ClinVar Miner

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

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656 0.00342
NM_000142.5(FGFR3):c.169G>A (p.Val57Met) rs61735064 0.00163
NM_000142.5(FGFR3):c.2043G>A (p.Gly681=) rs17883356 0.00101
NM_000142.5(FGFR3):c.193G>A (p.Gly65Arg) rs2305178 0.00097
NM_000142.5(FGFR3):c.2149G>A (p.Ala717Thr) rs17882190 0.00095
NM_000142.5(FGFR3):c.1959+8C>T rs371666188 0.00048
NM_000142.5(FGFR3):c.130G>A (p.Gly44Ser) rs146080119 0.00036
NM_000142.5(FGFR3):c.2169-13G>A rs370060233 0.00014
NM_000142.5(FGFR3):c.616-6G>A rs17883400 0.00014
NM_000142.5(FGFR3):c.1534+15G>T rs367781042 0.00013
NM_000142.5(FGFR3):c.2168+12C>T rs369096713 0.00013
NM_000142.5(FGFR3):c.2270C>G (p.Thr757Ser) rs748763892 0.00010
NM_000142.5(FGFR3):c.740-17G>A rs371424896 0.00010
NM_000142.5(FGFR3):c.1227C>T (p.Pro409=) rs533316478 0.00008
NM_000142.5(FGFR3):c.739+16C>T rs757999433 0.00008
NM_000142.5(FGFR3):c.1535-14C>T rs3135895 0.00007
NM_000142.5(FGFR3):c.272C>T (p.Pro91Leu) rs144995231 0.00006
NM_000142.5(FGFR3):c.21C>T (p.Ala7=) rs779195790 0.00004
NM_000142.5(FGFR3):c.2249G>T (p.Arg750Leu) rs762888506 0.00003
NM_000142.5(FGFR3):c.740-9C>T rs886038257 0.00003
NM_000142.5(FGFR3):c.1332C>T (p.Ser444=) rs769521432 0.00002
NM_000142.5(FGFR3):c.1576A>G (p.Met526Val) rs766053734 0.00002
NM_000142.5(FGFR3):c.1645+17C>T rs765768657 0.00002
NM_000142.5(FGFR3):c.1223C>T (p.Ser408Phe) rs761877926 0.00001
NM_000142.5(FGFR3):c.1290C>T (p.Ser430=) rs3135891 0.00001
NM_000142.5(FGFR3):c.1645+4G>C rs1367336734 0.00001
NM_000142.5(FGFR3):c.2274+50C>T rs756761813 0.00001
NM_000142.5(FGFR3):c.379+18G>A rs775716751 0.00001
NM_000142.5(FGFR3):c.381C>T (p.Asp127=) rs762778478 0.00001
NM_000142.5(FGFR3):c.615+11C>T rs780810190 0.00001
NM_000142.5(FGFR3):c.615+20T>C rs1374050784 0.00001
NM_000142.5(FGFR3):c.616-14G>T rs886038256 0.00001
NM_000142.5(FGFR3):c.666C>T (p.Asp222=) rs201081464 0.00001
NM_000142.5(FGFR3):c.1534+14G>T rs374221323
NM_000142.5(FGFR3):c.188C>G (p.Pro63Arg) rs371729802
NM_000142.5(FGFR3):c.894G>T (p.Val298=) rs886038258
NM_000142.5(FGFR3):c.931-712G>C

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