Limk2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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71 records found for search term Limk2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405655245	CV3276918	single nucleotide variant	NM_005569.4(LIMK2):c.117-9538T>G	not specified [RCV004415263]	uncertain significance	22	31248753	31248753	Human		name
8586878	CV121501	single nucleotide variant	NM_005569.3(LIMK2):c.116+13367A>G	Lung cancer [RCV000102021]	uncertain significance	22	31239186	31239186	Human		name
155958935	CV2313856	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1164A>G	not specified [RCV004164175]	uncertain significance	22	31277133	31277133	Human		name
156274954	CV2318190	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1293T>G	not specified [RCV004179376]	uncertain significance	22	31277004	31277004	Human		name
156184519	CV2324592	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1236A>T	not specified [RCV004172848]	uncertain significance	22	31277061	31277061	Human		name
155965536	CV2330584	single nucleotide variant	NM_005569.4(LIMK2):c.1772+1489C>G	not specified [RCV004183182]	uncertain significance	22	31276797	31276797	Human		name
156387017	CV2364913	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1479C>T	not specified [RCV004221813]	uncertain significance	22	31276818	31276818	Human		name
156257597	CV2368960	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1312G>A	not specified [RCV004207908]	uncertain significance	22	31276985	31276985	Human		name
329391788	CV2453129	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1204G>C	not specified [RCV004279516]	uncertain significance	22	31277093	31277093	Human		name
329393389	CV2453329	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1204G>A	not specified [RCV004266956]	uncertain significance	22	31277093	31277093	Human		name
401856054	CV2764300	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1318A>G	not specified [RCV004336832]	uncertain significance	22	31276979	31276979	Human		name
405655242	CV3276916	single nucleotide variant	NM_005569.4(LIMK2):c.1772+1483C>A	not specified [RCV004415261]	uncertain significance	22	31276791	31276791	Human		name
405655243	CV3276917	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1350A>G	not specified [RCV004415262]	uncertain significance	22	31276947	31276947	Human		name
597642839	CV3692999	single nucleotide variant	NM_005569.4(LIMK2):c.1772+1488C>A	not specified [RCV004941960]	uncertain significance	22	31276796	31276796	Human		name
597642844	CV3693000	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1236A>G	not specified [RCV004941961]	uncertain significance	22	31277061	31277061	Human		name
597642849	CV3693001	single nucleotide variant	NM_005569.4(LIMK2):c.1772+1488C>G	not specified [RCV004941962]	uncertain significance	22	31276796	31276796	Human		name
597642878	CV3693006	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1334G>T	not specified [RCV004941967]	uncertain significance	22	31276963	31276963	Human		name
598237363	CV3980809	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1363A>G	not specified [RCV005364061]	uncertain significance	22	31276934	31276934	Human		name
598260742	CV3980810	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1191C>A	not specified [RCV005347688]	uncertain significance	22	31277106	31277106	Human		name
598260746	CV3980812	single nucleotide variant	NM_005569.4(LIMK2):c.1773-1269C>G	not specified [RCV005347689]	uncertain significance	22	31277028	31277028	Human		name
598230244	CV3980814	single nucleotide variant	NM_005569.4(LIMK2):c.1772+1486C>A	not specified [RCV005362675]	uncertain significance	22	31276794	31276794	Human		name
155942953	CV2298369	single nucleotide variant	NM_005569.4(LIMK2):c.24T>A (p.Asp8Glu)	not specified [RCV004160261]	uncertain significance	22	31225727	31225727	Human		name
156188730	CV2328684	single nucleotide variant	NM_005569.4(LIMK2):c.26T>A (p.Val9Asp)	not specified [RCV004177924]	uncertain significance	22	31225729	31225729	Human		name
156004329	CV2295912	single nucleotide variant	NM_005569.4(LIMK2):c.47G>A (p.Gly16Glu)	not specified [RCV004151815]	uncertain significance	22	31225750	31225750	Human		name
