Vcp Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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803 records found for search term Vcp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
11578900	CV268541	single nucleotide variant	NM_007126.5(VCP):c.*4G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000291446]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000376145]\|Intellectual disability [RCV001252622]\|not provided [RCV001559813]\|not specified [RCV000301970]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35057113	35057113	Human	4	name , alternate_id
596938947	CV3549911	single nucleotide variant	NM_007126.5(VCP):c.-1C>T	not provided [RCV004812952]	uncertain significance	9	35072354	35072354	Human		name
11601818	CV308247	single nucleotide variant	NM_007126.5(VCP):c.*64C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000340221]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000285114]\|not provided [RCV004696139]	uncertain significance	9	35057053	35057053	Human	2	name , alternate_id
11603345	CV319056	single nucleotide variant	NM_007126.5(VCP):c.-53C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000400582]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000298964]	uncertain significance	9	35072406	35072406	Human	2	name , alternate_id
596946791	CV3548622	single nucleotide variant	NM_007126.5(VCP):c.*55G>A	not provided [RCV004810450]	uncertain significance	9	35057062	35057062	Human		name
28875882	CV901967	single nucleotide variant	NM_007126.5(VCP):c.*63G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001165971]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001167533]\|not provided [RCV004584856]	uncertain significance	9	35057054	35057054	Human	2	name , alternate_id
28881129	CV901968	single nucleotide variant	NM_007126.5(VCP):c.*15C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001167535]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001167534]	benign\|likely benign	9	35057102	35057102	Human	2	name , alternate_id
28881136	CV901969	single nucleotide variant	NM_007126.5(VCP):c.*12C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001167536]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001167537]	benign\|likely benign	9	35057105	35057105	Human	2	name , alternate_id
150431938	CV1246123	single nucleotide variant	NM_007126.5(VCP):c.18-4C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002538570]\|not provided [RCV001663535]	likely benign\|uncertain significance	9	35068366	35068366	Human	1	name , alternate_id
155995490	CV2023593	single nucleotide variant	NM_007126.5(VCP):c.18-6T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002755940]	likely benign	9	35068368	35068368	Human	1	name , alternate_id
156180632	CV2167507	single nucleotide variant	NM_007126.5(VCP):c.18-8C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003023815]	likely benign	9	35068370	35068370	Human	1	name , alternate_id
11607424	CV308235	single nucleotide variant	NM_007126.5(VCP):c.*596C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000401604]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000343505]	benign\|likely benign	9	35056521	35056521	Human	2	name , alternate_id
11603816	CV308243	single nucleotide variant	NM_007126.5(VCP):c.*438A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000303765]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000339601]	benign\|likely benign	9	35056679	35056679	Human	2	name , alternate_id
11599930	CV308244	single nucleotide variant	NM_007126.5(VCP):c.*382C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000269388]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000363922]	uncertain significance	9	35056735	35056735	Human	2	name , alternate_id
11647267	CV308246	single nucleotide variant	NM_007126.5(VCP):c.*184G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000275373]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000319333]	uncertain significance	9	35056933	35056933	Human	2	name , alternate_id
11648561	CV312609	single nucleotide variant	NM_007126.5(VCP):c.*788G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000337724]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000282676]	uncertain significance	9	35056329	35056329	Human	2	name , alternate_id
11604440	CV312615	deletion	NM_007126.5(VCP):c.*384del	Amyotrophic Lateral Sclerosis, Dominant [RCV000390511]\|Inclusion Body Myopathy, Dominant [RCV000309265]	uncertain significance	9	35056733	35056733	Human	2	name
11654150	CV312619	single nucleotide variant	NM_007126.5(VCP):c.*347C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000315190]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000369915]	uncertain significance	9	35056770	35056770	Human	2	name , alternate_id
11644555	CV312628	single nucleotide variant	NM_007126.5(VCP):c.*172C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000373981]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000260516]	uncertain significance	9	35056945	35056945	Human	2	name , alternate_id
11659737	CV312631	single nucleotide variant	NM_007126.5(VCP):c.-215A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000407512]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000360664]	uncertain significance	9	35072568	35072568	Human	2	name , alternate_id
11646696	CV312632	single nucleotide variant	NM_007126.5(VCP):c.-250C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000272098]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000329052]	uncertain significance	9	35072603	35072603	Human	2	name , alternate_id
11600054	CV312633	single nucleotide variant	NM_007126.5(VCP):c.-267C>T	Amyotrophic Lateral Sclerosis, Dominant [RCV000270492]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001166090]\|Inclusion Body Myopathy, Dominant [RCV000362697]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001166091]\|not provided [RCV ... (more) 004705493]	benign\|likely benign	9	35072620	35072620	Human	4	name , alternate_id
11606388	CV318524	single nucleotide variant	NM_007126.5(VCP):c.*906A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000330855]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000386372]	benign\|likely benign	9	35056211	35056211	Human	2	name , alternate_id
11601083	CV318528	single nucleotide variant	NM_007126.5(VCP):c.*700C>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000373728]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000279189]\|not provided [RCV003430970]	benign\|uncertain significance	9	35056417	35056417	Human	2	name , alternate_id
11605101	CV318529	single nucleotide variant	NM_007126.5(VCP):c.*153G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000315799]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000379622]\|not provided [RCV001675887]	benign\|likely benign	9	35056964	35056964	Human	2	name , alternate_id
11602759	CV318534	single nucleotide variant	NM_007126.5(VCP):c.18-5T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000293440]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001086142]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000338806]\|not provided [RCV000548347]\|not specified [ ... (more) RCV001699407]	benign\|likely benign	9	35068367	35068367	Human	3	name , alternate_id
11656370	CV318546	single nucleotide variant	NM_007126.4(VCP):c.-370G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000332626]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000389517]	uncertain significance	9	35072723	35072723	Human	2	name , alternate_id
408378040	CV3511664	single nucleotide variant	NM_007126.4(VCP):c.-360G>C	VCP-related disorder [RCV004735146]	uncertain significance	9	35072713	35072713	Human		name , trait , alternate_id
15172190	CV775544	single nucleotide variant	NM_007126.5(VCP):c.18-6T>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001411367]	likely benign	9	35068368	35068368	Human	1	name , alternate_id
28883045	CV901964	single nucleotide variant	NM_007126.5(VCP):c.*367G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168092]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168854]	uncertain significance	9	35056750	35056750	Human	2	name , alternate_id
28885719	CV901965	single nucleotide variant	NM_007126.5(VCP):c.*217G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168856]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168855]	uncertain significance	9	35056900	35056900	Human	2	name , alternate_id
28885727	CV901966	single nucleotide variant	NM_007126.5(VCP):c.*216G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168857]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168858]	uncertain significance	9	35056901	35056901	Human	2	name , alternate_id
28880910	CV903397	single nucleotide variant	NM_007126.5(VCP):c.*885G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001167477]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001167478]	uncertain significance	9	35056232	35056232	Human	2	name , alternate_id
126763407	CV1029188	single nucleotide variant	NM_007126.5(VCP):c.577-2A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001341264]	likely pathogenic\|uncertain significance	9	35064287	35064287	Human	1	name , alternate_id
126734212	CV1029190	single nucleotide variant	NM_007126.5(VCP):c.130-3C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001349905]	uncertain significance	9	35068066	35068066	Human	1	name , alternate_id
127248218	CV1076441	single nucleotide variant	NM_007126.5(VCP):c.446-5C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001394423]\|Inborn genetic diseases [RCV002329415]	likely benign\|uncertain significance	9	35065386	35065386	Human	2	name , alternate_id
150535142	CV1293688	single nucleotide variant	NM_007126.5(VCP):c.709-2A>G	not provided [RCV001757965]	uncertain significance	9	35063082	35063082	Human		name
151818982	CV1385798	single nucleotide variant	NM_007126.5(VCP):c.946-8T>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002013183]	likely benign\|uncertain significance	9	35062146	35062146	Human	1	name , alternate_id
151813616	CV1448031	single nucleotide variant	NM_007126.5(VCP):c.811+5G>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001918858]	uncertain significance	9	35062973	35062973	Human	1	name , alternate_id
152171443	CV1552749	single nucleotide variant	NM_007126.5(VCP):c.446-7C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002143448]	likely benign	9	35065388	35065388	Human	1	name , alternate_id
152101766	CV1645894	single nucleotide variant	NM_007126.5(VCP):c.577-9C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002173197]	likely benign	9	35064294	35064294	Human	1	name , alternate_id
155673272	CV1820238	single nucleotide variant	NM_007126.5(VCP):c.812-6T>G	Inborn genetic diseases [RCV002421307]	uncertain significance	9	35062356	35062356	Human	1	name
156029849	CV1893528	single nucleotide variant	NM_007126.5(VCP):c.446-7C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003078047]	likely benign	9	35065388	35065388	Human	1	name , alternate_id
156354903	CV1974996	single nucleotide variant	NM_007126.5(VCP):c.130-6C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002602091]	likely benign	9	35068069	35068069	Human	1	name , alternate_id
156351238	CV2018953	single nucleotide variant	NM_007126.5(VCP):c.302+8T>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002720197]	likely benign	9	35067883	35067883	Human	1	name , alternate_id
156072207	CV2172690	single nucleotide variant	NM_007126.5(VCP):c.445+8C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003053751]	uncertain significance	9	35066667	35066667	Human	1	name , alternate_id
156233750	CV2173205	single nucleotide variant	NM_007126.5(VCP):c.303-5C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003059405]	likely benign	9	35066822	35066822	Human	1	name , alternate_id
156107633	CV2181108	single nucleotide variant	NM_007126.5(VCP):c.812-9T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003054964]	likely benign	9	35062359	35062359	Human	1	name , alternate_id
156288602	CV2327424	single nucleotide variant	NM_007126.5(VCP):c.445+5G>C	Inborn genetic diseases [RCV002935431]	uncertain significance	9	35066670	35066670	Human	1	name
11545296	CV253532	single nucleotide variant	NM_007126.5(VCP):c.811+3G>A	Charcot-Marie-Tooth disease type 2Y [RCV002244629]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000294534]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001520363]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000 ... (more) 382040]\|not provided [RCV000710281]\|not specified [RCV000244946]	benign	9	35062975	35062975	Human	4	name , alternate_id
11647417	CV308234	duplication	NM_007126.5(VCP):c.*1035dup	Amyotrophic Lateral Sclerosis, Dominant [RCV000275786]\|Inclusion Body Myopathy, Dominant [RCV000388903]	uncertain significance	9	35056081	35056082	Human	2	name
405008568	CV3083194	single nucleotide variant	NM_007126.5(VCP):c.446-4G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003784141]	likely benign	9	35065385	35065385	Human	1	name , alternate_id
404989675	CV3094590	single nucleotide variant	NM_007126.5(VCP):c.303-4T>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003792601]	likely benign	9	35066821	35066821	Human	1	name , alternate_id
405057472	CV3102405	single nucleotide variant	NM_007126.5(VCP):c.811+9T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003798547]	likely benign	9	35062969	35062969	Human	1	name , alternate_id
405093823	CV3105487	single nucleotide variant	NM_007126.5(VCP):c.811+8A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003801204]	likely benign	9	35062970	35062970	Human	1	name , alternate_id
597850980	CV3873338	single nucleotide variant	NM_007126.5(VCP):c.945+6A>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005212780]	uncertain significance	9	35062211	35062211	Human	1	name , alternate_id
597856808	CV3877714	single nucleotide variant	NM_007126.5(VCP):c.17+17C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005229023]	likely benign	9	35072320	35072320	Human	1	name , alternate_id
13482016	CV459547	single nucleotide variant	NM_007126.5(VCP):c.303-3C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002231754]	uncertain significance	9	35066820	35066820	Human	1	name , alternate_id
13837453	CV588742	single nucleotide variant	NM_007126.5(VCP):c.811+2T>C	Inborn genetic diseases [RCV002422632]\|not provided [RCV000733871]	uncertain significance	9	35062976	35062976	Human	1	name
15111993	CV775389	single nucleotide variant	NM_007126.5(VCP):c.709-4A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001431016]	likely benign	9	35063084	35063084	Human	1	name , alternate_id
28875738	CV903395	single nucleotide variant	NM_007126.5(VCP):c.*1040T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001165910]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001165911]\|not provided [RCV002264211]	benign\|likely benign\|uncertain significance	9	35056077	35056077	Human	2	name , alternate_id
28875741	CV903396	single nucleotide variant	NM_007126.5(VCP):c.*1001C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001165912]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001167476]	benign\|likely benign	9	35056116	35056116	Human	2	name , alternate_id
28876066	CV903398	single nucleotide variant	NM_007126.5(VCP):c.812-7C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001166036]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002068014]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001166037]	benign\|likely benign	9	35062357	35062357	Human	3	name , alternate_id
28883532	CV903399	single nucleotide variant	NM_007126.5(VCP):c.446-4G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168237]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001873558]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168236]	likely benign\|uncertain significance	9	35065385	35065385	Human	3	name , alternate_id
28886172	CV903400	single nucleotide variant	NM_007126.5(VCP):c.130-9T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168985]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168986]	uncertain significance	9	35068072	35068072	Human	2	name , alternate_id
127274244	CV1098111	single nucleotide variant	NM_007126.5(VCP):c.2316-8G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001431897]	likely benign	9	35057230	35057230	Human	1	name , alternate_id
127245366	CV1098115	single nucleotide variant	NM_007126.5(VCP):c.577-15C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001424295]	likely benign	9	35064300	35064300	Human	1	name , alternate_id
127292598	CV1119688	single nucleotide variant	NM_007126.5(VCP):c.2161-5T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001451790]	likely benign	9	35057535	35057535	Human	1	name , alternate_id
127300158	CV1119689	single nucleotide variant	NM_007126.5(VCP):c.1360-9C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001478363]	likely benign	9	35060932	35060932	Human	1	name , alternate_id
127316554	CV1119690	single nucleotide variant	NM_007126.5(VCP):c.1081+8C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001465574]	likely benign	9	35061995	35061995	Human	1	name , alternate_id
127332448	CV1140512	duplication	NM_007126.5(VCP):c.1696-5dup	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001489492]	likely benign	9	35059805	35059806	Human	1	name , alternate_id
150422631	CV1180579	single nucleotide variant	NM_007126.5(VCP):c.811+97C>T	not provided [RCV001552901]	likely benign	9	35062881	35062881	Human		name
150408964	CV1190959	single nucleotide variant	NM_007126.5(VCP):c.811+96G>A	not provided [RCV001565508]	likely benign	9	35062882	35062882	Human		name
150417226	CV1194223	deletion	NM_007126.5(VCP):c.445+92del	not provided [RCV001568677]	likely benign	9	35066583	35066583	Human		name
150463063	CV1214733	single nucleotide variant	NM_007126.5(VCP):c.129+35G>A	not provided [RCV001613726]	benign	9	35068216	35068216	Human		name
150435040	CV1221544	single nucleotide variant	NM_007126.5(VCP):c.18-281T>A	not provided [RCV001609232]	benign	9	35068643	35068643	Human		name
150485978	CV1250339	duplication	NM_007126.5(VCP):c.445+80dup	not provided [RCV001673952]	benign	9	35066582	35066583	Human		name
150490755	CV1274559	single nucleotide variant	NM_007126.5(VCP):c.446-17A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002077140]\|not provided [RCV001700898]	likely benign	9	35065398	35065398	Human	1	name , alternate_id
151777365	CV1381156	single nucleotide variant	NM_007126.5(VCP):c.1482+4G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002045813]\|not provided [RCV003138045]	uncertain significance	9	35060797	35060797	Human	1	name , alternate_id
152088606	CV1527532	single nucleotide variant	NM_007126.5(VCP):c.1482+9A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002093858]	likely benign	9	35060792	35060792	Human	1	name , alternate_id
152063693	CV1542532	single nucleotide variant	NM_007126.5(VCP):c.129+12C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002209019]	likely benign	9	35068239	35068239	Human	1	name , alternate_id
152035375	CV1545714	single nucleotide variant	NM_007126.5(VCP):c.129+16A>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002164852]	likely benign	9	35068235	35068235	Human	1	name , alternate_id
152155085	CV1560910	single nucleotide variant	NM_007126.5(VCP):c.1360-5T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002102823]	likely benign	9	35060928	35060928	Human	1	name , alternate_id
152047112	CV1561552	single nucleotide variant	NM_007126.5(VCP):c.577-10C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002108472]	likely benign	9	35064295	35064295	Human	1	name , alternate_id
152030223	CV1566091	single nucleotide variant	NM_007126.5(VCP):c.446-15T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002086071]	likely benign	9	35065396	35065396	Human	1	name , alternate_id
152092390	CV1567775	single nucleotide variant	NM_007126.5(VCP):c.577-15C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002212904]	likely benign	9	35064300	35064300	Human	1	name , alternate_id
152130823	CV1567846	single nucleotide variant	NM_007126.5(VCP):c.302+12G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002218047]	likely benign	9	35067879	35067879	Human	1	name , alternate_id
152092771	CV1571311	single nucleotide variant	NM_007126.5(VCP):c.708+19G>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002150804]	likely benign	9	35064135	35064135	Human	1	name , alternate_id
152031670	CV1571828	single nucleotide variant	NM_007126.5(VCP):c.708+14G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002186749]	likely benign	9	35064140	35064140	Human	1	name , alternate_id
152086758	CV1573953	deletion	NM_007126.5(VCP):c.946-12del	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002150036]	likely benign	9	35062150	35062150	Human	1	name , alternate_id
152107655	CV1577964	single nucleotide variant	NM_007126.5(VCP):c.1696-8T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002096398]	likely benign	9	35059809	35059809	Human	1	name , alternate_id
152154394	CV1579473	single nucleotide variant	NM_007126.5(VCP):c.2315+8G>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002158655]	likely benign	9	35057368	35057368	Human	1	name , alternate_id
152067916	CV1588943	single nucleotide variant	NM_007126.5(VCP):c.129+11G>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002209596]	likely benign	9	35068240	35068240	Human	1	name , alternate_id
152091846	CV1602929	single nucleotide variant	NM_007126.5(VCP):c.446-11T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002194401]	likely benign	9	35065392	35065392	Human	1	name , alternate_id
152077125	CV1604661	single nucleotide variant	NM_007126.5(VCP):c.2161-4A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002092372]\|Inborn genetic diseases [RCV002427525]	likely benign\|uncertain significance	9	35057534	35057534	Human	2	name , alternate_id
