ClinVar Miner

List of variants in gene PIK3CA reported as likely pathogenic by Precision Medicine Oncology, Rutgers Cancer Institute of New Jersey

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_006218.4(PIK3CA):c.3074C>G (p.Thr1025Ser)	rs1553826166

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