List of variants in gene VCP reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_007126.5(VCP):c.79A>G (p.Ile27Val)	rs140913250	0.00151
NM_007126.5(VCP):c.1081+17C>T	rs200756991	0.00113
NM_007126.5(VCP):c.1584C>T (p.Ala528=)	rs147623367	0.00064
NM_007126.5(VCP):c.2316-48C>T	rs369994179	0.00029
NM_007126.5(VCP):c.1202A>G (p.Asn401Ser)	rs148329626	0.00009
NM_007126.5(VCP):c.1875G>T (p.Arg625=)	rs201410035	0.00009
NM_007126.5(VCP):c.1194+3G>A	rs183223259	0.00008
NM_007126.5(VCP):c.54A>G (p.Lys18=)	rs766042571	0.00003
NM_007126.5(VCP):c.330C>T (p.Tyr110=)	rs1259531489	0.00002
NM_007126.5(VCP):c.1696-4A>G	rs963637081	0.00001
NM_007126.5(VCP):c.1194+9ATG[2]	rs886038581
NM_007126.5(VCP):c.1359+10A>C
NM_007126.5(VCP):c.1383A>G (p.Pro461=)
NM_007126.5(VCP):c.1696-3C>T
NM_007126.5(VCP):c.1896C>A (p.Ala632=)	rs141275388
NM_007126.5(VCP):c.2148C>T (p.Asn716=)
NM_007126.5(VCP):c.291G>A (p.Gly97=)
NM_007126.5(VCP):c.426G>C (p.Ala142=)	rs577812326
NM_007126.5(VCP):c.577-21_577-18del	rs763622603

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