152161140	CV1619303	single nucleotide variant	NM_007126.5(VCP):c.446-11T>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002159661]	likely benign	9	35065392	35065392	Human	1	name , alternate_id
152066264	CV1620152	single nucleotide variant	NM_007126.5(VCP):c.446-16C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002209385]	likely benign	9	35065397	35065397	Human	1	name , alternate_id
152175105	CV1637524	single nucleotide variant	NM_007126.5(VCP):c.1081+9T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002144669]\|VCP-related disorder [RCV004734452]	likely benign	9	35061994	35061994	Human	2	name , trait , alternate_id
152172258	CV1650641	duplication	NM_007126.5(VCP):c.946-17dup	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002162392]	likely benign	9	35062154	35062155	Human	1	name , alternate_id
152115029	CV1659737	single nucleotide variant	NM_007126.5(VCP):c.946-15A>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002080776]	likely benign	9	35062153	35062153	Human	1	name , alternate_id
156059101	CV1867949	single nucleotide variant	NM_007126.5(VCP):c.945+11A>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003037196]	likely benign	9	35062206	35062206	Human	1	name , alternate_id
156386340	CV1891861	single nucleotide variant	NM_007126.5(VCP):c.1194+9A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003067589]	likely benign	9	35061568	35061568	Human	1	name , alternate_id
156306570	CV1898677	single nucleotide variant	NM_007126.5(VCP):c.708+12G>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003088207]	likely benign	9	35064142	35064142	Human	1	name , alternate_id
156413854	CV1901119	single nucleotide variant	NM_007126.5(VCP):c.2316-5C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002588296]	likely benign	9	35057227	35057227	Human	1	name , alternate_id
156419068	CV1929317	single nucleotide variant	NM_007126.5(VCP):c.811+14T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002612285]	likely benign	9	35062964	35062964	Human	1	name , alternate_id
156447110	CV1944749	single nucleotide variant	NM_007126.5(VCP):c.811+13G>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003118637]	likely benign	9	35062965	35062965	Human	1	name , alternate_id
155967938	CV1967880	single nucleotide variant	NM_007126.5(VCP):c.946-17A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002617042]	likely benign	9	35062155	35062155	Human	1	name , alternate_id
155968020	CV1967899	single nucleotide variant	NM_007126.5(VCP):c.946-20C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002617045]	likely benign	9	35062158	35062158	Human	1	name , alternate_id
156052045	CV1974409	single nucleotide variant	NM_007126.5(VCP):c.2005-6T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002590693]	likely benign	9	35059225	35059225	Human	1	name , alternate_id
156211414	CV2000988	single nucleotide variant	NM_007126.5(VCP):c.302+11G>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002666859]	likely benign	9	35067880	35067880	Human	1	name , alternate_id
156124915	CV2012325	single nucleotide variant	NM_007126.5(VCP):c.945+16A>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002696182]	likely benign	9	35062201	35062201	Human	1	name , alternate_id
156381315	CV2060828	single nucleotide variant	NM_007126.5(VCP):c.1194+8G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002815105]	likely benign	9	35061569	35061569	Human	1	name , alternate_id
156307945	CV2085638	single nucleotide variant	NM_007126.5(VCP):c.2005-9T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002898552]	likely benign	9	35059228	35059228	Human	1	name , alternate_id
156110909	CV2092889	single nucleotide variant	NM_007126.5(VCP):c.1359+8C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002913773]	likely benign	9	35061007	35061007	Human	1	name , alternate_id
156162020	CV2095290	single nucleotide variant	NM_007126.5(VCP):c.812-17A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002891035]	likely benign	9	35062367	35062367	Human	1	name , alternate_id
156234085	CV2108753	single nucleotide variant	NM_007126.5(VCP):c.811+19C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002932950]	likely benign	9	35062959	35062959	Human	1	name , alternate_id
156340467	CV2127335	single nucleotide variant	NM_007126.5(VCP):c.709-18C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002938870]	likely benign	9	35063098	35063098	Human	1	name , alternate_id
155905840	CV2130756	single nucleotide variant	NM_007126.5(VCP):c.708+16T>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002967704]	likely benign	9	35064138	35064138	Human	1	name , alternate_id
156334937	CV2168292	single nucleotide variant	NM_007126.5(VCP):c.708+20G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003029969]	likely benign	9	35064134	35064134	Human	1	name , alternate_id
11552395	CV253526	single nucleotide variant	NM_007126.5(VCP):c.1695+8A>G	Charcot-Marie-Tooth disease type 2Y [RCV002244628]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000367237]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001520362]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000 ... (more) 393728]\|not provided [RCV000710280]\|not specified [RCV000254320]	benign	9	35060305	35060305	Human	7	name , alternate_id
11552395	CV253526	single nucleotide variant	NM_007126.5(VCP):c.1695+8A>G	Charcot-Marie-Tooth disease type 2Y [RCV002244628]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000367237]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001520362]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000 ... (more) 393728]\|not provided [RCV000710280]\|not specified [RCV000254320]	benign	9	35060305	35060306	Human	7	name , alternate_id
11551995	CV253534	single nucleotide variant	NM_007126.5(VCP):c.129+47G>A	Charcot-Marie-Tooth disease type 2Y [RCV002244624]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002244623]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV002244622]\|not provided [RCV001660302]\|not specified [RCV000253783]	benign	9	35068204	35068204	Human	3	name , alternate_id
11603429	CV308255	single nucleotide variant	NM_007126.5(VCP):c.1360-6T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000299794]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003766109]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000354748]	likely benign\|uncertain significance	9	35060929	35060929	Human	3	name , alternate_id
404990838	CV3084232	single nucleotide variant	NM_007126.5(VCP):c.1696-3C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003782425]\|VCP-related disorder [RCV004539134]	likely benign\|uncertain significance	9	35059804	35059804	Human	2	name , trait , alternate_id
402504812	CV3088771	single nucleotide variant	NM_007126.5(VCP):c.2315+6T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003779480]	uncertain significance	9	35057370	35057370	Human	1	name , alternate_id
402492306	CV3091187	single nucleotide variant	NM_007126.5(VCP):c.2004+8C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003787693]	uncertain significance	9	35059485	35059485	Human	1	name , alternate_id
404980095	CV3099531	single nucleotide variant	NM_007126.5(VCP):c.812-19C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003791360]	likely benign	9	35062369	35062369	Human	1	name , alternate_id
404980519	CV3099602	single nucleotide variant	NM_007126.5(VCP):c.811+13G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003791431]	likely benign	9	35062965	35062965	Human	1	name , alternate_id
405072929	CV3099936	single nucleotide variant	NM_007126.5(VCP):c.130-20C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003799651]	likely benign	9	35068083	35068083	Human	1	name , alternate_id
405036922	CV3108698	single nucleotide variant	NM_007126.5(VCP):c.576+10C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003807156]	likely benign	9	35065241	35065241	Human	1	name , alternate_id
405066400	CV3110920	single nucleotide variant	NM_007126.5(VCP):c.811+17A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003809424]	likely benign	9	35062961	35062961	Human	1	name , alternate_id
405083204	CV3113573	single nucleotide variant	NM_007126.5(VCP):c.446-19G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003810590]	likely benign	9	35065400	35065400	Human	1	name , alternate_id
408368571	CV3513740	deletion	NM_007126.5(VCP):c.2161-9del	VCP-related disorder [RCV004735310]	likely benign	9	35057539	35057539	Human		name , trait , alternate_id
408368690	CV3514470	duplication	NM_007126.5(VCP):c.2004+6dup	VCP-related disorder [RCV004735367]	likely benign	9	35059486	35059487	Human		name , trait , alternate_id
597843392	CV3865237	single nucleotide variant	NM_007126.5(VCP):c.946-13C>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005211686]	likely benign	9	35062151	35062151	Human	1	name , alternate_id
597882825	CV3865943	single nucleotide variant	NM_007126.5(VCP):c.1696-9C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005217608]	likely benign	9	35059810	35059810	Human	1	name , alternate_id
597838298	CV3866966	single nucleotide variant	NM_007126.5(VCP):c.576+12C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005225958]	likely benign	9	35065239	35065239	Human	1	name , alternate_id
597837789	CV3870935	single nucleotide variant	NM_007126.5(VCP):c.445+10A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005210594]	likely benign	9	35066665	35066665	Human	1	name , alternate_id
597875691	CV3871368	single nucleotide variant	NM_007126.5(VCP):c.576+15T>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005216582]	likely benign	9	35065236	35065236	Human	1	name , alternate_id
597849413	CV3872953	single nucleotide variant	NM_007126.5(VCP):c.708+16T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005212590]	likely benign	9	35064138	35064138	Human	1	name , alternate_id
597898042	CV3875985	single nucleotide variant	NM_007126.5(VCP):c.302+10G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005219875]	likely benign	9	35067881	35067881	Human	1	name , alternate_id
597857807	CV3877866	single nucleotide variant	NM_007126.5(VCP):c.130-12T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005229175]	likely benign	9	35068075	35068075	Human	1	name , alternate_id
597841987	CV3878184	single nucleotide variant	NM_007126.5(VCP):c.1483-6T>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005226672]	likely benign	9	35060531	35060531	Human	1	name , alternate_id
597834750	CV3878725	single nucleotide variant	NM_007126.5(VCP):c.709-16C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005225097]	likely benign	9	35063096	35063096	Human	1	name , alternate_id
597929510	CV3879194	single nucleotide variant	NM_007126.5(VCP):c.812-19C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005224691]	likely benign	9	35062369	35062369	Human	1	name , alternate_id
597925479	CV3879786	single nucleotide variant	NM_007126.5(VCP):c.2161-3T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005224148]	uncertain significance	9	35057533	35057533	Human	1	name , alternate_id
597913313	CV3879973	single nucleotide variant	NM_007126.5(VCP):c.130-11T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005222212]	uncertain significance	9	35068074	35068074	Human	1	name , alternate_id
13482752	CV459451	single nucleotide variant	NM_007126.5(VCP):c.576+10C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001496176]	likely benign	9	35065241	35065241	Human	1	name , alternate_id
13494913	CV459539	single nucleotide variant	NM_007126.5(VCP):c.1696-7C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002231753]	likely benign	9	35059808	35059808	Human	1	name , alternate_id
13470598	CV459541	single nucleotide variant	NM_007126.5(VCP):c.1082-9G>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000546267]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001166032]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001166033]\|not provided [RCV001702503]\|not specified [ ... (more) RCV001289413]	benign	9	35061698	35061698	Human	3	name , alternate_id
13515778	CV492871	single nucleotide variant	NM_007126.5(VCP):c.1483-5C>T	not provided [RCV000594707]	uncertain significance	9	35060530	35060530	Human		name
13607704	CV524547	single nucleotide variant	NM_007126.5(VCP):c.2316-4A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000639664]	likely benign	9	35057226	35057226	Human	1	name , alternate_id
13607689	CV524945	single nucleotide variant	NM_007126.5(VCP):c.1360-4C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002232621]	likely benign\|uncertain significance	9	35060927	35060927	Human	1	name , alternate_id
13607701	CV525095	single nucleotide variant	NM_007126.5(VCP):c.2161-6C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000639661]	likely benign	9	35057536	35057536	Human	1	name , alternate_id
13804038	CV563957	single nucleotide variant	NM_007126.5(VCP):c.1194+3G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000685579]\|Inborn genetic diseases [RCV002334250]\|VCP-related disorder [RCV004535704]\|not provided [RCV000733640]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35061574	35061574	Human	3	name , trait , alternate_id
15109041	CV730637	single nucleotide variant	NM_007126.5(VCP):c.1081+8C>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002065603]	likely benign	9	35061995	35061995	Human	1	name , alternate_id
15123776	CV759748	single nucleotide variant	NM_007126.5(VCP):c.2160+8T>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000918877]\|not provided [RCV001580009]	benign\|likely benign	9	35059056	35059056	Human	1	name , alternate_id
15179123	CV779588	single nucleotide variant	NM_007126.5(VCP):c.1696-4A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000973833]\|VCP-related disorder [RCV004543636]	likely benign	9	35059805	35059805	Human	2	name , trait , alternate_id
150429021	CV1187485	single nucleotide variant	NM_007126.5(VCP):c.577-266T>C	not provided [RCV001563047]	likely benign	9	35064551	35064551	Human		name
150406395	CV1194225	single nucleotide variant	NM_007126.5(VCP):c.303-160C>T	not provided [RCV001572012]	likely benign	9	35066977	35066977	Human		name
150448186	CV1201997	single nucleotide variant	NM_007126.5(VCP):c.1081+27C>T	not provided [RCV001584867]	likely benign	9	35061976	35061976	Human		name
150442446	CV1204708	single nucleotide variant	NM_007126.5(VCP):c.2005-71G>A	not provided [RCV001583815]	likely benign	9	35059290	35059290	Human		name
150480694	CV1208067	single nucleotide variant	NM_007126.5(VCP):c.302+198C>T	not provided [RCV001590344]	likely benign	9	35067693	35067693	Human		name
150468461	CV1218916	single nucleotide variant	NM_007126.5(VCP):c.445+217G>T	not provided [RCV001614668]	benign	9	35066458	35066458	Human		name
150451170	CV1220825	single nucleotide variant	NM_007126.5(VCP):c.1482+52T>C	not provided [RCV001611919]	benign	9	35060749	35060749	Human		name
150494992	CV1256555	single nucleotide variant	NM_007126.5(VCP):c.1194+71A>G	not provided [RCV001675520]	benign	9	35061506	35061506	Human		name
150452634	CV1260419	single nucleotide variant	NM_007126.5(VCP):c.1194+84G>T	not provided [RCV001680909]	benign	9	35061493	35061493	Human		name
150467156	CV1269183	single nucleotide variant	NM_007126.5(VCP):c.812-266T>C	not provided [RCV001694591]	benign	9	35062616	35062616	Human		name
150489844	CV1279289	single nucleotide variant	NM_007126.5(VCP):c.302+287A>G	not provided [RCV001716368]	benign	9	35067604	35067604	Human		name
152064987	CV1539672	single nucleotide variant	NM_007126.5(VCP):c.1359+15C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002147290]	likely benign	9	35061000	35061000	Human	1	name , alternate_id
152114217	CV1574765	single nucleotide variant	NM_007126.5(VCP):c.1483-20C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002116967]	likely benign	9	35060545	35060545	Human	1	name , alternate_id
152125446	CV1580839	single nucleotide variant	NM_007126.5(VCP):c.2160+14C>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002082149]	likely benign	9	35059050	35059050	Human	1	name , alternate_id
152128394	CV1584126	single nucleotide variant	NM_007126.5(VCP):c.1360-12C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002082531]	likely benign	9	35060935	35060935	Human	1	name , alternate_id
152068860	CV1589099	single nucleotide variant	NM_007126.5(VCP):c.1695+11A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002209716]	likely benign	9	35060302	35060302	Human	1	name , alternate_id
152034781	CV1590206	microsatellite	NM_007126.5(VCP):c.302+2TG[3]	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002205404]	likely benign	9	35067882	35067883	Human		name , alternate_id
152026346	CV1594398	single nucleotide variant	NM_007126.5(VCP):c.1696-15C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002104525]	likely benign	9	35059816	35059816	Human	1	name , alternate_id
152125358	CV1630175	single nucleotide variant	NM_007126.5(VCP):c.1482+18A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002154795]	benign	9	35060783	35060783	Human	1	name , alternate_id
152120158	CV1664937	single nucleotide variant	NM_007126.5(VCP):c.1483-14C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002117749]	likely benign	9	35060539	35060539	Human	1	name , alternate_id
156155126	CV1931372	single nucleotide variant	NM_007126.5(VCP):c.1081+15T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002664037]	likely benign	9	35061988	35061988	Human	1	name , alternate_id
156393731	CV1934092	single nucleotide variant	NM_007126.5(VCP):c.1194+12A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002654655]	likely benign	9	35061565	35061565	Human	1	name , alternate_id
156442365	CV1938591	single nucleotide variant	NM_007126.5(VCP):c.1695+18G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003112706]	likely benign	9	35060295	35060295	Human	1	name , alternate_id
156442571	CV1938803	single nucleotide variant	NM_007126.5(VCP):c.1081+17C>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003112917]	likely benign	9	35061986	35061986	Human	1	name , alternate_id
156254734	CV2060596	single nucleotide variant	NM_007126.5(VCP):c.1195-12C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002791814]	likely benign	9	35061191	35061191	Human	1	name , alternate_id
156049108	CV2091348	single nucleotide variant	NM_007126.5(VCP):c.1482+10C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002886098]	likely benign	9	35060791	35060791	Human	1	name , alternate_id
156312311	CV2107616	single nucleotide variant	NM_007126.5(VCP):c.1359+17T>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002937243]	likely benign	9	35060998	35060998	Human	1	name , alternate_id
156123505	CV2112214	single nucleotide variant	NM_007126.5(VCP):c.2005-20A>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002927915]	likely benign	9	35059239	35059239	Human	1	name , alternate_id
156375426	CV2124061	single nucleotide variant	NM_007126.5(VCP):c.2316-11C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002942670]	likely benign	9	35057233	35057233	Human	1	name , alternate_id
11548843	CV253524	single nucleotide variant	NM_007126.5(VCP):c.2316-48C>T	not specified [RCV000249624]	likely benign	9	35057270	35057270	Human		name
11544847	CV253527	single nucleotide variant	NM_007126.5(VCP):c.1360-14C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000324520]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002058220]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000259903]\|not provided [RCV001579713]\|not specified [ ... (more) RCV000244337]	benign\|likely benign	9	35060937	35060937	Human	3	name , alternate_id
11548452	CV253528	single nucleotide variant	NM_007126.5(VCP):c.1360-35A>G	Charcot-Marie-Tooth disease type 2Y [RCV002244627]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002244626]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV002244625]\|not provided [RCV001610680]\|not specified [RCV000249111]	benign	9	35060958	35060958	Human	3	name , alternate_id
11550693	CV253531	single nucleotide variant	NM_007126.5(VCP):c.1081+17C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002058218]\|not provided [RCV001579998]\|not specified [RCV000252085]	benign\|likely benign	9	35061986	35061986	Human	1	name , alternate_id
405008319	CV3083174	single nucleotide variant	NM_007126.5(VCP):c.1359+16G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003784121]	likely benign	9	35060999	35060999	Human	1	name , alternate_id
405044728	CV3103868	single nucleotide variant	NM_007126.5(VCP):c.2005-14G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003797586]	likely benign	9	35059233	35059233	Human	1	name , alternate_id
405169650	CV3104249	single nucleotide variant	NM_007126.5(VCP):c.2315+10T>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003802926]	likely benign	9	35057366	35057366	Human	1	name , alternate_id
405056455	CV3107820	single nucleotide variant	NM_007126.5(VCP):c.2161-20T>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003808565]	likely benign	9	35057550	35057550	Human	1	name , alternate_id
405104439	CV3114414	single nucleotide variant	NM_007126.5(VCP):c.1359+11C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003812253]	likely benign	9	35061004	35061004	Human	1	name , alternate_id
405261535	CV3210016	single nucleotide variant	NM_007126.5(VCP):c.1359+10A>C	VCP-related disorder [RCV004544108]	likely benign	9	35061005	35061005	Human		name , trait , alternate_id
597859015	CV3864868	single nucleotide variant	NM_007126.5(VCP):c.1482+14G>A	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005213925]	likely benign	9	35060787	35060787	Human	1	name , alternate_id
