Lmna Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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1002 records found for search term Lmna

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
10398662	CV204464	single nucleotide variant	LMNA, ARG225GLN	Emery-Dreifuss muscular dystrophy 3, autosomal recessive [RCV000190400]\|Emery-dreifuss muscular dystrophy 3, autosomal recessive [RCV000190400]	pathogenic				Human		name
10401605	CV205355	variation	LMNA, GLN656GLN	Hutchinson-Gilford progeria syndrome, atypical [RCV000190822]	pathogenic				Human		name
14352091	CV608839	fusion	LMNA-NTRK1 fusion	Congenital fibrosarcoma [RCV000754610]	pathogenic				Human		name
8564278	CV29536	single nucleotide variant	LMNA, IVS9, G-C, +5	Limb-girdle muscular dystrophy, type 1B [RCV000015589]	pathogenic				Human		name
8564286	CV29544	insertion	LMNA, 1-BP INS, 28A	Dilated cardiomyopathy 1A [RCV000015599]	pathogenic				Human	1	name , alternate_id
8564296	CV29554	single nucleotide variant	LMNA, IVS8, G-C, +5	Lipodystrophy, familial partial, type 2 [RCV000015610]	pathogenic				Human		name
8564293	CV29551	single nucleotide variant	LMNA, IVS11, G-A, +1	Lethal tight skin contracture syndrome [RCV000015606]\|Hutchinson-Gilford syndrome [RCV000015607]	pathogenic				Human		name
10401606	CV205356	single nucleotide variant	LMNA, IVS11DS, G-A, +5	Hutchinson-Gilford progeria syndrome, atypical [RCV000190823]	pathogenic				Human		name
8564277	CV29535	deletion	LMNA, 3-BP DEL, EXON 3	Limb-girdle muscular dystrophy, type 1B [RCV000015588]	pathogenic				Human		name
8564302	CV29560	single nucleotide variant	LMNA, IVS9AS, T-G, -12	Heart-hand syndrome, Slovenian type [RCV000015618]	pathogenic				Human		name
11639762	CV270508	single nucleotide variant	NM_170707.4(LMNA):c.-1C>A	Cardiomyopathy [RCV001184771]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002494855]\|not provided [RCV000725824]	uncertain significance	1	156114918	156114918	Human	4	name
11644289	CV277447	single nucleotide variant	NM_170707.4(LMNA):c.-5C>A	Charcot-Marie-Tooth disease type 2 [RCV000347563]\|Congenital muscular dystrophy due to LMNA mutation [RCV000340631]\|Dilated Cardiomyopathy, Dominant [RCV000391566]\|Emery-Dreifuss muscular dystrophy [RCV000259413]\|Familial partial lipodystrophy [RCV000313589]\|Hut ... (more) chinson-Gilford syndrome [RCV000287946]\|Lethal tight skin contracture syndrome [RCV000319307]\|Limb-girdle muscular dystrophy, recessive [RCV000391573]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000312458]\|Mandibuloacral dysplasia [RCV000404736]	uncertain significance	1	156114914	156114914	Human	9	name
405738578	CV3228815	single nucleotide variant	NM_170707.4(LMNA):c.-6C>T	Primary dilated cardiomyopathy [RCV004014736]	uncertain significance	1	156114913	156114913	Human	1	name
405722477	CV3231941	single nucleotide variant	NM_170707.4(LMNA):c.-5C>G	Primary dilated cardiomyopathy [RCV004012963]	uncertain significance	1	156114914	156114914	Human	1	name
8610892	CV57191	single nucleotide variant	NM_170707.4(LMNA):c.*6G>A	Primary dilated cardiomyopathy [RCV003996452]\|not specified [RCV000041304]	uncertain significance	1	156139112	156139112	Human	1	name
34896017	CV906396	single nucleotide variant	NM_170707.4(LMNA):c.-4G>A	Cardiomyopathy [RCV001185591]	uncertain significance	1	156114915	156114915	Human	2	name
34901293	CV906466	single nucleotide variant	NM_170707.4(LMNA):c.*5G>A	Cardiomyopathy [RCV001191474]	uncertain significance	1	156139111	156139111	Human	2	name
150446981	CV1261450	single nucleotide variant	NM_170707.4(LMNA):c.-98G>C	not provided [RCV001680124]	benign	1	156114821	156114821	Human		name
11644792	CV276601	single nucleotide variant	NM_170707.4(LMNA):c.-62C>A	Charcot-Marie-Tooth disease type 2 [RCV000323065]\|Congenital muscular dystrophy due to LMNA mutation [RCV000319491]\|Dilated Cardiomyopathy, Dominant [RCV000369092]\|Emery-Dreifuss muscular dystrophy [RCV000261953]\|Familial partial lipodystrophy [RCV000379964]\|Hut ... (more) chinson-Gilford syndrome [RCV000279605]\|Lethal tight skin contracture syndrome [RCV000277124]\|Limb-girdle muscular dystrophy, recessive [RCV000307684]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000283250]\|Mandibuloacral dysplasia [RCV000371719]	uncertain significance	1	156114857	156114857	Human	9	name
11585687	CV277446	single nucleotide variant	NM_170707.4(LMNA):c.-88G>T	Charcot-Marie-Tooth disease type 2B1 [RCV000293288]\|Congenital muscular dystrophy due to LMNA mutation [RCV000390806]\|Dilated cardiomyopathy 1A [RCV000350000]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001101680]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV000335300]\|Familial partial lipodystrophy, Dunnigan type [RCV000365735]\|Hutchinson-Gilford syndrome [RCV000282647]\|Lethal tight skin contracture syndrome [RCV000406475]\|Limb-girdle muscular dystrophy, recessive [RCV000374360]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000304900]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000391862]\|Maturity onset diabetes mellitus in young [RCV002465611]\|not provided [RCV001651330]	benign\|likely benign	1	156114831	156114831	Human	13	name
405063055	CV2934264	single nucleotide variant	NM_170707.4(LMNA):c.-14C>T	Cardiomyopathy [RCV003532548]	uncertain significance	1	156114905	156114905	Human	2	name
405736941	CV3228610	single nucleotide variant	NM_170707.4(LMNA):c.-11A>G	Primary dilated cardiomyopathy [RCV004014529]	uncertain significance	1	156114908	156114908	Human	1	name
407502099	CV3495648	single nucleotide variant	NM_170707.4(LMNA):c.-17C>A	not provided [RCV004697488]	uncertain significance	1	156114902	156114902	Human		name
13532255	CV496593	single nucleotide variant	NM_170707.4(LMNA):c.-12A>T	not specified [RCV000606737]	uncertain significance	1	156114907	156114907	Human		name
13539212	CV498068	single nucleotide variant	NM_170707.4(LMNA):c.-28C>T	not specified [RCV000612961]	likely benign	1	156114891	156114891	Human		name
13529513	CV498119	single nucleotide variant	NM_170707.4(LMNA):c.-42C>T	not provided [RCV001698440]	likely benign	1	156114877	156114877	Human		name
8622630	CV77652	single nucleotide variant	NM_170707.4(LMNA):c.*27G>A	not provided [RCV000057211]	not provided	1	156139133	156139133	Human		name
8622631	CV77653	single nucleotide variant	NM_170707.4(LMNA):c.*79G>C	not provided [RCV000057212]\|not specified [RCV001698955]	benign\|not provided	1	156139185	156139185	Human		name
28879523	CV862420	single nucleotide variant	NM_170707.4(LMNA):c.-44T>A	Charcot-Marie-Tooth disease type 2B1 [RCV001096252]\|Congenital muscular dystrophy due to LMNA mutation [RCV001096253]\|Dilated cardiomyopathy 1A [RCV001096250]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001096251]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV001098000]\|Familial partial lipodystrophy, Dunnigan type [RCV001096255]\|Hutchinson-Gilford syndrome [RCV001096254]\|Lethal tight skin contracture syndrome [RCV001096248]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001097999]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001096249]	uncertain significance	1	156114875	156114875	Human	11	name
126732616	CV1000153	single nucleotide variant	NM_170707.4(LMNA):c.*710G>A	not provided [RCV001310874]	uncertain significance	1	156139816	156139816	Human		name
150406006	CV1189497	single nucleotide variant	NM_170707.4(LMNA):c.*130T>G	not provided [RCV001564546]	likely benign	1	156139236	156139236	Human		name
150469934	CV1209232	single nucleotide variant	NM_170707.4(LMNA):c.*639G>A	not provided [RCV001588343]	likely benign	1	156139745	156139745	Human		name
150445542	CV1215512	single nucleotide variant	NM_170707.4(LMNA):c.*365C>T	not provided [RCV001611105]	benign	1	156139471	156139471	Human		name
150443763	CV1232921	single nucleotide variant	NM_170707.4(LMNA):c.*393T>C	not provided [RCV001645593]	benign	1	156139499	156139499	Human		name
150431632	CV1234223	single nucleotide variant	NM_170707.4(LMNA):c.-148C>A	not provided [RCV001641876]	benign	1	156114771	156114771	Human		name
150468159	CV1257014	duplication	NM_170707.4(LMNA):c.*211dup	not provided [RCV001670660]	benign	1	156139303	156139304	Human		name
150493888	CV1257647	deletion	NM_170707.4(LMNA):c.*211del	not provided [RCV001675320]	benign	1	156139304	156139304	Human		name
150491985	CV1267866	single nucleotide variant	NM_170707.4(LMNA):c.*192A>C	not provided [RCV001687892]	benign	1	156139298	156139298	Human		name
150471705	CV1281051	single nucleotide variant	NM_170707.4(LMNA):c.-147C>A	not provided [RCV001713240]	benign	1	156114772	156114772	Human		name
10046793	CV190106	single nucleotide variant	NM_170707.4(LMNA):c.*747G>A	not provided [RCV004714526]\|not specified [RCV000126635]	benign	1	156139853	156139853	Human		name
329350417	CV2421684	single nucleotide variant	NM_170707.4(LMNA):c.*663G>C	not provided [RCV003159387]	uncertain significance	1	156139769	156139769	Human		name
11523558	CV244240	single nucleotide variant	NM_170707.4(LMNA):c.*672T>C	not specified [RCV000236119]	uncertain significance	1	156139778	156139778	Human		name
11644568	CV276591	single nucleotide variant	NM_170707.4(LMNA):c.-138T>C	Charcot-Marie-Tooth disease type 2B1 [RCV000300718]\|Congenital muscular dystrophy due to LMNA mutation [RCV000347305]\|Dilated cardiomyopathy 1A [RCV000368285]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001096152]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV000323133]\|Familial partial lipodystrophy, Dunnigan type [RCV000393952]\|Hutchinson-Gilford syndrome [RCV000260842]\|Lethal tight skin contracture syndrome [RCV000307448]\|Limb-girdle muscular dystrophy, recessive [RCV000403626]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000261874]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000369173]	uncertain significance	1	156114781	156114781	Human	12	name
11644660	CV276876	single nucleotide variant	NM_005572.3(LMNA):c.-226C>T	Charcot-Marie-Tooth disease type 2B1 [RCV000265425]\|Congenital muscular dystrophy due to LMNA mutation [RCV000301121]\|Dilated cardiomyopathy 1A [RCV000261321]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001096027]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV000402614]\|Familial partial lipodystrophy, Dunnigan type [RCV000274059]\|Hutchinson-Gilford syndrome [RCV000316510]\|Lethal tight skin contracture syndrome [RCV000344641]\|Limb-girdle muscular dystrophy, recessive [RCV000313835]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000368648]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000355952]	uncertain significance	1	156114693	156114693	Human	12	name
11649849	CV277430	single nucleotide variant	NM_005572.3(LMNA):c.-225C>A	Charcot-Marie-Tooth disease type 2 [RCV000311246]\|Congenital muscular dystrophy due to LMNA mutation [RCV000344756]\|Dilated Cardiomyopathy, Dominant [RCV000407508]\|Emery-Dreifuss muscular dystrophy [RCV000298571]\|Familial partial lipodystrophy [RCV000295779]\|Hut ... (more) chinson-Gilford syndrome [RCV000351009]\|Lethal tight skin contracture syndrome [RCV000353336]\|Limb-girdle muscular dystrophy, recessive [RCV000289831]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000338085]\|Mandibuloacral dysplasia [RCV000404192]	uncertain significance	1	156114694	156114694	Human	9	name
11645253	CV277432	single nucleotide variant	NM_005572.3(LMNA):c.-210T>C	Charcot-Marie-Tooth disease type 2B1 [RCV000329086]\|Congenital muscular dystrophy due to LMNA mutation [RCV000268032]\|Dilated cardiomyopathy 1A [RCV000326415]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001096151]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV000264625]\|Familial partial lipodystrophy, Dunnigan type [RCV000387923]\|Hutchinson-Gilford syndrome [RCV000269044]\|Lethal tight skin contracture syndrome [RCV000329887]\|Limb-girdle muscular dystrophy, recessive [RCV000295891]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000359267]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000386597]	uncertain significance	1	156114709	156114709	Human	12	name
11647488	CV277433	single nucleotide variant	NM_170707.4(LMNA):c.-183C>A	Charcot-Marie-Tooth disease type 2 [RCV000402632]\|Congenital muscular dystrophy due to LMNA mutation [RCV000280598]\|Dilated Cardiomyopathy, Dominant [RCV000279288]\|Emery-Dreifuss muscular dystrophy [RCV000307337]\|Familial partial lipodystrophy [RCV000365322]\|Hut ... (more) chinson-Gilford syndrome [RCV000364405]\|Lethal tight skin contracture syndrome [RCV000337822]\|Limb-girdle muscular dystrophy, recessive [RCV000276841]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000341353]\|Mandibuloacral dysplasia [RCV000303668]	uncertain significance	1	156114736	156114736	Human	9	name
11647179	CV277434	single nucleotide variant	NM_170707.4(LMNA):c.-142C>A	Charcot-Marie-Tooth disease type 2 [RCV000334255]\|Congenital muscular dystrophy due to LMNA mutation [RCV000367390]\|Dilated Cardiomyopathy, Dominant [RCV000318600]\|Emery-Dreifuss muscular dystrophy [RCV000279052]\|Familial partial lipodystrophy [RCV000287177]\|Hut ... (more) chinson-Gilford syndrome [RCV000290029]\|Lethal tight skin contracture syndrome [RCV000375572]\|Limb-girdle muscular dystrophy, recessive [RCV000379268]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000275157]\|Mandibuloacral dysplasia [RCV000393819]	uncertain significance	1	156114777	156114777	Human	9	name
11583289	CV277441	single nucleotide variant	NM_170707.4(LMNA):c.-128T>C	Charcot-Marie-Tooth disease type 2B1 [RCV000387993]\|Congenital muscular dystrophy due to LMNA mutation [RCV000265737]\|Dilated cardiomyopathy 1A [RCV000345153]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001099691]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV000299347]\|Familial partial lipodystrophy, Dunnigan type [RCV000348567]\|Hutchinson-Gilford syndrome [RCV000287889]\|Lethal tight skin contracture syndrome [RCV000407148]\|Limb-girdle muscular dystrophy, recessive [RCV000384802]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000380050]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000295952]	likely benign	1	156114791	156114791	Human	12	name
11645836	CV277445	single nucleotide variant	NM_170707.4(LMNA):c.-109G>T	Charcot-Marie-Tooth disease type 2 [RCV000332962]\|Congenital muscular dystrophy due to LMNA mutation [RCV000298025]\|Dilated Cardiomyopathy, Dominant [RCV000359848]\|Emery-Dreifuss muscular dystrophy [RCV000267691]\|Familial partial lipodystrophy [RCV000381613]\|Hut ... (more) chinson-Gilford syndrome [RCV000301697]\|Lethal tight skin contracture syndrome [RCV000359648]\|Limb-girdle muscular dystrophy, recessive [RCV000405878]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000270930]\|Mandibuloacral dysplasia [RCV000272013]	uncertain significance	1	156114810	156114810	Human	9	name
401942856	CV2839882	single nucleotide variant	NM_170707.4(LMNA):c.*694A>G	not provided [RCV003456669]	likely benign	1	156139800	156139800	Human		name
12846195	CV364529	single nucleotide variant	NM_170707.4(LMNA):c.*749G>A	not specified [RCV000441187]	likely benign	1	156139855	156139855	Human		name
616936130	CV4010613	single nucleotide variant	NM_170707.4(LMNA):c.*664A>G	Cardiovascular phenotype [RCV005403959]	uncertain significance	1	156139770	156139770	Human		name
12899525	CV404953	single nucleotide variant	NM_170707.4(LMNA):c.*707A>G	not specified [RCV000480406]	uncertain significance	1	156139813	156139813	Human		name
14975458	CV672373	single nucleotide variant	NM_170707.4(LMNA):c.*722T>C	Cardiovascular phenotype [RCV005400749]\|not specified [RCV003317389]	uncertain significance	1	156139828	156139828	Human		name
28884398	CV862419	single nucleotide variant	NM_005572.3(LMNA):c.-223C>T	Charcot-Marie-Tooth disease type 2B1 [RCV001099600]\|Congenital muscular dystrophy due to LMNA mutation [RCV001099598]\|Dilated cardiomyopathy 1A [RCV001097799]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001097800]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV001099597]\|Familial partial lipodystrophy, Dunnigan type [RCV001099595]\|Hutchinson-Gilford syndrome [RCV001099596]\|Lethal tight skin contracture syndrome [RCV001099594]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001099599]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001099593]\|not provided [RCV001564412]	benign\|likely benign\|uncertain significance	1	156114696	156114696	Human	11	name
126919116	CV1039477	single nucleotide variant	NM_170707.4(LMNA):c.639+5G>C	Charcot-Marie-Tooth disease type 2 [RCV001362111]	uncertain significance	1	156134533	156134533	Human	1	name
126908435	CV1039478	single nucleotide variant	NM_170707.4(LMNA):c.937-7C>A	Cardiomyopathy [RCV005401831]\|Charcot-Marie-Tooth disease type 2 [RCV001367857]\|not specified [RCV001820069]	likely benign\|uncertain significance	1	156135894	156135894	Human	3	name
127245217	CV1054743	single nucleotide variant	NM_170707.4(LMNA):c.513+2T>C	Charcot-Marie-Tooth disease type 2 [RCV001377378]	likely pathogenic	1	156130775	156130775	Human	1	name
127238597	CV1066295	single nucleotide variant	NM_170707.4(LMNA):c.357-9C>T	Charcot-Marie-Tooth disease type 2 [RCV001397354]	likely benign	1	156130608	156130608	Human	1	name
127337720	CV1109552	single nucleotide variant	NM_170707.4(LMNA):c.811-4C>G	Charcot-Marie-Tooth disease type 2 [RCV001475819]	likely benign	1	156135183	156135183	Human	1	name
127308312	CV1130453	single nucleotide variant	NM_170707.4(LMNA):c.357-8T>C	Cardiomyopathy [RCV005401845]\|Cardiovascular phenotype [RCV003160946]\|Charcot-Marie-Tooth disease type 2 [RCV001480589]\|LMNA-related disorder [RCV004533842]\|Primary dilated cardiomyopathy [RCV004007148]	likely benign	1	156130609	156130609	Human	4	name , alternate_id
127326894	CV1160080	single nucleotide variant	NM_170707.4(LMNA):c.810+4C>A	Cardiomyopathy [RCV001526276]\|Charcot-Marie-Tooth disease type 2 [RCV001873700]	uncertain significance	1	156134979	156134979	Human	3	name
150542758	CV1314937	single nucleotide variant	NM_170707.4(LMNA):c.513+1G>T	not provided [RCV001782389]	likely pathogenic	1	156130774	156130774	Human		name
151235639	CV1318988	single nucleotide variant	NM_170707.4(LMNA):c.937-5T>A	not provided [RCV001795804]	uncertain significance	1	156135896	156135896	Human		name
151354196	CV1329329	single nucleotide variant	NM_170707.4(LMNA):c.810+2T>C	Charcot-Marie-Tooth disease type 2 [RCV002542701]\|not provided [RCV001817692]	pathogenic	1	156134977	156134977	Human	1	name
151864863	CV1356722	single nucleotide variant	NM_170707.4(LMNA):c.811-2A>G	Charcot-Marie-Tooth disease type 2 [RCV001959700]	likely pathogenic	1	156135185	156135185	Human	1	name
151773966	CV1402283	single nucleotide variant	NM_170707.4(LMNA):c.811-8C>T	Charcot-Marie-Tooth disease type 2 [RCV001929795]	likely benign	1	156135179	156135179	Human	1	name
152172225	CV1598086	single nucleotide variant	NM_170707.4(LMNA):c.937-6C>A	Charcot-Marie-Tooth disease type 2 [RCV002162381]\|Primary dilated cardiomyopathy [RCV004011195]	likely benign\|uncertain significance	1	156135895	156135895	Human	2	name
152085805	CV1617386	single nucleotide variant	NM_170707.4(LMNA):c.937-7C>T	Charcot-Marie-Tooth disease type 2 [RCV002076965]\|Primary dilated cardiomyopathy [RCV004011188]	likely benign	1	156135894	156135894	Human	2	name
155684675	CV1824967	single nucleotide variant	NM_170707.4(LMNA):c.937-2A>G	Cardiovascular phenotype [RCV002371739]	likely pathogenic	1	156135899	156135899	Human		name
155684677	CV1824968	single nucleotide variant	NM_170707.4(LMNA):c.937-3C>T	Cardiomyopathy [RCV003533213]\|Cardiovascular phenotype [RCV002371740]	likely benign\|uncertain significance	1	156135898	156135898	Human	2	name
156311711	CV1928508	single nucleotide variant	NM_170707.4(LMNA):c.356+2T>G	Charcot-Marie-Tooth disease type 2 [RCV002648207]	pathogenic	1	156115276	156115276	Human	1	name
10056808	CV196457	single nucleotide variant	NM_170707.4(LMNA):c.356+1G>A	Cardiovascular phenotype [RCV005404350]\|Charcot-Marie-Tooth disease type 2 [RCV000689313]\|not provided [RCV000182355]	pathogenic	1	156115275	156115275	Human	1	name
10401328	CV205007	single nucleotide variant	NM_170707.4(LMNA):c.936+2T>C	Cardiomyopathy [RCV001798660]\|Cardiovascular phenotype [RCV003165426]\|Charcot-Marie-Tooth disease type 2 [RCV003743622]\|Hutchinson-Gilford syndrome [RCV000986430]	pathogenic\|likely pathogenic\|uncertain significance	1	156135314	156135314	Human	4	name
10406135	CV213515	single nucleotide variant	NM_170707.4(LMNA):c.810+1G>C	Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV000199480]	pathogenic\|likely pathogenic	1	156134976	156134976	Human	1	name
11040278	CV224183	single nucleotide variant	NM_170707.4(LMNA):c.937-8C>A	Cardiomyopathy [RCV000777940]\|Charcot-Marie-Tooth disease type 2 [RCV000545586]\|Charcot-Marie-Tooth disease type 2B1 [RCV001096750]\|Congenital muscular dystrophy due to LMNA mutation [RCV001098487]\|Dilated cardiomyopathy 1A [RCV001096746]\|Emery-Dreifuss muscular ... (more) dystrophy 2, autosomal dominant [RCV001096752]\|Emery-Dreifuss muscular dystrophy [RCV001096747]\|Familial partial lipodystrophy, Dunnigan type [RCV001096748]\|Hutchinson-Gilford syndrome [RCV001098486]\|Lethal tight skin contracture syndrome [RCV001096749]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001096751]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001098488]\|Primary dilated cardiomyopathy [RCV000207998]\|not provided [RCV001697242]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156135893	156135893	Human	15	name
11092334	CV228273	single nucleotide variant	NM_170707.4(LMNA):c.356+1G>C	Primary dilated cardiomyopathy [RCV000218409]\|not provided [RCV000592631]	pathogenic\|likely pathogenic	1	156115275	156115275	Human	1	name
11523040	CV244219	single nucleotide variant	NM_170707.4(LMNA):c.513+1G>A	Cardiovascular phenotype [RCV004020919]\|Charcot-Marie-Tooth disease type 2 [RCV001379216]\|not provided [RCV000235237]	pathogenic\|likely pathogenic\|uncertain significance	1	156130774	156130774	Human	1	name
401933333	CV2804032	single nucleotide variant	NM_170707.4(LMNA):c.936+4A>G	LMNA-related disorder [RCV004531725]	uncertain significance	1	156135316	156135316	Human		name , trait , alternate_id
405083846	CV2863077	single nucleotide variant	NM_170707.4(LMNA):c.811-9C>A	Charcot-Marie-Tooth disease type 2 [RCV003582318]	likely benign	1	156135178	156135178	Human	1	name
405084101	CV2877288	single nucleotide variant	NM_170707.4(LMNA):c.356+2T>A	Charcot-Marie-Tooth disease type 2 [RCV003582339]	pathogenic	1	156115276	156115276	Human	1	name
405088633	CV2906416	single nucleotide variant	NM_170707.4(LMNA):c.640-7C>G	Charcot-Marie-Tooth disease type 2 [RCV003582694]\|Primary dilated cardiomyopathy [RCV004011425]	likely benign	1	156134798	156134798	Human	2	name
405092816	CV2925049	single nucleotide variant	NM_170707.4(LMNA):c.639+3G>A	Charcot-Marie-Tooth disease type 2 [RCV003583025]	uncertain significance	1	156134531	156134531	Human	1	name
405095233	CV2953621	single nucleotide variant	NM_170707.4(LMNA):c.357-6C>G	Charcot-Marie-Tooth disease type 2 [RCV003745783]	likely benign	1	156130611	156130611	Human	1	name
405085600	CV2994353	single nucleotide variant	NM_170707.4(LMNA):c.640-9C>G	Charcot-Marie-Tooth disease type 2 [RCV003744323]	uncertain significance	1	156134796	156134796	Human	1	name
405077836	CV3023825	single nucleotide variant	NM_170707.4(LMNA):c.639+6G>A	Charcot-Marie-Tooth disease type 2 [RCV003743262]	uncertain significance	1	156134534	156134534	Human	1	name
405732200	CV3229404	duplication	NM_170707.4(LMNA):c.937-6dup	Primary dilated cardiomyopathy [RCV004013971]	likely benign	1	156135889	156135890	Human	1	name
405725487	CV3230524	deletion	NM_170707.4(LMNA):c.640-7del	Primary dilated cardiomyopathy [RCV004013277]	likely benign	1	156134796	156134796	Human	1	name
405722560	CV3231950	single nucleotide variant	NM_170707.4(LMNA):c.357-9C>A	Primary dilated cardiomyopathy [RCV004012972]	uncertain significance	1	156130608	156130608	Human	1	name
405728830	CV3391195	single nucleotide variant	NM_170707.4(LMNA):c.356+9G>A	Cardiovascular phenotype [RCV004524856]	likely benign	1	156115283	156115283	Human		name
407504633	CV3495911	deletion	NM_170707.4(LMNA):c.514-1del	not provided [RCV004697751]	likely pathogenic	1	156134402	156134402	Human		name
596941205	CV3546138	single nucleotide variant	NM_170707.4(LMNA):c.514-5C>T	Primary dilated cardiomyopathy [RCV004806767]	likely benign	1	156134398	156134398	Human	1	name
596941225	CV3546143	deletion	NM_170707.4(LMNA):c.937-6del	Primary dilated cardiomyopathy [RCV004806772]	likely benign	1	156135890	156135890	Human	1	name
597959051	CV3797461	single nucleotide variant	NM_170707.4(LMNA):c.811-1G>C	Charcot-Marie-Tooth disease type 2 [RCV005138148]	likely pathogenic	1	156135186	156135186	Human	1	name
597864222	CV3814153	single nucleotide variant	NM_170707.4(LMNA):c.937-6C>G	Charcot-Marie-Tooth disease type 2 [RCV005147222]	likely benign	1	156135895	156135895	Human	1	name
12884455	CV390833	single nucleotide variant	NM_170707.4(LMNA):c.513+8C>T	Charcot-Marie-Tooth disease type 2 [RCV001407282]	likely benign	1	156130781	156130781	Human	1	name
12890955	CV390837	single nucleotide variant	NM_170707.4(LMNA):c.936+7C>T	Charcot-Marie-Tooth disease type 2 [RCV000475659]	likely benign	1	156135319	156135319	Human	1	name
598238081	CV3981074	single nucleotide variant	NM_170707.4(LMNA):c.514-2A>G	Cardiovascular phenotype [RCV005364192]	likely pathogenic	1	156134401	156134401	Human		name
616935671	CV4010250	single nucleotide variant	NM_170707.4(LMNA):c.811-3C>A	Cardiomyopathy [RCV005403551]	uncertain significance	1	156135184	156135184	Human	2	name
13215764	CV427647	single nucleotide variant	NM_170707.4(LMNA):c.810+4C>G	Cardiomyopathy [RCV005401471]\|Charcot-Marie-Tooth disease type 2 [RCV001247016]\|not specified [RCV000502911]	uncertain significance	1	156134979	156134979	Human	3	name
13483987	CV447315	single nucleotide variant	NM_170707.4(LMNA):c.936+1G>A	Charcot-Marie-Tooth disease type 2 [RCV000552554]	pathogenic	1	156135313	156135313	Human	1	name
13533891	CV509113	single nucleotide variant	NM_170707.4(LMNA):c.513+2T>G	Cardiovascular phenotype [RCV000618096]\|Charcot-Marie-Tooth disease type 2 [RCV003581698]\|not provided [RCV000786357]	likely pathogenic\|uncertain significance	1	156130775	156130775	Human	1	name
13625797	CV515117	single nucleotide variant	NM_170707.4(LMNA):c.937-9C>T	Cardiomyopathy [RCV001176893]\|Cardiovascular phenotype [RCV003163011]\|Charcot-Marie-Tooth disease type 2 [RCV002532007]	likely benign	1	156135892	156135892	Human	3	name
13625728	CV515280	single nucleotide variant	NM_170707.4(LMNA):c.937-1G>A	Cardiovascular phenotype [RCV002369757]\|Charcot-Marie-Tooth disease type 2 [RCV000653870]	likely pathogenic	1	156135900	156135900	Human	1	name
8610933	CV57233	single nucleotide variant	NM_170707.4(LMNA):c.513+1G>C	Charcot-Marie-Tooth disease type 2 [RCV002513582]\|Primary dilated cardiomyopathy [RCV000041353]	likely pathogenic	1	156130774	156130774	Human	2	name
14692638	CV619051	single nucleotide variant	NM_170707.4(LMNA):c.937-8C>G	Cardiomyopathy [RCV000774196]\|Charcot-Marie-Tooth disease type 2 [RCV001456120]\|Primary dilated cardiomyopathy [RCV003231611]\|not provided [RCV001796209]\|not specified [RCV001796210]	benign\|likely benign\|uncertain significance	1	156135893	156135893	Human	4	name
14690779	CV621704	single nucleotide variant	NM_170707.4(LMNA):c.639+1G>A	Cardiomyopathy [RCV000781511]\|Charcot-Marie-Tooth disease type 2 [RCV000797832]\|not provided [RCV004702414]	likely pathogenic	1	156134529	156134529	Human	3	name
14699239	CV624746	single nucleotide variant	NM_170707.4(LMNA):c.639+9T>C	Charcot-Marie-Tooth disease type 2 [RCV001501103]\|not provided [RCV000788525]	likely benign\|uncertain significance	1	156134537	156134537	Human	1	name
14740383	CV650582	single nucleotide variant	NM_170707.4(LMNA):c.640-2A>G	Charcot-Marie-Tooth disease type 2 [RCV000821778]	likely pathogenic	1	156134803	156134803	Human	1	name
14703842	CV650588	single nucleotide variant	NM_170707.4(LMNA):c.357-2A>G	Charcot-Marie-Tooth disease type 2 [RCV000807553]	pathogenic	1	156130615	156130615	Human	1	name
14741157	CV650632	single nucleotide variant	NM_170707.4(LMNA):c.356+5G>A	Cardiovascular phenotype [RCV004029093]\|Charcot-Marie-Tooth disease type 2 [RCV000822120]\|Dilated cardiomyopathy 1A [RCV004776298]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005049712]	likely pathogenic\|uncertain significance	1	156115279	156115279	Human	16	name
14730539	CV650636	single nucleotide variant	NM_170707.4(LMNA):c.811-1G>A	Cardiovascular phenotype [RCV004028046]\|Charcot-Marie-Tooth disease type 2 [RCV000800997]	likely pathogenic	1	156135186	156135186	Human	1	name
15128176	CV695005	single nucleotide variant	NM_170707.4(LMNA):c.937-6C>T	Cardiomyopathy [RCV003532301]\|Charcot-Marie-Tooth disease type 2 [RCV001412121]\|LMNA-related disorder [RCV004530835]	likely benign	1	156135895	156135895	Human	3	name , alternate_id
15188188	CV777019	single nucleotide variant	NM_170707.4(LMNA):c.937-5T>C	Cardiomyopathy [RCV001180881]\|Cardiovascular phenotype [RCV003169470]\|Charcot-Marie-Tooth disease type 2 [RCV000953808]\|Dilated cardiomyopathy 1A [RCV001198844]	likely benign\|uncertain significance	1	156135896	156135896	Human	6	name
8622766	CV77790	single nucleotide variant	NM_170707.4(LMNA):c.357-1G>T	Charcot-Marie-Tooth disease type 2 [RCV001387325]\|not provided [RCV000057393]	pathogenic\|not provided	1	156130616	156130616	Human	1	name
8622776	CV77800	single nucleotide variant	NM_170707.4(LMNA):c.514-1G>A	Dilated cardiomyopathy 1A [RCV004786334]\|not provided [RCV000057413]	pathogenic\|not provided	1	156134402	156134402	Human	2	name
8622812	CV77836	single nucleotide variant	NM_170707.4(LMNA):c.810+1G>A	Charcot-Marie-Tooth disease type 2 [RCV000477527]\|not provided [RCV000057465]	pathogenic\|likely pathogenic\|not provided	1	156134976	156134976	Human	1	name
8622829	CV77853	single nucleotide variant	NM_170707.4(LMNA):c.936+1G>T	not provided [RCV000057485]	not provided	1	156135313	156135313	Human		name
8622832	CV77856	single nucleotide variant	NM_170707.4(LMNA):c.937-7C>G	Cardiomyopathy [RCV000772012]\|Charcot-Marie-Tooth disease [RCV001172638]\|Charcot-Marie-Tooth disease type 2 [RCV000530832]\|Dilated cardiomyopathy 1A [RCV004786335]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005042176]\|Primary dilated cardiomyopathy [RCV003996513]\|not provided ... (more) [RCV000057488]\|not specified [RCV000440584]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156135894	156135894	Human	8	name
