ClinVar Miner

List of variants in gene FGFR2 reported by Invitae

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Gene type:
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Total variants: 52
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HGVS dbSNP
NC_000010.10:g.(?_123353203)_(123353351_?)del
NM_022970.3(FGFR2):c.1087+1217A>G rs1057519041
NM_022970.3(FGFR2):c.1087+1218G>A rs879253719
NM_022970.3(FGFR2):c.1087+1219G>T rs1358919643
NM_022970.3(FGFR2):c.1087+1249A>G rs1443966407
NM_022970.3(FGFR2):c.1087+1262A>G rs121918493
NM_022970.3(FGFR2):c.1087+1268G>A
NM_022970.3(FGFR2):c.1087+1291G>A
NM_022970.3(FGFR2):c.1087+1291G>T rs1057519043
NM_022970.3(FGFR2):c.1087+1291_1087+1292delinsAA rs1554928905
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+1304G>C rs121918487
NM_022970.3(FGFR2):c.1087+1304G>T rs121918487
NM_022970.3(FGFR2):c.1087+1305C>G rs121918496
NM_022970.3(FGFR2):c.1087+1311G>A rs121918491
NM_022970.3(FGFR2):c.1087+1313G>A rs1554928838
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+1363_1087+1364insTCAACA rs1554928786
NM_022970.3(FGFR2):c.109+10T>G rs3135722
NM_022970.3(FGFR2):c.1127A>G (p.Tyr376Cys) rs121913478
NM_022970.3(FGFR2):c.1153G>A (p.Gly385Arg) rs1554927408
NM_022970.3(FGFR2):c.1155G>A (p.Gly385=) rs772014466
NM_022970.3(FGFR2):c.159G>A (p.Ala53=) rs1047102
NM_022970.3(FGFR2):c.170C>T (p.Ser57Leu) rs56226109
NM_022970.3(FGFR2):c.1756G>C (p.Glu586Gln) rs1564875398
NM_022970.3(FGFR2):c.17G>C (p.Arg6Pro) rs3750819
NM_022970.3(FGFR2):c.1821C>T (p.Cys607=) rs371395564
NM_022970.3(FGFR2):c.1944C>T (p.Leu648=) rs35337478
NM_022970.3(FGFR2):c.1980G>C (p.Lys660Asn)
NM_022970.3(FGFR2):c.2004C>G (p.Val668=) rs61731218
NM_022970.3(FGFR2):c.2155G>A (p.Glu719Lys)
NM_022970.3(FGFR2):c.23T>G (p.Ile8Ser) rs147307031
NM_022970.3(FGFR2):c.294G>A (p.Thr98=) rs1047101
NM_022970.3(FGFR2):c.314A>G (p.Tyr105Cys) rs1434545235
NM_022970.3(FGFR2):c.557T>C (p.Met186Thr) rs755793
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.812G>T (p.Gly271Val) rs1564919048
NM_022970.3(FGFR2):c.823G>C (p.Glu275Gln) rs1258584689
NM_022970.3(FGFR2):c.826T>G (p.Phe276Val) rs1057519036
NM_022970.3(FGFR2):c.833G>T (p.Cys278Phe) rs776587763
NM_022970.3(FGFR2):c.833_834delinsTT (p.Cys278Phe) rs1057519037
NM_022970.3(FGFR2):c.834C>G (p.Cys278Trp) rs1554930790
NM_022970.3(FGFR2):c.868T>C (p.Trp290Arg) rs121918501
NM_022970.3(FGFR2):c.870G>T (p.Trp290Cys) rs121918499
NM_022970.3(FGFR2):c.902A>G (p.Tyr301Cys) rs1554930684
NM_022970.3(FGFR2):c.910G>A (p.Asp304Asn)

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