156286630	CV2360939	single nucleotide variant	NM_005569.4(LIMK2):c.31A>G (p.Arg11Gly)	not specified [RCV004215752]	uncertain significance	22	31225734	31225734	Human		name
401912349	CV2822131	single nucleotide variant	NM_005569.4(LIMK2):c.342G>A (p.Val114=)	not provided [RCV003427231]	benign	22	31259210	31259210	Human		name
155958942	CV2313857	single nucleotide variant	NM_005569.4(LIMK2):c.106T>C (p.Ser36Pro)	not specified [RCV004164176]	uncertain significance	22	31225809	31225809	Human		name
156153580	CV2394997	single nucleotide variant	NM_005569.4(LIMK2):c.112T>G (p.Phe38Val)	not specified [RCV004236691]	uncertain significance	22	31225815	31225815	Human		name
598237375	CV3980815	single nucleotide variant	NM_005569.4(LIMK2):c.182C>G (p.Pro61Arg)	not specified [RCV005364063]	uncertain significance	22	31258356	31258356	Human		name
15163624	CV705887	single nucleotide variant	NM_005569.4(LIMK2):c.1242G>A (p.Lys414=)	not provided [RCV000948131]	benign	22	31267889	31267889	Human		name
156316166	CV2250875	single nucleotide variant	NM_005569.4(LIMK2):c.754C>T (p.Arg252Trp)	not specified [RCV004123467]	uncertain significance	22	31262691	31262691	Human		name
155953958	CV2303210	single nucleotide variant	NM_005569.4(LIMK2):c.974T>A (p.Ile325Asn)	not specified [RCV004156969]	uncertain significance	22	31266065	31266065	Human		name
156079353	CV2384515	single nucleotide variant	NM_005569.4(LIMK2):c.634G>A (p.Val212Ile)	not specified [RCV004232315]	uncertain significance	22	31262216	31262216	Human		name
156051136	CV2386272	single nucleotide variant	NM_005569.4(LIMK2):c.607C>T (p.Arg203Cys)	not specified [RCV004228623]	uncertain significance	22	31262189	31262189	Human		name
156040554	CV2387620	single nucleotide variant	NM_005569.4(LIMK2):c.920G>A (p.Arg307His)	not specified [RCV004234170]	uncertain significance	22	31266011	31266011	Human		name
329362567	CV2464009	single nucleotide variant	NM_005569.4(LIMK2):c.538G>A (p.Val180Met)	not specified [RCV004273721]	uncertain significance	22	31260064	31260064	Human		name
329398430	CV2464570	single nucleotide variant	NM_005569.4(LIMK2):c.931C>T (p.Arg311Cys)	not specified [RCV004278263]	uncertain significance	22	31266022	31266022	Human		name
401759669	CV2701664	single nucleotide variant	NM_005569.4(LIMK2):c.742C>T (p.Arg248Trp)	not specified [RCV004314077]	uncertain significance	22	31262679	31262679	Human		name
401882280	CV2781638	single nucleotide variant	NM_005569.4(LIMK2):c.844C>T (p.Arg282Cys)	not specified [RCV004354841]	uncertain significance	22	31262781	31262781	Human		name
405655247	CV3276919	single nucleotide variant	NM_005569.4(LIMK2):c.515C>G (p.Ala172Gly)	not specified [RCV004415264]	uncertain significance	22	31260041	31260041	Human		name
405655248	CV3276920	single nucleotide variant	NM_005569.4(LIMK2):c.755G>A (p.Arg252Gln)	not specified [RCV004415265]	likely benign	22	31262692	31262692	Human		name
405655250	CV3276921	single nucleotide variant	NM_005569.4(LIMK2):c.793G>A (p.Ala265Thr)	not specified [RCV004415266]	likely benign	22	31262730	31262730	Human		name
405655252	CV3276922	single nucleotide variant	NM_005569.4(LIMK2):c.904C>T (p.Pro302Ser)	not specified [RCV004415267]	uncertain significance	22	31265995	31265995	Human		name
405655254	CV3276923	single nucleotide variant	NM_005569.4(LIMK2):c.947G>A (p.Arg316His)	not specified [RCV004415268]	uncertain significance	22	31266038	31266038	Human		name
407460935	CV3449043	single nucleotide variant	NM_005569.4(LIMK2):c.928A>G (p.Ser310Gly)	not specified [RCV004633995]	uncertain significance	22	31266019	31266019	Human		name
407492732	CV3449044	single nucleotide variant	NM_005569.4(LIMK2):c.488G>A (p.Arg163Gln)	not specified [RCV004642574]	uncertain significance	22	31260014	31260014	Human		name
407492737	CV3449045	single nucleotide variant	NM_005569.4(LIMK2):c.839G>A (p.Arg280Lys)	not specified [RCV004642575]	uncertain significance	22	31262776	31262776	Human		name
407492751	CV3449048	single nucleotide variant	NM_005569.4(LIMK2):c.781G>A (p.Gly261Arg)	not specified [RCV004642578]	uncertain significance	22	31262718	31262718	Human		name
