List of variants in gene PIK3CA 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006218.4(PIK3CA):c.*29T>C	rs141178472	0.00333
NM_006218.4(PIK3CA):c.1104T>C (p.Cys368=)	rs202162121	0.00029
NM_006218.4(PIK3CA):c.1056T>C (p.Asp352=)	rs1131681	0.00022
NM_006218.4(PIK3CA):c.318C>A (p.Gly106=)	rs201193059	0.00016
NM_006218.4(PIK3CA):c.225A>G (p.Gln75=)	rs202176973	0.00009
NM_006218.4(PIK3CA):c.2445A>G (p.Gln815=)	rs1400861611	0.00002
NM_006218.4(PIK3CA):c.2592C>T (p.Gly864=)	rs780492649	0.00002
NM_006218.4(PIK3CA):c.1029C>T (p.Tyr343=)	rs375577477	0.00001
NM_006218.4(PIK3CA):c.1060-9T>C	rs750875731	0.00001
NM_006218.4(PIK3CA):c.1512A>T (p.Ala504=)	rs201108344	0.00001
NM_006218.4(PIK3CA):c.*27A>G
NM_006218.4(PIK3CA):c.2439A>G (p.Thr813=)	rs201600506
NM_006218.4(PIK3CA):c.747G>A (p.Lys249=)

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