List of variants in gene ZNF335 reported as uncertain significance for bone disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022095.4(ZNF335):c.3998A>G (p.Glu1333Gly)	rs200635860	0.00025
NM_022095.4(ZNF335):c.808C>T (p.Arg270Cys)	rs145110365	0.00022
NM_022095.4(ZNF335):c.1441C>G (p.Arg481Gly)	rs141481390	0.00010
NM_022095.4(ZNF335):c.857G>A (p.Arg286Gln)	rs559354455	0.00005
NM_022095.4(ZNF335):c.1508G>A (p.Arg503His)	rs765260747	0.00003
NM_022095.4(ZNF335):c.1856G>A (p.Arg619His)	rs555774487	0.00003
NM_022095.4(ZNF335):c.1471G>C (p.Asp491His)
NM_022095.4(ZNF335):c.1665+61G>A	rs2083829211
NM_022095.4(ZNF335):c.1665G>C (p.Pro555=)	rs1201395437
NM_022095.4(ZNF335):c.1748C>T (p.Thr583Met)
NM_022095.4(ZNF335):c.2047T>C (p.Cys683Arg)
NM_022095.4(ZNF335):c.2062C>T (p.Arg688Trp)
NM_022095.4(ZNF335):c.235C>T (p.Pro79Ser)	rs768996558
NM_022095.4(ZNF335):c.2891G>A (p.Cys964Tyr)	rs148007831
NM_022095.4(ZNF335):c.3158C>T (p.Pro1053Leu)	rs768092083
NM_022095.4(ZNF335):c.3206A>G (p.His1069Arg)
NM_022095.4(ZNF335):c.3274C>T (p.Arg1092Trp)
NM_022095.4(ZNF335):c.3589C>T (p.Gln1197Ter)	rs1600517442
NM_022095.4(ZNF335):c.3887_3888del (p.His1296fs)
NM_022095.4(ZNF335):c.715GTG[3] (p.Val242del)	rs759141702

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.