597642854	CV3693002	single nucleotide variant	NM_005569.4(LIMK2):c.607C>G (p.Arg203Gly)	not specified [RCV004941963]	uncertain significance	22	31262189	31262189	Human		name
597642866	CV3693004	single nucleotide variant	NM_005569.4(LIMK2):c.718G>A (p.Val240Ile)	not specified [RCV004941965]	uncertain significance	22	31262655	31262655	Human		name
597642873	CV3693005	single nucleotide variant	NM_005569.4(LIMK2):c.761C>T (p.Ala254Val)	not specified [RCV004941966]	uncertain significance	22	31262698	31262698	Human		name
598237352	CV3980805	single nucleotide variant	NM_005569.4(LIMK2):c.728G>A (p.Arg243His)	not specified [RCV005364059]	uncertain significance	22	31262665	31262665	Human		name
598260738	CV3980807	single nucleotide variant	NM_005569.4(LIMK2):c.950G>A (p.Cys317Tyr)	not specified [RCV005347687]	uncertain significance	22	31266041	31266041	Human		name
598237357	CV3980808	single nucleotide variant	NM_005569.4(LIMK2):c.308T>C (p.Val103Ala)	not specified [RCV005364060]	uncertain significance	22	31259176	31259176	Human		name
156057280	CV2239067	single nucleotide variant	NM_005569.4(LIMK2):c.1619T>C (p.Ile540Thr)	not specified [RCV004112073]	uncertain significance	22	31275155	31275155	Human		name
156243340	CV2283262	single nucleotide variant	NM_005569.4(LIMK2):c.1426A>C (p.Ile476Leu)	not specified [RCV004145930]	uncertain significance	22	31272572	31272572	Human		name
156080133	CV2300979	single nucleotide variant	NM_005569.4(LIMK2):c.1825G>C (p.Gly609Arg)	not specified [RCV004158151]	uncertain significance	22	31278349	31278349	Human		name
156053128	CV2320358	single nucleotide variant	NM_005569.4(LIMK2):c.1627G>A (p.Val543Met)	not specified [RCV004178519]	uncertain significance	22	31275163	31275163	Human		name
155969772	CV2337990	single nucleotide variant	NM_005569.4(LIMK2):c.1253G>A (p.Arg418His)	not specified [RCV004186034]	uncertain significance	22	31267900	31267900	Human		name
156199804	CV2362898	single nucleotide variant	NM_005569.4(LIMK2):c.1252C>T (p.Arg418Cys)	not specified [RCV004209006]	uncertain significance	22	31267899	31267899	Human		name
155936871	CV2376149	single nucleotide variant	NM_005569.4(LIMK2):c.1660C>G (p.Leu554Val)	not specified [RCV004220379]	uncertain significance	22	31275196	31275196	Human		name
156083206	CV2381862	single nucleotide variant	NM_005569.4(LIMK2):c.1004A>T (p.Glu335Val)	not specified [RCV004225807]	uncertain significance	22	31266095	31266095	Human		name
329370521	CV2461748	single nucleotide variant	NM_005569.4(LIMK2):c.1874C>T (p.Thr625Ile)	not specified [RCV004269896]	uncertain significance	22	31278398	31278398	Human		name
401755343	CV2682457	single nucleotide variant	NM_005569.4(LIMK2):c.1306G>A (p.Ala436Thr)	not specified [RCV004290483]	uncertain significance	22	31268189	31268189	Human		name
401881505	CV2783858	single nucleotide variant	NM_005569.4(LIMK2):c.1174A>C (p.Ile392Leu)	not specified [RCV004360758]	uncertain significance	22	31267821	31267821	Human		name
405655238	CV3276914	single nucleotide variant	NM_005569.4(LIMK2):c.1099G>A (p.Glu367Lys)	not specified [RCV004415259]	uncertain significance	22	31267041	31267041	Human		name
407492726	CV3449042	single nucleotide variant	NM_005569.4(LIMK2):c.1901G>A (p.Arg634Gln)	not specified [RCV004642573]	uncertain significance	22	31278425	31278425	Human		name
407492742	CV3449046	single nucleotide variant	NM_005569.4(LIMK2):c.1091G>T (p.Arg364Leu)	not specified [RCV004642576]	uncertain significance	22	31267033	31267033	Human		name
598237368	CV3980811	single nucleotide variant	NM_005569.4(LIMK2):c.1165C>G (p.Leu389Val)	not specified [RCV005364062]	uncertain significance	22	31267812	31267812	Human		name
598260751	CV3980813	single nucleotide variant	NM_005569.4(LIMK2):c.1361C>T (p.Ser454Leu)	not specified [RCV005347690]	uncertain significance	22	31271179	31271179	Human		name
598260756	CV3980816	single nucleotide variant	NM_005569.4(LIMK2):c.1000G>A (p.Gly334Arg)	not specified [RCV005347691]	uncertain significance	22	31266091	31266091	Human		name

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