ClinVar Miner

List of variants in gene FGFR3 reported as uncertain significance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 97
Download table as spreadsheet
HGVS dbSNP
NM_000142.4(FGFR3):c.1534+6G>C rs1213940166
NM_000142.4(FGFR3):c.1645+4G>C rs1367336734
NM_000142.4(FGFR3):c.1756G>A (p.Glu586Lys) rs576023546
NM_000142.4(FGFR3):c.2417C>T (p.Thr806Met) rs374547489
NM_000142.4(FGFR3):c.436_445+2del rs1030059712
NM_000142.4(FGFR3):c.445+2_445+5del rs756854039
NM_000142.4(FGFR3):c.446-8G>T rs868082562
NM_000142.4(FGFR3):c.615+6C>T rs2305182
NM_000142.4(FGFR3):c.616-6G>A rs17883400
NM_000142.5(FGFR3):c.1000G>A (p.Ala334Thr) rs373496046
NM_000142.5(FGFR3):c.1002C>T (p.Ala334=) rs376787929
NM_000142.5(FGFR3):c.1055C>T (p.Ala352Val) rs886043604
NM_000142.5(FGFR3):c.1056G>A (p.Ala352=) rs765849160
NM_000142.5(FGFR3):c.1078G>A (p.Glu360Lys) rs757013992
NM_000142.5(FGFR3):c.1099G>T (p.Asp367Tyr) rs1444200455
NM_000142.5(FGFR3):c.109G>A (p.Glu37Lys) rs1553842213
NM_000142.5(FGFR3):c.1106C>T (p.Ala369Val)
NM_000142.5(FGFR3):c.1118A>G (p.Tyr373Cys) rs121913485
NM_000142.5(FGFR3):c.1138G>A rs28931614
NM_000142.5(FGFR3):c.1181C>T (p.Thr394Met) rs747694886
NM_000142.5(FGFR3):c.1190G>A (p.Arg397His)
NM_000142.5(FGFR3):c.1210A>G (p.Lys404Glu)
NM_000142.5(FGFR3):c.1223C>T (p.Ser408Phe) rs761877926
NM_000142.5(FGFR3):c.1238A>G (p.Lys413Arg)
NM_000142.5(FGFR3):c.1263A>G (p.Arg421=) rs866774930
NM_000142.5(FGFR3):c.1266+25C>T
NM_000142.5(FGFR3):c.1331C>G (p.Ser444Cys) rs761325047
NM_000142.5(FGFR3):c.1366G>A (p.Glu456Lys) rs1201375716
NM_000142.5(FGFR3):c.1379C>T (p.Pro460Leu)
NM_000142.5(FGFR3):c.1480A>G (p.Ile494Val) rs1057519048
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.1519G>A (p.Val507Met) rs1560437651
NM_000142.5(FGFR3):c.1537G>A (p.Asp513Asn) rs121913112
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.1606A>G (p.Lys536Glu)
NM_000142.5(FGFR3):c.1618A>G (p.Asn540Asp) rs1057519049
NM_000142.5(FGFR3):c.1619A>G (p.Asn540Ser) rs77722678
NM_000142.5(FGFR3):c.1657G>A (p.Val553Met) rs199544087
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.1733C>T (p.Ser578Phe) rs989826317
NM_000142.5(FGFR3):c.1742C>T (p.Thr581Ile)
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.1837-3C>T
NM_000142.5(FGFR3):c.1879G>A (p.Glu627Lys) rs200849753
NM_000142.5(FGFR3):c.188C>G (p.Pro63Arg) rs371729802
NM_000142.5(FGFR3):c.188C>T (p.Pro63Leu)
NM_000142.5(FGFR3):c.1921_1922delinsAT (p.Asp641Ile)
NM_000142.5(FGFR3):c.1922A>T (p.Asp641Val)
NM_000142.5(FGFR3):c.1923C>T (p.Asp641=) rs148104605
NM_000142.5(FGFR3):c.1948A>C (p.Lys650Gln) rs78311289
NM_000142.5(FGFR3):c.1960-16T>C
NM_000142.5(FGFR3):c.1993G>T (p.Ala665Ser) rs764892330
NM_000142.5(FGFR3):c.2005C>G (p.Arg669Gly) rs1490564667
NM_000142.5(FGFR3):c.200G>A (p.Gly67Asp) rs369232922
NM_000142.5(FGFR3):c.200G>C (p.Gly67Ala)
NM_000142.5(FGFR3):c.2150C>T (p.Ala717Val) rs749192018
NM_000142.5(FGFR3):c.2153A>G (p.Asn718Ser) rs139773438
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.2294C>T (p.Ala765Val) rs140211846
NM_000142.5(FGFR3):c.2374dup (p.Asp792fs) rs1057518205
NM_000142.5(FGFR3):c.2396C>T (p.Pro799Leu) rs150452037
NM_000142.5(FGFR3):c.2413C>T (p.Arg805Trp) rs369758941
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.335G>A (p.Arg112Gln) rs758163128
NM_000142.5(FGFR3):c.343C>G (p.Gln115Glu)
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.433G>A (p.Gly145Ser)
NM_000142.5(FGFR3):c.517C>T (p.Arg173Cys)
NM_000142.5(FGFR3):c.518G>A (p.Arg173His) rs1441656357
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.667C>T (p.Arg223Cys)
NM_000142.5(FGFR3):c.712C>T (p.Arg238Trp) rs766423062
NM_000142.5(FGFR3):c.739G>A (p.Glu247Lys) rs565612580
NM_000142.5(FGFR3):c.749C>T (p.Pro250Leu) rs4647924
NM_000142.5(FGFR3):c.77G>A (p.Gly26Glu) rs1221876688
NM_000142.5(FGFR3):c.875A>T (p.Glu292Val)
NM_000142.5(FGFR3):c.916G>A (p.Val306Ile) rs774047997
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.989C>T (p.Thr330Ile)
NM_022965.3(FGFR3):c.276_277delinsAT (p.Arg93Trp) rs1560406964
NM_022965.3(FGFR3):c.931-398C>T rs28931615

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.