Lrrn3 Variant Search Result - Rat Genome Database

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55 records found for search term Lrrn3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156135842	CV2379983	single nucleotide variant	NM_001099658.2(LRRN3):c.7G>T (p.Asp3Tyr)	not specified [RCV004222124]	uncertain significance	7	111122779	111122779	Human		name
155974488	CV2211177	single nucleotide variant	NM_001099658.2(LRRN3):c.13C>A (p.Pro5Thr)	not specified [RCV004088339]	uncertain significance	7	111122785	111122785	Human		name
156346678	CV2305428	single nucleotide variant	NM_001099658.2(LRRN3):c.91C>T (p.Arg31Trp)	not specified [RCV004165152]	uncertain significance	7	111122863	111122863	Human		name
15100879	CV699749	single nucleotide variant	NM_001099658.2(LRRN3):c.92G>A (p.Arg31Gln)	not provided [RCV000958981]	benign	7	111122864	111122864	Human		name
15197654	CV699750	single nucleotide variant	NM_001099658.2(LRRN3):c.900C>T (p.Ile300=)	not provided [RCV000956525]	benign	7	111123672	111123672	Human		name
15164702	CV710712	single nucleotide variant	NM_001099658.2(LRRN3):c.675A>G (p.Thr225=)	not provided [RCV000970785]	benign	7	111123447	111123447	Human		name
8632282	CV87490	single nucleotide variant	NM_001099658.1(LRRN3):c.651G>A (p.Leu217=)	Malignant melanoma [RCV000067581]	not provided	7	111123423	111123423	Human		name
155991771	CV2355522	single nucleotide variant	NM_001099658.2(LRRN3):c.265G>A (p.Asp89Asn)	not specified [RCV004205372]	uncertain significance	7	111123037	111123037	Human		name
597634393	CV3702418	single nucleotide variant	NM_001099658.2(LRRN3):c.101C>A (p.Thr34Lys)	not specified [RCV004940416]	uncertain significance	7	111122873	111122873	Human		name
598223441	CV3984996	single nucleotide variant	NM_001099658.2(LRRN3):c.208A>C (p.Asn70His)	not specified [RCV005380051]	uncertain significance	7	111122980	111122980	Human		name
15197658	CV699751	single nucleotide variant	NM_001099658.2(LRRN3):c.1131T>C (p.Arg377=)	not provided [RCV000956526]	benign	7	111123903	111123903	Human		name
156168844	CV2247276	single nucleotide variant	NM_001099658.2(LRRN3):c.328A>G (p.Ile110Val)	not specified [RCV004115053]	uncertain significance	7	111123100	111123100	Human		name
156038338	CV2313632	single nucleotide variant	NM_001099658.2(LRRN3):c.862G>C (p.Glu288Gln)	not specified [RCV004157564]	uncertain significance	7	111123634	111123634	Human		name
156207635	CV2382394	single nucleotide variant	NM_001099658.2(LRRN3):c.827G>A (p.Arg276Gln)	not specified [RCV004230732]	uncertain significance	7	111123599	111123599	Human		name
329382787	CV2424555	single nucleotide variant	NM_001099658.2(LRRN3):c.476C>G (p.Ala159Gly)	not specified [RCV004254056]	uncertain significance	7	111123248	111123248	Human		name
401895770	CV2778764	single nucleotide variant	NM_001099658.2(LRRN3):c.781A>C (p.Asn261His)	not specified [RCV004346669]	uncertain significance	7	111123553	111123553	Human		name
405810544	CV3284312	single nucleotide variant	NM_001099658.2(LRRN3):c.691G>A (p.Ala231Thr)	not specified [RCV004408040]	uncertain significance	7	111123463	111123463	Human		name
597634432	CV3702425	single nucleotide variant	NM_001099658.2(LRRN3):c.491A>G (p.His164Arg)	not specified [RCV004940423]	uncertain significance	7	111123263	111123263	Human		name
