List of variants in gene CCNF reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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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.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.1638C>T (p.Ser546=)	rs778768659	0.00001

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