Lrrn2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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69 records found for search term Lrrn2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401936712	CV2815980	single nucleotide variant	NM_201630.2(LRRN2):c.453C>T (p.Asn151=)	not provided [RCV003414706]	benign	1	204619540	204619540	Human		name
15138382	CV732029	single nucleotide variant	NM_201630.2(LRRN2):c.687C>T (p.Ser229=)	not provided [RCV000898970]	benign	1	204619306	204619306	Human		name
156041381	CV2279199	single nucleotide variant	NM_201630.2(LRRN2):c.143G>T (p.Arg48Leu)	not specified [RCV004139431]	uncertain significance	1	204619850	204619850	Human		name
156087406	CV2299137	single nucleotide variant	NM_201630.2(LRRN2):c.262G>C (p.Glu88Gln)	not specified [RCV004152484]	uncertain significance	1	204619731	204619731	Human		name
156101630	CV2352194	single nucleotide variant	NM_201630.2(LRRN2):c.130C>T (p.Arg44Cys)	not specified [RCV004200679]	uncertain significance	1	204619863	204619863	Human		name
156344773	CV2364336	single nucleotide variant	NM_201630.2(LRRN2):c.241A>G (p.Ile81Val)	not specified [RCV004223556]	uncertain significance	1	204619752	204619752	Human		name
401717892	CV2728359	single nucleotide variant	NM_201630.2(LRRN2):c.133T>G (p.Ser45Ala)	not specified [RCV004333412]	uncertain significance	1	204619860	204619860	Human		name
401936711	CV2815979	single nucleotide variant	NM_201630.2(LRRN2):c.1194G>A (p.Ala398=)	not provided [RCV003414705]	likely benign	1	204618799	204618799	Human		name
405810514	CV3288255	single nucleotide variant	NM_201630.2(LRRN2):c.134C>T (p.Ser45Leu)	not specified [RCV004408025]	uncertain significance	1	204619859	204619859	Human		name
405810521	CV3288259	single nucleotide variant	NM_201630.2(LRRN2):c.218C>T (p.Thr73Ile)	not specified [RCV004408029]	uncertain significance	1	204619775	204619775	Human		name
407482363	CV3453018	single nucleotide variant	NM_201630.2(LRRN2):c.127C>A (p.Pro43Thr)	not specified [RCV004640119]	uncertain significance	1	204619866	204619866	Human		name
597634340	CV3702408	single nucleotide variant	NM_201630.2(LRRN2):c.113G>A (p.Arg38Gln)	not specified [RCV004940406]	uncertain significance	1	204619880	204619880	Human		name
597634346	CV3702409	single nucleotide variant	NM_201630.2(LRRN2):c.175T>C (p.Phe59Leu)	not specified [RCV004940407]	uncertain significance	1	204619818	204619818	Human		name
155930932	CV2220941	single nucleotide variant	NM_201630.2(LRRN2):c.647G>A (p.Arg216His)	not specified [RCV004092632]	uncertain significance	1	204619346	204619346	Human		name
156076829	CV2291559	single nucleotide variant	NM_201630.2(LRRN2):c.994C>A (p.His332Asn)	not specified [RCV004155861]	uncertain significance	1	204618999	204618999	Human		name
156356316	CV2320761	single nucleotide variant	NM_201630.2(LRRN2):c.836G>A (p.Gly279Glu)	not specified [RCV004172599]	uncertain significance	1	204619157	204619157	Human		name
156053032	CV2333266	single nucleotide variant	NM_201630.2(LRRN2):c.628C>T (p.Arg210Trp)	not specified [RCV004197016]	uncertain significance	1	204619365	204619365	Human		name
156294197	CV2336712	single nucleotide variant	NM_201630.2(LRRN2):c.392G>A (p.Arg131Gln)	not specified [RCV004196952]	uncertain significance	1	204619601	204619601	Human		name
156390934	CV2384961	single nucleotide variant	NM_201630.2(LRRN2):c.815C>T (p.Pro272Leu)	not specified [RCV004226189]	uncertain significance	1	204619178	204619178	Human		name
156265554	CV2389072	single nucleotide variant	NM_201630.2(LRRN2):c.901A>G (p.Ile301Val)	not specified [RCV004235410]	uncertain significance	1	204619092	204619092	Human		name
156091563	CV2389478	single nucleotide variant	NM_201630.2(LRRN2):c.547C>T (p.Arg183Cys)	not specified [RCV004238196]	uncertain significance	1	204619446	204619446	Human		name
329371669	CV2442818	single nucleotide variant	NM_201630.2(LRRN2):c.751C>T (p.Arg251Trp)	not specified [RCV004251643]	uncertain significance	1	204619242	204619242	Human		name
329372432	CV2443020	single nucleotide variant	NM_201630.2(LRRN2):c.463C>T (p.Arg155Cys)	not specified [RCV004253611]	uncertain significance	1	204619530	204619530	Human		name