26885530	CV850728	single nucleotide variant	NM_170707.4(LMNA):c.639+1G>T	Cardiovascular phenotype [RCV002355077]\|Charcot-Marie-Tooth disease type 2 [RCV001065501]	likely pathogenic	1	156134529	156134529	Human	1	name
26891460	CV850734	single nucleotide variant	NM_170707.4(LMNA):c.937-9C>A	Charcot-Marie-Tooth disease type 2 [RCV001068265]\|Primary dilated cardiomyopathy [RCV004000174]	likely benign\|uncertain significance	1	156135892	156135892	Human	2	name
34897685	CV915099	duplication	NM_170707.4(LMNA):c.514-7dup	Cardiomyopathy [RCV001179363]\|Charcot-Marie-Tooth disease type 2 [RCV001422955]	likely benign	1	156134394	156134395	Human	3	name
34894608	CV915100	deletion	NM_170707.4(LMNA):c.513+8del	Cardiomyopathy [RCV001177453]	likely benign	1	156130780	156130780	Human	2	name
34895402	CV915104	single nucleotide variant	NM_170707.4(LMNA):c.810+5T>C	Cardiomyopathy [RCV001178054]	likely benign	1	156134980	156134980	Human	2	name
34897428	CV915113	single nucleotide variant	NM_170707.4(LMNA):c.640-8C>G	Cardiomyopathy [RCV001179156]\|Cardiovascular phenotype [RCV004033031]\|Charcot-Marie-Tooth disease type 2 [RCV005093811]	likely benign	1	156134797	156134797	Human	3	name
34896777	CV915224	single nucleotide variant	NM_170707.4(LMNA):c.937-8C>T	Cardiomyopathy [RCV001185904]\|Charcot-Marie-Tooth disease type 2 [RCV001401080]	likely benign	1	156135893	156135893	Human	3	name
38480747	CV959524	single nucleotide variant	NM_170707.4(LMNA):c.513+6G>A	Charcot-Marie-Tooth disease type 2 [RCV001234834]	uncertain significance	1	156130779	156130779	Human	1	name
38598012	CV964644	single nucleotide variant	NM_170707.4(LMNA):c.937-3C>A	Hutchinson-Gilford syndrome [RCV001253332]	uncertain significance	1	156135898	156135898	Human	1	name
126744544	CV1019195	single nucleotide variant	NM_170707.4(LMNA):c.810+17G>A	Charcot-Marie-Tooth disease type 2 [RCV003745314]\|Dilated cardiomyopathy 1A [RCV001337052]	likely benign\|uncertain significance	1	156134992	156134992	Human	3	name
127266514	CV1058442	single nucleotide variant	NM_170707.4(LMNA):c.1608+2T>G	Cardiovascular phenotype [RCV002395876]\|Charcot-Marie-Tooth disease type 2 [RCV001388734]	pathogenic\|likely pathogenic	1	156137234	156137234	Human	1	name
127269632	CV1088036	single nucleotide variant	NM_170707.4(LMNA):c.356+10C>A	Charcot-Marie-Tooth disease type 2 [RCV001441125]	likely benign	1	156115284	156115284	Human	1	name
127255983	CV1088038	single nucleotide variant	NM_170707.4(LMNA):c.639+10G>C	Charcot-Marie-Tooth disease type 2 [RCV001426721]	likely benign	1	156134538	156134538	Human	1	name
127258489	CV1088040	single nucleotide variant	NM_170707.4(LMNA):c.1158-6C>T	Charcot-Marie-Tooth disease type 2 [RCV001427336]\|Primary dilated cardiomyopathy [RCV004006965]	likely benign	1	156136208	156136208	Human	2	name
127261032	CV1088044	single nucleotide variant	NM_170707.4(LMNA):c.1609-6C>T	Charcot-Marie-Tooth disease type 2 [RCV001428005]	likely benign	1	156137648	156137648	Human	1	name
127302611	CV1109554	single nucleotide variant	NM_170707.4(LMNA):c.1158-4C>A	Charcot-Marie-Tooth disease type 2 [RCV001461686]	likely benign	1	156136210	156136210	Human	1	name
127326653	CV1160082	single nucleotide variant	NM_170707.4(LMNA):c.1158-5C>G	Cardiomyopathy [RCV001526137]\|Charcot-Marie-Tooth disease type 2 [RCV003745337]	likely benign\|uncertain significance	1	156136209	156136209	Human	3	name
150428346	CV1186059	duplication	NM_170707.4(LMNA):c.1380+5dup	Primary dilated cardiomyopathy [RCV004008933]\|not provided [RCV001562144]	likely benign\|uncertain significance	1	156136439	156136440	Human	1	name
150428803	CV1186060	microsatellite	NM_170707.4(LMNA):c.*484AG[9]	not provided [RCV001562748]	likely benign	1	156139588	156139589	Human		name
150478234	CV1250853	single nucleotide variant	NM_170707.4(LMNA):c.936+66C>T	not provided [RCV001672343]	benign	1	156135378	156135378	Human		name
150452867	CV1275346	single nucleotide variant	NM_170707.4(LMNA):c.1699-2A>G	Familial partial lipodystrophy, Dunnigan type [RCV001706860]	likely pathogenic	1	156138486	156138486	Human	1	name
151348743	CV1322693	single nucleotide variant	NM_170707.4(LMNA):c.357-13C>A	Cardiomyopathy [RCV001804489]\|Charcot-Marie-Tooth disease type 2 [RCV002074188]	likely benign\|uncertain significance	1	156130604	156130604	Human	3	name
151348003	CV1325230	single nucleotide variant	NM_170707.4(LMNA):c.1698+1G>A	Charcot-Marie-Tooth disease type 2 [RCV001885299]\|Primary dilated cardiomyopathy [RCV004009160]\|not provided [RCV001813872]	likely pathogenic\|uncertain significance	1	156137744	156137744	Human	2	name
151819212	CV1385827	single nucleotide variant	NM_170707.4(LMNA):c.811-18C>G	Charcot-Marie-Tooth disease type 2 [RCV002013204]\|not specified [RCV003331268]	likely benign	1	156135169	156135169	Human	1	name
151841685	CV1438255	single nucleotide variant	NM_170707.4(LMNA):c.1488+3G>A	Charcot-Marie-Tooth disease type 2 [RCV001921607]	uncertain significance	1	156137031	156137031	Human	1	name
151837578	CV1469883	single nucleotide variant	NM_170707.4(LMNA):c.1609-9C>A	Charcot-Marie-Tooth disease type 2 [RCV001880965]	likely benign\|uncertain significance	1	156137645	156137645	Human	1	name
151727872	CV1517442	single nucleotide variant	NM_170707.4(LMNA):c.1608+2T>A	Dilated cardiomyopathy 1A [RCV002052057]	likely pathogenic	1	156137234	156137234	Human	2	name
152057509	CV1523197	single nucleotide variant	NM_170707.4(LMNA):c.513+11C>A	Charcot-Marie-Tooth disease type 2 [RCV002167620]	likely benign	1	156130784	156130784	Human	1	name
152161229	CV1534688	single nucleotide variant	NM_170707.4(LMNA):c.1380+8C>T	Charcot-Marie-Tooth disease type 2 [RCV002140955]\|LMNA-related disorder [RCV004734468]	likely benign	1	156136444	156136444	Human	1	name , alternate_id
152053662	CV1557666	single nucleotide variant	NM_170707.4(LMNA):c.936+19C>T	Charcot-Marie-Tooth disease type 2 [RCV002141542]\|not provided [RCV002225965]	likely benign	1	156135331	156135331	Human	1	name
152061051	CV1558313	deletion	NM_170707.4(LMNA):c.640-15del	Charcot-Marie-Tooth disease type 2 [RCV002128347]	likely benign	1	156134789	156134789	Human	1	name
152092609	CV1571250	single nucleotide variant	NM_170707.4(LMNA):c.936+15C>T	Charcot-Marie-Tooth disease type 2 [RCV002150785]	likely benign	1	156135327	156135327	Human	1	name
152124203	CV1587385	single nucleotide variant	NM_170707.4(LMNA):c.1381-4G>T	Charcot-Marie-Tooth disease type 2 [RCV002136107]\|Primary dilated cardiomyopathy [RCV004005478]	likely benign	1	156136917	156136917	Human	2	name
155266192	CV1684188	single nucleotide variant	NM_170707.4(LMNA):c.1381-2A>C	Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV002281663]	pathogenic	1	156136919	156136919	Human	1	name
10408192	CV172114	single nucleotide variant	NM_170707.4(LMNA):c.1968+1G>C	Hutchinson-Gilford syndrome [RCV000192016]	pathogenic\|not provided	1	156138758	156138758	Human	1	name
10408193	CV172115	single nucleotide variant	NM_170707.4(LMNA):c.1968+2T>A	Hutchinson-Gilford syndrome [RCV000192017]	pathogenic\|not provided	1	156138759	156138759	Human	1	name
10408194	CV172116	single nucleotide variant	NM_170707.4(LMNA):c.1968+2T>C	Hutchinson-Gilford syndrome [RCV000192018]	pathogenic\|not provided	1	156138759	156138759	Human	1	name
10407829	CV172117	single nucleotide variant	NM_170707.4(LMNA):c.1968+5G>A	Hutchinson-Gilford progeria syndrome, atypical [RCV000190823]\|Hutchinson-Gilford syndrome [RCV000192020]	pathogenic\|likely pathogenic\|not provided	1	156138762	156138762	Human	1	name
10407828	CV172118	single nucleotide variant	NM_170707.4(LMNA):c.1968+5G>C	Hutchinson-Gilford syndrome [RCV000192019]	pathogenic\|not provided	1	156138762	156138762	Human	1	name
9690639	CV172344	single nucleotide variant	NM_170707.4(LMNA):c.640-11A>C	Cardiomyopathy [RCV001186918]\|Charcot-Marie-Tooth disease type 2 [RCV002056124]\|Primary dilated cardiomyopathy [RCV003998309]\|not specified [RCV000156325]	likely benign\|uncertain significance	1	156134794	156134794	Human	4	name
9690913	CV172349	single nucleotide variant	NM_170707.4(LMNA):c.1609-1G>A	Charcot-Marie-Tooth disease type 2 [RCV001850165]\|Primary dilated cardiomyopathy [RCV000156608]\|not provided [RCV000182373]	pathogenic\|likely pathogenic	1	156137653	156137653	Human	2	name
9691772	CV172486	single nucleotide variant	NM_170707.4(LMNA):c.1158-3C>T	Charcot-Marie-Tooth disease type 2 [RCV005055621]\|Primary dilated cardiomyopathy [RCV003998207]\|not specified [RCV000150951]	pathogenic\|likely benign\|uncertain significance	1	156136211	156136211	Human	2	name
9691773	CV172490	single nucleotide variant	NM_170707.4(LMNA):c.1699-8C>G	Cardiomyopathy [RCV000769731]\|Cardiovascular phenotype [RCV004639144]\|Charcot-Marie-Tooth disease [RCV001173401]\|Charcot-Marie-Tooth disease type 2 [RCV000876929]\|not provided [RCV001775636]\|not specified [RCV000150956]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156138480	156138480	Human	4	name
9832408	CV178432	single nucleotide variant	NM_170707.4(LMNA):c.1381-5G>A	Cardiomyopathy [RCV001185511]\|Cardiovascular phenotype [RCV002381508]\|Charcot-Marie-Tooth disease type 2 [RCV000815746]\|Dilated cardiomyopathy 1A [RCV001775087]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002478468]\|Primary familial hypertrophic cardiomyopathy [RCV000157297]\|n ... (more) ot provided [RCV000484067]\|not specified [RCV005237592]	uncertain significance	1	156136916	156136916	Human	20	name
155684668	CV1824965	single nucleotide variant	NM_170707.4(LMNA):c.937-15C>T	Cardiomyopathy [RCV003533212]\|Cardiovascular phenotype [RCV002371737]\|Charcot-Marie-Tooth disease type 2 [RCV003094796]\|Primary dilated cardiomyopathy [RCV004007284]	likely benign	1	156135886	156135886	Human	4	name
156408765	CV1870294	single nucleotide variant	NM_170707.4(LMNA):c.810+19T>C	Charcot-Marie-Tooth disease type 2 [RCV003071400]	likely benign	1	156134994	156134994	Human	1	name
156412434	CV1890584	single nucleotide variant	NM_170707.4(LMNA):c.937-20A>G	Charcot-Marie-Tooth disease type 2 [RCV003072890]	likely benign	1	156135881	156135881	Human	1	name
156333570	CV1905778	single nucleotide variant	NM_170707.4(LMNA):c.936+16A>G	Charcot-Marie-Tooth disease type 2 [RCV003089937]	likely benign	1	156135328	156135328	Human	1	name
156406248	CV1921512	single nucleotide variant	NM_170707.4(LMNA):c.356+15G>A	Charcot-Marie-Tooth disease type 2 [RCV002606534]	likely benign	1	156115289	156115289	Human	1	name
156270813	CV1957177	single nucleotide variant	NM_170707.4(LMNA):c.513+11C>T	Charcot-Marie-Tooth disease type 2 [RCV002577153]	likely benign	1	156130784	156130784	Human	1	name
10055555	CV196458	single nucleotide variant	NM_170707.4(LMNA):c.357-19T>C	Charcot-Marie-Tooth disease type 2 [RCV002054166]\|not specified [RCV000182346]	benign\|likely benign	1	156130598	156130598	Human	1	name
10055556	CV196471	single nucleotide variant	NM_170707.4(LMNA):c.810+12C>T	Charcot-Marie-Tooth disease [RCV001172629]\|Charcot-Marie-Tooth disease type 2 [RCV002054167]\|not specified [RCV000182347]	benign\|likely benign	1	156134987	156134987	Human	2	name
10055557	CV196477	single nucleotide variant	NM_170707.4(LMNA):c.1157+6C>G	Cardiomyopathy [RCV001182769]\|Cardiovascular phenotype [RCV005404349]\|Charcot-Marie-Tooth disease type 2 [RCV000821919]\|Primary dilated cardiomyopathy [RCV003996713]\|not specified [RCV000182348]	benign\|likely benign\|uncertain significance	1	156136127	156136127	Human	4	name
156315739	CV2028028	single nucleotide variant	NM_170707.4(LMNA):c.639+11T>C	Charcot-Marie-Tooth disease type 2 [RCV002716788]	likely benign	1	156134539	156134539	Human	1	name
156211157	CV2036900	single nucleotide variant	NM_170707.4(LMNA):c.1489-8C>T	Cardiomyopathy [RCV003533299]\|Charcot-Marie-Tooth disease type 2 [RCV002790246]	likely benign	1	156137105	156137105	Human	3	name
156215107	CV2039024	single nucleotide variant	NM_170707.4(LMNA):c.1969-8T>C	Charcot-Marie-Tooth disease type 2 [RCV002766763]	likely benign	1	156139072	156139072	Human	1	name
155902121	CV2043664	single nucleotide variant	NM_170707.4(LMNA):c.640-11A>T	Charcot-Marie-Tooth disease type 2 [RCV002771041]	likely benign	1	156134794	156134794	Human	1	name
156136423	CV2044389	deletion	NM_170707.4(LMNA):c.639+13del	Charcot-Marie-Tooth disease type 2 [RCV002786364]	likely benign	1	156134541	156134541	Human	1	name
156333026	CV2061483	single nucleotide variant	NM_170707.4(LMNA):c.936+17C>T	Charcot-Marie-Tooth disease type 2 [RCV002810790]	likely benign	1	156135329	156135329	Human	1	name
156060795	CV2069226	single nucleotide variant	NM_170707.4(LMNA):c.1609-2A>G	Charcot-Marie-Tooth disease type 2 [RCV002846766]	likely pathogenic	1	156137652	156137652	Human	1	name
155977557	CV2073171	single nucleotide variant	NM_170707.4(LMNA):c.513+45T>C	Charcot-Marie-Tooth disease type 2 [RCV002842362]	likely benign	1	156130818	156130818	Human	1	name
11093743	CV228278	single nucleotide variant	NM_170707.4(LMNA):c.1488+8G>A	Cardiovascular phenotype [RCV002390573]\|Charcot-Marie-Tooth disease [RCV001173413]\|Charcot-Marie-Tooth disease type 2 [RCV001088656]\|not provided [RCV000725758]\|not specified [RCV000220172]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156137036	156137036	Human	2	name
11090269	CV228280	single nucleotide variant	NM_170707.4(LMNA):c.1381-6C>T	Cardiomyopathy [RCV001180052]\|Charcot-Marie-Tooth disease type 2 [RCV001087904]\|Primary dilated cardiomyopathy [RCV003997704]\|not provided [RCV000416195]\|not specified [RCV000215844]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156136915	156136915	Human	4	name
11345550	CV237758	single nucleotide variant	NM_170707.4(LMNA):c.513+45T>G	Charcot-Marie-Tooth disease type 2 [RCV003581587]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV000225043]	pathogenic\|uncertain significance	1	156130818	156130818	Human	2	name
156436072	CV2403685	single nucleotide variant	NM_170707.4(LMNA):c.356+12C>T	Cardiomyopathy [RCV003128184]\|Charcot-Marie-Tooth disease type 2 [RCV005099272]	likely benign\|uncertain significance	1	156115286	156115286	Human	3	name
243058644	CV2413108	single nucleotide variant	NM_170707.4(LMNA):c.1157+3G>A	Cardiovascular phenotype [RCV004636709]\|Charcot-Marie-Tooth disease type 2 [RCV003745552]\|not provided [RCV003134078]	uncertain significance	1	156136124	156136124	Human	1	name
329355394	CV2430046	single nucleotide variant	NM_170707.4(LMNA):c.1381-1G>A	Cardiovascular phenotype [RCV003177759]	likely pathogenic	1	156136920	156136920	Human		name
11523671	CV244228	single nucleotide variant	NM_170707.4(LMNA):c.1157+1G>T	Charcot-Marie-Tooth disease type 2 [RCV001857811]\|not provided [RCV000236305]	pathogenic\|likely pathogenic	1	156136122	156136122	Human	1	name
11523984	CV244233	single nucleotide variant	NM_170707.4(LMNA):c.1489-2A>G	Cardiovascular phenotype [RCV002392730]\|Charcot-Marie-Tooth disease type 2 [RCV002518441]\|not provided [RCV000236890]	pathogenic\|likely pathogenic	1	156137111	156137111	Human	1	name
11523433	CV244236	single nucleotide variant	NM_170707.4(LMNA):c.1609-8C>G	Charcot-Marie-Tooth disease type 2 [RCV002518429]\|not provided [RCV000235897]	likely benign\|uncertain significance	1	156137646	156137646	Human	1	name
11549562	CV249418	single nucleotide variant	NM_170707.4(LMNA):c.936+47C>T	not specified [RCV000250579]	likely benign	1	156135359	156135359	Human		name
11642947	CV269951	single nucleotide variant	NM_170707.4(LMNA):c.1609-8C>T	not provided [RCV000385066]	uncertain significance	1	156137646	156137646	Human		name
401857135	CV2750436	single nucleotide variant	NM_170707.4(LMNA):c.1157+1G>C	Cardiovascular phenotype [RCV004992599]\|not provided [RCV003334109]	pathogenic\|uncertain significance	1	156136122	156136122	Human		name
11577521	CV276610	single nucleotide variant	NM_170707.4(LMNA):c.936+12C>T	Cardiovascular phenotype [RCV003165785]\|Charcot-Marie-Tooth disease [RCV001172628]\|Charcot-Marie-Tooth disease type 2 [RCV000342630]\|Congenital muscular dystrophy due to LMNA mutation [RCV000408245]\|Dilated Cardiomyopathy, Dominant [RCV000262176]\|Emery-Dreifuss ... (more) muscular dystrophy [RCV000307693]\|Familial partial lipodystrophy [RCV000274234]\|Hutchinson-Gilford syndrome [RCV000277642]\|Lethal tight skin contracture syndrome [RCV000370046]\|Limb-girdle muscular dystrophy, recessive [RCV000313011]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000316315]\|Mandibuloacral dysplasia [RCV000373251]\|not specified [RCV000611471]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156135324	156135324	Human	12	name
11644331	CV277453	single nucleotide variant	NM_170707.4(LMNA):c.514-11C>T	Cardiomyopathy [RCV005402898]\|Cardiovascular phenotype [RCV004639205]\|Charcot-Marie-Tooth disease type 2 [RCV002061154]\|Charcot-Marie-Tooth disease type 2B1 [RCV000319234]\|Congenital muscular dystrophy due to LMNA mutation [RCV000338954]\|Dilated cardiomyopathy 1 ... (more) A [RCV000277232]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001096563]\|Emery-Dreifuss muscular dystrophy [RCV000259634]\|Familial partial lipodystrophy, Dunnigan type [RCV000312526]\|Hutchinson-Gilford syndrome [RCV000271579]\|Lethal tight skin contracture syndrome [RCV000367228]\|Limb-girdle muscular dystrophy, recessive [RCV000366122]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000372986]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000373949]\|not provided [RCV000828218]	likely benign\|uncertain significance	1	156134392	156134392	Human	17	name
405173925	CV2853541	deletion	NM_170707.4(LMNA):c.1968+1del	not provided [RCV003542577]	uncertain significance	1	156138757	156138757	Human		name
405071124	CV2885329	single nucleotide variant	NM_170707.4(LMNA):c.357-18C>G	Charcot-Marie-Tooth disease type 2 [RCV003581128]	likely benign	1	156130599	156130599	Human	1	name
405075631	CV2898334	single nucleotide variant	NM_170707.4(LMNA):c.1608+4A>G	Charcot-Marie-Tooth disease type 2 [RCV003581429]	uncertain significance	1	156137236	156137236	Human	1	name
405088459	CV2900196	single nucleotide variant	NM_170707.4(LMNA):c.639+18C>T	Charcot-Marie-Tooth disease type 2 [RCV003582679]	likely benign	1	156134546	156134546	Human	1	name
405063090	CV2934268	single nucleotide variant	NM_170707.4(LMNA):c.357-15C>T	Cardiomyopathy [RCV003532552]	likely benign	1	156130602	156130602	Human	2	name
405063147	CV2934274	single nucleotide variant	NM_170707.4(LMNA):c.1157+5G>T	Cardiomyopathy [RCV003532558]\|Primary dilated cardiomyopathy [RCV004011491]	uncertain significance	1	156136126	156136126	Human	3	name
405246395	CV2971184	single nucleotide variant	NM_170707.4(LMNA):c.1381-5G>T	Charcot-Marie-Tooth disease type 2 [RCV003745962]	likely benign	1	156136916	156136916	Human	1	name
405083119	CV2972671	single nucleotide variant	NM_170707.4(LMNA):c.356+17G>T	Charcot-Marie-Tooth disease type 2 [RCV003744063]	likely benign	1	156115291	156115291	Human	1	name
405085173	CV2983490	single nucleotide variant	NM_170707.4(LMNA):c.937-14C>T	Charcot-Marie-Tooth disease type 2 [RCV003744291]	likely benign	1	156135887	156135887	Human	1	name
405075589	CV3007465	single nucleotide variant	NM_170707.4(LMNA):c.513+19G>T	Charcot-Marie-Tooth disease type 2 [RCV003743127]	likely benign	1	156130792	156130792	Human	1	name
405077057	CV3023083	single nucleotide variant	NM_170707.4(LMNA):c.640-16C>T	Charcot-Marie-Tooth disease type 2 [RCV003743223]	likely benign	1	156134789	156134789	Human	1	name
405079697	CV3043902	single nucleotide variant	NM_170707.4(LMNA):c.936+10C>T	Charcot-Marie-Tooth disease type 2 [RCV003743430]	likely benign	1	156135322	156135322	Human	1	name
405046427	CV3154562	single nucleotide variant	NM_170707.4(LMNA):c.640-20C>T	Charcot-Marie-Tooth disease type 2 [RCV003849238]	likely benign	1	156134785	156134785	Human	1	name
405248636	CV3169678	single nucleotide variant	NM_170707.4(LMNA):c.1157+7T>C	Charcot-Marie-Tooth disease type 2 [RCV003869491]	likely benign	1	156136128	156136128	Human	1	name
405264251	CV3189965	single nucleotide variant	NM_170707.4(LMNA):c.513+36C>T	LMNA-related disorder [RCV004534463]	likely benign	1	156130809	156130809	Human		name , trait , alternate_id
405280624	CV3195646	single nucleotide variant	NM_170707.4(LMNA):c.936+49G>C	LMNA-related disorder [RCV004536990]	likely benign	1	156135361	156135361	Human		name , trait , alternate_id
405723406	CV3230313	single nucleotide variant	NM_170707.4(LMNA):c.1158-8C>T	Primary dilated cardiomyopathy [RCV004013065]	likely benign	1	156136206	156136206	Human	1	name
405712265	CV3231821	single nucleotide variant	NM_170707.4(LMNA):c.1489-5T>C	Primary dilated cardiomyopathy [RCV004011851]	uncertain significance	1	156137108	156137108	Human	1	name
405728811	CV3391192	single nucleotide variant	NM_170707.4(LMNA):c.1489-1G>A	Cardiovascular phenotype [RCV004524853]	likely pathogenic	1	156137112	156137112	Human		name
405728843	CV3391197	single nucleotide variant	NM_170707.4(LMNA):c.937-10C>T	Cardiovascular phenotype [RCV004524858]	likely benign	1	156135891	156135891	Human		name
405852361	CV3395977	single nucleotide variant	NM_170707.4(LMNA):c.1157+2T>A	Primary dilated cardiomyopathy [RCV004556980]	pathogenic	1	156136123	156136123	Human	1	name
407573696	CV3498063	single nucleotide variant	NM_170707.4(LMNA):c.1608+1G>T	not provided [RCV004702049]	pathogenic	1	156137233	156137233	Human		name
408386377	CV3522490	single nucleotide variant	NM_170707.4(LMNA):c.1608+4A>T	not provided [RCV004767850]	uncertain significance	1	156137236	156137236	Human		name
596941233	CV3546145	single nucleotide variant	NM_170707.4(LMNA):c.1158-7T>C	Charcot-Marie-Tooth disease type 2 [RCV005105200]\|Primary dilated cardiomyopathy [RCV004806774]	likely benign	1	156136207	156136207	Human	2	name
12838868	CV364452	single nucleotide variant	NM_170707.4(LMNA):c.1609-9C>T	Charcot-Marie-Tooth disease type 2 [RCV002521808]\|not specified [RCV000427759]	likely benign	1	156137645	156137645	Human	1	name
12842226	CV364493	single nucleotide variant	NM_170707.4(LMNA):c.811-12C>T	Cardiomyopathy [RCV001187601]\|Cardiovascular phenotype [RCV003168655]\|Charcot-Marie-Tooth disease type 2 [RCV002062661]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002480303]\|Primary dilated cardiomyopathy [RCV004000400]\|not specified [RCV000434017]	likely benign	1	156135175	156135175	Human	18	name
12844198	CV364549	single nucleotide variant	NM_170707.4(LMNA):c.356+18G>T	Charcot-Marie-Tooth disease type 2 [RCV002062441]\|not specified [RCV000437571]	likely benign	1	156115292	156115292	Human	1	name
597831702	CV3759788	single nucleotide variant	NM_170707.4(LMNA):c.937-13C>T	Charcot-Marie-Tooth disease type 2 [RCV005084726]	likely benign	1	156135888	156135888	Human	1	name
597854601	CV3762511	single nucleotide variant	NM_170707.4(LMNA):c.1158-1G>A	Primary familial dilated cardiomyopathy [RCV005088427]	pathogenic	1	156136213	156136213	Human	1	name
597924444	CV3777943	single nucleotide variant	NM_170707.4(LMNA):c.639+12G>T	Charcot-Marie-Tooth disease type 2 [RCV005130667]	likely benign	1	156134540	156134540	Human	1	name
597913256	CV3778678	single nucleotide variant	NM_170707.4(LMNA):c.811-13T>C	Charcot-Marie-Tooth disease type 2 [RCV005129023]	likely benign	1	156135174	156135174	Human	1	name
597966713	CV3794301	single nucleotide variant	NM_170707.4(LMNA):c.513+20C>T	Charcot-Marie-Tooth disease type 2 [RCV005140477]	likely benign	1	156130793	156130793	Human	1	name
597894612	CV3810080	single nucleotide variant	NM_170707.4(LMNA):c.810+15T>C	Charcot-Marie-Tooth disease type 2 [RCV005151801]	likely benign	1	156134990	156134990	Human	1	name
597916856	CV3811071	single nucleotide variant	NM_170707.4(LMNA):c.1157+8G>T	Charcot-Marie-Tooth disease type 2 [RCV005155106]	likely benign	1	156136129	156136129	Human	1	name
597840141	CV3825264	single nucleotide variant	NM_170707.4(LMNA):c.1380+9C>T	Charcot-Marie-Tooth disease type 2 [RCV005171947]	likely benign	1	156136445	156136445	Human	1	name
597920054	CV3842592	single nucleotide variant	NM_170707.4(LMNA):c.357-18C>T	Charcot-Marie-Tooth disease type 2 [RCV005184077]	likely benign	1	156130599	156130599	Human	1	name
597912646	CV3850541	single nucleotide variant	NM_170707.4(LMNA):c.1969-1G>A	Charcot-Marie-Tooth disease type 2 [RCV005203690]	uncertain significance	1	156139079	156139079	Human	1	name
597908893	CV3853769	single nucleotide variant	NM_170707.4(LMNA):c.1380+5G>C	Charcot-Marie-Tooth disease type 2 [RCV005203252]	uncertain significance	1	156136441	156136441	Human	1	name
597881366	CV3857409	single nucleotide variant	NM_170707.4(LMNA):c.513+18G>A	Charcot-Marie-Tooth disease type 2 [RCV005199025]	likely benign	1	156130791	156130791	Human	1	name
12896591	CV389323	single nucleotide variant	NM_170707.4(LMNA):c.1969-1G>T	Cardiomyopathy [RCV001188692]\|Charcot-Marie-Tooth disease type 2 [RCV001303566]\|Primary dilated cardiomyopathy [RCV004000603]\|not provided [RCV003441856]\|not specified [RCV000455558]	uncertain significance	1	156139079	156139079	Human	4	name
616937359	CV4010998	single nucleotide variant	NM_170707.4(LMNA):c.937-46A>T	not specified [RCV005404842]	likely benign	1	156135855	156135855	Human		name
13213592	CV427645	single nucleotide variant	NM_170707.4(LMNA):c.513+12C>A	Charcot-Marie-Tooth disease type 2 [RCV002060129]\|not specified [RCV000500206]	likely benign\|uncertain significance	1	156130785	156130785	Human	1	name
13504434	CV442640	single nucleotide variant	NM_170707.4(LMNA):c.1698+1G>C	Cardiomyopathy [RCV001524187]\|Cardiovascular phenotype [RCV004992297]\|Charcot-Marie-Tooth disease type 2 [RCV003581682]\|LMNA-related disorder [RCV004527626]\|Primary dilated cardiomyopathy [RCV004806384]\|not provided [RCV000519351]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	1	156137744	156137744	Human	4	name , alternate_id
8569612	CV45137	single nucleotide variant	NM_170707.4(LMNA):c.1381-2A>G	Cardiovascular phenotype [RCV005403727]\|Congenital muscular dystrophy due to LMNA mutation [RCV000030147]\|not provided [RCV000057284]	pathogenic\|likely pathogenic\|not provided	1	156136919	156136919	Human	1	name
8569614	CV45140	single nucleotide variant	NM_170707.4(LMNA):c.357-20C>T	Charcot-Marie-Tooth disease type 2 [RCV002054501]\|not provided [RCV000057394]\|not specified [RCV005414257]	likely benign\|uncertain significance\|not provided	1	156130597	156130597	Human	1	name
8569616	CV45142	single nucleotide variant	NM_170707.4(LMNA):c.810+13G>T	Cardiomyopathy [RCV000030152]\|Cardiovascular phenotype [RCV002415432]\|Charcot-Marie-Tooth disease [RCV001173419]\|Charcot-Marie-Tooth disease type 2 [RCV002054502]\|Charcot-Marie-Tooth disease type 2B1 [RCV000263860]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000325879]\|Dilated cardiomyopathy 1A [RCV000319052]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002482919]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001096665]\|Emery-Dreifuss muscular dystrophy [RCV000265060]\|Familial partial lipodystrophy, Dunnigan type [RCV000398608]\|Hutchinson-Gilford syndrome [RCV000324727]\|Lethal tight skin contracture syndrome [RCV000383154]\|Limb-girdle muscular dystrophy, recessive [RCV000379234]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000289568]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000293408]\|Primary dilated cardiomyopathy [RCV002464077]\|not provided [RCV000057464]\|not specified [RCV000041371]	benign\|not provided	1	156134988	156134988	Human	22	name
13521507	CV495086	single nucleotide variant	NM_170707.4(LMNA):c.1488+6T>G	Cardiomyopathy [RCV001178645]\|Charcot-Marie-Tooth disease type 2 [RCV001236548]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002476345]\|Primary dilated cardiomyopathy [RCV004002472]\|not provided [RCV000599507]\|not specified [RCV003155244]	uncertain significance	1	156137034	156137034	Human	6	name
13535681	CV498122	single nucleotide variant	NM_170707.4(LMNA):c.639+12G>A	not specified [RCV000607945]	likely benign	1	156134540	156134540	Human		name
13538904	CV498124	deletion	NM_170707.4(LMNA):c.811-18del	not specified [RCV000612522]	likely benign	1	156135167	156135167	Human		name
13534772	CV509123	single nucleotide variant	NM_170707.4(LMNA):c.1608+5G>A	Cardiovascular phenotype [RCV000619007]	likely pathogenic	1	156137237	156137237	Human		name
13625858	CV515122	single nucleotide variant	NM_170707.4(LMNA):c.1609-4C>T	Cardiomyopathy [RCV003532226]\|Charcot-Marie-Tooth disease type 2 [RCV000654022]\|Primary dilated cardiomyopathy [RCV004004117]	likely benign	1	156137650	156137650	Human	4	name
13625804	CV515138	single nucleotide variant	NM_170707.4(LMNA):c.1609-7C>T	Charcot-Marie-Tooth disease type 2 [RCV000654019]	likely benign	1	156137647	156137647	Human	1	name
13625781	CV515284	single nucleotide variant	NM_170707.4(LMNA):c.1380+2T>G	Charcot-Marie-Tooth disease type 2 [RCV000653953]	pathogenic\|likely pathogenic	1	156136438	156136438	Human	1	name
8610947	CV57249	single nucleotide variant	NM_170707.4(LMNA):c.810+13G>A	Charcot-Marie-Tooth disease type 2 [RCV002054811]\|not specified [RCV000041370]	likely benign	1	156134988	156134988	Human	1	name
8610948	CV57250	single nucleotide variant	NM_170707.4(LMNA):c.811-13T>A	Cardiomyopathy [RCV000771102]\|Cardiovascular phenotype [RCV002415485]\|Charcot-Marie-Tooth disease [RCV001173418]\|Charcot-Marie-Tooth disease type 2 [RCV002054812]\|Charcot-Marie-Tooth disease type 2B1 [RCV000294723]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000335689]\|Dilated cardiomyopathy 1A [RCV000406731]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001100168]\|Emery-Dreifuss muscular dystrophy [RCV000361342]\|Familial partial lipodystrophy, Dunnigan type [RCV000406740]\|Hutchinson-Gilford syndrome [RCV000300601]\|Lethal tight skin contracture syndrome [RCV000268196]\|Limb-girdle muscular dystrophy, recessive [RCV000325561]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000271656]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000301904]\|not provided [RCV000057470]\|not specified [RCV000041372]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|no classifications from unflagged records\|not provided	1	156135174	156135174	Human	18	name
13835705	CV586967	single nucleotide variant	NM_170707.4(LMNA):c.640-52C>T	Charcot-Marie-Tooth disease type 2 [RCV001511690]\|LMNA-related disorder [RCV004540059]\|not provided [RCV000731588]\|not specified [RCV001700299]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156134753	156134753	Human	1	name , alternate_id
14688734	CV615184	single nucleotide variant	NM_170707.4(LMNA):c.1381-6C>A	Cardiomyopathy [RCV000769729]\|Charcot-Marie-Tooth disease type 2 [RCV001309848]	uncertain significance	1	156136915	156136915	Human	3	name
14728330	CV657113	single nucleotide variant	NM_170707.4(LMNA):c.639+56G>T	not provided [RCV000834725]	benign	1	156134584	156134584	Human		name
14728333	CV657118	single nucleotide variant	NM_170707.4(LMNA):c.639+73C>T	not provided [RCV000834726]	benign	1	156134601	156134601	Human		name
