ClinVar Miner

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

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Total variants: 21
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HGVS dbSNP
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

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