ClinVar Miner

List of variants in gene FGFR2 reported by GeneDx

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Total variants: 57
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HGVS dbSNP
NM_022970.3(FGFR2):c.*259C>T rs1047057
NM_022970.3(FGFR2):c.-150-522C>T
NM_022970.3(FGFR2):c.-151+19G>T rs974988741
NM_022970.3(FGFR2):c.-157A>G rs41258305
NM_022970.3(FGFR2):c.-46G>A rs201606812
NM_022970.3(FGFR2):c.1087+1221C>T rs201717227
NM_022970.3(FGFR2):c.1087+1298A>G rs1554928884
NM_022970.3(FGFR2):c.1087+1303T>A rs121918488
NM_022970.3(FGFR2):c.1087+1331C>G rs121918502
NM_022970.3(FGFR2):c.1087+1383T>C rs1554928776
NM_022970.3(FGFR2):c.1089G>A (p.Ala363=) rs151250769
NM_022970.3(FGFR2):c.109+10T>G rs3135722
NM_022970.3(FGFR2):c.110-54C>T
NM_022970.3(FGFR2):c.1127A>G (p.Tyr376Cys) rs121913478
NM_022970.3(FGFR2):c.1145A>G (p.Tyr382Cys) rs1064796452
NM_022970.3(FGFR2):c.1175T>G (p.Met392Arg) rs387906677
NM_022970.3(FGFR2):c.1291-161G>A
NM_022970.3(FGFR2):c.1291-23G>C
NM_022970.3(FGFR2):c.1365G>A (p.Thr455=) rs200183009
NM_022970.3(FGFR2):c.1443-231C>T
NM_022970.3(FGFR2):c.149A>T (p.Tyr50Phe) rs1398842143
NM_022970.3(FGFR2):c.159G>A (p.Ala53=) rs1047102
NM_022970.3(FGFR2):c.1626T>G (p.Ile542Met) rs1057524807
NM_022970.3(FGFR2):c.1676-12C>T rs41293763
NM_022970.3(FGFR2):c.1760_1761delinsGA (p.Tyr587Ter) rs1554914180
NM_022970.3(FGFR2):c.17G>C (p.Arg6Pro) rs3750819
NM_022970.3(FGFR2):c.1867-125dup
NM_022970.3(FGFR2):c.1867-17T>G rs3135802
NM_022970.3(FGFR2):c.1885G>A (p.Ala629Thr) rs121918509
NM_022970.3(FGFR2):c.1928T>A (p.Ile643Lys) rs1064796413
NM_022970.3(FGFR2):c.1944C>T (p.Leu648=) rs35337478
NM_022970.3(FGFR2):c.1989+7C>T rs199697707
NM_022970.3(FGFR2):c.2060+256C>T
NM_022970.3(FGFR2):c.2061-10T>C
NM_022970.3(FGFR2):c.2193C>T (p.Asn731=) rs55637244
NM_022970.3(FGFR2):c.2286C>T (p.Leu762=) rs753103160
NM_022970.3(FGFR2):c.2304+1186A>G
NM_022970.3(FGFR2):c.2304+15C>T rs2278202
NM_022970.3(FGFR2):c.2304+1716A>G
NM_022970.3(FGFR2):c.2304+1829G>A
NM_022970.3(FGFR2):c.2305-1838G>A
NM_022970.3(FGFR2):c.234C>T (p.His78=)
NM_022970.3(FGFR2):c.314A>G (p.Tyr105Cys) rs1434545235
NM_022970.3(FGFR2):c.376G>A (p.Asp126Asn) rs1057523040
NM_022970.3(FGFR2):c.377-10T>C
NM_022970.3(FGFR2):c.420G>A (p.Ala140=) rs765024365
NM_022970.3(FGFR2):c.455-315T>A
NM_022970.3(FGFR2):c.557T>C (p.Met186Thr) rs755793
NM_022970.3(FGFR2):c.608G>A (p.Arg203His) rs747502397
NM_022970.3(FGFR2):c.624+139A>G
NM_022970.3(FGFR2):c.624+140T>C
NM_022970.3(FGFR2):c.696A>G (p.Val232=) rs1047100
NM_022970.3(FGFR2):c.749-183G>A
NM_022970.3(FGFR2):c.755C>G (p.Ser252Trp) rs79184941
NM_022970.3(FGFR2):c.758C>G (p.Pro253Arg) rs77543610
NM_022970.3(FGFR2):c.799T>C (p.Ser267Pro) rs121918505
NM_022970.3(FGFR2):c.833G>T (p.Cys278Phe) rs776587763

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