15111419	CV695006	single nucleotide variant	NM_170707.4(LMNA):c.1488+7G>A	Cardiovascular phenotype [RCV003169178]\|Charcot-Marie-Tooth disease type 2 [RCV000872310]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002507521]	likely benign	1	156137035	156137035	Human	16	name
15141133	CV758864	single nucleotide variant	NM_170707.4(LMNA):c.1969-4T>C	Cardiomyopathy [RCV001179743]\|Charcot-Marie-Tooth disease [RCV001173404]\|Charcot-Marie-Tooth disease type 2 [RCV000921791]\|Primary dilated cardiomyopathy [RCV004807222]\|not provided [RCV001702860]	likely benign\|uncertain significance	1	156139076	156139076	Human	5	name
15108822	CV774381	single nucleotide variant	NM_170707.4(LMNA):c.1489-9C>T	Cardiomyopathy [RCV003532329]\|Charcot-Marie-Tooth disease type 2 [RCV001453406]\|not provided [RCV000938223]	likely benign	1	156137104	156137104	Human	3	name
15097727	CV774391	single nucleotide variant	NM_170707.4(LMNA):c.1381-6C>G	Charcot-Marie-Tooth disease type 2 [RCV000936113]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002489250]	likely benign	1	156136915	156136915	Human	3	name
8622656	CV77678	single nucleotide variant	NM_170707.4(LMNA):c.1157+1G>A	Cardiovascular phenotype [RCV000621430]\|Charcot-Marie-Tooth disease type 2 [RCV002513736]\|not provided [RCV000057242]	pathogenic\|likely pathogenic\|not provided	1	156136122	156136122	Human	1	name
8622659	CV77681	single nucleotide variant	NM_170707.4(LMNA):c.1158-2A>G	not provided [RCV000057245]	likely pathogenic\|not provided	1	156136212	156136212	Human		name
8622692	CV77714	single nucleotide variant	NM_170707.4(LMNA):c.1380+1G>A	Cardiovascular phenotype [RCV002381366]\|Charcot-Marie-Tooth disease type 2 [RCV000697969]\|Dilated cardiomyopathy 1A [RCV001535753]\|not provided [RCV000057283]	pathogenic\|not provided	1	156136437	156136437	Human	13	name
8622693	CV77715	single nucleotide variant	NM_170707.4(LMNA):c.1381-8C>G	not provided [RCV000057285]	not provided	1	156136913	156136913	Human		name
8622706	CV77728	single nucleotide variant	NM_170707.4(LMNA):c.1488+1G>A	Cardiovascular phenotype [RCV003298103]\|Charcot-Marie-Tooth disease type 2 [RCV003581574]\|not provided [RCV000057305]	pathogenic\|likely pathogenic\|uncertain significance\|not provided	1	156137029	156137029	Human	1	name
8622707	CV77729	single nucleotide variant	NM_170707.4(LMNA):c.1488+5G>A	not provided [RCV000057306]	not provided	1	156137033	156137033	Human		name
8622708	CV77730	single nucleotide variant	NM_170707.4(LMNA):c.1488+5G>C	Charcot-Marie-Tooth disease type 2 [RCV003581575]\|Familial partial lipodystrophy, Dunnigan type [RCV000015610]\|not provided [RCV000057307]	pathogenic\|uncertain significance\|not provided	1	156137033	156137033	Human	2	name
8622727	CV77750	single nucleotide variant	NM_170707.4(LMNA):c.1608+1G>A	Cardiovascular phenotype [RCV004629146]\|Charcot-Marie-Tooth disease type 2 [RCV000693979]\|Dilated cardiomyopathy 1A [RCV001196083]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002490641]\|Neuromuscular disease [RCV000150954]\|not provided [RCV000057335]	pathogenic\|not provided	1	156137233	156137233	Human	17	name
8622728	CV77751	single nucleotide variant	NM_170707.4(LMNA):c.1608+5G>C	Cardiovascular phenotype [RCV002390205]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV000015589]\|not provided [RCV000057336]	pathogenic\|not provided	1	156137237	156137237	Human	2	name
8622730	CV77753	single nucleotide variant	NM_170707.4(LMNA):c.1609-3C>G	Cardiovascular phenotype [RCV002390206]\|Charcot-Marie-Tooth disease [RCV001174242]\|Charcot-Marie-Tooth disease type 2 [RCV001854174]\|Dilated cardiomyopathy 1A [RCV000503283]\|LMNA-related disorder [RCV004537257]\|Primary dilated cardiomyopathy [RCV000154514]\|not p ... (more) rovided [RCV000057338]	pathogenic\|likely pathogenic\|not provided	1	156137651	156137651	Human	5	name , alternate_id
8622731	CV77754	single nucleotide variant	NM_170707.4(LMNA):c.1609-5A>G	not provided [RCV000057339]	not provided	1	156137649	156137649	Human		name
8622753	CV77776	single nucleotide variant	NM_170707.4(LMNA):c.1968+1G>A	Hutchinson-Gilford syndrome [RCV000015607]\|Restrictive dermopathy 2 [RCV001847645]\|not provided [RCV000057377]	pathogenic\|not provided	1	156138758	156138758	Human	2	name
8622793	CV77817	single nucleotide variant	NM_170707.4(LMNA):c.640-10A>C	not provided [RCV000057436]	not provided	1	156134795	156134795	Human		name
8622794	CV77818	single nucleotide variant	NM_170707.4(LMNA):c.640-10A>G	Cardiovascular phenotype [RCV002362690]\|Charcot-Marie-Tooth disease type 2 [RCV001221904]\|Dilated cardiomyopathy 1A [RCV001029824]\|not provided [RCV000057437]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|not provided	1	156134795	156134795	Human	4	name
8622813	CV77837	single nucleotide variant	NM_170707.4(LMNA):c.810+61C>T	not provided [RCV000057466]	benign\|not provided	1	156135036	156135036	Human		name
8622814	CV77838	single nucleotide variant	NM_170707.4(LMNA):c.810+63C>A	not provided [RCV000057467]	not provided	1	156135038	156135038	Human		name
8622816	CV77840	single nucleotide variant	NM_170707.4(LMNA):c.811-10T>A	not provided [RCV000057469]	not provided	1	156135177	156135177	Human		name
8622830	CV77854	single nucleotide variant	NM_170707.4(LMNA):c.937-11C>G	Charcot-Marie-Tooth disease type 2 [RCV001854178]\|not provided [RCV000057486]	pathogenic\|not provided	1	156135890	156135890	Human	1	name
8622831	CV77855	single nucleotide variant	NM_170707.4(LMNA):c.937-46A>G	not provided [RCV000057487]\|not specified [RCV005403746]	likely benign\|not provided	1	156135855	156135855	Human		name
15116337	CV787005	single nucleotide variant	NM_170707.4(LMNA):c.1699-4C>T	Cardiomyopathy [RCV001184431]\|Cardiovascular phenotype [RCV005359710]\|Charcot-Marie-Tooth disease type 2 [RCV000978573]\|LMNA-related disorder [RCV004543651]\|not specified [RCV005405468]	likely benign	1	156138484	156138484	Human	3	name , alternate_id
21070486	CV789856	single nucleotide variant	NM_170707.4(LMNA):c.1969-2A>T	Dilated cardiomyopathy 1A [RCV002249095]	likely pathogenic	1	156139078	156139078	Human	2	name
26898622	CV850729	single nucleotide variant	NM_170707.4(LMNA):c.1488+1G>T	Charcot-Marie-Tooth disease type 2 [RCV001048954]	pathogenic\|likely pathogenic	1	156137029	156137029	Human	1	name
26901136	CV851103	single nucleotide variant	NM_170707.4(LMNA):c.1158-1G>T	Charcot-Marie-Tooth disease type 2 [RCV001049778]	likely pathogenic	1	156136213	156136213	Human	1	name
28880911	CV858855	single nucleotide variant	NM_170707.4(LMNA):c.1968+3G>A	Cardiomyopathy [RCV001177999]\|not provided [RCV001092176]	likely benign\|uncertain significance	1	156138760	156138760	Human	2	name
28890643	CV864995	single nucleotide variant	NM_170707.4(LMNA):c.356+12C>A	Charcot-Marie-Tooth disease type 2B1 [RCV001099884]\|Congenital muscular dystrophy due to LMNA mutation [RCV001101875]\|Dilated cardiomyopathy 1A [RCV001099885]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001101876]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV001099883]\|Familial partial lipodystrophy, Dunnigan type [RCV001099887]\|Hutchinson-Gilford syndrome [RCV001101877]\|Lethal tight skin contracture syndrome [RCV001101874]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001099886]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001099888]	uncertain significance	1	156115286	156115286	Human	11	name
34891054	CV915102	single nucleotide variant	NM_170707.4(LMNA):c.937-11C>A	Cardiomyopathy [RCV001182360]\|Charcot-Marie-Tooth disease type 2 [RCV002559022]	likely benign	1	156135890	156135890	Human	3	name
34896520	CV915114	single nucleotide variant	NM_170707.4(LMNA):c.1380+3A>G	Cardiomyopathy [RCV001185770]\|Cardiovascular phenotype [RCV002379715]\|Charcot-Marie-Tooth disease type 2 [RCV005057043]	uncertain significance	1	156136439	156136439	Human	3	name
34893278	CV915118	single nucleotide variant	NM_170707.4(LMNA):c.1699-8C>T	Cardiomyopathy [RCV001176405]	likely benign	1	156138480	156138480	Human	2	name
34888723	CV915170	single nucleotide variant	NM_170707.4(LMNA):c.1699-7T>C	Cardiomyopathy [RCV001180930]\|Charcot-Marie-Tooth disease type 2 [RCV001469235]\|Dilated cardiomyopathy 1A [RCV001262512]\|Primary dilated cardiomyopathy [RCV004006700]\|not provided [RCV002264213]	likely benign\|uncertain significance	1	156138481	156138481	Human	6	name
34897190	CV915226	single nucleotide variant	NM_170707.4(LMNA):c.1699-9C>T	Cardiomyopathy [RCV001186264]\|Cardiovascular phenotype [RCV003163447]\|Charcot-Marie-Tooth disease type 2 [RCV001399224]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002484016]\|Primary dilated cardiomyopathy [RCV004807404]	likely benign	1	156138479	156138479	Human	18	name
38481520	CV959525	single nucleotide variant	NM_170707.4(LMNA):c.937-10C>A	Charcot-Marie-Tooth disease type 2 [RCV001235144]	uncertain significance	1	156135891	156135891	Human	1	name
41406915	CV982361	single nucleotide variant	NM_170707.4(LMNA):c.1968+8G>T	not provided [RCV001289080]	uncertain significance	1	156138765	156138765	Human		name
127326282	CV1160087	single nucleotide variant	NM_170707.4(LMNA):c.1698+26G>A	Cardiomyopathy [RCV001525867]	uncertain significance	1	156137769	156137769	Human	2	name
150334638	CV1170595	single nucleotide variant	NM_170707.4(LMNA):c.357-778C>G	not provided [RCV001540154]	benign	1	156129839	156129839	Human		name
150414780	CV1175762	single nucleotide variant	NM_170707.4(LMNA):c.1698+25C>G	not provided [RCV001548285]	likely benign	1	156137768	156137768	Human		name
150481259	CV1222129	duplication	NM_170707.4(LMNA):c.1968+20dup	not provided [RCV001616927]	benign	1	156138776	156138777	Human		name
150436290	CV1234039	duplication	NM_170707.4(LMNA):c.357-171dup	not provided [RCV001644166]	benign	1	156130443	156130444	Human		name
151880272	CV1421298	single nucleotide variant	NM_170707.4(LMNA):c.1699-10C>A	Charcot-Marie-Tooth disease type 2 [RCV001886372]\|Primary dilated cardiomyopathy [RCV004010748]	likely benign\|uncertain significance	1	156138478	156138478	Human	2	name
151756540	CV1426151	single nucleotide variant	NM_170707.4(LMNA):c.1380+14C>T	Charcot-Marie-Tooth disease type 2 [RCV002007383]	likely benign	1	156136450	156136450	Human	1	name
152101591	CV1540225	deletion	NM_170707.4(LMNA):c.1489-16del	Charcot-Marie-Tooth disease type 2 [RCV002095603]	likely benign	1	156137096	156137096	Human	1	name
152109130	CV1563820	single nucleotide variant	NM_170707.4(LMNA):c.1609-12T>C	Charcot-Marie-Tooth disease type 2 [RCV002174103]\|Primary dilated cardiomyopathy [RCV004808227]	likely benign	1	156137642	156137642	Human	2	name
152131369	CV1568003	single nucleotide variant	NM_170707.4(LMNA):c.1608+17C>T	Charcot-Marie-Tooth disease type 2 [RCV002218118]	likely benign	1	156137249	156137249	Human	1	name
152121157	CV1574411	single nucleotide variant	NM_170707.4(LMNA):c.1489-16C>T	Charcot-Marie-Tooth disease type 2 [RCV002175596]	likely benign	1	156137097	156137097	Human	1	name
152087047	CV1578262	single nucleotide variant	NM_170707.4(LMNA):c.1381-17C>A	Charcot-Marie-Tooth disease type 2 [RCV002171312]	likely benign	1	156136904	156136904	Human	1	name
152027313	CV1626862	single nucleotide variant	NM_170707.4(LMNA):c.1158-19T>G	Charcot-Marie-Tooth disease type 2 [RCV002185455]	likely benign	1	156136195	156136195	Human	1	name
152154848	CV1658021	single nucleotide variant	NM_170707.4(LMNA):c.1699-15T>C	Charcot-Marie-Tooth disease type 2 [RCV002179993]	likely benign	1	156138473	156138473	Human	1	name
152066287	CV1659899	single nucleotide variant	NM_170707.4(LMNA):c.1380+17G>A	Charcot-Marie-Tooth disease type 2 [RCV002147470]	likely benign	1	156136453	156136453	Human	1	name
9689215	CV172350	single nucleotide variant	NM_170707.4(LMNA):c.1698+25C>T	Cardiomyopathy [RCV001189963]\|not provided [RCV004710561]\|not specified [RCV000154674]	likely benign\|uncertain significance\|not provided	1	156137768	156137768	Human	2	name
9689275	CV172488	single nucleotide variant	NM_170707.4(LMNA):c.1488+14C>T	Cardiovascular phenotype [RCV003162630]\|Charcot-Marie-Tooth disease [RCV001173408]\|Charcot-Marie-Tooth disease type 2 [RCV001850119]\|Charcot-Marie-Tooth disease type 2B1 [RCV001097148]\|Congenital muscular dystrophy due to LMNA mutation [RCV001098891]\|Dilated car ... (more) diomyopathy 1A [RCV001098890]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001097152]\|Emery-Dreifuss muscular dystrophy [RCV001097150]\|Familial partial lipodystrophy, Dunnigan type [RCV001097151]\|Hutchinson-Gilford syndrome [RCV001098892]\|LMNA-related disorder [RCV004734724]\|Lethal tight skin contracture syndrome [RCV001098893]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001097149]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001098889]\|not provided [RCV001795278]\|not specified [RCV000154749]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156137042	156137042	Human	15	name , alternate_id
156377691	CV1876557	single nucleotide variant	NM_170707.4(LMNA):c.1158-16G>A	Charcot-Marie-Tooth disease type 2 [RCV003066880]	likely benign	1	156136198	156136198	Human	1	name
156412073	CV1890310	single nucleotide variant	NM_170707.4(LMNA):c.1489-17C>A	Charcot-Marie-Tooth disease type 2 [RCV003072744]	likely benign	1	156137096	156137096	Human	1	name
10046097	CV189381	single nucleotide variant	NM_170707.4(LMNA):c.357-739T>G	Hutchinson-Gilford syndrome [RCV000986428]\|not provided [RCV004713393]\|not specified [RCV000172758]	benign	1	156129878	156129878	Human	1	name
156403490	CV1920082	single nucleotide variant	NM_170707.4(LMNA):c.1608+16C>T	Charcot-Marie-Tooth disease type 2 [RCV002605906]	likely benign	1	156137248	156137248	Human	1	name
156311750	CV1928512	single nucleotide variant	NM_170707.4(LMNA):c.1608+14G>A	Charcot-Marie-Tooth disease type 2 [RCV002648210]	likely benign	1	156137246	156137246	Human	1	name
156288916	CV2012985	single nucleotide variant	NM_170707.4(LMNA):c.1157+12A>G	Charcot-Marie-Tooth disease type 2 [RCV002715572]	likely benign	1	156136133	156136133	Human	1	name
156115643	CV2020724	single nucleotide variant	NM_170707.4(LMNA):c.1380+13T>C	Charcot-Marie-Tooth disease type 2 [RCV002739999]	likely benign	1	156136449	156136449	Human	1	name
155948414	CV2029103	single nucleotide variant	NM_170707.4(LMNA):c.1157+16G>T	Charcot-Marie-Tooth disease type 2 [RCV002730541]	likely benign	1	156136137	156136137	Human	1	name
156127909	CV2036418	single nucleotide variant	NM_170707.4(LMNA):c.1489-17C>T	Charcot-Marie-Tooth disease type 2 [RCV002786053]	likely benign	1	156137096	156137096	Human	1	name
156224973	CV2064254	single nucleotide variant	NM_170707.4(LMNA):c.1609-19G>A	Charcot-Marie-Tooth disease type 2 [RCV002829833]	uncertain significance	1	156137635	156137635	Human	1	name
156075735	CV2083459	single nucleotide variant	NM_170707.4(LMNA):c.1699-18C>G	Charcot-Marie-Tooth disease type 2 [RCV002847218]	likely benign	1	156138470	156138470	Human	1	name
156261800	CV2100669	single nucleotide variant	NM_170707.4(LMNA):c.1158-16G>T	Charcot-Marie-Tooth disease type 2 [RCV002877298]	likely benign	1	156136198	156136198	Human	1	name
156348182	CV2128932	deletion	NM_170707.4(LMNA):c.1608+15del	Charcot-Marie-Tooth disease type 2 [RCV002966094]	likely benign	1	156137245	156137245	Human	1	name
156092988	CV2151915	single nucleotide variant	NM_170707.4(LMNA):c.1699-17C>T	Charcot-Marie-Tooth disease type 2 [RCV003020754]	likely benign	1	156138471	156138471	Human	1	name
329351476	CV2476407	single nucleotide variant	NM_170707.4(LMNA):c.1968+62G>T	not provided [RCV003222639]	likely benign	1	156138819	156138819	Human		name
11550985	CV249419	single nucleotide variant	NM_170707.4(LMNA):c.1158-43A>G	not provided [RCV000830547]\|not specified [RCV000252459]	benign\|likely benign	1	156136171	156136171	Human		name
11547170	CV249420	single nucleotide variant	NM_170707.4(LMNA):c.1380+37C>T	not specified [RCV000247416]	likely benign	1	156136473	156136473	Human		name
11550600	CV249421	single nucleotide variant	NM_170707.4(LMNA):c.1488+33G>T	not specified [RCV000251971]	likely benign	1	156137061	156137061	Human		name
401829081	CV2743586	single nucleotide variant	NM_170707.4(LMNA):c.1968+80G>T	not provided [RCV003326762]	benign\|likely benign	1	156138837	156138837	Human		name
11583021	CV277461	single nucleotide variant	NM_170707.4(LMNA):c.1698+57G>A	Charcot-Marie-Tooth disease type 2B1 [RCV000361986]\|Congenital muscular dystrophy due to LMNA mutation [RCV000267234]\|Dilated cardiomyopathy 1A [RCV000293451]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001099085]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV000358640]\|Familial partial lipodystrophy, Dunnigan type [RCV000263913]\|Hutchinson-Gilford syndrome [RCV000318957]\|Lethal tight skin contracture syndrome [RCV000333140]\|Limb-girdle muscular dystrophy, recessive [RCV000322274]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000278097]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000373664]	likely benign\|uncertain significance	1	156137800	156137800	Human	12	name
405083154	CV2855722	single nucleotide variant	NM_170707.4(LMNA):c.1969-14G>C	Charcot-Marie-Tooth disease type 2 [RCV003582264]	likely benign	1	156139066	156139066	Human	1	name
405084825	CV2874423	single nucleotide variant	NM_170707.4(LMNA):c.1158-46G>A	Charcot-Marie-Tooth disease type 2 [RCV003582395]	likely benign	1	156136168	156136168	Human	1	name
405075243	CV2883482	single nucleotide variant	NM_170707.4(LMNA):c.1969-11T>C	Charcot-Marie-Tooth disease type 2 [RCV003581324]	likely benign	1	156139069	156139069	Human	1	name
405071872	CV2885672	single nucleotide variant	NM_170707.4(LMNA):c.1609-16T>C	Charcot-Marie-Tooth disease type 2 [RCV003581174]	likely benign	1	156137638	156137638	Human	1	name
405083606	CV2977672	single nucleotide variant	NM_170707.4(LMNA):c.1157+13G>A	Charcot-Marie-Tooth disease type 2 [RCV003744171]	likely benign	1	156136134	156136134	Human	1	name
405086819	CV2994018	single nucleotide variant	NM_170707.4(LMNA):c.1488+17T>C	Charcot-Marie-Tooth disease type 2 [RCV003744445]	likely benign	1	156137045	156137045	Human	1	name
405086112	CV2995328	single nucleotide variant	NM_170707.4(LMNA):c.1380+14C>G	Charcot-Marie-Tooth disease type 2 [RCV003744365]	likely benign	1	156136450	156136450	Human	1	name
405079747	CV3054088	single nucleotide variant	NM_170707.4(LMNA):c.1157+46C>T	Charcot-Marie-Tooth disease type 2 [RCV003743434]	likely benign	1	156136167	156136167	Human	1	name
405080449	CV3055906	single nucleotide variant	NM_170707.4(LMNA):c.1157+22G>A	Charcot-Marie-Tooth disease type 2 [RCV003743512]	likely benign	1	156136143	156136143	Human	1	name
405209458	CV3162559	single nucleotide variant	NM_170707.4(LMNA):c.1157+30G>A	Charcot-Marie-Tooth disease type 2 [RCV003861858]	likely benign	1	156136151	156136151	Human	1	name
405242456	CV3173332	single nucleotide variant	NM_170707.4(LMNA):c.1968+19G>C	Charcot-Marie-Tooth disease type 2 [RCV003867617]	likely benign	1	156138776	156138776	Human	1	name
405704993	CV3231582	single nucleotide variant	NM_170707.4(LMNA):c.1381-15C>T	Primary dilated cardiomyopathy [RCV004010125]	likely benign	1	156136906	156136906	Human	1	name
12847077	CV364503	single nucleotide variant	NM_170707.4(LMNA):c.1157+18C>T	Charcot-Marie-Tooth disease type 2 [RCV002061420]\|not provided [RCV004711040]\|not specified [RCV000442840]	likely benign	1	156136139	156136139	Human	1	name
12842725	CV364504	single nucleotide variant	NM_170707.4(LMNA):c.1488+15G>A	Charcot-Marie-Tooth disease type 2 [RCV002521790]\|not specified [RCV000434948]	likely benign	1	156137043	156137043	Human	1	name
12833039	CV364522	single nucleotide variant	NM_170707.4(LMNA):c.1157+19G>A	Charcot-Marie-Tooth disease [RCV001173412]\|Charcot-Marie-Tooth disease type 2 [RCV002061584]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002488896]\|not provided [RCV001810900]\|not specified [RCV000417739]	likely benign	1	156136140	156136140	Human	4	name
597844344	CV3736135	single nucleotide variant	NM_170707.4(LMNA):c.1158-17G>T	Charcot-Marie-Tooth disease type 2 [RCV005065483]	likely benign	1	156136197	156136197	Human	1	name
597964837	CV3751023	single nucleotide variant	NM_170707.4(LMNA):c.1609-19G>C	Charcot-Marie-Tooth disease type 2 [RCV005082585]	likely benign	1	156137635	156137635	Human	1	name
597949164	CV3772288	single nucleotide variant	NM_170707.4(LMNA):c.1381-14T>G	Charcot-Marie-Tooth disease type 2 [RCV005120607]	likely benign	1	156136907	156136907	Human	1	name
597926087	CV3783254	single nucleotide variant	NM_170707.4(LMNA):c.1157+40T>G	Charcot-Marie-Tooth disease type 2 [RCV005115940]	likely benign	1	156136161	156136161	Human	1	name
597855408	CV3821745	single nucleotide variant	NM_170707.4(LMNA):c.1488+12G>C	Charcot-Marie-Tooth disease type 2 [RCV005174223]	likely benign	1	156137040	156137040	Human	1	name
597861943	CV3860462	single nucleotide variant	NM_170707.4(LMNA):c.1157+45C>G	Charcot-Marie-Tooth disease type 2 [RCV005195990]	likely benign	1	156136166	156136166	Human	1	name
616936964	CV4010892	single nucleotide variant	NM_170707.4(LMNA):c.357-714A>G	not specified [RCV005404239]	likely benign	1	156129903	156129903	Human		name
13481821	CV447163	single nucleotide variant	NM_170707.4(LMNA):c.1608+10C>T	Charcot-Marie-Tooth disease type 2 [RCV000529134]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002483494]	likely benign\|uncertain significance	1	156137242	156137242	Human	3	name
8569611	CV45136	single nucleotide variant	NM_170707.4(LMNA):c.1157+16G>A	Charcot-Marie-Tooth disease [RCV001173416]\|Charcot-Marie-Tooth disease type 2 [RCV002054500]\|Primary dilated cardiomyopathy [RCV000030146]\|not provided [RCV000057241]\|not specified [RCV000041310]	benign\|likely benign\|conflicting interpretations of pathogenicity\|conflicting data from submitters\|not provided	1	156136137	156136137	Human	3	name
13516951	CV491093	single nucleotide variant	NM_170707.4(LMNA):c.1698+28G>A	not provided [RCV000596153]	uncertain significance	1	156137771	156137771	Human		name
13536627	CV498073	single nucleotide variant	NM_170707.4(LMNA):c.1381-13A>G	Cardiomyopathy [RCV001179649]\|Cardiovascular phenotype [RCV003343948]\|Charcot-Marie-Tooth disease type 2 [RCV002066699]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002476367]\|Primary dilated cardiomyopathy [RCV004002608]\|not provided [RCV001811111]\|not specified [RCV000609274]	benign\|likely benign	1	156136908	156136908	Human	18	name
13539977	CV498076	single nucleotide variant	NM_170707.4(LMNA):c.1968+12C>G	not specified [RCV000614046]	likely benign	1	156138769	156138769	Human		name
13832621	CV586866	single nucleotide variant	NM_170707.4(LMNA):c.1968+37C>T	Charcot-Marie-Tooth disease type 2 [RCV002067118]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005046993]\|not provided [RCV000731456]	likely benign\|uncertain significance	1	156138794	156138794	Human	3	name
14745833	CV657048	single nucleotide variant	NM_170707.4(LMNA):c.356+310T>C	not provided [RCV000843795]	benign	1	156115584	156115584	Human	1	name
14722309	CV657051	single nucleotide variant	NM_170707.4(LMNA):c.514-197A>C	not provided [RCV000832045]	benign	1	156134206	156134206	Human		name
14728204	CV657054	single nucleotide variant	NM_170707.4(LMNA):c.514-111C>T	not provided [RCV000834675]	benign	1	156134292	156134292	Human		name
14711254	CV657066	single nucleotide variant	NM_170707.4(LMNA):c.937-275A>G	not provided [RCV000827977]	benign	1	156135626	156135626	Human		name
14714443	CV657068	single nucleotide variant	NM_170707.4(LMNA):c.1380+18G>A	Charcot-Marie-Tooth disease type 2 [RCV002062227]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002495199]\|not provided [RCV000829041]	likely benign	1	156136454	156136454	Human	3	name
14710991	CV657104	single nucleotide variant	NM_170707.4(LMNA):c.357-269T>C	not provided [RCV000827889]	benign	1	156130348	156130348	Human		name
14745185	CV657105	single nucleotide variant	NM_170707.4(LMNA):c.936+234C>T	not provided [RCV000843210]	benign	1	156135546	156135546	Human		name
14722306	CV657111	single nucleotide variant	NM_170707.4(LMNA):c.513+175T>C	not provided [RCV000832044]	benign	1	156130948	156130948	Human		name
14745825	CV657115	single nucleotide variant	NM_170707.4(LMNA):c.513+274C>G	not provided [RCV000843787]	benign	1	156131047	156131047	Human		name
15180006	CV774395	single nucleotide variant	NM_170707.4(LMNA):c.1158-10C>T	Charcot-Marie-Tooth disease type 2 [RCV000929780]	likely benign	1	156136204	156136204	Human	1	name
8622660	CV77682	single nucleotide variant	NM_170707.4(LMNA):c.1158-38G>A	not provided [RCV000057246]	not provided	1	156136176	156136176	Human		name
8622661	CV77683	single nucleotide variant	NM_170707.4(LMNA):c.1158-44C>T	Charcot-Marie-Tooth disease type 2 [RCV000233008]\|LMNA-related disorder [RCV004537255]\|not provided [RCV000057247]\|not specified [RCV000275328]	benign\|likely benign\|not provided	1	156136170	156136170	Human	1	name , alternate_id
8622709	CV77731	single nucleotide variant	NM_170707.4(LMNA):c.1489-41C>T	not provided [RCV000057308]\|not specified [RCV000243967]	benign\|not provided	1	156137072	156137072	Human		name
8622729	CV77752	single nucleotide variant	NM_170707.4(LMNA):c.1609-12T>G	Heart-hand syndrome, Slovenian type [RCV000015618]\|Primary dilated cardiomyopathy [RCV005250008]\|not provided [RCV000057337]	pathogenic\|likely pathogenic\|not provided	1	156137642	156137642	Human	2	name
8622754	CV77777	single nucleotide variant	NM_170707.4(LMNA):c.1968+26A>G	not provided [RCV000057378]\|not specified [RCV000508292]	benign\|not provided	1	156138783	156138783	Human		name
28888694	CV862423	single nucleotide variant	NM_170707.4(LMNA):c.1698+83G>A	Charcot-Marie-Tooth disease type 2B1 [RCV001101162]\|Congenital muscular dystrophy due to LMNA mutation [RCV001101164]\|Dilated cardiomyopathy 1A [RCV001101163]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001101161]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV001101165]\|Familial partial lipodystrophy, Dunnigan type [RCV001099174]\|Hutchinson-Gilford syndrome [RCV001099171]\|Lethal tight skin contracture syndrome [RCV001099170]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001099173]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001099172]	uncertain significance	1	156137826	156137826	Human	11	name
34890000	CV905557	single nucleotide variant	NM_170707.4(LMNA):c.1157+15C>T	Cardiovascular phenotype [RCV004032951]\|Charcot-Marie-Tooth disease [RCV001173406]\|Charcot-Marie-Tooth disease type 2 [RCV002067847]	likely benign	1	156136136	156136136	Human	2	name
34889586	CV905558	single nucleotide variant	NM_170707.4(LMNA):c.1489-16C>G	Charcot-Marie-Tooth disease [RCV001172630]\|Charcot-Marie-Tooth disease type 2 [RCV002068061]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002497605]\|not provided [RCV001528967]\|not specified [RCV001700712]	benign\|likely benign	1	156137097	156137097	Human	4	name
34889999	CV905560	duplication	NM_170707.4(LMNA):c.1968+18dup	Charcot-Marie-Tooth disease [RCV001173403]\|Charcot-Marie-Tooth disease type 2 [RCV002068081]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002491487]\|not provided [RCV001712866]\|not specified [RCV005236652]	benign\|likely benign	1	156138772	156138773	Human	4	name
34891633	CV915106	single nucleotide variant	NM_170707.4(LMNA):c.1158-12C>G	Cardiomyopathy [RCV001182607]\|Cardiovascular phenotype [RCV003380863]\|Charcot-Marie-Tooth disease type 2 [RCV002068323]	likely benign	1	156136202	156136202	Human	3	name
34894429	CV915108	single nucleotide variant	NM_170707.4(LMNA):c.1158-14C>T	Cardiomyopathy [RCV001184602]\|Charcot-Marie-Tooth disease type 2 [RCV002559866]	likely benign	1	156136200	156136200	Human	3	name
34899392	CV915174	single nucleotide variant	NM_170707.4(LMNA):c.1969-11T>G	Cardiomyopathy [RCV001188283]	uncertain significance	1	156139069	156139069	Human	2	name
150419662	CV1196484	single nucleotide variant	NM_170707.4(LMNA):c.1699-133C>T	not provided [RCV001577275]	likely benign	1	156138355	156138355	Human		name
150448703	CV1215015	single nucleotide variant	NM_170707.4(LMNA):c.1609-108G>A	not provided [RCV001611604]	benign	1	156137546	156137546	Human		name
150506829	CV1226441	single nucleotide variant	NM_170707.4(LMNA):c.1608+143A>G	not provided [RCV001635809]	benign	1	156137375	156137375	Human		name
150483855	CV1247020	single nucleotide variant	NM_170707.4(LMNA):c.357-3431G>A	not provided [RCV001673516]	benign	1	156127186	156127186	Human		name
150436033	CV1274117	single nucleotide variant	NM_170707.4(LMNA):c.357-3717A>G	not provided [RCV001724387]\|not specified [RCV001700802]	benign\|likely benign	1	156126900	156126900	Human		name
150472826	CV1281295	single nucleotide variant	NM_170707.4(LMNA):c.357-4599C>A	not provided [RCV001713431]	benign	1	156126018	156126018	Human		name
150540994	CV1297388	single nucleotide variant	NM_170707.4(LMNA):c.357-3734G>A	not provided [RCV001767070]	uncertain significance	1	156126883	156126883	Human		name
8691861	CV141828	single nucleotide variant	NM_170707.4(LMNA):c.357-4426G>A	not specified [RCV000126633]	benign	1	156126191	156126191	Human		name
152038471	CV1669280	single nucleotide variant	NM_170707.4(LMNA):c.357-3748C>T	not provided [RCV002224332]\|not specified [RCV004700694]	conflicting interpretations of pathogenicity\|uncertain significance	1	156126869	156126869	Human		name
155641327	CV1709645	single nucleotide variant	NM_170707.4(LMNA):c.1968+130C>T	not provided [RCV002292745]	uncertain significance	1	156138887	156138887	Human		name
11523756	CV244213	single nucleotide variant	NM_170707.4(LMNA):c.357-4406A>G	not provided [RCV000236483]	uncertain significance	1	156126211	156126211	Human		name
401933069	CV2806056	single nucleotide variant	NM_170707.4(LMNA):c.1969-130C>A	not provided [RCV003409142]	uncertain significance	1	156138950	156138950	Human		name
401948467	CV2832580	single nucleotide variant	NM_170707.4(LMNA):c.357-3669G>A	Familial partial lipodystrophy, Dunnigan type [RCV003448560]	uncertain significance	1	156126948	156126948	Human	1	name
405277853	CV3196151	single nucleotide variant	NM_170707.4(LMNA):c.357-3720C>T	LMNA-related disorder [RCV004537112]	uncertain significance	1	156126897	156126897	Human		name , trait , alternate_id
405869475	CV3396752	single nucleotide variant	NM_170707.4(LMNA):c.357-3735G>A	Emery-Dreifuss muscular dystrophy 3, autosomal recessive [RCV004566631]	uncertain significance	1	156126882	156126882	Human	1	name
408369094	CV3508375	single nucleotide variant	NM_170707.4(LMNA):c.357-3820A>T	LMNA-related disorder [RCV004736564]	likely benign	1	156126797	156126797	Human		name , trait , alternate_id
408368893	CV3517353	single nucleotide variant	NM_170707.4(LMNA):c.357-3719G>A	LMNA-related disorder [RCV004736100]	likely benign	1	156126898	156126898	Human		name , trait , alternate_id
