ClinVar Miner

List of variants in gene FGFR2 reported as uncertain significance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
Download table as spreadsheet
HGVS dbSNP
NC_000010.10:g.(?_123353203)_(123353351_?)del
NM_000141.5(FGFR2):c.418G>A (p.Ala140Thr)
NM_022970.3(FGFR2):c.*1070T>C rs886046761
NM_022970.3(FGFR2):c.*1126T>C rs370106008
NM_022970.3(FGFR2):c.*1287A>C rs886046760
NM_022970.3(FGFR2):c.*1369C>T rs886046759
NM_022970.3(FGFR2):c.*1402T>C rs886046758
NM_022970.3(FGFR2):c.*1489C>T rs886046757
NM_022970.3(FGFR2):c.*497T>C rs3135827
NM_022970.3(FGFR2):c.*674G>T rs566155088
NM_022970.3(FGFR2):c.*736dup rs886046762
NM_022970.3(FGFR2):c.-128G>A rs547739869
NM_022970.3(FGFR2):c.-129C>T rs886046765
NM_022970.3(FGFR2):c.-165G>A rs886046766
NM_022970.3(FGFR2):c.-371C>T rs527570655
NM_022970.3(FGFR2):c.-535G>C rs886046767
NM_022970.3(FGFR2):c.-622G>A rs886046768
NM_022970.3(FGFR2):c.1087+1268G>A rs199757302
NM_022970.3(FGFR2):c.1087+1288G>A rs387906676
NM_022970.3(FGFR2):c.1087+1291_1087+1292delinsAA rs1554928905
NM_022970.3(FGFR2):c.1087+1313G>A rs1554928838
NM_022970.3(FGFR2):c.1087+1363_1087+1364insTCAACA rs1554928786
NM_022970.3(FGFR2):c.1089G>C (p.Ala363=) rs151250769
NM_022970.3(FGFR2):c.110-22TC[3] rs773932794
NM_022970.3(FGFR2):c.1147T>C (p.Cys383Arg) rs121913474
NM_022970.3(FGFR2):c.1182A>T (p.Val394=) rs886046763
NM_022970.3(FGFR2):c.1208A>G (p.Asn403Ser) rs764748528
NM_022970.3(FGFR2):c.138A>C (p.Gln46His) rs748117555
NM_022970.3(FGFR2):c.149A>T (p.Tyr50Phe) rs1398842143
NM_022970.3(FGFR2):c.1542C>A (p.Thr514=) rs74160617
NM_022970.3(FGFR2):c.1565-11A>G rs41293744
NM_022970.3(FGFR2):c.1626T>G (p.Ile542Met) rs1057524807
NM_022970.3(FGFR2):c.1738C>T (p.Arg580Trp) rs1564875549
NM_022970.3(FGFR2):c.1756G>C (p.Glu586Gln) rs1564875398
NM_022970.3(FGFR2):c.1994G>A (p.Arg665Gln) rs1554907364
NM_022970.3(FGFR2):c.2043C>T (p.Tyr681=) rs751495618
NM_022970.3(FGFR2):c.204C>T (p.Ala68=) rs747982371
NM_022970.3(FGFR2):c.2073G>T (p.Gly691=) rs1281525856
NM_022970.3(FGFR2):c.2109G>A (p.Ser703=) rs794727163
NM_022970.3(FGFR2):c.2127C>T (p.Pro709=) rs140813163
NM_022970.3(FGFR2):c.2155G>A (p.Glu719Lys)
NM_022970.3(FGFR2):c.2419G>A (p.Glu807Lys) rs764959117
NM_022970.3(FGFR2):c.289G>A (p.Ala97Thr) rs372430349
NM_022970.3(FGFR2):c.351T>C (p.Thr117=) rs886046764
NM_022970.3(FGFR2):c.376G>A (p.Asp126Asn) rs1057523040
NM_022970.3(FGFR2):c.560C>T (p.Pro187Leu) rs1564972481
NM_022970.3(FGFR2):c.568C>T (p.Arg190Trp) rs147987917
NM_022970.3(FGFR2):c.608G>A (p.Arg203His) rs747502397
NM_022970.3(FGFR2):c.759T>G (p.Pro253=) rs3135755
NM_022970.3(FGFR2):c.823G>C (p.Glu275Gln) rs1258584689
NM_022970.3(FGFR2):c.834C>G (p.Cys278Trp) rs1554930790
NM_022970.3(FGFR2):c.902A>G (p.Tyr301Cys) rs1554930684
NM_022970.3(FGFR2):c.910G>A (p.Asp304Asn) rs370877537

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.