"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "VCP"[ge - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 583788	NC_000009.11:g.(?_34645556)_(36277059_?)dup	CCIN, SPATA31F1 +138 more	Duplication	Anauxetic dysplasia	GUncertain significance
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 464107	NM_007126.5(VCP):c.2412G>A (p.Leu804=)	VCP	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 194756	NM_007126.5(VCP):c.2406T>C (p.Asp802=)	VCP	Single nucleotide variant (synonymous variant)	not provided +5 more	GBenign/Likely benign
Select item 568017	NM_007126.5(VCP):c.2397C>G (p.Asp799Glu)	VCP (D799E +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2930112	NM_007126.5(VCP):c.2391A>G (p.Thr797=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2017821	NM_007126.5(VCP):c.2385A>G (p.Val795=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 1986151	NM_007126.5(VCP):c.2381G>A (p.Ser794Asn)	VCP (S749N +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 2926569	NM_007126.5(VCP):c.2373A>G (p.Thr791=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2939485	NM_007126.5(VCP):c.2370C>T (p.Gly790=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2925170	NM_007126.5(VCP):c.2367C>T (p.Gly789=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 1058517	NM_007126.5(VCP):c.2345G>T (p.Gly782Val)	VCP (G737V +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 835129	NM_007126.5(VCP):c.2345G>C (p.Gly782Ala)	VCP (G782A +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1956782	NM_007126.5(VCP):c.2343T>C (p.Ala781=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2127553	NM_007126.5(VCP):c.2334G>A (p.Gln778=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 532767	NM_007126.5(VCP):c.2316-4A>G	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2174979	NM_007126.5(VCP):c.2316-5C>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 1106973	NM_007126.5(VCP):c.2316-8G>A	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2061369	NM_007126.5(VCP):c.2316-11C>G	VCP	Single nucleotide variant (intron 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)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 1652973	NM_007126.5(VCP):c.2315+8G>C	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2921393	NM_007126.5(VCP):c.2315+6T>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2928269	NM_007126.5(VCP):c.2298G>A (p.Arg766=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 653332	NM_007126.5(VCP):c.2266G>A (p.Glu756Lys)	VCP (E711K +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 2053864	NM_007126.5(VCP):c.2244T>C (p.Ser748=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 940463	NM_007126.5(VCP):c.2242A>T (p.Ser748Cys)	VCP (S748C +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2925445	NM_007126.5(VCP):c.2234G>A (p.Arg745His)	VCP (R745H +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1349844	NM_007126.5(VCP):c.2233C>T (p.Arg745Cys)	VCP (R700C +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 1167285	NM_007126.5(VCP):c.2229G>A (p.Ala743=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GBenign
Select item 837640	NM_007126.5(VCP):c.2228C>T (p.Ala743Val)	VCP (A698V +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 1124905	NM_007126.5(VCP):c.2223C>T (p.Arg741=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2169829	NM_007126.5(VCP):c.2221C>T (p.Arg741Cys)	VCP (R696C +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +2 more	GUncertain significance
Select item 194645	NM_007126.5(VCP):c.2214A>G (p.Glu738=)	VCP	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +5 more	GBenign/Likely benign
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 1160158	NM_007126.5(VCP):c.2197C>A (p.Arg733=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 952496	NM_007126.5(VCP):c.2194C>T (p.Arg732Cys)	VCP (R687C +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 1169485	NM_007126.5(VCP):c.2193C>T (p.Ile731=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GBenign
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 1626465	NM_007126.5(VCP):c.2175T>C (p.Asp725=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 705822	NM_007126.5(VCP):c.2166A>G (p.Val722=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +2 more	GLikely benign
Select item 1531243	NM_007126.5(VCP):c.2161-4A>G	VCP	Single nucleotide variant (intron variant)	Inborn genetic diseases +2 more	GConflicting classifications of pathogenicity
Select item 1121489	NM_007126.5(VCP):c.2161-5T>C	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 532766	NM_007126.5(VCP):c.2161-6C>T	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +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 1618706	NM_007126.5(VCP):c.2160+14C>A	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 742604	NM_007126.5(VCP):c.2160+8T>G	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GBenign
Select item 1910993	NM_007126.5(VCP):c.2151A>G (p.Pro717=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2004286	NM_007126.5(VCP):c.2143A>G (p.Thr715Ala)	VCP (T715A +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 2047295	NM_007126.5(VCP):c.2134G>C (p.Glu712Gln)	VCP (E667Q +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 966733	NM_007126.5(VCP):c.2132G>A (p.Arg711Gln)	VCP (R666Q +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +2 more	GUncertain significance
