Lmo7 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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191 records found for search term Lmo7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598238265	CV3981129	single nucleotide variant	NM_001306080.2(LMO7):c.*1T>G	not specified [RCV005364220]	uncertain significance	13	75857944	75857944	Human		name
401748160	CV2698944	single nucleotide variant	NM_001306080.2(LMO7):c.*48T>C	not specified [RCV004303480]	uncertain significance	13	75857991	75857991	Human		name
405809877	CV3287762	single nucleotide variant	NM_001306080.2(LMO7):c.*65C>G	not specified [RCV004407724]	uncertain significance	13	75858008	75858008	Human		name
597623243	CV3701720	single nucleotide variant	NM_001306080.2(LMO7):c.*15C>T	not specified [RCV004936274]	uncertain significance	13	75857958	75857958	Human		name
8583169	CV117729	single nucleotide variant	NM_005358.5(LMO7):c.296+4372G>T	Lung cancer [RCV000098250]	uncertain significance	13	75717624	75717624	Human		name
401926720	CV2798738	single nucleotide variant	NM_001306080.2(LMO7):c.140+4A>G	LMO7-related disorder [RCV003406024]	uncertain significance	13	75713256	75713256	Human		name , trait , alternate_id
15179389	CV730923	single nucleotide variant	NM_001306080.2(LMO7):c.2641-8T>A	not provided [RCV000885278]	benign	13	75823557	75823557	Human		name
405274960	CV3199922	duplication	NM_001306080.2(LMO7):c.4771-10dup	LMO7-related disorder [RCV003973950]	likely benign	13	75856486	75856487	Human		name , trait , alternate_id
408375800	CV3511097	deletion	NM_001306080.2(LMO7):c.3582+10del	LMO7-related disorder [RCV004748305]	likely benign	13	75840504	75840504	Human		name , trait , alternate_id
408376082	CV3512020	deletion	NM_001306080.2(LMO7):c.4771-10del	LMO7-related disorder [RCV004748418]	likely benign	13	75856487	75856487	Human		name , trait , alternate_id
155930626	CV2399692	single nucleotide variant	NM_005358.5(LMO7):c.53A>G (p.Tyr18Cys)	not specified [RCV004245511]	uncertain significance	13	75621746	75621746	Human		name
598230578	CV3981120	single nucleotide variant	NM_005358.5(LMO7):c.89T>C (p.Leu30Pro)	not specified [RCV005362729]	uncertain significance	13	75621782	75621782	Human		name
156257805	CV2204612	single nucleotide variant	NM_005358.5(LMO7):c.112T>C (p.Cys38Arg)	not specified [RCV004081720]	uncertain significance	13	75621805	75621805	Human		name
329350263	CV2470683	single nucleotide variant	NM_005358.5(LMO7):c.214A>T (p.Ile72Phe)	not specified [RCV004275933]	uncertain significance	13	75623309	75623309	Human		name
401746151	CV2693725	single nucleotide variant	NM_005358.5(LMO7):c.179T>C (p.Ile60Thr)	not specified [RCV004298051]	uncertain significance	13	75623274	75623274	Human		name
401744954	CV2704230	single nucleotide variant	NM_005358.5(LMO7):c.169A>G (p.Lys57Glu)	not specified [RCV004311230]	uncertain significance	13	75621862	75621862	Human		name
401857324	CV2774620	single nucleotide variant	NM_005358.5(LMO7):c.156C>A (p.Asp52Glu)	not specified [RCV004350089]	likely benign	13	75621849	75621849	Human		name
405809788	CV3287745	single nucleotide variant	NM_005358.5(LMO7):c.136G>C (p.Gly46Arg)	not specified [RCV004407707]	uncertain significance	13	75621829	75621829	Human		name
407484247	CV3449278	single nucleotide variant	NM_005358.5(LMO7):c.102G>T (p.Arg34Ser)	not specified [RCV004637269]	uncertain significance	13	75621795	75621795	Human		name
598230572	CV3981119	single nucleotide variant	NM_005358.5(LMO7):c.154G>A (p.Asp52Asn)	not specified [RCV005362728]	uncertain significance	13	75621847	75621847	Human		name
8635082	CV90304	single nucleotide variant	NM_005358.5(LMO7):c.3186G>A (p.Arg1062=)	Malignant melanoma [RCV000070402]	not provided	13	75842851	75842851	Human		name
598261192	CV3981112	single nucleotide variant	NM_001306080.2(LMO7):c.77C>A (p.Thr26Lys)	not specified [RCV005347788]	uncertain significance	13	75713189	75713189	Human		name
15132265	CV739076	single nucleotide variant	NM_001306080.2(LMO7):c.513C>T (p.Tyr171=)	not provided [RCV000897926]	likely benign	13	75800734	75800734	Human		name
15192895	CV739077	single nucleotide variant	NM_001306080.2(LMO7):c.684G>A (p.Ser228=)	not provided [RCV000910678]	benign	13	75804311	75804311	Human		name
