List of variants in gene FGFR2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000141.5(FGFR2):c.170C>T (p.Ser57Leu)	rs56226109	0.00322
NM_000141.5(FGFR2):c.2001C>G (p.Val667=)	rs61731218	0.00187
NM_000141.5(FGFR2):c.23T>G (p.Ile8Ser)	rs147307031	0.00107
NM_000141.5(FGFR2):c.34G>A (p.Val12Met)	rs143978938	0.00043
NM_000141.5(FGFR2):c.789G>A (p.Pro263=)	rs138315382	0.00038
NM_000141.5(FGFR2):c.2190C>T (p.Asn730=)	rs55637244	0.00036
NM_000141.5(FGFR2):c.1986+7C>T	rs199697707	0.00032
NM_000141.5(FGFR2):c.1911C>T (p.Asn637=)	rs149008039	0.00026
NM_022970.4(FGFR2):c.1035T>C (p.Tyr345=)	rs187206427	0.00021
NM_000141.5(FGFR2):c.625-10A>G	rs201512833	0.00013
NM_000141.5(FGFR2):c.1361C>T (p.Thr454Met)	rs148672240	0.00011
NM_000141.5(FGFR2):c.201C>T (p.Ala67=)	rs200386134	0.00006
NM_000141.5(FGFR2):c.780C>T (p.Ala260=)	rs778288494	0.00005
NM_022970.4(FGFR2):c.993C>T (p.Thr331=)	rs752595302	0.00005
NM_000141.5(FGFR2):c.*282A>G	rs577983786	0.00004
NM_000141.5(FGFR2):c.-7C>T	rs773626594	0.00004
NM_000141.5(FGFR2):c.1086G>A (p.Ala362=)	rs151250769	0.00003
NM_000141.5(FGFR2):c.1239G>A (p.Pro413=)	rs147674677	0.00003
NM_000141.5(FGFR2):c.1673-8C>T	rs756716480	0.00003
NM_000141.5(FGFR2):c.940-4C>G	rs527592748	0.00002
NM_000141.5(FGFR2):c.1431A>G (p.Pro477=)	rs1436326576	0.00001
NM_000141.5(FGFR2):c.855G>A (p.Gln285=)	rs1161520202	0.00001
NM_000141.5(FGFR2):c.*255C>T	rs1368902748
NM_000141.5(FGFR2):c.1011T>C (p.Ala337=)	rs886038254
NM_000141.5(FGFR2):c.1716C>T (p.Leu572=)	rs1222100043
NM_000141.5(FGFR2):c.1746C>T (p.Pro582=)	rs369850306
NM_000141.5(FGFR2):c.2301+1512dup	rs775759591
NM_000141.5(FGFR2):c.2328C>T (p.Leu776=)	rs148478597
NM_000141.5(FGFR2):c.309C>A (p.Gly103=)	rs749255726
NM_000141.5(FGFR2):c.543C>T (p.Ala181=)	rs150598483
NM_000141.5(FGFR2):c.749-6590C>T	rs2540226763
NM_000141.5(FGFR2):c.831C>T (p.Val277=)	rs886038255
NM_022970.4(FGFR2):c.1008G>C (p.Gly336=)	rs944656551
NM_022970.4(FGFR2):c.942C>T (p.His314=)	rs1051324390

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