Lims1 Variant Search Result - Rat Genome Database

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42 records found for search term Lims1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15169319	CV743787	single nucleotide variant	NM_001193483.3(LIMS1):c.824-6C>G	not provided [RCV000905033]	benign	2	108680689	108680689	Human		name
156075067	CV2321741	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4401A>G	not specified [RCV004179736]	uncertain significance	2	108655204	108655204	Human		name
156222820	CV2343993	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4403G>T	not specified [RCV004195610]	uncertain significance	2	108655202	108655202	Human		name
155931096	CV2399779	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4413A>C	not specified [RCV004245591]	uncertain significance	2	108655192	108655192	Human		name
329392335	CV2470626	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4355C>T	not specified [RCV004273620]	uncertain significance	2	108655250	108655250	Human		name
401780826	CV2681778	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4472G>A	not specified [RCV004296783]	likely benign	2	108655133	108655133	Human		name
401726248	CV2695622	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4389G>A	not specified [RCV004299440]	uncertain significance	2	108655216	108655216	Human		name
401749174	CV2709865	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4433A>G	not provided [RCV004696461]\|not specified [RCV004321162]	uncertain significance	2	108655172	108655172	Human		name
405655269	CV3276932	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4450C>G	not specified [RCV004415277]	uncertain significance	2	108655155	108655155	Human		name
407492756	CV3449049	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4428G>A	not specified [RCV004642579]	uncertain significance	2	108655177	108655177	Human		name
597642891	CV3693008	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4458A>G	not specified [RCV004941969]	uncertain significance	2	108655147	108655147	Human		name
598237381	CV3980820	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4511C>T	not specified [RCV005364064]	likely benign	2	108655094	108655094	Human		name
598237394	CV3980824	single nucleotide variant	NM_001193483.3(LIMS1):c.33-4485G>A	not specified [RCV005364066]	uncertain significance	2	108655120	108655120	Human		name
8576257	CV110615	single nucleotide variant	NM_001193483.2(LIMS1):c.32+50334G>C	Lung cancer [RCV000091138]	uncertain significance	2	108584928	108584928	Human		name
405655264	CV3276929	single nucleotide variant	NM_001193483.3(LIMS1):c.33-38201G>A	not specified [RCV004415274]	uncertain significance	2	108621404	108621404	Human		name
405655266	CV3276930	single nucleotide variant	NM_001193483.3(LIMS1):c.33-38184G>A	not specified [RCV004415275]	uncertain significance	2	108621421	108621421	Human		name
598260774	CV3980821	single nucleotide variant	NM_001193483.3(LIMS1):c.33-38189G>A	not specified [RCV005347695]	uncertain significance	2	108621416	108621416	Human		name
156271333	CV2315712	single nucleotide variant	NM_001193483.3(LIMS1):c.61A>G (p.Thr21Ala)	not specified [RCV004169729]	uncertain significance	2	108659633	108659633	Human		name
156066827	CV2340926	single nucleotide variant	NM_001193483.3(LIMS1):c.94G>A (p.Ala32Thr)	not specified [RCV004181420]	uncertain significance	2	108659666	108659666	Human		name
155925646	CV2348463	single nucleotide variant	NM_001193483.3(LIMS1):c.70C>T (p.Arg24Cys)	not provided [RCV004695629]\|not specified [RCV004193653]	uncertain significance	2	108659642	108659642	Human		name
329386954	CV2436165	single nucleotide variant	NM_001193483.3(LIMS1):c.67G>A (p.Glu23Lys)	not specified [RCV004249798]	uncertain significance	2	108659639	108659639	Human		name
