ClinVar Miner

List of variants in gene FGFR3 reported as likely benign for not specified

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Gene type:
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Total variants: 42
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HGVS dbSNP
NM_000142.4(FGFR3):c.-102-9C>T rs1035034826
NM_000142.4(FGFR3):c.1534+14G>T rs374221323
NM_000142.4(FGFR3):c.1534+15G>T rs367781042
NM_000142.4(FGFR3):c.1535-14C>T rs3135895
NM_000142.4(FGFR3):c.1645+17C>T rs765768657
NM_000142.4(FGFR3):c.1645+4G>C rs1367336734
NM_000142.4(FGFR3):c.1959+8C>T rs371666188
NM_000142.4(FGFR3):c.2168+12C>T rs369096713
NM_000142.4(FGFR3):c.2169-13G>A rs370060233
NM_000142.4(FGFR3):c.2274+50C>T rs756761813
NM_000142.4(FGFR3):c.379+18G>A rs775716751
NM_000142.4(FGFR3):c.615+11C>T rs780810190
NM_000142.4(FGFR3):c.615+20T>C rs1374050784
NM_000142.4(FGFR3):c.616-14G>T rs886038256
NM_000142.4(FGFR3):c.616-6G>A rs17883400
NM_000142.4(FGFR3):c.739+16C>T rs757999433
NM_000142.4(FGFR3):c.740-17G>A rs371424896
NM_000142.4(FGFR3):c.740-9C>T rs886038257
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656
NM_000142.5(FGFR3):c.1205C>G (p.Pro402Arg) rs752194597
NM_000142.5(FGFR3):c.1223C>T (p.Ser408Phe) rs761877926
NM_000142.5(FGFR3):c.1227C>T (p.Pro409=) rs533316478
NM_000142.5(FGFR3):c.1290C>T (p.Ser430=) rs3135891
NM_000142.5(FGFR3):c.130G>A (p.Gly44Ser) rs146080119
NM_000142.5(FGFR3):c.1332C>T (p.Ser444=) rs769521432
NM_000142.5(FGFR3):c.1576A>G (p.Met526Val) rs766053734
NM_000142.5(FGFR3):c.169G>A (p.Val57Met) rs61735064
NM_000142.5(FGFR3):c.188C>G (p.Pro63Arg) rs371729802
NM_000142.5(FGFR3):c.193G>A (p.Gly65Arg) rs2305178
NM_000142.5(FGFR3):c.201T>C (p.Gly67=) rs752621056
NM_000142.5(FGFR3):c.2043G>A (p.Gly681=) rs17883356
NM_000142.5(FGFR3):c.2088C>T (p.Pro696=) rs142884145
NM_000142.5(FGFR3):c.2149G>A (p.Ala717Thr) rs17882190
NM_000142.5(FGFR3):c.21C>T (p.Ala7=) rs779195790
NM_000142.5(FGFR3):c.2249G>T (p.Arg750Leu) rs762888506
NM_000142.5(FGFR3):c.2270C>G (p.Thr757Ser) rs748763892
NM_000142.5(FGFR3):c.272C>T (p.Pro91Leu) rs144995231
NM_000142.5(FGFR3):c.381C>T (p.Asp127=) rs762778478
NM_000142.5(FGFR3):c.573C>T (p.Asn191=) rs377492283
NM_000142.5(FGFR3):c.666C>T (p.Asp222=) rs201081464
NM_000142.5(FGFR3):c.808G>A (p.Asp270Asn) rs780147591
NM_000142.5(FGFR3):c.894G>T (p.Val298=) rs886038258

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