ClinVar Miner

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

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_000141.5(FGFR2):c.2301+15C>T rs2278202 0.45747
NM_000141.5(FGFR2):c.557T>C (p.Met186Thr) rs755793 0.10553
NM_000141.5(FGFR2):c.1941C>T (p.Leu647=) rs35337478 0.02240
NM_000141.5(FGFR2):c.1864-17T>G rs3135802 0.02120
NM_000141.5(FGFR2):c.109+10T>G rs3135722 0.00799
NM_000141.5(FGFR2):c.294G>A (p.Thr98=) rs1047101 0.00776
NM_000141.5(FGFR2):c.170C>T (p.Ser57Leu) rs56226109 0.00271
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.2190C>T (p.Asn730=) rs55637244 0.00040
NM_000141.5(FGFR2):c.789G>A (p.Pro263=) rs138315382 0.00038
NM_000141.5(FGFR2):c.1986+7C>T rs199697707 0.00032
NM_000141.5(FGFR2):c.1911C>T (p.Asn637=) rs149008039 0.00026
NM_000141.5(FGFR2):c.1361C>T (p.Thr454Met) rs148672240 0.00012
NM_000141.5(FGFR2):c.625-10A>G rs201512833 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_000141.5(FGFR2):c.1086G>A (p.Ala362=) rs151250769 0.00003
NM_000141.5(FGFR2):c.1239G>A (p.Pro413=) rs147674677 0.00001
NM_000141.5(FGFR2):c.755C>T (p.Ser252Leu) rs79184941 0.00001
NM_000141.5(FGFR2):c.*255C>T
NM_000141.5(FGFR2):c.*256G>A rs763095219
NM_000141.5(FGFR2):c.*282A>G
NM_000141.5(FGFR2):c.-7C>T
NM_000141.5(FGFR2):c.1011T>C (p.Ala337=) rs886038254
NM_000141.5(FGFR2):c.1070T>C (p.Leu357Ser) rs2134254345
NM_000141.5(FGFR2):c.1084+1G>A
NM_000141.5(FGFR2):c.1124A>G (p.Tyr375Cys) rs121913478
NM_000141.5(FGFR2):c.1141T>G (p.Tyr381Asp) rs387906678
NM_000141.5(FGFR2):c.1431A>G (p.Pro477=)
NM_000141.5(FGFR2):c.1673-8C>T
NM_000141.5(FGFR2):c.1694A>C (p.Glu565Ala) rs121918506
NM_000141.5(FGFR2):c.1716C>T (p.Leu572=)
NM_000141.5(FGFR2):c.1746C>T (p.Pro582=) rs369850306
NM_000141.5(FGFR2):c.1949A>G (p.Asp650Gly)
NM_000141.5(FGFR2):c.1977G>C (p.Lys659Asn) rs1589722765
NM_000141.5(FGFR2):c.2301+1512dup
NM_000141.5(FGFR2):c.2328C>T (p.Leu776=) rs148478597
NM_000141.5(FGFR2):c.2415C>A (p.Tyr805Ter)
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.696A>G (p.Val232=) rs1047100
NM_000141.5(FGFR2):c.749-6576T>G
NM_000141.5(FGFR2):c.749-6590C>T
NM_000141.5(FGFR2):c.755C>G (p.Ser252Trp) rs79184941
NM_000141.5(FGFR2):c.758C>G (p.Pro253Arg) rs77543610
NM_000141.5(FGFR2):c.820G>A (p.Val274Ile)
NM_000141.5(FGFR2):c.831C>T (p.Val277=) rs886038255
NM_000141.5(FGFR2):c.842A>G (p.Tyr281Cys) rs1057519038
NM_000141.5(FGFR2):c.855G>A (p.Gln285=)
NM_000141.5(FGFR2):c.857_877del (p.Pro286_Lys292del)
NM_000141.5(FGFR2):c.870G>C (p.Trp290Cys) rs121918499
NM_000141.5(FGFR2):c.940-4C>G
NM_022970.4(FGFR2):c.1008G>C (p.Gly336=)
NM_022970.4(FGFR2):c.1035T>C (p.Tyr345=)
NM_022970.4(FGFR2):c.1067C>G (p.Thr356Ser)
NM_022970.4(FGFR2):c.942C>T (p.His314=)
NM_022970.4(FGFR2):c.993C>T (p.Thr331=)

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