"OMIM"[submitter] AND "FANCF"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1169400	NM_022725.4(FANCF):c.534del (p.Lys179fs)	FANCF (K179fs)	Deletion (frameshift variant)	Fanconi anemia complementation group F	GPathogenic
Select item 6343	NM_022725.4(FANCF):c.484_485del (p.Leu162fs)	FANCF (L162fs)	Microsatellite (frameshift variant)	Fanconi anemia +2 more	GPathogenic
Select item 1169397	NM_022725.4(FANCF):c.438_451del (p.Leu146_Arg147insTer)	FANCF	Deletion (frameshift variant)	Fanconi anemia complementation group F	GPathogenic
Select item 6341	NM_022725.4(FANCF):c.351_397del (p.Gly120fs)	FANCF (G120fs)	Deletion (frameshift variant)	Fanconi anemia +1 more	GPathogenic
Select item 6344	NM_022725.4(FANCF):c.327C>G (p.Tyr109Ter)	FANCF (Y109*)	Single nucleotide variant (nonsense)	Fanconi anemia complementation group F	GPathogenic
Select item 6340	NM_022725.4(FANCF):c.230_252del (p.Val77fs)	FANCF	Deletion (frameshift variant)	Fanconi anemia complementation group F +1 more	GPathogenic
Select item 929562	NM_022725.4(FANCF):c.219del (p.Arg74fs)	FANCF (R74fs)	Deletion (frameshift variant)	Fanconi anemia complementation group F +1 more	GPathogenic
Select item 6342	NM_022725.4(FANCF):c.16C>T (p.Gln6Ter)	FANCF (Q6*)	Single nucleotide variant (nonsense)	Fanconi anemia complementation group F	GPathogenic

ClinVar