ClinVar Miner

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:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.