597839101	CV3867642	single nucleotide variant	NM_007126.5(VCP):c.1081+11C>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005210837]	likely benign	9	35061992	35061992	Human	1	name , alternate_id
597844541	CV3875788	single nucleotide variant	NM_007126.5(VCP):c.1195-15G>C	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005211870]	likely benign	9	35061194	35061194	Human	1	name , alternate_id
597849382	CV3876838	single nucleotide variant	NM_007126.5(VCP):c.1360-20A>T	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005228065]	likely benign	9	35060943	35060943	Human	1	name , alternate_id
597916055	CV3879074	single nucleotide variant	NM_007126.5(VCP):c.1482+10C>G	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005222610]	likely benign	9	35060791	35060791	Human	1	name , alternate_id
150428104	CV1187484	single nucleotide variant	NM_007126.5(VCP):c.2160+297T>G	not provided [RCV001561815]	likely benign	9	35058767	35058767	Human		name
150411276	CV1190958	deletion	NM_007126.5(VCP):c.1695+167del	not provided [RCV001566488]	likely benign	9	35060146	35060146	Human		name
150419391	CV1194222	single nucleotide variant	NM_007126.5(VCP):c.1081+154C>G	not provided [RCV001569665]	likely benign	9	35061849	35061849	Human		name
150513901	CV1210758	single nucleotide variant	NM_007126.5(VCP):c.2161-241C>T	not provided [RCV001598799]	benign	9	35057771	35057771	Human		name
150504177	CV1240702	single nucleotide variant	NM_007126.5(VCP):c.2160+222A>G	not provided [RCV001657545]	benign	9	35058842	35058842	Human		name
150451305	CV1261528	single nucleotide variant	NM_007126.5(VCP):c.1696-223G>T	not provided [RCV001680730]	benign	9	35060024	35060024	Human		name
150475173	CV1263465	deletion	NM_007126.5(VCP):c.2160+272del	not provided [RCV001684988]	benign	9	35058792	35058792	Human		name
150462819	CV1273065	single nucleotide variant	NM_007126.5(VCP):c.1695+210G>A	not provided [RCV001693822]	benign	9	35060103	35060103	Human		name
156189339	CV1934030	deletion	NM_007126.5(VCP):c.18-9_18-8del	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002625308]	likely benign	9	35068370	35068371	Human	1	name , alternate_id
11548392	CV253529	microsatellite	NM_007126.5(VCP):c.1194+9ATG[2]	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002058219]\|not specified [RCV000249024]	likely benign	9	35061560	35061562	Human		name , alternate_id
402493016	CV3091146	microsatellite	NM_007126.5(VCP):c.17+8_17+9del	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003787651]	likely benign	9	35072328	35072329	Human		name , alternate_id
329353339	CV2477067	microsatellite	NM_007126.5(VCP):c.-219TGCCAC[4]	not provided [RCV003223299]	benign	9	35072554	35072555	Human		name
329353342	CV2477068	microsatellite	NM_007126.5(VCP):c.-233GCTGCC[5]	not provided [RCV003223300]	likely benign	9	35072568	35072569	Human		name
11635086	CV318542	microsatellite	NM_007126.5(VCP):c.-233GCTGCC[4]	Amyotrophic Lateral Sclerosis, Dominant [RCV000359673]\|Inclusion Body Myopathy, Dominant [RCV000302695]\|not provided [RCV004696140]	uncertain significance	9	35072568	35072569	Human		name
402516176	CV3087705	single nucleotide variant	NM_007126.5(VCP):c.9T>C (p.Ser3=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003790056]	likely benign	9	35072345	35072345	Human	1	name , alternate_id
13499490	CV460015	inversion	NM_007126.5(VCP):c.811+2_811+3inv	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000539857]	uncertain significance	9	35062975	35062976	Human		name , alternate_id
151811138	CV1350411	duplication	NM_007126.5(VCP):c.1696-34_1716dup	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002048865]	uncertain significance	9	35059780	35059781	Human	1	name , alternate_id
152172944	CV1641787	single nucleotide variant	NM_007126.5(VCP):c.15C>T (p.Ala5=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002184012]	likely benign	9	35072339	35072339	Human	1	name , alternate_id
127292103	CV1156216	single nucleotide variant	NM_007126.5(VCP):c.54A>G (p.Lys18=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001510720]\|VCP-related disorder [RCV004540476]	benign\|likely benign	9	35068326	35068326	Human	2	name , trait , alternate_id
150404996	CV1194224	duplication	NM_007126.5(VCP):c.445+80_445+81dup	not provided [RCV001571426]	likely benign	9	35066582	35066583	Human		name
152124891	CV1532244	deletion	NM_007126.5(VCP):c.303-21_303-19del	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002118321]	likely benign	9	35066836	35066838	Human	1	name , alternate_id
152045105	CV1590645	single nucleotide variant	NM_007126.5(VCP):c.45C>T (p.Ala15=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002108251]	likely benign	9	35068335	35068335	Human	1	name , alternate_id
152076565	CV1604553	single nucleotide variant	NM_007126.5(VCP):c.87T>C (p.Asp29=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002092302]	likely benign	9	35068293	35068293	Human	1	name , alternate_id
156310674	CV1925143	single nucleotide variant	NM_007126.5(VCP):c.34C>T (p.Leu12=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002629747]	likely benign	9	35068346	35068346	Human	1	name , alternate_id
11552473	CV253533	microsatellite	NM_007126.5(VCP):c.577-21_577-18del	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002058221]\|not specified [RCV000254424]	likely benign	9	35064303	35064306	Human		name , alternate_id
402517032	CV3087770	microsatellite	NM_007126.5(VCP):c.709-19_709-18del	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003790123]	likely benign	9	35063098	35063099	Human		name , alternate_id
405021948	CV3088140	deletion	NM_007126.5(VCP):c.576+14_576+15del	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003795700]	likely benign	9	35065236	35065237	Human	1	name , alternate_id
597922057	CV3867244	microsatellite	NM_007126.5(VCP):c.709-16_709-15del	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005223670]	likely benign	9	35063095	35063096	Human		name , alternate_id
14705308	CV638221	single nucleotide variant	NM_007126.5(VCP):c.84T>A (p.Val28=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002233819]	uncertain significance	9	35068296	35068296	Human	1	name , alternate_id
126736738	CV1000668	single nucleotide variant	NM_007126.5(VCP):c.234T>C (p.Ser78=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003770634]\|not provided [RCV001311775]\|not specified [RCV004770031]	likely benign	9	35067959	35067959	Human	1	name , alternate_id
127277996	CV1076442	single nucleotide variant	NM_007126.5(VCP):c.210C>T (p.Ile70=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001408207]\|VCP-related disorder [RCV004734176]	likely benign	9	35067983	35067983	Human	2	name , trait , alternate_id
127242301	CV1076443	single nucleotide variant	NM_007126.5(VCP):c.168A>C (p.Thr56=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001393317]	likely benign	9	35068025	35068025	Human	1	name , alternate_id
127280802	CV1076444	single nucleotide variant	NM_007126.5(VCP):c.120C>T (p.Ser40=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001410057]	likely benign	9	35068260	35068260	Human	1	name , alternate_id
127332187	CV1140516	single nucleotide variant	NM_007126.5(VCP):c.147G>A (p.Leu49=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001489347]	likely benign	9	35068046	35068046	Human	1	name , alternate_id
150528065	CV1299050	single nucleotide variant	NM_007126.5(VCP):c.10G>A (p.Gly4Arg)	not provided [RCV001754958]	uncertain significance	9	35072344	35072344	Human		name
152075923	CV1653292	single nucleotide variant	NM_007126.5(VCP):c.192A>G (p.Arg64=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002075730]	likely benign	9	35068001	35068001	Human	1	name , alternate_id
156406089	CV1894710	single nucleotide variant	NM_007126.5(VCP):c.207C>T (p.Cys69=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003070227]	likely benign	9	35067986	35067986	Human	1	name , alternate_id
243062000	CV2407190	single nucleotide variant	NM_007126.5(VCP):c.11G>A (p.Gly4Glu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003778817]\|not provided [RCV003139273]	uncertain significance	9	35072343	35072343	Human	1	name , alternate_id
11544505	CV253530	duplication	NM_007126.5(VCP):c.1082-18_1082-8dup	Amyotrophic Lateral Sclerosis, Dominant [RCV000321686]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000639658]\|Inclusion Body Myopathy, Dominant [RCV000383262]\|VCP-related disorder [RCV004529437]\|not provided [RCV001597014]\|not specified [R ... (more) CV000243886]	benign	9	35061696	35061697	Human	4	name , trait , alternate_id
402516837	CV3089881	single nucleotide variant	NM_007126.5(VCP):c.291G>A (p.Gly97=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003780758]\|VCP-related disorder [RCV004542256]	likely benign	9	35067902	35067902	Human	2	name , trait , alternate_id
405003755	CV3095710	single nucleotide variant	NM_007126.5(VCP):c.288A>G (p.Leu96=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003794015]	likely benign	9	35067905	35067905	Human	1	name , alternate_id
405020012	CV3100986	single nucleotide variant	NM_007126.5(VCP):c.255T>C (p.Asn85=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003805734]	likely benign	9	35067938	35067938	Human	1	name , alternate_id
405078340	CV3114667	single nucleotide variant	NM_007126.5(VCP):c.168A>G (p.Thr56=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003810230]	likely benign	9	35068025	35068025	Human	1	name , alternate_id
597875657	CV3871363	single nucleotide variant	NM_007126.5(VCP):c.165C>T (p.Asp55=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005216577]	likely benign	9	35068028	35068028	Human	1	name , alternate_id
13607699	CV525108	single nucleotide variant	NM_007126.5(VCP):c.213C>T (p.Val71=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002233478]\|Inborn genetic diseases [RCV002424422]	likely benign	9	35067980	35067980	Human	2	name , alternate_id
13834087	CV585329	single nucleotide variant	NM_007126.5(VCP):c.258A>G (p.Arg86=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001408701]\|Inborn genetic diseases [RCV002424743]\|not provided [RCV000729518]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35067935	35067935	Human	2	name , alternate_id
126762910	CV1008635	single nucleotide variant	NM_007126.5(VCP):c.94A>G (p.Ile32Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001319074]	uncertain significance	9	35068286	35068286	Human	1	name , alternate_id
127238248	CV1076440	single nucleotide variant	NM_007126.5(VCP):c.664C>T (p.Leu222=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001392438]	likely benign	9	35064198	35064198	Human	1	name , alternate_id
127249065	CV1098114	single nucleotide variant	NM_007126.5(VCP):c.675A>G (p.Arg225=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001436016]	likely benign	9	35064187	35064187	Human	1	name , alternate_id
127243796	CV1098116	single nucleotide variant	NM_007126.5(VCP):c.351G>T (p.Leu117=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001434907]	likely benign	9	35066769	35066769	Human	1	name , alternate_id
127325975	CV1119691	single nucleotide variant	NM_007126.5(VCP):c.975A>G (p.Val325=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001468641]\|not provided [RCV003426124]	likely benign	9	35062109	35062109	Human	1	name , alternate_id
127301701	CV1119692	single nucleotide variant	NM_007126.5(VCP):c.711T>G (p.Pro237=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001454230]	likely benign	9	35063078	35063078	Human	1	name , alternate_id
127291942	CV1119693	single nucleotide variant	NM_007126.5(VCP):c.349C>T (p.Leu117=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001458866]	likely benign	9	35066771	35066771	Human	1	name , alternate_id
127322130	CV1140514	single nucleotide variant	NM_007126.5(VCP):c.897C>G (p.Ala299=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001484849]	likely benign	9	35062265	35062265	Human	1	name , alternate_id
127328095	CV1140515	single nucleotide variant	NM_007126.5(VCP):c.804G>A (p.Leu268=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001506907]	likely benign	9	35062985	35062985	Human	1	name , alternate_id
127307857	CV1156215	single nucleotide variant	NM_007126.5(VCP):c.465T>G (p.Arg155=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001517278]	benign	9	35065362	35065362	Human	1	name , alternate_id
150553114	CV1298138	single nucleotide variant	NM_007126.5(VCP):c.91G>T (p.Ala31Ser)	Inborn genetic diseases [RCV002449411]\|not provided [RCV001768751]	uncertain significance	9	35068289	35068289	Human	1	name
151348140	CV1322401	deletion	NM_007126.5(VCP):c.265del (p.Arg89fs)	not provided [RCV001804206]	uncertain significance	9	35067928	35067928	Human		name
151821479	CV1338547	single nucleotide variant	NM_007126.5(VCP):c.62A>G (p.Asn21Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001900926]\|Inborn genetic diseases [RCV005298921]	uncertain significance	9	35068318	35068318	Human	2	name , alternate_id
151885822	CV1340998	single nucleotide variant	NM_007126.5(VCP):c.73C>T (p.Arg25Trp)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001962627]\|not provided [RCV003136340]	uncertain significance	9	35068307	35068307	Human	1	name , alternate_id
151795474	CV1404384	single nucleotide variant	NM_007126.5(VCP):c.810T>C (p.Asn270=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002011084]	uncertain significance	9	35062979	35062979	Human	1	name , alternate_id
151814697	CV1444527	single nucleotide variant	NM_007126.5(VCP):c.82G>A (p.Val28Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001933553]	uncertain significance	9	35068298	35068298	Human	1	name , alternate_id
152083187	CV1526317	single nucleotide variant	NM_007126.5(VCP):c.792C>T (p.Ala264=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002170813]	likely benign	9	35062997	35062997	Human	1	name , alternate_id
152091233	CV1528685	single nucleotide variant	NM_007126.5(VCP):c.670C>T (p.Leu224=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002094207]	likely benign	9	35064192	35064192	Human	1	name , alternate_id
152036221	CV1545953	single nucleotide variant	NM_007126.5(VCP):c.702T>C (p.Gly234=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002164984]	likely benign	9	35064160	35064160	Human	1	name , alternate_id
152076539	CV1581490	single nucleotide variant	NM_007126.5(VCP):c.418C>T (p.Leu140=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002112180]	likely benign	9	35066702	35066702	Human	1	name , alternate_id
152035739	CV1590470	single nucleotide variant	NM_007126.5(VCP):c.330C>T (p.Tyr110=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002205545]\|VCP-related disorder [RCV004531318]	likely benign	9	35066790	35066790	Human	2	name , trait , alternate_id
152098112	CV1611653	single nucleotide variant	NM_007126.5(VCP):c.312A>G (p.Pro104=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002172739]	likely benign	9	35066808	35066808	Human	1	name , alternate_id
152121391	CV1613188	single nucleotide variant	NM_007126.5(VCP):c.531T>A (p.Ala177=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002154306]	likely benign	9	35065296	35065296	Human	1	name , alternate_id
152055597	CV1633220	single nucleotide variant	NM_007126.5(VCP):c.738T>A (p.Pro246=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002127735]	likely benign	9	35063051	35063051	Human	1	name , alternate_id
152139027	CV1637982	single nucleotide variant	NM_007126.5(VCP):c.366A>G (p.Thr122=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002177807]	likely benign	9	35066754	35066754	Human	1	name , alternate_id
156189015	CV1882740	single nucleotide variant	NM_007126.5(VCP):c.684C>T (p.Ala228=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003083811]	likely benign	9	35064178	35064178	Human	1	name , alternate_id
156195373	CV1912276	single nucleotide variant	NM_007126.5(VCP):c.606G>A (p.Gly202=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002595516]	likely benign	9	35064256	35064256	Human	1	name , alternate_id
156290695	CV1929227	single nucleotide variant	NM_007126.5(VCP):c.756C>T (p.Thr252=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002647180]	likely benign	9	35063033	35063033	Human	1	name , alternate_id
156188231	CV1933953	single nucleotide variant	NM_007126.5(VCP):c.411G>C (p.Pro137=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002625273]	likely benign	9	35066709	35066709	Human	1	name , alternate_id
156072891	CV1968918	single nucleotide variant	NM_007126.5(VCP):c.522C>T (p.Cys174=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002621297]	likely benign	9	35065305	35065305	Human	1	name , alternate_id
156395593	CV2012222	single nucleotide variant	NM_007126.5(VCP):c.318T>C (p.Pro106=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002725514]	likely benign	9	35066802	35066802	Human	1	name , alternate_id
156097132	CV2050925	single nucleotide variant	NM_007126.5(VCP):c.663A>G (p.Glu221=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002824416]	likely benign	9	35064199	35064199	Human	1	name , alternate_id
156314070	CV2087605	single nucleotide variant	NM_007126.5(VCP):c.726G>A (p.Leu242=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002857834]	likely benign	9	35063063	35063063	Human	1	name , alternate_id
156218990	CV2104692	single nucleotide variant	NM_007126.5(VCP):c.894T>A (p.Pro298=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002932380]	likely benign	9	35062268	35062268	Human	1	name , alternate_id
156369411	CV2109604	single nucleotide variant	NM_007126.5(VCP):c.807C>T (p.Ile269=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002942207]	likely benign	9	35062982	35062982	Human	1	name , alternate_id
156288811	CV2115093	single nucleotide variant	NM_007126.5(VCP):c.571C>A (p.Arg191=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002922064]	likely benign	9	35065256	35065256	Human	1	name , alternate_id
156255189	CV2117222	single nucleotide variant	NM_007126.5(VCP):c.729T>G (p.Leu243=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002933690]	likely benign	9	35063060	35063060	Human	1	name , alternate_id
155948874	CV2123345	single nucleotide variant	NM_007126.5(VCP):c.393C>T (p.Phe131=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002971744]	likely benign	9	35066727	35066727	Human	1	name , alternate_id
156256366	CV2159217	single nucleotide variant	NM_007126.5(VCP):c.840T>C (p.Gly280=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003026512]	likely benign\|uncertain significance	9	35062322	35062322	Human	1	name , alternate_id
156050137	CV2186694	single nucleotide variant	NM_007126.5(VCP):c.375C>T (p.Gly125=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003036880]	likely benign	9	35066745	35066745	Human	1	name , alternate_id
155998022	CV2287099	single nucleotide variant	NM_007126.5(VCP):c.60G>T (p.Lys20Asn)	Inborn genetic diseases [RCV002865098]	uncertain significance	9	35068320	35068320	Human	1	name
243061997	CV2407187	single nucleotide variant	NM_007126.5(VCP):c.56A>G (p.Gln19Arg)	not provided [RCV003139270]	uncertain significance	9	35068324	35068324	Human		name
329353335	CV2477066	single nucleotide variant	NM_007126.5(VCP):c.816T>G (p.Pro272=)	not provided [RCV003223298]	likely benign	9	35062346	35062346	Human		name
11643254	CV268539	single nucleotide variant	NM_007126.5(VCP):c.79A>G (p.Ile27Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000639655]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168490]\|Inborn genetic diseases [RCV002418113]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168987]\|Inte ... (more) llectual disability [RCV001252623]\|VCP-related disorder [RCV004543043]\|not provided [RCV001642885]\|not specified [RCV000390549]	benign\|likely benign\|uncertain significance	9	35068301	35068301	Human	6	name , trait , alternate_id
11640458	CV271637	single nucleotide variant	NM_007126.5(VCP):c.954C>T (p.Gly318=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001069332]\|not provided [RCV000338106]	likely benign\|uncertain significance	9	35062130	35062130	Human	1	name , alternate_id
402503570	CV3090091	single nucleotide variant	NM_007126.5(VCP):c.951T>C (p.His317=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003788858]	likely benign	9	35062133	35062133	Human	1	name , alternate_id
402493806	CV3092210	single nucleotide variant	NM_007126.5(VCP):c.735A>G (p.Gly245=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003787829]	likely benign	9	35063054	35063054	Human	1	name , alternate_id
404999974	CV3099219	single nucleotide variant	NM_007126.5(VCP):c.666G>A (p.Leu222=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003793640]	likely benign	9	35064196	35064196	Human	1	name , alternate_id
405060670	CV3102805	single nucleotide variant	NM_007126.5(VCP):c.555A>G (p.Glu185=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003798795]	likely benign	9	35065272	35065272	Human	1	name , alternate_id
405039086	CV3103254	single nucleotide variant	NM_007126.5(VCP):c.399A>G (p.Val133=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003797131]	likely benign	9	35066721	35066721	Human	1	name , alternate_id
405013188	CV3106513	single nucleotide variant	NM_007126.5(VCP):c.627C>T (p.Cys209=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003794850]	likely benign	9	35064235	35064235	Human	1	name , alternate_id
405156663	CV3110502	single nucleotide variant	NM_007126.5(VCP):c.672G>C (p.Leu224=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003818023]	likely benign	9	35064190	35064190	Human	1	name , alternate_id
405110213	CV3110582	single nucleotide variant	NM_007126.5(VCP):c.759G>C (p.Leu253=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003813485]	likely benign	9	35063030	35063030	Human	1	name , alternate_id
405126807	CV3111985	single nucleotide variant	NM_007126.5(VCP):c.411G>A (p.Pro137=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003815458]\|not provided [RCV004585066]	likely benign	9	35066709	35066709	Human	1	name , alternate_id
