628	Human		name
8628396	CV83540	single nucleotide variant	NM_001081450.2(LILRB3):c.1339G>A (p.Gly447Arg)	Malignant melanoma [RCV000063621]	not provided	19	54219216	54219216	Human		name

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