"CFP-related condition"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043044	NM_001145252.3(CFP):c.*2A>T	CFP	Single nucleotide variant (3 prime UTR variant)	CFP-related condition	GBenign
Select item 1497624	NM_001145252.3(CFP):c.1360C>G (p.Pro454Ala)	CFP (P454A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 726140	NM_001145252.3(CFP):c.895G>A (p.Asp299Asn)	CFP (D299N)	Single nucleotide variant (missense variant)	CFP-related condition +1 more	GBenign/Likely benign
Select item 1381377	NM_001145252.3(CFP):c.665G>A (p.Arg222His)	CFP (R222H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1608881	NM_001145252.3(CFP):c.391C>G (p.Gln131Glu)	CFP (Q131E)	Single nucleotide variant (missense variant)	CFP-related condition +1 more	GBenign
Select item 235395	NM_001145252.3(CFP):c.236G>A (p.Arg79Gln)	CFP (R79Q)	Single nucleotide variant (missense variant)	CFP-related condition +1 more	GBenign
Select item 1166179	NM_001145252.3(CFP):c.121G>A (p.Gly41Ser)	CFP (G41S)	Single nucleotide variant (missense variant)	CFP-related condition +1 more	GBenign/Likely benign
Select item 1543780	NM_001145252.3(CFP):c.88G>A (p.Val30Met)	CFP (V30M)	Single nucleotide variant (missense variant)	CFP-related condition +1 more	GBenign/Likely benign

ClinVar