8627469	CV82613	single nucleotide variant	NM_005358.5(LMO7):c.2588C>T (p.Ser863Leu)	Malignant melanoma [RCV000062693]	not provided	13	75838179	75838179	Human		name
156152360	CV2194255	single nucleotide variant	NM_001306080.2(LMO7):c.166G>A (p.Val56Ile)	not specified [RCV004079376]	likely benign	13	75727054	75727054	Human		name
156400231	CV2199050	single nucleotide variant	NM_001306080.2(LMO7):c.182A>G (p.Asn61Ser)	not specified [RCV004080452]	uncertain significance	13	75727070	75727070	Human		name
156116318	CV2221662	single nucleotide variant	NM_001306080.2(LMO7):c.194C>T (p.Thr65Ile)	not specified [RCV004096903]	uncertain significance	13	75727082	75727082	Human		name
155992050	CV2253418	single nucleotide variant	NM_001306080.2(LMO7):c.110C>T (p.Ala37Val)	not specified [RCV004125145]	uncertain significance	13	75713222	75713222	Human		name
405809857	CV3287753	single nucleotide variant	NM_001306080.2(LMO7):c.205G>C (p.Gly69Arg)	not specified [RCV004407715]	uncertain significance	13	75727093	75727093	Human		name
407471032	CV3449276	single nucleotide variant	NM_001306080.2(LMO7):c.101A>G (p.Asp34Gly)	not specified [RCV004637267]	uncertain significance	13	75713213	75713213	Human		name
597623246	CV3701723	single nucleotide variant	NM_001306080.2(LMO7):c.103T>A (p.Phe35Ile)	not specified [RCV004936277]	uncertain significance	13	75713215	75713215	Human		name
598230558	CV3981115	single nucleotide variant	NM_001306080.2(LMO7):c.107G>A (p.Arg36Gln)	not specified [RCV005362726]	uncertain significance	13	75713219	75713219	Human		name
598238251	CV3981122	single nucleotide variant	NM_001306080.2(LMO7):c.146T>C (p.Ile49Thr)	not specified [RCV005364218]	uncertain significance	13	75727034	75727034	Human		name
15191315	CV702730	single nucleotide variant	NM_001306080.2(LMO7):c.1260T>C (p.His420=)	LMO7-related disorder [RCV003915851]\|not provided [RCV000954739]	benign\|likely benign	13	75807543	75807543	Human		name , trait , alternate_id
15119019	CV713971	single nucleotide variant	NM_001306080.2(LMO7):c.1632C>T (p.Pro544=)	not provided [RCV000962479]	benign	13	75807915	75807915	Human		name
156339585	CV2351604	single nucleotide variant	NM_001306080.2(LMO7):c.778C>T (p.Arg260Cys)	not specified [RCV004195321]	uncertain significance	13	75804405	75804405	Human		name
156274727	CV2351743	single nucleotide variant	NM_001306080.2(LMO7):c.838A>G (p.Lys280Glu)	not specified [RCV004197901]	uncertain significance	13	75804465	75804465	Human		name
156156192	CV2388845	single nucleotide variant	NM_001306080.2(LMO7):c.943G>A (p.Val315Met)	not specified [RCV004239691]	uncertain significance	13	75805507	75805507	Human		name
401774779	CV2688284	single nucleotide variant	NM_001306080.2(LMO7):c.743C>T (p.Ser248Leu)	not specified [RCV004299294]	uncertain significance	13	75804370	75804370	Human		name
401901928	CV2813932	single nucleotide variant	NM_001306080.2(LMO7):c.3750C>G (p.Thr1250=)	not provided [RCV003393344]	likely benign	13	75841702	75841702	Human		name
405271500	CV3202835	single nucleotide variant	NM_001306080.2(LMO7):c.656G>C (p.Arg219Pro)	LMO7-related disorder [RCV003913898]	uncertain significance	13	75800877	75800877	Human		name , trait , alternate_id
405809803	CV3287752	single nucleotide variant	NM_001306080.2(LMO7):c.728C>T (p.Ser243Leu)	not specified [RCV004407714]	uncertain significance	13	75804355	75804355	Human		name
597623253	CV3701733	single nucleotide variant	NM_001306080.2(LMO7):c.860A>G (p.Asn287Ser)	not specified [RCV004936284]	uncertain significance	13	75804487	75804487	Human		name
598261211	CV3981126	single nucleotide variant	NM_001306080.2(LMO7):c.889A>G (p.Thr297Ala)	not specified [RCV005347792]	uncertain significance	13	75804516	75804516	Human		name
15152566	CV753885	single nucleotide variant	NM_001306080.2(LMO7):c.3966G>A (p.Ala1322=)	not provided [RCV000923896]	likely benign	13	75841918	75841918	Human		name
156322607	CV2205151	single nucleotide variant	NM_001306080.2(LMO7):c.2704G>T (p.Val902Phe)	not specified [RCV004077748]	uncertain significance	13	75823628	75823628	Human		name
155934802	CV2225413	single nucleotide variant	NM_001306080.2(LMO7):c.2600C>T (p.Ser867Phe)	not specified [RCV004100818]	uncertain significance	13	75821569	75821569	Human		name