11602508	CV319044	single nucleotide variant	NM_007126.5(VCP):c.927C>T (p.Ile309=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000325072]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001080044]\|Inborn genetic diseases [RCV002374609]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000291230]\|not ... (more) provided [RCV000714167]\|not specified [RCV000728435]	benign\|likely benign	9	35062235	35062235	Human	4	name , alternate_id
597834668	CV3864312	single nucleotide variant	NM_007126.5(VCP):c.724C>T (p.Leu242=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005209948]	likely benign	9	35063065	35063065	Human	1	name , alternate_id
597840597	CV3864507	single nucleotide variant	NM_007126.5(VCP):c.963G>A (p.Glu321=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005211118]	likely benign	9	35062121	35062121	Human	1	name , alternate_id
597891953	CV3867973	single nucleotide variant	NM_007126.5(VCP):c.807C>A (p.Ile269=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005219001]	likely benign	9	35062982	35062982	Human	1	name , alternate_id
597863153	CV3875333	single nucleotide variant	NM_007126.5(VCP):c.300C>T (p.Ile100=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005214510]	likely benign	9	35067893	35067893	Human	1	name , alternate_id
597899935	CV3876250	single nucleotide variant	NM_007126.5(VCP):c.978A>G (p.Ser326=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005220140]	likely benign	9	35062106	35062106	Human	1	name , alternate_id
597841698	CV3878123	single nucleotide variant	NM_007126.5(VCP):c.879T>C (p.Ala293=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005226610]	likely benign	9	35062283	35062283	Human	1	name , alternate_id
597915780	CV3879035	single nucleotide variant	NM_007126.5(VCP):c.74G>A (p.Arg25Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005222571]	uncertain significance	9	35068306	35068306	Human	1	name , alternate_id
597910933	CV3879460	single nucleotide variant	NM_007126.5(VCP):c.510T>G (p.Pro170=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005221861]	likely benign	9	35065317	35065317	Human	1	name , alternate_id
616939854	CV4014429	single nucleotide variant	NM_007126.5(VCP):c.98A>G (p.Asn33Ser)	not provided [RCV005413923]	uncertain significance	9	35068282	35068282	Human		name
13474610	CV459155	single nucleotide variant	NM_007126.5(VCP):c.426G>A (p.Ala142=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000525916]\|Inborn genetic diseases [RCV002330872]\|not provided [RCV000598290]	likely benign\|uncertain significance	9	35066694	35066694	Human	2	name , alternate_id
13607698	CV524557	single nucleotide variant	NM_007126.5(VCP):c.552C>T (p.Cys184=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002232623]\|Inborn genetic diseases [RCV002343262]	likely benign	9	35065275	35065275	Human	2	name , alternate_id
15135819	CV692665	single nucleotide variant	NM_007126.5(VCP):c.832T>C (p.Leu278=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000876711]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001166034]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001166035]\|not provided [RCV004584819]\|not specified [ ... (more) RCV001664521]	benign\|likely benign	9	35062330	35062330	Human	3	name , alternate_id
15154961	CV700987	single nucleotide variant	NM_007126.5(VCP):c.924C>T (p.Ala308=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000946395]\|not provided [RCV004707497]	likely benign	9	35062238	35062238	Human	1	name , alternate_id
15153357	CV700988	single nucleotide variant	NM_007126.5(VCP):c.732C>T (p.Tyr244=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001395321]\|VCP-related disorder [RCV004726741]\|not provided [RCV000946065]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35063057	35063057	Human	2	name , trait , alternate_id
15116891	CV737122	single nucleotide variant	NM_007126.5(VCP):c.426G>C (p.Ala142=)	VCP-related disorder [RCV004541847]\|not provided [RCV000895281]	likely benign	9	35066694	35066694	Human		name , trait , alternate_id
15113416	CV751686	single nucleotide variant	NM_007126.5(VCP):c.982T>C (p.Leu328=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003768823]	likely benign	9	35062102	35062102	Human	1	name , alternate_id
15132218	CV751687	single nucleotide variant	NM_007126.5(VCP):c.628A>C (p.Arg210=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001502771]\|not provided [RCV005243414]	likely benign	9	35064234	35064234	Human	1	name , alternate_id
15119188	CV751688	single nucleotide variant	NM_007126.5(VCP):c.345T>C (p.His115=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001415753]	likely benign	9	35066775	35066775	Human	1	name , alternate_id
15182333	CV767391	single nucleotide variant	NM_007126.5(VCP):c.624C>T (p.Gly208=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000930336]	likely benign	9	35064238	35064238	Human	1	name , alternate_id
15142474	CV767392	single nucleotide variant	NM_007126.5(VCP):c.618T>C (p.Ile206=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001498468]	likely benign	9	35064244	35064244	Human	1	name , alternate_id
15115538	CV783400	single nucleotide variant	NM_007126.5(VCP):c.519T>C (p.Tyr173=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002066471]	likely benign	9	35065308	35065308	Human	1	name , alternate_id
15140976	CV783401	single nucleotide variant	NM_007126.5(VCP):c.390C>G (p.Leu130=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001496783]	likely benign	9	35066730	35066730	Human	1	name , alternate_id
15118796	CV783402	single nucleotide variant	NM_007126.5(VCP):c.372A>G (p.Glu124=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001505470]	likely benign	9	35066748	35066748	Human	1	name , alternate_id
21069963	CV796308	single nucleotide variant	NM_007126.5(VCP):c.888T>C (p.Asn296=)	not provided [RCV000999153]	uncertain significance	9	35062274	35062274	Human		name
28876472	CV861363	single nucleotide variant	NM_007126.5(VCP):c.41C>T (p.Thr14Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002555974]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001196071]\|not provided [RCV003425917]\|not specified [RCV001095442]	uncertain significance	9	35068339	35068339	Human	3	name , alternate_id
8633339	CV88553	single nucleotide variant	NM_007126.3(VCP):c.489C>T (p.Phe163=)	Malignant melanoma [RCV000068646]	not provided	9	35065338	35065338	Human		name
28883525	CV901973	single nucleotide variant	NM_007126.5(VCP):c.591C>G (p.Ser197=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168235]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168234]	uncertain significance	9	35064271	35064271	Human	2	name , alternate_id
28883540	CV901974	single nucleotide variant	NM_007126.5(VCP):c.384T>C (p.Gly128=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168238]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002067829]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168239]\|VCP-r ... (more) elated disorder [RCV004545096]	benign\|likely benign\|uncertain significance	9	35066736	35066736	Human	3	name , trait , alternate_id
38462114	CV919228	single nucleotide variant	NM_007126.5(VCP):c.30T>A (p.Asp10Glu)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001198195]	uncertain significance	9	35068350	35068350	Human	1	name
126739301	CV1008633	single nucleotide variant	NM_007126.5(VCP):c.268A>G (p.Asn90Asp)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001325031]	uncertain significance	9	35067925	35067925	Human	1	name , alternate_id
126735127	CV1008634	single nucleotide variant	NM_007126.5(VCP):c.237T>A (p.Asp79Glu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001313680]\|not provided [RCV003222301]	uncertain significance	9	35067956	35067956	Human	1	name , alternate_id
127249979	CV1076437	single nucleotide variant	NM_007126.5(VCP):c.2109C>T (p.Ile703=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001417459]\|VCP-related disorder [RCV004734179]\|not provided [RCV001579543]	likely benign	9	35059115	35059115	Human	2	name , trait , alternate_id
127231068	CV1076438	single nucleotide variant	NM_007126.5(VCP):c.1839A>C (p.Thr613=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001412878]	likely benign	9	35059658	35059658	Human	1	name , alternate_id
127278801	CV1076439	single nucleotide variant	NM_007126.5(VCP):c.1611C>G (p.Ala537=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001408717]	likely benign	9	35060397	35060397	Human	1	name , alternate_id
127272715	CV1098112	single nucleotide variant	NM_007126.5(VCP):c.1776T>C (p.Asp592=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001431388]	likely benign	9	35059721	35059721	Human	1	name , alternate_id
127240321	CV1098113	single nucleotide variant	NM_007126.5(VCP):c.1474C>T (p.Leu492=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001423300]	likely benign	9	35060809	35060809	Human	1	name , alternate_id
127309891	CV1119687	single nucleotide variant	NM_007126.5(VCP):c.2223C>T (p.Arg741=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001456473]	likely benign	9	35057468	35057468	Human	1	name , alternate_id
127319765	CV1140511	single nucleotide variant	NM_007126.5(VCP):c.2197C>A (p.Arg733=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001504164]	likely benign	9	35057494	35057494	Human	1	name , alternate_id
127287170	CV1140513	single nucleotide variant	NM_007126.5(VCP):c.1437C>T (p.Ile479=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001494783]	likely benign	9	35060846	35060846	Human	1	name , alternate_id
127305654	CV1156212	single nucleotide variant	NM_007126.5(VCP):c.2229G>A (p.Ala743=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001516356]	benign	9	35057462	35057462	Human	1	name , alternate_id
127316974	CV1156213	single nucleotide variant	NM_007126.5(VCP):c.2193C>T (p.Ile731=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001520804]	benign	9	35057498	35057498	Human	1	name , alternate_id
127304475	CV1156214	single nucleotide variant	NM_007126.5(VCP):c.1407A>G (p.Val469=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001515901]	benign	9	35060876	35060876	Human	1	name , alternate_id
151842130	CV1363068	single nucleotide variant	NM_007126.5(VCP):c.273C>A (p.Asn91Lys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002015462]	likely pathogenic\|uncertain significance	9	35067920	35067920	Human	1	name , alternate_id
151747172	CV1367857	single nucleotide variant	NM_007126.5(VCP):c.233C>G (p.Ser78Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001927107]	uncertain significance	9	35067960	35067960	Human	1	name , alternate_id
151715408	CV1392697	single nucleotide variant	NM_007126.5(VCP):c.273C>G (p.Asn91Lys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001908873]	likely pathogenic\|uncertain significance	9	35067920	35067920	Human	1	name , alternate_id
151865888	CV1472233	single nucleotide variant	NM_007126.5(VCP):c.284G>A (p.Arg95His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002018336]	likely pathogenic	9	35067909	35067909	Human	1	name , alternate_id
151720718	CV1494548	single nucleotide variant	NM_007126.5(VCP):c.1521C>T (p.Gly507=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001965932]	likely benign\|uncertain significance	9	35060487	35060487	Human	1	name , alternate_id
152046320	CV1526990	single nucleotide variant	NM_007126.5(VCP):c.1617C>T (p.Phe539=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002166313]	likely benign	9	35060391	35060391	Human	1	name , alternate_id
152060529	CV1540639	single nucleotide variant	NM_007126.5(VCP):c.1569G>A (p.Gly523=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002110057]	likely benign	9	35060439	35060439	Human	1	name , alternate_id
152101798	CV1547026	single nucleotide variant	NM_007126.5(VCP):c.1182G>A (p.Val394=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002151899]	likely benign	9	35061589	35061589	Human	1	name , alternate_id
152119678	CV1576061	single nucleotide variant	NM_007126.5(VCP):c.1332T>C (p.Ser444=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002197875]	likely benign	9	35061042	35061042	Human	1	name , alternate_id
152065608	CV1583470	single nucleotide variant	NM_007126.5(VCP):c.2175T>C (p.Asp725=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002110744]	likely benign	9	35057516	35057516	Human	1	name , alternate_id
152146390	CV1590469	single nucleotide variant	NM_007126.5(VCP):c.1566T>C (p.Cys522=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002220112]	likely benign	9	35060442	35060442	Human	1	name , alternate_id
152030219	CV1622071	single nucleotide variant	NM_007126.5(VCP):c.1317C>T (p.Ala439=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002186411]	likely benign	9	35061057	35061057	Human	1	name , alternate_id
152044170	CV1624494	single nucleotide variant	NM_007126.5(VCP):c.1494G>A (p.Glu498=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002126463]\|not provided [RCV005412377]	likely benign	9	35060514	35060514	Human	1	name , alternate_id
152085654	CV1633548	single nucleotide variant	NM_007126.5(VCP):c.2028T>C (p.Ala676=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002113352]	likely benign	9	35059196	35059196	Human	1	name , alternate_id
152147047	CV1635577	single nucleotide variant	NM_007126.5(VCP):c.1944T>C (p.Pro648=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002201391]	likely benign	9	35059553	35059553	Human	1	name , alternate_id
152110707	CV1651023	single nucleotide variant	NM_007126.5(VCP):c.1512G>A (p.Leu504=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002134446]	likely benign	9	35060496	35060496	Human	1	name , alternate_id
155645699	CV1709053	single nucleotide variant	NM_007126.5(VCP):c.1359G>A (p.Arg453=)	not provided [RCV002291929]	uncertain significance	9	35061015	35061015	Human		name
156376292	CV1868927	single nucleotide variant	NM_007126.5(VCP):c.211G>A (p.Val71Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003066759]	uncertain significance	9	35067982	35067982	Human	1	name , alternate_id
156272506	CV1899525	single nucleotide variant	NM_007126.5(VCP):c.1587A>G (p.Lys529=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003086835]	likely benign	9	35060421	35060421	Human	1	name , alternate_id
156287113	CV1900704	single nucleotide variant	NM_007126.5(VCP):c.1050C>G (p.Pro350=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002598599]	likely benign	9	35062034	35062034	Human	1	name , alternate_id
156407795	CV1915090	single nucleotide variant	NM_007126.5(VCP):c.1896C>G (p.Ala632=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002607007]	likely benign	9	35059601	35059601	Human	1	name , alternate_id
10047969	CV191808	single nucleotide variant	NM_007126.5(VCP):c.2214A>G (p.Glu738=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000399763]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001087937]\|Inborn genetic diseases [RCV002426834]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000346373]\|not ... (more) provided [RCV000526744]\|not specified [RCV000175065]	benign\|likely benign	9	35057477	35057477	Human	4	name , alternate_id
10050434	CV191919	single nucleotide variant	NM_007126.5(VCP):c.2406T>C (p.Asp802=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001085623]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168166]\|Inborn genetic diseases [RCV002444698]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001167538]\|not ... (more) provided [RCV000762559]\|not specified [RCV000175197]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35057132	35057132	Human	4	name , alternate_id
156449936	CV1938443	single nucleotide variant	NM_007126.5(VCP):c.1137G>A (p.Glu379=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003122067]	likely benign	9	35061634	35061634	Human	1	name , alternate_id
156434123	CV1946845	single nucleotide variant	NM_007126.5(VCP):c.1854C>T (p.Phe618=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003104306]	likely benign	9	35059643	35059643	Human	1	name , alternate_id
156416107	CV1966464	single nucleotide variant	NM_007126.5(VCP):c.2151A>G (p.Pro717=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002589531]	likely benign	9	35059073	35059073	Human	1	name , alternate_id
156047541	CV1978113	single nucleotide variant	NM_007126.5(VCP):c.1467A>G (p.Leu489=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002590550]	likely benign	9	35060816	35060816	Human	1	name , alternate_id
156370683	CV2007712	single nucleotide variant	NM_007126.5(VCP):c.1680A>G (p.Arg560=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002676872]	likely benign	9	35060328	35060328	Human	1	name , alternate_id
156074919	CV2011754	single nucleotide variant	NM_007126.5(VCP):c.2343T>C (p.Ala781=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002705801]	likely benign	9	35057195	35057195	Human	1	name , alternate_id
156019246	CV2019251	single nucleotide variant	NM_007126.5(VCP):c.1818A>G (p.Thr606=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002690918]	likely benign	9	35059679	35059679	Human	1	name , alternate_id
156131395	CV2036578	single nucleotide variant	NM_007126.5(VCP):c.1479C>G (p.Val493=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002786185]	likely benign	9	35060804	35060804	Human	1	name , alternate_id
156014980	CV2038719	single nucleotide variant	NM_007126.5(VCP):c.1884C>T (p.Ile628=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002780351]	likely benign	9	35059613	35059613	Human	1	name , alternate_id
156298466	CV2075739	single nucleotide variant	NM_007126.5(VCP):c.2385A>G (p.Val795=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002857053]	likely benign	9	35057153	35057153	Human	1	name , alternate_id
155905799	CV2084180	single nucleotide variant	NM_007126.5(VCP):c.1299G>A (p.Glu433=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002858146]	likely benign	9	35061075	35061075	Human	1	name , alternate_id
156207896	CV2103147	single nucleotide variant	NM_007126.5(VCP):c.1416A>G (p.Pro472=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002918045]	likely benign	9	35060867	35060867	Human	1	name , alternate_id
155999689	CV2106683	single nucleotide variant	NM_007126.5(VCP):c.1107T>C (p.Ile369=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002947727]	likely benign	9	35061664	35061664	Human	1	name , alternate_id
156108632	CV2108130	single nucleotide variant	NM_007126.5(VCP):c.266G>A (p.Arg89Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002927327]	pathogenic\|uncertain significance	9	35067927	35067927	Human	1	name , alternate_id
156237740	CV2115616	single nucleotide variant	NM_007126.5(VCP):c.2244T>C (p.Ser748=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002919181]	likely benign	9	35057447	35057447	Human	1	name , alternate_id
155967380	CV2131207	single nucleotide variant	NM_007126.5(VCP):c.1338A>G (p.Ala446=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002972682]	likely benign	9	35061036	35061036	Human	1	name , alternate_id
10448452	CV214539	single nucleotide variant	NM_007126.5(VCP):c.271A>T (p.Asn91Tyr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001271088]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002519583]\|INCLUSION BODY MYOPATHY WITHOUT EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA 1 [RCV001271081]\|Inclusion body myopathy with Paget diseas ... (more) e of bone and frontotemporal dementia type 1 [RCV000201935]	pathogenic\|likely pathogenic	9	35067922	35067922	Human	3	name , alternate_id
156303788	CV2146605	single nucleotide variant	NM_007126.5(VCP):c.194G>A (p.Arg65Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003028220]\|not provided [RCV003138441]	uncertain significance	9	35067999	35067999	Human	1	name , alternate_id
156300298	CV2149667	single nucleotide variant	NM_007126.5(VCP):c.1179T>C (p.Asp393=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003028058]	likely benign	9	35061592	35061592	Human	1	name , alternate_id
10449615	CV215002	single nucleotide variant	NM_007126.5(VCP):c.290G>A (p.Gly97Glu)	Charcot-Marie-Tooth disease type 2Y [RCV000202492]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001853259]	pathogenic\|likely pathogenic	9	35067903	35067903	Human	2	name , alternate_id
155980807	CV2163064	single nucleotide variant	NM_007126.5(VCP):c.1623C>T (p.Ser541=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003033869]	likely benign	9	35060385	35060385	Human	1	name , alternate_id
156123421	CV2175091	single nucleotide variant	NM_007126.5(VCP):c.2334G>A (p.Gln778=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003055556]	likely benign	9	35057204	35057204	Human	1	name , alternate_id
156181808	CV2182390	insertion	NM_007126.5(VCP):c.1696-11_1696-10insA	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003057553]	likely benign	9	35059811	35059812	Human	1	name , alternate_id
8597938	CV23510	single nucleotide variant	NM_007126.5(VCP):c.283C>G (p.Arg95Gly)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005222674]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000008992]	pathogenic	9	35067910	35067910	Human	3	name , alternate_id
11546177	CV253525	single nucleotide variant	NM_007126.5(VCP):c.1704A>G (p.Gln568=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000390268]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001083290]\|Inborn genetic diseases [RCV002401958]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000312517]\|... (more) n style='font-weight:700;'>VCP-related disorder [RCV004529438]\|not provided [RCV000714165]\|not specified [RCV000246121]	benign\|likely benign	9	35059793	35059793	Human	4	name , trait , alternate_id
