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: 26
Download table as spreadsheet
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.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.1668G>A (p.Glu556=) rs1388294342
NM_000142.4(FGFR3):c.1959+22G>A rs3135898
NM_000142.4(FGFR3):c.1959+8C>T rs371666188
NM_000142.4(FGFR3):c.2169-5C>T
NM_000142.4(FGFR3):c.445+158T>C rs3135869
NM_000142.4(FGFR3):c.616-40T>C rs2305183
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_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656
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.1497C>T (p.Ala499=) rs140594137
NM_000142.5(FGFR3):c.2259C>T (p.Thr753=) rs146662137
NM_000142.5(FGFR3):c.417C>T (p.Asp139=) rs3135867
NM_000142.5(FGFR3):c.771G>A (p.Ala257=) rs138334098
NM_000142.5(FGFR3):c.882T>C (p.Asn294=) rs2234909
NM_001163213.1(FGFR3):c.1652-4C>T rs200428838

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.