Select item 1039720	NM_007126.5(VCP):c.2126G>A (p.Arg709Gln)	VCP (R709Q +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2921507	NM_007126.5(VCP):c.2111A>C (p.Glu704Ala)	VCP (E704A +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 1716921	NM_007126.5(VCP):c.2110G>A (p.Glu704Lys)	VCP (E659K +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 1096276	NM_007126.5(VCP):c.2109C>T (p.Ile703=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 709727	NM_007126.5(VCP):c.2052A>G (p.Gly684=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2033936	NM_007126.5(VCP):c.2036C>T (p.Thr679Ile)	VCP (T634I +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 1596465	NM_007126.5(VCP):c.2028T>C (p.Ala676=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 647081	NM_007126.5(VCP):c.2014T>G (p.Leu672Val)	VCP (L627V +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +1 more	GUncertain significance
Select item 1916783	NM_007126.5(VCP):c.2005-6T>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 2030291	NM_007126.5(VCP):c.2005-9T>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 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 2054332	NM_007126.5(VCP):c.2005-20A>G	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2930335	NM_007126.5(VCP):c.2004+8C>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 847962	NM_007126.5(VCP):c.1996G>A (p.Val666Ile)	VCP (V621I +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 1470708	NM_007126.5(VCP):c.1993C>T (p.Pro665Ser)	VCP (P620S +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 1390232	NM_007126.5(VCP):c.1985G>A (p.Arg662His)	VCP (R617H +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +2 more	GUncertain significance
Select item 572697	NM_007126.5(VCP):c.1984C>T (p.Arg662Cys)	VCP (R662C +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 586925	NM_007126.5(VCP):c.1973A>C (p.Lys658Thr)	VCP (K658T +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +3 more	GUncertain significance
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 532763	NM_007126.5(VCP):c.1950G>A (p.Glu650=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +2 more	GLikely benign
Select item 1670212	NM_007126.5(VCP):c.1944T>C (p.Pro648=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2090326	NM_007126.5(VCP):c.1915C>A (p.Leu639Ile)	VCP (L594I +1 more)	Single nucleotide variant (missense variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 2188978	NM_007126.5(VCP):c.1896C>G (p.Ala632=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 501835	NM_007126.5(VCP):c.1896C>A (p.Ala632=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +3 more	GConflicting classifications of pathogenicity
Select item 733166	NM_007126.5(VCP):c.1887T>C (p.Ile629=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 1980848	NM_007126.5(VCP):c.1884C>T (p.Ile628=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 501479	NM_007126.5(VCP):c.1875G>T (p.Arg625=)	VCP	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 972527	NM_007126.5(VCP):c.1864G>T (p.Ala622Ser)	VCP (A577S +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 593323	NM_007126.5(VCP):c.1863C>T (p.Gly621=)	VCP	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 2413510	NM_007126.5(VCP):c.1854C>T (p.Phe618=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 718252	NM_007126.5(VCP):c.1847dup (p.Asn616fs)	VCP (N571fs +1 more)	Duplication (frameshift variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +2 more	GConflicting classifications of pathogenicity
Select item 2931374	NM_007126.5(VCP):c.1842A>G (p.Lys614=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 1092902	NM_007126.5(VCP):c.1839A>C (p.Thr613=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 1509783	NM_007126.5(VCP):c.1837A>G (p.Thr613Ala)	VCP (T613A +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 1957826	NM_007126.5(VCP):c.1818A>G (p.Thr606=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 1431328	NM_007126.5(VCP):c.1790C>T (p.Ala597Val)	VCP (A552V +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 1106594	NM_007126.5(VCP):c.1776T>C (p.Asp592=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 1359439	NM_007126.5(VCP):c.1768A>G (p.Ile590Val)	VCP (I590V +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 2939293	NM_007126.5(VCP):c.1743G>T (p.Ser581=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 2925195	NM_007126.5(VCP):c.1743G>A (p.Ser581=)	VCP	Single nucleotide variant (synonymous 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 2927785	NM_007126.5(VCP):c.1722A>G (p.Leu574=)	VCP	Single nucleotide variant (synonymous variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 1523242	NM_007126.5(VCP):c.1696-34_1716dup	VCP	Duplication (splice acceptor variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 260125	NM_007126.5(VCP):c.1704A>G (p.Gln568=)	VCP	Single nucleotide variant (synonymous variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1 +5 more	GBenign/Likely benign
Select item 2924884	NM_007126.5(VCP):c.1699C>T (p.Arg567Cys)	VCP (R567C +1 more)	Single nucleotide variant (missense variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GUncertain significance
Select item 2931163	NM_007126.5(VCP):c.1696-3C>T	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GUncertain significance
Select item 1149313	NM_007126.5(VCP):c.1696-5dup	VCP	Duplication (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign
Select item 790949	NM_007126.5(VCP):c.1696-4A>G	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 464106	NM_007126.5(VCP):c.1696-7C>T	VCP	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 +1 more	GLikely benign
Select item 1591848	NM_007126.5(VCP):c.1696-8T>C	VCP	Single nucleotide variant (intron variant)	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia +1 more	GLikely benign

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