329391356	CV2452265	single nucleotide variant	NM_201630.2(LRRN2):c.354G>C (p.Gln118His)	not specified [RCV004278952]	uncertain significance	1	204619639	204619639	Human		name
401737129	CV2717964	single nucleotide variant	NM_201630.2(LRRN2):c.349C>A (p.Pro117Thr)	not specified [RCV004321914]	uncertain significance	1	204619644	204619644	Human		name
405810524	CV3288260	single nucleotide variant	NM_201630.2(LRRN2):c.415G>A (p.Gly139Arg)	not specified [RCV004408030]	uncertain significance	1	204619578	204619578	Human		name
405810528	CV3288262	single nucleotide variant	NM_201630.2(LRRN2):c.548G>A (p.Arg183His)	not specified [RCV004408032]	uncertain significance	1	204619445	204619445	Human		name
407468422	CV3453016	single nucleotide variant	NM_201630.2(LRRN2):c.326G>A (p.Arg109Gln)	not specified [RCV004636274]	uncertain significance	1	204619667	204619667	Human		name
597634303	CV3702401	single nucleotide variant	NM_201630.2(LRRN2):c.965G>A (p.Arg322Gln)	not specified [RCV004940399]	uncertain significance	1	204619028	204619028	Human		name
597634308	CV3702402	single nucleotide variant	NM_201630.2(LRRN2):c.749C>A (p.Ala250Asp)	not specified [RCV004940400]	uncertain significance	1	204619244	204619244	Human		name
597634313	CV3702403	single nucleotide variant	NM_201630.2(LRRN2):c.506G>A (p.Arg169Gln)	not specified [RCV004940401]	uncertain significance	1	204619487	204619487	Human		name
597634366	CV3702413	single nucleotide variant	NM_201630.2(LRRN2):c.833C>T (p.Pro278Leu)	not specified [RCV004940411]	uncertain significance	1	204619160	204619160	Human		name
597634821	CV3702414	single nucleotide variant	NM_201630.2(LRRN2):c.422C>G (p.Ala141Gly)	not specified [RCV004940412]	uncertain significance	1	204619571	204619571	Human		name
598223384	CV3984985	single nucleotide variant	NM_201630.2(LRRN2):c.629G>A (p.Arg210Gln)	not specified [RCV005380043]	uncertain significance	1	204619364	204619364	Human		name
156272698	CV2195336	single nucleotide variant	NM_201630.2(LRRN2):c.1948C>G (p.Leu650Val)	not specified [RCV004080257]	uncertain significance	1	204618045	204618045	Human		name
156121630	CV2227048	single nucleotide variant	NM_201630.2(LRRN2):c.1226G>A (p.Arg409His)	not specified [RCV004097416]	uncertain significance	1	204618767	204618767	Human		name
156318298	CV2260668	single nucleotide variant	NM_201630.2(LRRN2):c.1594C>T (p.Arg532Trp)	not specified [RCV004123690]	uncertain significance	1	204618399	204618399	Human		name
155926992	CV2285027	single nucleotide variant	NM_201630.2(LRRN2):c.1696G>A (p.Gly566Ser)	not specified [RCV004143452]	uncertain significance	1	204618297	204618297	Human		name
155961998	CV2285600	single nucleotide variant	NM_201630.2(LRRN2):c.1291C>G (p.Pro431Ala)	not specified [RCV004141470]	uncertain significance	1	204618702	204618702	Human		name
155942396	CV2301168	single nucleotide variant	NM_201630.2(LRRN2):c.1645C>T (p.Pro549Ser)	not specified [RCV004160077]	uncertain significance	1	204618348	204618348	Human		name
156065626	CV2317781	single nucleotide variant	NM_201630.2(LRRN2):c.1280G>A (p.Arg427Gln)	not specified [RCV004175032]	uncertain significance	1	204618713	204618713	Human		name
155974234	CV2342528	single nucleotide variant	NM_201630.2(LRRN2):c.1148C>T (p.Thr383Met)	not specified [RCV004196626]	uncertain significance	1	204618845	204618845	Human		name
156105350	CV2361205	single nucleotide variant	NM_201630.2(LRRN2):c.1915G>A (p.Val639Ile)	not specified [RCV004216384]	uncertain significance	1	204618078	204618078	Human		name
156342451	CV2368555	single nucleotide variant	NM_201630.2(LRRN2):c.1241G>A (p.Arg414Gln)	not specified [RCV004221344]	uncertain significance	1	204618752	204618752	Human		name
155994431	CV2379543	single nucleotide variant	NM_201630.2(LRRN2):c.1889G>T (p.Gly630Val)	not specified [RCV004603385]	uncertain significance	1	204618104	204618104	Human		name
156004063	CV2400947	single nucleotide variant	NM_201630.2(LRRN2):c.1424G>A (p.Arg475Gln)	not specified [RCV004244235]	uncertain significance	1	204618569	204618569	Human		name