11578384	CV264531	single nucleotide variant	NM_007126.5(VCP):c.283C>T (p.Arg95Cys)	Amyotrophic lateral sclerosis [RCV001095441]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001215048]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV004556775]\|Inborn genetic diseases [RCV002436094]\|Inclusion body myopathy with Paget disease of bone and front ... (more) otemporal dementia type 1 [RCV000761344]\|Spastic paraplegia [RCV001391611]\|VCP-related disorder [RCV004734912]\|not provided [RCV000280148]	pathogenic\|likely pathogenic\|uncertain significance	9	35067910	35067910	Human	8	name , trait , alternate_id
329954254	CV2669490	single nucleotide variant	NM_007126.5(VCP):c.230G>T (p.Cys77Phe)	not provided [RCV003231998]	uncertain significance	9	35067963	35067963	Human		name
329954255	CV2669491	single nucleotide variant	NM_007126.5(VCP):c.146T>C (p.Leu49Ser)	not provided [RCV003231999]	uncertain significance	9	35068047	35068047	Human		name
11639469	CV267452	single nucleotide variant	NM_007126.5(VCP):c.1584C>T (p.Ala528=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001081085]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168167]\|Inborn genetic diseases [RCV002401981]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168925]\|... (more) n style='font-weight:700;'>VCP-related disorder [RCV004535294]\|not provided [RCV000321351]\|not specified [RCV001580089]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35060424	35060424	Human	4	name , trait , alternate_id
11643588	CV275114	single nucleotide variant	NM_007126.5(VCP):c.1197A>G (p.Val399=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003765688]\|not provided [RCV000395681]	uncertain significance	9	35061177	35061177	Human	1	name , alternate_id
401910984	CV2828862	single nucleotide variant	NM_007126.5(VCP):c.166A>G (p.Thr56Ala)	not provided [RCV003425656]	likely pathogenic	9	35068027	35068027	Human		name
401916748	CV2829471	single nucleotide variant	NM_007126.5(VCP):c.124T>C (p.Ser42Pro)	not provided [RCV003443515]	uncertain significance	9	35068256	35068256	Human		name
405011797	CV3083468	single nucleotide variant	NM_007126.5(VCP):c.1722A>G (p.Leu574=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003784415]	likely benign	9	35059775	35059775	Human	1	name , alternate_id
405050651	CV3084614	single nucleotide variant	NM_007126.5(VCP):c.1383A>G (p.Pro461=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003798021]\|VCP-related disorder [RCV004542268]	likely benign	9	35060900	35060900	Human	2	name , trait , alternate_id
404999993	CV3085970	single nucleotide variant	NM_007126.5(VCP):c.1569G>T (p.Gly523=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003783341]	likely benign	9	35060439	35060439	Human	1	name , alternate_id
402517991	CV3086078	single nucleotide variant	NM_007126.5(VCP):c.1743G>A (p.Ser581=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003780849]	likely benign	9	35059754	35059754	Human	1	name , alternate_id
402517655	CV3089946	single nucleotide variant	NM_007126.5(VCP):c.2367C>T (p.Gly789=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003780824]	likely benign	9	35057171	35057171	Human	1	name , alternate_id
402503067	CV3090041	single nucleotide variant	NM_007126.5(VCP):c.2373A>G (p.Thr791=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003788807]	likely benign	9	35057165	35057165	Human	1	name , alternate_id
402486665	CV3090431	single nucleotide variant	NM_007126.5(VCP):c.2298G>A (p.Arg766=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003787091]	likely benign	9	35057393	35057393	Human	1	name , alternate_id
402508516	CV3090737	single nucleotide variant	NM_007126.5(VCP):c.1333C>T (p.Leu445=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003789354]	likely benign	9	35061041	35061041	Human	1	name , alternate_id
402490336	CV3090968	single nucleotide variant	NM_007126.5(VCP):c.2391A>G (p.Thr797=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003787470]	likely benign	9	35057147	35057147	Human	1	name , alternate_id
402484563	CV3093686	single nucleotide variant	NM_007126.5(VCP):c.230G>A (p.Cys77Tyr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003786885]	uncertain significance	9	35067963	35067963	Human	1	name , alternate_id
405018401	CV3094386	single nucleotide variant	NM_007126.5(VCP):c.1842A>G (p.Lys614=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003785076]	likely benign	9	35059655	35059655	Human	1	name , alternate_id
405056167	CV3095137	single nucleotide variant	NM_007126.5(VCP):c.244A>C (p.Ile82Leu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003798451]	uncertain significance	9	35067949	35067949	Human	1	name , alternate_id
404984504	CV3096470	single nucleotide variant	NM_007126.5(VCP):c.1743G>T (p.Ser581=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003792019]	likely benign	9	35059754	35059754	Human	1	name , alternate_id
405011059	CV3096662	single nucleotide variant	NM_007126.5(VCP):c.2370C>T (p.Gly790=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003794651]	likely benign	9	35057168	35057168	Human	1	name , alternate_id
405051565	CV3097881	single nucleotide variant	NM_007126.5(VCP):c.1341T>C (p.Val447=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003808294]	likely benign	9	35061033	35061033	Human	1	name , alternate_id
405072127	CV3099809	single nucleotide variant	NM_007126.5(VCP):c.1095G>A (p.Arg365=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003799524]	likely benign	9	35061676	35061676	Human	1	name , alternate_id
405041540	CV3106811	single nucleotide variant	NM_007126.5(VCP):c.1287C>T (p.Leu429=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003797341]	likely benign	9	35061087	35061087	Human	1	name , alternate_id
405166020	CV3107103	single nucleotide variant	NM_007126.5(VCP):c.2420A>G (p.Ter807=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003802594]	likely benign	9	35057118	35057118	Human	1	name , alternate_id
405111584	CV3110799	single nucleotide variant	NM_007126.5(VCP):c.283C>A (p.Arg95Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003813702]	likely pathogenic	9	35067910	35067910	Human	1	name , alternate_id
405081999	CV3113504	single nucleotide variant	NM_007126.5(VCP):c.1731T>C (p.Asp577=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003810521]	likely benign	9	35059766	35059766	Human	1	name , alternate_id
405107451	CV3113805	single nucleotide variant	NM_007126.5(VCP):c.2205C>T (p.His735=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003812928]	likely benign	9	35057486	35057486	Human	1	name , alternate_id
405013924	CV3114297	single nucleotide variant	NM_007126.5(VCP):c.1465C>T (p.Leu489=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003805151]	uncertain significance	9	35060818	35060818	Human	1	name , alternate_id
405262665	CV3189376	single nucleotide variant	NM_007126.5(VCP):c.2148C>T (p.Asn716=)	VCP-related disorder [RCV004539274]	likely benign	9	35059076	35059076	Human		name , trait , alternate_id
11599280	CV319032	single nucleotide variant	NM_007126.5(VCP):c.1092C>T (p.Asp364=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000264259]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000560152]\|Inborn genetic diseases [RCV002446629]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000360586]\|... (more) n style='font-weight:700;'>VCP-related disorder [RCV004530485]\|not provided [RCV001559823]\|not specified [RCV001700365]	benign\|likely benign	9	35061679	35061679	Human	4	name , trait , alternate_id
11658814	CV319050	single nucleotide variant	NM_007126.5(VCP):c.185A>G (p.Lys62Arg)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000351753]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005222912]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000396114]	uncertain significance	9	35068008	35068008	Human	3	name , alternate_id
408369026	CV3507603	single nucleotide variant	NM_007126.5(VCP):c.1839A>G (p.Thr613=)	VCP-related disorder [RCV004736490]	likely benign	9	35059658	35059658	Human		name , trait , alternate_id
408368274	CV3509390	single nucleotide variant	NM_007126.5(VCP):c.1390C>T (p.Leu464=)	VCP-related disorder [RCV004734988]	likely benign	9	35060893	35060893	Human		name , trait , alternate_id
597834828	CV3864370	single nucleotide variant	NM_007126.5(VCP):c.272A>G (p.Asn91Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005210006]	uncertain significance	9	35067921	35067921	Human	1	name , alternate_id
597843579	CV3865263	single nucleotide variant	NM_007126.5(VCP):c.1404G>T (p.Val468=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005211712]	likely benign	9	35060879	35060879	Human	1	name , alternate_id
597841512	CV3868286	single nucleotide variant	NM_007126.5(VCP):c.2121T>A (p.Ile707=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005211319]	likely benign	9	35059103	35059103	Human	1	name , alternate_id
597841759	CV3868335	single nucleotide variant	NM_007126.5(VCP):c.1392G>T (p.Leu464=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005211368]	likely benign	9	35060891	35060891	Human	1	name , alternate_id
597865666	CV3868821	single nucleotide variant	NM_007126.5(VCP):c.115G>A (p.Val39Met)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005214941]	uncertain significance	9	35068265	35068265	Human	1	name , alternate_id
597870844	CV3869972	single nucleotide variant	NM_007126.5(VCP):c.296T>C (p.Val99Ala)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005215702]	uncertain significance	9	35067897	35067897	Human	1	name , alternate_id
597852863	CV3870123	single nucleotide variant	NM_007126.5(VCP):c.2172G>A (p.Glu724=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005228515]	likely benign	9	35057519	35057519	Human	1	name , alternate_id
597908217	CV3870439	single nucleotide variant	NM_007126.5(VCP):c.2010G>C (p.Val670=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005221490]	likely benign	9	35059214	35059214	Human	1	name , alternate_id
597891162	CV3871696	single nucleotide variant	NM_007126.5(VCP):c.1212C>T (p.His404=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005218865]	likely benign	9	35061162	35061162	Human	1	name , alternate_id
597845427	CV3872197	single nucleotide variant	NM_007126.5(VCP):c.269A>G (p.Asn90Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005212026]	uncertain significance	9	35067924	35067924	Human	1	name , alternate_id
597845433	CV3872198	single nucleotide variant	NM_007126.5(VCP):c.112G>A (p.Val38Met)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005212027]	uncertain significance	9	35068268	35068268	Human	1	name , alternate_id
597857708	CV3877854	single nucleotide variant	NM_007126.5(VCP):c.1083T>C (p.Gly361=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005229163]	likely benign	9	35061688	35061688	Human	1	name , alternate_id
597860198	CV3879874	single nucleotide variant	NM_007126.5(VCP):c.254A>G (p.Asn85Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005229453]	uncertain significance	9	35067939	35067939	Human	1	name , alternate_id
597913661	CV3880022	single nucleotide variant	NM_007126.5(VCP):c.2187T>G (p.Pro729=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005222261]	benign	9	35057504	35057504	Human	1	name , alternate_id
598124041	CV3884057	single nucleotide variant	NM_007126.5(VCP):c.286C>G (p.Leu96Val)	Progressive muscle weakness [RCV005234868]	likely pathogenic	9	35067907	35067907	Human	2	name
13475943	CV444478	single nucleotide variant	NM_007126.5(VCP):c.278G>A (p.Arg93His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002231635]\|not provided [RCV000520021]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	9	35067915	35067915	Human	1	name , alternate_id
13501817	CV459154	single nucleotide variant	NM_007126.5(VCP):c.2412G>A (p.Leu804=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001463039]\|Inborn genetic diseases [RCV002448686]	likely benign	9	35057126	35057126	Human	2	name , alternate_id
13469461	CV459544	single nucleotide variant	NM_007126.5(VCP):c.1017A>G (p.Ala339=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001467986]\|Inborn genetic diseases [RCV002350261]	likely benign	9	35062067	35062067	Human	2	name , alternate_id
13515365	CV492903	single nucleotide variant	NM_007126.5(VCP):c.1875G>T (p.Arg625=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000639662]\|Inborn genetic diseases [RCV002413681]\|VCP-related disorder [RCV004543374]\|not provided [RCV002292570]\|not specified [RCV000594187]	benign\|likely benign	9	35059622	35059622	Human	3	name , trait , alternate_id
13520305	CV493259	single nucleotide variant	NM_007126.5(VCP):c.1896C>A (p.Ala632=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001403231]\|Inborn genetic diseases [RCV002413682]\|VCP-related disorder [RCV004530715]\|not provided [RCV000598527]	likely benign\|uncertain significance	9	35059601	35059601	Human	3	name , trait , alternate_id
13522568	CV493563	single nucleotide variant	NM_007126.5(VCP):c.1929C>T (p.Ile643=)	Inborn genetic diseases [RCV002413684]\|not provided [RCV000591899]	likely benign\|uncertain significance	9	35059568	35059568	Human	1	name
13607695	CV524550	single nucleotide variant	NM_007126.5(VCP):c.1329C>T (p.Asn443=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002232786]\|Inborn genetic diseases [RCV002386046]	likely benign	9	35061045	35061045	Human	2	name , alternate_id
13607697	CV525101	single nucleotide variant	NM_007126.5(VCP):c.1950G>A (p.Glu650=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002232622]\|Inborn genetic diseases [RCV002420727]	likely benign	9	35059547	35059547	Human	2	name , alternate_id
13832909	CV584135	single nucleotide variant	NM_007126.5(VCP):c.277C>T (p.Arg93Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002233733]\|not provided [RCV000728008]	pathogenic	9	35067916	35067916	Human	1	name , alternate_id
13833159	CV584387	single nucleotide variant	NM_007126.5(VCP):c.1863C>T (p.Gly621=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001462593]\|Inborn genetic diseases [RCV002406659]\|not provided [RCV000728329]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35059634	35059634	Human	2	name , alternate_id
13834190	CV585434	single nucleotide variant	NM_007126.5(VCP):c.1242G>A (p.Leu414=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001221457]\|Inborn genetic diseases [RCV002386295]\|not provided [RCV000729642]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35061132	35061132	Human	2	name , alternate_id
13835235	CV586492	single nucleotide variant	NM_007126.5(VCP):c.1488T>C (p.Pro496=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001402342]\|Inborn genetic diseases [RCV002388365]\|not provided [RCV000730972]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35060520	35060520	Human	2	name , alternate_id
13835543	CV586803	single nucleotide variant	NM_007126.5(VCP):c.2283C>T (p.Thr761=)	Inborn genetic diseases [RCV002442556]\|not provided [RCV000731379]	likely benign\|uncertain significance	9	35057408	35057408	Human	1	name
13835710	CV586972	single nucleotide variant	NM_007126.5(VCP):c.284G>C (p.Arg95Pro)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001046936]\|not provided [RCV000731593]	likely pathogenic\|uncertain significance	9	35067909	35067909	Human	1	name , alternate_id
15132979	CV692664	single nucleotide variant	NM_007126.5(VCP):c.2166A>G (p.Val722=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001422418]\|VCP-related disorder [RCV004735854]\|not specified [RCV004782590]	likely benign	9	35057525	35057525	Human	2	name , trait , alternate_id
15159397	CV723557	single nucleotide variant	NM_007126.5(VCP):c.2052A>G (p.Gly684=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000881188]	likely benign	9	35059172	35059172	Human	1	name , alternate_id
15185010	CV737120	single nucleotide variant	NM_007126.5(VCP):c.1887T>C (p.Ile629=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000908412]	likely benign	9	35059610	35059610	Human	1	name , alternate_id
15185797	CV737121	single nucleotide variant	NM_007126.5(VCP):c.1476G>A (p.Leu492=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001496255]\|VCP-related disorder [RCV004735882]	likely benign	9	35060807	35060807	Human	2	name , trait , alternate_id
15155005	CV751685	single nucleotide variant	NM_007126.5(VCP):c.1401C>T (p.Thr467=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001407364]	likely benign	9	35060882	35060882	Human	1	name , alternate_id
15136184	CV767388	single nucleotide variant	NM_007126.5(VCP):c.1371C>T (p.Ser457=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001423429]	likely benign	9	35060912	35060912	Human	1	name , alternate_id
15143941	CV767389	single nucleotide variant	NM_007126.5(VCP):c.1191A>G (p.Glu397=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001469773]	likely benign	9	35061580	35061580	Human	1	name , alternate_id
15141787	CV767390	single nucleotide variant	NM_007126.5(VCP):c.1017A>T (p.Ala339=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001493134]	likely benign	9	35062067	35062067	Human	1	name , alternate_id
26888991	CV851337	indel	NM_007126.5(VCP):c.446-4_446-3delinsAT	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001045459]	uncertain significance	9	35065384	35065385	Human		name , alternate_id
28885946	CV901970	single nucleotide variant	NM_007126.5(VCP):c.1293C>T (p.Asp431=)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168927]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168926]	uncertain significance	9	35061081	35061081	Human	2	name , alternate_id
38597833	CV964331	single nucleotide variant	NM_007126.5(VCP):c.294T>A (p.Asp98Glu)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001253196]	likely pathogenic	9	35067899	35067899	Human	1	name
126756485	CV993443	single nucleotide variant	NM_007126.5(VCP):c.265C>T (p.Arg89Trp)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001308126]\|not provided [RCV004720847]	likely pathogenic\|uncertain significance	9	35067928	35067928	Human	1	name , alternate_id
126729265	CV1008632	single nucleotide variant	NM_007126.5(VCP):c.460G>T (p.Val154Phe)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001312665]	uncertain significance	9	35065367	35065367	Human	1	name , alternate_id
126774958	CV1029189	single nucleotide variant	NM_007126.5(VCP):c.331G>A (p.Gly111Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001347828]	uncertain significance	9	35066789	35066789	Human	1	name , alternate_id
126918806	CV1046163	single nucleotide variant	NM_007126.5(VCP):c.512G>A (p.Ser171Asn)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001361941]	uncertain significance	9	35065315	35065315	Human	1	name , alternate_id
150336791	CV1171983	single nucleotide variant	NM_007126.5(VCP):c.511A>C (p.Ser171Arg)	not provided [RCV001541190]	uncertain significance	9	35065316	35065316	Human		name
150500644	CV1213196	deletion	NM_007126.5(VCP):c.1695+181_1695+182del	not provided [RCV001594608]	benign	9	35060131	35060132	Human		name
150554047	CV1297139	single nucleotide variant	NM_007126.5(VCP):c.811G>C (p.Gly271Arg)	not provided [RCV001770660]	uncertain significance	9	35062978	35062978	Human		name
151768185	CV1345420	single nucleotide variant	NM_007126.5(VCP):c.310C>T (p.Pro104Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001863821]	uncertain significance	9	35066810	35066810	Human	1	name , alternate_id
151845557	CV1389875	single nucleotide variant	NM_007126.5(VCP):c.677A>T (p.His226Leu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001881889]	uncertain significance	9	35064185	35064185	Human	1	name , alternate_id
151810052	CV1393319	single nucleotide variant	NM_007126.5(VCP):c.472A>G (p.Met158Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001953725]	pathogenic	9	35065355	35065355	Human	1	name , alternate_id
151786802	CV1393320	single nucleotide variant	NM_007126.5(VCP):c.469G>A (p.Gly157Arg)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001972632]	pathogenic	9	35065358	35065358	Human	1	name , alternate_id
151761738	CV1393321	single nucleotide variant	NM_007126.5(VCP):c.463C>A (p.Arg155Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001949225]	pathogenic	9	35065364	35065364	Human	1	name , alternate_id
151723778	CV1425155	single nucleotide variant	NM_007126.5(VCP):c.367G>A (p.Val123Met)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001891465]	uncertain significance	9	35066753	35066753	Human	1	name , alternate_id
151855878	CV1473921	single nucleotide variant	NM_007126.5(VCP):c.365C>T (p.Thr122Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001904683]	uncertain significance	9	35066755	35066755	Human	1	name , alternate_id
151716249	CV1513031	single nucleotide variant	NM_007126.5(VCP):c.451A>G (p.Ile151Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001890377]\|Inborn genetic diseases [RCV003355609]	uncertain significance	9	35065376	35065376	Human	2	name , alternate_id
155267089	CV1699423	single nucleotide variant	NM_007126.5(VCP):c.338G>A (p.Arg113His)	not provided [RCV002283218]	uncertain significance	9	35066782	35066782	Human		name
155717884	CV1772088	single nucleotide variant	NM_007126.5(VCP):c.298A>G (p.Ile100Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002296567]	uncertain significance	9	35067895	35067895	Human	1	name , alternate_id
155749424	CV1773778	single nucleotide variant	NM_007126.5(VCP):c.380C>T (p.Thr127Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002304637]	uncertain significance	9	35066740	35066740	Human	1	name , alternate_id
155733900	CV1774366	single nucleotide variant	NM_007126.5(VCP):c.760A>T (p.Ile254Phe)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002301822]	uncertain significance	9	35063029	35063029	Human	1	name , alternate_id
155692171	CV1775212	single nucleotide variant	NM_007126.5(VCP):c.407A>C (p.Lys136Thr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002299369]	uncertain significance	9	35066713	35066713	Human	1	name , alternate_id
