List of variants in gene PIK3CA reported as likely pathogenic for not provided

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006218.4(PIK3CA):c.1048G>A (p.Asp350Asn)	rs1064793349
NM_006218.4(PIK3CA):c.1090G>A (p.Gly364Arg)	rs1576935161
NM_006218.4(PIK3CA):c.1259_1261dup (p.Cys420_Pro421insArg)	rs1057518041
NM_006218.4(PIK3CA):c.1625A>G (p.Glu542Gly)	rs1057519927
NM_006218.4(PIK3CA):c.2740G>A (p.Gly914Arg)	rs587776932
NM_006218.4(PIK3CA):c.2758A>G (p.Asn920Asp)	rs1064795304
NM_006218.4(PIK3CA):c.2816A>G (p.Asp939Gly)	rs2108424902
NM_006218.4(PIK3CA):c.3073A>G (p.Thr1025Ala)	rs397517202
NM_006218.4(PIK3CA):c.311_322del (p.Pro104_Asn107del)	rs1553820381
NM_006218.4(PIK3CA):c.3140A>G (p.His1047Arg)	rs121913279
NM_006218.4(PIK3CA):c.32_52del (p.Trp11_Pro18delinsSer)	rs2108385065

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