329358776	CV2450701	single nucleotide variant	NM_201630.2(LRRN2):c.1912G>A (p.Ala638Thr)	not specified [RCV004267649]	uncertain significance	1	204618081	204618081	Human		name
401730688	CV2677261	single nucleotide variant	NM_201630.2(LRRN2):c.1640C>T (p.Thr547Ile)	not specified [RCV004295882]	uncertain significance	1	204618353	204618353	Human		name
401758559	CV2694163	single nucleotide variant	NM_201630.2(LRRN2):c.1225C>T (p.Arg409Cys)	not specified [RCV004302589]	uncertain significance	1	204618768	204618768	Human		name
401772613	CV2712823	single nucleotide variant	NM_201630.2(LRRN2):c.1678A>G (p.Ser560Gly)	not specified [RCV004314245]	uncertain significance	1	204618315	204618315	Human		name
401875996	CV2777617	single nucleotide variant	NM_201630.2(LRRN2):c.1928C>T (p.Ala643Val)	not specified [RCV004343462]	uncertain significance	1	204618065	204618065	Human		name
405810516	CV3288256	single nucleotide variant	NM_201630.2(LRRN2):c.1360G>A (p.Glu454Lys)	not specified [RCV004408026]	uncertain significance	1	204618633	204618633	Human		name
405810518	CV3288257	single nucleotide variant	NM_201630.2(LRRN2):c.1615T>C (p.Tyr539His)	not specified [RCV004408027]	uncertain significance	1	204618378	204618378	Human		name
405810519	CV3288258	single nucleotide variant	NM_201630.2(LRRN2):c.1940C>T (p.Ala647Val)	not specified [RCV004408028]	uncertain significance	1	204618053	204618053	Human		name
407482350	CV3453015	single nucleotide variant	NM_201630.2(LRRN2):c.1595G>A (p.Arg532Gln)	not specified [RCV004640117]	uncertain significance	1	204618398	204618398	Human		name
407482357	CV3453017	single nucleotide variant	NM_201630.2(LRRN2):c.1882C>A (p.Arg628Ser)	not specified [RCV004640118]	uncertain significance	1	204618111	204618111	Human		name
597634319	CV3702404	single nucleotide variant	NM_201630.2(LRRN2):c.1895T>C (p.Ile632Thr)	not specified [RCV004940402]	uncertain significance	1	204618098	204618098	Human		name
597634324	CV3702405	single nucleotide variant	NM_201630.2(LRRN2):c.1287C>G (p.Phe429Leu)	not specified [RCV004940403]	uncertain significance	1	204618706	204618706	Human		name
597634329	CV3702406	single nucleotide variant	NM_201630.2(LRRN2):c.1250C>T (p.Thr417Met)	not specified [RCV004940404]	uncertain significance	1	204618743	204618743	Human		name
597634334	CV3702407	single nucleotide variant	NM_201630.2(LRRN2):c.1883G>A (p.Arg628His)	not specified [RCV004940405]	uncertain significance	1	204618110	204618110	Human		name
597634351	CV3702410	single nucleotide variant	NM_201630.2(LRRN2):c.1202C>T (p.Pro401Leu)	not specified [RCV004940408]	uncertain significance	1	204618791	204618791	Human		name
597634357	CV3702411	single nucleotide variant	NM_201630.2(LRRN2):c.1697G>T (p.Gly566Val)	not specified [RCV004940409]	uncertain significance	1	204618296	204618296	Human		name
597634361	CV3702412	single nucleotide variant	NM_201630.2(LRRN2):c.1066G>A (p.Glu356Lys)	not specified [RCV004940410]	uncertain significance	1	204618927	204618927	Human		name
598223391	CV3984986	single nucleotide variant	NM_201630.2(LRRN2):c.1879G>A (p.Asp627Asn)	not specified [RCV005380044]	uncertain significance	1	204618114	204618114	Human		name
598223396	CV3984987	single nucleotide variant	NM_201630.2(LRRN2):c.1538T>C (p.Val513Ala)	not specified [RCV005380045]	uncertain significance	1	204618455	204618455	Human		name
598251653	CV3984988	single nucleotide variant	NM_201630.2(LRRN2):c.1730G>A (p.Arg577Gln)	not specified [RCV005366734]	uncertain significance	1	204618263	204618263	Human		name
598223405	CV3984989	single nucleotide variant	NM_201630.2(LRRN2):c.1337G>A (p.Arg446Gln)	not specified [RCV005380046]	uncertain significance	1	204618656	204618656	Human		name
598223413	CV3984990	single nucleotide variant	NM_201630.2(LRRN2):c.1742G>C (p.Ser581Thr)	not specified [RCV005380047]	uncertain significance	1	204618251	204618251	Human		name
598223420	CV3984991	single nucleotide variant	NM_201630.2(LRRN2):c.1115G>A (p.Arg372His)	not specified [RCV005380048]	uncertain significance	1	204618878	204618878	Human		name

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