ClinVar Miner

List of variants in gene FGFR2 reported by Ambry Genetics

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000141.5(FGFR2):c.263T>C (p.Ile88Thr) rs200369248 0.00022
NM_000141.5(FGFR2):c.16C>T (p.Arg6Cys) rs141724446 0.00005
NM_000141.5(FGFR2):c.469A>G (p.Thr157Ala) rs770169545 0.00005
NM_000141.5(FGFR2):c.1061C>G (p.Ser354Cys) rs121918490
NM_000141.5(FGFR2):c.1085C>A (p.Ala362Glu)
NM_000141.5(FGFR2):c.1117C>T (p.Pro373Ser)
NM_000141.5(FGFR2):c.1141T>G (p.Tyr381Asp) rs387906678
NM_000141.5(FGFR2):c.1313T>C (p.Met438Thr)
NM_000141.5(FGFR2):c.1351C>G (p.Leu451Val)
NM_000141.5(FGFR2):c.1394A>G (p.Glu465Gly)
NM_000141.5(FGFR2):c.1537A>G (p.Thr513Ala)
NM_000141.5(FGFR2):c.160C>T (p.Pro54Ser)
NM_000141.5(FGFR2):c.1852G>A (p.Ala618Thr)
NM_000141.5(FGFR2):c.1991G>A (p.Arg664Gln) rs1554907364
NM_000141.5(FGFR2):c.2108C>T (p.Pro703Leu)
NM_000141.5(FGFR2):c.2205G>C (p.Met735Ile)
NM_000141.5(FGFR2):c.2290A>G (p.Thr764Ala)
NM_000141.5(FGFR2):c.2389G>T (p.Val797Phe)
NM_000141.5(FGFR2):c.454+3A>G
NM_000141.5(FGFR2):c.532C>T (p.Arg178Cys)
NM_000141.5(FGFR2):c.554C>T (p.Pro185Leu)
NM_000141.5(FGFR2):c.562A>G (p.Thr188Ala)
NM_000141.5(FGFR2):c.758C>T (p.Pro253Leu) rs77543610
NM_000141.5(FGFR2):c.803C>T (p.Thr268Ile)
NM_000141.5(FGFR2):c.940-165_978del rs1554928978

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