ClinVar Miner

List of variants in gene FGFR3 reported as likely benign by GeneDx

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Gene type:
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Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_000142.5(FGFR3):c.380-101G>C rs3135866 0.01766
NM_000142.5(FGFR3):c.1075+185G>A rs3135887 0.01661
NM_000142.5(FGFR3):c.2169-33G>A rs3135899 0.01105
NM_000142.5(FGFR3):c.109+26G>A rs17884282 0.00910
NM_000142.5(FGFR3):c.1836+44C>T rs17878554 0.00809
NM_000142.5(FGFR3):c.931-470C>T rs377192087 0.00786
NM_000142.5(FGFR3):c.446-126C>T rs368240567 0.00754
NM_000142.5(FGFR3):c.445+78C>T rs184080582 0.00744
NM_000142.5(FGFR3):c.*138C>T rs73202816 0.00739
NM_000142.5(FGFR3):c.110-218C>T rs149321012 0.00704
NM_000142.5(FGFR3):c.1266+64C>T rs78940694 0.00626
NM_000142.5(FGFR3):c.1075+168C>T rs115088677 0.00503
NM_000142.5(FGFR3):c.-102-181G>A rs565525693 0.00420
NM_000142.5(FGFR3):c.930+180G>A rs150056292 0.00353
NM_000142.5(FGFR3):c.678C>T (p.Tyr226=) rs141575580 0.00142
NM_000142.5(FGFR3):c.-102-9C>T rs1035034826 0.00063
NM_000142.5(FGFR3):c.1371C>T (p.Leu457=) rs199758988 0.00057
NM_000142.5(FGFR3):c.2088C>T (p.Pro696=) rs142884145 0.00052
NM_000142.5(FGFR3):c.154G>A (p.Gly52Ser) rs140087676 0.00043
NM_000142.5(FGFR3):c.713G>A (p.Arg238Gln) rs199944818 0.00037
NM_000142.5(FGFR3):c.130G>A (p.Gly44Ser) rs146080119 0.00036
NM_000142.5(FGFR3):c.616-8C>T rs372304346 0.00034
NM_000142.5(FGFR3):c.159C>T (p.Ser53=) rs143548893 0.00025
NM_000142.5(FGFR3):c.725C>T (p.Thr242Met) rs150916178 0.00021
NM_000142.5(FGFR3):c.807C>T (p.Ser269=) rs199614237 0.00021
NM_000142.5(FGFR3):c.490C>G (p.Leu164Val) rs577990843 0.00020
NM_000142.5(FGFR3):c.2272G>A (p.Asp758Asn) rs56266857 0.00019
NM_000142.5(FGFR3):c.967G>A (p.Val323Ile) rs753520867 0.00017
NM_000142.5(FGFR3):c.933G>A (p.Thr311=) rs142805104 0.00015
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.1320C>T (p.Ile440=) rs190111780 0.00013
NM_000142.5(FGFR3):c.616-18G>C rs372940259 0.00013
NM_000142.5(FGFR3):c.2082G>A (p.Pro694=) rs765659195 0.00011
NM_000142.5(FGFR3):c.1206C>A (p.Pro402=) rs779554720 0.00010
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.2207C>A (p.Ser736Tyr) rs148631462 0.00009
NM_000142.5(FGFR3):c.808G>A (p.Asp270Asn) rs780147591 0.00009
NM_000142.5(FGFR3):c.1227C>T (p.Pro409=) rs533316478 0.00008
NM_000142.5(FGFR3):c.1830C>G (p.Ser610=) rs758618182 0.00008
NM_000142.5(FGFR3):c.335G>A (p.Arg112Gln) rs758163128 0.00008
NM_000142.5(FGFR3):c.739+16C>T rs757999433 0.00008
NM_000142.5(FGFR3):c.1182G>A (p.Thr394=) rs771495510 0.00007
NM_000142.5(FGFR3):c.1701G>C (p.Leu567=) rs372367824 0.00007
NM_000142.5(FGFR3):c.416A>C (p.Asp139Ala) rs376268669 0.00007
NM_000142.5(FGFR3):c.1733C>T (p.Ser578Phe) rs989826317 0.00006
NM_000142.5(FGFR3):c.272C>T (p.Pro91Leu) rs144995231 0.00006
NM_000142.5(FGFR3):c.329G>A (p.Arg110Gln) rs556916370 0.00006
NM_000142.5(FGFR3):c.1646-10G>A rs201317043 0.00005
NM_000142.5(FGFR3):c.1752G>A (p.Pro584=) rs139020690 0.00004
NM_000142.5(FGFR3):c.21C>T (p.Ala7=) rs779195790 0.00004
NM_000142.5(FGFR3):c.2412G>A (p.Ser804=) rs375563964 0.00004
NM_000142.5(FGFR3):c.573C>T (p.Asn191=) rs377492283 0.00004
NM_000142.5(FGFR3):c.985G>A (p.Val329Ile) rs188723332 0.00004
NM_000142.5(FGFR3):c.2249G>T (p.Arg750Leu) rs762888506 0.00003
NM_000142.5(FGFR3):c.534C>T (p.Ala178=) rs567597726 0.00003
NM_000142.5(FGFR3):c.1205C>G (p.Pro402Arg) rs752194597 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.2169-4G>A rs758292253 0.00002
NM_000142.5(FGFR3):c.870C>T (p.His290=) rs370518637 0.00002
NM_000142.5(FGFR3):c.*287C>T rs17882030 0.00001
NM_000142.5(FGFR3):c.1560G>A (p.Ser520=) rs776527776 0.00001
NM_000142.5(FGFR3):c.192C>T (p.Pro64=) rs766462409 0.00001
NM_000142.5(FGFR3):c.200G>A (p.Gly67Asp) rs369232922 0.00001
NM_000142.5(FGFR3):c.201T>C (p.Gly67=) rs752621056 0.00001
NM_000142.5(FGFR3):c.379+18G>A rs775716751 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.666C>T (p.Asp222=) rs201081464 0.00001
NM_000142.5(FGFR3):c.*140TG[3] rs34562534
NM_000142.5(FGFR3):c.*204AG[1]
NM_000142.5(FGFR3):c.1076-41G>C rs373591344
NM_000142.5(FGFR3):c.1076-42G>C rs17884871
NM_000142.5(FGFR3):c.1076-43G>T rs547904954
NM_000142.5(FGFR3):c.109+297C>A rs3135833
NM_000142.5(FGFR3):c.1371C>G (p.Leu457=) rs199758988
NM_000142.5(FGFR3):c.1534+14G>T rs374221323
NM_000142.5(FGFR3):c.1674G>A (p.Ala558=) rs557734169
NM_000142.5(FGFR3):c.189G>A (p.Pro63=) rs140377760
NM_000142.5(FGFR3):c.615+6C>A rs2305182
NM_000142.5(FGFR3):c.912C>G (p.Pro304=) rs201012537
NM_000142.5(FGFR3):c.921C>T (p.Thr307=) rs148518372

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