ClinVar Miner

List of variants in gene FGFR3 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 99
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000142.5(FGFR3):c.1953G>A (p.Thr651=) rs7688609 0.95729
NM_000142.5(FGFR3):c.931-123G>A rs3135883 0.91705
NM_000142.5(FGFR3):c.930+625G>A rs3135878 0.82366
NM_000142.5(FGFR3):c.-103+129C>A rs4450996 0.59323
NM_000142.5(FGFR3):c.616-40T>C rs2305183 0.21932
NM_000142.5(FGFR3):c.882T>C (p.Asn294=) rs2234909 0.20412
NM_000142.5(FGFR3):c.930+72C>G rs2305184 0.19439
NM_000142.5(FGFR3):c.109+309C>T rs3135834 0.10213
NM_000142.5(FGFR3):c.445+3A>G rs3135868 0.09950
NM_000142.5(FGFR3):c.1267-32C>T rs3135890 0.09901
NM_000142.5(FGFR3):c.603T>C (p.Ile201=) rs2305181 0.09854
NM_000142.5(FGFR3):c.445+158T>C rs3135869 0.08952
NM_000142.5(FGFR3):c.*184C>T rs3135901 0.04173
NM_000142.5(FGFR3):c.417C>T (p.Asp139=) rs3135867 0.03551
NM_000142.5(FGFR3):c.1075+236T>C rs3135888 0.03378
NM_000142.5(FGFR3):c.588C>T (p.Arg196=) rs2305180 0.03125
NM_000142.5(FGFR3):c.930+174T>C rs3135874 0.02902
NM_000142.5(FGFR3):c.109+174T>C rs17884005 0.02494
NM_000142.5(FGFR3):c.*36A>G rs3135900 0.02388
NM_000142.5(FGFR3):c.615+8C>G rs17878375 0.02283
NM_000142.5(FGFR3):c.1076-17C>T rs17881967 0.02051
NM_000142.5(FGFR3):c.348C>T (p.Arg116=) rs2305179 0.01752
NM_000142.5(FGFR3):c.1959+22G>A rs3135898 0.01743
NM_000142.5(FGFR3):c.1075+5C>T rs3135885 0.01659
NM_000142.5(FGFR3):c.2169-33G>A rs3135899 0.01105
NM_000142.5(FGFR3):c.1345C>T (p.Pro449Ser) rs61735104 0.00867
NM_000142.5(FGFR3):c.654G>C (p.Val218=) rs147769045 0.00703
NM_000142.5(FGFR3):c.1076-13C>T rs114754024 0.00661
NM_000142.5(FGFR3):c.1645+15G>A rs192433202 0.00533
NM_000142.5(FGFR3):c.616-15C>T rs17883683 0.00494
NM_000142.5(FGFR3):c.663G>A (p.Ser221=) rs114421370 0.00485
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656 0.00342
NM_000142.5(FGFR3):c.1535-8G>T rs111460786 0.00332
NM_000142.5(FGFR3):c.1014C>T (p.Thr338=) rs4647928 0.00328
NM_000142.5(FGFR3):c.1076-16G>A rs3135889 0.00296
NM_000142.5(FGFR3):c.393G>A (p.Ser131=) rs55662109 0.00292
NM_000142.5(FGFR3):c.2205C>G (p.Pro735=) rs145020302 0.00287
NM_000142.5(FGFR3):c.*5C>G rs17879364 0.00201
NM_000142.5(FGFR3):c.1535-20G>A rs113557371 0.00174
NM_000142.5(FGFR3):c.169G>A (p.Val57Met) rs61735064 0.00163
NM_000142.5(FGFR3):c.1959+15G>C rs17886888 0.00158
NM_000142.5(FGFR3):c.678C>T (p.Tyr226=) rs141575580 0.00142
NM_000142.5(FGFR3):c.1413-16C>G rs201702411 0.00114
NM_000142.5(FGFR3):c.2169-5C>T rs17884617 0.00112
NM_000142.5(FGFR3):c.739+15G>T rs373101038 0.00108
NM_000142.5(FGFR3):c.1497C>T (p.Ala499=) rs140594137 0.00106