11665231	CV353062	single nucleotide variant	NM_170707.4(LMNA):c.1698+124C>T	Charcot-Marie-Tooth disease type 2 [RCV000343251]\|Congenital muscular dystrophy due to LMNA mutation [RCV000405500]\|Dilated Cardiomyopathy, Dominant [RCV000398598]\|Emery-Dreifuss muscular dystrophy [RCV000394847]\|Familial partial lipodystrophy [RCV000353940]\|Hut ... (more) chinson-Gilford syndrome [RCV000260405]\|Lethal tight skin contracture syndrome [RCV000317932]\|Limb-girdle muscular dystrophy, recessive [RCV000315427]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000346677]\|Mandibuloacral dysplasia [RCV000311797]	uncertain significance	1	156137867	156137867	Human	9	name
598128144	CV3883163	single nucleotide variant	NM_170707.4(LMNA):c.357-4385G>A	not provided [RCV005234696]	likely benign	1	156126232	156126232	Human		name
616936561	CV4010487	single nucleotide variant	NM_170707.4(LMNA):c.357-3723G>A	Cardiovascular phenotype [RCV005403833]	uncertain significance	1	156126894	156126894	Human		name
14728757	CV657072	single nucleotide variant	NM_170707.4(LMNA):c.1608+152A>G	not provided [RCV000834916]	benign	1	156137384	156137384	Human		name
14710987	CV657087	single nucleotide variant	NM_170707.4(LMNA):c.357-4760T>C	not provided [RCV000827888]	benign	1	156125857	156125857	Human		name
14745824	CV657090	single nucleotide variant	NM_170707.4(LMNA):c.357-4696T>C	not provided [RCV000843786]	benign	1	156125921	156125921	Human		name
14722229	CV657094	single nucleotide variant	NM_170707.4(LMNA):c.357-4652C>T	not provided [RCV000832013]	benign	1	156125965	156125965	Human		name
14722230	CV657095	single nucleotide variant	NM_170707.4(LMNA):c.357-4560C>T	not provided [RCV000832014]	benign	1	156126057	156126057	Human		name
14722298	CV657096	single nucleotide variant	NM_170707.4(LMNA):c.357-3991T>G	not provided [RCV000832041]\|not specified [RCV005405332]	benign	1	156126626	156126626	Human		name
14728327	CV657101	single nucleotide variant	NM_170707.4(LMNA):c.357-4032G>A	not provided [RCV000834724]\|not specified [RCV005405334]	benign	1	156126585	156126585	Human		name
14722296	CV657102	single nucleotide variant	NM_170707.4(LMNA):c.357-4021G>A	not provided [RCV000832040]\|not specified [RCV005405331]	benign	1	156126596	156126596	Human		name
14722303	CV657110	single nucleotide variant	NM_170707.4(LMNA):c.357-3489G>A	not provided [RCV000832043]	benign	1	156127128	156127128	Human		name
14722300	CV657112	single nucleotide variant	NM_170707.4(LMNA):c.357-3535T>C	not provided [RCV000832042]	benign	1	156127082	156127082	Human		name
14745826	CV657114	single nucleotide variant	NM_170707.4(LMNA):c.1699-260C>T	not provided [RCV000843788]	benign	1	156138228	156138228	Human		name
14722310	CV657120	single nucleotide variant	NM_170707.4(LMNA):c.1380+142G>A	not provided [RCV000832046]	benign	1	156136578	156136578	Human		name
14745187	CV657123	single nucleotide variant	NM_170707.4(LMNA):c.1699-231T>C	not provided [RCV000843211]	benign	1	156138257	156138257	Human		name
152980614	CV1678807	deletion	NM_170707.4(LMNA):c.666_667del	not provided [RCV002247202]	uncertain significance	1	156139772	156139773	Human		name
150520684	CV1290558	insertion	NM_170707.4(LMNA):c.196_197insA	not provided [RCV001732249]	benign	1	156139302	156139303	Human		name
405076947	CV3016429	deletion	NM_170707.4(LMNA):c.758_810+70del	Charcot-Marie-Tooth disease type 2 [RCV003743089]	pathogenic	1	156134923	156135045	Human	1	name
597901828	CV3851351	deletion	NM_170707.4(LMNA):c.640-67_718del	Charcot-Marie-Tooth disease type 2 [RCV005202127]	likely pathogenic	1	156134736	156134881	Human	1	name
10407826	CV172111	deletion	NM_170707.4(LMNA):c.1700_1968+1del	Hutchinson-Gilford syndrome [RCV000192013]	pathogenic\|not provided	1	156138483	156138752	Human	1	name
597720712	CV3726807	duplication	NM_170707.4(LMNA):c.1699-1_1706dup	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005049888]	uncertain significance	1	156138481	156138482	Human	2	name
597883072	CV3857666	deletion	NM_170707.4(LMNA):c.357-396_434del	Charcot-Marie-Tooth disease type 2 [RCV005199293]	pathogenic	1	156130221	156130694	Human	1	name
13516578	CV488416	deletion	NM_170707.4(LMNA):c.1142_1157+1del	Cardiovascular phenotype [RCV002456296]\|Charcot-Marie-Tooth disease type 2 [RCV001231259]\|not provided [RCV000599189]	pathogenic\|likely pathogenic	1	156136104	156136120	Human	1	name
13818057	CV556965	deletion	NM_170707.4(LMNA):c.810+32_1323del	Charcot-Marie-Tooth disease type 2 [RCV000693456]	pathogenic	1	156135004	156136376	Human	1	name
14709258	CV657092	microsatellite	NM_170707.4(LMNA):c.357-4646AAT[3]	not provided [RCV000834764]	benign	1	156125971	156125973	Human		name
38459035	CV959523	deletion	NM_170707.4(LMNA):c.356+3_356+6del	Charcot-Marie-Tooth disease type 2 [RCV001229061]\|not provided [RCV002265012]	likely pathogenic\|uncertain significance	1	156115275	156115278	Human	1	name
41408108	CV980754	deletion	NM_170707.4(LMNA):c.1158-9_1173del	Proximal muscle weakness [RCV001281579]	likely pathogenic	1	156136202	156136226	Human	1	name
127276640	CV1066294	single nucleotide variant	NM_170707.4(LMNA):c.21G>C (p.Arg7=)	Charcot-Marie-Tooth disease type 2 [RCV001407234]	likely benign	1	156114939	156114939	Human	1	name
127317272	CV1130450	single nucleotide variant	NM_170707.4(LMNA):c.12G>C (p.Pro4=)	Charcot-Marie-Tooth disease type 2 [RCV001503343]	likely benign	1	156114930	156114930	Human	1	name
156161327	CV2096891	duplication	NM_170707.4(LMNA):c.640-11_640-7dup	Charcot-Marie-Tooth disease type 2 [RCV002872671]	likely benign	1	156134791	156134792	Human	1	name
405086587	CV3000282	duplication	NM_170707.4(LMNA):c.513+6_513+20dup	Charcot-Marie-Tooth disease type 2 [RCV003744426]	likely benign	1	156130778	156130779	Human	1	name
405093702	CV3077515	single nucleotide variant	NM_170707.4(LMNA):c.21G>A (p.Arg7=)	Charcot-Marie-Tooth disease type 2 [RCV003745271]	likely benign	1	156114939	156114939	Human	1	name
408380599	CV3501214	single nucleotide variant	NM_170707.4(LMNA):c.24C>T (p.Arg8=)	not provided [RCV004727303]	likely benign	1	156114942	156114942	Human		name
12836042	CV364449	single nucleotide variant	NM_170707.4(LMNA):c.12G>A (p.Pro4=)	Cardiomyopathy [RCV000768707]\|Cardiovascular phenotype [RCV002379298]\|Charcot-Marie-Tooth disease [RCV001173407]\|Charcot-Marie-Tooth disease type 2 [RCV000527270]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002488882]\|Primary dilated cardiomyopathy [RCV003995962]\|not specified ... (more) [RCV000422715]	benign\|likely benign	1	156114930	156114930	Human	19	name
597735893	CV3719645	deletion	NM_170707.4(LMNA):c.5del (p.Glu2fs)	Charcot-Marie-Tooth disease type 2 [RCV005105305]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005051628]	pathogenic	1	156114923	156114923	Human	3	name
15159805	CV685572	single nucleotide variant	NM_170707.4(LMNA):c.15C>T (p.Ser5=)	Cardiovascular phenotype [RCV004639396]\|Charcot-Marie-Tooth disease type 2 [RCV001441179]\|Primary dilated cardiomyopathy [RCV004807217]	likely benign	1	156114933	156114933	Human	2	name
34896465	CV906398	single nucleotide variant	NM_170707.4(LMNA):c.24C>A (p.Arg8=)	Cardiomyopathy [RCV001178467]\|Charcot-Marie-Tooth disease type 2 [RCV002068224]	likely benign	1	156114942	156114942	Human	3	name
127273132	CV1058424	single nucleotide variant	NM_170707.4(LMNA):c.1A>T (p.Met1Leu)	Charcot-Marie-Tooth disease type 2 [RCV001390690]	pathogenic	1	156114919	156114919	Human	1	name
127329509	CV1130451	single nucleotide variant	NM_170707.4(LMNA):c.90G>A (p.Gln30=)	Charcot-Marie-Tooth disease type 2 [RCV001487448]	likely benign	1	156115008	156115008	Human	1	name
151813909	CV1373301	single nucleotide variant	NM_170707.4(LMNA):c.7A>G (p.Thr3Ala)	Charcot-Marie-Tooth disease type 2 [RCV001900220]\|not provided [RCV003130563]	uncertain significance	1	156114925	156114925	Human	1	name
9691200	CV172880	deletion	NM_170707.2(LMNA):c.(?_1)_(356_?)del	Primary dilated cardiomyopathy [RCV000156910]	pathogenic	1	156114919	156115274	Human	1	name
155704449	CV1810689	single nucleotide variant	NM_170707.4(LMNA):c.57T>C (p.Thr19=)	Cardiovascular phenotype [RCV002359878]	likely benign	1	156114975	156114975	Human		name
155669429	CV1822075	single nucleotide variant	NM_170707.4(LMNA):c.66G>A (p.Ser22=)	Cardiovascular phenotype [RCV002367147]\|Charcot-Marie-Tooth disease type 2 [RCV005096986]	likely benign	1	156114984	156114984	Human	1	name
10056824	CV196446	single nucleotide variant	NM_170707.4(LMNA):c.3G>T (p.Met1Ile)	Charcot-Marie-Tooth disease type 2 [RCV002515313]\|not provided [RCV000182378]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity	1	156114921	156114921	Human	1	name
11347665	CV238145	single nucleotide variant	NM_170707.4(LMNA):c.93G>A (p.Glu31=)	Cardiomyopathy [RCV001176602]\|Cardiovascular phenotype [RCV005365197]\|Charcot-Marie-Tooth disease type 2 [RCV000232909]\|Primary dilated cardiomyopathy [RCV004806267]	likely benign	1	156115011	156115011	Human	4	name
11523697	CV244206	single nucleotide variant	NM_170707.4(LMNA):c.3G>C (p.Met1Ile)	not provided [RCV000236357]\|not specified [RCV000678713]	pathogenic\|likely pathogenic	1	156114921	156114921	Human		name
329392321	CV2470608	single nucleotide variant	NM_170707.4(LMNA):c.2T>A (p.Met1Lys)	Cardiovascular phenotype [RCV003217711]\|not provided [RCV004719317]	pathogenic	1	156114920	156114920	Human		name
11638176	CV269995	deletion	NM_170707.4(LMNA):c.937-22_937-10del	Congenital muscular dystrophy due to LMNA mutation [RCV001255625]\|not provided [RCV000298699]	likely pathogenic\|uncertain significance	1	156135875	156135887	Human	1	name
11639145	CV270683	single nucleotide variant	NM_170707.4(LMNA):c.75C>T (p.Arg25=)	Charcot-Marie-Tooth disease type 2 [RCV001452238]\|not provided [RCV000316060]	likely benign\|uncertain significance	1	156114993	156114993	Human	1	name
11641831	CV272023	single nucleotide variant	NM_170707.4(LMNA):c.66G>T (p.Ser22=)	not provided [RCV000364039]	uncertain significance	1	156114984	156114984	Human		name
401862413	CV2753889	single nucleotide variant	NM_170707.4(LMNA):c.4G>A (p.Glu2Lys)	Cardiovascular phenotype [RCV003358470]	uncertain significance	1	156114922	156114922	Human		name
405077856	CV2887510	single nucleotide variant	NM_170707.4(LMNA):c.39G>A (p.Gly13=)	Cardiomyopathy [RCV003534211]\|Cardiovascular phenotype [RCV005363141]\|Charcot-Marie-Tooth disease type 2 [RCV003582651]\|Primary dilated cardiomyopathy [RCV004011375]	likely benign	1	156114957	156114957	Human	4	name
405093297	CV2925632	single nucleotide variant	NM_170707.4(LMNA):c.87G>T (p.Leu29=)	Charcot-Marie-Tooth disease type 2 [RCV003583066]	likely benign	1	156115005	156115005	Human	1	name
405063067	CV2934265	single nucleotide variant	NM_170707.4(LMNA):c.72C>G (p.Thr24=)	Cardiomyopathy [RCV003532549]	likely benign	1	156114990	156114990	Human	2	name
405728821	CV3391194	single nucleotide variant	NM_170707.4(LMNA):c.1A>G (p.Met1Val)	Cardiovascular phenotype [RCV004524855]	pathogenic	1	156114919	156114919	Human		name
407509063	CV3496432	deletion	NM_170707.4(LMNA):c.1609-3_1609-2del	not provided [RCV004698273]	likely pathogenic	1	156137651	156137652	Human		name
597722699	CV3693381	single nucleotide variant	NM_170707.4(LMNA):c.99G>A (p.Glu33=)	Cardiovascular phenotype [RCV004993753]	likely benign	1	156115017	156115017	Human		name
597893769	CV3857128	single nucleotide variant	NM_170707.4(LMNA):c.36C>T (p.Ser12=)	Charcot-Marie-Tooth disease type 2 [RCV005200991]	likely benign	1	156114954	156114954	Human	1	name
8569615	CV45141	single nucleotide variant	NM_170707.4(LMNA):c.51C>T (p.Ser17=)	Cardiomyopathy [RCV000768708]\|Cardiovascular phenotype [RCV000246550]\|Charcot-Marie-Tooth disease [RCV001173421]\|Charcot-Marie-Tooth disease type 2 [RCV000204379]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093839]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000351657]\|Dilated cardiomyopathy 1A [RCV001028068]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002496461]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001098001]\|Emery-Dreifuss muscular dystrophy [RCV000355480]\|Familial partial lipodystrophy, Dunnigan type [RCV000385116]\|Hutchinson-Gilford syndrome [RCV000290770]\|Hypertrophic cardiomyopathy 2 [RCV004595890]\|Lethal tight skin contracture syndrome [RCV000285289]\|Limb-girdle muscular dystrophy, recessive [RCV000265426]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000320485]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000350387]\|Primary dilated cardiomyopathy [RCV000030151]\|not provided [RCV000057414]\|not specified [RCV000041354]	benign\|likely benign\|not provided	1	156114969	156114969	Human	23	name
13509208	CV481568	single nucleotide variant	NM_170707.4(LMNA):c.3G>A (p.Met1Ile)	Charcot-Marie-Tooth disease type 2 [RCV000653926]\|Dilated cardiomyopathy 1A [RCV001594399]\|See cases [RCV001268969]\|not provided [RCV000579197]	pathogenic\|likely pathogenic	1	156114921	156114921	Human	3	name
13527231	CV509108	single nucleotide variant	NM_170707.4(LMNA):c.42G>A (p.Ala14=)	Cardiomyopathy [RCV003532204]\|Cardiovascular phenotype [RCV000619598]\|Charcot-Marie-Tooth disease type 2 [RCV001499333]	likely benign	1	156114960	156114960	Human	3	name
13625796	CV515135	single nucleotide variant	NM_170707.4(LMNA):c.96G>A (p.Lys32=)	Cardiomyopathy [RCV001185033]\|Cardiovascular phenotype [RCV002369758]\|Charcot-Marie-Tooth disease type 2 [RCV000653976]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002493055]\|Primary dilated cardiomyopathy [RCV004004116]	likely benign	1	156115014	156115014	Human	18	name
13810505	CV556669	single nucleotide variant	NM_170707.4(LMNA):c.4G>T (p.Glu2Ter)	Cardiovascular phenotype [RCV002343440]\|Charcot-Marie-Tooth disease type 2 [RCV000688289]	pathogenic	1	156114922	156114922	Human	1	name
8610945	CV57247	single nucleotide variant	NM_170707.4(LMNA):c.78C>T (p.Ile26=)	Cardiomyopathy [RCV001188883]\|Cardiovascular phenotype [RCV002415484]\|Charcot-Marie-Tooth disease type 2 [RCV001079073]\|not provided [RCV000725413]\|not specified [RCV000041368]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156114996	156114996	Human	3	name
14712178	CV626901	duplication	NM_170707.4(LMNA):c.11dup (p.Ser5fs)	Charcot-Marie-Tooth disease type 2 [RCV000793718]	pathogenic	1	156114925	156114926	Human	1	name
15123993	CV695007	deletion	NM_170707.4(LMNA):c.1699-9_1699-8del	Cardiomyopathy [RCV001179741]\|Cardiovascular phenotype [RCV004027848]\|Charcot-Marie-Tooth disease type 2 [RCV001409456]	likely benign\|uncertain significance	1	156138478	156138479	Human	3	name
34890864	CV905876	single nucleotide variant	NM_170707.4(LMNA):c.72C>T (p.Thr24=)	Charcot-Marie-Tooth disease type 2 [RCV003744740]\|not specified [RCV001174564]	likely benign	1	156114990	156114990	Human	1	name
34889890	CV906397	single nucleotide variant	NM_170707.4(LMNA):c.8C>A (p.Thr3Asn)	Cardiomyopathy [RCV001181741]\|Charcot-Marie-Tooth disease type 2 [RCV003769991]\|Dilated cardiomyopathy 1A [RCV004789426]\|Primary dilated cardiomyopathy [RCV004006760]	uncertain significance	1	156114926	156114926	Human	6	name
38483655	CV930059	deletion	NM_170707.4(LMNA):c.13del (p.Ser5fs)	Charcot-Marie-Tooth disease type 2 [RCV001207729]	pathogenic	1	156114931	156114931	Human	1	name
38486254	CV930060	deletion	NM_170707.4(LMNA):c.16del (p.Gln6fs)	Charcot-Marie-Tooth disease type 2 [RCV001208820]	pathogenic	1	156114932	156114932	Human	1	name
126772226	CV1022657	single nucleotide variant	NM_170707.4(LMNA):c.22C>G (p.Arg8Gly)	Charcot-Marie-Tooth disease type 2 [RCV001345496]	uncertain significance	1	156114940	156114940	Human	1	name
126908348	CV1039475	single nucleotide variant	NM_170707.4(LMNA):c.10C>T (p.Pro4Ser)	Charcot-Marie-Tooth disease type 2 [RCV001367763]	uncertain significance	1	156114928	156114928	Human	1	name
127290415	CV1109549	single nucleotide variant	NM_170707.4(LMNA):c.141C>T (p.Asp47=)	Charcot-Marie-Tooth disease type 2 [RCV001451238]	likely benign	1	156115059	156115059	Human	1	name
127301260	CV1109550	single nucleotide variant	NM_170707.4(LMNA):c.189C>A (p.Ile63=)	Charcot-Marie-Tooth disease type 2 [RCV001461350]	likely benign	1	156115107	156115107	Human	1	name
150544717	CV1313526	deletion	NM_170707.4(LMNA):c.65del (p.Ser22fs)	not provided [RCV001783604]	pathogenic	1	156114983	156114983	Human		name
151791957	CV1398589	single nucleotide variant	NM_170707.4(LMNA):c.11C>A (p.Pro4Gln)	Cardiovascular phenotype [RCV004990559]\|Charcot-Marie-Tooth disease type 2 [RCV002010787]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005050511]	likely pathogenic\|uncertain significance	1	156114929	156114929	Human	16	name
151773530	CV1402849	single nucleotide variant	NM_170707.4(LMNA):c.11C>T (p.Pro4Leu)	Charcot-Marie-Tooth disease type 2 [RCV001896572]\|Primary dilated cardiomyopathy [RCV004010788]	uncertain significance	1	156114929	156114929	Human	2	name
151871591	CV1429730	single nucleotide variant	NM_170707.4(LMNA):c.19C>T (p.Arg7Trp)	Charcot-Marie-Tooth disease type 2 [RCV002019020]	uncertain significance	1	156114937	156114937	Human	1	name
151721041	CV1491648	single nucleotide variant	NM_170707.4(LMNA):c.22C>T (p.Arg8Cys)	Charcot-Marie-Tooth disease type 2 [RCV002003671]	uncertain significance	1	156114940	156114940	Human	1	name
152086692	CV1531799	single nucleotide variant	NM_170707.4(LMNA):c.243C>T (p.Tyr81=)	Charcot-Marie-Tooth disease type 2 [RCV002077079]	likely benign	1	156115161	156115161	Human	1	name
152121985	CV1562591	single nucleotide variant	NM_170707.4(LMNA):c.147G>A (p.Val49=)	Charcot-Marie-Tooth disease type 2 [RCV002098281]	likely benign	1	156115065	156115065	Human	1	name
152151435	CV1631400	single nucleotide variant	NM_170707.4(LMNA):c.132C>T (p.Val44=)	Cardiovascular phenotype [RCV005370149]\|Charcot-Marie-Tooth disease type 2 [RCV002179511]	likely benign	1	156115050	156115050	Human	1	name
152028171	CV1642682	single nucleotide variant	NM_170707.4(LMNA):c.249C>G (p.Ala83=)	Charcot-Marie-Tooth disease type 2 [RCV002185747]	likely benign	1	156115167	156115167	Human	1	name
155264950	CV1704500	single nucleotide variant	NM_170707.4(LMNA):c.10C>G (p.Pro4Ala)	Charcot-Marie-Tooth disease type 2 [RCV003101634]\|not provided [RCV002284716]	uncertain significance	1	156114928	156114928	Human	1	name
155683225	CV1830198	single nucleotide variant	NM_170707.4(LMNA):c.103C>T (p.Leu35=)	Cardiovascular phenotype [RCV002389609]\|Charcot-Marie-Tooth disease type 2 [RCV005097546]	likely benign	1	156115021	156115021	Human	1	name
156049999	CV1868968	single nucleotide variant	NM_170707.4(LMNA):c.25G>A (p.Ala9Thr)	Cardiomyopathy [RCV003533333]\|Charcot-Marie-Tooth disease type 2 [RCV003052963]\|Primary dilated cardiomyopathy [RCV004009309]\|not provided [RCV003134603]	uncertain significance	1	156114943	156114943	Human	4	name
10047549	CV190480	deletion	NM_170707.4(LMNA):c.48del (p.Ser17fs)	not provided [RCV000173379]	pathogenic	1	156114965	156114965	Human		name
156415128	CV1983197	single nucleotide variant	NM_170707.4(LMNA):c.207G>A (p.Val69=)	Cardiomyopathy [RCV003533286]\|Charcot-Marie-Tooth disease type 2 [RCV002609524]\|Primary dilated cardiomyopathy [RCV004007512]	likely benign	1	156115125	156115125	Human	4	name
156332485	CV2061450	single nucleotide variant	NM_170707.4(LMNA):c.22C>A (p.Arg8Ser)	Charcot-Marie-Tooth disease type 2 [RCV002810761]	uncertain significance	1	156114940	156114940	Human	1	name
156074511	CV2102137	single nucleotide variant	NM_170707.4(LMNA):c.124T>C (p.Leu42=)	Charcot-Marie-Tooth disease type 2 [RCV002912492]	likely benign	1	156115042	156115042	Human	1	name
156333061	CV2171999	single nucleotide variant	NM_170707.4(LMNA):c.25G>C (p.Ala9Pro)	Charcot-Marie-Tooth disease type 2 [RCV003029877]	uncertain significance	1	156114943	156114943	Human	1	name
243062332	CV2404745	deletion	NM_170707.4(LMNA):c.91del (p.Glu31fs)	Congenital muscular dystrophy due to LMNA mutation [RCV003140302]	uncertain significance	1	156115008	156115008	Human	1	name
11547536	CV257922	single nucleotide variant	NM_170707.4(LMNA):c.111G>A (p.Glu37=)	Cardiomyopathy [RCV003532072]\|Cardiovascular phenotype [RCV000247889]\|Primary dilated cardiomyopathy [RCV003999033]\|not provided [RCV000726524]	likely benign\|uncertain significance	1	156115029	156115029	Human	3	name
11549564	CV257929	single nucleotide variant	NM_170707.4(LMNA):c.207G>C (p.Val69=)	Cardiovascular phenotype [RCV000250582]	likely benign	1	156115125	156115125	Human		name
11640939	CV267009	single nucleotide variant	NM_170707.4(LMNA):c.192C>T (p.Thr64=)	Cardiomyopathy [RCV001183039]\|Cardiovascular phenotype [RCV002411149]\|Charcot-Marie-Tooth disease type 2 [RCV001087778]\|Primary dilated cardiomyopathy [RCV003995762]\|not provided [RCV000725140]\|not specified [RCV000348112]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156115110	156115110	Human	4	name
11645970	CV277537	single nucleotide variant	NM_170707.4(LMNA):c.294G>A (p.Glu98=)	Charcot-Marie-Tooth disease type 2B1 [RCV000268830]\|Congenital muscular dystrophy due to LMNA mutation [RCV000268358]\|Dilated cardiomyopathy 1A [RCV000404276]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001101770]\|Emery-Dreifuss muscular dystroph ... (more) y [RCV000364211]\|Familial partial lipodystrophy, Dunnigan type [RCV000338865]\|Hutchinson-Gilford syndrome [RCV000297999]\|Lethal tight skin contracture syndrome [RCV000358456]\|Limb-girdle muscular dystrophy, recessive [RCV000407235]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000304893]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000303772]\|Primary dilated cardiomyopathy [RCV003231435]\|not provided [RCV001718593]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156115212	156115212	Human	13	name
405085917	CV2868212	single nucleotide variant	NM_170707.4(LMNA):c.195G>A (p.Glu65=)	Charcot-Marie-Tooth disease type 2 [RCV003582457]	likely benign	1	156115113	156115113	Human	1	name
405093326	CV2921977	single nucleotide variant	NM_170707.4(LMNA):c.297C>T (p.Arg99=)	Charcot-Marie-Tooth disease type 2 [RCV003583068]	likely benign	1	156115215	156115215	Human	1	name
405093116	CV2942841	single nucleotide variant	NM_170707.4(LMNA):c.175C>T (p.Leu59=)	Charcot-Marie-Tooth disease type 2 [RCV003745618]	likely benign	1	156115093	156115093	Human	1	name
8564259	CV29516	single nucleotide variant	NM_170707.4(LMNA):c.16C>T (p.Gln6Ter)	Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV000015564]\|Primary dilated cardiomyopathy [RCV000041328]\|not provided [RCV000057350]	pathogenic\|not provided	1	156114934	156114934	Human	2	name
405095705	CV2958586	single nucleotide variant	NM_170707.4(LMNA):c.129G>C (p.Ala43=)	Charcot-Marie-Tooth disease type 2 [RCV003745853]	likely benign	1	156115047	156115047	Human	1	name
405087909	CV3015658	deletion	NM_170707.4(LMNA):c.40del (p.Ala14fs)	Charcot-Marie-Tooth disease type 2 [RCV003744526]	pathogenic	1	156114955	156114955	Human	1	name
405075867	CV3021407	single nucleotide variant	NM_170707.4(LMNA):c.102C>T (p.Asp34=)	Charcot-Marie-Tooth disease type 2 [RCV003743145]	likely benign	1	156115020	156115020	Human	1	name
405081959	CV3056932	single nucleotide variant	NM_170707.4(LMNA):c.282A>G (p.Ser94=)	Cardiovascular phenotype [RCV004992765]\|Charcot-Marie-Tooth disease type 2 [RCV003743540]	likely benign	1	156115200	156115200	Human	1	name
405089112	CV3064030	single nucleotide variant	NM_170707.4(LMNA):c.204G>A (p.Glu68=)	Charcot-Marie-Tooth disease type 2 [RCV003745052]	likely benign	1	156115122	156115122	Human	1	name
405091418	CV3071763	single nucleotide variant	NM_170707.4(LMNA):c.210C>A (p.Val70=)	Charcot-Marie-Tooth disease type 2 [RCV003745231]	likely benign	1	156115128	156115128	Human	1	name
405711660	CV3231726	single nucleotide variant	NM_170707.4(LMNA):c.174G>T (p.Gly58=)	Cardiovascular phenotype [RCV004994416]\|Primary dilated cardiomyopathy [RCV004011756]	likely benign\|uncertain significance	1	156115092	156115092	Human	1	name
405715504	CV3232394	single nucleotide variant	NM_170707.4(LMNA):c.189C>T (p.Ile63=)	Primary dilated cardiomyopathy [RCV004012247]	likely benign	1	156115107	156115107	Human	1	name
405702677	CV3233463	single nucleotide variant	NM_170707.4(LMNA):c.273C>A (p.Thr91=)	Primary dilated cardiomyopathy [RCV004009919]	likely benign	1	156115191	156115191	Human	1	name
596928413	CV3540185	duplication	NM_170707.4(LMNA):c.75dup (p.Ile26fs)	not provided [RCV004791178]	likely pathogenic	1	156114992	156114993	Human		name
596941196	CV3546136	single nucleotide variant	NM_170707.4(LMNA):c.126G>A (p.Leu42=)	Primary dilated cardiomyopathy [RCV004806765]	likely benign	1	156115044	156115044	Human	1	name
597722660	CV3693373	single nucleotide variant	NM_170707.4(LMNA):c.264C>T (p.Ala88=)	Cardiovascular phenotype [RCV004993745]	likely benign	1	156115182	156115182	Human		name
597722669	CV3693375	single nucleotide variant	NM_170707.4(LMNA):c.231C>A (p.Ile77=)	Cardiovascular phenotype [RCV004993747]	likely benign	1	156115149	156115149	Human		name
597722675	CV3693376	single nucleotide variant	NM_170707.4(LMNA):c.285A>G (p.Val95=)	Cardiovascular phenotype [RCV004993748]	likely benign	1	156115203	156115203	Human		name
597722676	CV3693377	single nucleotide variant	NM_170707.4(LMNA):c.105G>A (p.Leu35=)	Cardiovascular phenotype [RCV004993749]	likely benign	1	156115023	156115023	Human		name
597722685	CV3693378	single nucleotide variant	NM_170707.4(LMNA):c.150C>G (p.Arg50=)	Cardiovascular phenotype [RCV004993750]	likely benign	1	156115068	156115068	Human		name
597722689	CV3693379	single nucleotide variant	NM_170707.4(LMNA):c.168C>T (p.Asn56=)	Cardiovascular phenotype [RCV004993751]	likely benign	1	156115086	156115086	Human		name
597722694	CV3693380	single nucleotide variant	NM_170707.4(LMNA):c.120T>C (p.Asp40=)	Cardiovascular phenotype [RCV004993752]	likely benign	1	156115038	156115038	Human		name
597722705	CV3693382	single nucleotide variant	NM_170707.4(LMNA):c.201A>G (p.Glu67=)	Cardiovascular phenotype [RCV004993754]	likely benign	1	156115119	156115119	Human		name
597722709	CV3701638	single nucleotide variant	NM_170707.4(LMNA):c.225C>T (p.Ser75=)	Cardiovascular phenotype [RCV004993755]	likely benign	1	156115143	156115143	Human		name
597722713	CV3701639	single nucleotide variant	NM_170707.4(LMNA):c.129G>T (p.Ala43=)	Cardiovascular phenotype [RCV004993756]	likely benign	1	156115047	156115047	Human		name
597722719	CV3701640	single nucleotide variant	NM_170707.4(LMNA):c.255C>G (p.Leu85=)	Cardiovascular phenotype [RCV004993757]	likely benign	1	156115173	156115173	Human		name
12891620	CV390818	single nucleotide variant	NM_170707.4(LMNA):c.20G>A (p.Arg7Gln)	Cardiomyopathy [RCV001181379]\|Charcot-Marie-Tooth disease type 2 [RCV000476932]\|not specified [RCV001823729]	uncertain significance	1	156114938	156114938	Human	3	name
616934556	CV4009636	single nucleotide variant	NM_170707.4(LMNA):c.105G>C (p.Leu35=)	Cardiomyopathy [RCV005400794]	likely benign	1	156115023	156115023	Human	2	name
616934768	CV4009962	single nucleotide variant	NM_170707.4(LMNA):c.129G>A (p.Ala43=)	Cardiomyopathy [RCV005401120]	likely benign	1	156115047	156115047	Human	2	name
616935631	CV4010220	single nucleotide variant	NM_170707.4(LMNA):c.213C>T (p.Ser71=)	Cardiomyopathy [RCV005403521]	likely benign	1	156115131	156115131	Human	2	name
13541950	CV498064	single nucleotide variant	NM_170707.4(LMNA):c.153G>T (p.Ser51=)	Cardiomyopathy [RCV001176365]\|Cardiovascular phenotype [RCV002404668]\|Charcot-Marie-Tooth disease type 2 [RCV000654002]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002476361]\|Primary dilated cardiomyopathy [RCV004002571]\|not provided [RCV003411457]\|not specified [RCV000616855]	likely benign	1	156115071	156115071	Human	18	name
13625792	CV515136	single nucleotide variant	NM_170707.4(LMNA):c.138C>T (p.Ile46=)	Cardiovascular phenotype [RCV002388147]\|Charcot-Marie-Tooth disease type 2 [RCV000653981]\|not provided [RCV000994131]	likely benign	1	156115056	156115056	Human	1	name
13821372	CV556671	deletion	NM_170707.4(LMNA):c.73del (p.Arg25fs)	Charcot-Marie-Tooth disease type 2 [RCV000695793]	pathogenic	1	156114989	156114989	Human	1	name
8610905	CV57204	single nucleotide variant	NM_170707.4(LMNA):c.150C>T (p.Arg50=)	Cardiomyopathy [RCV001181344]\|Cardiovascular phenotype [RCV002390178]\|Charcot-Marie-Tooth disease type 2 [RCV000874140]\|Primary dilated cardiomyopathy [RCV003996455]\|not provided [RCV001697065]\|not specified [RCV000041319]	likely benign	1	156115068	156115068	Human	4	name
8610922	CV57221	single nucleotide variant	NM_170707.4(LMNA):c.198T>C (p.Ser66=)	not specified [RCV000041339]	likely benign	1	156115116	156115116	Human		name
8610923	CV57222	single nucleotide variant	NM_170707.4(LMNA):c.261T>C (p.Asp87=)	Charcot-Marie-Tooth disease type 2 [RCV002054810]\|not specified [RCV000041341]	likely benign	1	156115179	156115179	Human	1	name
14692664	CV616005	single nucleotide variant	NM_170707.4(LMNA):c.249C>T (p.Ala83=)	Cardiomyopathy [RCV000774239]\|Charcot-Marie-Tooth disease type 2 [RCV001422093]\|Primary dilated cardiomyopathy [RCV004001371]	likely benign	1	156115167	156115167	Human	4	name
14711560	CV655044	single nucleotide variant	NM_170707.4(LMNA):c.240C>T (p.Ala80=)	Cardiovascular phenotype [RCV004029207]\|Charcot-Marie-Tooth disease type 2 [RCV002067475]\|Primary dilated cardiomyopathy [RCV004002880]\|not provided [RCV000828086]	likely benign	1	156115158	156115158	Human	2	name
8622670	CV77692	single nucleotide variant	NM_170707.4(LMNA):c.11C>G (p.Pro4Arg)	Charcot-Marie-Tooth disease type 2 [RCV000818990]\|not provided [RCV000057257]	pathogenic\|not provided	1	156114929	156114929	Human	1	name
8654990	CV77784	duplication	NM_170707.4(LMNA):c.28dup (p.Thr10fs)	not provided [RCV000057386]	not provided	1	156114945	156114946	Human		name
8622763	CV77787	deletion	NM_170707.4(LMNA):c.31del (p.Arg11fs)	not provided [RCV000057389]	not provided	1	156114947	156114947	Human		name
26903217	CV822789	single nucleotide variant	NM_170707.4(LMNA):c.23G>A (p.Arg8His)	Cardiomyopathy [RCV003532873]\|Cardiovascular phenotype [RCV002445371]\|Charcot-Marie-Tooth disease type 2 [RCV001072091]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005047288]\|Primary dilated cardiomyopathy [RCV004000209]	uncertain significance	1	156114941	156114941	Human	18	name
34892772	CV906400	single nucleotide variant	NM_170707.4(LMNA):c.162G>A (p.Thr54=)	Cardiomyopathy [RCV001176007]\|Charcot-Marie-Tooth disease type 2 [RCV003744742]	likely benign	1	156115080	156115080	Human	3	name
34897392	CV906401	single nucleotide variant	NM_170707.4(LMNA):c.165G>A (p.Glu55=)	Cardiomyopathy [RCV001186429]	likely benign	1	156115083	156115083	Human	2	name
