List of variants studied for benign neoplasm by GeneReviews

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004985.5(KRAS):c.35G>A (p.Gly12Asp)	rs121913529	0.00001
NM_004985.5(KRAS):c.38G>A (p.Gly13Asp)	rs112445441	0.00001
NM_004985.5(KRAS):c.437C>T (p.Ala146Val)	rs1057519725	0.00001
NM_004985.5(KRAS):c.57G>C (p.Leu19Phe)	rs121913538	0.00001
NM_004985.5(KRAS):c.436G>A (p.Ala146Thr)	rs121913527
NM_006218.4(PIK3CA):c.1258T>C (p.Cys420Arg)	rs121913272
NM_006218.4(PIK3CA):c.1624G>A (p.Glu542Lys)	rs121913273
NM_006218.4(PIK3CA):c.3140A>G (p.His1047Arg)	rs121913279
NM_006218.4(PIK3CA):c.3140A>T (p.His1047Leu)	rs121913279
NM_015922.3(NSDHL):c.1046A>G (p.Tyr349Cys)	rs137853863
NM_015922.3(NSDHL):c.262C>T (p.Arg88Ter)	rs104894903
NM_015922.3(NSDHL):c.314C>T (p.Ala105Val)	rs104894909
NM_015922.3(NSDHL):c.613G>A (p.Gly205Ser)	rs104894901
NM_023110.3(FGFR1):c.1638C>A (p.Asn546Lys)	rs779707422
NM_023110.3(FGFR1):c.1966A>G (p.Lys656Glu)	rs869320694

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