598223426	CV3984992	single nucleotide variant	NM_001099658.2(LRRN3):c.631C>T (p.Leu211Phe)	not specified [RCV005380049]	uncertain significance	7	111123403	111123403	Human		name
598251660	CV3984993	single nucleotide variant	NM_001099658.2(LRRN3):c.370G>C (p.Glu124Gln)	not specified [RCV005366735]	uncertain significance	7	111123142	111123142	Human		name
156109750	CV2211332	single nucleotide variant	NM_001099658.2(LRRN3):c.1358A>T (p.Glu453Val)	not specified [RCV004090259]	uncertain significance	7	111124130	111124130	Human		name
156127565	CV2234723	single nucleotide variant	NM_001099658.2(LRRN3):c.2036C>A (p.Pro679His)	not specified [RCV004102667]	uncertain significance	7	111124808	111124808	Human		name
155988384	CV2285376	single nucleotide variant	NM_001099658.2(LRRN3):c.1199C>A (p.Pro400His)	not specified [RCV004139244]	uncertain significance	7	111123971	111123971	Human		name
156091662	CV2302673	single nucleotide variant	NM_001099658.2(LRRN3):c.1594A>C (p.Ile532Leu)	not specified [RCV004162615]	uncertain significance	7	111124366	111124366	Human		name
155912338	CV2308757	single nucleotide variant	NM_001099658.2(LRRN3):c.1853A>C (p.Gln618Pro)	not specified [RCV004169078]	uncertain significance	7	111124625	111124625	Human		name
156155254	CV2328747	single nucleotide variant	NM_001099658.2(LRRN3):c.1529T>C (p.Met510Thr)	not specified [RCV004177976]	uncertain significance	7	111124301	111124301	Human		name
156036192	CV2373966	single nucleotide variant	NM_001099658.2(LRRN3):c.1510G>A (p.Ala504Thr)	not specified [RCV004227098]	uncertain significance	7	111124282	111124282	Human		name
329386185	CV2428216	single nucleotide variant	NM_001099658.2(LRRN3):c.1898T>G (p.Leu633Arg)	not specified [RCV004251250]	uncertain significance	7	111124670	111124670	Human		name
329394923	CV2457732	single nucleotide variant	NM_001099658.2(LRRN3):c.1484C>T (p.Thr495Ile)	not specified [RCV004269571]	uncertain significance	7	111124256	111124256	Human		name
401747376	CV2679085	single nucleotide variant	NM_001099658.2(LRRN3):c.1976A>G (p.His659Arg)	not specified [RCV004295079]	uncertain significance	7	111124748	111124748	Human		name
401743481	CV2687963	single nucleotide variant	NM_001099658.2(LRRN3):c.2075C>A (p.Thr692Lys)	not specified [RCV004305045]	uncertain significance	7	111124847	111124847	Human		name
401731948	CV2690225	single nucleotide variant	NM_001099658.2(LRRN3):c.1304A>C (p.Glu435Ala)	not specified [RCV004302233]	uncertain significance	7	111124076	111124076	Human		name
401775620	CV2710640	single nucleotide variant	NM_001099658.2(LRRN3):c.1090A>G (p.Ser364Gly)	not specified [RCV004319551]	uncertain significance	7	111123862	111123862	Human		name
401894211	CV2780450	single nucleotide variant	NM_001099658.2(LRRN3):c.1243A>G (p.Met415Val)	not specified [RCV004358152]	uncertain significance	7	111124015	111124015	Human		name
405810542	CV3284311	single nucleotide variant	NM_001099658.2(LRRN3):c.2020G>T (p.Gly674Cys)	not specified [RCV004408039]	uncertain significance	7	111124792	111124792	Human		name
405810530	CV3288263	single nucleotide variant	NM_001099658.2(LRRN3):c.1061T>C (p.Ile354Thr)	not specified [RCV004408033]	uncertain significance	7	111123833	111123833	Human		name
405810532	CV3288264	single nucleotide variant	NM_001099658.2(LRRN3):c.1222C>T (p.Arg408Trp)	not specified [RCV004408034]	uncertain significance	7	111123994	111123994	Human		name
