ClinVar Miner

List of variants in gene FGFR2 reported as uncertain significance by GeneDx

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_000141.5(FGFR2):c.2230C>T (p.Pro744Ser) rs747941020 0.00004
NM_000141.5(FGFR2):c.494G>A (p.Arg165Gln) rs146244307 0.00004
NM_000141.5(FGFR2):c.1382C>T (p.Ala461Val) rs376451171 0.00003
NM_000141.5(FGFR2):c.362T>C (p.Met121Thr) rs748322657 0.00003
NM_000141.5(FGFR2):c.1348C>T (p.Arg450Cys) rs536181987 0.00002
NM_000141.5(FGFR2):c.1267C>T (p.Pro423Ser) rs1207716999 0.00001
NM_000141.5(FGFR2):c.1448T>C (p.Leu483Pro) rs767430380 0.00001
NM_000141.5(FGFR2):c.1637A>C (p.Asn546Thr) rs765658636 0.00001
NM_000141.5(FGFR2):c.2077A>G (p.Met693Val) rs774682374 0.00001
NM_000141.5(FGFR2):c.2189A>G (p.Asn730Ser) rs200453002 0.00001
NM_000141.5(FGFR2):c.256G>A (p.Val86Met) rs1396687223 0.00001
NM_000141.5(FGFR2):c.376G>A (p.Asp126Asn) rs1057523040 0.00001
NM_000141.5(FGFR2):c.608G>A (p.Arg203His) rs747502397 0.00001
NM_000141.5(FGFR2):c.67C>A (p.Pro23Thr) rs1309596973 0.00001
NM_000141.5(FGFR2):c.755C>T (p.Ser252Leu) rs79184941 0.00001
NM_000141.5(FGFR2):c.*197del rs748777325
NM_000141.5(FGFR2):c.1001T>A (p.Phe334Tyr)
NM_000141.5(FGFR2):c.109G>C (p.Glu37Gln)
NM_000141.5(FGFR2):c.1173G>A (p.Met391Ile)
NM_000141.5(FGFR2):c.1207A>G (p.Thr403Ala)
NM_000141.5(FGFR2):c.1225T>G (p.Phe409Val)
NM_000141.5(FGFR2):c.1342A>G (p.Thr448Ala)
NM_000141.5(FGFR2):c.149A>T (p.Tyr50Phe) rs1398842143
NM_000141.5(FGFR2):c.1562-9_1562-7delinsAA rs2133978031
NM_000141.5(FGFR2):c.1623T>G (p.Ile541Met) rs1057524807
NM_000141.5(FGFR2):c.1690G>A (p.Val564Ile) rs1057519797
NM_000141.5(FGFR2):c.1699G>A (p.Ala567Thr)
NM_000141.5(FGFR2):c.1718G>A (p.Arg573Gln) rs2133942636
NM_000141.5(FGFR2):c.1721_1732del (p.Glu574_Arg577del) rs2133941864
NM_000141.5(FGFR2):c.1723T>C (p.Tyr575His) rs2133942461
NM_000141.5(FGFR2):c.17G>A (p.Arg6His) rs3750819
NM_000141.5(FGFR2):c.1808T>A (p.Leu603Ter)
NM_000141.5(FGFR2):c.1891A>G (p.Asn631Asp) rs2133838683
NM_000141.5(FGFR2):c.1A>G (p.Met1Val) rs774885289
NM_000141.5(FGFR2):c.2200A>T (p.Met734Leu)
NM_000141.5(FGFR2):c.2210G>C (p.Arg737Thr)
NM_000141.5(FGFR2):c.2368T>C (p.Cys790Arg) rs2133682792
NM_000141.5(FGFR2):c.2410C>T (p.Pro804Ser) rs575812178
NM_000141.5(FGFR2):c.2416G>A (p.Glu806Lys) rs764959117
NM_000141.5(FGFR2):c.287G>A (p.Gly96Asp) rs1277734487
NM_000141.5(FGFR2):c.318T>A (p.Ala106=)
NM_000141.5(FGFR2):c.326C>A (p.Ala109Asp)
NM_000141.5(FGFR2):c.394G>C (p.Asp132His)
NM_000141.5(FGFR2):c.454+3A>G
NM_000141.5(FGFR2):c.544G>A (p.Gly182Arg)
NM_000141.5(FGFR2):c.544G>T (p.Gly182Trp)
NM_000141.5(FGFR2):c.56C>T (p.Ser19Phe)
NM_000141.5(FGFR2):c.589G>C (p.Glu197Gln)
NM_000141.5(FGFR2):c.671C>G (p.Ser224Cys) rs2134606046
NM_000141.5(FGFR2):c.67C>G (p.Pro23Ala)
NM_000141.5(FGFR2):c.715T>A (p.Ser239Thr)
NM_000141.5(FGFR2):c.781G>A (p.Gly261Arg) rs2134317947
NM_000141.5(FGFR2):c.796G>C (p.Ala266Pro) rs1375799439
NM_000141.5(FGFR2):c.914G>T (p.Gly305Val) rs2134308697
NM_000141.5(FGFR2):c.940G>T (p.Ala314Ser) rs1358919643
NM_000141.5(FGFR2):c.959C>T (p.Thr320Met) rs2134259953
NM_022970.4(FGFR2):c.984C>A (p.Phe328Leu)

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