ClinVar Miner

List of variants in gene WNT10B studied for bone development disease

Included ClinVar conditions (618):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003394.4(WNT10B):c.1059C>T (p.His353=) rs1051886 0.32338
NM_003394.4(WNT10B):c.995G>A (p.Arg332Gln) rs768477854 0.00002
NM_003394.4(WNT10B):c.458_461dup (p.Asp155fs) rs763548858 0.00001
NM_003394.4(WNT10B):c.676C>T (p.Arg226Ter) rs763991433 0.00001
NM_003394.4(WNT10B):c.994C>T (p.Arg332Trp) rs121918349 0.00001
NM_003394.4(WNT10B):c.115G>T (p.Glu39Ter)
NM_003394.4(WNT10B):c.117_136del (p.Glu39fs) rs2137615101
NM_003394.4(WNT10B):c.257A>C (p.Gln86Pro) rs1592252556
NM_003394.4(WNT10B):c.290T>C (p.Leu97Pro) rs1458667581
NM_003394.4(WNT10B):c.337G>C (p.Gly113Arg)
NM_003394.4(WNT10B):c.338-1G>C rs1163162816
NM_003394.4(WNT10B):c.499_500del (p.Leu167fs) rs2137612860
NM_003394.4(WNT10B):c.53T>A (p.Leu18Gln)
NM_003394.4(WNT10B):c.689ACA[2] (p.Asn232del) rs776938956
NM_003394.4(WNT10B):c.741del (p.Lys246_Cys247insTer) rs2137611223
NM_003394.4(WNT10B):c.746G>T (p.Cys249Phe)
NM_003394.4(WNT10B):c.817del (p.Ala273fs)
NM_003394.4(WNT10B):c.817dup (p.Ala273fs)
NM_003394.4(WNT10B):c.949T>A (p.Phe317Ile)

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.