ClinVar Miner

List of variants in gene FGFR2 reported as pathogenic by OMIM

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Total variants: 42
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HGVS dbSNP
FGFR2, ALU INS
NM_022970.3(FGFR2):c.1087+1216_1087+1225delinsACC
NM_022970.3(FGFR2):c.1087+1218G>A rs879253719
NM_022970.3(FGFR2):c.1087+1222G>T rs121918504
NM_022970.3(FGFR2):c.1087+1241A>C rs121918510
NM_022970.3(FGFR2):c.1087+1262A>G rs121918493
NM_022970.3(FGFR2):c.1087+1288G>C rs387906676
NM_022970.3(FGFR2):c.1087+1297T>C rs121918489
NM_022970.3(FGFR2):c.1087+1300A>C rs121918495
NM_022970.3(FGFR2):c.1087+1303T>A rs121918488
NM_022970.3(FGFR2):c.1087+1303T>C rs121918488
NM_022970.3(FGFR2):c.1087+1304G>A rs121918487
NM_022970.3(FGFR2):c.1087+1305C>G rs121918496
NM_022970.3(FGFR2):c.1087+1310C>G rs121918492
NM_022970.3(FGFR2):c.1087+1311G>A rs121918491
NM_022970.3(FGFR2):c.1087+1319C>G rs121918494
NM_022970.3(FGFR2):c.1087+1331C>G rs121918502
NM_022970.3(FGFR2):c.1087+1340C>G rs121918490
NM_022970.3(FGFR2):c.1087+1366A>G rs879253721
NM_022970.3(FGFR2):c.1118C>G (p.Ser373Cys) rs121913477
NM_022970.3(FGFR2):c.1127A>G (p.Tyr376Cys) rs121913478
NM_022970.3(FGFR2):c.1144T>G (p.Tyr382Asp) rs387906678
NM_022970.3(FGFR2):c.1175T>G (p.Met392Arg) rs387906677
NM_022970.3(FGFR2):c.1579A>G (p.Lys527Glu) rs121918507
NM_022970.3(FGFR2):c.1697A>C (p.Glu566Ala) rs121918506
NM_022970.3(FGFR2):c.1885G>A (p.Ala629Thr) rs121918509
NM_022970.3(FGFR2):c.1945G>A (p.Ala649Thr) rs121918508
NM_022970.3(FGFR2):c.1950_1952del (p.Arg650_Asp651delinsSer) rs879253720
NM_022970.3(FGFR2):c.755C>G (p.Ser252Trp) rs79184941
NM_022970.3(FGFR2):c.755_756delinsTT (p.Ser252Phe) rs121918498
NM_022970.3(FGFR2):c.755_757delinsTCT (p.Ser252_Pro253delinsPheSer) rs281865420
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.804_809del (p.Val269_Val270del) rs879253718
NM_022970.3(FGFR2):c.818_820del (p.Asp273del) rs121918503
NM_022970.3(FGFR2):c.859_921del (p.His287_Pro307del) rs1554930637
NM_022970.3(FGFR2):c.866A>C (p.Gln289Pro) rs121918497
NM_022970.3(FGFR2):c.868T>C (p.Trp290Arg) rs121918501
NM_022970.3(FGFR2):c.868T>G (p.Trp290Gly) rs121918501
NM_022970.3(FGFR2):c.870G>C (p.Trp290Cys) rs121918499
NM_022970.3(FGFR2):c.870G>T (p.Trp290Cys) rs121918499
NM_022970.3(FGFR2):c.874A>G (p.Lys292Glu) rs121918500

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