List of variants in gene CFP reported as 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

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HGVS	dbSNP	gnomAD frequency
NM_001145252.3(CFP):c.1284C>T (p.Asn428=)	rs1048118	0.23155
NM_001145252.3(CFP):c.748G>A (p.Gly250Ser)	rs8177077	0.00366
NM_001145252.3(CFP):c.157G>A (p.Val53Met)	rs8177068	0.00274
NM_001145252.3(CFP):c.403+9G>A	rs8177075	0.00217
NM_001145252.3(CFP):c.895G>A (p.Asp299Asn)	rs61737993	0.00182
NM_001145252.3(CFP):c.940+7A>G	rs375455564	0.00046
NM_001145252.3(CFP):c.121G>A (p.Gly41Ser)	rs374687577	0.00030
NM_001145252.3(CFP):c.663C>T (p.Ser221=)	rs367635632	0.00023
NM_001145252.3(CFP):c.716C>T (p.Pro239Leu)	rs200036265	0.00022
NM_001145252.3(CFP):c.88G>A (p.Val30Met)	rs138456565	0.00013
NM_001145252.3(CFP):c.1332G>T (p.Gly444=)	rs141133000	0.00012
NM_001145252.3(CFP):c.135C>T (p.Gly45=)	rs767157838	0.00004
NM_001145252.3(CFP):c.236G>A (p.Arg79Gln)	rs761962858	0.00002
NM_001145252.3(CFP):c.391C>G (p.Gln131Glu)	rs371132642	0.00001
NM_001145252.3(CFP):c.611C>T (p.Pro204Leu)	rs8177076
NM_001145252.3(CFP):c.717G>A (p.Pro239=)

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