156190766	CV2325523	single nucleotide variant	NM_001306080.2(LMO7):c.2731G>A (p.Ala911Thr)	not specified [RCV004179962]	likely benign	13	75823655	75823655	Human		name
156281667	CV2338478	single nucleotide variant	NM_001306080.2(LMO7):c.1063A>C (p.Ser355Arg)	not specified [RCV004188519]	uncertain significance	13	75805627	75805627	Human		name
156304331	CV2341503	single nucleotide variant	NM_001306080.2(LMO7):c.2902T>C (p.Ser968Pro)	not specified [RCV004188896]	uncertain significance	13	75823826	75823826	Human		name
156337671	CV2343084	single nucleotide variant	NM_001306080.2(LMO7):c.2458C>A (p.Gln820Lys)	not specified [RCV004192680]	uncertain significance	13	75821427	75821427	Human		name
156109762	CV2355521	single nucleotide variant	NM_001306080.2(LMO7):c.1606G>A (p.Asp536Asn)	not specified [RCV004205371]	uncertain significance	13	75807889	75807889	Human		name
156384763	CV2371590	single nucleotide variant	NM_001306080.2(LMO7):c.2893A>G (p.Met965Val)	not specified [RCV004216837]	uncertain significance	13	75823817	75823817	Human		name
156162363	CV2371698	single nucleotide variant	NM_001306080.2(LMO7):c.2945C>T (p.Ser982Phe)	not specified [RCV004218982]	uncertain significance	13	75823869	75823869	Human		name
156048093	CV2382607	single nucleotide variant	NM_001306080.2(LMO7):c.2381A>G (p.Asp794Gly)	not specified [RCV004232932]	uncertain significance	13	75821350	75821350	Human		name
156053202	CV2385487	single nucleotide variant	NM_001306080.2(LMO7):c.2410C>T (p.Arg804Cys)	not specified [RCV004233133]	uncertain significance	13	75821379	75821379	Human		name
156005220	CV2393967	single nucleotide variant	NM_001306080.2(LMO7):c.1577A>G (p.Lys526Arg)	not specified [RCV004236195]	uncertain significance	13	75807860	75807860	Human		name
329382456	CV2424474	single nucleotide variant	NM_001306080.2(LMO7):c.2641A>G (p.Met881Val)	not specified [RCV004252364]	uncertain significance	13	75823565	75823565	Human		name
329373799	CV2434592	single nucleotide variant	NM_001306080.2(LMO7):c.2623C>A (p.Leu875Ile)	not specified [RCV004248320]	uncertain significance	13	75821592	75821592	Human		name
329370802	CV2435691	single nucleotide variant	NM_001306080.2(LMO7):c.2338G>A (p.Glu780Lys)	not specified [RCV004254925]	uncertain significance	13	75821307	75821307	Human		name
329353793	CV2439692	single nucleotide variant	NM_001306080.2(LMO7):c.1028A>G (p.Asn343Ser)	not specified [RCV004255705]	uncertain significance	13	75805592	75805592	Human		name
329366900	CV2441965	single nucleotide variant	NM_001306080.2(LMO7):c.1436G>A (p.Arg479Gln)	not specified [RCV004262139]	uncertain significance	13	75807719	75807719	Human		name
329356269	CV2442558	single nucleotide variant	NM_001306080.2(LMO7):c.1153A>G (p.Arg385Gly)	not specified [RCV004266780]	uncertain significance	13	75805717	75805717	Human		name
329355304	CV2449313	single nucleotide variant	NM_001306080.2(LMO7):c.1198C>A (p.Gln400Lys)	not specified [RCV004257443]	uncertain significance	13	75807481	75807481	Human		name
401723550	CV2674993	single nucleotide variant	NM_001306080.2(LMO7):c.1972G>A (p.Ala658Thr)	not specified [RCV004296299]	uncertain significance	13	75817186	75817186	Human		name
401722916	CV2677135	single nucleotide variant	NM_001306080.2(LMO7):c.1300C>T (p.Arg434Cys)	not specified [RCV004295769]	uncertain significance	13	75807583	75807583	Human		name
401737247	CV2679264	single nucleotide variant	NM_001306080.2(LMO7):c.1595C>G (p.Ser532Cys)	not specified [RCV004285812]	uncertain significance	13	75807878	75807878	Human		name
401782095	CV2686528	single nucleotide variant	NM_001306080.2(LMO7):c.2281G>A (p.Gly761Arg)	not specified [RCV004299967]	uncertain significance	13	75821250	75821250	Human		name
401736452	CV2688793	single nucleotide variant	NM_001306080.2(LMO7):c.2693C>A (p.Pro898Gln)	not specified [RCV004303816]	likely benign	13	75823617	75823617	Human		name
401757427	CV2692997	single nucleotide variant	NM_001306080.2(LMO7):c.2503A>G (p.Met835Val)	not specified [RCV004306506]	uncertain significance	13	75821472	75821472	Human		name
401726147	CV2699121	single nucleotide variant	NM_001306080.2(LMO7):c.2828C>A (p.Ser943Tyr)	not specified [RCV004303629]	uncertain significance	13	75823752	75823752	Human		name