34893426	CV906405	single nucleotide variant	NM_170707.4(LMNA):c.237C>T (p.Ala79=)	Cardiomyopathy [RCV001183831]	likely benign	1	156115155	156115155	Human	2	name
34895667	CV906406	single nucleotide variant	NM_170707.4(LMNA):c.273C>T (p.Thr91=)	Cardiomyopathy [RCV001185448]\|Charcot-Marie-Tooth disease type 2 [RCV001396397]	likely benign	1	156115191	156115191	Human	3	name
126733256	CV1002170	single nucleotide variant	NM_170707.4(LMNA):c.32G>T (p.Arg11Leu)	Charcot-Marie-Tooth disease type 2 [RCV001313361]	uncertain significance	1	156114950	156114950	Human	1	name
126763679	CV1022658	single nucleotide variant	NM_170707.4(LMNA):c.44A>C (p.Gln15Pro)	Charcot-Marie-Tooth disease type 2 [RCV001341373]\|Primary dilated cardiomyopathy [RCV004808019]	uncertain significance	1	156114962	156114962	Human	2	name
127247805	CV1058425	duplication	NM_170707.4(LMNA):c.186dup (p.Ile63fs)	Charcot-Marie-Tooth disease type 2 [RCV001384798]	pathogenic	1	156115103	156115104	Human	1	name
127238609	CV1066296	single nucleotide variant	NM_170707.4(LMNA):c.495G>T (p.Leu165=)	Charcot-Marie-Tooth disease type 2 [RCV001397356]	likely benign	1	156130755	156130755	Human	1	name
127267955	CV1088037	single nucleotide variant	NM_170707.4(LMNA):c.366G>A (p.Lys122=)	Cardiovascular phenotype [RCV002456730]\|Charcot-Marie-Tooth disease type 2 [RCV001440657]	likely benign	1	156130626	156130626	Human	1	name
127312372	CV1109551	single nucleotide variant	NM_170707.4(LMNA):c.435G>A (p.Glu145=)	Charcot-Marie-Tooth disease type 2 [RCV001464373]\|not specified [RCV001823774]	likely benign	1	156130695	156130695	Human	1	name
127295873	CV1130452	single nucleotide variant	NM_170707.4(LMNA):c.354G>A (p.Ala118=)	Charcot-Marie-Tooth disease type 2 [RCV001497356]	likely benign	1	156115272	156115272	Human	1	name
127286624	CV1130454	single nucleotide variant	NM_170707.4(LMNA):c.472C>T (p.Leu158=)	Charcot-Marie-Tooth disease type 2 [RCV001494477]	likely benign	1	156130732	156130732	Human	1	name
127308807	CV1130455	single nucleotide variant	NM_170707.4(LMNA):c.570G>C (p.Arg190=)	Charcot-Marie-Tooth disease type 2 [RCV001480696]	likely benign	1	156134459	156134459	Human	1	name
127302165	CV1130456	single nucleotide variant	NM_170707.4(LMNA):c.750C>T (p.Ala250=)	Cardiovascular phenotype [RCV002388541]\|Charcot-Marie-Tooth disease type 2 [RCV001499026]	likely benign	1	156134915	156134915	Human	1	name
127323623	CV1160081	single nucleotide variant	NM_170707.4(LMNA):c.927C>T (p.Leu309=)	Cardiomyopathy [RCV001524156]\|Charcot-Marie-Tooth disease type 2 [RCV002070303]\|Primary dilated cardiomyopathy [RCV004007261]	likely benign	1	156135303	156135303	Human	4	name
150334251	CV1164065	single nucleotide variant	NM_170707.4(LMNA):c.71C>T (p.Thr24Ile)	Cardiovascular phenotype [RCV003284369]\|Charcot-Marie-Tooth disease type 2 [RCV003745339]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002495854]\|Primary dilated cardiomyopathy [RCV004008915]\|not provided [RCV001529465]	uncertain significance	1	156114989	156114989	Human	16	name
150432338	CV1246258	single nucleotide variant	NM_170707.4(LMNA):c.41C>A (p.Ala14Glu)	not provided [RCV001663671]	uncertain significance	1	156114959	156114959	Human		name
150487802	CV1274266	single nucleotide variant	NM_170707.4(LMNA):c.876G>A (p.Leu292=)	Charcot-Marie-Tooth disease type 2 [RCV005094889]\|not provided [RCV001699935]\|not specified [RCV001699639]	benign\|likely benign	1	156135252	156135252	Human	1	name
151350000	CV1322915	single nucleotide variant	NM_170707.4(LMNA):c.606G>A (p.Glu202=)	Cardiomyopathy [RCV001805242]\|Cardiovascular phenotype [RCV003163943]\|Charcot-Marie-Tooth disease type 2 [RCV002077250]\|Primary dilated cardiomyopathy [RCV004808127]	likely benign	1	156134495	156134495	Human	4	name
151782458	CV1342008	single nucleotide variant	NM_170707.4(LMNA):c.540G>A (p.Lys180=)	Cardiovascular phenotype [RCV002343962]\|Charcot-Marie-Tooth disease type 2 [RCV001897371]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005040472]\|Primary dilated cardiomyopathy [RCV004010754]	likely benign	1	156134429	156134429	Human	16	name
151790919	CV1394430	single nucleotide variant	NM_170707.4(LMNA):c.936G>A (p.Gln312=)	Charcot-Marie-Tooth disease type 2 [RCV002047096]	uncertain significance	1	156135312	156135312	Human	1	name
8691862	CV141829	single nucleotide variant	NM_005572.3(LMNA):c.747G>A (p.Arg249=)	not provided [RCV000126635]	benign	1	156134912	156134912	Human		name
151762605	CV1471332	single nucleotide variant	NM_170707.4(LMNA):c.43C>T (p.Gln15Ter)	Charcot-Marie-Tooth disease type 2 [RCV001949326]	pathogenic	1	156114961	156114961	Human	1	name
151740203	CV1474867	single nucleotide variant	NM_170707.4(LMNA):c.88C>G (p.Gln30Glu)	Charcot-Marie-Tooth disease type 2 [RCV001968068]	uncertain significance	1	156115006	156115006	Human	1	name
151739273	CV1492295	single nucleotide variant	NM_170707.4(LMNA):c.47C>A (p.Ala16Asp)	Cardiovascular phenotype [RCV005350661]\|Charcot-Marie-Tooth disease type 2 [RCV002042071]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002489934]\|Primary dilated cardiomyopathy [RCV004009185]	uncertain significance	1	156114965	156114965	Human	16	name
152135843	CV1528375	single nucleotide variant	NM_170707.4(LMNA):c.852G>C (p.Leu284=)	Cardiovascular phenotype [RCV004045790]\|Charcot-Marie-Tooth disease type 2 [RCV002100104]	likely benign	1	156135228	156135228	Human	1	name
152153876	CV1539910	single nucleotide variant	NM_170707.4(LMNA):c.379C>T (p.Leu127=)	Cardiomyopathy [RCV003533135]\|Charcot-Marie-Tooth disease type 2 [RCV002139919]	likely benign\|uncertain significance	1	156130639	156130639	Human	3	name
152150996	CV1567573	single nucleotide variant	NM_170707.4(LMNA):c.774G>A (p.Gln258=)	Cardiomyopathy [RCV003533124]\|Cardiovascular phenotype [RCV002409541]\|Charcot-Marie-Tooth disease type 2 [RCV002158189]	likely benign	1	156134939	156134939	Human	3	name
152070981	CV1570192	single nucleotide variant	NM_170707.4(LMNA):c.699G>A (p.Lys233=)	Charcot-Marie-Tooth disease type 2 [RCV002191776]	likely benign	1	156134864	156134864	Human	1	name
152079845	CV1579929	single nucleotide variant	NM_170707.4(LMNA):c.966C>T (p.Asp322=)	Charcot-Marie-Tooth disease type 2 [RCV002076222]	likely benign	1	156135930	156135930	Human	1	name
152080507	CV1620745	single nucleotide variant	NM_170707.4(LMNA):c.967C>T (p.Leu323=)	Charcot-Marie-Tooth disease type 2 [RCV002112686]\|LMNA-related disorder [RCV004543792]	likely benign	1	156135931	156135931	Human	1	name , alternate_id
152027232	CV1626823	single nucleotide variant	NM_170707.4(LMNA):c.423G>A (p.Leu141=)	Charcot-Marie-Tooth disease type 2 [RCV002185426]	likely benign	1	156130683	156130683	Human	1	name
152115604	CV1640043	single nucleotide variant	NM_170707.4(LMNA):c.375T>C (p.Gly125=)	Cardiomyopathy [RCV003533110]\|Charcot-Marie-Tooth disease type 2 [RCV002080847]	likely benign	1	156130635	156130635	Human	3	name
152028299	CV1642732	single nucleotide variant	NM_170707.4(LMNA):c.687T>C (p.Ile229=)	Charcot-Marie-Tooth disease type 2 [RCV002185789]	likely benign	1	156134852	156134852	Human	1	name
152173033	CV1652866	single nucleotide variant	NM_170707.4(LMNA):c.609A>G (p.Glu203=)	Charcot-Marie-Tooth disease type 2 [RCV002143978]	likely benign	1	156134498	156134498	Human	1	name
9691770	CV172343	single nucleotide variant	NM_170707.4(LMNA):c.486G>A (p.Leu162=)	Cardiomyopathy [RCV001188346]\|Charcot-Marie-Tooth disease [RCV001173411]\|Primary dilated cardiomyopathy [RCV003998205]\|not specified [RCV000150938]	likely benign	1	156130746	156130746	Human	4	name
9690991	CV172485	single nucleotide variant	NM_170707.4(LMNA):c.837G>A (p.Glu279=)	Cardiomyopathy [RCV001188633]\|Charcot-Marie-Tooth disease type 2 [RCV001465034]\|not specified [RCV000156690]	likely benign	1	156135213	156135213	Human	3	name
155702006	CV1776924	single nucleotide variant	NM_170707.4(LMNA):c.76A>G (p.Ile26Val)	Charcot-Marie-Tooth disease type 2 [RCV002300019]	uncertain significance	1	156114994	156114994	Human	1	name
155736289	CV1798661	single nucleotide variant	NM_170707.4(LMNA):c.468C>T (p.Arg156=)	Cardiovascular phenotype [RCV002330560]	likely benign	1	156130728	156130728	Human		name
155722450	CV1817635	single nucleotide variant	NM_170707.4(LMNA):c.873G>A (p.Glu291=)	Cardiovascular phenotype [RCV002449754]\|Charcot-Marie-Tooth disease type 2 [RCV003744027]	likely benign	1	156135249	156135249	Human	1	name
155694573	CV1821363	single nucleotide variant	NM_170707.4(LMNA):c.945C>G (p.Ala315=)	Cardiovascular phenotype [RCV002443471]	likely benign	1	156135909	156135909	Human		name
155694598	CV1821371	single nucleotide variant	NM_170707.4(LMNA):c.945C>T (p.Ala315=)	Cardiovascular phenotype [RCV002443477]\|Charcot-Marie-Tooth disease type 2 [RCV003094814]	likely benign	1	156135909	156135909	Human	1	name
155742642	CV1823840	single nucleotide variant	NM_170707.4(LMNA):c.807C>T (p.Ala269=)	Cardiovascular phenotype [RCV002412483]\|Primary dilated cardiomyopathy [RCV004005763]	likely benign	1	156134972	156134972	Human	1	name
155698867	CV1824480	single nucleotide variant	NM_170707.4(LMNA):c.888C>T (p.Arg296=)	Cardiovascular phenotype [RCV002375996]\|Charcot-Marie-Tooth disease type 2 [RCV003100048]	likely benign	1	156135264	156135264	Human	1	name
155684002	CV1825261	single nucleotide variant	NM_170707.4(LMNA):c.930G>A (p.Gln310=)	Cardiomyopathy [RCV005401971]\|Cardiovascular phenotype [RCV002371573]	likely benign	1	156135306	156135306	Human	2	name
155801833	CV1864144	single nucleotide variant	NM_170707.4(LMNA):c.807C>G (p.Ala269=)	Primary dilated cardiomyopathy [RCV004007474]\|not provided [RCV002475097]	conflicting interpretations of pathogenicity\|uncertain significance	1	156134972	156134972	Human	1	name
156301370	CV1902100	single nucleotide variant	NM_170707.4(LMNA):c.597C>T (p.Thr199=)	Charcot-Marie-Tooth disease type 2 [RCV003087944]	likely benign	1	156134486	156134486	Human	1	name
156043272	CV1914702	single nucleotide variant	NM_170707.4(LMNA):c.564G>A (p.Leu188=)	Charcot-Marie-Tooth disease type 2 [RCV002620343]\|Primary dilated cardiomyopathy [RCV004009478]	likely benign	1	156134453	156134453	Human	2	name
10052160	CV194416	single nucleotide variant	NM_170707.4(LMNA):c.643C>T (p.Leu215=)	Cardiomyopathy [RCV001804907]\|Cardiovascular phenotype [RCV002362912]\|Charcot-Marie-Tooth disease type 2 [RCV001429120]\|Primary dilated cardiomyopathy [RCV003996573]\|not provided [RCV000585450]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156134808	156134808	Human	4	name
10056825	CV196447	single nucleotide variant	NM_170707.4(LMNA):c.64T>G (p.Ser22Ala)	not provided [RCV000182379]	likely pathogenic\|conflicting interpretations of pathogenicity	1	156114982	156114982	Human		name
10056826	CV196448	single nucleotide variant	NM_170707.4(LMNA):c.77T>C (p.Ile26Thr)	Cardiovascular phenotype [RCV004992063]\|not provided [RCV000182380]	likely pathogenic\|uncertain significance	1	156114995	156114995	Human		name
10056811	CV196463	single nucleotide variant	NM_170707.4(LMNA):c.471G>A (p.Thr157=)	Cardiomyopathy [RCV000778038]\|Cardiovascular phenotype [RCV002336452]\|Charcot-Marie-Tooth disease type 2 [RCV001081191]\|Charcot-Marie-Tooth disease type 2B1 [RCV001101972]\|Congenital muscular dystrophy due to LMNA mutation [RCV001101973]\|Dilated cardiomyopathy 1 ... (more) A [RCV001099964]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001099966]\|Emery-Dreifuss muscular dystrophy [RCV001101971]\|Familial partial lipodystrophy, Dunnigan type [RCV001099969]\|Hutchinson-Gilford syndrome [RCV001099963]\|Lethal tight skin contracture syndrome [RCV001099968]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001099965]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001099967]\|not provided [RCV000727266]\|not specified [RCV000182358]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156130731	156130731	Human	16	name
10056816	CV196470	single nucleotide variant	NM_170707.4(LMNA):c.768G>A (p.Val256=)	Cardiovascular phenotype [RCV002399655]\|Charcot-Marie-Tooth disease type 2 [RCV000806148]\|Dilated cardiomyopathy 1A [RCV001199263]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005042396]\|Primary dilated cardiomyopathy [RCV000219229]\|not provided [RCV000182364]	pathogenic\|likely pathogenic\|uncertain significance	1	156134933	156134933	Human	16	name
156288560	CV1964774	single nucleotide variant	NM_170707.4(LMNA):c.40G>A (p.Ala14Thr)	Charcot-Marie-Tooth disease type 2 [RCV002577738]	uncertain significance	1	156114958	156114958	Human	1	name
156347138	CV1995326	single nucleotide variant	NM_170707.4(LMNA):c.28A>C (p.Thr10Pro)	Charcot-Marie-Tooth disease type 2 [RCV002650630]	likely pathogenic	1	156114946	156114946	Human	1	name
156025521	CV2078050	single nucleotide variant	NM_170707.4(LMNA):c.744G>C (p.Leu248=)	Charcot-Marie-Tooth disease type 2 [RCV002866818]	likely benign	1	156134909	156134909	Human	1	name
155911910	CV2085018	single nucleotide variant	NM_170707.4(LMNA):c.678G>T (p.Leu226=)	Charcot-Marie-Tooth disease type 2 [RCV002858557]	likely benign	1	156134843	156134843	Human	1	name
156243850	CV2086106	single nucleotide variant	NM_170707.4(LMNA):c.312G>C (p.Leu104=)	Charcot-Marie-Tooth disease type 2 [RCV002876694]	likely benign	1	156115230	156115230	Human	1	name
156128443	CV2104328	single nucleotide variant	NM_170707.4(LMNA):c.696G>C (p.Gly232=)	Charcot-Marie-Tooth disease type 2 [RCV002914457]	likely benign	1	156134861	156134861	Human	1	name
156096702	CV2110650	single nucleotide variant	NM_170707.4(LMNA):c.97G>C (p.Glu33Gln)	Charcot-Marie-Tooth disease type 2 [RCV002926889]	uncertain significance	1	156115015	156115015	Human	1	name
10448435	CV214482	single nucleotide variant	NM_170707.4(LMNA):c.80C>G (p.Thr27Ser)	Charcot-Marie-Tooth disease type 2 [RCV002517317]\|Paroxysmal familial ventricular fibrillation [RCV000201884]	uncertain significance	1	156114998	156114998	Human	2	name
155932162	CV2156784	single nucleotide variant	NM_170707.4(LMNA):c.378C>T (p.Asp126=)	Charcot-Marie-Tooth disease type 2 [RCV003013694]	likely benign	1	156130638	156130638	Human	1	name
156303722	CV2187787	single nucleotide variant	NM_170707.4(LMNA):c.645G>A (p.Leu215=)	Charcot-Marie-Tooth disease type 2 [RCV003062084]	likely benign	1	156134810	156134810	Human	1	name
156331995	CV2188104	deletion	NM_170707.4(LMNA):c.205del (p.Val69fs)	Charcot-Marie-Tooth disease type 2 [RCV003063750]	pathogenic	1	156115122	156115122	Human	1	name
11060030	CV226866	single nucleotide variant	NM_170707.4(LMNA):c.82C>G (p.Arg28Gly)	Inborn genetic diseases [RCV000210645]	likely pathogenic	1	156115000	156115000	Human	1	name
11088327	CV228272	single nucleotide variant	NM_170707.4(LMNA):c.346C>T (p.Leu116=)	Cardiomyopathy [RCV000771953]\|Cardiovascular phenotype [RCV002336594]\|Charcot-Marie-Tooth disease type 2 [RCV000904865]\|Primary dilated cardiomyopathy [RCV003997707]\|not specified [RCV000213438]	likely benign\|uncertain significance	1	156115264	156115264	Human	4	name
243062374	CV2404746	single nucleotide variant	NM_170707.4(LMNA):c.89A>C (p.Gln30Pro)	Congenital muscular dystrophy due to LMNA mutation [RCV003140303]	uncertain significance	1	156115007	156115007	Human	1	name
11523598	CV244207	single nucleotide variant	NM_170707.4(LMNA):c.74G>T (p.Arg25Leu)	Cardiomyopathy [RCV001182288]\|Cardiovascular phenotype [RCV002392726]\|Charcot-Marie-Tooth disease type 2 [RCV001079756]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005044491]\|Primary dilated cardiomyopathy [RCV003998902]\|not provided [RCV000236179]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156114992	156114992	Human	18	name
11544634	CV257936	single nucleotide variant	NM_170707.4(LMNA):c.927C>A (p.Leu309=)	Cardiomyopathy [RCV001180367]\|Cardiovascular phenotype [RCV000244053]\|Charcot-Marie-Tooth disease type 2 [RCV000950061]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002500943]\|Primary dilated cardiomyopathy [RCV003999028]\|not specified [RCV000433510]	likely benign	1	156135303	156135303	Human	18	name
11640808	CV265812	single nucleotide variant	NM_170707.4(LMNA):c.726G>A (p.Ala242=)	Cardiomyopathy [RCV001525715]\|Cardiovascular phenotype [RCV002379110]\|Charcot-Marie-Tooth disease type 2 [RCV001088674]\|Primary dilated cardiomyopathy [RCV003995754]\|not provided [RCV000345591]\|not specified [RCV000780388]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156134891	156134891	Human	4	name
401829050	CV2668630	single nucleotide variant	NM_170707.4(LMNA):c.95A>C (p.Lys32Thr)	Congenital muscular dystrophy due to LMNA mutation [RCV003326722]	pathogenic	1	156115013	156115013	Human	1	name
11642690	CV269705	single nucleotide variant	NM_170707.4(LMNA):c.83G>A (p.Arg28Gln)	Charcot-Marie-Tooth disease type 2 [RCV000809047]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV004577329]\|not provided [RCV000380269]	pathogenic\|likely pathogenic\|uncertain significance	1	156115001	156115001	Human	2	name
11643493	CV269962	single nucleotide variant	NM_170707.4(LMNA):c.498G>A (p.Arg166=)	Cardiovascular phenotype [RCV002338846]\|Charcot-Marie-Tooth disease type 2 [RCV002059182]\|not provided [RCV000395106]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156130758	156130758	Human	1	name
401718752	CV2730929	single nucleotide variant	NM_170707.4(LMNA):c.31C>T (p.Arg11Cys)	Cardiovascular phenotype [RCV003311164]\|Charcot-Marie-Tooth disease type 2 [RCV003745581]\|LMNA-related disorder [RCV004540639]\|not provided [RCV004763640]	uncertain significance	1	156114949	156114949	Human	1	name , alternate_id
11639574	CV273191	single nucleotide variant	NM_170707.4(LMNA):c.591G>A (p.Leu197=)	Cardiomyopathy [RCV003532078]\|Charcot-Marie-Tooth disease type 2 [RCV002059252]\|Primary dilated cardiomyopathy [RCV003995787]\|not provided [RCV000323285]	likely benign\|uncertain significance	1	156134480	156134480	Human	4	name
11637023	CV274945	single nucleotide variant	NM_170707.4(LMNA):c.732G>A (p.Ala244=)	Cardiomyopathy [RCV000769725]\|Cardiovascular phenotype [RCV004992167]\|Charcot-Marie-Tooth disease type 2 [RCV001416242]\|Primary dilated cardiomyopathy [RCV003995794]\|not provided [RCV000278718]	likely benign\|uncertain significance	1	156134897	156134897	Human	4	name
401933068	CV2806055	single nucleotide variant	NM_170707.4(LMNA):c.528A>G (p.Leu176=)	not provided [RCV003409141]	likely benign	1	156134417	156134417	Human		name
404978759	CV2852226	single nucleotide variant	NM_170707.4(LMNA):c.957G>A (p.Lys319=)	Cardiomyopathy [RCV003487232]	likely benign	1	156135921	156135921	Human	2	name
405084039	CV2856618	single nucleotide variant	NM_170707.4(LMNA):c.852G>T (p.Leu284=)	Charcot-Marie-Tooth disease type 2 [RCV003582333]	likely benign	1	156135228	156135228	Human	1	name
405083132	CV2859414	single nucleotide variant	NM_170707.4(LMNA):c.504G>A (p.Gln168=)	Cardiovascular phenotype [RCV004992627]\|Charcot-Marie-Tooth disease type 2 [RCV003582262]	likely benign	1	156130764	156130764	Human	1	name
405079968	CV2863655	single nucleotide variant	NM_170707.4(LMNA):c.582G>A (p.Glu194=)	Charcot-Marie-Tooth disease type 2 [RCV003581948]	likely benign	1	156134471	156134471	Human	1	name
405085341	CV2874138	single nucleotide variant	NM_170707.4(LMNA):c.516T>A (p.Leu172=)	Charcot-Marie-Tooth disease type 2 [RCV003582356]	uncertain significance	1	156134405	156134405	Human	1	name
405073939	CV2887018	single nucleotide variant	NM_170707.4(LMNA):c.894C>T (p.Arg298=)	Charcot-Marie-Tooth disease type 2 [RCV003581317]	likely benign	1	156135270	156135270	Human	1	name
405075033	CV2894287	single nucleotide variant	NM_170707.4(LMNA):c.304C>T (p.Leu102=)	Charcot-Marie-Tooth disease type 2 [RCV003581391]	likely benign	1	156115222	156115222	Human	1	name
405091925	CV2909640	single nucleotide variant	NM_170707.4(LMNA):c.756T>C (p.His252=)	Charcot-Marie-Tooth disease type 2 [RCV003582926]	likely benign	1	156134921	156134921	Human	1	name
405092216	CV2909921	single nucleotide variant	NM_170707.4(LMNA):c.74G>A (p.Arg25His)	Charcot-Marie-Tooth disease type 2 [RCV003582949]	likely pathogenic	1	156114992	156114992	Human	1	name
405063078	CV2934266	single nucleotide variant	NM_170707.4(LMNA):c.76A>C (p.Ile26Leu)	Cardiomyopathy [RCV003532550]	uncertain significance	1	156114994	156114994	Human	2	name
405063084	CV2934267	single nucleotide variant	NM_170707.4(LMNA):c.336G>A (p.Glu112=)	Cardiomyopathy [RCV003532551]	likely benign	1	156115254	156115254	Human	2	name
405063126	CV2934272	single nucleotide variant	NM_170707.4(LMNA):c.900C>T (p.Asp300=)	Cardiomyopathy [RCV003532556]	likely benign	1	156135276	156135276	Human	2	name
405093505	CV2943847	single nucleotide variant	NM_170707.4(LMNA):c.570G>A (p.Arg190=)	Charcot-Marie-Tooth disease type 2 [RCV003745651]	likely benign	1	156134459	156134459	Human	1	name
405095936	CV2950364	single nucleotide variant	NM_170707.4(LMNA):c.507G>A (p.Val169=)	Charcot-Marie-Tooth disease type 2 [RCV003745797]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005047727]	uncertain significance	1	156130767	156130767	Human	3	name
405081988	CV2975731	deletion	NM_170707.4(LMNA):c.274del (p.Asp93fs)	Charcot-Marie-Tooth disease type 2 [RCV003744060]	pathogenic	1	156115190	156115190	Human	1	name
405083708	CV2984813	single nucleotide variant	NM_170707.4(LMNA):c.409C>T (p.Leu137=)	Charcot-Marie-Tooth disease type 2 [RCV003744179]\|not provided [RCV004765932]	likely benign\|uncertain significance	1	156130669	156130669	Human	1	name
405086144	CV2991706	single nucleotide variant	NM_170707.4(LMNA):c.610C>T (p.Leu204=)	Charcot-Marie-Tooth disease type 2 [RCV003744368]	likely benign	1	156134499	156134499	Human	1	name
405086473	CV2993173	microsatellite	NM_170707.4(LMNA):c.1969-18_1969-16del	Charcot-Marie-Tooth disease type 2 [RCV003744417]	likely benign	1	156139059	156139061	Human		name
405088316	CV3004161	single nucleotide variant	NM_170707.4(LMNA):c.47C>T (p.Ala16Val)	Charcot-Marie-Tooth disease type 2 [RCV003744450]	uncertain significance	1	156114965	156114965	Human	1	name
405086933	CV3011404	single nucleotide variant	NM_170707.4(LMNA):c.786G>A (p.Glu262=)	Charcot-Marie-Tooth disease type 2 [RCV003744454]	likely benign	1	156134951	156134951	Human	1	name
405076719	CV3026023	duplication	NM_170707.4(LMNA):c.241dup (p.Tyr81fs)	Charcot-Marie-Tooth disease type 2 [RCV003743200]	pathogenic	1	156115158	156115159	Human	1	name
405078461	CV3040883	single nucleotide variant	NM_170707.4(LMNA):c.318G>C (p.Leu106=)	Charcot-Marie-Tooth disease type 2 [RCV003743316]	likely benign	1	156115236	156115236	Human	1	name
405091136	CV3079424	single nucleotide variant	NM_170707.4(LMNA):c.531T>C (p.Gly177=)	Charcot-Marie-Tooth disease type 2 [RCV003745210]	likely benign	1	156134420	156134420	Human	1	name
405020586	CV3139162	single nucleotide variant	NM_170707.4(LMNA):c.55A>T (p.Thr19Ser)	Charcot-Marie-Tooth disease type 2 [RCV003829804]	uncertain significance	1	156114973	156114973	Human	1	name
405236218	CV3166442	single nucleotide variant	NM_170707.4(LMNA):c.996C>T (p.Asp332=)	Charcot-Marie-Tooth disease type 2 [RCV003853891]	likely benign	1	156135960	156135960	Human	1	name
405213003	CV3169763	single nucleotide variant	NM_170707.4(LMNA):c.645G>C (p.Leu215=)	Cardiovascular phenotype [RCV004369571]\|Charcot-Marie-Tooth disease type 2 [RCV003862362]	likely benign	1	156134810	156134810	Human	1	name
405254390	CV3175106	single nucleotide variant	NM_170707.4(LMNA):c.615C>T (p.Asp205=)	Charcot-Marie-Tooth disease type 2 [RCV003871558]\|Primary dilated cardiomyopathy [RCV004006165]	likely benign	1	156134504	156134504	Human	2	name
405656728	CV3227954	deletion	NM_170707.4(LMNA):c.174del (p.Leu59fs)	Primary dilated cardiomyopathy [RCV003994696]	pathogenic	1	156115090	156115090	Human	1	name
405738986	CV3228842	single nucleotide variant	NM_170707.4(LMNA):c.58C>T (p.Pro20Ser)	Cardiovascular phenotype [RCV004994419]\|Primary dilated cardiomyopathy [RCV004014763]	uncertain significance	1	156114976	156114976	Human	1	name
405740332	CV3229216	single nucleotide variant	NM_170707.4(LMNA):c.562C>T (p.Leu188=)	Primary dilated cardiomyopathy [RCV004014959]	likely benign	1	156134451	156134451	Human	1	name
405723204	CV3230289	single nucleotide variant	NM_170707.4(LMNA):c.777T>C (p.Tyr259=)	Primary dilated cardiomyopathy [RCV004013041]	likely benign	1	156134942	156134942	Human	1	name
405736047	CV3230646	single nucleotide variant	NM_170707.4(LMNA):c.306G>A (p.Leu102=)	Charcot-Marie-Tooth disease type 2 [RCV005103243]\|Primary dilated cardiomyopathy [RCV004014392]	likely benign	1	156115224	156115224	Human	2	name
405754004	CV3232475	single nucleotide variant	NM_170707.4(LMNA):c.46G>T (p.Ala16Ser)	Primary dilated cardiomyopathy [RCV004016610]	uncertain significance	1	156114964	156114964	Human	1	name
596941209	CV3546139	single nucleotide variant	NM_170707.4(LMNA):c.565C>A (p.Arg189=)	Primary dilated cardiomyopathy [RCV004806768]	likely benign	1	156134454	156134454	Human	1	name
12837347	CV364520	single nucleotide variant	NM_170707.4(LMNA):c.948G>A (p.Lys316=)	Cardiomyopathy [RCV001524079]\|Cardiovascular phenotype [RCV002374685]\|Charcot-Marie-Tooth disease type 2 [RCV000473779]\|not provided [RCV001712277]	benign\|likely benign	1	156135912	156135912	Human	3	name
597722732	CV3701644	single nucleotide variant	NM_170707.4(LMNA):c.330T>A (p.Arg110=)	Cardiovascular phenotype [RCV004993760]	likely benign	1	156115248	156115248	Human		name
597722737	CV3701645	single nucleotide variant	NM_170707.4(LMNA):c.492T>C (p.Asp164=)	Cardiovascular phenotype [RCV004993761]	likely benign	1	156130752	156130752	Human		name
597722743	CV3701646	single nucleotide variant	NM_170707.4(LMNA):c.501C>G (p.Gly167=)	Cardiovascular phenotype [RCV004993762]	likely benign	1	156130761	156130761	Human		name
597653027	CV3719774	single nucleotide variant	NM_170707.4(LMNA):c.41C>T (p.Ala14Val)	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005041310]	uncertain significance	1	156114959	156114959	Human	2	name
597653294	CV3719797	single nucleotide variant	NM_170707.4(LMNA):c.64T>C (p.Ser22Pro)	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005041342]	uncertain significance	1	156114982	156114982	Human	2	name
597921590	CV3738402	single nucleotide variant	NM_170707.4(LMNA):c.28A>T (p.Thr10Ser)	Charcot-Marie-Tooth disease type 2 [RCV005074809]	likely pathogenic	1	156114946	156114946	Human	1	name
597852650	CV3747081	single nucleotide variant	NM_170707.4(LMNA):c.882G>A (p.Gln294=)	Charcot-Marie-Tooth disease type 2 [RCV005060710]	likely benign	1	156135258	156135258	Human	1	name
597938748	CV3759980	single nucleotide variant	NM_170707.4(LMNA):c.393G>A (p.Gln131=)	Charcot-Marie-Tooth disease type 2 [RCV005076902]	likely benign	1	156130653	156130653	Human	1	name
597910454	CV3770377	single nucleotide variant	NM_170707.4(LMNA):c.29C>G (p.Thr10Ser)	Charcot-Marie-Tooth disease type 2 [RCV005113678]	likely pathogenic	1	156114947	156114947	Human	1	name
597910460	CV3770378	single nucleotide variant	NM_170707.4(LMNA):c.44A>G (p.Gln15Arg)	Charcot-Marie-Tooth disease type 2 [RCV005113679]	uncertain significance	1	156114962	156114962	Human	1	name
597928489	CV3779743	deletion	NM_170707.4(LMNA):c.208del (p.Val70fs)	Charcot-Marie-Tooth disease type 2 [RCV005116272]	pathogenic	1	156115125	156115125	Human	1	name
597883781	CV3784310	single nucleotide variant	NM_170707.4(LMNA):c.441A>T (p.Ala147=)	Charcot-Marie-Tooth disease type 2 [RCV005124598]	likely benign	1	156130701	156130701	Human	1	name
597975846	CV3795960	single nucleotide variant	NM_170707.4(LMNA):c.381G>C (p.Leu127=)	Charcot-Marie-Tooth disease type 2 [RCV005144791]	likely benign	1	156130641	156130641	Human	1	name
597954970	CV3809374	single nucleotide variant	NM_170707.4(LMNA):c.525C>T (p.Ala175=)	Charcot-Marie-Tooth disease type 2 [RCV005162098]	likely benign	1	156134414	156134414	Human	1	name
597888749	CV3839484	single nucleotide variant	NM_170707.4(LMNA):c.85C>A (p.Leu29Met)	Charcot-Marie-Tooth disease type 2 [RCV005179376]	uncertain significance	1	156115003	156115003	Human	1	name
597899839	CV3850854	single nucleotide variant	NM_170707.4(LMNA):c.384A>T (p.Ile128=)	Charcot-Marie-Tooth disease type 2 [RCV005201838]	likely benign	1	156130644	156130644	Human	1	name
597938558	CV3852858	duplication	NM_170707.4(LMNA):c.282dup (p.Val95fs)	Charcot-Marie-Tooth disease type 2 [RCV005187259]	pathogenic	1	156115199	156115200	Human	1	name
597915859	CV3860922	single nucleotide variant	NM_170707.4(LMNA):c.891C>T (p.Ile297=)	Charcot-Marie-Tooth disease type 2 [RCV005204285]	likely benign	1	156135267	156135267	Human	1	name
12886895	CV390813	single nucleotide variant	NM_170707.4(LMNA):c.711T>C (p.Phe237=)	Cardiovascular phenotype [RCV002367595]\|Charcot-Marie-Tooth disease type 2 [RCV001481809]	likely benign	1	156134876	156134876	Human	1	name
12883611	CV390829	single nucleotide variant	NM_170707.4(LMNA):c.681G>A (p.Val227=)	Charcot-Marie-Tooth disease type 2 [RCV001455501]\|not specified [RCV005404609]	likely benign	1	156134846	156134846	Human	1	name
616934662	CV4009801	single nucleotide variant	NM_170707.4(LMNA):c.306G>C (p.Leu102=)	Cardiomyopathy [RCV005400959]	likely benign	1	156115224	156115224	Human	2	name
616937358	CV4010999	single nucleotide variant	NM_170707.4(LMNA):c.906C>T (p.Leu302=)	not specified [RCV005404843]	likely benign	1	156135282	156135282	Human		name
13482605	CV447227	single nucleotide variant	NM_170707.4(LMNA):c.94A>G (p.Lys32Glu)	Charcot-Marie-Tooth disease type 2 [RCV000529491]\|Congenital muscular dystrophy due to LMNA mutation [RCV000785916]	pathogenic\|likely pathogenic	1	156115012	156115012	Human	2	name
13498378	CV447231	single nucleotide variant	NM_170707.4(LMNA):c.771G>A (p.Glu257=)	Cardiovascular phenotype [RCV002404568]\|Charcot-Marie-Tooth disease type 2 [RCV001493413]\|Primary dilated cardiomyopathy [RCV003999470]	likely benign	1	156134936	156134936	Human	2	name
13480829	CV447240	single nucleotide variant	NM_170707.4(LMNA):c.477G>A (p.Glu159=)	Cardiovascular phenotype [RCV002341465]\|Charcot-Marie-Tooth disease type 2 [RCV001432751]	likely benign	1	156130737	156130737	Human	1	name
13486847	CV447243	single nucleotide variant	NM_170707.4(LMNA):c.870G>A (p.Glu290=)	Cardiomyopathy [RCV001191882]\|Cardiovascular phenotype [RCV002448795]\|Charcot-Marie-Tooth disease type 2 [RCV000553950]\|Primary dilated cardiomyopathy [RCV003999471]\|not provided [RCV000597468]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156135246	156135246	Human	4	name
13464666	CV447254	single nucleotide variant	NM_170707.4(LMNA):c.897C>T (p.Ile299=)	Cardiomyopathy [RCV001185071]\|Cardiovascular phenotype [RCV000617823]\|Charcot-Marie-Tooth disease type 2 [RCV000542339]\|Primary dilated cardiomyopathy [RCV003999472]	likely benign\|conflicting interpretations of pathogenicity	1	156135273	156135273	Human	4	name
