ClinVar Miner

List of variants in gene FGFR3 studied for not provided

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Total variants: 124
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HGVS dbSNP
NM_000142.4(FGFR3):c.-103+129C>A rs4450996
NM_000142.4(FGFR3):c.1023G>A (p.Ala341=) rs147833498
NM_000142.4(FGFR3):c.1146C>T (p.Gly382=) rs762689187
NM_000142.4(FGFR3):c.1320C>T (p.Ile440=) rs190111780
NM_000142.4(FGFR3):c.1356C>A (p.Ala452=) rs149555011
NM_000142.4(FGFR3):c.1404T>G (p.Ser468=) rs1391284081
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.1431C>T (p.Pro477=) rs1351116736
NM_000142.4(FGFR3):c.1476C>T (p.Ile492=) rs373254179
NM_000142.4(FGFR3):c.1551G>A (p.Lys517=) rs142622642
NM_000142.4(FGFR3):c.159C>T (p.Ser53=) rs143548893
NM_000142.4(FGFR3):c.1644C>T (p.Gly548=) rs756321317
NM_000142.4(FGFR3):c.1668G>A (p.Glu556=) rs1388294342
NM_000142.4(FGFR3):c.1671C>T (p.Tyr557=) rs370408732
NM_000142.4(FGFR3):c.1706C>T (p.Ala569Val) rs146672976
NM_000142.4(FGFR3):c.1764G>A (p.Gln588=) rs765360194
NM_000142.4(FGFR3):c.1845C>T (p.His615=) rs375856533
NM_000142.4(FGFR3):c.1878C>T (p.Thr626=) rs369137031
NM_000142.4(FGFR3):c.1959+22G>A rs3135898
NM_000142.4(FGFR3):c.1959+8C>T rs371666188
NM_000142.4(FGFR3):c.1971C>T (p.Pro657=) rs922106076
NM_000142.4(FGFR3):c.2082G>A (p.Pro694=) rs765659195
NM_000142.4(FGFR3):c.2148C>T (p.Pro716=) rs373967853
NM_000142.4(FGFR3):c.2169-5C>T
NM_000142.4(FGFR3):c.2265G>A (p.Thr755=) rs755791719
NM_000142.4(FGFR3):c.2316G>A (p.Pro772=) rs200629304
NM_000142.4(FGFR3):c.2418G>A (p.Thr806=) rs779088139
NM_000142.4(FGFR3):c.304G>A (p.Glu102Lys) rs558935109
NM_000142.4(FGFR3):c.445+158T>C rs3135869
NM_000142.4(FGFR3):c.446-8G>T rs868082562
NM_000142.4(FGFR3):c.615+6C>T rs2305182
NM_000142.4(FGFR3):c.616-18G>C rs372940259
NM_000142.4(FGFR3):c.616-40T>C rs2305183
NM_000142.4(FGFR3):c.616-6G>A rs17883400
NM_000142.4(FGFR3):c.660C>A (p.Pro220=) rs146927248
NM_000142.4(FGFR3):c.669C>T (p.Arg223=) rs749024125
NM_000142.4(FGFR3):c.726G>C (p.Thr242=) rs1399793508
NM_000142.4(FGFR3):c.740-9C>T rs886038257
NM_000142.4(FGFR3):c.921C>G (p.Thr307=) rs148518372
NM_000142.4(FGFR3):c.930+10C>T rs534857289
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_000142.4(FGFR3):c.933G>A (p.Thr311=) rs142805104
NM_000142.4(FGFR3):c.963A>G (p.Leu321=) rs201221388
NM_000142.5(FGFR3):c.1002C>T (p.Ala334=) rs376787929
NM_000142.5(FGFR3):c.1052C>G (p.Ser351Cys) rs1057517964
NM_000142.5(FGFR3):c.1055C>T (p.Ala352Val) rs886043604
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.1138G>C (p.Gly380Arg) 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.1263A>G (p.Arg421=) rs866774930
NM_000142.5(FGFR3):c.130G>A (p.Gly44Ser) rs146080119
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104
NM_000142.5(FGFR3):c.1349C>T (p.Thr450Met) rs56240927
NM_000142.5(FGFR3):c.1366G>A (p.Glu456Lys) rs1201375716
