List of variants in gene CCNF reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001761.3(CCNF):c.16+214A>C	rs13337091	0.76461
NM_001761.3(CCNF):c.346+22A>G	rs12928789	0.75715
NM_001761.3(CCNF):c.699+75T>G	rs28647184	0.75714
NM_001761.3(CCNF):c.540+161C>T	rs28758190	0.75712
NM_001761.3(CCNF):c.594+87T>C	rs12926008	0.75702
NM_001761.3(CCNF):c.347-132A>T	rs12921396	0.75672
NM_001761.3(CCNF):c.1095-28A>G	rs28417759	0.75558
NM_001761.3(CCNF):c.1218+32T>C	rs8060813	0.75557
NM_001761.3(CCNF):c.540+97G>T	rs28550541	0.71416
NM_001761.3(CCNF):c.1095-7G>A	rs28670436	0.71160
NM_001761.3(CCNF):c.17-183A>G	rs12923030	0.16502
NM_001761.3(CCNF):c.-1G>C	rs13331598	0.04207
NM_001761.3(CCNF):c.17-27C>G	rs9936014	0.04071
NM_001761.3(CCNF):c.1392C>T (p.His464=)	rs147242999	0.00178
NM_001761.3(CCNF):c.111A>G (p.Glu37=)	rs151217933	0.00140
NM_001761.3(CCNF):c.1217G>A (p.Arg406Gln)	rs146438723	0.00120
NM_001761.3(CCNF):c.1773G>A (p.Ala591=)	rs118173479	0.00098
NM_001761.3(CCNF):c.1188G>T (p.Glu396Asp)	rs36008785	0.00051

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