ClinVar for MedGen (Select 1759760) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3763976	NM_007126.5(VCP):c.709-16C>T	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3763570	NM_007126.5(VCP):c.812-19C>T	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3763450	NM_007126.5(VCP):c.1482+10C>G	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3763411	NM_007126.5(VCP):c.74G>A (p.Arg25Gln)	VCP (R25Q)	Single nucleotide variant (5 prime UTR variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 3763101	NM_007126.5(VCP):c.2187T>G (p.Pro729=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GBenign
Select item 3763052	NM_007126.5(VCP):c.130-11T>C	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 3762953	NM_007126.5(VCP):c.254A>G (p.Asn85Ser)	VCP (N40S +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 3762675	NM_007126.5(VCP):c.130-12T>C	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3762663	NM_007126.5(VCP):c.1083T>C (p.Gly361=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3762523	NM_007126.5(VCP):c.17+17C>T	LOC130001690, VCP	Single nucleotide variant (5 prime UTR variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3762130	NM_007126.5(VCP):c.1483-6T>A	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3762068	NM_007126.5(VCP):c.879T>C (p.Ala293=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3761793	NM_007126.5(VCP):c.907A>G (p.Ile303Val)	VCP (I258V +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 3761564	NM_007126.5(VCP):c.2161-3T>C	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 3761238	NM_007126.5(VCP):c.510T>G (p.Pro170=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3760690	NM_007126.5(VCP):c.1358G>A (p.Arg453Gln)	VCP (R408Q +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 3759622	NM_007126.5(VCP):c.709-16_709-15del	VCP	Microsatellite (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3759403	NM_007126.5(VCP):c.2010G>C (p.Val670=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3759087	NM_007126.5(VCP):c.2172G>A (p.Glu724=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 3758637	NM_007126.5(VCP):c.1360-20A>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3758488	NM_007126.5(VCP):c.576+12C>G	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3758076	NM_007126.5(VCP):c.296T>C (p.Val99Ala)	VCP (V54A +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3757599	NM_007126.5(VCP):c.945+6A>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3757511	NM_007126.5(VCP):c.389T>C (p.Leu130Pro)	VCP (L130P +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3755958	NM_007126.5(VCP):c.1858A>G (p.Ile620Val)	VCP (I575V +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3755945	NM_007126.5(VCP):c.708+16T>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3755499	NM_007126.5(VCP):c.978A>G (p.Ser326=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3755234	NM_007126.5(VCP):c.302+10G>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3755011	NM_007126.5(VCP):c.665T>G (p.Leu222Arg)	VCP (L177R +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3754919	NM_007126.5(VCP):c.1696-9C>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3754387	NM_007126.5(VCP):c.115G>A (p.Val39Met)	VCP (V39M)	Single nucleotide variant (5 prime UTR variant +1 more)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3753918	NM_007126.5(VCP):c.112G>A (p.Val38Met)	VCP (V38M)	Single nucleotide variant (5 prime UTR variant +1 more)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3753917	NM_007126.5(VCP):c.269A>G (p.Asn90Ser)	VCP (N45S +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3753916	NM_007126.5(VCP):c.2123G>A (p.Arg708Lys)	VCP (R663K +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3753761	NM_007126.5(VCP):c.1195-15G>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3752995	NM_007126.5(VCP):c.1343C>T (p.Thr448Ile)	VCP (T403I +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3752013	NM_007126.5(VCP):c.300C>T (p.Ile100=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3751660	NM_007126.5(VCP):c.1404G>T (p.Val468=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3751634	NM_007126.5(VCP):c.946-13C>A	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3751316	NM_007126.5(VCP):c.1392G>T (p.Leu464=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3751267	NM_007126.5(VCP):c.2121T>A (p.Ile707=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3750953	NM_007126.5(VCP):c.807C>A (p.Ile269=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3750817	NM_007126.5(VCP):c.1212C>T (p.His404=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3750486	NM_007126.5(VCP):c.576+15T>A	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3750481	NM_007126.5(VCP):c.165C>T (p.Asp55=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3749972	NM_007126.5(VCP):c.1648A>G (p.Met550Val)	VCP (M505V +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3749964	NM_007126.5(VCP):c.1482+14G>A	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3749602	NM_007126.5(VCP):c.963G>A (p.Glu321=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3749321	NM_007126.5(VCP):c.1081+11C>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3748754	NM_007126.5(VCP):c.445+10A>G	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3748166	NM_007126.5(VCP):c.272A>G (p.Asn91Ser)	VCP (N46S +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3748108	NM_007126.5(VCP):c.724C>T (p.Leu242=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 3354975	NM_007126.5(VCP):c.2149C>T (p.Pro717Ser)	VCP (P672S +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 3346187	NM_007126.5(VCP):c.481G>A (p.Val161Met)	VCP (V116M +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 2954479	NM_007126.5(VCP):c.283C>A (p.Arg95Ser)	VCP (R50S +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely pathogenic
