ClinVar Miner

List of variants in gene FGFR3 reported by GeneDx

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Total variants: 78
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HGVS dbSNP
NM_000142.4(FGFR3):c.-102-3T>C rs10023340
NM_000142.4(FGFR3):c.-102-9C>T rs1035034826
NM_000142.4(FGFR3):c.-103+129C>A rs4450996
NM_000142.4(FGFR3):c.1075+5C>T rs3135885
NM_000142.4(FGFR3):c.1076-13C>T rs114754024
NM_000142.4(FGFR3):c.1076-16G>A rs3135889
NM_000142.4(FGFR3):c.1076-17C>T rs17881967
NM_000142.4(FGFR3):c.1412+138G>C rs4865476
NM_000142.4(FGFR3):c.1413-16C>G rs201702411
NM_000142.4(FGFR3):c.1413-29A>G rs3135894
NM_000142.4(FGFR3):c.1534+14G>T rs374221323
NM_000142.4(FGFR3):c.1535-20G>A rs113557371
NM_000142.4(FGFR3):c.1535-8G>T rs111460786
NM_000142.4(FGFR3):c.1645+15G>A rs192433202
NM_000142.4(FGFR3):c.1645+17C>T rs765768657
NM_000142.4(FGFR3):c.1959+22G>A rs3135898
NM_000142.4(FGFR3):c.379+18G>A rs775716751
NM_000142.4(FGFR3):c.445+158T>C rs3135869
NM_000142.4(FGFR3):c.445+3A>G rs3135868
NM_000142.4(FGFR3):c.615+11C>T rs780810190
NM_000142.4(FGFR3):c.615+20T>C rs1374050784
NM_000142.4(FGFR3):c.615+8C>G rs17878375
NM_000142.4(FGFR3):c.616-15C>T rs17883683
NM_000142.4(FGFR3):c.616-18G>C rs372940259
NM_000142.4(FGFR3):c.616-40T>C rs2305183
NM_000142.4(FGFR3):c.739+16C>T rs757999433
NM_000142.4(FGFR3):c.740-17G>A rs371424896
NM_000142.4(FGFR3):c.930+625G>A rs3135878
NM_000142.4(FGFR3):c.930+72C>G rs2305184
NM_000142.4(FGFR3):c.931-123G>A rs3135883
NM_000142.5(FGFR3):c.1014C>T (p.Thr338=) rs4647928
NM_000142.5(FGFR3):c.1052C>G (p.Ser351Cys) rs1057517964
NM_000142.5(FGFR3):c.1099G>T (p.Asp367Tyr) rs1444200455
NM_000142.5(FGFR3):c.1108G>T (p.Gly370Cys) rs121913479
NM_000142.5(FGFR3):c.1118A>G (p.Tyr373Cys) rs121913485
NM_000142.5(FGFR3):c.1138G>A rs28931614
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656
NM_000142.5(FGFR3):c.1172C>A (p.Ala391Glu) rs28931615
NM_000142.5(FGFR3):c.1205C>G (p.Pro402Arg) rs752194597
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104
NM_000142.5(FGFR3):c.1497C>T (p.Ala499=) rs140594137
NM_000142.5(FGFR3):c.1576A>G (p.Met526Val) rs766053734
NM_000142.5(FGFR3):c.1620C>A (p.Asn540Lys) rs28933068
NM_000142.5(FGFR3):c.1620C>G (p.Asn540Lys) rs28933068
NM_000142.5(FGFR3):c.1647G>T (p.Gly549=) rs3135897
NM_000142.5(FGFR3):c.1675G>C (p.Ala559Pro) rs768385286
NM_000142.5(FGFR3):c.1753C>T (p.Pro585Ser) rs761163163
NM_000142.5(FGFR3):c.1808G>A (p.Arg603Gln) rs1462697338
NM_000142.5(FGFR3):c.1948A>G (p.Lys650Glu) rs78311289
NM_000142.5(FGFR3):c.1953= (p.Thr651=) rs7688609
NM_000142.5(FGFR3):c.200G>A (p.Gly67Asp) rs369232922
NM_000142.5(FGFR3):c.201T>C (p.Gly67=) rs752621056
NM_000142.5(FGFR3):c.2088C>T (p.Pro696=) rs142884145
NM_000142.5(FGFR3):c.21C>T (p.Ala7=) rs779195790
NM_000142.5(FGFR3):c.2205C>G (p.Pro735=) rs145020302
NM_000142.5(FGFR3):c.2222T>C (p.Phe741Ser) rs768999235
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.2374dup (p.Asp792fs) rs1057518205
NM_000142.5(FGFR3):c.2407_*5delinsCCCTG (p.Gly803_Ter807delinsProXaa) rs1064796266
NM_000142.5(FGFR3):c.2419T>A (p.Ter807Arg) rs121913101
NM_000142.5(FGFR3):c.2419T>G (p.Ter807Gly) rs121913101
NM_000142.5(FGFR3):c.2420G>T (p.Ter807Leu) rs397515514
NM_000142.5(FGFR3):c.348C>T (p.Arg116=) rs2305179
NM_000142.5(FGFR3):c.389C>T (p.Ser130Phe) rs113172184
NM_000142.5(FGFR3):c.393G>A (p.Ser131=) rs55662109
NM_000142.5(FGFR3):c.417C>T (p.Asp139=) rs3135867
NM_000142.5(FGFR3):c.573C>T (p.Asn191=) rs377492283
NM_000142.5(FGFR3):c.588C>T (p.Arg196=) rs2305180
NM_000142.5(FGFR3):c.603T>C (p.Ile201=) rs2305181
NM_000142.5(FGFR3):c.654G>C (p.Val218=) rs147769045
NM_000142.5(FGFR3):c.663G>A (p.Ser221=) rs114421370
NM_000142.5(FGFR3):c.666C>T (p.Asp222=) rs201081464
NM_000142.5(FGFR3):c.742C>T (p.Arg248Cys) rs121913482
NM_000142.5(FGFR3):c.749C>G (p.Pro250Arg) rs4647924
NM_000142.5(FGFR3):c.808G>A (p.Asp270Asn) rs780147591
NM_000142.5(FGFR3):c.882T>C (p.Asn294=) rs2234909
NM_001163213.1(FGFR3):c.746C>G (p.Ser249Cys) rs121913483

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