155743730	CV1839529	deletion	NM_007126.5(VCP):c.1847del (p.Asn616fs)	Inborn genetic diseases [RCV002412949]\|not provided [RCV004820252]	uncertain significance	9	35059650	35059650	Human	1	name
156062881	CV1877770	single nucleotide variant	NM_007126.5(VCP):c.466G>A (p.Gly156Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003037322]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005227805]	pathogenic\|likely pathogenic	9	35065361	35065361	Human	1	name , alternate_id
156322542	CV1885873	single nucleotide variant	NM_007126.5(VCP):c.397G>T (p.Val133Leu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003089263]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV004763532]	uncertain significance	9	35066723	35066723	Human	3	name , alternate_id
156024338	CV1895982	single nucleotide variant	NM_007126.5(VCP):c.565A>G (p.Ile189Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003100354]\|not provided [RCV004697252]	uncertain significance	9	35065262	35065262	Human	1	name , alternate_id
156365369	CV1908399	single nucleotide variant	NM_007126.5(VCP):c.355A>G (p.Ile119Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002582023]	uncertain significance	9	35066765	35066765	Human	1	name , alternate_id
155968040	CV2059084	single nucleotide variant	NM_007126.5(VCP):c.636G>C (p.Gln212His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002776601]	uncertain significance	9	35064226	35064226	Human	1	name , alternate_id
156233913	CV2085473	single nucleotide variant	NM_007126.5(VCP):c.382G>A (p.Gly128Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002876342]	likely pathogenic	9	35066738	35066738	Human	1	name , alternate_id
10406111	CV213592	single nucleotide variant	NM_007126.5(VCP):c.463C>G (p.Arg155Gly)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002229498]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000196145]\|not provided [RCV000494556]	pathogenic\|likely pathogenic\|uncertain significance	9	35065364	35065364	Human	3	name , alternate_id
156001715	CV2145919	single nucleotide variant	NM_007126.5(VCP):c.584A>G (p.Glu195Gly)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002997055]	uncertain significance	9	35064278	35064278	Human	1	name , alternate_id
10449611	CV215001	single nucleotide variant	NM_007126.5(VCP):c.553G>A (p.Glu185Lys)	Charcot-Marie-Tooth disease type 2Y [RCV000202444]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002229147]\|Inborn genetic diseases [RCV002345722]	pathogenic\|likely pathogenic\|uncertain significance	9	35065274	35065274	Human	3	name , alternate_id
156066849	CV2166952	single nucleotide variant	NM_007126.5(VCP):c.486G>C (p.Glu162Asp)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003019916]	uncertain significance	9	35065341	35065341	Human	1	name , alternate_id
156337485	CV2190164	single nucleotide variant	NM_007126.5(VCP):c.400T>C (p.Tyr134His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003064048]	uncertain significance	9	35066720	35066720	Human	1	name , alternate_id
8597935	CV23507	single nucleotide variant	NM_007126.5(VCP):c.464G>A (p.Arg155His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000540496]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001271089]\|Inborn genetic diseases [RCV002336080]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000008989]\|not ... (more) provided [RCV000523065]	pathogenic	9	35065363	35065363	Human	4	name , alternate_id
8597936	CV23508	single nucleotide variant	NM_007126.5(VCP):c.463C>T (p.Arg155Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000685660]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001095424]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000008990]\|not provided [RCV000372207]	pathogenic\|likely pathogenic	9	35065364	35065364	Human	3	name , alternate_id
8597937	CV23509	single nucleotide variant	NM_007126.5(VCP):c.695C>A (p.Ala232Glu)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000008991]\|not provided [RCV001172005]	pathogenic	9	35064167	35064167	Human	1	name
8597939	CV23511	single nucleotide variant	NM_007126.5(VCP):c.464G>C (p.Arg155Pro)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001387337]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000008993]\|not provided [RCV003137504]	pathogenic\|uncertain significance	9	35065363	35065363	Human	3	name , alternate_id
8597940	CV23512	single nucleotide variant	NM_007126.5(VCP):c.572G>A (p.Arg191Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000023064]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000555373]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000008994]\|Inclusion body myopathy with Paget disease ... (more) of bone and frontotemporal dementia type 1 [RCV002496309]\|not provided [RCV000516636]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity	9	35065255	35065255	Human	4	name , alternate_id
8597941	CV23513	single nucleotide variant	NM_007126.5(VCP):c.476G>A (p.Arg159His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000639653]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003335021]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000008995]\|VCP-r ... (more) elated disorder [RCV004532314]\|not provided [RCV000276565]	pathogenic	9	35065351	35065351	Human	3	name , trait , alternate_id
156435722	CV2403247	single nucleotide variant	NM_007126.5(VCP):c.812G>A (p.Gly271Asp)	not provided [RCV003127198]	likely pathogenic	9	35062350	35062350	Human		name
243061995	CV2407185	single nucleotide variant	NM_007126.5(VCP):c.478G>A (p.Ala160Thr)	not provided [RCV003139268]	uncertain significance	9	35065349	35065349	Human		name
243061996	CV2407186	single nucleotide variant	NM_007126.5(VCP):c.392T>C (p.Phe131Ser)	not provided [RCV003139269]	uncertain significance	9	35066728	35066728	Human		name
243061998	CV2407188	single nucleotide variant	NM_007126.5(VCP):c.887A>G (p.Asn296Ser)	not provided [RCV003139271]	uncertain significance	9	35062275	35062275	Human		name
243062001	CV2407191	single nucleotide variant	NM_007126.5(VCP):c.722T>C (p.Ile241Thr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003778818]\|not provided [RCV003139274]	uncertain significance	9	35063067	35063067	Human	1	name , alternate_id
243051455	CV2415789	single nucleotide variant	NM_007126.5(VCP):c.961G>A (p.Glu321Lys)	Charcot-Marie-Tooth disease type 2Y [RCV003148399]	uncertain significance	9	35062123	35062123	Human	1	name
11580449	CV264328	single nucleotide variant	NM_007126.5(VCP):c.475C>T (p.Arg159Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001095425]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002229732]\|not provided [RCV000333881]	pathogenic\|likely pathogenic	9	35065352	35065352	Human	1	name , alternate_id
401796323	CV2740505	single nucleotide variant	NM_007126.5(VCP):c.892C>T (p.Pro298Ser)	not provided [RCV003321175]	uncertain significance	9	35062270	35062270	Human		name
401854271	CV2750246	single nucleotide variant	NM_007126.5(VCP):c.685C>T (p.Leu229Phe)	Childhood Onset VCP-related Neurodevelopmental Disorder [RCV003333705]	uncertain significance	9	35064177	35064177	Human		name , trait
401854272	CV2750247	single nucleotide variant	NM_007126.5(VCP):c.753G>T (p.Lys251Asn)	Childhood Onset VCP-related Neurodevelopmental Disorder [RCV003333706]	likely pathogenic	9	35063036	35063036	Human		name , trait
401854273	CV2750248	single nucleotide variant	NM_007126.5(VCP):c.766C>G (p.Arg256Gly)	Childhood Onset VCP-related Neurodevelopmental Disorder [RCV003333707]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV003883215]	likely pathogenic	9	35063023	35063023	Human	3	name , trait , alternate_id
401873178	CV2752041	single nucleotide variant	NM_007126.5(VCP):c.742G>A (p.Gly248Arg)	VCP-related disorder [RCV003335918]	likely pathogenic	9	35063047	35063047	Human		name , trait , alternate_id
404996726	CV2851472	single nucleotide variant	NM_007126.5(VCP):c.722T>G (p.Ile241Ser)	not provided [RCV003491846]	uncertain significance	9	35063067	35063067	Human		name
404993772	CV3089092	single nucleotide variant	NM_007126.5(VCP):c.382G>C (p.Gly128Arg)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003782738]	uncertain significance	9	35066738	35066738	Human	1	name , alternate_id
405051476	CV3097874	single nucleotide variant	NM_007126.5(VCP):c.605G>A (p.Gly202Glu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003808287]	uncertain significance	9	35064257	35064257	Human	1	name , alternate_id
405175658	CV3101084	single nucleotide variant	NM_007126.5(VCP):c.467G>T (p.Gly156Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003803471]	uncertain significance	9	35065360	35065360	Human	1	name , alternate_id
405002561	CV3102086	single nucleotide variant	NM_007126.5(VCP):c.367G>C (p.Val123Leu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003804131]	uncertain significance	9	35066753	35066753	Human	1	name , alternate_id
405060898	CV3102823	single nucleotide variant	NM_007126.5(VCP):c.401A>T (p.Tyr134Phe)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003798813]	uncertain significance	9	35066719	35066719	Human	1	name , alternate_id
405039154	CV3112705	single nucleotide variant	NM_007126.5(VCP):c.487T>A (p.Phe163Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003807372]	uncertain significance	9	35065340	35065340	Human	1	name , alternate_id
405656494	CV3227876	single nucleotide variant	NM_007126.5(VCP):c.563C>T (p.Pro188Leu)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV003994618]	uncertain significance	9	35065264	35065264	Human	1	name
407426304	CV3409838	single nucleotide variant	NM_007126.5(VCP):c.782A>C (p.Glu261Ala)	not provided [RCV004585770]	likely pathogenic	9	35063007	35063007	Human		name
408370986	CV3504598	single nucleotide variant	NM_007126.5(VCP):c.524T>C (p.Ile175Thr)	VCP-related disorder [RCV004724333]	uncertain significance	9	35065303	35065303	Human		name , trait , alternate_id
408370919	CV3505855	single nucleotide variant	NM_007126.5(VCP):c.481G>A (p.Val161Met)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005218268]\|VCP-related disorder [RCV004724291]	uncertain significance	9	35065346	35065346	Human	2	name , trait , alternate_id
596929153	CV3530980	single nucleotide variant	NM_007126.5(VCP):c.511A>G (p.Ser171Gly)	not provided [RCV004779554]	uncertain significance	9	35065316	35065316	Human		name
596927434	CV3532590	single nucleotide variant	NM_007126.5(VCP):c.482T>G (p.Val161Gly)	not provided [RCV004778688]	uncertain significance	9	35065345	35065345	Human		name
596921226	CV3534844	single nucleotide variant	NM_007126.5(VCP):c.551G>A (p.Cys184Tyr)	not provided [RCV004784402]	uncertain significance	9	35065276	35065276	Human		name
596946420	CV3548241	single nucleotide variant	NM_007126.5(VCP):c.397G>A (p.Val133Ile)	not provided [RCV004810066]	uncertain significance	9	35066723	35066723	Human		name
597657127	CV3731645	single nucleotide variant	NM_007126.5(VCP):c.446G>A (p.Gly149Glu)	not provided [RCV005001826]	uncertain significance	9	35065381	35065381	Human		name
597883681	CV3866035	single nucleotide variant	NM_007126.5(VCP):c.665T>G (p.Leu222Arg)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005217700]	uncertain significance	9	35064197	35064197	Human	1	name , alternate_id
597903701	CV3873250	single nucleotide variant	NM_007126.5(VCP):c.389T>C (p.Leu130Pro)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005220688]	uncertain significance	9	35066731	35066731	Human	1	name , alternate_id
597927287	CV3874105	single nucleotide variant	NM_007126.5(VCP):c.907A>G (p.Ile303Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005224377]	uncertain significance	9	35062255	35062255	Human	1	name , alternate_id
598123253	CV3885091	single nucleotide variant	NM_007126.5(VCP):c.410C>T (p.Pro137Leu)	Charcot-Marie-Tooth disease type 2Y [RCV005238702]	pathogenic	9	35066710	35066710	Human	1	name
8602144	CV39108	single nucleotide variant	NM_007126.5(VCP):c.475C>G (p.Arg159Gly)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000023065]	pathogenic	9	35065352	35065352	Human	1	name , alternate_id
598240316	CV3929490	single nucleotide variant	NM_007126.5(VCP):c.799T>A (p.Phe267Ile)	Inborn genetic diseases [RCV005296750]	uncertain significance	9	35062990	35062990	Human	1	name
616938427	CV4012940	single nucleotide variant	NM_007126.5(VCP):c.830A>G (p.Lys277Arg)	not provided [RCV005410405]	uncertain significance	9	35062332	35062332	Human		name
617153604	CV4016678	single nucleotide variant	NM_007126.5(VCP):c.578A>G (p.Asp193Gly)	not provided [RCV005415775]	uncertain significance	9	35064284	35064284	Human		name
617150610	CV4018917	single nucleotide variant	NM_007126.5(VCP):c.308A>G (p.Gln103Arg)	not provided [RCV005423325]	uncertain significance	9	35066812	35066812	Human		name
617154022	CV4022185	single nucleotide variant	NM_007126.5(VCP):c.965G>A (p.Arg322Gln)	not provided [RCV005429541]	uncertain significance	9	35062119	35062119	Human		name
12900955	CV407691	single nucleotide variant	NM_007126.5(VCP):c.812G>C (p.Gly271Ala)	not provided [RCV000483569]	uncertain significance	9	35062350	35062350	Human		name
13212347	CV425845	single nucleotide variant	NM_007126.5(VCP):c.383G>C (p.Gly128Ala)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003766796]\|not provided [RCV000498690]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	9	35066737	35066737	Human	1	name , alternate_id
13485702	CV441332	single nucleotide variant	NM_007126.5(VCP):c.827G>C (p.Ser276Thr)	not specified [RCV000518809]	uncertain significance	9	35062335	35062335	Human		name
13607693	CV524559	single nucleotide variant	NM_007126.5(VCP):c.478G>C (p.Ala160Pro)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000639654]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia [RCV001535609]\|not provided [RCV000993545]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	9	35065349	35065349	Human	2	name , alternate_id
13607687	CV525102	single nucleotide variant	NM_007126.5(VCP):c.479C>T (p.Ala160Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002233477]	uncertain significance	9	35065348	35065348	Human	1	name , alternate_id
13705930	CV536773	single nucleotide variant	NM_007126.5(VCP):c.860G>T (p.Arg287Leu)	not provided [RCV000658477]	uncertain significance	9	35062302	35062302	Human		name
13804184	CV565887	single nucleotide variant	NM_007126.5(VCP):c.374G>A (p.Gly125Asp)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002233201]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001809749]	likely pathogenic\|uncertain significance	9	35066746	35066746	Human	3	name , alternate_id
13804387	CV569010	single nucleotide variant	NM_007126.5(VCP):c.320A>T (p.Asp107Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002233639]	uncertain significance	9	35066800	35066800	Human	1	name , alternate_id
13834782	CV586032	single nucleotide variant	NM_007126.5(VCP):c.555A>C (p.Glu185Asp)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005223150]\|not provided [RCV000730388]	uncertain significance	9	35065272	35065272	Human	1	name , alternate_id
13837269	CV588557	single nucleotide variant	NM_007126.5(VCP):c.340A>G (p.Ile114Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000801185]\|Inborn genetic diseases [RCV002332532]\|VCP-related disorder [RCV004535869]\|not provided [RCV000733637]	likely benign\|uncertain significance	9	35066780	35066780	Human	3	name , trait , alternate_id
14349926	CV590945	single nucleotide variant	NM_007126.5(VCP):c.409C>T (p.Pro137Ser)	Alzheimer disease [RCV000736269]	likely pathogenic	9	35066711	35066711	Human	2	name
14710209	CV638220	single nucleotide variant	NM_007126.5(VCP):c.512G>T (p.Ser171Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000793063]	uncertain significance	9	35065315	35065315	Human	1	name , alternate_id
15201373	CV723558	duplication	NM_007126.5(VCP):c.1847dup (p.Asn616fs)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002065572]\|Inborn genetic diseases [RCV002409141]	likely benign\|uncertain significance	9	35059649	35059650	Human	2	name , alternate_id
26902775	CV836086	single nucleotide variant	NM_007126.5(VCP):c.995T>C (p.Met332Thr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001050288]\|not provided [RCV004797894]	uncertain significance	9	35062089	35062089	Human	1	name , alternate_id
26907724	CV836087	single nucleotide variant	NM_007126.5(VCP):c.648A>G (p.Ile216Met)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001038094]\|Lewy body dementia [RCV002463580]	likely pathogenic\|uncertain significance	9	35064214	35064214	Human	3	name , alternate_id
28886147	CV859757	single nucleotide variant	NM_007126.5(VCP):c.469G>C (p.Gly157Arg)	not provided [RCV001091822]	pathogenic	9	35065358	35065358	Human		name
28877003	CV861362	single nucleotide variant	NM_007126.5(VCP):c.572G>C (p.Arg191Pro)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001095426]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003769035]	pathogenic\|likely pathogenic	9	35065255	35065255	Human	1	name , alternate_id
28881375	CV901971	single nucleotide variant	NM_007126.5(VCP):c.794T>C (p.Phe265Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001167605]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001167604]\|not provided [RCV004768884]	likely pathogenic\|uncertain significance	9	35062995	35062995	Human	2	name , alternate_id
28881379	CV901972	single nucleotide variant	NM_007126.5(VCP):c.697A>G (p.Ile233Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001167607]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001220592]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001167606]\|not provided [RCV001664718]	uncertain significance	9	35064165	35064165	Human	3	name , alternate_id
28883546	CV901975	single nucleotide variant	NM_007126.5(VCP):c.335A>G (p.Lys112Arg)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001168241]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003769818]\|Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV001168240]	uncertain significance	9	35066785	35066785	Human	3	name , alternate_id
38479415	CV925569	single nucleotide variant	NM_007126.5(VCP):c.767G>A (p.Arg256Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001217063]	uncertain significance	9	35063022	35063022	Human	1	name , alternate_id
38464788	CV934748	single nucleotide variant	NM_007126.5(VCP):c.523A>G (p.Ile175Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001212543]	uncertain significance	9	35065304	35065304	Human	1	name , alternate_id
38467139	CV934749	single nucleotide variant	NM_007126.5(VCP):c.453T>G (p.Ile151Met)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001212890]	uncertain significance	9	35065374	35065374	Human	1	name , alternate_id
38462299	CV934750	single nucleotide variant	NM_007126.5(VCP):c.377T>G (p.Ile126Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001212180]	uncertain significance	9	35066743	35066743	Human	1	name , alternate_id
38479683	CV946602	single nucleotide variant	NM_007126.5(VCP):c.313T>C (p.Cys105Arg)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001234395]	uncertain significance	9	35066807	35066807	Human	1	name , alternate_id
40903629	CV977364	single nucleotide variant	NM_007126.5(VCP):c.475C>A (p.Arg159Ser)	Amyotrophic lateral sclerosis type 6 [RCV001271083]	pathogenic	9	35065352	35065352	Human	1	name
126747928	CV993442	single nucleotide variant	NM_007126.5(VCP):c.401A>G (p.Tyr134Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001296826]\|Inborn genetic diseases [RCV002357086]\|not provided [RCV003135925]	uncertain significance	9	35066719	35066719	Human	2	name , alternate_id
126736732	CV1000667	single nucleotide variant	NM_007126.5(VCP):c.1153A>G (p.Thr385Ala)	not provided [RCV001311774]	uncertain significance	9	35061618	35061618	Human		name
126770674	CV1008631	single nucleotide variant	NM_007126.5(VCP):c.1144C>G (p.Gln382Glu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001322715]\|not provided [RCV003135972]	uncertain significance	9	35061627	35061627	Human	1	name , alternate_id
126768266	CV1029186	single nucleotide variant	NM_007126.5(VCP):c.2126G>A (p.Arg709Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001343252]	uncertain significance	9	35059098	35059098	Human	1	name , alternate_id
126768811	CV1029187	single nucleotide variant	NM_007126.5(VCP):c.1318G>A (p.Glu440Lys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001343566]	uncertain significance	9	35061056	35061056	Human	1	name , alternate_id
126908172	CV1046162	single nucleotide variant	NM_007126.5(VCP):c.2345G>T (p.Gly782Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001367667]\|not provided [RCV003318686]	uncertain significance	9	35057193	35057193	Human	1	name , alternate_id
150509050	CV1284438	insertion	NM_007126.5(VCP):c.2160+293_2160+294insG	not provided [RCV001720546]	benign	9	35058770	35058771	Human		name
150548829	CV1293924	single nucleotide variant	NM_007126.5(VCP):c.2257C>T (p.Arg753Trp)	not provided [RCV001764763]	uncertain significance	9	35057434	35057434	Human		name
150549259	CV1295059	single nucleotide variant	NM_007126.5(VCP):c.1709C>T (p.Ala570Val)	not provided [RCV001765020]	uncertain significance	9	35059788	35059788	Human		name
150534682	CV1300693	single nucleotide variant	NM_007126.5(VCP):c.1809G>C (p.Gln603His)	not provided [RCV001758821]	uncertain significance	9	35059688	35059688	Human		name
150528011	CV1301033	single nucleotide variant	NM_007126.5(VCP):c.2173G>A (p.Asp725Asn)	not provided [RCV001754893]	uncertain significance	9	35057518	35057518	Human		name
150547323	CV1302997	single nucleotide variant	NM_007126.5(VCP):c.2118G>T (p.Glu706Asp)	not provided [RCV001763742]	uncertain significance	9	35059106	35059106	Human		name
150553484	CV1303487	single nucleotide variant	NM_007126.5(VCP):c.1357C>T (p.Arg453Trp)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001868584]\|not provided [RCV001769177]	uncertain significance	9	35061017	35061017	Human	1	name , alternate_id
