ClinVar Miner

List of variants in gene FGFR1 reported by OMIM

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_023110.3(FGFR1):c.899T>C (p.Ile300Thr) rs121909633 0.00042
NM_023110.3(FGFR1):c.1409G>T (p.Arg470Leu) rs121909637 0.00010
NM_023110.2(FGFR1):c.[2165C>A;2172C>G]
NM_023110.3(FGFR1):c.1025T>C (p.Leu342Ser) rs121909638
NM_023110.3(FGFR1):c.1042G>A (p.Gly348Arg) rs886037634
NM_023110.3(FGFR1):c.1097C>T (p.Pro366Leu) rs121909641
NM_023110.3(FGFR1):c.1121A>G (p.Tyr374Cys) rs121909631
NM_023110.3(FGFR1):c.1141T>C (p.Cys381Arg) rs121909634
NM_023110.3(FGFR1):c.1317_1318del (p.Val441fs) rs587776835
NM_023110.3(FGFR1):c.142G>A (p.Gly48Ser) rs121909640
NM_023110.3(FGFR1):c.1447C>A (p.Pro483Thr) rs397515444
NM_023110.3(FGFR1):c.1638C>A (p.Asn546Lys) rs779707422
NM_023110.3(FGFR1):c.1819G>A (p.Val607Met) rs121909629
NM_023110.3(FGFR1):c.1825C>T (p.Arg609Ter) rs121909639
NM_023110.3(FGFR1):c.1864C>T (p.Arg622Ter) rs121909628
NM_023110.3(FGFR1):c.1867G>T (p.Asp623Tyr) rs398122946
NM_023110.3(FGFR1):c.1966A>G (p.Lys656Glu) rs869320694
NM_023110.3(FGFR1):c.1970_1971del (p.Thr657fs) rs1586111679
NM_023110.3(FGFR1):c.1996T>A (p.Trp666Arg) rs1563433902
NM_023110.3(FGFR1):c.2008G>A (p.Glu670Lys) rs397515446
NM_023110.3(FGFR1):c.2038C>T (p.Gln680Ter) rs121909636
NM_023110.3(FGFR1):c.2075A>G (p.Glu692Gly) rs397515445
NM_023110.3(FGFR1):c.2164C>T (p.Pro722Ser) rs121909642
NM_023110.3(FGFR1):c.2174G>A (p.Cys725Tyr) rs398122945
NM_023110.3(FGFR1):c.2292G>T (p.Gln764His) rs121909643
NM_023110.3(FGFR1):c.2302G>T (p.Asp768Tyr) rs121909644
NM_023110.3(FGFR1):c.494T>C (p.Leu165Ser) rs397515481
NM_023110.3(FGFR1):c.499G>T (p.Ala167Ser) rs121909630
NM_023110.3(FGFR1):c.709G>A (p.Gly237Ser) rs121909635
NM_023110.3(FGFR1):c.749G>A (p.Arg250Gln) rs121909645
NM_023110.3(FGFR1):c.755C>G (p.Pro252Arg) rs121909627
NM_023110.3(FGFR1):c.936G>A (p.Lys312=) rs1586287678
NM_023110.3(FGFR1):c.989A>T (p.Asn330Ile) rs121909632

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