List of variants in gene GPC3 reported as likely benign by Ambry Genetics

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_004484.4(GPC3):c.826G>A (p.Gly276Ser)	rs141100113	0.00082
NM_004484.4(GPC3):c.660C>T (p.Ser220=)	rs138450923	0.00050
NM_004484.4(GPC3):c.1232G>T (p.Ser411Ile)	rs139206747	0.00010
NM_004484.4(GPC3):c.358C>T (p.Arg120Cys)	rs587778392	0.00006
NM_004484.4(GPC3):c.168C>G (p.Pro56=)	rs188592483	0.00005
NM_004484.4(GPC3):c.648G>C (p.Met216Ile)	rs752516966	0.00004
NM_004484.4(GPC3):c.608G>A (p.Arg203His)	rs375160737	0.00003
NM_004484.4(GPC3):c.485A>G (p.Asn162Ser)	rs780431445	0.00002
NM_004484.4(GPC3):c.1162A>G (p.Arg388Gly)	rs199812705	0.00001
NM_004484.4(GPC3):c.1248G>A (p.Ala416=)	rs201677091	0.00001
NM_004484.4(GPC3):c.1550A>G (p.Lys517Arg)	rs758464784	0.00001
NM_004484.4(GPC3):c.1698C>T (p.Thr566=)	rs201310379	0.00001
NM_004484.4(GPC3):c.543G>A (p.Gln181=)	rs1266410074	0.00001
NM_004484.4(GPC3):c.192A>G (p.Val64=)	rs2076401014
NM_004484.4(GPC3):c.59T>G (p.Phe20Cys)
NM_004484.4(GPC3):c.79CCG[4] (p.Pro31del)

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