401720435	CV2701884	single nucleotide variant	NM_001306080.2(LMO7):c.1720T>G (p.Cys574Gly)	not specified [RCV004320504]	uncertain significance	13	75808003	75808003	Human		name
401883614	CV2754507	single nucleotide variant	NM_001306080.2(LMO7):c.1505G>T (p.Cys502Phe)	not specified [RCV004336714]	uncertain significance	13	75807788	75807788	Human		name
401881080	CV2763235	single nucleotide variant	NM_001306080.2(LMO7):c.2486G>A (p.Arg829His)	not specified [RCV004336269]	likely benign	13	75821455	75821455	Human		name
401868736	CV2767326	single nucleotide variant	NM_001306080.2(LMO7):c.1937G>T (p.Gly646Val)	not specified [RCV004349492]	uncertain significance	13	75809174	75809174	Human		name
401877020	CV2767798	single nucleotide variant	NM_001306080.2(LMO7):c.2485C>T (p.Arg829Cys)	not specified [RCV004345920]	uncertain significance	13	75821454	75821454	Human		name
401871204	CV2783446	single nucleotide variant	NM_001306080.2(LMO7):c.2375A>G (p.Lys792Arg)	not specified [RCV004365790]	uncertain significance	13	75821344	75821344	Human		name
401879457	CV2785098	single nucleotide variant	NM_001306080.2(LMO7):c.2449G>A (p.Val817Met)	not specified [RCV004355111]	uncertain significance	13	75821418	75821418	Human		name
401918045	CV2795513	single nucleotide variant	NM_001306080.2(LMO7):c.1883G>C (p.Arg628Thr)	Bladder exstrophy-epispadias-cloacal extrophy complex [RCV003389437]	uncertain significance	13	75808166	75808166	Human	1	name
401934589	CV2795925	single nucleotide variant	NM_001306080.2(LMO7):c.2992G>A (p.Gly998Arg)	LMO7-related disorder [RCV003412012]	uncertain significance	13	75833093	75833093	Human		name , trait , alternate_id
401906182	CV2802674	single nucleotide variant	NM_001306080.2(LMO7):c.2708G>A (p.Ser903Asn)	LMO7-related disorder [RCV003421125]	uncertain significance	13	75823632	75823632	Human		name , trait , alternate_id
405284660	CV3190452	single nucleotide variant	NM_001306080.2(LMO7):c.1286C>G (p.Pro429Arg)	LMO7-related disorder [RCV003909263]	uncertain significance	13	75807569	75807569	Human		name , trait , alternate_id
405293294	CV3221397	single nucleotide variant	NM_001306080.2(LMO7):c.2263G>A (p.Asp755Asn)	LMO7-related disorder [RCV003966888]	likely benign	13	75821232	75821232	Human		name , trait , alternate_id
405809781	CV3287742	single nucleotide variant	NM_001306080.2(LMO7):c.1745G>A (p.Arg582Gln)	not specified [RCV004407704]	uncertain significance	13	75808028	75808028	Human		name
405809784	CV3287743	single nucleotide variant	NM_001306080.2(LMO7):c.1804G>A (p.Val602Met)	not specified [RCV004407705]	uncertain significance	13	75808087	75808087	Human		name
405809786	CV3287744	single nucleotide variant	NM_001306080.2(LMO7):c.1870C>T (p.Arg624Trp)	not specified [RCV004407706]	uncertain significance	13	75808153	75808153	Human		name
405809790	CV3287746	single nucleotide variant	NM_001306080.2(LMO7):c.2545C>T (p.Arg849Trp)	not specified [RCV004407708]	uncertain significance	13	75821514	75821514	Human		name
405809793	CV3287747	single nucleotide variant	NM_001306080.2(LMO7):c.2677G>C (p.Asp893His)	not specified [RCV004407709]	uncertain significance	13	75823601	75823601	Human		name
405809795	CV3287748	single nucleotide variant	NM_001306080.2(LMO7):c.2899G>C (p.Glu967Gln)	not specified [RCV004407710]	uncertain significance	13	75823823	75823823	Human		name
405809879	CV3287763	single nucleotide variant	NM_001306080.2(LMO7):c.1301G>A (p.Arg434His)	not specified [RCV004407725]	uncertain significance	13	75807584	75807584	Human		name
405809881	CV3287764	single nucleotide variant	NM_001306080.2(LMO7):c.1308G>T (p.Lys436Asn)	not specified [RCV004407726]	uncertain significance	13	75807591	75807591	Human		name
405809884	CV3287765	single nucleotide variant	NM_001306080.2(LMO7):c.1513G>A (p.Gly505Ser)	not specified [RCV004407727]	uncertain significance	13	75807796	75807796	Human		name
407471007	CV3449271	single nucleotide variant	NM_001306080.2(LMO7):c.2543A>G (p.Tyr848Cys)	not specified [RCV004637262]	uncertain significance	13	75821512	75821512	Human		name
407471016	CV3449273	single nucleotide variant	NM_001306080.2(LMO7):c.2961T>G (p.Ser987Arg)	not specified [RCV004637264]	uncertain significance	13	75833062	75833062	Human		name
407471026	CV3449275	single nucleotide variant	NM_001306080.2(LMO7):c.1055G>A (p.Arg352His)	not specified [RCV004637266]	uncertain significance	13	75805619	75805619	Human		name
