List of variants in gene PIK3CA reported as likely pathogenic by Clinical Genomics Laboratory, Washington University in St. Louis

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006218.4(PIK3CA):c.1340_1366del (p.Pro447_Leu455del)
NM_006218.4(PIK3CA):c.1636C>A (p.Gln546Lys)	rs121913286
NM_006218.4(PIK3CA):c.3073A>G (p.Thr1025Ala)	rs397517202
NM_006218.4(PIK3CA):c.311C>T (p.Pro104Leu)	rs863225060
NM_006218.4(PIK3CA):c.3203dup (p.Asn1068fs)	rs587776802
NM_006218.4(PIK3CA):c.344G>C (p.Arg115Pro)	rs200018596
NM_006218.4(PIK3CA):c.344G>T (p.Arg115Leu)

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