ClinVar Miner

List of variants in gene FGFR2 reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
NM_022970.3(FGFR2):c.1087+1319C>G rs121918494
NM_022970.3(FGFR2):c.1089G>C (p.Ala363=) rs151250769
NM_022970.3(FGFR2):c.1144T>G (p.Tyr382Asp) rs387906678
NM_022970.3(FGFR2):c.1208A>G (p.Asn403Ser) rs764748528
NM_022970.3(FGFR2):c.1542C>T (p.Thr514=) rs74160617
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.170C>T (p.Ser57Leu) rs56226109
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.1925A>G (p.Lys642Arg) rs1057519047
NM_022970.3(FGFR2):c.2043C>T (p.Tyr681=) rs751495618
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.23T>G (p.Ile8Ser) rs147307031
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.557T>C (p.Met186Thr) rs755793
NM_022970.3(FGFR2):c.568C>T (p.Arg190Trp) rs147987917
NM_022970.3(FGFR2):c.759T>G (p.Pro253=) rs3135755

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.