407471036	CV3449277	single nucleotide variant	NM_001306080.2(LMO7):c.1372T>G (p.Leu458Val)	not specified [RCV004637268]	uncertain significance	13	75807655	75807655	Human		name
597623234	CV3701707	single nucleotide variant	NM_001306080.2(LMO7):c.2016G>A (p.Met672Ile)	not specified [RCV004936265]	uncertain significance	13	75817230	75817230	Human		name
597623236	CV3701710	single nucleotide variant	NM_001306080.2(LMO7):c.1345C>G (p.Leu449Val)	not specified [RCV004936267]	uncertain significance	13	75807628	75807628	Human		name
597623239	CV3701713	single nucleotide variant	NM_001306080.2(LMO7):c.2536A>G (p.Arg846Gly)	not specified [RCV004936270]	uncertain significance	13	75821505	75821505	Human		name
597623247	CV3701724	single nucleotide variant	NM_001306080.2(LMO7):c.2120A>G (p.Lys707Arg)	not specified [RCV004936278]	uncertain significance	13	75819448	75819448	Human		name
597795957	CV3701726	single nucleotide variant	NM_001306080.2(LMO7):c.2468C>A (p.Ala823Asp)	not specified [RCV004935052]	uncertain significance	13	75821437	75821437	Human		name
597623249	CV3701727	single nucleotide variant	NM_001306080.2(LMO7):c.2406G>T (p.Glu802Asp)	not specified [RCV004936280]	uncertain significance	13	75821375	75821375	Human		name
597795959	CV3701729	single nucleotide variant	NM_001306080.2(LMO7):c.2842C>G (p.Gln948Glu)	not specified [RCV004935053]	uncertain significance	13	75823766	75823766	Human		name
597623250	CV3701730	single nucleotide variant	NM_001306080.2(LMO7):c.2468C>T (p.Ala823Val)	not specified [RCV004936281]	uncertain significance	13	75821437	75821437	Human		name
597623252	CV3701732	single nucleotide variant	NM_001306080.2(LMO7):c.1231T>C (p.Ser411Pro)	not specified [RCV004936283]	uncertain significance	13	75807514	75807514	Human		name
597795962	CV3701734	single nucleotide variant	NM_001306080.2(LMO7):c.2152G>A (p.Ala718Thr)	not specified [RCV004935054]	uncertain significance	13	75819480	75819480	Human		name
597623254	CV3701735	single nucleotide variant	NM_001306080.2(LMO7):c.1789A>G (p.Lys597Glu)	not specified [RCV004936285]	uncertain significance	13	75808072	75808072	Human		name
598238208	CV3981111	single nucleotide variant	NM_001306080.2(LMO7):c.2491C>T (p.Arg831Trp)	not specified [RCV005364212]	uncertain significance	13	75821460	75821460	Human		name
598261197	CV3981123	single nucleotide variant	NM_001306080.2(LMO7):c.1851G>T (p.Leu617Phe)	not specified [RCV005347789]	uncertain significance	13	75808134	75808134	Human		name
598261202	CV3981124	single nucleotide variant	NM_001306080.2(LMO7):c.1522G>T (p.Val508Leu)	not specified [RCV005347790]	uncertain significance	13	75807805	75807805	Human		name
598261206	CV3981125	single nucleotide variant	NM_001306080.2(LMO7):c.2222A>G (p.Gln741Arg)	not specified [RCV005347791]	uncertain significance	13	75821191	75821191	Human		name
598261216	CV3981127	single nucleotide variant	NM_001306080.2(LMO7):c.2952T>G (p.Asp984Glu)	not specified [RCV005347793]	uncertain significance	13	75833053	75833053	Human		name
15170020	CV702731	single nucleotide variant	NM_001306080.2(LMO7):c.2650G>A (p.Ala884Thr)	not provided [RCV000949573]	benign	13	75823574	75823574	Human		name
15151916	CV725522	single nucleotide variant	NM_001306080.2(LMO7):c.1610G>A (p.Arg537Lys)	not provided [RCV000879698]	benign	13	75807893	75807893	Human		name
15124871	CV739078	single nucleotide variant	NM_001306080.2(LMO7):c.2711C>T (p.Thr904Ile)	not provided [RCV000896664]	benign	13	75823635	75823635	Human		name
156398926	CV2194872	single nucleotide variant	NM_001306080.2(LMO7):c.3621G>T (p.Glu1207Asp)	not specified [RCV004075405]	uncertain significance	13	75841147	75841147	Human		name
156326240	CV2209637	single nucleotide variant	NM_001306080.2(LMO7):c.3410C>T (p.Ser1137Phe)	not specified [RCV004093716]	uncertain significance	13	75838155	75838155	Human		name
155971706	CV2214168	single nucleotide variant	NM_001306080.2(LMO7):c.3142G>A (p.Asp1048Asn)	not specified [RCV004086166]	uncertain significance	13	75834303	75834303	Human		name
156031377	CV2239123	single nucleotide variant	NM_001306080.2(LMO7):c.4213G>A (p.Glu1405Lys)	not specified [RCV004112120]	uncertain significance	13	75849141	75849141	Human		name