597643394	CV3693009	single nucleotide variant	NM_001193483.3(LIMS1):c.89C>T (p.Ala30Val)	not specified [RCV004941970]	uncertain significance	2	108659661	108659661	Human		name
155923612	CV2351779	single nucleotide variant	NM_001193483.3(LIMS1):c.211T>C (p.Cys71Arg)	not specified [RCV004197936]	uncertain significance	2	108670799	108670799	Human		name
597642909	CV3693011	single nucleotide variant	NM_001193483.3(LIMS1):c.244T>A (p.Cys82Ser)	not specified [RCV004941972]	uncertain significance	2	108670832	108670832	Human		name
598260763	CV3980818	single nucleotide variant	NM_001193483.3(LIMS1):c.119G>T (p.Gly40Val)	not specified [RCV005347693]	uncertain significance	2	108659691	108659691	Human		name
598230250	CV3980823	single nucleotide variant	NM_001193483.3(LIMS1):c.218A>T (p.His73Leu)	not specified [RCV005362676]	uncertain significance	2	108670806	108670806	Human		name
156229649	CV2209404	single nucleotide variant	NM_001193483.3(LIMS1):c.535G>C (p.Glu179Gln)	not specified [RCV004093568]	uncertain significance	2	108675882	108675882	Human		name
156229676	CV2209405	single nucleotide variant	NM_001193483.3(LIMS1):c.536A>T (p.Glu179Val)	not specified [RCV004093569]	uncertain significance	2	108675883	108675883	Human		name
156333630	CV2214630	single nucleotide variant	NM_001193483.3(LIMS1):c.944G>A (p.Cys315Tyr)	not specified [RCV004090461]	uncertain significance	2	108683929	108683929	Human		name
156180256	CV2258425	single nucleotide variant	NM_001193483.3(LIMS1):c.475C>G (p.Leu159Val)	not specified [RCV004115623]	uncertain significance	2	108672974	108672974	Human		name
156239330	CV2269133	single nucleotide variant	NM_001193483.3(LIMS1):c.626G>A (p.Arg209Gln)	not specified [RCV004130307]	uncertain significance	2	108675973	108675973	Human		name
155983598	CV2348048	single nucleotide variant	NM_001193483.3(LIMS1):c.436A>G (p.Ile146Val)	not specified [RCV004197730]	uncertain significance	2	108672935	108672935	Human		name
405655257	CV3276925	single nucleotide variant	NM_001193483.3(LIMS1):c.875C>T (p.Thr292Ile)	not specified [RCV004415270]	uncertain significance	2	108680746	108680746	Human		name
405655259	CV3276926	single nucleotide variant	NM_001193483.3(LIMS1):c.898A>G (p.Lys300Glu)	not specified [RCV004415271]	uncertain significance	2	108680769	108680769	Human		name
405655260	CV3276927	single nucleotide variant	NM_001193483.3(LIMS1):c.919G>T (p.Asp307Tyr)	not specified [RCV004415272]	uncertain significance	2	108683904	108683904	Human		name
405655271	CV3276933	single nucleotide variant	NM_001193483.3(LIMS1):c.701G>A (p.Cys234Tyr)	not specified [RCV004415278]	uncertain significance	2	108676625	108676625	Human		name
597642885	CV3693007	single nucleotide variant	NM_001193483.3(LIMS1):c.643C>T (p.Arg215Cys)	not specified [RCV004941968]	uncertain significance	2	108675990	108675990	Human		name
597642903	CV3693010	single nucleotide variant	NM_001193483.3(LIMS1):c.463G>A (p.Asp155Asn)	not specified [RCV004941971]	uncertain significance	2	108672962	108672962	Human		name
597642922	CV3693013	single nucleotide variant	NM_001193483.3(LIMS1):c.572T>A (p.Leu191Gln)	not specified [RCV004941974]	uncertain significance	2	108675919	108675919	Human		name
598260768	CV3980819	single nucleotide variant	NM_001193483.3(LIMS1):c.806G>A (p.Arg269His)	not specified [RCV005347694]	uncertain significance	2	108678010	108678010	Human		name
598237387	CV3980822	single nucleotide variant	NM_001193483.3(LIMS1):c.407G>A (p.Arg136His)	not specified [RCV005364065]	uncertain significance	2	108672906	108672906	Human		name
15190841	CV696948	single nucleotide variant	NM_001193483.3(LIMS1):c.853G>A (p.Val285Met)	not provided [RCV000954596]	benign	2	108680724	108680724	Human		name

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