405810534	CV3288265	single nucleotide variant	NM_001099658.2(LRRN3):c.1228G>A (p.Val410Met)	not specified [RCV004408035]	uncertain significance	7	111124000	111124000	Human		name
405810536	CV3288266	single nucleotide variant	NM_001099658.2(LRRN3):c.1709G>A (p.Arg570Gln)	not specified [RCV004408036]	uncertain significance	7	111124481	111124481	Human		name
405810538	CV3288267	single nucleotide variant	NM_001099658.2(LRRN3):c.1802A>T (p.Lys601Ile)	not specified [RCV004408037]	uncertain significance	7	111124574	111124574	Human		name
405810540	CV3288268	single nucleotide variant	NM_001099658.2(LRRN3):c.2014G>C (p.Ala672Pro)	not specified [RCV004408038]	uncertain significance	7	111124786	111124786	Human		name
407480475	CV3453019	single nucleotide variant	NM_001099658.2(LRRN3):c.1697C>T (p.Ala566Val)	not specified [RCV004636275]	uncertain significance	7	111124469	111124469	Human		name
597634376	CV3702415	single nucleotide variant	NM_001099658.2(LRRN3):c.1417T>C (p.Phe473Leu)	not specified [RCV004940413]	uncertain significance	7	111124189	111124189	Human		name
597634382	CV3702416	single nucleotide variant	NM_001099658.2(LRRN3):c.1204T>C (p.Phe402Leu)	not specified [RCV004940414]	uncertain significance	7	111123976	111123976	Human		name
597634388	CV3702417	single nucleotide variant	NM_001099658.2(LRRN3):c.1420T>C (p.Tyr474His)	not specified [RCV004940415]	uncertain significance	7	111124192	111124192	Human		name
597634398	CV3702419	single nucleotide variant	NM_001099658.2(LRRN3):c.1299T>A (p.Asn433Lys)	not specified [RCV004940417]	uncertain significance	7	111124071	111124071	Human		name
597634404	CV3702420	single nucleotide variant	NM_001099658.2(LRRN3):c.1151C>G (p.Thr384Ser)	not specified [RCV004940418]	uncertain significance	7	111123923	111123923	Human		name
597634409	CV3702421	single nucleotide variant	NM_001099658.2(LRRN3):c.1124T>C (p.Val375Ala)	not specified [RCV004940419]	uncertain significance	7	111123896	111123896	Human		name
597634415	CV3702422	single nucleotide variant	NM_001099658.2(LRRN3):c.1402A>T (p.Thr468Ser)	not specified [RCV004940420]	uncertain significance	7	111124174	111124174	Human		name
597634420	CV3702423	single nucleotide variant	NM_001099658.2(LRRN3):c.1063G>A (p.Glu355Lys)	not specified [RCV004940421]	uncertain significance	7	111123835	111123835	Human		name
597634426	CV3702424	single nucleotide variant	NM_001099658.2(LRRN3):c.1328A>T (p.His443Leu)	not specified [RCV004940422]	uncertain significance	7	111124100	111124100	Human		name
597634438	CV3702426	single nucleotide variant	NM_001099658.2(LRRN3):c.1043C>T (p.Ala348Val)	not specified [RCV004940424]	uncertain significance	7	111123815	111123815	Human		name
598223434	CV3984994	single nucleotide variant	NM_001099658.2(LRRN3):c.1845C>A (p.His615Gln)	not specified [RCV005380050]	uncertain significance	7	111124617	111124617	Human		name
598251666	CV3984995	single nucleotide variant	NM_001099658.2(LRRN3):c.1343C>T (p.Ala448Val)	not specified [RCV005366736]	uncertain significance	7	111124115	111124115	Human		name
8626309	CV81453	single nucleotide variant	NM_001099658.1(LRRN3):c.1084G>A (p.Glu362Lys)	Malignant melanoma [RCV000061531]	not provided	7	111123856	111123856	Human		name

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