156203329	CV2256303	single nucleotide variant	NM_001306080.2(LMO7):c.3998G>A (p.Arg1333Gln)	not specified [RCV004116546]	uncertain significance	13	75841950	75841950	Human		name
156039182	CV2278999	single nucleotide variant	NM_001306080.2(LMO7):c.4322G>A (p.Ser1441Asn)	not specified [RCV004145688]	uncertain significance	13	75849250	75849250	Human		name
156348481	CV2312815	single nucleotide variant	NM_001306080.2(LMO7):c.4588G>A (p.Ala1530Thr)	not specified [RCV004171316]	uncertain significance	13	75853315	75853315	Human		name
156260850	CV2322329	single nucleotide variant	NM_001306080.2(LMO7):c.4141A>G (p.Asn1381Asp)	not specified [RCV004176085]	uncertain significance	13	75845370	75845370	Human		name
156057475	CV2322851	single nucleotide variant	NM_001306080.2(LMO7):c.3148A>C (p.Lys1050Gln)	not specified [RCV004185311]	uncertain significance	13	75834309	75834309	Human		name
156333665	CV2336029	single nucleotide variant	NM_001306080.2(LMO7):c.4654C>T (p.Arg1552Cys)	not specified [RCV004189634]	uncertain significance	13	75853381	75853381	Human		name
156342926	CV2344195	single nucleotide variant	NM_001306080.2(LMO7):c.3535C>T (p.Arg1179Trp)	not specified [RCV004197836]	uncertain significance	13	75840448	75840448	Human		name
156279156	CV2348306	single nucleotide variant	NM_001306080.2(LMO7):c.4510C>T (p.Arg1504Cys)	LMO7-related disorder [RCV003963762]\|not specified [RCV004193506]	uncertain significance	13	75853237	75853237	Human		name , trait , alternate_id
155906594	CV2357351	single nucleotide variant	NM_001306080.2(LMO7):c.4657A>G (p.Asn1553Asp)	not specified [RCV004200240]	uncertain significance	13	75853384	75853384	Human		name
156307673	CV2369793	single nucleotide variant	NM_001306080.2(LMO7):c.3254C>T (p.Ala1085Val)	not specified [RCV004215180]	uncertain significance	13	75835260	75835260	Human		name
156337724	CV2370486	single nucleotide variant	NM_001306080.2(LMO7):c.3325C>G (p.Gln1109Glu)	not specified [RCV004215832]	uncertain significance	13	75835331	75835331	Human		name
156347956	CV2383014	single nucleotide variant	NM_001306080.2(LMO7):c.3857C>G (p.Pro1286Arg)	not specified [RCV004217599]	uncertain significance	13	75841809	75841809	Human		name
156044598	CV2397135	single nucleotide variant	NM_001306080.2(LMO7):c.4410G>T (p.Trp1470Cys)	not specified [RCV004236636]	uncertain significance	13	75853137	75853137	Human		name
155996365	CV2398527	single nucleotide variant	NM_001306080.2(LMO7):c.3307G>T (p.Asp1103Tyr)	not specified [RCV004237846]	uncertain significance	13	75835313	75835313	Human		name
155997175	CV2398673	single nucleotide variant	NM_001306080.2(LMO7):c.4564G>C (p.Val1522Leu)	not specified [RCV004240021]	uncertain significance	13	75853291	75853291	Human		name
329375968	CV2431683	single nucleotide variant	NM_001306080.2(LMO7):c.3050C>G (p.Ala1017Gly)	not specified [RCV004248851]	uncertain significance	13	75833151	75833151	Human		name
329354094	CV2436942	single nucleotide variant	NM_001306080.2(LMO7):c.3965C>T (p.Ala1322Val)	not specified [RCV004260320]	uncertain significance	13	75841917	75841917	Human		name
329373238	CV2439367	single nucleotide variant	NM_001306080.2(LMO7):c.3791G>A (p.Arg1264Gln)	not specified [RCV004249666]	uncertain significance	13	75841743	75841743	Human		name
329371871	CV2454964	single nucleotide variant	NM_001306080.2(LMO7):c.3509G>T (p.Arg1170Leu)	not specified [RCV004272238]	uncertain significance	13	75840422	75840422	Human		name
329393386	CV2466910	single nucleotide variant	NM_001306080.2(LMO7):c.3056T>C (p.Val1019Ala)	not specified [RCV004282679]	uncertain significance	13	75833157	75833157	Human		name
329381944	CV2467432	single nucleotide variant	NM_001306080.2(LMO7):c.3536G>A (p.Arg1179Gln)	not specified [RCV004287047]	uncertain significance	13	75840449	75840449	Human		name
401736199	CV2672848	single nucleotide variant	NM_001306080.2(LMO7):c.3512G>C (p.Trp1171Ser)	not specified [RCV004281623]	uncertain significance	13	75840425	75840425	Human		name
401724400	CV2677868	single nucleotide variant	NM_001306080.2(LMO7):c.3148A>G (p.Lys1050Glu)	not specified [RCV004294363]	uncertain significance	13	75834309	75834309	Human		name
