ClinVar Miner

List of variants in gene FGFR2 studied for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 91
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 10q26.13(chr10:123343892-123348355)x1
NM_000141.5(FGFR2):c.1084+8C>T
NM_000141.5(FGFR2):c.1545C>T (p.Ala515=)
NM_000141.5(FGFR2):c.1561+7G>A
NM_000141.5(FGFR2):c.159G>T (p.Ala53=)
NM_000141.5(FGFR2):c.1761C>T (p.Ser587=)
NM_000141.5(FGFR2):c.1911C>T (p.Asn637=)
NM_000141.5(FGFR2):c.1987-5T>G
NM_000141.5(FGFR2):c.2232C>T (p.Pro744=)
NM_000141.5(FGFR2):c.2247G>A (p.Thr749=)
NM_000141.5(FGFR2):c.252G>A (p.Arg84=)
NM_000141.5(FGFR2):c.377-6A>T
NM_000141.5(FGFR2):c.390C>G (p.Ser130=)
NM_000141.5(FGFR2):c.418G>A (p.Ala140Thr)
NM_000141.5(FGFR2):c.64C>T (p.Arg22Trp)
NM_000141.5(FGFR2):c.714G>A (p.Gly238=)
NM_000141.5(FGFR2):c.780C>T (p.Ala260=)
NM_000141.5(FGFR2):c.789G>A (p.Pro263=)
NM_022970.3(FGFR2):c.*259C>T rs1047057
NM_022970.3(FGFR2):c.-150-522C>T
NM_022970.3(FGFR2):c.-46G>A rs201606812
NM_022970.3(FGFR2):c.1087+1298A>G rs1554928884
NM_022970.3(FGFR2):c.1087+1303T>A rs121918488
NM_022970.3(FGFR2):c.1087+1319C>G rs121918494
NM_022970.3(FGFR2):c.1087+1331C>G rs121918502
NM_022970.3(FGFR2):c.1089G>C (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.1144T>G (p.Tyr382Asp) rs387906678
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.1208A>G (p.Asn403Ser) rs764748528
NM_022970.3(FGFR2):c.1242G>A (p.Pro414=) rs147674677
NM_022970.3(FGFR2):c.1291-161G>A
NM_022970.3(FGFR2):c.1291-23G>C
NM_022970.3(FGFR2):c.1443-231C>T
NM_022970.3(FGFR2):c.149A>T (p.Tyr50Phe) rs1398842143
NM_022970.3(FGFR2):c.1542C>T (p.Thr514=) rs74160617
NM_022970.3(FGFR2):c.1551G>A (p.Val517=) rs200522893
NM_022970.3(FGFR2):c.1575A>G (p.Thr525=) rs74160613
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.170C>T (p.Ser57Leu) rs56226109
NM_022970.3(FGFR2):c.1720C>T (p.Arg574Ter) rs1564875577
NM_022970.3(FGFR2):c.1738C>T (p.Arg580Trp) rs1564875549
NM_022970.3(FGFR2):c.1760_1761delinsGA (p.Tyr587Ter) rs1554914180
NM_022970.3(FGFR2):c.1791G>A (p.Glu597=) rs56335660
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.1867-125dup
NM_022970.3(FGFR2):c.1885G>A (p.Ala629Thr) rs121918509
NM_022970.3(FGFR2):c.1925A>G (p.Lys642Arg) rs1057519047
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.2004C>G (p.Val668=) rs61731218
NM_022970.3(FGFR2):c.2043C>T (p.Tyr681=) rs751495618
NM_022970.3(FGFR2):c.2060+256C>T
NM_022970.3(FGFR2):c.2061-10T>C
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.2304+1186A>G
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.23T>G (p.Ile8Ser) rs147307031
NM_022970.3(FGFR2):c.2418C>T (p.Tyr806=) rs558460047
NM_022970.3(FGFR2):c.289G>A (p.Ala97Thr) rs372430349
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.34G>A (p.Val12Met) rs143978938
NM_022970.3(FGFR2):c.376G>A (p.Asp126Asn) rs1057523040
NM_022970.3(FGFR2):c.377-10T>C
NM_022970.3(FGFR2):c.455-315T>A
NM_022970.3(FGFR2):c.557T>C (p.Met186Thr) rs755793
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.624+139A>G
NM_022970.3(FGFR2):c.624+140T>C
NM_022970.3(FGFR2):c.625-10A>G rs201512833
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.759T>G (p.Pro253=) rs3135755
NM_022970.3(FGFR2):c.799T>C (p.Ser267Pro) rs121918505
NM_022970.3(FGFR2):c.833G>T (p.Cys278Phe) rs776587763
NM_022970.3(FGFR2):c.879C>T (p.His293=) rs55745510

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.