Lipk Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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34 records found for search term Lipk

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8652390	CV128965	single nucleotide variant	NM_001080518.1(LIPK):c.669+861A>G	Lung cancer [RCV000109452]	uncertain significance	10	88733412	88733412	Human		name
156333505	CV2336004	single nucleotide variant	NM_001080518.2(LIPK):c.11T>C (p.Leu4Pro)	not specified [RCV004189610]	uncertain significance	10	88724554	88724554	Human		name
598237615	CV3980914	single nucleotide variant	NM_001080518.2(LIPK):c.16G>T (p.Ala6Ser)	not specified [RCV005364109]	uncertain significance	10	88724559	88724559	Human		name
156378454	CV2207728	single nucleotide variant	NM_001080518.2(LIPK):c.77A>G (p.Asn26Ser)	not specified [RCV004084171]	uncertain significance	10	88724620	88724620	Human		name
156041705	CV2219594	single nucleotide variant	NM_001080518.2(LIPK):c.91G>A (p.Ala31Thr)	not specified [RCV004095322]	uncertain significance	10	88724634	88724634	Human		name
156195512	CV2322383	single nucleotide variant	NM_001080518.2(LIPK):c.56G>A (p.Gly19Asp)	not specified [RCV004176132]	uncertain significance	10	88724599	88724599	Human		name
8633760	CV88976	single nucleotide variant	NM_001080518.1(LIPK):c.312C>T (p.Phe104=)	Malignant melanoma [RCV000069073]	not provided	10	88731071	88731071	Human		name
405295191	CV3211145	single nucleotide variant	NM_001080518.2(LIPK):c.107G>A (p.Ser36Asn)	LIPK-related disorder [RCV003937134]	likely benign	10	88726796	88726796	Human		name , trait , alternate_id
597643643	CV3693166	single nucleotide variant	NM_001080518.2(LIPK):c.232C>T (p.Pro78Ser)	not specified [RCV004942069]	uncertain significance	10	88730991	88730991	Human		name
156033064	CV2214575	single nucleotide variant	NM_001080518.2(LIPK):c.472A>G (p.Ile158Val)	not specified [RCV004088622]	likely benign	10	88732227	88732227	Human		name
156262600	CV2216584	single nucleotide variant	NM_001080518.2(LIPK):c.833A>T (p.Tyr278Phe)	not specified [RCV004097348]	uncertain significance	10	88740012	88740012	Human		name
156125981	CV2223627	single nucleotide variant	NM_001080518.2(LIPK):c.837G>T (p.Leu279Phe)	not specified [RCV004093764]	uncertain significance	10	88740016	88740016	Human		name
155929158	CV2224504	single nucleotide variant	NM_001080518.2(LIPK):c.892G>T (p.Val298Phe)	not specified [RCV004098092]	uncertain significance	10	88743253	88743253	Human		name
156060949	CV2236046	single nucleotide variant	NM_001080518.2(LIPK):c.953T>G (p.Phe318Cys)	not specified [RCV004114208]	uncertain significance	10	88743314	88743314	Human		name
156279413	CV2316754	single nucleotide variant	NM_001080518.2(LIPK):c.469A>T (p.Ile157Phe)	not specified [RCV004171975]	uncertain significance	10	88732224	88732224	Human		name
156276612	CV2328056	single nucleotide variant	NM_001080518.2(LIPK):c.445G>A (p.Asp149Asn)	not specified [RCV004173181]	uncertain significance	10	88732200	88732200	Human		name
156110085	CV2355553	single nucleotide variant	NM_001080518.2(LIPK):c.632T>C (p.Met211Thr)	not specified [RCV004205400]	uncertain significance	10	88732514	88732514	Human		name
156146415	CV2357933	single nucleotide variant	NM_001080518.2(LIPK):c.872T>G (p.Met291Arg)	not specified [RCV004209716]	uncertain significance	10	88740051	88740051	Human		name
156063320	CV2380478	single nucleotide variant	NM_001080518.2(LIPK):c.803A>C (p.Gln268Pro)	not specified [RCV004218073]	uncertain significance	10	88737768	88737768	Human		name
156043265	CV2387954	single nucleotide variant	NM_001080518.2(LIPK):c.758G>A (p.Arg253His)	not specified [RCV004236492]	likely benign	10	88737723	88737723	Human		name
329369420	CV2424815	single nucleotide variant	NM_001080518.2(LIPK):c.351C>A (p.Asn117Lys)	not specified [RCV004248703]	uncertain significance	10	88731110	88731110	Human		name
401756547	CV2734114	single nucleotide variant	NM_001080518.2(LIPK):c.631A>G (p.Met211Val)	not specified [RCV004330658]	uncertain significance	10	88732513	88732513	Human		name
401889442	CV2758113	single nucleotide variant	NM_001080518.2(LIPK):c.965C>G (p.Thr322Arg)	not specified [RCV004341494]	uncertain significance	10	88752521	88752521	Human		name
405809266	CV3287477	single nucleotide variant	NM_001080518.2(LIPK):c.511C>A (p.His171Asn)	not specified [RCV004407439]	uncertain significance	10	88732266	88732266	Human		name
405809270	CV3287479	single nucleotide variant	NM_001080518.2(LIPK):c.827A>T (p.Asp276Val)	not specified [RCV004407441]	uncertain significance	10	88740006	88740006	Human		name
407461002	CV3449119	single nucleotide variant	NM_001080518.2(LIPK):c.320C>T (p.Ala107Val)	not specified [RCV004634012]	uncertain significance	10	88731079	88731079	Human		name
597795999	CV3693162	single nucleotide variant	NM_001080518.2(LIPK):c.715C>A (p.Gln239Lys)	not specified [RCV004935020]	likely benign	10	88737680	88737680	Human		name
597643627	CV3693163	single nucleotide variant	NM_001080518.2(LIPK):c.426G>T (p.Leu142Phe)	not specified [RCV004942066]	uncertain significance	10	88732181	88732181	Human		name
597643638	CV3693165	single nucleotide variant	NM_001080518.2(LIPK):c.649C>T (p.Leu217Phe)	not specified [RCV004942068]	uncertain significance	10	88732531	88732531	Human		name
597643649	CV3693167	single nucleotide variant	NM_001080518.2(LIPK):c.337G>A (p.Val113Met)	not specified [RCV004942070]	uncertain significance	10	88731096	88731096	Human		name
598237604	CV3980912	single nucleotide variant	NM_001080518.2(LIPK):c.392C>T (p.Ser131Leu)	not specified [RCV005364107]	uncertain significance	10	88731151	88731151	Human		name
156384569	CV2231122	single nucleotide variant	NM_001080518.2(LIPK):c.1112A>G (p.Asn371Ser)	not specified [RCV004094337]	uncertain significance	10	88752668	88752668	Human		name
156094326	CV2252944	single nucleotide variant	NM_001080518.2(LIPK):c.1091A>G (p.Tyr364Cys)	not specified [RCV004120764]	uncertain significance	10	88752647	88752647	Human		name
405809262	CV3287475	single nucleotide variant	NM_001080518.2(LIPK):c.1180G>A (p.Glu394Lys)	not specified [RCV004407437]	uncertain significance	10	88752736	88752736	Human		name

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