Select item 2954262	NM_007126.5(VCP):c.759G>C (p.Leu253=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2954125	NM_007126.5(VCP):c.1637A>G (p.Glu546Gly)	VCP (E501G +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 2953705	NM_007126.5(VCP):c.2205C>T (p.His735=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2953472	NM_007126.5(VCP):c.446-19G>T	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2953403	NM_007126.5(VCP):c.1731T>C (p.Asp577=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2953121	NM_007126.5(VCP):c.2190G>T (p.Glu730Asp)	VCP (E685D +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 2953112	NM_007126.5(VCP):c.168A>G (p.Thr56=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2952889	NM_007126.5(VCP):c.672G>C (p.Leu224=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2952307	NM_007126.5(VCP):c.411G>A (p.Pro137=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +2 more	GLikely benign
Select item 2951566	NM_007126.5(VCP):c.1359+11C>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2951449	NM_007126.5(VCP):c.1465C>T (p.Leu489=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2950014	NM_007126.5(VCP):c.487T>A (p.Phe163Ile)	VCP (F118I +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2948650	NM_007126.5(VCP):c.811+17A>G	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2948646	NM_007126.5(VCP):c.1115C>T (p.Pro372Leu)	VCP (P327L +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2948334	NM_007126.5(VCP):c.576+10C>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2947501	NM_007126.5(VCP):c.367G>C (p.Val123Leu)	VCP (V78L +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2947014	NM_007126.5(VCP):c.811+8A>G	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2944863	NM_007126.5(VCP):c.2161-20T>A	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2944592	NM_007126.5(VCP):c.1341T>C (p.Val447=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2944585	NM_007126.5(VCP):c.605G>A (p.Gly202Glu)	VCP (G157E +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2943913	NM_007126.5(VCP):c.467G>T (p.Gly156Val)	VCP (G156V +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2942975	NM_007126.5(VCP):c.1309A>G (p.Ile437Val)	VCP (I392V +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2942520	NM_007126.5(VCP):c.255T>C (p.Asn85=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2941904	NM_007126.5(VCP):c.2315+10T>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2941572	NM_007126.5(VCP):c.2420A>G (p.Ter807=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2941213	NM_007126.5(VCP):c.1972A>C (p.Lys658Gln)	VCP (K658Q +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2940228	NM_007126.5(VCP):c.2005-14G>A	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2939983	NM_007126.5(VCP):c.1287C>T (p.Leu429=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2939684	NM_007126.5(VCP):c.627C>T (p.Cys209=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2939485	NM_007126.5(VCP):c.2370C>T (p.Gly790=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2939293	NM_007126.5(VCP):c.1743G>T (p.Ser581=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2938877	NM_007126.5(VCP):c.130-20C>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2938750	NM_007126.5(VCP):c.1095G>A (p.Arg365=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2938309	NM_007126.5(VCP):c.399A>G (p.Val133=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2937349	NM_007126.5(VCP):c.1031T>C (p.Met344Thr)	VCP (M299T +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2937241	NM_007126.5(VCP):c.811+13G>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2937170	NM_007126.5(VCP):c.812-19C>G	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2936575	NM_007126.5(VCP):c.401A>T (p.Tyr134Phe)	VCP (Y134F +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2936557	NM_007126.5(VCP):c.555A>G (p.Glu185=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2935921	NM_007126.5(VCP):c.288A>G (p.Leu96=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2935546	NM_007126.5(VCP):c.666G>A (p.Leu222=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2934845	NM_007126.5(VCP):c.811+9T>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2934749	NM_007126.5(VCP):c.244A>C (p.Ile82Leu)	VCP (I82L +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2933056	NM_007126.5(VCP):c.1528C>T (p.Pro510Ser)	VCP (P465S +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2932855	NM_007126.5(VCP):c.1383A>G (p.Pro461=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign

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