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.990C>T (p.Thr330=) rs2305185 0.00097
NM_000142.5(FGFR3):c.2149G>A (p.Ala717Thr) rs17882190 0.00095
NM_000142.5(FGFR3):c.1349C>T (p.Thr450Met) rs56240927 0.00083
NM_000142.5(FGFR3):c.1923C>T (p.Asp641=) rs148104605 0.00081
NM_000142.5(FGFR3):c.1671C>T (p.Tyr557=) rs370408732 0.00057
NM_000142.5(FGFR3):c.1646-4C>T rs200428838 0.00054
NM_000142.5(FGFR3):c.446-17C>T rs376137178 0.00053
NM_000142.5(FGFR3):c.2088C>T (p.Pro696=) rs142884145 0.00052
NM_000142.5(FGFR3):c.1023G>A (p.Ala341=) rs147833498 0.00050
NM_000142.5(FGFR3):c.1959+8C>T rs371666188 0.00048
NM_000142.5(FGFR3):c.1686C>T (p.Asn562=) rs761445231 0.00046
NM_000142.5(FGFR3):c.252G>A (p.Ser84=) rs367973461 0.00039
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.446-5C>T rs144211980 0.00021
NM_000142.5(FGFR3):c.771G>A (p.Ala257=) rs138334098 0.00021
NM_000142.5(FGFR3):c.490C>G (p.Leu164Val) rs577990843 0.00020
NM_000142.5(FGFR3):c.2259C>T (p.Thr753=) rs146662137 0.00015
NM_000142.5(FGFR3):c.933G>A (p.Thr311=) rs142805104 0.00015
NM_000142.5(FGFR3):c.1449C>T (p.Phe483=) rs545617229 0.00014
NM_000142.5(FGFR3):c.930+10C>T rs534857289 0.00014
NM_000142.5(FGFR3):c.616-18G>C rs372940259 0.00013
NM_000142.5(FGFR3):c.1413-20C>T rs367942098 0.00011
NM_000142.5(FGFR3):c.1960-13C>T rs377604726 0.00011
NM_000142.5(FGFR3):c.1719G>A (p.Pro573=) rs772157613 0.00010
NM_000142.5(FGFR3):c.1227C>T (p.Pro409=) rs533316478 0.00008
NM_000142.5(FGFR3):c.1285G>A (p.Ala429Thr) rs182935140 0.00008
NM_000142.5(FGFR3):c.639G>A (p.Leu213=) rs138707520 0.00007
NM_000142.5(FGFR3):c.1287G>A (p.Ala429=) rs187229103 0.00006
NM_000142.5(FGFR3):c.684C>T (p.Cys228=) rs769248723 0.00003
NM_000142.5(FGFR3):c.1935C>T (p.Leu645=) rs104886006 0.00002
NM_000142.5(FGFR3):c.1290C>T (p.Ser430=) rs3135891 0.00001
NM_000142.5(FGFR3):c.1668G>A (p.Glu556=) rs1388294342 0.00001
NM_000142.5(FGFR3):c.*140TG[8] rs34562534
NM_000142.5(FGFR3):c.-102-18_-102-11del rs1452696194
NM_000142.5(FGFR3):c.-103+141C>T rs17879199
NM_000142.5(FGFR3):c.1075+11CTG[6]
NM_000142.5(FGFR3):c.1075+30G>C rs3135886
NM_000142.5(FGFR3):c.1076-34del rs4647926
NM_000142.5(FGFR3):c.1076-34dup rs4647926
NM_000142.5(FGFR3):c.110-67C>T
NM_000142.5(FGFR3):c.1218G>C (p.Leu406=)
NM_000142.5(FGFR3):c.1412+138G>C rs4865476
NM_000142.5(FGFR3):c.1413-29A>G rs3135894
NM_000142.5(FGFR3):c.1647G>T (p.Gly549=) rs3135897
NM_000142.5(FGFR3):c.1837-20_1837-9dup
NM_000142.5(FGFR3):c.1959+11C>T
NM_000142.5(FGFR3):c.2275-8G>A
NM_000142.5(FGFR3):c.615+6C>A rs2305182
NM_000142.5(FGFR3):c.912C>G (p.Pro304=) rs201012537
NM_000142.5(FGFR3):c.930+218G>A rs3135875

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.