List of variants in gene ZNF335 reported as benign 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: 31

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022095.4(ZNF335):c.201+10C>G	rs6017715	0.92719
NM_022095.4(ZNF335):c.2021-37C>T	rs3746507	0.92505
NM_022095.4(ZNF335):c.881G>C (p.Ser294Thr)	rs6032606	0.88895
NM_022095.4(ZNF335):c.642C>T (p.Ser214=)	rs3848719	0.32130
NM_022095.4(ZNF335):c.1102+39C>T	rs3746513	0.27648
NM_022095.4(ZNF335):c.1103-7G>A	rs3746512	0.20987
NM_022095.4(ZNF335):c.3522A>T (p.Pro1174=)	rs16990951	0.16743
NM_022095.4(ZNF335):c.3384T>C (p.Pro1128=)	rs3746503	0.10253
NM_022095.4(ZNF335):c.1355+13G>A	rs3746511	0.10246
NM_022095.4(ZNF335):c.2703C>T (p.Ser901=)	rs3746504	0.04113
NM_022095.4(ZNF335):c.2595C>A (p.Asp865Glu)	rs41280276	0.04003
NM_022095.4(ZNF335):c.1623C>T (p.His541=)	rs16990964	0.03634
NM_022095.4(ZNF335):c.2253+10G>T	rs6130977	0.03629
NM_022095.4(ZNF335):c.3487+14G>C	rs73622634	0.02822
NM_022095.4(ZNF335):c.3187C>A (p.Arg1063=)	rs11905235	0.02316
NM_022095.4(ZNF335):c.2167T>G (p.Phe723Val)	rs41305805	0.01608
NM_022095.4(ZNF335):c.3354C>T (p.Leu1118=)	rs35156034	0.01110
NM_022095.4(ZNF335):c.1102+9T>C	rs112458662	0.00945
NM_022095.4(ZNF335):c.3800C>A (p.Pro1267Gln)	rs113958814	0.00829
NM_022095.4(ZNF335):c.3180C>T (p.Pro1060=)	rs61729182	0.00669
NM_022095.4(ZNF335):c.3489T>C (p.Thr1163=)	rs116077790	0.00620
NM_022095.4(ZNF335):c.3507C>T (p.His1169=)	rs141812371	0.00420
NM_022095.4(ZNF335):c.826G>A (p.Ala276Thr)	rs117802609	0.00417
NM_022095.4(ZNF335):c.3488-6G>A	rs201983124	0.00311
NM_022095.4(ZNF335):c.103G>T (p.Val35Leu)	rs114356103	0.00300
NM_022095.4(ZNF335):c.3820-11C>T	rs191147826	0.00194
NM_022095.4(ZNF335):c.1830C>G (p.Leu610=)	rs60180055	0.00009
NM_022095.4(ZNF335):c.2500C>T (p.Pro834Ser)	rs549937846	0.00008
NM_022095.4(ZNF335):c.3670-16dup	rs201440041
NM_022095.4(ZNF335):c.3820-7_3820-6del	rs150750750
NM_022095.4(ZNF335):c.815-3del	rs551678383

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.