151353539	CV1326698	single nucleotide variant	NM_007126.5(VCP):c.1460G>A (p.Arg487His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003772278]\|not provided [RCV001816505]	pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	9	35060823	35060823	Human	1	name , alternate_id
151796671	CV1347942	single nucleotide variant	NM_007126.5(VCP):c.1265C>G (p.Ala422Gly)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001990570]	uncertain significance	9	35061109	35061109	Human	1	name , alternate_id
151877837	CV1360544	single nucleotide variant	NM_007126.5(VCP):c.1459C>T (p.Arg487Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001907289]\|VCP-related disorder [RCV004536387]	uncertain significance	9	35060824	35060824	Human	2	name , trait , alternate_id
151802672	CV1364596	single nucleotide variant	NM_007126.5(VCP):c.1402G>A (p.Val468Met)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001991096]	uncertain significance	9	35060881	35060881	Human	1	name , alternate_id
151766895	CV1366283	single nucleotide variant	NM_007126.5(VCP):c.1294C>G (p.Leu432Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001949771]	uncertain significance	9	35061080	35061080	Human	1	name , alternate_id
151778230	CV1370619	single nucleotide variant	NM_007126.5(VCP):c.1768A>G (p.Ile590Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001864719]	uncertain significance	9	35059729	35059729	Human	1	name , alternate_id
151799142	CV1373831	single nucleotide variant	NM_007126.5(VCP):c.1985G>A (p.Arg662His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001917549]\|Inborn genetic diseases [RCV003375409]\|not provided [RCV005409845]	uncertain significance	9	35059512	35059512	Human	2	name , alternate_id
151845603	CV1394935	single nucleotide variant	NM_007126.5(VCP):c.1993C>T (p.Pro665Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001995288]	uncertain significance	9	35059504	35059504	Human	1	name , alternate_id
151824228	CV1397865	single nucleotide variant	NM_007126.5(VCP):c.1283A>T (p.Asp428Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001976035]	uncertain significance	9	35061091	35061091	Human	1	name , alternate_id
151726665	CV1445702	single nucleotide variant	NM_007126.5(VCP):c.1837A>G (p.Thr613Ala)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002040767]	uncertain significance	9	35059660	35059660	Human	1	name , alternate_id
151715769	CV1472667	single nucleotide variant	NM_007126.5(VCP):c.2233C>T (p.Arg745Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002039309]	uncertain significance	9	35057458	35057458	Human	1	name , alternate_id
151862250	CV1474203	single nucleotide variant	NM_007126.5(VCP):c.1211A>C (p.His404Pro)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001884072]\|not provided [RCV003136256]	uncertain significance	9	35061163	35061163	Human	1	name , alternate_id
151815624	CV1475792	single nucleotide variant	NM_007126.5(VCP):c.1202A>T (p.Asn401Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001992255]	uncertain significance	9	35061172	35061172	Human	1	name , alternate_id
151787026	CV1479005	single nucleotide variant	NM_007126.5(VCP):c.1186C>G (p.Leu396Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002046718]\|not provided [RCV003136195]	uncertain significance	9	35061585	35061585	Human	1	name , alternate_id
151753191	CV1480130	single nucleotide variant	NM_007126.5(VCP):c.1162A>G (p.Met388Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001927729]	uncertain significance	9	35061609	35061609	Human	1	name , alternate_id
151755885	CV1490627	single nucleotide variant	NM_007126.5(VCP):c.1790C>T (p.Ala597Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001948610]	uncertain significance	9	35059707	35059707	Human	1	name , alternate_id
155265192	CV1704651	single nucleotide variant	NM_007126.5(VCP):c.1712C>T (p.Pro571Leu)	not provided [RCV002284867]	uncertain significance	9	35059785	35059785	Human		name
155692416	CV1775240	single nucleotide variant	NM_007126.5(VCP):c.1198G>T (p.Ala400Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002299384]	uncertain significance	9	35061176	35061176	Human	1	name , alternate_id
155709549	CV1775746	single nucleotide variant	NM_007126.5(VCP):c.2110G>A (p.Glu704Lys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002296134]	uncertain significance	9	35059114	35059114	Human	1	name , alternate_id
155695229	CV1797088	single nucleotide variant	NM_007126.5(VCP):c.1160A>G (p.Asn387Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003775778]\|Inborn genetic diseases [RCV002357701]\|not provided [RCV003320884]	uncertain significance	9	35061611	35061611	Human	2	name , alternate_id
155701554	CV1832968	single nucleotide variant	NM_007126.5(VCP):c.1457A>T (p.Lys486Ile)	Inborn genetic diseases [RCV002394729]	uncertain significance	9	35060826	35060826	Human	1	name
155720669	CV1834470	single nucleotide variant	NM_007126.5(VCP):c.1708G>T (p.Ala570Ser)	Inborn genetic diseases [RCV002398837]	uncertain significance	9	35059789	35059789	Human	1	name
155682030	CV1839740	single nucleotide variant	NM_007126.5(VCP):c.1972A>G (p.Lys658Glu)	Inborn genetic diseases [RCV002423516]	uncertain significance	9	35059525	35059525	Human	1	name
155695062	CV1844547	single nucleotide variant	NM_007126.5(VCP):c.2254A>G (p.Ile752Val)	Inborn genetic diseases [RCV002443596]	uncertain significance	9	35057437	35057437	Human	1	name
155698893	CV1847397	single nucleotide variant	NM_007126.5(VCP):c.2222G>A (p.Arg741His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005227752]\|Inborn genetic diseases [RCV002428099]	uncertain significance	9	35057469	35057469	Human	2	name , alternate_id
156043978	CV1887329	single nucleotide variant	NM_007126.5(VCP):c.1058T>C (p.Ile353Thr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003078630]	uncertain significance	9	35062026	35062026	Human	1	name , alternate_id
156221922	CV1899851	single nucleotide variant	NM_007126.5(VCP):c.2221C>T (p.Arg741Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003085031]\|not provided [RCV004823105]	uncertain significance	9	35057470	35057470	Human	1	name , alternate_id
155961615	CV1936560	single nucleotide variant	NM_007126.5(VCP):c.1256C>G (p.Ala419Gly)	not provided [RCV002512378]	uncertain significance	9	35061118	35061118	Human		name
156125720	CV2036301	single nucleotide variant	NM_007126.5(VCP):c.2381G>A (p.Ser794Asn)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002785969]	uncertain significance	9	35057157	35057157	Human	1	name , alternate_id
155946152	CV2062221	single nucleotide variant	NM_007126.5(VCP):c.2143A>G (p.Thr715Ala)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002815993]	uncertain significance	9	35059081	35059081	Human	1	name , alternate_id
156163579	CV2096996	single nucleotide variant	NM_007126.5(VCP):c.2036C>T (p.Thr679Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002872751]	uncertain significance	9	35059188	35059188	Human	1	name , alternate_id
156094742	CV2114238	single nucleotide variant	NM_007126.5(VCP):c.2134G>C (p.Glu712Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002926813]	uncertain significance	9	35059090	35059090	Human	1	name , alternate_id
156185003	CV2152109	single nucleotide variant	NM_007126.5(VCP):c.1915C>A (p.Leu639Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003005826]	uncertain significance	9	35059582	35059582	Human	1	name , alternate_id
156335096	CV2191784	single nucleotide variant	NM_007126.5(VCP):c.1310T>C (p.Ile437Thr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003063918]	uncertain significance	9	35061064	35061064	Human	1	name , alternate_id
243061992	CV2407182	single nucleotide variant	NM_007126.5(VCP):c.1129C>T (p.Arg377Cys)	not provided [RCV003139265]	uncertain significance	9	35061642	35061642	Human		name
243061993	CV2407183	single nucleotide variant	NM_007126.5(VCP):c.2118G>C (p.Glu706Asp)	not provided [RCV003139266]	uncertain significance	9	35059106	35059106	Human		name
243061994	CV2407184	single nucleotide variant	NM_007126.5(VCP):c.2101G>A (p.Glu701Lys)	not provided [RCV003139267]	uncertain significance	9	35059123	35059123	Human		name
243061999	CV2407189	single nucleotide variant	NM_007126.5(VCP):c.1433A>T (p.Asp478Val)	not provided [RCV003139272]	uncertain significance	9	35060850	35060850	Human		name
243059208	CV2418186	single nucleotide variant	NM_007126.5(VCP):c.1874G>C (p.Arg625Pro)	Global developmental delay [RCV003153238]	pathogenic	9	35059623	35059623	Human	2	name
11637351	CV271001	single nucleotide variant	NM_007126.5(VCP):c.1121C>A (p.Ala374Asp)	not provided [RCV000284424]	uncertain significance	9	35061650	35061650	Human		name
401754703	CV2719720	single nucleotide variant	NM_007126.5(VCP):c.2352T>G (p.Ser784Arg)	Inborn genetic diseases [RCV003278107]	uncertain significance	9	35057186	35057186	Human	1	name
401828115	CV2744485	single nucleotide variant	NM_007126.5(VCP):c.1550A>G (p.Tyr517Cys)	not provided [RCV003327882]	uncertain significance	9	35060458	35060458	Human		name
401854275	CV2750250	single nucleotide variant	NM_007126.5(VCP):c.1084C>T (p.Arg362Cys)	Childhood Onset VCP-related Neurodevelopmental Disorder [RCV003333709]	likely pathogenic	9	35061687	35061687	Human		name , trait
401854276	CV2750251	single nucleotide variant	NM_007126.5(VCP):c.1622C>A (p.Ser541Tyr)	Childhood Onset VCP-related Neurodevelopmental Disorder [RCV003333710]	likely pathogenic	9	35060386	35060386	Human		name , trait
401917254	CV2829753	single nucleotide variant	NM_007126.5(VCP):c.2179C>A (p.Pro727Thr)	not provided [RCV003443797]	uncertain significance	9	35057512	35057512	Human		name
405008743	CV3082937	single nucleotide variant	NM_007126.5(VCP):c.1307C>T (p.Thr436Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003784038]	uncertain significance	9	35061067	35061067	Human	1	name , alternate_id
402521159	CV3086326	single nucleotide variant	NM_007126.5(VCP):c.2234G>A (p.Arg745His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003781099]\|not specified [RCV004783111]	uncertain significance	9	35057457	35057457	Human	1	name , alternate_id
402509127	CV3088885	single nucleotide variant	NM_007126.5(VCP):c.2111A>C (p.Glu704Ala)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003780089]	uncertain significance	9	35059113	35059113	Human	1	name , alternate_id
402501058	CV3089663	single nucleotide variant	NM_007126.5(VCP):c.1699C>T (p.Arg567Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003788586]	uncertain significance	9	35059798	35059798	Human	1	name , alternate_id
402518409	CV3091728	single nucleotide variant	NM_007126.5(VCP):c.1528C>T (p.Pro510Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003790174]	uncertain significance	9	35060480	35060480	Human	1	name , alternate_id
404988466	CV3097086	single nucleotide variant	NM_007126.5(VCP):c.1972A>C (p.Lys658Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003792475]	uncertain significance	9	35059525	35059525	Human	1	name , alternate_id
405049545	CV3097561	single nucleotide variant	NM_007126.5(VCP):c.1309A>G (p.Ile437Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003808141]	uncertain significance	9	35061065	35061065	Human	1	name , alternate_id
404981141	CV3099710	single nucleotide variant	NM_007126.5(VCP):c.1031T>C (p.Met344Thr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003791539]	uncertain significance	9	35062053	35062053	Human	1	name , alternate_id
405066334	CV3110916	single nucleotide variant	NM_007126.5(VCP):c.1115C>T (p.Pro372Leu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003809420]	uncertain significance	9	35061656	35061656	Human	1	name , alternate_id
405109439	CV3112505	single nucleotide variant	NM_007126.5(VCP):c.1637A>G (p.Glu546Gly)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003813348]\|VCP-related disorder [RCV004736410]	uncertain significance	9	35060371	35060371	Human	2	name , trait , alternate_id
405078455	CV3114676	single nucleotide variant	NM_007126.5(VCP):c.2190G>T (p.Glu730Asp)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003810239]	uncertain significance	9	35057501	35057501	Human	1	name , alternate_id
11652713	CV318533	single nucleotide variant	NM_007126.5(VCP):c.1856T>C (p.Ile619Thr)	Amyotrophic Lateral Sclerosis, Dominant [RCV000306523]\|Inclusion Body Myopathy, Dominant [RCV000352284]	uncertain significance	9	35059641	35059641	Human	2	name
405806559	CV3345482	single nucleotide variant	NM_007126.5(VCP):c.1394G>A (p.Arg465Gln)	Inborn genetic diseases [RCV004480269]	uncertain significance	9	35060889	35060889	Human	1	name
408380610	CV3501217	single nucleotide variant	NM_007126.5(VCP):c.2214A>C (p.Glu738Asp)	not provided [RCV004727306]	uncertain significance	9	35057477	35057477	Human		name
408372843	CV3502152	single nucleotide variant	NM_007126.5(VCP):c.1916T>A (p.Leu639His)	not provided [RCV004725739]	uncertain significance	9	35059581	35059581	Human		name
408368605	CV3514196	single nucleotide variant	NM_007126.5(VCP):c.2149C>T (p.Pro717Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005221027]\|VCP-related disorder [RCV004735344]	uncertain significance	9	35059075	35059075	Human	2	name , trait , alternate_id
408391481	CV3523215	single nucleotide variant	NM_007126.5(VCP):c.1228G>A (p.Asp410Asn)	not provided [RCV004770587]	uncertain significance	9	35061146	35061146	Human		name
408392616	CV3525300	single nucleotide variant	NM_007126.5(VCP):c.1988A>G (p.Lys663Arg)	not provided [RCV004771186]	uncertain significance	9	35059509	35059509	Human		name
596922837	CV3537424	single nucleotide variant	NM_007126.5(VCP):c.2248A>G (p.Asn750Asp)	not provided [RCV004787394]	uncertain significance	9	35057443	35057443	Human		name
596944907	CV3543561	single nucleotide variant	NM_007126.5(VCP):c.1947T>A (p.Asp649Glu)	not provided [RCV004801683]	uncertain significance	9	35059550	35059550	Human		name
596945834	CV3548086	single nucleotide variant	NM_007126.5(VCP):c.1072C>T (p.Arg358Trp)	not provided [RCV004809417]	uncertain significance	9	35062012	35062012	Human		name
597632540	CV3552860	single nucleotide variant	NM_007126.5(VCP):c.1063C>A (p.Pro355Thr)	not provided [RCV004823688]	uncertain significance	9	35062021	35062021	Human		name
597643120	CV3633358	single nucleotide variant	NM_007126.5(VCP):c.1996G>C (p.Val666Leu)	Inborn genetic diseases [RCV004972119]	uncertain significance	9	35059501	35059501	Human	1	name
597643125	CV3633359	single nucleotide variant	NM_007126.5(VCP):c.2403T>G (p.Asp801Glu)	Inborn genetic diseases [RCV004972120]	uncertain significance	9	35057135	35057135	Human	1	name
597833855	CV3735631	single nucleotide variant	NM_007126.5(VCP):c.2078G>T (p.Arg693Leu)	not provided [RCV005063493]	uncertain significance	9	35059146	35059146	Human		name
12854208	CV384436	single nucleotide variant	NM_007126.5(VCP):c.1374G>C (p.Gln458His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000449528]	uncertain significance	9	35060909	35060909	Human	1	name , alternate_id
597859075	CV3864876	single nucleotide variant	NM_007126.5(VCP):c.1648A>G (p.Met550Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005213933]	uncertain significance	9	35060360	35060360	Human	1	name , alternate_id
597895030	CV3868725	single nucleotide variant	NM_007126.5(VCP):c.1343C>T (p.Thr448Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005219431]	uncertain significance	9	35061031	35061031	Human	1	name , alternate_id
597845423	CV3872196	single nucleotide variant	NM_007126.5(VCP):c.2123G>A (p.Arg708Lys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005212025]	uncertain significance	9	35059101	35059101	Human	1	name , alternate_id
597849524	CV3872966	single nucleotide variant	NM_007126.5(VCP):c.1858A>G (p.Ile620Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005212603]	uncertain significance	9	35059639	35059639	Human	1	name , alternate_id
597854204	CV3873869	single nucleotide variant	NM_007126.5(VCP):c.1358G>A (p.Arg453Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV005228654]	uncertain significance	9	35061016	35061016	Human	1	name , alternate_id
598124551	CV3883587	single nucleotide variant	NM_007126.5(VCP):c.1901T>A (p.Leu634His)	not provided [RCV005235941]	uncertain significance	9	35059596	35059596	Human		name
598123385	CV3890318	single nucleotide variant	NM_007126.5(VCP):c.1594G>A (p.Ala532Thr)	not provided [RCV005250837]	uncertain significance	9	35060414	35060414	Human		name
8602145	CV39109	single nucleotide variant	NM_007126.5(VCP):c.1774G>A (p.Asp592Asn)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000023066]	pathogenic	9	35059723	35059723	Human	1	name , alternate_id
598205686	CV3929489	single nucleotide variant	NM_007126.5(VCP):c.1217A>G (p.His406Arg)	Inborn genetic diseases [RCV005290890]	uncertain significance	9	35061157	35061157	Human	1	name
598205689	CV3929491	single nucleotide variant	NM_007126.5(VCP):c.1618A>G (p.Ile540Val)	Inborn genetic diseases [RCV005290891]	uncertain significance	9	35060390	35060390	Human	1	name
616937816	CV4013188	single nucleotide variant	NM_007126.5(VCP):c.2162A>C (p.Glu721Ala)	not provided [RCV005410655]	uncertain significance	9	35057529	35057529	Human		name
617150710	CV4018821	single nucleotide variant	NM_007126.5(VCP):c.1000G>A (p.Gly334Ser)	not provided [RCV005423229]	uncertain significance	9	35062084	35062084	Human		name
617154081	CV4022244	single nucleotide variant	NM_007126.5(VCP):c.2333A>G (p.Gln778Arg)	not provided [RCV005429600]	uncertain significance	9	35057205	35057205	Human		name
13211526	CV425844	single nucleotide variant	NM_007126.5(VCP):c.1614C>G (p.Asn538Lys)	not provided [RCV000497568]	uncertain significance	9	35060394	35060394	Human		name
13482381	CV441331	single nucleotide variant	NM_007126.5(VCP):c.1160A>C (p.Asn387Thr)	not specified [RCV000517850]	uncertain significance	9	35061611	35061611	Human		name
13487202	CV444477	single nucleotide variant	NM_007126.5(VCP):c.2077C>T (p.Arg693Cys)	not provided [RCV000523151]	likely pathogenic	9	35059147	35059147	Human		name
13491613	CV460014	single nucleotide variant	NM_007126.5(VCP):c.1202A>G (p.Asn401Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000534353]\|Inborn genetic diseases [RCV002350262]\|VCP-related disorder [RCV004537963]\|not provided [RCV001579523]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	9	35061172	35061172	Human	3	name , trait , alternate_id
13523179	CV493633	single nucleotide variant	NM_007126.5(VCP):c.2121T>G (p.Ile707Met)	not provided [RCV000592679]	uncertain significance	9	35059103	35059103	Human		name
13516577	CV493837	single nucleotide variant	NM_007126.5(VCP):c.1433A>G (p.Asp478Gly)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001860219]\|not provided [RCV000595705]	uncertain significance	9	35060850	35060850	Human	1	name , alternate_id
13607691	CV524552	single nucleotide variant	NM_007126.5(VCP):c.1327A>C (p.Asn443His)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV000639652]\|Inborn genetic diseases [RCV004678774]\|not provided [RCV004800501]	uncertain significance	9	35061047	35061047	Human	2	name , alternate_id
13804134	CV563943	single nucleotide variant	NM_007126.5(VCP):c.2397C>G (p.Asp799Glu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002233165]	uncertain significance	9	35057141	35057141	Human	1	name , alternate_id
13804301	CV563947	single nucleotide variant	NM_007126.5(VCP):c.1984C>T (p.Arg662Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002233265]\|not provided [RCV003140101]	uncertain significance	9	35059513	35059513	Human	1	name , alternate_id
13802571	CV577121	single nucleotide variant	NM_007126.5(VCP):c.1973A>C (p.Lys658Thr)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003768116]\|Inborn genetic diseases [RCV003353004]\|not provided [RCV000714166]	uncertain significance	9	35059524	35059524	Human	2	name , alternate_id
13833966	CV585206	single nucleotide variant	NM_007126.5(VCP):c.1156A>G (p.Lys386Glu)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001346989]\|not provided [RCV000729360]	uncertain significance	9	35061615	35061615	Human	1	name , alternate_id
14688242	CV620329	single nucleotide variant	NM_007126.5(VCP):c.1318G>T (p.Glu440Ter)	VCP-related disorder [RCV000779579]	uncertain significance	9	35061056	35061056	Human		name , trait , alternate_id
14708454	CV638217	single nucleotide variant	NM_007126.5(VCP):c.2266G>A (p.Glu756Lys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002235557]	uncertain significance	9	35057425	35057425	Human	1	name , alternate_id
14731649	CV638218	single nucleotide variant	NM_007126.5(VCP):c.2014T>G (p.Leu672Val)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 [RCV000801506]	uncertain significance	9	35059210	35059210	Human	2	name , alternate_id
14720383	CV638219	single nucleotide variant	NM_007126.5(VCP):c.1180G>A (p.Val394Met)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002234843]	uncertain significance	9	35061591	35061591	Human	1	name , alternate_id
26902364	CV836083	single nucleotide variant	NM_007126.5(VCP):c.2345G>C (p.Gly782Ala)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001035947]\|not provided [RCV003141942]	uncertain significance	9	35057193	35057193	Human	1	name , alternate_id
26912144	CV836084	single nucleotide variant	NM_007126.5(VCP):c.2228C>T (p.Ala743Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001039023]\|not provided [RCV005250126]	uncertain significance	9	35057463	35057463	Human	1	name , alternate_id
26906202	CV836085	single nucleotide variant	NM_007126.5(VCP):c.1996G>A (p.Val666Ile)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001051610]	uncertain significance	9	35059501	35059501	Human	1	name , alternate_id
28878003	CV861633	single nucleotide variant	NM_007126.5(VCP):c.1349A>T (p.Asp450Val)	VCP-related multisystem proteinopathy [RCV001095775]	uncertain significance	9	35061025	35061025	Human		name , trait
