List of variants in gene PIK3CA reported as likely pathogenic for embryonal neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_006218.4(PIK3CA):c.1636C>A (p.Gln546Lys)	rs121913286
NM_006218.4(PIK3CA):c.1636C>G (p.Gln546Glu)	rs121913286
NM_006218.4(PIK3CA):c.1637A>C (p.Gln546Pro)	rs397517201
NM_006218.4(PIK3CA):c.1637A>G (p.Gln546Arg)	rs397517201
NM_006218.4(PIK3CA):c.1637A>T (p.Gln546Leu)	rs397517201
NM_006218.4(PIK3CA):c.1638G>T (p.Gln546His)	rs1057519940
NM_006218.4(PIK3CA):c.241G>A (p.Glu81Lys)	rs1057519929
NM_006218.4(PIK3CA):c.3139C>T (p.His1047Tyr)	rs121913281
NM_006218.4(PIK3CA):c.3140A>G (p.His1047Arg)	rs121913279
NM_006218.4(PIK3CA):c.3140A>T (p.His1047Leu)	rs121913279
NM_006218.4(PIK3CA):c.3141T>G (p.His1047Gln)	rs1057519932
NM_006218.4(PIK3CA):c.331A>G (p.Lys111Glu)	rs1057519933
NM_006218.4(PIK3CA):c.332A>G (p.Lys111Arg)	rs1057519935
NM_006218.4(PIK3CA):c.333G>C (p.Lys111Asn)	rs1057519934

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