List of variants in gene PIK3CA reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_006218.4(PIK3CA):c.3075C>T (p.Thr1025=)	rs17849079	0.01239
NM_006218.4(PIK3CA):c.323G>A (p.Arg108His)	rs886042002	0.00001
NM_006218.4(PIK3CA):c.1252G>A (p.Glu418Lys)	rs397517199
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg)	rs121913272
NM_006218.4(PIK3CA):c.1359_1373del (p.Glu453_Pro458delinsAsp)	rs397517200
NM_006218.4(PIK3CA):c.1624G>A (p.Glu542Lys)	rs121913273
NM_006218.4(PIK3CA):c.1633G>A (p.Glu545Lys)	rs104886003
NM_006218.4(PIK3CA):c.1634A>C (p.Glu545Ala)	rs121913274
NM_006218.4(PIK3CA):c.1637A>G (p.Gln546Arg)	rs397517201
NM_006218.4(PIK3CA):c.3073A>G (p.Thr1025Ala)	rs397517202
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile)	rs121913283
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr)	rs121913281
NM_006218.4(PIK3CA):c.3140A>G (p.His1047Arg)	rs121913279

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