38493933	CV925568	single nucleotide variant	NM_007126.5(VCP):c.2194C>T (p.Arg732Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001224616]	uncertain significance	9	35057497	35057497	Human	1	name , alternate_id
38489110	CV934747	single nucleotide variant	NM_007126.5(VCP):c.2242A>T (p.Ser748Cys)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001210057]	uncertain significance	9	35057449	35057449	Human	1	name , alternate_id
38480450	CV946600	single nucleotide variant	NM_007126.5(VCP):c.1324A>G (p.Met442Val)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001234713]	uncertain significance	9	35061050	35061050	Human	1	name , alternate_id
38487415	CV946601	single nucleotide variant	NM_007126.5(VCP):c.1106T>C (p.Ile369Thr)	Charcot-Marie-Tooth disease type 2Y [RCV002471052]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001237563]\|not provided [RCV001760253]	uncertain significance	9	35061665	35061665	Human	2	name , alternate_id
38494717	CV955811	single nucleotide variant	NM_007126.5(VCP):c.2132G>A (p.Arg711Gln)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001241484]\|Inborn genetic diseases [RCV002418829]	uncertain significance	9	35059092	35059092	Human	2	name , alternate_id
38471139	CV955812	single nucleotide variant	NM_007126.5(VCP):c.1864G>T (p.Ala622Ser)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001248579]	uncertain significance	9	35059633	35059633	Human	1	name , alternate_id
40903630	CV977365	single nucleotide variant	NM_007126.5(VCP):c.1184A>G (p.Asp395Gly)	FRONTOTEMPORAL DEMENTIA WITHOUT AMYOTROPHIC LATERAL SCLEROSIS 6, WITH NEUROFIBRILLARY TANGLES [RCV001271084]\|not provided [RCV004797923]	pathogenic\|likely pathogenic	9	35061587	35061587	Human	1	name
156134270	CV1977190	microsatellite	NM_007126.5(VCP):c.792CTT[3] (p.Phe267del)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002593607]	uncertain significance	9	35062986	35062988	Human		name , alternate_id
401854274	CV2750249	microsatellite	NM_007126.5(VCP):c.898ATC[1] (p.Ile301del)	Childhood Onset VCP-related Neurodevelopmental Disorder [RCV003333708]	uncertain significance	9	35062259	35062261	Human		name , trait
598175816	CV3891052	microsatellite	NM_007126.5(VCP):c.909TGA[1] (p.Asp304del)	not provided [RCV005251905]	uncertain significance	9	35062248	35062250	Human		name
156225499	CV1981564	insertion	NM_007126.5(VCP):c.1082-8_1082-7insTGTTTGTGTAT	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV002626601]	likely benign	9	35061696	35061697	Human	1	name , alternate_id
155802978	CV1857877	deletion	NM_007126.5(VCP):c.1397_1402del (p.Glu466_Thr467del)	not provided [RCV002461727]	uncertain significance	9	35060881	35060886	Human		name
126773459	CV1022311	duplication	NC_000009.11:g.(?_34458994)_(35072710_?)dup	Autosomal recessive distal spinal muscular atrophy 2 [RCV001374141]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV001346193]	uncertain significance				Human	2	alternate_id
156439645	CV1939697	duplication	NC_000009.11:g.(?_32453279)_(35068379_?)dup	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003109611]	uncertain significance				Human	1	alternate_id
156439269	CV1942518	duplication	NC_000009.11:g.(?_32453279)_(37785041_?)dup	Acromesomelic dysplasia 1, Maroteaux type [RCV003109230]\|Arthrogryposis, distal, type 1A [RCV003119438]\|Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase [RCV003119437]\|Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 [RCV003109231]\|Primary ciliary dyskinesia [RCV00311943 ... (more) 9]\|not provided [RCV003154083]	uncertain significance\|no classifications from unflagged records				Human	5	alternate_id
405806583	CV3345494	single nucleotide variant	NM_024558.3(VCPKMT):c.26T>C (p.Leu9Pro)	not specified [RCV004480281]	uncertain significance	14	50116527	50116527	Human		name
598240371	CV3929501	single nucleotide variant	NM_024558.3(VCPKMT):c.16G>A (p.Glu6Lys)	not specified [RCV005296758]	uncertain significance	14	50116537	50116537	Human		name
156077211	CV2331863	single nucleotide variant	NM_024558.3(VCPKMT):c.35C>T (p.Pro12Leu)	not specified [RCV004186519]	uncertain significance	14	50116518	50116518	Human		name
329392688	CV2439120	single nucleotide variant	NM_024558.3(VCPKMT):c.52C>G (p.Arg18Gly)	not specified [RCV004266407]	uncertain significance	14	50116501	50116501	Human		name
401781661	CV2722210	single nucleotide variant	NM_025054.5(VCPIP1):c.46C>T (p.Pro16Ser)	not specified [RCV004328775]	uncertain significance	8	66666913	66666913	Human		name
405806579	CV3345492	single nucleotide variant	NM_025054.5(VCPIP1):c.67A>G (p.Thr23Ala)	not specified [RCV004480279]	uncertain significance	8	66666892	66666892	Human		name
407529524	CV3493418	single nucleotide variant	NM_024558.3(VCPKMT):c.35C>A (p.Pro12Gln)	not specified [RCV004680956]	uncertain significance	14	50116518	50116518	Human		name
407529532	CV3493422	single nucleotide variant	NM_024558.3(VCPKMT):c.29A>C (p.Glu10Ala)	not specified [RCV004680960]	uncertain significance	14	50116524	50116524	Human		name
597803781	CV3633377	single nucleotide variant	NM_024558.3(VCPKMT):c.74G>A (p.Gly25Asp)	not specified [RCV004881917]	uncertain significance	14	50116479	50116479	Human		name
598205714	CV3929503	single nucleotide variant	NM_024558.3(VCPKMT):c.31G>A (p.Asp11Asn)	not specified [RCV005290895]	uncertain significance	14	50116522	50116522	Human		name
14703951	CV642469	single nucleotide variant	NM_024558.3(VCPKMT):c.99T>G (p.Tyr33Ter)	not provided [RCV000807596]\|not specified [RCV001005055]	uncertain significance	14	50116454	50116454	Human		name
156367556	CV2203539	single nucleotide variant	NM_024558.3(VCPKMT):c.140T>C (p.Ile47Thr)	not specified [RCV004072742]	uncertain significance	14	50116413	50116413	Human		name
156151534	CV2268961	single nucleotide variant	NM_025054.5(VCPIP1):c.153T>A (p.Asp51Glu)	not specified [RCV004128363]	uncertain significance	8	66666806	66666806	Human		name
156333683	CV2336032	single nucleotide variant	NM_024558.3(VCPKMT):c.209C>T (p.Ser70Leu)	not specified [RCV004189637]	uncertain significance	14	50116344	50116344	Human		name
155995434	CV2375817	single nucleotide variant	NM_025054.5(VCPIP1):c.100G>C (p.Gly34Arg)	not specified [RCV004224398]	uncertain significance	8	66666859	66666859	Human		name
329377547	CV2453474	single nucleotide variant	NM_024558.3(VCPKMT):c.283A>C (p.Thr95Pro)	not specified [RCV004267075]	uncertain significance	14	50116163	50116163	Human		name
405806561	CV3345483	single nucleotide variant	NM_025054.5(VCPIP1):c.107T>C (p.Leu36Pro)	not specified [RCV004480270]	uncertain significance	8	66666852	66666852	Human		name
405806569	CV3345487	single nucleotide variant	NM_025054.5(VCPIP1):c.262G>A (p.Val88Met)	not specified [RCV004480274]	uncertain significance	8	66666697	66666697	Human		name
597698258	CV3629495	single nucleotide variant	NM_024558.3(VCPKMT):c.202C>T (p.Arg68Trp)	not specified [RCV004885356]	uncertain significance	14	50116351	50116351	Human		name
597803783	CV3633378	single nucleotide variant	NM_024558.3(VCPKMT):c.219G>C (p.Glu73Asp)	not specified [RCV004881918]	uncertain significance	14	50116334	50116334	Human		name
598240319	CV3929493	single nucleotide variant	NM_025054.5(VCPIP1):c.290A>G (p.Asn97Ser)	not specified [RCV005296751]	uncertain significance	8	66666669	66666669	Human		name
155916331	CV2197361	single nucleotide variant	NM_024558.3(VCPKMT):c.666G>C (p.Lys222Asn)	not specified [RCV004081103]	uncertain significance	14	50112624	50112624	Human		name
156056658	CV2265853	single nucleotide variant	NM_024558.3(VCPKMT):c.605C>A (p.Pro202His)	not specified [RCV004126719]	uncertain significance	14	50112685	50112685	Human		name
156301756	CV2307101	single nucleotide variant	NM_024558.3(VCPKMT):c.443A>G (p.Tyr148Cys)	not specified [RCV004159583]	uncertain significance	14	50115846	50115846	Human		name
155997282	CV2398692	single nucleotide variant	NM_024558.3(VCPKMT):c.672A>C (p.Lys224Asn)	not specified [RCV004240037]	uncertain significance	14	50112618	50112618	Human		name
401763607	CV2704005	single nucleotide variant	NM_024558.3(VCPKMT):c.508A>G (p.Ile170Val)	not specified [RCV004308897]	uncertain significance	14	50114347	50114347	Human		name
401771745	CV2711875	single nucleotide variant	NM_025054.5(VCPIP1):c.500C>T (p.Ala167Val)	not specified [RCV004309501]	uncertain significance	8	66666459	66666459	Human		name
401772161	CV2719553	single nucleotide variant	NM_024558.3(VCPKMT):c.394G>A (p.Gly132Ser)	not specified [RCV004327233]	uncertain significance	14	50115895	50115895	Human		name
401870484	CV2762782	single nucleotide variant	NM_024558.3(VCPKMT):c.574C>T (p.Leu192Phe)	not specified [RCV004340334]	uncertain significance	14	50112716	50112716	Human		name
405806586	CV3345495	single nucleotide variant	NM_024558.3(VCPKMT):c.386A>G (p.Glu129Gly)	not specified [RCV004480282]	uncertain significance	14	50115903	50115903	Human		name
405806588	CV3345496	single nucleotide variant	NM_024558.3(VCPKMT):c.433T>A (p.Cys145Ser)	not specified [RCV004480283]	uncertain significance	14	50115856	50115856	Human		name
405806589	CV3345497	single nucleotide variant	NM_024558.3(VCPKMT):c.490G>A (p.Gly164Arg)	not specified [RCV004480284]	uncertain significance	14	50114365	50114365	Human		name
405806591	CV3345498	single nucleotide variant	NM_024558.3(VCPKMT):c.604C>T (p.Pro202Ser)	not specified [RCV004480285]	uncertain significance	14	50112686	50112686	Human		name
407529526	CV3493419	single nucleotide variant	NM_024558.3(VCPKMT):c.482A>G (p.Asp161Gly)	not specified [RCV004680957]	uncertain significance	14	50114373	50114373	Human		name
407529529	CV3493420	single nucleotide variant	NM_024558.3(VCPKMT):c.680T>C (p.Phe227Ser)	not specified [RCV004680958]	uncertain significance	14	50109709	50109709	Human		name
407529530	CV3493421	single nucleotide variant	NM_024558.3(VCPKMT):c.674C>T (p.Ser225Leu)	not specified [RCV004680959]	uncertain significance	14	50112616	50112616	Human		name
407529534	CV3493423	single nucleotide variant	NM_024558.3(VCPKMT):c.635G>A (p.Ser212Asn)	not specified [RCV004680961]	uncertain significance	14	50112655	50112655	Human		name
597804035	CV3629494	single nucleotide variant	NM_024558.3(VCPKMT):c.391G>C (p.Glu131Gln)	not specified [RCV004881923]	uncertain significance	14	50115898	50115898	Human		name
597804033	CV3629496	single nucleotide variant	NM_024558.3(VCPKMT):c.307T>G (p.Leu103Val)	not specified [RCV004881924]	uncertain significance	14	50116139	50116139	Human		name
597803766	CV3633362	single nucleotide variant	NM_025054.5(VCPIP1):c.515C>G (p.Pro172Arg)	not specified [RCV004881909]	uncertain significance	8	66666444	66666444	Human		name
597698172	CV3633364	single nucleotide variant	NM_025054.5(VCPIP1):c.760C>G (p.Gln254Glu)	not specified [RCV004885347]	uncertain significance	8	66666199	66666199	Human		name
597803777	CV3633372	single nucleotide variant	NM_025054.5(VCPIP1):c.998C>G (p.Thr333Ser)	not specified [RCV004881915]	uncertain significance	8	66665961	66665961	Human		name
597698217	CV3633374	single nucleotide variant	NM_025054.5(VCPIP1):c.378C>G (p.His126Gln)	not specified [RCV004885352]	uncertain significance	8	66666581	66666581	Human		name
597698236	CV3633379	single nucleotide variant	NM_024558.3(VCPKMT):c.314A>G (p.Lys105Arg)	not specified [RCV004885354]	uncertain significance	14	50116132	50116132	Human		name
597698247	CV3633380	single nucleotide variant	NM_024558.3(VCPKMT):c.448G>A (p.Glu150Lys)	not specified [RCV004885355]	uncertain significance	14	50115841	50115841	Human		name
597803785	CV3633381	single nucleotide variant	NM_024558.3(VCPKMT):c.617A>G (p.His206Arg)	not specified [RCV004881919]	uncertain significance	14	50112673	50112673	Human		name
597803787	CV3633382	single nucleotide variant	NM_024558.3(VCPKMT):c.488G>T (p.Ser163Ile)	not specified [RCV004881920]	uncertain significance	14	50114367	50114367	Human		name
597803788	CV3633383	single nucleotide variant	NM_024558.3(VCPKMT):c.317T>C (p.Met106Thr)	not specified [RCV004881921]	uncertain significance	14	50116129	50116129	Human		name
598240335	CV3929495	single nucleotide variant	NM_025054.5(VCPIP1):c.505C>T (p.Leu169Phe)	not specified [RCV005296753]	uncertain significance	8	66666454	66666454	Human		name
598205707	CV3929502	single nucleotide variant	NM_024558.3(VCPKMT):c.442T>C (p.Tyr148His)	not specified [RCV005290894]	uncertain significance	14	50115847	50115847	Human		name
156377635	CV2217088	single nucleotide variant	NM_025054.5(VCPIP1):c.2962G>A (p.Ala988Thr)	not specified [RCV004085765]	uncertain significance	8	66635208	66635208	Human		name
155947999	CV2245831	single nucleotide variant	NM_025054.5(VCPIP1):c.2510C>G (p.Pro837Arg)	not specified [RCV004111681]	uncertain significance	8	66664449	66664449	Human		name
156162817	CV2246564	single nucleotide variant	NM_025054.5(VCPIP1):c.1384A>T (p.Met462Leu)	not specified [RCV004110312]	uncertain significance	8	66665575	66665575	Human		name
156245580	CV2283432	single nucleotide variant	NM_025054.5(VCPIP1):c.2210A>G (p.Gln737Arg)	not specified [RCV004139655]	uncertain significance	8	66664749	66664749	Human		name
155927644	CV2365962	single nucleotide variant	NM_025054.5(VCPIP1):c.2242C>T (p.Pro748Ser)	not specified [RCV004207570]	uncertain significance	8	66664717	66664717	Human		name
156288447	CV2370656	single nucleotide variant	NM_025054.5(VCPIP1):c.1840A>C (p.Ser614Arg)	not specified [RCV004209064]	uncertain significance	8	66665119	66665119	Human		name
156168062	CV2399104	single nucleotide variant	NM_025054.5(VCPIP1):c.1403A>G (p.Lys468Arg)	not specified [RCV004246540]	uncertain significance	8	66665556	66665556	Human		name
329360549	CV2443615	single nucleotide variant	NM_025054.5(VCPIP1):c.2426A>G (p.Asn809Ser)	not specified [RCV004262436]	uncertain significance	8	66664533	66664533	Human		name
401756957	CV2692715	single nucleotide variant	NM_025054.5(VCPIP1):c.1510A>C (p.Thr504Pro)	not specified [RCV004306267]	likely benign	8	66665449	66665449	Human		name
401748127	CV2700009	single nucleotide variant	NM_025054.5(VCPIP1):c.1694C>T (p.Ser565Phe)	not specified [RCV004310438]	uncertain significance	8	66665265	66665265	Human		name
401855417	CV2757316	single nucleotide variant	NM_025054.5(VCPIP1):c.1388A>G (p.Asp463Gly)	not specified [RCV004340725]	uncertain significance	8	66665571	66665571	Human		name
401890683	CV2778290	single nucleotide variant	NM_025054.5(VCPIP1):c.1970A>C (p.Lys657Thr)	not specified [RCV004350345]	uncertain significance	8	66664989	66664989	Human		name
405806563	CV3345484	single nucleotide variant	NM_025054.5(VCPIP1):c.1651G>A (p.Gly551Arg)	not specified [RCV004480271]	uncertain significance	8	66665308	66665308	Human		name
405806565	CV3345485	single nucleotide variant	NM_025054.5(VCPIP1):c.2285C>A (p.Pro762His)	not specified [RCV004480272]	uncertain significance	8	66664674	66664674	Human		name
405806910	CV3345486	single nucleotide variant	NM_025054.5(VCPIP1):c.2296C>T (p.Pro766Ser)	not specified [RCV004480273]	uncertain significance	8	66664663	66664663	Human		name
405806571	CV3345488	single nucleotide variant	NM_025054.5(VCPIP1):c.2846C>A (p.Thr949Asn)	not specified [RCV004480275]	uncertain significance	8	66635324	66635324	Human		name
407529504	CV3493405	single nucleotide variant	NM_025054.5(VCPIP1):c.2311A>C (p.Thr771Pro)	not specified [RCV004680946]	uncertain significance	8	66664648	66664648	Human		name
407529508	CV3493408	single nucleotide variant	NM_025054.5(VCPIP1):c.2792C>A (p.Thr931Asn)	not specified [RCV004680948]	uncertain significance	8	66651463	66651463	Human		name
407529510	CV3493409	single nucleotide variant	NM_025054.5(VCPIP1):c.2016C>A (p.His672Gln)	not specified [RCV004680949]	uncertain significance	8	66664943	66664943	Human		name
407529512	CV3493410	single nucleotide variant	NM_025054.5(VCPIP1):c.1527C>G (p.Ser509Arg)	not specified [RCV004680950]	uncertain significance	8	66665432	66665432	Human		name
407464835	CV3493414	single nucleotide variant	NM_025054.5(VCPIP1):c.2417G>C (p.Arg806Thr)	not specified [RCV004688611]	uncertain significance	8	66664542	66664542	Human		name
407529520	CV3493416	single nucleotide variant	NM_025054.5(VCPIP1):c.2711G>A (p.Gly904Glu)	not specified [RCV004680954]	uncertain significance	8	66651544	66651544	Human		name
597803763	CV3633360	single nucleotide variant	NM_025054.5(VCPIP1):c.1561T>A (p.Ser521Thr)	not specified [RCV004881907]	uncertain significance	8	66665398	66665398	Human		name
597803765	CV3633361	single nucleotide variant	NM_025054.5(VCPIP1):c.1841G>A (p.Ser614Asn)	not specified [RCV004881908]	uncertain significance	8	66665118	66665118	Human		name
597698181	CV3633365	single nucleotide variant	NM_025054.5(VCPIP1):c.2144C>T (p.Thr715Ile)	not specified [RCV004885348]	uncertain significance	8	66664815	66664815	Human		name
597803770	CV3633366	single nucleotide variant	NM_025054.5(VCPIP1):c.2201A>G (p.Lys734Arg)	not specified [RCV004881911]	uncertain significance	8	66664758	66664758	Human		name
597698200	CV3633368	single nucleotide variant	NM_025054.5(VCPIP1):c.1625A>G (p.His542Arg)	not specified [RCV004885350]	uncertain significance	8	66665334	66665334	Human		name
597803772	CV3633369	single nucleotide variant	NM_025054.5(VCPIP1):c.2132A>G (p.Lys711Arg)	not specified [RCV004881912]	uncertain significance	8	66664827	66664827	Human		name
597803774	CV3633370	single nucleotide variant	NM_025054.5(VCPIP1):c.1509G>T (p.Arg503Ser)	not specified [RCV004881913]	uncertain significance	8	66665450	66665450	Human		name
597803776	CV3633371	single nucleotide variant	NM_025054.5(VCPIP1):c.2293G>C (p.Ala765Pro)	not specified [RCV004881914]	uncertain significance	8	66664666	66664666	Human		name
597803779	CV3633375	single nucleotide variant	NM_025054.5(VCPIP1):c.2503A>G (p.Lys835Glu)	not specified [RCV004881916]	uncertain significance	8	66664456	66664456	Human		name
597698227	CV3633376	single nucleotide variant	NM_025054.5(VCPIP1):c.1588T>C (p.Tyr530His)	not specified [RCV004885353]	uncertain significance	8	66665371	66665371	Human		name
598205694	CV3929492	single nucleotide variant	NM_025054.5(VCPIP1):c.2312C>A (p.Thr771Asn)	not specified [RCV005290892]	uncertain significance	8	66664647	66664647	Human		name
598240328	CV3929494	single nucleotide variant	NM_025054.5(VCPIP1):c.2579C>T (p.Ser860Phe)	not specified [RCV005296752]	uncertain significance	8	66664380	66664380	Human		name
598205701	CV3929496	single nucleotide variant	NM_025054.5(VCPIP1):c.2108A>G (p.His703Arg)	not specified [RCV005290893]	uncertain significance	8	66664851	66664851	Human		name
598240343	CV3929497	single nucleotide variant	NM_025054.5(VCPIP1):c.2491G>A (p.Ala831Thr)	not specified [RCV005296754]	uncertain significance	8	66664468	66664468	Human		name
156231050	CV2348733	single nucleotide variant	NM_025054.5(VCPIP1):c.3374G>A (p.Arg1125Gln)	not specified [RCV004201143]	uncertain significance	8	66634796	66634796	Human		name
401773642	CV2695313	single nucleotide variant	NM_025054.5(VCPIP1):c.3506A>T (p.Asn1169Ile)	not specified [RCV004303436]	uncertain significance	8	66634664	66634664	Human		name
401865124	CV2757539	single nucleotide variant	NM_025054.5(VCPIP1):c.3416G>A (p.Arg1139Lys)	not specified [RCV004340915]	uncertain significance	8	66634754	66634754	Human		name
405806573	CV3345489	single nucleotide variant	NM_025054.5(VCPIP1):c.3229A>G (p.Ser1077Gly)	not specified [RCV004480276]	uncertain significance	8	66634941	66634941	Human		name
405806575	CV3345490	single nucleotide variant	NM_025054.5(VCPIP1):c.3257C>T (p.Pro1086Leu)	not specified [RCV004480277]	uncertain significance	8	66634913	66634913	Human		name
405806577	CV3345491	single nucleotide variant	NM_025054.5(VCPIP1):c.3363C>G (p.Asp1121Glu)	not specified [RCV004480278]	uncertain significance	8	66634807	66634807	Human		name
407529506	CV3493406	single nucleotide variant	NM_025054.5(VCPIP1):c.3434G>A (p.Ser1145Asn)	not specified [RCV004680947]	uncertain significance	8	66634736	66634736	Human		name
407464827	CV3493407	single nucleotide variant	NM_025054.5(VCPIP1):c.3545C>T (p.Ala1182Val)	not specified [RCV004688609]	uncertain significance	8	66634625	66634625	Human		name
407464831	CV3493411	single nucleotide variant	NM_025054.5(VCPIP1):c.3190T>A (p.Ser1064Thr)	not specified [RCV004688610]	uncertain significance	8	66634980	66634980	Human		name
407529514	CV3493412	single nucleotide variant	NM_025054.5(VCPIP1):c.3539C>T (p.Ala1180Val)	not specified [RCV004680951]	uncertain significance	8	66634631	66634631	Human		name
407529516	CV3493413	single nucleotide variant	NM_025054.5(VCPIP1):c.3451G>C (p.Gly1151Arg)	not specified [RCV004680952]	uncertain significance	8	66634719	66634719	Human		name
407529522	CV3493417	single nucleotide variant	NM_025054.5(VCPIP1):c.3115C>A (p.Pro1039Thr)	not specified [RCV004680955]	uncertain significance	8	66635055	66635055	Human		name
597698190	CV3633367	single nucleotide variant	NM_025054.5(VCPIP1):c.3547C>G (p.Leu1183Val)	not specified [RCV004885349]	uncertain significance	8	66634623	66634623	Human		name
598240350	CV3929498	single nucleotide variant	NM_025054.5(VCPIP1):c.3274A>G (p.Arg1092Gly)	not specified [RCV005296755]	uncertain significance	8	66634896	66634896	Human		name
598240358	CV3929499	single nucleotide variant	NM_025054.5(VCPIP1):c.3637A>G (p.Thr1213Ala)	not specified [RCV005296756]	uncertain significance	8	66634533	66634533	Human		name
598240365	CV3929500	single nucleotide variant	NM_025054.5(VCPIP1):c.3643A>G (p.Thr1215Ala)	not specified [RCV005296757]	uncertain significance	8	66634527	66634527	Human		name
8635223	CV90445	single nucleotide variant	NM_001040662.1(VCPKMT):c.104C>T (p.Ser35Phe)	Malignant melanoma [RCV000070543]	not provided	14	50116449	50116449	Human		name

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