List of variants in gene CCNF reported as likely benign for not provided

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001761.3(CCNF):c.111A>G (p.Glu37=)	rs151217933	0.00140
NM_001761.3(CCNF):c.1773G>A (p.Ala591=)	rs118173479	0.00098
NM_001761.3(CCNF):c.1287C>T (p.His429=)	rs151164394	0.00054
NM_001761.3(CCNF):c.1715+9C>T	rs201692958	0.00019
NM_001761.3(CCNF):c.540+3G>A	rs772207315	0.00013
NM_001761.3(CCNF):c.1677C>T (p.His559=)	rs555465125	0.00006
NM_001761.3(CCNF):c.498C>T (p.Ala166=)	rs150541774	0.00006
NM_001761.3(CCNF):c.1500C>T (p.Asp500=)	rs749156038	0.00005
NM_001761.3(CCNF):c.1362C>T (p.Ala454=)	rs373935407	0.00002
NM_001761.3(CCNF):c.1335C>T (p.Ser445=)	rs529445674	0.00001
NM_001761.3(CCNF):c.1464C>T (p.Cys488=)	rs753110068	0.00001
NM_001761.3(CCNF):c.1638C>T (p.Ser546=)	rs778768659	0.00001
NM_001761.3(CCNF):c.1715+10C>T	rs184804277	0.00001
NM_001761.3(CCNF):c.1737G>A (p.Gln579=)	rs761337879	0.00001
NM_001761.3(CCNF):c.177C>T (p.His59=)	rs772632798
NM_001761.3(CCNF):c.278+7C>G	rs1596914265

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.