List of variants in gene CCNF reported as likely benign for CCNF-related disorder

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

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001761.3(CCNF):c.1233G>A (p.Val411=)	rs111543933	0.00119
NM_001761.3(CCNF):c.1188G>T (p.Glu396Asp)	rs36008785	0.00051
NM_001761.3(CCNF):c.1592T>G (p.Leu531Arg)	rs372723774	0.00014
NM_001761.3(CCNF):c.540+3G>A	rs772207315	0.00013
NM_001761.3(CCNF):c.1047G>T (p.Arg349=)	rs144631476	0.00010
NM_001761.3(CCNF):c.435C>T (p.Ala145=)	rs200978756	0.00007
NM_001761.3(CCNF):c.1056C>T (p.Leu352=)	rs2141824569
NM_001761.3(CCNF):c.347-4G>A	rs374319260
NM_001761.3(CCNF):c.750C>T (p.Tyr250=)

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