13494446	CV447317	single nucleotide variant	NM_170707.4(LMNA):c.990G>A (p.Glu330=)	Cardiomyopathy [RCV001805190]\|Cardiovascular phenotype [RCV000621804]\|Charcot-Marie-Tooth disease type 2 [RCV001078841]\|not provided [RCV000831068]\|not specified [RCV005239219]	likely benign	1	156135954	156135954	Human	3	name
13518522	CV486016	single nucleotide variant	NM_170707.4(LMNA):c.867C>T (p.His289=)	Cardiomyopathy [RCV001178182]\|Cardiovascular phenotype [RCV002448816]\|Charcot-Marie-Tooth disease type 2 [RCV001454538]\|LMNA-related disorder [RCV004530631]\|Primary dilated cardiomyopathy [RCV004002385]\|not provided [RCV000584877]	likely benign\|uncertain significance	1	156135243	156135243	Human	4	name , alternate_id
13519723	CV490436	single nucleotide variant	NM_170707.4(LMNA):c.483G>A (p.Glu161=)	Cardiovascular phenotype [RCV002341521]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002483600]\|not provided [RCV000598095]	likely benign\|uncertain significance	1	156130743	156130743	Human	15	name
13520060	CV490807	single nucleotide variant	NM_170707.4(LMNA):c.528A>T (p.Leu176=)	Cardiomyopathy [RCV001178641]\|Charcot-Marie-Tooth disease type 2 [RCV001448884]\|Primary dilated cardiomyopathy [RCV004002459]\|not provided [RCV000598349]	likely benign\|uncertain significance	1	156134417	156134417	Human	4	name
13541965	CV498067	single nucleotide variant	NM_170707.4(LMNA):c.657G>A (p.Lys219=)	Cardiovascular phenotype [RCV002368042]\|not specified [RCV000616882]	likely benign	1	156134822	156134822	Human		name
13538466	CV498071	single nucleotide variant	NM_170707.4(LMNA):c.526C>T (p.Leu176=)	Charcot-Marie-Tooth disease type 2 [RCV001440390]\|not specified [RCV000611876]	likely benign	1	156134415	156134415	Human	1	name
13533485	CV509112	single nucleotide variant	NM_170707.4(LMNA):c.480C>T (p.Gly160=)	Cardiomyopathy [RCV003532203]\|Cardiovascular phenotype [RCV000617617]\|Charcot-Marie-Tooth disease type 2 [RCV001314765]\|Primary dilated cardiomyopathy [RCV004002700]	likely benign\|uncertain significance	1	156130740	156130740	Human	4	name
13528917	CV509114	single nucleotide variant	NM_170707.4(LMNA):c.579T>C (p.Ala193=)	Cardiomyopathy [RCV001185528]\|Cardiovascular phenotype [RCV000621074]\|Charcot-Marie-Tooth disease [RCV001173405]\|Charcot-Marie-Tooth disease type 2 [RCV001485044]\|Primary dilated cardiomyopathy [RCV004002685]\|not provided [RCV000712225]	likely benign	1	156134468	156134468	Human	5	name
13533310	CV509116	single nucleotide variant	NM_170707.4(LMNA):c.729T>C (p.Asp243=)	Cardiomyopathy [RCV001176482]\|Cardiovascular phenotype [RCV000617357]\|Charcot-Marie-Tooth disease type 2 [RCV003581699]\|Primary dilated cardiomyopathy [RCV004002712]	likely benign	1	156134894	156134894	Human	4	name
13529144	CV513494	single nucleotide variant	NM_170707.4(LMNA):c.59C>T (p.Pro20Leu)	Charcot-Marie-Tooth disease type 2 [RCV003581701]\|Congenital muscular dystrophy due to LMNA mutation [RCV000626229]	likely pathogenic\|uncertain significance	1	156114977	156114977	Human	2	name
13821187	CV556955	single nucleotide variant	NM_170707.4(LMNA):c.91G>A (p.Glu31Lys)	Charcot-Marie-Tooth disease type 2 [RCV000695532]\|not provided [RCV003456423]	pathogenic	1	156115009	156115009	Human	1	name
8610926	CV57226	single nucleotide variant	NM_170707.4(LMNA):c.357C>T (p.Arg119=)	Cardiomyopathy [RCV000768710]\|Cardiovascular phenotype [RCV000249770]\|Charcot-Marie-Tooth disease [RCV001173420]\|Charcot-Marie-Tooth disease type 2 [RCV001081311]\|Charcot-Marie-Tooth disease type 2B1 [RCV001101880]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV001101879]\|Dilated cardiomyopathy 1A [RCV001101878]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001096445]\|Emery-Dreifuss muscular dystrophy [RCV000148598]\|Familial partial lipodystrophy, Dunnigan type [RCV001096443]\|Hutchinson-Gilford syndrome [RCV001096446]\|LMNA-related disorder [RCV004528231]\|Lethal tight skin contracture syndrome [RCV001096444]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001101881]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001096447]\|Primary dilated cardiomyopathy [RCV000211467]\|not provided [RCV000057395]\|not specified [RCV000041345]	pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156130617	156130617	Human	17	name , alternate_id
8610930	CV57230	single nucleotide variant	NM_170707.4(LMNA):c.438C>T (p.Ala146=)	Cardiomyopathy [RCV000768711]\|Cardiovascular phenotype [RCV000617451]\|Charcot-Marie-Tooth disease type 2 [RCV001086851]\|LMNA-related disorder [RCV004528232]\|Primary dilated cardiomyopathy [RCV003996463]\|not provided [RCV000587594]\|not specified [RCV000041349]	benign\|likely benign\|conflicting interpretations of pathogenicity\|conflicting data from submitters	1	156130698	156130698	Human	4	name , alternate_id
8610934	CV57235	single nucleotide variant	NM_170707.4(LMNA):c.612G>A (p.Leu204=)	Cardiomyopathy [RCV000768713]\|Cardiovascular phenotype [RCV000253205]\|Charcot-Marie-Tooth disease [RCV001173422]\|Charcot-Marie-Tooth disease type 2 [RCV000226227]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093797]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000379768]\|Dilated cardiomyopathy 1A [RCV000390872]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001096564]\|Emery-Dreifuss muscular dystrophy [RCV000403709]\|Familial partial lipodystrophy, Dunnigan type [RCV000346784]\|Hutchinson-Gilford syndrome [RCV000285363]\|Lethal tight skin contracture syndrome [RCV000344918]\|Limb-girdle muscular dystrophy, recessive [RCV000371234]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000311894]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000291863]\|Primary dilated cardiomyopathy [RCV003996464]\|not provided [RCV000057430]\|not specified [RCV000041356]	likely pathogenic\|benign\|likely benign\|not provided	1	156134501	156134501	Human	18	name
8610944	CV57246	single nucleotide variant	NM_170707.4(LMNA):c.789G>A (p.Leu263=)	Cardiomyopathy [RCV001178117]\|Cardiovascular phenotype [RCV000617711]\|Charcot-Marie-Tooth disease type 2 [RCV001085667]\|Primary dilated cardiomyopathy [RCV003996465]\|not provided [RCV000723485]\|not specified [RCV000041367]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156134954	156134954	Human	4	name
8610950	CV57252	single nucleotide variant	NM_170707.4(LMNA):c.861T>C (p.Ala287=)	Cardiomyopathy [RCV000776003]\|Cardiovascular phenotype [RCV000249986]\|Charcot-Marie-Tooth disease [RCV001173415]\|Charcot-Marie-Tooth disease type 2 [RCV000408212]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093907]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000332471]\|Dilated cardiomyopathy 1A [RCV000303946]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001102163]\|Emery-Dreifuss muscular dystrophy [RCV000335802]\|Familial partial lipodystrophy, Dunnigan type [RCV000389150]\|Hutchinson-Gilford syndrome [RCV000281700]\|Lethal tight skin contracture syndrome [RCV000278366]\|Limb-girdle muscular dystrophy, recessive [RCV000385848]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000339029]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000374142]\|Primary dilated cardiomyopathy [RCV003125877]\|not provided [RCV000057475]\|not specified [RCV000041374]	benign\|conflicting interpretations of pathogenicity\|conflicting data from submitters\|not provided	1	156135237	156135237	Human	18	name
8610956	CV57258	single nucleotide variant	NM_170707.4(LMNA):c.954G>A (p.Ala318=)	Charcot-Marie-Tooth disease type 2 [RCV001447601]\|Primary dilated cardiomyopathy [RCV003996466]\|not provided [RCV002225280]\|not specified [RCV000041380]	likely benign\|uncertain significance	1	156135918	156135918	Human	2	name
13810277	CV576411	single nucleotide variant	NM_170707.4(LMNA):c.65C>T (p.Ser22Leu)	Cardiomyopathy [RCV001798969]\|Cardiovascular phenotype [RCV005348205]\|Charcot-Marie-Tooth disease type 2 [RCV001318123]\|Dilated cardiomyopathy 1A [RCV003147538]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002477648]\|Primary dilated cardiomyopathy [RCV003999795]\|not provided [R ... (more) CV000712226]	likely pathogenic\|uncertain significance	1	156114983	156114983	Human	18	name
14692153	CV616007	single nucleotide variant	NM_170707.4(LMNA):c.969G>A (p.Leu323=)	Cardiomyopathy [RCV000773421]\|Charcot-Marie-Tooth disease type 2 [RCV002067266]	likely benign	1	156135933	156135933	Human	3	name
14725840	CV626902	single nucleotide variant	NM_170707.4(LMNA):c.71C>G (p.Thr24Ser)	Cardiomyopathy [RCV003532266]\|Cardiovascular phenotype [RCV002370101]\|Charcot-Marie-Tooth disease type 2 [RCV000798982]	uncertain significance	1	156114989	156114989	Human	3	name
14718637	CV626903	single nucleotide variant	NM_170707.4(LMNA):c.94A>T (p.Lys32Ter)	Charcot-Marie-Tooth disease type 2 [RCV000812291]\|Dilated cardiomyopathy 1A [RCV004789213]	pathogenic	1	156115012	156115012	Human	3	name
14728493	CV626910	single nucleotide variant	NM_170707.4(LMNA):c.573G>A (p.Val191=)	Cardiovascular phenotype [RCV003166354]\|Charcot-Marie-Tooth disease type 2 [RCV000816543]\|Primary dilated cardiomyopathy [RCV004807203]	likely benign\|uncertain significance	1	156134462	156134462	Human	2	name
14977180	CV677482	deletion	NM_170707.4(LMNA):c.1157+23_1158-45del	LMNA-associated condition [RCV000850629]	likely pathogenic	1	156136142	156136167	Human		name
28881792	CV682590	single nucleotide variant	NM_170707.4(LMNA):c.58C>A (p.Pro20Thr)	Hypertrophic cardiomyopathy [RCV001093543]	likely pathogenic	1	156114976	156114976	Human	1	name
15139146	CV685573	single nucleotide variant	NM_170707.4(LMNA):c.885G>A (p.Ser295=)	Cardiomyopathy [RCV001176530]\|Cardiovascular phenotype [RCV002372417]\|Charcot-Marie-Tooth disease type 2 [RCV000864955]\|Primary dilated cardiomyopathy [RCV004002953]\|not specified [RCV001000647]	likely benign	1	156135261	156135261	Human	4	name
15156050	CV685574	single nucleotide variant	NM_170707.4(LMNA):c.951G>A (p.Glu317=)	Charcot-Marie-Tooth disease type 2 [RCV001417843]\|LMNA-related disorder [RCV004538266]	likely benign	1	156135915	156135915	Human	1	name , alternate_id
15124023	CV690376	single nucleotide variant	NM_170707.4(LMNA):c.852G>A (p.Leu284=)	Charcot-Marie-Tooth disease type 2 [RCV001442109]	likely benign	1	156135228	156135228	Human	1	name
15123797	CV745732	single nucleotide variant	NM_170707.4(LMNA):c.339T>C (p.Phe113=)	Cardiovascular phenotype [RCV004994109]\|Charcot-Marie-Tooth disease type 2 [RCV001436785]	likely benign	1	156115257	156115257	Human	1	name
15200919	CV745733	single nucleotide variant	NM_170707.4(LMNA):c.496C>A (p.Arg166=)	Charcot-Marie-Tooth disease type 2 [RCV001436333]	likely benign	1	156130756	156130756	Human	1	name
15133783	CV745734	single nucleotide variant	NM_170707.4(LMNA):c.822C>G (p.Ala274=)	Charcot-Marie-Tooth disease type 2 [RCV000920575]\|Primary dilated cardiomyopathy [RCV004003185]	likely benign	1	156135198	156135198	Human	2	name
15107115	CV761249	single nucleotide variant	NM_170707.4(LMNA):c.372G>A (p.Glu124=)	Cardiovascular phenotype [RCV003363020]\|Charcot-Marie-Tooth disease type 2 [RCV001405568]	likely benign	1	156130632	156130632	Human	1	name
15116320	CV761250	single nucleotide variant	NM_170707.4(LMNA):c.909T>A (p.Ser303=)	Charcot-Marie-Tooth disease type 2 [RCV001451208]	likely benign	1	156135285	156135285	Human	1	name
8622761	CV77785	single nucleotide variant	NM_170707.4(LMNA):c.29C>T (p.Thr10Ile)	Dilated cardiomyopathy 1A [RCV000015599]\|Familial partial lipodystrophy, Dunnigan type [RCV000502816]\|Inborn genetic diseases [RCV000622546]\|Lipodystrophy [RCV000755005]\|not provided [RCV000057387]	pathogenic\|likely pathogenic\|not provided	1	156114947	156114947	Human	6	name
8622775	CV77799	single nucleotide variant	NM_170707.4(LMNA):c.513G>A (p.Lys171=)	Charcot-Marie-Tooth disease type 2 [RCV001231297]\|not provided [RCV000057412]	likely pathogenic\|not provided	1	156130773	156130773	Human	1	name
8622799	CV77823	single nucleotide variant	NM_170707.4(LMNA):c.723G>A (p.Leu241=)	not provided [RCV000057447]	not provided	1	156134888	156134888	Human		name
8622801	CV77825	single nucleotide variant	NM_170707.4(LMNA):c.73C>G (p.Arg25Gly)	Cardiovascular phenotype [RCV002381367]\|Charcot-Marie-Tooth disease type 2 [RCV001048135]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV005409613]\|not provided [RCV000057449]	pathogenic\|likely pathogenic\|uncertain significance\|not provided	1	156114991	156114991	Human	3	name
8622802	CV77826	single nucleotide variant	NM_170707.4(LMNA):c.73C>T (p.Arg25Cys)	Cardiovascular phenotype [RCV002381368]\|Charcot-Marie-Tooth disease type 2 [RCV001049614]\|Dilated cardiomyopathy 1A [RCV005001985]\|not provided [RCV000057450]	likely pathogenic\|uncertain significance\|not provided	1	156114991	156114991	Human	4	name
8622805	CV77829	single nucleotide variant	NM_170707.4(LMNA):c.74G>C (p.Arg25Pro)	Charcot-Marie-Tooth disease type 2 [RCV002513740]\|not provided [RCV000057454]	likely pathogenic\|not provided	1	156114992	156114992	Human	1	name
8622815	CV77839	single nucleotide variant	NM_170707.4(LMNA):c.810G>A (p.Lys270=)	Charcot-Marie-Tooth disease type 2 [RCV005089471]\|not provided [RCV000057468]	uncertain significance\|not provided	1	156134975	156134975	Human	1	name
8622819	CV77843	single nucleotide variant	NM_170707.4(LMNA):c.82C>T (p.Arg28Trp)	Charcot-Marie-Tooth disease type 2 [RCV000653924]\|not provided [RCV000057473]	pathogenic\|not provided	1	156115000	156115000	Human	1	name
8622835	CV77859	single nucleotide variant	NM_170707.4(LMNA):c.98A>G (p.Glu33Gly)	Charcot-Marie-Tooth disease type 2 [RCV002513742]\|not provided [RCV000057495]	pathogenic\|not provided	1	156115016	156115016	Human	1	name
8622837	CV77861	single nucleotide variant	NM_170707.4(LMNA):c.99G>C (p.Glu33Asp)	not provided [RCV000057497]	likely pathogenic\|not provided	1	156115017	156115017	Human		name
8622838	CV77862	single nucleotide variant	NM_170707.4(LMNA):c.99G>T (p.Glu33Asp)	Charcot-Marie-Tooth disease [RCV000790002]\|Charcot-Marie-Tooth disease type 2 [RCV001854179]\|not provided [RCV000057498]	pathogenic\|uncertain significance\|not provided	1	156115017	156115017	Human	2	name
21069316	CV792654	single nucleotide variant	NM_170707.4(LMNA):c.80C>T (p.Thr27Ile)	Charcot-Marie-Tooth disease type 2 [RCV005092985]\|Dilated cardiomyopathy 1A [RCV000991275]	likely pathogenic	1	156114998	156114998	Human	3	name
26887248	CV822791	deletion	NM_170707.4(LMNA):c.210del (p.Ser71fs)	Charcot-Marie-Tooth disease type 2 [RCV001044761]	pathogenic	1	156115128	156115128	Human	1	name
28880312	CV858766	single nucleotide variant	NM_170707.4(LMNA):c.62T>C (p.Leu21Pro)	Charcot-Marie-Tooth disease type 2 [RCV002298871]\|Developmental regression [RCV001090180]	uncertain significance	1	156114980	156114980	Human	4	name
28893325	CV903710	single nucleotide variant	NM_170707.4(LMNA):c.37G>A (p.Gly13Arg)	Cardiomyopathy [RCV001170448]	uncertain significance	1	156114955	156114955	Human	2	name
34899852	CV906408	single nucleotide variant	NM_170707.4(LMNA):c.300C>G (p.Ala100=)	Cardiomyopathy [RCV001189057]	likely benign	1	156115218	156115218	Human	2	name
34894715	CV906409	single nucleotide variant	NM_170707.4(LMNA):c.369G>A (p.Lys123=)	Cardiomyopathy [RCV001184852]\|Cardiovascular phenotype [RCV002356847]\|Charcot-Marie-Tooth disease type 2 [RCV001426027]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002480613]\|Primary dilated cardiomyopathy [RCV004008491]	likely benign	1	156130629	156130629	Human	18	name
34899994	CV906411	single nucleotide variant	NM_170707.4(LMNA):c.480C>A (p.Gly160=)	Cardiomyopathy [RCV001189286]\|Charcot-Marie-Tooth disease type 2 [RCV003117829]\|Primary dilated cardiomyopathy [RCV004010354]	likely benign	1	156130740	156130740	Human	4	name
34900601	CV906416	single nucleotide variant	NM_170707.4(LMNA):c.537C>T (p.Ala179=)	Cardiomyopathy [RCV001190328]	likely benign	1	156134426	156134426	Human	2	name
34893927	CV906418	single nucleotide variant	NM_170707.4(LMNA):c.624G>A (p.Lys208=)	Cardiomyopathy [RCV001176943]\|Charcot-Marie-Tooth disease type 2 [RCV002559708]	likely benign	1	156134513	156134513	Human	3	name
34889326	CV906419	single nucleotide variant	NM_170707.4(LMNA):c.660C>T (p.Arg220=)	Cardiomyopathy [RCV001181411]\|Cardiovascular phenotype [RCV004994282]	likely benign	1	156134825	156134825	Human	2	name
34892775	CV906420	single nucleotide variant	NM_170707.4(LMNA):c.678G>A (p.Leu226=)	Cardiomyopathy [RCV001176008]\|Cardiovascular phenotype [RCV002365834]\|Charcot-Marie-Tooth disease type 2 [RCV001426917]\|Primary dilated cardiomyopathy [RCV004000313]	likely benign	1	156134843	156134843	Human	4	name
34898880	CV906421	single nucleotide variant	NM_170707.4(LMNA):c.693T>C (p.Asn231=)	Cardiomyopathy [RCV001180344]	likely benign	1	156134858	156134858	Human	2	name
34893214	CV906422	single nucleotide variant	NM_170707.4(LMNA):c.765G>A (p.Gln255=)	Cardiomyopathy [RCV001183665]\|Charcot-Marie-Tooth disease type 2 [RCV002068360]\|Primary dilated cardiomyopathy [RCV004008398]	likely benign	1	156134930	156134930	Human	4	name
34898705	CV906424	single nucleotide variant	NM_170707.4(LMNA):c.843C>T (p.Asn281=)	Cardiomyopathy [RCV001180196]\|Charcot-Marie-Tooth disease type 2 [RCV001401182]	likely benign	1	156135219	156135219	Human	3	name
38473845	CV921664	single nucleotide variant	NM_170707.4(LMNA):c.92A>G (p.Glu31Gly)	Charcot-Marie-Tooth disease type 2 [RCV001214508]	pathogenic	1	156115010	156115010	Human	1	name
38484734	CV941494	single nucleotide variant	NM_170707.4(LMNA):c.471G>T (p.Thr157=)	Charcot-Marie-Tooth disease type 2 [RCV001236489]	uncertain significance	1	156130731	156130731	Human	1	name
8642203	CV101187	single nucleotide variant	NM_170707.4(LMNA):c.148C>T (p.Arg50Cys)	Congenital muscular dystrophy due to LMNA mutation [RCV003987355]\|not provided [RCV000081302]	pathogenic\|uncertain significance	1	156115066	156115066	Human	1	name
152135338	CV1571870	single nucleotide variant	NM_170707.4(LMNA):c.1578G>T (p.Leu526=)	Cardiovascular phenotype [RCV002398163]\|Charcot-Marie-Tooth disease type 2 [RCV002177348]	likely benign	1	156137202	156137202	Human	1	name
152159467	CV1588091	single nucleotide variant	NM_170707.4(LMNA):c.1116G>A (p.Glu372=)	Charcot-Marie-Tooth disease type 2 [RCV002180673]	likely benign	1	156136080	156136080	Human	1	name
153304346	CV1686963	single nucleotide variant	NM_170707.4(LMNA):c.1179T>C (p.Pro393=)	Charcot-Marie-Tooth disease type 2 [RCV005058195]\|not provided [RCV002262250]	likely benign	1	156136235	156136235	Human	1	name
155643878	CV1708188	single nucleotide variant	NM_170707.4(LMNA):c.145G>T (p.Val49Leu)	Congenital muscular dystrophy due to LMNA mutation [RCV002290177]	uncertain significance	1	156115063	156115063	Human	1	name
9691068	CV172341	single nucleotide variant	NM_170707.4(LMNA):c.178C>T (p.Arg60Cys)	Cardiomyopathy [RCV000768709]\|Charcot-Marie-Tooth disease type 2 [RCV001206073]\|Dilated cardiomyopathy 1A [RCV004786415]\|not specified [RCV000156772]	pathogenic\|likely pathogenic\|uncertain significance	1	156115096	156115096	Human	5	name
9690775	CV172342	single nucleotide variant	NM_170707.4(LMNA):c.234G>C (p.Lys78Asn)	Charcot-Marie-Tooth disease type 2 [RCV003581579]\|not specified [RCV000156465]	uncertain significance	1	156115152	156115152	Human	1	name
9687837	CV172346	single nucleotide variant	NM_170707.4(LMNA):c.1122C>T (p.His374=)	Cardiomyopathy [RCV001182014]\|Cardiovascular phenotype [RCV000242405]\|Charcot-Marie-Tooth disease type 2 [RCV001046037]\|not provided [RCV000725445]\|not specified [RCV000150949]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156136086	156136086	Human	3	name
9689040	CV172481	single nucleotide variant	NM_170707.4(LMNA):c.215G>T (p.Arg72Leu)	Cardiovascular phenotype [RCV002426738]\|Charcot-Marie-Tooth disease type 2 [RCV001059604]\|not specified [RCV000154457]	pathogenic\|likely pathogenic\|uncertain significance	1	156115133	156115133	Human	1	name
155743706	CV1806923	duplication	NM_170707.4(LMNA):c.561dup (p.Leu188fs)	Cardiovascular phenotype [RCV002345004]	pathogenic	1	156134449	156134450	Human		name
155722927	CV1831433	single nucleotide variant	NM_170707.4(LMNA):c.1725C>T (p.Asp575=)	Cardiovascular phenotype [RCV002399113]\|Charcot-Marie-Tooth disease type 2 [RCV003097178]\|Primary dilated cardiomyopathy [RCV004808318]	likely benign	1	156138514	156138514	Human	2	name
155737920	CV1831777	single nucleotide variant	NM_170707.4(LMNA):c.1806C>T (p.Gly602=)	Cardiovascular phenotype [RCV002410074]	likely benign	1	156138595	156138595	Human		name
155732296	CV1835092	single nucleotide variant	NM_170707.4(LMNA):c.1800C>T (p.Ala600=)	Cardiovascular phenotype [RCV002407906]	likely benign	1	156138589	156138589	Human		name
155732548	CV1835391	single nucleotide variant	NM_170707.4(LMNA):c.1887G>C (p.Val629=)	Cardiovascular phenotype [RCV002407951]	likely benign	1	156138676	156138676	Human		name
155733945	CV1842744	single nucleotide variant	NM_170707.4(LMNA):c.1005G>C (p.Arg335=)	Cardiovascular phenotype [RCV002408315]	likely benign	1	156135969	156135969	Human		name
155739261	CV1842947	single nucleotide variant	NM_170707.4(LMNA):c.1914G>A (p.Gly638=)	Cardiovascular phenotype [RCV002410596]	likely benign	1	156138703	156138703	Human		name
155748461	CV1847127	single nucleotide variant	NM_170707.4(LMNA):c.212G>T (p.Ser71Ile)	Cardiovascular phenotype [RCV002417754]\|Charcot-Marie-Tooth disease type 2 [RCV003775107]\|not provided [RCV004765511]\|not specified [RCV003121030]	uncertain significance	1	156115130	156115130	Human	1	name
155669094	CV1848870	single nucleotide variant	NM_170707.4(LMNA):c.257G>A (p.Gly86Glu)	Cardiovascular phenotype [RCV002452831]	uncertain significance	1	156115175	156115175	Human		name
156217246	CV1903428	single nucleotide variant	NM_170707.4(LMNA):c.208G>A (p.Val70Ile)	Charcot-Marie-Tooth disease type 2 [RCV003084847]	uncertain significance	1	156115126	156115126	Human	1	name
156159310	CV1928507	single nucleotide variant	NM_170707.4(LMNA):c.115A>G (p.Asn39Asp)	Charcot-Marie-Tooth disease type 2 [RCV002664185]\|Congenital muscular dystrophy due to LMNA mutation [RCV005254717]	likely pathogenic	1	156115033	156115033	Human	2	name
156397247	CV1934314	single nucleotide variant	NM_170707.4(LMNA):c.1239C>A (p.Gly413=)	Cardiomyopathy [RCV003533363]\|Charcot-Marie-Tooth disease type 2 [RCV002655053]\|Primary dilated cardiomyopathy [RCV004009528]	likely benign	1	156136295	156136295	Human	4	name
156440578	CV1943681	single nucleotide variant	NM_170707.4(LMNA):c.1257C>T (p.Arg419=)	Charcot-Marie-Tooth disease type 2 [RCV003110614]	likely benign	1	156136313	156136313	Human	1	name
156219296	CV2015419	single nucleotide variant	NM_170707.4(LMNA):c.193G>A (p.Glu65Lys)	Charcot-Marie-Tooth disease type 2 [RCV002700942]\|Primary dilated cardiomyopathy [RCV004007552]	likely pathogenic\|uncertain significance	1	156115111	156115111	Human	2	name
155910915	CV2033023	single nucleotide variant	NM_170707.4(LMNA):c.1119C>T (p.Ile373=)	Charcot-Marie-Tooth disease type 2 [RCV002750129]\|Primary dilated cardiomyopathy [RCV004007570]	likely benign	1	156136083	156136083	Human	2	name
156031113	CV2036914	single nucleotide variant	NM_170707.4(LMNA):c.1062G>A (p.Gln354=)	Cardiovascular phenotype [RCV003367881]\|Charcot-Marie-Tooth disease type 2 [RCV002781114]	likely benign	1	156136026	156136026	Human	1	name
156156973	CV2049345	deletion	NM_170707.4(LMNA):c.707del (p.Glu236fs)	Charcot-Marie-Tooth disease type 2 [RCV002801487]	pathogenic	1	156134872	156134872	Human	1	name
156119163	CV2055224	single nucleotide variant	NM_170707.4(LMNA):c.194A>T (p.Glu65Val)	Charcot-Marie-Tooth disease type 2 [RCV002825231]	likely pathogenic	1	156115112	156115112	Human	1	name
156198609	CV2062832	single nucleotide variant	NM_170707.4(LMNA):c.1272T>C (p.Thr424=)	Charcot-Marie-Tooth disease type 2 [RCV002828856]\|Primary dilated cardiomyopathy [RCV004007630]	likely benign	1	156136328	156136328	Human	2	name
155928764	CV2067152	single nucleotide variant	NM_170707.4(LMNA):c.1167G>A (p.Leu389=)	Charcot-Marie-Tooth disease type 2 [RCV002838657]	likely benign	1	156136223	156136223	Human	1	name
156219888	CV2078306	single nucleotide variant	NM_170707.4(LMNA):c.1413C>A (p.Arg471=)	Charcot-Marie-Tooth disease type 2 [RCV002894141]	likely benign	1	156136953	156136953	Human	1	name
156220129	CV2083861	single nucleotide variant	NM_170707.4(LMNA):c.1923G>C (p.Leu641=)	Charcot-Marie-Tooth disease type 2 [RCV002875836]	likely benign	1	156138712	156138712	Human	1	name
156316174	CV2104136	single nucleotide variant	NM_170707.4(LMNA):c.1215C>T (p.His405=)	Cardiomyopathy [RCV005403249]\|Charcot-Marie-Tooth disease type 2 [RCV002937461]	likely benign\|uncertain significance	1	156136271	156136271	Human	3	name
156007237	CV2126645	single nucleotide variant	NM_170707.4(LMNA):c.1335G>A (p.Val445=)	Charcot-Marie-Tooth disease type 2 [RCV002975459]	likely benign	1	156136391	156136391	Human	1	name
156125075	CV2144709	single nucleotide variant	NM_170707.4(LMNA):c.245A>G (p.Glu82Gly)	Charcot-Marie-Tooth disease type 2 [RCV003003137]	likely pathogenic	1	156115163	156115163	Human	1	name
156042458	CV2146938	single nucleotide variant	NM_170707.4(LMNA):c.117T>A (p.Asn39Lys)	Charcot-Marie-Tooth disease type 2 [RCV003019110]	pathogenic	1	156115035	156115035	Human	1	name
156285149	CV2187102	single nucleotide variant	NM_170707.4(LMNA):c.1926C>T (p.Val642=)	Charcot-Marie-Tooth disease type 2 [RCV003044914]	likely benign	1	156138715	156138715	Human	1	name
156371797	CV2188773	single nucleotide variant	NM_170707.4(LMNA):c.250G>T (p.Glu84Ter)	Charcot-Marie-Tooth disease type 2 [RCV003066344]	pathogenic	1	156115168	156115168	Human	1	name
156140796	CV2191812	duplication	NM_170707.4(LMNA):c.734dup (p.Gln246fs)	Charcot-Marie-Tooth disease type 2 [RCV003056175]	pathogenic	1	156134898	156134899	Human	1	name
243062305	CV2404698	single nucleotide variant	NM_170707.4(LMNA):c.104T>A (p.Leu35Gln)	Congenital muscular dystrophy due to LMNA mutation [RCV003140259]	uncertain significance	1	156115022	156115022	Human	1	name
243062333	CV2404747	single nucleotide variant	NM_170707.4(LMNA):c.117T>G (p.Asn39Lys)	Congenital muscular dystrophy due to LMNA mutation [RCV003140304]	uncertain significance	1	156115035	156115035	Human	1	name
243058649	CV2413110	single nucleotide variant	NM_170707.4(LMNA):c.148C>G (p.Arg50Gly)	Charcot-Marie-Tooth disease type 2 [RCV005099310]\|not provided [RCV003134080]	likely pathogenic\|uncertain significance	1	156115066	156115066	Human	1	name
243058656	CV2413113	single nucleotide variant	NM_170707.4(LMNA):c.107A>C (p.Gln36Pro)	not provided [RCV003134082]	uncertain significance	1	156115025	156115025	Human		name
329355388	CV2430043	single nucleotide variant	NM_170707.4(LMNA):c.1860C>T (p.Val620=)	Cardiovascular phenotype [RCV003177756]	likely benign	1	156138649	156138649	Human		name
329355392	CV2430045	single nucleotide variant	NM_170707.4(LMNA):c.1045C>A (p.Arg349=)	Cardiovascular phenotype [RCV003177758]	likely benign	1	156136009	156136009	Human		name
329355399	CV2430049	single nucleotide variant	NM_170707.4(LMNA):c.1677T>C (p.Asp559=)	Cardiovascular phenotype [RCV003177762]	likely benign	1	156137722	156137722	Human		name
401796153	CV2670278	deletion	NM_170707.4(LMNA):c.673del (p.Arg225fs)	Dilated cardiomyopathy 1A [RCV003319247]	likely pathogenic	1	156134836	156134836	Human	2	name
401755552	CV2730928	duplication	NM_170707.4(LMNA):c.383dup (p.Ala129fs)	Cardiovascular phenotype [RCV003278430]\|Charcot-Marie-Tooth disease type 2 [RCV003581919]	pathogenic	1	156130642	156130643	Human	1	name
401733780	CV2736896	single nucleotide variant	NM_170707.4(LMNA):c.139G>T (p.Asp47Tyr)	Familial partial lipodystrophy, Dunnigan type [RCV005254761]\|not provided [RCV003313659]	pathogenic\|uncertain significance	1	156115057	156115057	Human	1	name
401899644	CV2753890	single nucleotide variant	NM_170707.4(LMNA):c.251A>G (p.Glu84Gly)	Cardiovascular phenotype [RCV003377964]\|Charcot-Marie-Tooth disease type 2 [RCV003745590]	uncertain significance	1	156115169	156115169	Human	1	name
401869172	CV2753891	deletion	NM_170707.4(LMNA):c.679del (p.Val227fs)	Cardiovascular phenotype [RCV003360740]	pathogenic	1	156134843	156134843	Human		name
401948008	CV2832137	deletion	NM_170707.4(LMNA):c.324del (p.Val109fs)	Sick sinus syndrome [RCV003447662]	likely pathogenic	1	156115240	156115240	Human	2	name
404984752	CV2851669	deletion	NM_170707.4(LMNA):c.-1_22del (p.Met1fs)	not provided [RCV003489386]	likely pathogenic	1	156114914	156114936	Human		name
405082523	CV2855012	single nucleotide variant	NM_170707.4(LMNA):c.152C>G (p.Ser51Trp)	Charcot-Marie-Tooth disease type 2 [RCV003582210]	uncertain significance	1	156115070	156115070	Human	1	name
405070835	CV2888172	single nucleotide variant	NM_170707.4(LMNA):c.179G>A (p.Arg60His)	Charcot-Marie-Tooth disease type 2 [RCV003581110]\|Familial partial lipodystrophy, Dunnigan type [RCV005254823]	likely pathogenic\|uncertain significance	1	156115097	156115097	Human	2	name
405075511	CV2898323	single nucleotide variant	NM_170707.4(LMNA):c.121C>T (p.Arg41Cys)	Charcot-Marie-Tooth disease type 2 [RCV003581422]	pathogenic	1	156115039	156115039	Human	1	name
405089027	CV2900662	single nucleotide variant	NM_170707.4(LMNA):c.172G>A (p.Gly58Arg)	Charcot-Marie-Tooth disease type 2 [RCV003582726]	uncertain significance	1	156115090	156115090	Human	1	name
405089350	CV2901197	single nucleotide variant	NM_170707.4(LMNA):c.1089G>A (p.Leu363=)	Charcot-Marie-Tooth disease type 2 [RCV003582751]	likely benign	1	156136053	156136053	Human	1	name
405091039	CV2913399	single nucleotide variant	NM_170707.4(LMNA):c.1935C>T (p.Ser645=)	Charcot-Marie-Tooth disease type 2 [RCV003582882]	likely benign	1	156138724	156138724	Human	1	name
405089968	CV2918708	deletion	NM_170707.4(LMNA):c.940del (p.Ala314fs)	Charcot-Marie-Tooth disease type 2 [RCV003582799]	pathogenic	1	156135903	156135903	Human	1	name
405081316	CV2933596	deletion	NM_170707.4(LMNA):c.535del (p.Ala179fs)	Charcot-Marie-Tooth disease type 2 [RCV003582067]	pathogenic	1	156134423	156134423	Human	1	name
405063165	CV2934276	single nucleotide variant	NM_170707.4(LMNA):c.1209C>G (p.Ser403=)	Cardiomyopathy [RCV003532560]	likely benign	1	156136265	156136265	Human	2	name
405063208	CV2934283	single nucleotide variant	NM_170707.4(LMNA):c.1722G>A (p.Gly574=)	Cardiomyopathy [RCV003532565]\|Charcot-Marie-Tooth disease type 2 [RCV005063056]	likely benign	1	156138511	156138511	Human	3	name
405063218	CV2934284	single nucleotide variant	NM_170707.4(LMNA):c.1737C>T (p.Tyr579=)	Cardiomyopathy [RCV003532566]\|Charcot-Marie-Tooth disease type 2 [RCV005100360]	likely benign	1	156138526	156138526	Human	3	name
405063228	CV2934285	single nucleotide variant	NM_170707.4(LMNA):c.1752C>T (p.Arg584=)	Cardiomyopathy [RCV003532567]	likely benign	1	156138541	156138541	Human	2	name