NM_000142.5(FGFR3):c.1497C>T (p.Ala499=) rs140594137
NM_000142.5(FGFR3):c.150C>T (p.Val50=) rs750641928
NM_000142.5(FGFR3):c.1550A>G (p.Lys517Arg) rs139707740
NM_000142.5(FGFR3):c.158G>C (p.Ser53Thr) rs201433984
NM_000142.5(FGFR3):c.1596C>T (p.Ile532=) rs528979086
NM_000142.5(FGFR3):c.1612A>G (p.Ile538Val) rs80053154
NM_000142.5(FGFR3):c.1619A>G (p.Asn540Ser) rs77722678
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.1657G>A (p.Val553Met) rs199544087
NM_000142.5(FGFR3):c.1663G>C (p.Val555Leu)
NM_000142.5(FGFR3):c.1664T>A (p.Val555Glu) rs1254322699
NM_000142.5(FGFR3):c.1675G>C (p.Ala559Pro) rs768385286
NM_000142.5(FGFR3):c.1752G>A (p.Pro584=) rs139020690
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.1830C>G (p.Ser610=) rs758618182
NM_000142.5(FGFR3):c.1879G>A (p.Glu627Lys) rs200849753
NM_000142.5(FGFR3):c.1923C>T (p.Asp641=) rs148104605
NM_000142.5(FGFR3):c.1948A>G (p.Lys650Glu) rs78311289
NM_000142.5(FGFR3):c.1950G>C (p.Lys650Asn) rs28928868
NM_000142.5(FGFR3):c.200G>A (p.Gly67Asp) rs369232922
NM_000142.5(FGFR3):c.2149G>A (p.Ala717Thr) rs17882190
NM_000142.5(FGFR3):c.2183G>A (p.Arg728Gln) rs149924317
NM_000142.5(FGFR3):c.2201C>T (p.Ala734Val) rs555257146
NM_000142.5(FGFR3):c.2222T>C (p.Phe741Ser) rs768999235
NM_000142.5(FGFR3):c.2259C>T (p.Thr753=) rs146662137
NM_000142.5(FGFR3):c.2396C>T (p.Pro799Leu) rs150452037
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.252G>A (p.Ser84=) rs367973461
NM_000142.5(FGFR3):c.272C>T (p.Pro91Leu) rs144995231
NM_000142.5(FGFR3):c.312C>T (p.Ser104=) rs377018654
NM_000142.5(FGFR3):c.335G>A (p.Arg112Gln) rs758163128
NM_000142.5(FGFR3):c.346C>T (p.Arg116Cys) rs886042775
NM_000142.5(FGFR3):c.389C>T (p.Ser130Phe) rs113172184
NM_000142.5(FGFR3):c.3G>T (p.Met1Ile) rs1560384106
NM_000142.5(FGFR3):c.416A>C (p.Asp139Ala)
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.598C>T (p.Arg200Cys) rs886043613
NM_000142.5(FGFR3):c.666C>T (p.Asp222=) rs201081464
NM_000142.5(FGFR3):c.712C>T (p.Arg238Trp) rs766423062
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.771G>A (p.Ala257=) rs138334098
NM_000142.5(FGFR3):c.792G>A (p.Thr264=) rs754400359
NM_000142.5(FGFR3):c.835A>T (p.Ser279Cys) rs121913114
NM_000142.5(FGFR3):c.882T>C (p.Asn294=) rs2234909
NM_000142.5(FGFR3):c.912C>G (p.Pro304=) rs201012537
NM_000142.5(FGFR3):c.931-634C>T rs755547723
NM_000142.5(FGFR3):c.931-640G>C rs747899858
NM_000142.5(FGFR3):c.940G>A (p.Ala314Thr)
NM_000142.5(FGFR3):c.967G>A (p.Val323Ile) rs753520867
NM_001163213.1(FGFR3):c.1652-4C>T rs200428838
NM_001163213.1(FGFR3):c.2036+9C>T rs373627757
NM_001163213.1(FGFR3):c.616-8C>T rs372304346
NM_001163213.1(FGFR3):c.746C>G (p.Ser249Cys) rs121913483
NM_022965.3(FGFR3):c.276_277delinsAT (p.Arg93Trp) rs1560406964
NM_022965.3(FGFR3):c.931-398C>T rs28931615

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