401745521	CV2681281	single nucleotide variant	NM_001306080.2(LMO7):c.3211C>T (p.Arg1071Cys)	not specified [RCV004289409]	uncertain significance	13	75834372	75834372	Human		name
401718561	CV2704662	single nucleotide variant	NM_001306080.2(LMO7):c.3928C>T (p.Arg1310Trp)	not specified [RCV004313692]	uncertain significance	13	75841880	75841880	Human		name
401762813	CV2710327	single nucleotide variant	NM_001306080.2(LMO7):c.3885G>T (p.Glu1295Asp)	not specified [RCV004317502]	uncertain significance	13	75841837	75841837	Human		name
401762816	CV2710328	single nucleotide variant	NM_001306080.2(LMO7):c.3886A>T (p.Arg1296Trp)	not specified [RCV004317503]	uncertain significance	13	75841838	75841838	Human		name
401862207	CV2766631	single nucleotide variant	NM_001306080.2(LMO7):c.3386A>T (p.Glu1129Val)	not specified [RCV004347241]	uncertain significance	13	75836449	75836449	Human		name
401897663	CV2776652	single nucleotide variant	NM_001306080.2(LMO7):c.3958C>T (p.Arg1320Cys)	not specified [RCV004357520]	uncertain significance	13	75841910	75841910	Human		name
401898674	CV2788017	single nucleotide variant	NM_001306080.2(LMO7):c.4175T>C (p.Ile1392Thr)	not specified [RCV004358669]	uncertain significance	13	75849103	75849103	Human		name
405275093	CV3204636	single nucleotide variant	NM_001306080.2(LMO7):c.3520G>C (p.Asp1174His)	LMO7-related disorder [RCV003952041]	likely benign	13	75840433	75840433	Human		name , trait , alternate_id
405265887	CV3220905	single nucleotide variant	NM_001306080.2(LMO7):c.3979C>T (p.Arg1327Cys)	LMO7-related disorder [RCV003969067]	likely benign	13	75841931	75841931	Human		name , trait , alternate_id
405809797	CV3287749	single nucleotide variant	NM_001306080.2(LMO7):c.3429G>T (p.Arg1143Ser)	not specified [RCV004407711]	uncertain significance	13	75838174	75838174	Human		name
405809799	CV3287750	single nucleotide variant	NM_001306080.2(LMO7):c.3508C>T (p.Arg1170Cys)	not specified [RCV004407712]	uncertain significance	13	75840421	75840421	Human		name
405809801	CV3287751	single nucleotide variant	NM_001306080.2(LMO7):c.3608A>T (p.Lys1203Ile)	not specified [RCV004407713]	uncertain significance	13	75841134	75841134	Human		name
405809859	CV3287754	single nucleotide variant	NM_001306080.2(LMO7):c.4357A>G (p.Met1453Val)	not specified [RCV004407716]	uncertain significance	13	75849285	75849285	Human		name
405809862	CV3287755	single nucleotide variant	NM_001306080.2(LMO7):c.4397G>A (p.Arg1466Gln)	not specified [RCV004407717]	uncertain significance	13	75853124	75853124	Human		name
405809864	CV3287756	single nucleotide variant	NM_001306080.2(LMO7):c.4522C>T (p.Arg1508Trp)	not specified [RCV004407718]	uncertain significance	13	75853249	75853249	Human		name
405809866	CV3287757	single nucleotide variant	NM_001306080.2(LMO7):c.4549C>T (p.Pro1517Ser)	not specified [RCV004407719]	uncertain significance	13	75853276	75853276	Human		name
405809868	CV3287758	single nucleotide variant	NM_001306080.2(LMO7):c.4559G>A (p.Gly1520Asp)	not specified [RCV004407720]	uncertain significance	13	75853286	75853286	Human		name
405809870	CV3287759	single nucleotide variant	NM_001306080.2(LMO7):c.4802C>A (p.Ser1601Tyr)	not specified [RCV004407721]	uncertain significance	13	75856537	75856537	Human		name
405809872	CV3287760	single nucleotide variant	NM_001306080.2(LMO7):c.4852G>A (p.Asp1618Asn)	not specified [RCV004407722]	likely benign	13	75856587	75856587	Human		name
405809875	CV3287761	single nucleotide variant	NM_001306080.2(LMO7):c.4879C>T (p.Arg1627Trp)	not specified [RCV004407723]	likely benign	13	75857926	75857926	Human		name
407470991	CV3449267	single nucleotide variant	NM_001306080.2(LMO7):c.4289A>G (p.Asn1430Ser)	not specified [RCV004637258]	uncertain significance	13	75849217	75849217	Human		name
407470995	CV3449268	single nucleotide variant	NM_001306080.2(LMO7):c.3725C>T (p.Pro1242Leu)	not specified [RCV004637259]	uncertain significance	13	75841677	75841677	Human		name
407470999	CV3449269	single nucleotide variant	NM_001306080.2(LMO7):c.3260C>T (p.Ser1087Phe)	not specified [RCV004637260]	uncertain significance	13	75835266	75835266	Human		name
407471003	CV3449270	single nucleotide variant	NM_001306080.2(LMO7):c.3571C>T (p.Arg1191Cys)	not specified [RCV004637261]	uncertain significance	13	75840484	75840484	Human		name