405063238	CV2934286	single nucleotide variant	NM_170707.4(LMNA):c.1788C>T (p.Asp596=)	Cardiomyopathy [RCV003532568]\|Charcot-Marie-Tooth disease type 2 [RCV005100361]\|Primary dilated cardiomyopathy [RCV004805533]	likely benign	1	156138577	156138577	Human	4	name
405094687	CV2941847	single nucleotide variant	NM_170707.4(LMNA):c.118G>A (p.Asp40Asn)	Charcot-Marie-Tooth disease type 2 [RCV003745733]	uncertain significance	1	156115036	156115036	Human	1	name
8564261	CV29518	single nucleotide variant	NM_170707.4(LMNA):c.178C>G (p.Arg60Gly)	Dilated cardiomyopathy 1A [RCV000015566]\|Familial partial lipodystrophy, Dunnigan type [RCV000015567]\|not provided [RCV000057359]	pathogenic\|not provided	1	156115096	156115096	Human	3	name
8564262	CV29519	single nucleotide variant	NM_170707.4(LMNA):c.254T>G (p.Leu85Arg)	Cardiovascular phenotype [RCV002453264]\|Dilated cardiomyopathy 1A [RCV000015568]\|not provided [RCV000057381]	pathogenic\|uncertain significance\|not provided	1	156115172	156115172	Human	3	name
8599851	CV29530	deletion	NM_170707.4(LMNA):c.960del (p.Arg321fs)	Dilated cardiomyopathy 1A [RCV000015581]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV000681609]\|not provided [RCV000057492]	pathogenic\|not provided	1	156135923	156135923	Human	3	name
405095267	CV2953785	single nucleotide variant	NM_170707.4(LMNA):c.1197T>C (p.Arg399=)	Charcot-Marie-Tooth disease type 2 [RCV003745787]	likely benign	1	156136253	156136253	Human	1	name
8564281	CV29539	single nucleotide variant	NM_170707.4(LMNA):c.1824C>T (p.Gly608=)	Charcot-Marie-Tooth disease type 2 [RCV000806737]\|Hutchinson-Gilford syndrome [RCV000015593]\|Primary dilated cardiomyopathy [RCV000150957]\|Restrictive dermopathy 2 [RCV001847608]\|not provided [RCV000057364]	pathogenic	1	156138613	156138613	Human	4	name
8564287	CV29545	single nucleotide variant	NM_170707.4(LMNA):c.169G>C (p.Ala57Pro)	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV000015600]\|not provided [RCV000057349]	pathogenic\|not provided	1	156115087	156115087	Human	1	name
405096117	CV2955402	single nucleotide variant	NM_170707.4(LMNA):c.1182C>G (p.Thr394=)	Charcot-Marie-Tooth disease type 2 [RCV003745868]	likely benign	1	156136238	156136238	Human	1	name
8564297	CV29555	single nucleotide variant	NM_170707.4(LMNA):c.1821G>A (p.Val607=)	Hutchinson-Gilford syndrome [RCV000015611]\|not provided [RCV000057362]	pathogenic\|not provided	1	156138610	156138610	Human	1	name
405085320	CV2980264	single nucleotide variant	NM_170707.4(LMNA):c.176T>A (p.Leu59Gln)	Charcot-Marie-Tooth disease type 2 [RCV003744303]	uncertain significance	1	156115094	156115094	Human	1	name
405084447	CV2986410	deletion	NM_170707.4(LMNA):c.973del (p.Asp325fs)	Charcot-Marie-Tooth disease type 2 [RCV003744235]	pathogenic	1	156135936	156135936	Human	1	name
405087146	CV3004608	single nucleotide variant	NM_170707.4(LMNA):c.1278C>T (p.Ser426=)	Charcot-Marie-Tooth disease type 2 [RCV003744470]	likely benign	1	156136334	156136334	Human	1	name
405075168	CV3010446	single nucleotide variant	NM_170707.4(LMNA):c.1032G>A (p.Glu344=)	Charcot-Marie-Tooth disease type 2 [RCV003743102]	likely benign	1	156135996	156135996	Human	1	name
405077234	CV3029962	single nucleotide variant	NM_170707.4(LMNA):c.212G>C (p.Ser71Thr)	Charcot-Marie-Tooth disease type 2 [RCV003743236]	uncertain significance	1	156115130	156115130	Human	1	name
405077333	CV3030176	duplication	NM_170707.4(LMNA):c.755dup (p.His252fs)	Charcot-Marie-Tooth disease type 2 [RCV003743243]	pathogenic	1	156134919	156134920	Human	1	name
405078441	CV3032214	single nucleotide variant	NM_170707.4(LMNA):c.143G>A (p.Arg48His)	Charcot-Marie-Tooth disease type 2 [RCV003743314]	likely pathogenic	1	156115061	156115061	Human	1	name
407474958	CV3042731	single nucleotide variant	NM_170707.4(LMNA):c.215G>C (p.Arg72Pro)	Congenital muscular dystrophy due to LMNA mutation [RCV004690464]	likely pathogenic	1	156115133	156115133	Human	1	name
405082000	CV3056933	single nucleotide variant	NM_170707.4(LMNA):c.1920T>C (p.Asn640=)	Cardiovascular phenotype [RCV004992766]\|Charcot-Marie-Tooth disease type 2 [RCV003743541]	likely benign	1	156138709	156138709	Human	1	name
405188432	CV3121301	single nucleotide variant	NM_170707.4(LMNA):c.1203T>G (p.Arg401=)	Charcot-Marie-Tooth disease type 2 [RCV003820757]	likely benign	1	156136259	156136259	Human	1	name
405087662	CV3122178	single nucleotide variant	NM_170707.4(LMNA):c.1965C>T (p.Thr655=)	Charcot-Marie-Tooth disease type 2 [RCV003810933]	likely benign	1	156138754	156138754	Human	1	name
404979110	CV3127750	single nucleotide variant	NM_170707.4(LMNA):c.1398T>C (p.Asn466=)	Charcot-Marie-Tooth disease type 2 [RCV003825782]	likely benign	1	156136938	156136938	Human	1	name
405200626	CV3143466	single nucleotide variant	NM_170707.4(LMNA):c.1824C>A (p.Gly608=)	Cardiovascular phenotype [RCV004636864]\|Charcot-Marie-Tooth disease type 2 [RCV003844452]	likely benign	1	156138613	156138613	Human	1	name
405180598	CV3159428	single nucleotide variant	NM_170707.4(LMNA):c.1887G>T (p.Val629=)	Charcot-Marie-Tooth disease type 2 [RCV003858678]	likely benign	1	156138676	156138676	Human	1	name
402477995	CV3170206	single nucleotide variant	NM_170707.4(LMNA):c.1068G>A (p.Leu356=)	Charcot-Marie-Tooth disease type 2 [RCV003875594]	likely benign	1	156136032	156136032	Human	1	name
404982065	CV3184151	single nucleotide variant	NM_170707.4(LMNA):c.1026G>A (p.Glu342=)	Charcot-Marie-Tooth disease type 2 [RCV003880643]	likely benign	1	156135990	156135990	Human	1	name
405733515	CV3229547	single nucleotide variant	NM_170707.4(LMNA):c.1425T>C (p.Asp475=)	Primary dilated cardiomyopathy [RCV004014114]	likely benign	1	156136965	156136965	Human	1	name
405734432	CV3229646	single nucleotide variant	NM_170707.4(LMNA):c.1524C>A (p.Pro508=)	Charcot-Marie-Tooth disease type 2 [RCV005103341]\|Primary dilated cardiomyopathy [RCV004014213]	likely benign	1	156137148	156137148	Human	2	name
405723187	CV3230287	single nucleotide variant	NM_170707.4(LMNA):c.1435C>T (p.Leu479=)	Primary dilated cardiomyopathy [RCV004013039]	likely benign	1	156136975	156136975	Human	1	name
405723365	CV3230308	single nucleotide variant	NM_170707.4(LMNA):c.1221C>T (p.Ser407=)	Primary dilated cardiomyopathy [RCV004013060]	likely benign	1	156136277	156136277	Human	1	name
405725714	CV3230547	single nucleotide variant	NM_170707.4(LMNA):c.190A>G (p.Thr64Ala)	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005040625]\|Primary dilated cardiomyopathy [RCV004013300]	uncertain significance	1	156115108	156115108	Human	3	name
405715126	CV3232323	single nucleotide variant	NM_170707.4(LMNA):c.235G>A (p.Ala79Thr)	Primary dilated cardiomyopathy [RCV004012176]	uncertain significance	1	156115153	156115153	Human	1	name
405755420	CV3232677	single nucleotide variant	NM_170707.4(LMNA):c.173G>T (p.Gly58Val)	Primary dilated cardiomyopathy [RCV004016813]	uncertain significance	1	156115091	156115091	Human	1	name
405756290	CV3232973	single nucleotide variant	NM_170707.4(LMNA):c.1431C>T (p.Pro477=)	Primary dilated cardiomyopathy [RCV004016924]	likely benign	1	156136971	156136971	Human	1	name
405745406	CV3234545	single nucleotide variant	NM_170707.4(LMNA):c.295C>G (p.Arg99Gly)	Primary dilated cardiomyopathy [RCV004015418]	uncertain significance	1	156115213	156115213	Human	1	name
8564309	CV33496	single nucleotide variant	NM_170707.4(LMNA):c.176T>G (p.Leu59Arg)	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV000015627]\|not provided [RCV000057357]	pathogenic\|not provided	1	156115094	156115094	Human	1	name
407470942	CV3449247	single nucleotide variant	NM_170707.4(LMNA):c.238G>T (p.Ala80Ser)	Cardiovascular phenotype [RCV004637245]	uncertain significance	1	156115156	156115156	Human		name
407574605	CV3499616	single nucleotide variant	NM_170707.4(LMNA):c.161C>A (p.Thr54Lys)	not provided [RCV004720109]	uncertain significance	1	156115079	156115079	Human		name
408394850	CV3522100	single nucleotide variant	NM_170707.4(LMNA):c.165G>T (p.Glu55Asp)	Dilated cardiomyopathy 1A [RCV004765098]	uncertain significance	1	156115083	156115083	Human	2	name
596925581	CV3535854	deletion	NM_170707.4(LMNA):c.751del (p.Gln251fs)	Dilated cardiomyopathy 1A [RCV004788284]	pathogenic	1	156134914	156134914	Human	2	name
596941241	CV3546147	single nucleotide variant	NM_170707.4(LMNA):c.1444C>A (p.Arg482=)	Primary dilated cardiomyopathy [RCV004806776]	likely benign	1	156136984	156136984	Human	1	name
597655895	CV3552302	single nucleotide variant	NM_170707.4(LMNA):c.223T>C (p.Ser75Pro)	Congenital muscular dystrophy due to LMNA mutation [RCV004821160]	uncertain significance	1	156115141	156115141	Human	1	name
597722653	CV3693372	single nucleotide variant	NM_170707.4(LMNA):c.1974C>T (p.Pro658=)	Cardiovascular phenotype [RCV004993744]	likely benign	1	156139085	156139085	Human		name
597722724	CV3701641	single nucleotide variant	NM_170707.4(LMNA):c.1845T>C (p.Ser615=)	Cardiovascular phenotype [RCV004993758]	likely benign	1	156138634	156138634	Human		name
597722730	CV3701642	single nucleotide variant	NM_170707.4(LMNA):c.1848T>C (p.Ser616=)	Cardiovascular phenotype [RCV004993759]	likely benign	1	156138637	156138637	Human		name
597722748	CV3701647	single nucleotide variant	NM_170707.4(LMNA):c.1881C>A (p.Arg627=)	Cardiovascular phenotype [RCV004993763]	likely benign	1	156138670	156138670	Human		name
597930551	CV3745860	single nucleotide variant	NM_170707.4(LMNA):c.1785C>G (p.Ala595=)	Charcot-Marie-Tooth disease type 2 [RCV005075845]	likely benign	1	156138574	156138574	Human	1	name
597946878	CV3755536	single nucleotide variant	NM_170707.4(LMNA):c.1530C>A (p.Thr510=)	Charcot-Marie-Tooth disease type 2 [RCV005078546]	likely benign	1	156137154	156137154	Human	1	name
597837092	CV3761442	single nucleotide variant	NM_170707.4(LMNA):c.1227A>T (p.Thr409=)	Charcot-Marie-Tooth disease type 2 [RCV005085813]	likely benign	1	156136283	156136283	Human	1	name
597910467	CV3770379	single nucleotide variant	NM_170707.4(LMNA):c.238G>A (p.Ala80Thr)	Charcot-Marie-Tooth disease type 2 [RCV005113680]	uncertain significance	1	156115156	156115156	Human	1	name
597940218	CV3772725	single nucleotide variant	NM_170707.4(LMNA):c.1386G>A (p.Gln462=)	Charcot-Marie-Tooth disease type 2 [RCV005118355]	likely benign	1	156136926	156136926	Human	1	name
597877792	CV3776197	single nucleotide variant	NM_170707.4(LMNA):c.1627C>T (p.Leu543=)	Charcot-Marie-Tooth disease type 2 [RCV005123725]	likely benign	1	156137672	156137672	Human	1	name
597944140	CV3776511	single nucleotide variant	NM_170707.4(LMNA):c.1632G>A (p.Val544=)	Charcot-Marie-Tooth disease type 2 [RCV005119366]	likely benign	1	156137677	156137677	Human	1	name
597929896	CV3780178	single nucleotide variant	NM_170707.4(LMNA):c.1863G>C (p.Thr621=)	Charcot-Marie-Tooth disease type 2 [RCV005116498]	likely benign	1	156138652	156138652	Human	1	name
597937662	CV3787923	single nucleotide variant	NM_170707.4(LMNA):c.1923G>A (p.Leu641=)	Charcot-Marie-Tooth disease type 2 [RCV005132802]	likely benign	1	156138712	156138712	Human	1	name
597954929	CV3796108	single nucleotide variant	NM_170707.4(LMNA):c.1884T>C (p.Ser628=)	Charcot-Marie-Tooth disease type 2 [RCV005136925]	likely benign	1	156138673	156138673	Human	1	name
597964959	CV3797017	single nucleotide variant	NM_170707.4(LMNA):c.1377T>C (p.Asn459=)	Charcot-Marie-Tooth disease type 2 [RCV005139977]	likely benign	1	156136433	156136433	Human	1	name
597959111	CV3797479	single nucleotide variant	NM_170707.4(LMNA):c.1009C>T (p.Leu337=)	Charcot-Marie-Tooth disease type 2 [RCV005138166]	likely benign	1	156135973	156135973	Human	1	name
597949524	CV3801336	deletion	NM_170707.4(LMNA):c.814del (p.Asp272fs)	Charcot-Marie-Tooth disease type 2 [RCV005135516]	pathogenic	1	156135189	156135189	Human	1	name
597939065	CV3808375	single nucleotide variant	NM_170707.4(LMNA):c.271A>C (p.Thr91Pro)	Charcot-Marie-Tooth disease type 2 [RCV005158563]	uncertain significance	1	156115189	156115189	Human	1	name
597863066	CV3813580	single nucleotide variant	NM_170707.4(LMNA):c.1165C>T (p.Leu389=)	Charcot-Marie-Tooth disease type 2 [RCV005146842]	likely benign	1	156136221	156136221	Human	1	name
597940361	CV3819037	single nucleotide variant	NM_170707.4(LMNA):c.1323C>G (p.Ala441=)	Charcot-Marie-Tooth disease type 2 [RCV005158848]	likely benign	1	156136379	156136379	Human	1	name
597973057	CV3820070	single nucleotide variant	NM_170707.4(LMNA):c.118G>C (p.Asp40His)	Charcot-Marie-Tooth disease type 2 [RCV005167784]	uncertain significance	1	156115036	156115036	Human	1	name
597973628	CV3820616	single nucleotide variant	NM_170707.4(LMNA):c.1050A>G (p.Ala350=)	Charcot-Marie-Tooth disease type 2 [RCV005168133]	likely benign	1	156136014	156136014	Human	1	name
597920465	CV3842744	single nucleotide variant	NM_170707.4(LMNA):c.1995A>G (p.Ter665=)	Charcot-Marie-Tooth disease type 2 [RCV005184229]	likely benign	1	156139106	156139106	Human	1	name
597911367	CV3850480	deletion	NM_170707.4(LMNA):c.574del (p.Asp192fs)	Charcot-Marie-Tooth disease type 2 [RCV005203629]	pathogenic	1	156134462	156134462	Human	1	name
597897627	CV3854404	single nucleotide variant	NM_170707.4(LMNA):c.1095C>A (p.Ile365=)	Charcot-Marie-Tooth disease type 2 [RCV005201511]	likely benign	1	156136059	156136059	Human	1	name
597845489	CV3880440	single nucleotide variant	NM_170707.4(LMNA):c.101A>G (p.Asp34Gly)	not provided [RCV005227328]	uncertain significance	1	156115019	156115019	Human		name
616934879	CV4010131	single nucleotide variant	NM_170707.4(LMNA):c.1842C>T (p.Gly614=)	Cardiomyopathy [RCV005401752]	likely benign	1	156138631	156138631	Human	2	name
616932994	CV4012758	single nucleotide variant	NM_170707.4(LMNA):c.185G>C (p.Arg62Pro)	Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV005410220]	likely pathogenic	1	156115103	156115103	Human	1	name
616938859	CV4015195	single nucleotide variant	NM_170707.4(LMNA):c.175C>G (p.Leu59Val)	Hutchinson-Gilford syndrome [RCV005412209]	likely pathogenic	1	156115093	156115093	Human	1	name
8569613	CV45139	single nucleotide variant	NM_170707.4(LMNA):c.1761G>A (p.Leu587=)	Cardiomyopathy [RCV000030149]\|Cardiovascular phenotype [RCV000249377]\|Charcot-Marie-Tooth disease [RCV001172632]\|Charcot-Marie-Tooth disease type 2 [RCV001085192]\|Primary dilated cardiomyopathy [RCV003996128]\|not provided [RCV000710161]\|not specified [RCV000041331]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156138550	156138550	Human	5	name
8610897	CV57196	single nucleotide variant	NM_170707.4(LMNA):c.1146C>T (p.Gly382=)	Cardiovascular phenotype [RCV000620488]\|Charcot-Marie-Tooth disease type 2 [RCV000468865]\|Dilated cardiomyopathy 1A [RCV001775074]\|Primary dilated cardiomyopathy [RCV000041309]\|not provided [RCV000057239]	pathogenic\|likely pathogenic\|not provided	1	156136110	156136110	Human	5	name
8610898	CV57197	single nucleotide variant	NM_170707.4(LMNA):c.1185G>A (p.Ser395=)	Cardiomyopathy [RCV000777976]\|Charcot-Marie-Tooth disease type 2 [RCV001441153]\|not provided [RCV000725248]\|not specified [RCV000041311]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156136241	156136241	Human	3	name
8610899	CV57198	single nucleotide variant	NM_170707.4(LMNA):c.1242C>T (p.Ser414=)	Cardiomyopathy [RCV001184221]\|Charcot-Marie-Tooth disease type 2 [RCV005089373]\|not specified [RCV000041312]	likely benign	1	156136298	156136298	Human	3	name
8610902	CV57201	single nucleotide variant	NM_170707.4(LMNA):c.1338T>C (p.Asp446=)	Cardiomyopathy [RCV000776001]\|Cardiovascular phenotype [RCV000252403]\|Charcot-Marie-Tooth disease [RCV001173417]\|Charcot-Marie-Tooth disease type 2 [RCV000357954]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093809]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000278595]\|Dilated cardiomyopathy 1A [RCV000326241]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001098691]\|Emery-Dreifuss muscular dystrophy [RCV000351015]\|Familial partial lipodystrophy, Dunnigan type [RCV000268754]\|Hutchinson-Gilford syndrome [RCV000304015]\|Lethal tight skin contracture syndrome [RCV000392971]\|Limb-girdle muscular dystrophy, recessive [RCV000402362]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000300868]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000360967]\|Primary dilated cardiomyopathy [RCV003125875]\|not provided [RCV000057270]\|not specified [RCV000041315]	benign\|conflicting interpretations of pathogenicity\|conflicting data from submitters\|not provided	1	156136394	156136394	Human	19	name
8610902	CV57201	single nucleotide variant	NM_170707.4(LMNA):c.1338T>C (p.Asp446=)	Cardiomyopathy [RCV000776001]\|Cardiovascular phenotype [RCV000252403]\|Charcot-Marie-Tooth disease [RCV001173417]\|Charcot-Marie-Tooth disease type 2 [RCV000357954]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093809]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000278595]\|Dilated cardiomyopathy 1A [RCV000326241]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001098691]\|Emery-Dreifuss muscular dystrophy [RCV000351015]\|Familial partial lipodystrophy, Dunnigan type [RCV000268754]\|Hutchinson-Gilford syndrome [RCV000304015]\|Lethal tight skin contracture syndrome [RCV000392971]\|Limb-girdle muscular dystrophy, recessive [RCV000402362]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000300868]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000360967]\|Primary dilated cardiomyopathy [RCV003125875]\|not provided [RCV000057270]\|not specified [RCV000041315]	benign\|conflicting interpretations of pathogenicity\|conflicting data from submitters\|not provided	1	156136394	156136395	Human	19	name
8610907	CV57206	single nucleotide variant	NM_170707.4(LMNA):c.154C>G (p.Leu52Val)	Primary dilated cardiomyopathy [RCV000041321]	likely pathogenic	1	156115072	156115072	Human	1	name
8610908	CV57207	single nucleotide variant	NM_170707.4(LMNA):c.1566C>T (p.Cys522=)	Cardiomyopathy [RCV000777760]\|Cardiovascular phenotype [RCV000242680]\|Charcot-Marie-Tooth disease [RCV001172631]\|Charcot-Marie-Tooth disease type 2 [RCV000233927]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093764]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000380292]\|Dilated cardiomyopathy 1A [RCV000262946]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001098994]\|Emery-Dreifuss muscular dystrophy [RCV000289458]\|Familial partial lipodystrophy, Dunnigan type [RCV000320484]\|Hutchinson-Gilford syndrome [RCV000285909]\|Lethal tight skin contracture syndrome [RCV000399953]\|Limb-girdle muscular dystrophy, recessive [RCV000337260]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000377490]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000340752]\|not provided [RCV001310873]\|not specified [RCV000041322]	benign\|likely benign\|conflicting interpretations of pathogenicity	1	156137190	156137190	Human	18	name
8610909	CV57208	single nucleotide variant	NM_170707.4(LMNA):c.1584G>A (p.Thr528=)	Cardiomyopathy [RCV000771807]\|Cardiovascular phenotype [RCV002399396]\|Charcot-Marie-Tooth disease [RCV001172635]\|Charcot-Marie-Tooth disease type 2 [RCV000464925]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093817]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000272639]\|Dilated cardiomyopathy 1A [RCV000297337]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001100808]\|Emery-Dreifuss muscular dystrophy [RCV000312611]\|Familial partial lipodystrophy, Dunnigan type [RCV000327741]\|Hutchinson-Gilford syndrome [RCV000284072]\|Lethal tight skin contracture syndrome [RCV000268685]\|Limb-girdle muscular dystrophy, recessive [RCV000370762]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000276010]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000323895]\|Primary dilated cardiomyopathy [RCV002464006]\|not provided [RCV000827979]\|not specified [RCV000041323]	benign\|likely benign	1	156137208	156137208	Human	18	name
8610912	CV57211	single nucleotide variant	NM_170707.4(LMNA):c.1656C>T (p.Asp552=)	Cardiomyopathy [RCV001180815]\|Cardiovascular phenotype [RCV000619881]\|Charcot-Marie-Tooth disease type 2 [RCV001088399]\|LMNA-related disorder [RCV004734589]\|Primary dilated cardiomyopathy [RCV003996457]\|not provided [RCV000726458]\|not specified [RCV000041326]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156137701	156137701	Human	4	name , alternate_id
8610913	CV57212	single nucleotide variant	NM_170707.4(LMNA):c.1698C>T (p.His566=)	Cardiomyopathy [RCV000775990]\|Cardiovascular phenotype [RCV000252567]\|Charcot-Marie-Tooth disease [RCV001173414]\|Charcot-Marie-Tooth disease type 2 [RCV000393593]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093768]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000313972]\|Dilated cardiomyopathy 1A [RCV000375103]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001098384]\|Emery-Dreifuss muscular dystrophy [RCV000307278]\|Familial partial lipodystrophy, Dunnigan type [RCV000280696]\|Hutchinson-Gilford syndrome [RCV000335127]\|Lethal tight skin contracture syndrome [RCV000339153]\|Limb-girdle muscular dystrophy, recessive [RCV000350197]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000398387]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000225004]\|Primary dilated cardiomyopathy [RCV003125876]\|not provided [RCV000057348]\|not specified [RCV000041327]	pathogenic\|likely pathogenic\|benign\|conflicting interpretations of pathogenicity\|conflicting data from submitters\|not provided	1	156137743	156137743	Human	21	name
8610913	CV57212	single nucleotide variant	NM_170707.4(LMNA):c.1698C>T (p.His566=)	Cardiomyopathy [RCV000775990]\|Cardiovascular phenotype [RCV000252567]\|Charcot-Marie-Tooth disease [RCV001173414]\|Charcot-Marie-Tooth disease type 2 [RCV000393593]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093768]\|Congenital muscular dystrophy due to LMNA mutat ... (more) ion [RCV000313972]\|Dilated cardiomyopathy 1A [RCV000375103]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001098384]\|Emery-Dreifuss muscular dystrophy [RCV000307278]\|Familial partial lipodystrophy, Dunnigan type [RCV000280696]\|Hutchinson-Gilford syndrome [RCV000335127]\|Lethal tight skin contracture syndrome [RCV000339153]\|Limb-girdle muscular dystrophy, recessive [RCV000350197]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000398387]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000225004]\|Primary dilated cardiomyopathy [RCV003125876]\|not provided [RCV000057348]\|not specified [RCV000041327]	pathogenic\|likely pathogenic\|benign\|conflicting interpretations of pathogenicity\|conflicting data from submitters\|not provided	1	156137743	156137744	Human	21	name
8610915	CV57214	single nucleotide variant	NM_170707.4(LMNA):c.1770C>G (p.Thr590=)	Charcot-Marie-Tooth disease type 2 [RCV003743556]\|Primary dilated cardiomyopathy [RCV004806041]\|not provided [RCV003407414]\|not specified [RCV000041332]	likely benign	1	156138559	156138559	Human	2	name
8610916	CV57215	single nucleotide variant	NM_170707.4(LMNA):c.1773C>T (p.Cys591=)	Cardiomyopathy [RCV001184223]\|Cardiovascular phenotype [RCV002399397]\|Charcot-Marie-Tooth disease type 2 [RCV000530060]\|Primary dilated cardiomyopathy [RCV003996458]\|not specified [RCV000041333]	likely benign\|conflicting interpretations of pathogenicity	1	156138562	156138562	Human	4	name
8610919	CV57218	single nucleotide variant	NM_170707.4(LMNA):c.1851C>T (p.Ala617=)	Cardiomyopathy [RCV000769733]\|Cardiovascular phenotype [RCV002408539]\|Charcot-Marie-Tooth disease [RCV001173409]\|Charcot-Marie-Tooth disease type 2 [RCV000234314]\|Primary dilated cardiomyopathy [RCV003996460]\|not provided [RCV001701583]\|not specified [RCV000041336]	benign\|likely benign\|conflicting interpretations of pathogenicity	1	156138640	156138640	Human	5	name
8610920	CV57219	single nucleotide variant	NM_170707.4(LMNA):c.1911C>T (p.Phe637=)	Cardiomyopathy [RCV001170983]\|Cardiovascular phenotype [RCV000619457]\|Charcot-Marie-Tooth disease [RCV001173400]\|Charcot-Marie-Tooth disease type 2 [RCV000473263]\|Primary dilated cardiomyopathy [RCV003996461]\|not provided [RCV001529866]\|not specified [RCV000041337]	benign\|likely benign	1	156138700	156138700	Human	5	name
8610924	CV57223	single nucleotide variant	NM_170707.4(LMNA):c.266G>A (p.Arg89His)	Charcot-Marie-Tooth disease type 2 [RCV005089375]\|not specified [RCV000041342]	likely pathogenic\|uncertain significance	1	156115184	156115184	Human	1	name
8654928	CV57225	duplication	NM_170707.4(LMNA):c.348dup (p.Lys117fs)	Cardiovascular phenotype [RCV005364913]\|Charcot-Marie-Tooth disease type 2 [RCV000703206]\|Primary dilated cardiomyopathy [RCV000041344]\|not provided [RCV000057392]	pathogenic\|not provided	1	156115265	156115266	Human	2	name
8610941	CV57243	deletion	NM_170707.4(LMNA):c.763del (p.Gln255fs)	Charcot-Marie-Tooth disease type 2 [RCV003581569]\|Primary dilated cardiomyopathy [RCV000041364]	pathogenic\|likely pathogenic	1	156134927	156134927	Human	2	name
8610957	CV57259	deletion	NM_170707.4(LMNA):c.958del (p.Leu320fs)	Charcot-Marie-Tooth disease type 2 [RCV001069384]\|Primary dilated cardiomyopathy [RCV000041381]\|not provided [RCV000236709]	pathogenic	1	156135922	156135922	Human	2	name
8622636	CV77658	single nucleotide variant	NM_170707.4(LMNA):c.103C>G (p.Leu35Val)	not provided [RCV000057217]	not provided	1	156115021	156115021	Human		name
8622640	CV77662	single nucleotide variant	NM_170707.4(LMNA):c.104T>C (p.Leu35Pro)	Charcot-Marie-Tooth disease type 2 [RCV001231384]\|Muscular dystrophy [RCV000499410]\|not provided [RCV000057221]	pathogenic\|likely pathogenic\|uncertain significance\|not provided	1	156115022	156115022	Human	3	name
8622645	CV77667	single nucleotide variant	NM_170707.4(LMNA):c.106C>T (p.Gln36Ter)	not provided [RCV000057226]	not provided	1	156115024	156115024	Human		name
8622649	CV77671	single nucleotide variant	NM_170707.4(LMNA):c.1098G>A (p.Lys366=)	Cardiomyopathy [RCV001178173]\|Cardiovascular phenotype [RCV002453371]\|Charcot-Marie-Tooth disease type 2 [RCV001437348]\|Primary dilated cardiomyopathy [RCV003996496]\|not provided [RCV000057231]\|not specified [RCV000500477]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156136062	156136062	Human	4	name
8622655	CV77677	single nucleotide variant	NM_170707.4(LMNA):c.1149G>A (p.Glu383=)	Cardiomyopathy [RCV000776145]\|Cardiovascular phenotype [RCV000619516]\|Charcot-Marie-Tooth disease type 2 [RCV000536971]\|Charcot-Marie-Tooth disease type 2B1 [RCV001093854]\|Congenital muscular dystrophy due to LMNA mutation [RCV000327855]\|Dilated Cardiomyopathy, ... (more) Dominant [RCV000259414]\|Dilated cardiomyopathy 1A [RCV000355460]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001098597]\|Emery-Dreifuss muscular dystrophy [RCV000377531]\|Familial partial lipodystrophy, Dunnigan type [RCV000289312]\|Hutchinson-Gilford syndrome [RCV000263024]\|Lethal tight skin contracture syndrome [RCV000324542]\|Limb-girdle muscular dystrophy, recessive [RCV000384768]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV000298159]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV000293812]\|not provided [RCV000057240]\|not specified [RCV000259097]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156136113	156136113	Human	17	name
8622663	CV77685	single nucleotide variant	NM_170707.4(LMNA):c.115A>T (p.Asn39Tyr)	not provided [RCV000057249]	not provided	1	156115033	156115033	Human		name
8622666	CV77688	single nucleotide variant	NM_170707.4(LMNA):c.116A>G (p.Asn39Ser)	Charcot-Marie-Tooth disease type 2 [RCV000557302]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV005252725]\|LMNA-related disorder [RCV004545742]\|not provided [RCV000057252]	pathogenic\|not provided	1	156115034	156115034	Human	3	name , alternate_id
8622674	CV77696	single nucleotide variant	NM_170707.4(LMNA):c.127G>A (p.Ala43Thr)	Charcot-Marie-Tooth disease type 2 [RCV001225020]\|not provided [RCV000057262]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156115045	156115045	Human	1	name
8622676	CV77698	single nucleotide variant	NM_170707.4(LMNA):c.1299C>T (p.His433=)	Cardiomyopathy [RCV001187620]\|Charcot-Marie-Tooth disease type 2 [RCV001088311]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002490640]\|Primary dilated cardiomyopathy [RCV003996502]\|not provided [RCV000057264]\|not specified [RCV000504112]	benign\|likely benign\|not provided	1	156136355	156136355	Human	6	name
8622682	CV77704	single nucleotide variant	NM_170707.4(LMNA):c.134A>G (p.Tyr45Cys)	Charcot-Marie-Tooth disease type 2 [RCV000692072]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV002468560]\|not provided [RCV000057272]	pathogenic\|likely pathogenic\|uncertain significance\|not provided	1	156115052	156115052	Human	2	name
8622690	CV77712	single nucleotide variant	NM_170707.4(LMNA):c.136A>G (p.Ile46Val)	Charcot-Marie-Tooth disease type 2 [RCV001230439]\|not provided [RCV000057281]	pathogenic\|likely pathogenic\|uncertain significance\|not provided	1	156115054	156115054	Human	1	name
8622697	CV77719	single nucleotide variant	NM_170707.4(LMNA):c.139G>C (p.Asp47His)	Charcot-Marie-Tooth disease type 2 [RCV001319873]\|not provided [RCV000057290]	uncertain significance\|not provided	1	156115057	156115057	Human	1	name
8622710	CV77732	single nucleotide variant	NM_170707.4(LMNA):c.148C>A (p.Arg50Ser)	not provided [RCV000057309]	not provided	1	156115066	156115066	Human		name
8622715	CV77737	single nucleotide variant	NM_170707.4(LMNA):c.149G>C (p.Arg50Pro)	not provided [RCV000057314]	pathogenic\|not provided	1	156115067	156115067	Human		name
8622721	CV77744	single nucleotide variant	NM_170707.4(LMNA):c.155T>C (p.Leu52Pro)	not provided [RCV000057322]	not provided	1	156115073	156115073	Human		name
8622726	CV77749	single nucleotide variant	NM_170707.4(LMNA):c.158A>T (p.Glu53Val)	not provided [RCV000057334]	not provided	1	156115076	156115076	Human		name
8622741	CV77764	single nucleotide variant	NM_170707.4(LMNA):c.1803C>T (p.Ser601=)	Cardiomyopathy [RCV001189167]\|Cardiovascular phenotype [RCV002408561]\|Charcot-Marie-Tooth disease type 2 [RCV001082711]\|Primary dilated cardiomyopathy [RCV003996508]\|not provided [RCV000057360]	likely benign\|not provided	1	156138592	156138592	Human	4	name
8622742	CV77765	single nucleotide variant	NM_170707.4(LMNA):c.184C>G (p.Arg62Gly)	Charcot-Marie-Tooth disease type 2 [RCV001051802]\|Familial partial lipodystrophy, Dunnigan type [RCV000503031]\|not provided [RCV000057365]	pathogenic\|not provided	1	156115102	156115102	Human	2	name
8622745	CV77768	single nucleotide variant	NM_170707.4(LMNA):c.188T>A (p.Ile63Asn)	not provided [RCV000057368]	not provided	1	156115106	156115106	Human		name
8622746	CV77769	single nucleotide variant	NM_170707.4(LMNA):c.188T>G (p.Ile63Ser)	not provided [RCV000057369]	not provided	1	156115106	156115106	Human		name
