List of variants in gene PIK3CA reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006218.4(PIK3CA):c.178C>A (p.Gln60Lys)	rs71310379	0.00004
NM_006218.4(PIK3CA):c.341A>G (p.Asn114Ser)	rs746860750	0.00002
NM_006218.4(PIK3CA):c.436G>A (p.Val146Ile)	rs755969956	0.00001
NM_006218.4(PIK3CA):c.1244C>T (p.Ala415Val)	rs1576938120
NM_006218.4(PIK3CA):c.148T>C (p.Phe50Leu)	rs1064797300
NM_006218.4(PIK3CA):c.1795A>G (p.Met599Val)
NM_006218.4(PIK3CA):c.2382T>A (p.Phe794Leu)	rs2108418129
NM_006218.4(PIK3CA):c.3091A>G (p.Thr1031Ala)
NM_006218.4(PIK3CA):c.3172A>C (p.Ile1058Leu)	rs1576950003
NM_006218.4(PIK3CA):c.325GAA[1] (p.Glu110del)	rs1724343994
NM_006218.4(PIK3CA):c.519T>C (p.Ser173=)	rs1576932506

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