ClinVar Miner

List of variants in gene FGFR2 studied for not specified

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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_000141.5(FGFR2):c.696A>G (p.Val232=) rs1047100 0.76882
NM_000141.5(FGFR2):c.2301+15C>T rs2278202 0.46576
NM_000141.5(FGFR2):c.*259C>T rs1047057 0.44321
NM_000141.5(FGFR2):c.1864-125dup rs4647914 0.28413
NM_000141.5(FGFR2):c.1864-43del rs111564057 0.17733
NM_000141.5(FGFR2):c.-157A>G rs41258305 0.13622
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.110-54C>T rs3135732 0.01267
NM_000141.5(FGFR2):c.109+10T>G rs3135722 0.00759
NM_000141.5(FGFR2):c.294G>A (p.Thr98=) rs1047101 0.00734
NM_000141.5(FGFR2):c.1288-35A>G rs41295587 0.00467
NM_000141.5(FGFR2):c.159G>A (p.Ala53=) rs1047102 0.00414
NM_000141.5(FGFR2):c.170C>T (p.Ser57Leu) rs56226109 0.00322
NM_000141.5(FGFR2):c.1572A>G (p.Thr524=) rs74160613 0.00281
NM_000141.5(FGFR2):c.17G>C (p.Arg6Pro) rs3750819 0.00267
NM_000141.5(FGFR2):c.1539C>T (p.Thr513=) rs74160617 0.00228
NM_000141.5(FGFR2):c.939+11T>C rs145303463 0.00134
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.1788G>A (p.Glu596=) rs56335660 0.00036
NM_000141.5(FGFR2):c.1986+7C>T rs199697707 0.00032
NM_000141.5(FGFR2):c.2301+1526A>G rs189179463 0.00026
NM_000141.5(FGFR2):c.625-10A>G rs201512833 0.00013
NM_000141.5(FGFR2):c.748+18C>T rs377269009 0.00012
NM_000141.5(FGFR2):c.942C>T (p.Ala314=) rs201717227 0.00008
NM_000141.5(FGFR2):c.1441C>T (p.Leu481=) rs144116729 0.00005
NM_000141.5(FGFR2):c.202G>A (p.Ala68Thr) rs374996878 0.00003
NM_000141.5(FGFR2):c.2195+7G>A rs377397478 0.00003
NM_000141.5(FGFR2):c.*1A>G rs547079762 0.00001
NM_000141.5(FGFR2):c.1085-19C>T rs551301348 0.00001
NM_000141.5(FGFR2):c.181C>T (p.Arg61Cys) rs1354205157 0.00001
NM_000141.5(FGFR2):c.569G>A (p.Arg190Gln) rs759750319 0.00001
NM_000141.5(FGFR2):c.755C>T (p.Ser252Leu) rs79184941 0.00001
GRCh37/hg19 10q26.13(chr10:123346115-123425406)
NC_000010.10:g.(?_123237845)_(123357959_?)dup
NM_000141.5(FGFR2):c.-151+19G>T rs974988741
NM_000141.5(FGFR2):c.1011T>C (p.Ala337=) rs886038254
NM_000141.5(FGFR2):c.1084+20T>C rs1554928776
NM_000141.5(FGFR2):c.1084+8C>T rs1589827584
NM_000141.5(FGFR2):c.1448T>A (p.Leu483Gln)
NM_000141.5(FGFR2):c.1847A>G (p.Tyr616Cys) rs762545440
NM_000141.5(FGFR2):c.2329G>A (p.Glu777Lys) rs374993905
NM_000141.5(FGFR2):c.309C>A (p.Gly103=) rs749255726
NM_000141.5(FGFR2):c.455G>T (p.Arg152Ile) rs2134843752
NM_000141.5(FGFR2):c.560C>G (p.Pro187Arg) rs1564972481
NM_000141.5(FGFR2):c.831C>T (p.Val277=) rs886038255

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