8622749	CV77772	single nucleotide variant	NM_170707.4(LMNA):c.1908C>T (p.Ser636=)	Cardiomyopathy [RCV003531949]\|Cardiovascular phenotype [RCV002408562]\|Charcot-Marie-Tooth disease type 2 [RCV003743557]\|not provided [RCV000057372]	pathogenic\|likely benign\|not provided	1	156138697	156138697	Human	3	name
8622756	CV77779	single nucleotide variant	NM_170707.4(LMNA):c.244G>A (p.Glu82Lys)	Charcot-Marie-Tooth disease type 2 [RCV000457442]\|Primary dilated cardiomyopathy [RCV000156060]\|not provided [RCV000057380]	pathogenic\|not provided	1	156115162	156115162	Human	2	name
8622757	CV77780	single nucleotide variant	NM_170707.4(LMNA):c.265C>T (p.Arg89Cys)	Heart-hand syndrome, Slovenian type [RCV004767053]\|not provided [RCV000057382]	likely pathogenic\|not provided	1	156115183	156115183	Human	1	name
8622758	CV77781	single nucleotide variant	NM_170707.4(LMNA):c.266G>T (p.Arg89Leu)	Cardiovascular phenotype [RCV005364950]\|Charcot-Marie-Tooth disease type 2 [RCV000462640]\|not provided [RCV000057383]	pathogenic\|likely pathogenic\|not provided	1	156115184	156115184	Human	1	name
8622759	CV77782	single nucleotide variant	NM_170707.4(LMNA):c.274C>T (p.Leu92Phe)	Cardiovascular phenotype [RCV002433553]\|not provided [RCV000057384]	pathogenic\|likely pathogenic\|not provided	1	156115192	156115192	Human		name
8622760	CV77783	single nucleotide variant	NM_170707.4(LMNA):c.289A>G (p.Lys97Glu)	not provided [RCV000057385]	not provided	1	156115207	156115207	Human		name
8622792	CV77816	deletion	NM_170707.4(LMNA):c.626del (p.Asn209fs)	not provided [RCV000057434]	likely pathogenic\|not provided	1	156134514	156134514	Human		name
8622843	CV77867	deletion	NM_170707.4(LMNA):c.506del (p.Val169fs)	not provided [RCV000057505]	not provided	1	156130766	156130766	Human		name
21071842	CV794448	single nucleotide variant	NM_170707.4(LMNA):c.122G>C (p.Arg41Pro)	not provided [RCV000994130]	likely pathogenic	1	156115040	156115040	Human		name
21071848	CV794449	single nucleotide variant	NM_170707.4(LMNA):c.1146C>A (p.Gly382=)	not provided [RCV000994132]	likely pathogenic	1	156136110	156136110	Human		name
21071857	CV794451	single nucleotide variant	NM_170707.4(LMNA):c.1182C>T (p.Thr394=)	Cardiovascular phenotype [RCV002337050]\|Charcot-Marie-Tooth disease type 2 [RCV001439975]\|not provided [RCV000994134]	likely benign\|uncertain significance	1	156136238	156136238	Human	1	name
26918914	CV822790	single nucleotide variant	NM_170707.4(LMNA):c.136A>C (p.Ile46Leu)	Charcot-Marie-Tooth disease type 2 [RCV001058402]	uncertain significance	1	156115054	156115054	Human	1	name
26886629	CV822792	single nucleotide variant	NM_170707.4(LMNA):c.230T>G (p.Ile77Ser)	Charcot-Marie-Tooth disease type 2 [RCV001044350]\|Heart-hand syndrome, Slovenian type [RCV005253689]	uncertain significance	1	156115148	156115148	Human	2	name
26886998	CV822793	single nucleotide variant	NM_170707.4(LMNA):c.272C>T (p.Thr91Ile)	Cardiovascular phenotype [RCV004994236]\|Charcot-Marie-Tooth disease type 2 [RCV001066402]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002480424]\|Primary dilated cardiomyopathy [RCV004000159]\|not provided [RCV002469339]	uncertain significance	1	156115190	156115190	Human	16	name
26913126	CV822794	single nucleotide variant	NM_170707.4(LMNA):c.274C>G (p.Leu92Val)	Cardiomyopathy [RCV001170450]\|Cardiovascular phenotype [RCV004031698]\|Charcot-Marie-Tooth disease type 2 [RCV001054035]	likely pathogenic\|uncertain significance	1	156115192	156115192	Human	3	name
26901549	CV822801	deletion	NM_170707.4(LMNA):c.611del (p.Leu204fs)	Cardiovascular phenotype [RCV005348308]\|Charcot-Marie-Tooth disease type 2 [RCV001071612]	pathogenic	1	156134500	156134500	Human	1	name
28893335	CV903711	single nucleotide variant	NM_170707.4(LMNA):c.230T>A (p.Ile77Asn)	Cardiomyopathy [RCV001170449]	uncertain significance	1	156115148	156115148	Human	2	name
34891919	CV905108	single nucleotide variant	NM_170707.4(LMNA):c.1092C>T (p.Asp364=)	Cardiomyopathy [RCV001183172]\|Cardiovascular phenotype [RCV005348336]\|Charcot-Marie-Tooth disease [RCV001173399]\|Charcot-Marie-Tooth disease type 2 [RCV002067846]\|Primary dilated cardiomyopathy [RCV004000281]	likely benign	1	156136056	156136056	Human	5	name
34890496	CV906399	single nucleotide variant	NM_170707.4(LMNA):c.141C>A (p.Asp47Glu)	Cardiomyopathy [RCV001182106]	uncertain significance	1	156115059	156115059	Human	2	name
34898839	CV906402	single nucleotide variant	NM_170707.4(LMNA):c.202G>A (p.Glu68Lys)	Cardiomyopathy [RCV001187535]\|Primary dilated cardiomyopathy [RCV004008711]	uncertain significance	1	156115120	156115120	Human	3	name
34894419	CV906403	single nucleotide variant	NM_170707.4(LMNA):c.206T>C (p.Val69Ala)	Cardiomyopathy [RCV001177272]	uncertain significance	1	156115124	156115124	Human	2	name
34897752	CV906404	single nucleotide variant	NM_170707.4(LMNA):c.215G>A (p.Arg72His)	Cardiomyopathy [RCV001186710]\|Cardiovascular phenotype [RCV005405531]	likely pathogenic\|uncertain significance	1	156115133	156115133	Human	2	name
34898228	CV906407	single nucleotide variant	NM_170707.4(LMNA):c.293A>G (p.Glu98Gly)	Cardiomyopathy [RCV001187072]\|Charcot-Marie-Tooth disease type 2 [RCV001862947]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002484024]\|Primary dilated cardiomyopathy [RCV004008663]	uncertain significance	1	156115211	156115211	Human	6	name
34888796	CV906428	single nucleotide variant	NM_170707.4(LMNA):c.1014G>A (p.Leu338=)	Cardiomyopathy [RCV001181011]	likely benign	1	156135978	156135978	Human	2	name
34897483	CV906429	single nucleotide variant	NM_170707.4(LMNA):c.1077C>T (p.Tyr359=)	Cardiomyopathy [RCV001186500]\|Charcot-Marie-Tooth disease type 2 [RCV001405135]	likely benign	1	156136041	156136041	Human	3	name
34888776	CV906430	single nucleotide variant	NM_170707.4(LMNA):c.1083G>A (p.Glu361=)	Cardiomyopathy [RCV001180990]\|Cardiovascular phenotype [RCV003293935]	likely benign	1	156136047	156136047	Human	2	name
34899732	CV906431	single nucleotide variant	NM_170707.4(LMNA):c.1218A>G (p.Ser406=)	Cardiomyopathy [RCV001188839]\|Cardiovascular phenotype [RCV003163465]\|Charcot-Marie-Tooth disease type 2 [RCV001449256]\|Primary dilated cardiomyopathy [RCV004010319]	likely benign	1	156136274	156136274	Human	4	name
34898368	CV906432	single nucleotide variant	NM_170707.4(LMNA):c.1230G>A (p.Gln410=)	Cardiomyopathy [RCV001187184]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005040002]\|Primary dilated cardiomyopathy [RCV004008679]	likely benign\|uncertain significance	1	156136286	156136286	Human	5	name
34893147	CV906434	single nucleotide variant	NM_170707.4(LMNA):c.1236G>C (p.Gly412=)	Cardiomyopathy [RCV001176314]\|Cardiovascular phenotype [RCV002365839]\|Charcot-Marie-Tooth disease type 2 [RCV001446980]\|Primary dilated cardiomyopathy [RCV004006285]	likely benign	1	156136292	156136292	Human	4	name
34899848	CV906439	single nucleotide variant	NM_170707.4(LMNA):c.1323C>T (p.Ala441=)	Cardiomyopathy [RCV001189053]\|Cardiovascular phenotype [RCV002379730]\|Charcot-Marie-Tooth disease type 2 [RCV001402439]\|Primary dilated cardiomyopathy [RCV004010329]	likely benign	1	156136379	156136379	Human	4	name
34900004	CV906440	single nucleotide variant	NM_170707.4(LMNA):c.1359G>A (p.Arg453=)	Cardiomyopathy [RCV001189296]\|Charcot-Marie-Tooth disease type 2 [RCV002069066]	likely benign	1	156136415	156136415	Human	3	name
34897086	CV906442	single nucleotide variant	NM_170707.4(LMNA):c.1407C>T (p.Ile469=)	Cardiomyopathy [RCV001186168]	likely benign	1	156136947	156136947	Human	2	name
34897298	CV906443	single nucleotide variant	NM_170707.4(LMNA):c.1482G>A (p.Val494=)	Cardiomyopathy [RCV001186353]	likely benign	1	156137022	156137022	Human	2	name
34901491	CV906444	single nucleotide variant	NM_170707.4(LMNA):c.1485G>A (p.Val495=)	Cardiomyopathy [RCV001191754]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002504215]	likely benign	1	156137025	156137025	Human	4	name
34896549	CV906445	single nucleotide variant	NM_170707.4(LMNA):c.1536G>A (p.Leu512=)	Cardiomyopathy [RCV001178505]\|Cardiovascular phenotype [RCV002402533]\|Charcot-Marie-Tooth disease type 2 [RCV002555487]\|Primary dilated cardiomyopathy [RCV004006485]	likely benign	1	156137160	156137160	Human	4	name
34898714	CV906448	single nucleotide variant	NM_170707.4(LMNA):c.1602T>C (p.Thr534=)	Cardiomyopathy [RCV001180201]\|Charcot-Marie-Tooth disease type 2 [RCV002068271]	likely benign	1	156137226	156137226	Human	3	name
34894956	CV906452	single nucleotide variant	NM_170707.4(LMNA):c.1701C>A (p.Gly567=)	Cardiomyopathy [RCV001185040]	likely benign	1	156138490	156138490	Human	2	name
34900804	CV906453	single nucleotide variant	NM_170707.4(LMNA):c.1728C>T (p.Pro576=)	Cardiomyopathy [RCV001190694]\|Cardiovascular phenotype [RCV002411718]\|Charcot-Marie-Tooth disease type 2 [RCV001401960]\|Primary dilated cardiomyopathy [RCV004010452]\|not provided [RCV001724264]\|not specified [RCV001699519]	benign\|likely benign	1	156138517	156138517	Human	4	name
34896903	CV906455	single nucleotide variant	NM_170707.4(LMNA):c.1746C>T (p.Arg582=)	Cardiomyopathy [RCV001186008]\|Charcot-Marie-Tooth disease type 2 [RCV001455621]	likely benign	1	156138535	156138535	Human	3	name
34897461	CV906457	single nucleotide variant	NM_170707.4(LMNA):c.1827A>G (p.Gly609=)	Cardiomyopathy [RCV001179184]	likely benign	1	156138616	156138616	Human	2	name
34891600	CV906458	single nucleotide variant	NM_170707.4(LMNA):c.1830C>T (p.Pro610=)	Cardiomyopathy [RCV001182597]	likely benign	1	156138619	156138619	Human	2	name
34900308	CV906463	single nucleotide variant	NM_170707.4(LMNA):c.1932C>T (p.Arg644=)	Cardiomyopathy [RCV001189823]	likely benign	1	156138721	156138721	Human	2	name
34897389	CV906465	single nucleotide variant	NM_170707.4(LMNA):c.1947C>A (p.Gly649=)	Cardiomyopathy [RCV001186425]	likely benign	1	156138736	156138736	Human	2	name
38463012	CV918566	single nucleotide variant	NM_170707.4(LMNA):c.1488G>C (p.Thr496=)	Dilated cardiomyopathy 1A [RCV001198820]	uncertain significance	1	156137028	156137028	Human	2	name
38476043	CV930061	single nucleotide variant	NM_170707.4(LMNA):c.115A>C (p.Asn39His)	Charcot-Marie-Tooth disease type 2 [RCV001204509]	likely pathogenic\|uncertain significance	1	156115033	156115033	Human	1	name
38457670	CV930062	single nucleotide variant	NM_170707.4(LMNA):c.163G>T (p.Glu55Ter)	Charcot-Marie-Tooth disease type 2 [RCV001211199]	pathogenic	1	156115081	156115081	Human	1	name
38461660	CV930063	single nucleotide variant	NM_170707.4(LMNA):c.217G>T (p.Glu73Ter)	Charcot-Marie-Tooth disease type 2 [RCV001212067]\|not provided [RCV001780125]	pathogenic	1	156115135	156115135	Human	1	name
38480480	CV930066	deletion	NM_170707.4(LMNA):c.705del (p.Glu236fs)	Charcot-Marie-Tooth disease type 2 [RCV001206410]	pathogenic	1	156134870	156134870	Human	1	name
38476622	CV941490	single nucleotide variant	NM_170707.4(LMNA):c.151T>C (p.Ser51Pro)	Charcot-Marie-Tooth disease type 2 [RCV001233158]\|not specified [RCV001815027]	uncertain significance	1	156115069	156115069	Human	1	name
38480290	CV941491	single nucleotide variant	NM_170707.4(LMNA):c.200A>G (p.Glu67Gly)	Charcot-Marie-Tooth disease type 2 [RCV001234658]	uncertain significance	1	156115118	156115118	Human	1	name
38474647	CV941492	single nucleotide variant	NM_170707.4(LMNA):c.265C>G (p.Arg89Gly)	Charcot-Marie-Tooth disease type 2 [RCV001232305]	likely pathogenic\|uncertain significance	1	156115183	156115183	Human	1	name
38460210	CV941503	single nucleotide variant	NM_170707.4(LMNA):c.1767G>T (p.Gly589=)	Charcot-Marie-Tooth disease type 2 [RCV001229302]\|Primary dilated cardiomyopathy [RCV004807476]	likely benign\|uncertain significance	1	156138556	156138556	Human	2	name
38464591	CV952090	single nucleotide variant	NM_170707.4(LMNA):c.185G>T (p.Arg62Leu)	Charcot-Marie-Tooth disease type 2 [RCV001247423]	likely pathogenic\|uncertain significance	1	156115103	156115103	Human	1	name
38598113	CV964131	single nucleotide variant	NM_170707.4(LMNA):c.193G>C (p.Glu65Gln)	Dilated cardiomyopathy 1A [RCV001253415]	uncertain significance	1	156115111	156115111	Human	2	name
41405484	CV981241	single nucleotide variant	NM_170707.4(LMNA):c.1212T>C (p.Ser404=)	not provided [RCV001813019]	likely benign	1	156136268	156136268	Human		name
126767627	CV1022660	single nucleotide variant	NM_170707.4(LMNA):c.470C>T (p.Thr157Met)	Cardiovascular phenotype [RCV002341704]\|Charcot-Marie-Tooth disease type 2 [RCV001342901]\|LMNA-related disorder [RCV004734130]	uncertain significance	1	156130730	156130730	Human	1	alternate_id
126733026	CV1022666	single nucleotide variant	NM_170707.4(LMNA):c.1459T>C (p.Phe487Leu)	Charcot-Marie-Tooth disease type 2 [RCV001349706]\|LMNA-related disorder [RCV004727177]\|not provided [RCV003238864]	uncertain significance	1	156136999	156136999	Human	1	alternate_id
9687838	CV172489	single nucleotide variant	NM_170707.4(LMNA):c.1634G>A (p.Arg545His)	Autosomal semi-dominant severe lipodystrophic laminopathy [RCV003993830]\|Cardiomyopathy [RCV000771819]\|Cardiovascular phenotype [RCV000621850]\|Charcot-Marie-Tooth disease type 2 [RCV000468904]\|Charcot-Marie-Tooth disease type 2B1 [RCV001101060]\|Congenital muscular dystrophy due to LMNA ... (more) weight:700;'>LMNA mutation [RCV001101062]\|Dilated cardiomyopathy 1A [RCV001101058]\|Dilated cardiomyopathy 1S [RCV000491650]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005042294]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005359320]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001101055]\|Hutchinson-Gilford syndrome [RCV001101061]\|LMNA-related disorder [RCV004532675]\|Lethal tight skin contracture syndrome [RCV001101057]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001100810]\|Lipodystrophy [RCV001248958]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001101059]\|Peripheral neuropathy [RCV000449630]\|Primary dilated cardiomyopathy [RCV003998208]\|Short stature [RCV001781492]\|not provided [RCV000505801]\|not specified [RCV000150955]	pathogenic\|likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156137679	156137679	Human	34	alternate_id
10046349	CV189383	single nucleotide variant	NM_170707.4(LMNA):c.1017G>A (p.Ala339=)	Cardiomyopathy [RCV000771177]\|Cardiovascular phenotype [RCV000244350]\|Charcot-Marie-Tooth disease [RCV001172634]\|Charcot-Marie-Tooth disease type 2 [RCV001086138]\|LMNA-related disorder [RCV004535167]\|not provided [RCV000172001]\|not specified [RCV000276961]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156135981	156135981	Human	4	alternate_id
10056809	CV196461	single nucleotide variant	NM_170707.4(LMNA):c.398G>A (p.Arg133Gln)	Cardiomyopathy [RCV001191911]\|Cardiovascular phenotype [RCV002372114]\|Charcot-Marie-Tooth disease type 2 [RCV000204542]\|Charcot-Marie-Tooth disease type 2B1 [RCV001098187]\|Congenital muscular dystrophy due to LMNA mutation [RCV001098188]\|Dilated cardiomyopathy 1 ... (more) A [RCV001098191]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV005042395]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV001098184]\|Emery-Dreifuss muscular dystrophy [RCV001098186]\|Familial partial lipodystrophy, Dunnigan type [RCV001098189]\|Hutchinson-Gilford syndrome [RCV001098190]\|LMNA-related disorder [RCV004734805]\|Lethal tight skin contracture syndrome [RCV001096448]\|Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules [RCV001096449]\|Mandibuloacral dysplasia with type A lipodystrophy [RCV001098185]\|Primary dilated cardiomyopathy [RCV003996714]\|not provided [RCV000182356]	pathogenic\|likely pathogenic\|uncertain significance	1	156130658	156130658	Human	20	alternate_id
10056818	CV196479	single nucleotide variant	NM_170707.4(LMNA):c.1279C>T (p.Arg427Cys)	Cardiomyopathy [RCV001181813]\|Cardiovascular phenotype [RCV002381591]\|Charcot-Marie-Tooth disease type 2 [RCV000653931]\|Dilated cardiomyopathy 1A [RCV002463440]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002492808]\|LMNA-related disorder [ ... (more) RCV004539704]\|Primary dilated cardiomyopathy [RCV003996715]\|not provided [RCV000182369]\|not specified [RCV003479048]	likely pathogenic\|uncertain significance	1	156136335	156136335	Human	18	alternate_id
10056838	CV196485	indel	NM_005572.4(LMNA):c.1711_1712delinsTC (p.Arg571Ser)	Cardiomyopathy [RCV001191556]\|Cardiovascular phenotype [RCV000249124]\|Charcot-Marie-Tooth disease type 2 [RCV001300467]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV003333038]\|LMNA-related disorder [RCV004528958]\|not provided [RCV000725840]	pathogenic\|likely benign\|uncertain significance	1	156137756	156137757	Human		alternate_id
156010124	CV2045475	single nucleotide variant	NM_170707.4(LMNA):c.1900G>T (p.Gly634Cys)	Charcot-Marie-Tooth disease type 2 [RCV002780094]\|LMNA-related disorder [RCV004725370]	uncertain significance	1	156138689	156138689	Human	1	alternate_id
11093384	CV228279	single nucleotide variant	NM_170707.4(LMNA):c.1770C>T (p.Thr590=)	Cardiomyopathy [RCV001189149]\|Cardiovascular phenotype [RCV002399784]\|Charcot-Marie-Tooth disease [RCV001173402]\|Charcot-Marie-Tooth disease type 2 [RCV000459717]\|LMNA-related disorder [RCV004530298]\|Primary dilated cardiomyopathy [RCV003997706]\|not provided [RC ... (more) V001705194]\|not specified [RCV000219715]	likely benign	1	156138559	156138559	Human	5	alternate_id
11638010	CV272513	single nucleotide variant	NM_170707.4(LMNA):c.1919A>G (p.Asn640Ser)	Charcot-Marie-Tooth disease type 2 [RCV000533234]\|Familial partial lipodystrophy, Dunnigan type [RCV003335301]\|LMNA-related disorder [RCV004734939]\|Primary dilated cardiomyopathy [RCV003995784]\|not provided [RCV000658526]	likely benign\|uncertain significance	1	156138708	156138708	Human	4	alternate_id
401931700	CV2801582	single nucleotide variant	NM_170707.4(LMNA):c.631T>G (p.Tyr211Asp)	LMNA-related disorder [RCV004529272]	uncertain significance	1	156134520	156134520	Human		trait , alternate_id
8564268	CV29525	single nucleotide variant	NM_170707.4(LMNA):c.1445G>A (p.Arg482Gln)	Cardiomyopathy [RCV001179839]\|Cardiovascular phenotype [RCV002390111]\|Charcot-Marie-Tooth disease type 2 [RCV000459624]\|Dilated cardiomyopathy 1A [RCV001822996]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV000763258]\|Emery-Dreifuss muscular dystrophy 3, autosomal recessive [RCV ... (more) 000190399]\|Familial partial lipodystrophy, Dunnigan type [RCV000015575]\|LMNA-related disorder [RCV004532361]\|Laminopathy [RCV000041318]\|Monogenic diabetes [RCV000754814]\|Primary dilated cardiomyopathy [RCV004806012]\|not provided [RCV000057299]	pathogenic\|uncertain significance\|no classifications from unflagged records\|not provided	1	156136985	156136985	Human	20	alternate_id
8564271	CV29528	single nucleotide variant	NM_170707.4(LMNA):c.1444C>T (p.Arg482Trp)	Cardiovascular phenotype [RCV002390112]\|Charcot-Marie-Tooth disease [RCV001174239]\|Charcot-Marie-Tooth disease type 2 [RCV001235764]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002482872]\|Familial partial lipodystrophy [RCV001248961]\|Familial partial lipodystrophy, Dunnigan ty ... (more) pe [RCV000015579]\|LMNA-related disorder [RCV004532362]\|not provided [RCV000057298]	pathogenic\|likely pathogenic\|not provided	1	156136984	156136984	Human	17	alternate_id
8564275	CV29533	single nucleotide variant	NM_170707.4(LMNA):c.1745G>A (p.Arg582His)	Cardiomyopathy [RCV001804734]\|Cardiovascular phenotype [RCV002399327]\|Charcot-Marie-Tooth disease type 2 [RCV001068657]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV004795416]\|Familial partial lipodystrophy, Dunnigan type [RCV000015585]\|LMNA ... (more) >-related disorder [RCV004532363]\|Primary dilated cardiomyopathy [RCV003996099]\|not provided [RCV000057353]	pathogenic\|likely pathogenic\|uncertain significance\|not provided	1	156138534	156138534	Human	18	alternate_id
8564305	CV29563	single nucleotide variant	NM_170707.4(LMNA):c.745C>T (p.Arg249Trp)	Charcot-Marie-Tooth disease type 2 [RCV000814531]\|Congenital muscular dystrophy due to LMNA mutation [RCV000015621]\|LMNA-related disorder [RCV005229797]\|not provided [RCV000057452]	pathogenic\|likely pathogenic\|not provided	1	156134910	156134910	Human	2	alternate_id
8564308	CV29566	single nucleotide variant	NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys)	Cardiomyopathy [RCV000771143]\|Cardiovascular phenotype [RCV000245284]\|Charcot-Marie-Tooth disease [RCV000144868]\|Charcot-Marie-Tooth disease type 2 [RCV001084244]\|Dilated cardiomyopathy 1A [RCV000755679]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV003224100]\|Familial partial l ... (more) ipodystrophy, Dunnigan type [RCV002467497]\|LMNA-related disorder [RCV004528114]\|Monogenic diabetes [RCV001174411]\|Primary dilated cardiomyopathy [RCV000148602]\|Variant of unknown significance [RCV000015626]\|not provided [RCV000057374]\|not specified [RCV000041340]	likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156138719	156138719	Human	20	alternate_id
408375987	CV3506750	single nucleotide variant	NM_170707.4(LMNA):c.454C>T (p.Leu152Phe)	LMNA-related disorder [RCV004726488]	uncertain significance	1	156130714	156130714	Human		trait , alternate_id
408369052	CV3507873	single nucleotide variant	NM_170707.4(LMNA):c.1325T>A (p.Val442Glu)	LMNA-related disorder [RCV004736521]	likely pathogenic	1	156136381	156136381	Human		trait , alternate_id
12837964	CV364527	single nucleotide variant	NM_170707.4(LMNA):c.1857T>C (p.Ser619=)	Cardiomyopathy [RCV001180308]\|Cardiovascular phenotype [RCV002411298]\|Charcot-Marie-Tooth disease [RCV001172633]\|Charcot-Marie-Tooth disease type 2 [RCV000653988]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002502474]\|LMNA-related disorder ... (more) [RCV004530539]\|Primary dilated cardiomyopathy [RCV003995963]\|not provided [RCV004808703]\|not specified [RCV000426097]	likely benign	1	156138646	156138646	Human	19	alternate_id
12892167	CV390809	single nucleotide variant	NM_170707.4(LMNA):c.352G>T (p.Ala118Ser)	Charcot-Marie-Tooth disease type 2 [RCV000459194]\|LMNA-related disorder [RCV004735540]	uncertain significance	1	156115270	156115270	Human	1	alternate_id
616933308	CV4011407	single nucleotide variant	NM_170707.4(LMNA):c.1398T>G (p.Asn466Lys)	LMNA-related disorder [RCV005407488]	pathogenic	1	156136938	156136938	Human		trait , alternate_id
8602919	CV45135	single nucleotide variant	NM_170707.4(LMNA):c.1003C>T (p.Arg335Trp)	Arrhythmogenic right ventricular cardiomyopathy [RCV000852407]\|Cardiomyopathy [RCV003149579]\|Cardiovascular phenotype [RCV000620788]\|Charcot-Marie-Tooth disease type 2 [RCV000546102]\|Dilated cardiomyopathy 1A [RCV001196390]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002477025 ... (more) ]\|Heart-hand syndrome, Slovenian type [RCV000721960]\|LMNA-related disorder [RCV004532421]\|Left ventricular noncompaction [RCV000845456]\|Primary dilated cardiomyopathy [RCV000030145]\|Primary dilated cardiomyopathy [RCV000844672]\|Primary familial dilated cardiomyopathy [RCV003492303]\|not provided [RCV000182368]	pathogenic\|likely pathogenic	1	156135967	156135967	Human	23	alternate_id
13529871	CV509124	indel	NM_170707.4(LMNA):c.1873_1874delinsCC (p.Ser625Pro)	Cardiomyopathy [RCV001185275]\|Cardiovascular phenotype [RCV000622044]\|Charcot-Marie-Tooth disease type 2 [RCV000822504]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002498997]\|LMNA-related disorder [RCV004735679]\|not provided [RCV005429259]	uncertain significance	1	156138662	156138663	Human		alternate_id
8610917	CV57216	single nucleotide variant	NM_170707.4(LMNA):c.1804G>A (p.Gly602Ser)	Cardiomyopathy [RCV000771799]\|Cardiovascular phenotype [RCV000617798]\|Charcot-Marie-Tooth disease type 2 [RCV001088263]\|Congenital muscular dystrophy due to LMNA mutation [RCV004820827]\|Insulin-resistant diabetes mellitus AND acanthosis nigricans [RCV000148601]\| ... (more) LMNA-related disorder [RCV004541208]\|not provided [RCV000057361]\|not specified [RCV000041334]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156138593	156138593	Human	6	alternate_id
8610918	CV57217	single nucleotide variant	NM_170707.4(LMNA):c.1825G>A (p.Gly609Arg)	Cardiomyopathy [RCV001804765]\|Cardiovascular phenotype [RCV003162352]\|Charcot-Marie-Tooth disease type 2 [RCV001852840]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002483028]\|LMNA-related disorder [RCV004528230]\|Primary dilated cardiomyopa ... (more) thy [RCV003996459]\|not provided [RCV003320549]	uncertain significance	1	156138614	156138614	Human	18	alternate_id
8610921	CV57220	single nucleotide variant	NM_170707.4(LMNA):c.1912G>A (p.Gly638Arg)	Cardiomyopathy [RCV001188113]\|Cardiovascular phenotype [RCV005403744]\|Charcot-Marie-Tooth disease type 2 [RCV001084443]\|LMNA-related disorder [RCV004541209]\|not provided [RCV000725381]\|not specified [RCV000041338]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156138701	156138701	Human	3	alternate_id
8573365	CV57234	single nucleotide variant	NM_170707.4(LMNA):c.607G>A (p.Glu203Lys)	Cardiovascular phenotype [RCV000618699]\|Charcot-Marie-Tooth disease type 2 [RCV000653912]\|Dilated cardiomyopathy 1A [RCV000055999]\|Dilated cardiomyopathy 1A [RCV001824588]\|LMNA-related disorder [RCV004724769]\|Primary dilated cardiomyopathy [RCV000211790]\|not pro ... (more) vided [RCV000057427]	pathogenic\|likely pathogenic\|not provided	1	156134496	156134496	Human	13	alternate_id
8610954	CV57256	single nucleotide variant	NM_170707.4(LMNA):c.895A>G (p.Ile299Val)	Cardiomyopathy [RCV000777745]\|Cardiovascular phenotype [RCV000619864]\|Charcot-Marie-Tooth disease [RCV001174244]\|Charcot-Marie-Tooth disease type 2 [RCV001086902]\|Familial partial lipodystrophy, Dunnigan type [RCV000148604]\|LMNA-related disorder [RCV004734590]\|P ... (more) rimary dilated cardiomyopathy [RCV004806042]\|not provided [RCV000726532]\|not specified [RCV000041378]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	156135271	156135271	Human	7	alternate_id
8610955	CV57257	single nucleotide variant	NM_170707.4(LMNA):c.949G>A (p.Glu317Lys)	Cardiomyopathy [RCV000769726]\|Cardiovascular phenotype [RCV002371856]\|Charcot-Marie-Tooth disease type 2 [RCV000560270]\|Dilated cardiomyopathy 1A [RCV001775075]\|LMNA-related disorder [RCV004541210]\|Primary dilated cardiomyopathy [RCV000041379]\|Primary familial d ... (more) ilated cardiomyopathy [RCV001251293]\|not provided [RCV000057489]\|not specified [RCV001000784]	pathogenic\|likely pathogenic\|not provided	1	156135913	156135913	Human	7	alternate_id
8610960	CV57262	single nucleotide variant	NM_170707.4(LMNA):c.992G>A (p.Arg331Gln)	Cardiomyopathy [RCV000769727]\|Cardiovascular phenotype [RCV002381325]\|Charcot-Marie-Tooth disease type 2 [RCV001071970]\|Dilated cardiomyopathy 1A [RCV001265547]\|LMNA-related disorder [RCV003335073]\|Primary dilated cardiomyopathy [RCV000593819]\|Primary familial d ... (more) ilated cardiomyopathy [RCV003235003]\|See cases [RCV004797773]\|not provided [RCV000182367]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	1	156135956	156135956	Human	7	alternate_id
15165186	CV745738	single nucleotide variant	NM_170707.4(LMNA):c.1941C>T (p.Leu647=)	Cardiomyopathy [RCV001805932]\|Cardiovascular phenotype [RCV003363010]\|Charcot-Marie-Tooth disease type 2 [RCV002066044]\|LMNA-related disorder [RCV004533570]	likely benign	1	156138730	156138730	Human	3	alternate_id
8622488	CV77508	single nucleotide variant	NM_005572.4(LMNA):c.1711C>T (p.Arg571Cys)	Cardiomyopathy [RCV001176130]\|Cardiovascular phenotype [RCV004992003]\|Charcot-Marie-Tooth disease [RCV000790249]\|Charcot-Marie-Tooth disease type 2 [RCV001854169]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002504958]\|LMNA-related disorder ... (more) [RCV004734614]\|Primary dilated cardiomyopathy [RCV003996491]\|not provided [RCV000057045]	uncertain significance\|not provided	1	156137756	156137756	Human	19	alternate_id
8622679	CV77701	single nucleotide variant	NM_170707.4(LMNA):c.1315C>T (p.Arg439Cys)	Cardiomyopathy [RCV001182564]\|Cardiovascular phenotype [RCV002381365]\|Charcot-Marie-Tooth disease type 2 [RCV001225469]\|Charcot-Marie-Tooth disease type 2B1 [RCV004786333]\|Familial partial lipodystrophy, Dunnigan type [RCV003326119]\|LMNA-related disorder [RCV004 ... (more) 537256]\|Primary dilated cardiomyopathy [RCV003996503]\|not provided [RCV000057267]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156136371	156136371	Human	7	alternate_id
8622734	CV77757	single nucleotide variant	NM_170707.4(LMNA):c.1622G>A (p.Arg541His)	Cardiovascular phenotype [RCV000246865]\|Charcot-Marie-Tooth disease type 2 [RCV000230467]\|Congenital muscular dystrophy [RCV004018989]\|Dilated cardiomyopathy 1A [RCV001262710]\|Emery-Dreifuss muscular dystrophy 2, autosomal dominant [RCV005252726]\|Hutchinson-Gilford syndrome [RCV001836636]\|LMNA ... (more) e='font-weight:700;'>LMNA-related disorder [RCV003335086]\|Primary dilated cardiomyopathy [RCV000221013]\|not provided [RCV000057344]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	1	156137667	156137667	Human	9	alternate_id
8622781	CV77805	single nucleotide variant	NM_170707.4(LMNA):c.568C>T (p.Arg190Trp)	Cardiovascular phenotype [RCV000619878]\|Charcot-Marie-Tooth disease type 2 [RCV000535082]\|Dilated cardiomyopathy 1S [RCV000491585]\|LMNA-related disorder [RCV004528262]\|Primary dilated cardiomyopathy [RCV003996512]\|not provided [RCV000057419]	pathogenic\|not provided	1	156134457	156134457	Human	3	alternate_id
41406917	CV982360	single nucleotide variant	NM_170707.4(LMNA):c.832G>A (p.Ala278Thr)	Cardiomyopathy [RCV005403014]\|Charcot-Marie-Tooth disease type 2 [RCV001863151]\|LMNA-related disorder [RCV004528448]\|not provided [RCV001289083]	pathogenic\|likely pathogenic\|uncertain significance	1	156135208	156135208	Human	3	alternate_id
151761351	CV1496391	indel	NM_170707.4(LMNA):c.937-9_937-8delinsAG	Charcot-Marie-Tooth disease type 2 [RCV001895356]	uncertain significance	1	156135892	156135893	Human		name
150513313	CV1228967	deletion	NM_170707.4(LMNA):c.357-3588_357-3580del	not provided [RCV001637809]	benign	1	156127024	156127032	Human		name
151810145	CV1393340	deletion	NM_170707.4(LMNA):c.822del (p.Arg275fs)	Charcot-Marie-Tooth disease type 2 [RCV001953733]\|Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome [RCV002492131]	pathogenic\|likely pathogenic	1	156135197	156135197	Human	3	name
152085789	CV1645265	single nucleotide variant	NM_170707.4(LMNA):c.1200C>T (p.Gly400=)	Charcot-Marie-Tooth disease type 2 [RCV002131410]	likely benign	1	156136256	156136256	Human	1	name
155721469	CV1835936	single nucleotide variant	NM_170707.4(LMNA):c.1305C>T (p.Arg435=)	Cardiovascular phenotype [RCV002380939]\|Charcot-Marie-Tooth disease type 2 [RCV003094946]	likely benign	1	156136361	156136361	Human	1	name

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