407471012	CV3449272	single nucleotide variant	NM_001306080.2(LMO7):c.4543C>A (p.Pro1515Thr)	not specified [RCV004637263]	uncertain significance	13	75853270	75853270	Human		name
407471021	CV3449274	single nucleotide variant	NM_001306080.2(LMO7):c.3316G>A (p.Glu1106Lys)	not specified [RCV004637265]	uncertain significance	13	75835322	75835322	Human		name
408376563	CV3514810	deletion	NM_001306080.2(LMO7):c.283_295del (p.Asp95fs)	LMO7-related disorder [RCV004749278]	uncertain significance	13	75761004	75761016	Human		name , trait , alternate_id
597623235	CV3701708	single nucleotide variant	NM_001306080.2(LMO7):c.4061C>T (p.Thr1354Ile)	not specified [RCV004936266]	uncertain significance	13	75842880	75842880	Human		name
597623237	CV3701711	single nucleotide variant	NM_001306080.2(LMO7):c.4888G>A (p.Ala1630Thr)	not specified [RCV004936268]	likely benign	13	75857935	75857935	Human		name
597623238	CV3701712	single nucleotide variant	NM_001306080.2(LMO7):c.3857C>T (p.Pro1286Leu)	not specified [RCV004936269]	likely benign	13	75841809	75841809	Human		name
597795950	CV3701714	single nucleotide variant	NM_001306080.2(LMO7):c.3992T>C (p.Ile1331Thr)	not specified [RCV004935050]	uncertain significance	13	75841944	75841944	Human		name
597623240	CV3701715	single nucleotide variant	NM_001306080.2(LMO7):c.3689T>G (p.Leu1230Arg)	not specified [RCV004936271]	uncertain significance	13	75841641	75841641	Human		name
597623241	CV3701716	single nucleotide variant	NM_001306080.2(LMO7):c.4478G>A (p.Arg1493His)	not specified [RCV004936272]	uncertain significance	13	75853205	75853205	Human		name
597623242	CV3701718	single nucleotide variant	NM_001306080.2(LMO7):c.4483C>T (p.Pro1495Ser)	not specified [RCV004936273]	uncertain significance	13	75853210	75853210	Human		name
597795954	CV3701719	single nucleotide variant	NM_001306080.2(LMO7):c.4514C>G (p.Ala1505Gly)	not specified [RCV004935051]	uncertain significance	13	75853241	75853241	Human		name
597623244	CV3701721	single nucleotide variant	NM_001306080.2(LMO7):c.4523G>A (p.Arg1508Gln)	not specified [RCV004936275]	uncertain significance	13	75853250	75853250	Human		name
597623245	CV3701722	single nucleotide variant	NM_001306080.2(LMO7):c.3632C>A (p.Ala1211Asp)	not specified [RCV004936276]	uncertain significance	13	75841158	75841158	Human		name
597623248	CV3701725	single nucleotide variant	NM_001306080.2(LMO7):c.4478G>C (p.Arg1493Pro)	not specified [RCV004936279]	uncertain significance	13	75853205	75853205	Human		name
597623251	CV3701731	single nucleotide variant	NM_001306080.2(LMO7):c.3595C>A (p.Arg1199Ser)	not specified [RCV004936282]	uncertain significance	13	75841121	75841121	Human		name
598261188	CV3981110	single nucleotide variant	NM_001306080.2(LMO7):c.3374G>A (p.Ser1125Asn)	not specified [RCV005347787]	uncertain significance	13	75836437	75836437	Human		name
598238224	CV3981114	single nucleotide variant	NM_001306080.2(LMO7):c.4795G>A (p.Gly1599Arg)	not specified [RCV005364214]	likely benign	13	75856530	75856530	Human		name
598238232	CV3981116	single nucleotide variant	NM_001306080.2(LMO7):c.3511T>G (p.Trp1171Gly)	not specified [RCV005364215]	uncertain significance	13	75840424	75840424	Human		name
598238238	CV3981117	single nucleotide variant	NM_001306080.2(LMO7):c.3515T>G (p.Val1172Gly)	not specified [RCV005364216]	uncertain significance	13	75840428	75840428	Human		name
598230566	CV3981118	single nucleotide variant	NM_001306080.2(LMO7):c.3212G>A (p.Arg1071His)	not specified [RCV005362727]	uncertain significance	13	75834373	75834373	Human		name
598238244	CV3981121	single nucleotide variant	NM_001306080.2(LMO7):c.4430A>G (p.Asn1477Ser)	not specified [RCV005364217]	likely benign	13	75853157	75853157	Human		name
598238258	CV3981128	single nucleotide variant	NM_001306080.2(LMO7):c.4620T>A (p.His1540Gln)	not specified [RCV005364219]	uncertain significance	13	75853347	75853347	Human		name
401929808	CV2813933	single nucleotide variant	NR_164111.1(LMO7DN):n.218G>A	not provided [RCV003390376]	likely benign	13	75873668	75873668	Human		name
405866907	CV2842420	single nucleotide variant	NR_164111.1(LMO7DN):n.340T>A	EBV-positive nodal T- and NK-cell lymphoma [RCV004557777]	likely benign	13	75873907	75873907	Human		name

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