"Illumina Laboratory Services, Illumina"[submitter] AND "LOC130005443" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 418190	NM_022725.4(FANCF):c.1087C>T (p.Gln363Ter)	FANCF, LOC130005443 (Q363*)	Single nucleotide variant (nonsense)	not provided +3 more	GUncertain significance
Select item 877894	NM_022725.4(FANCF):c.1064G>A (p.Arg355His)	LOC130005443, FANCF (R355H)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group F +1 more	GUncertain significance
Select item 877895	NM_022725.4(FANCF):c.1063C>T (p.Arg355Cys)	FANCF, LOC130005443 (R355C)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group F	GUncertain significance
Select item 304200	NM_022725.4(FANCF):c.1006G>A (p.Asp336Asn)	FANCF, LOC130005443 (D336N)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group F	GUncertain significance
Select item 878061	NM_022725.4(FANCF):c.970A>G (p.Lys324Glu)	FANCF, LOC130005443 (K324E)	Single nucleotide variant (missense variant)	Fanconi anemia +1 more	GConflicting classifications of pathogenicity
Select item 134351	NM_022725.4(FANCF):c.959C>T (p.Pro320Leu)	FANCF, LOC130005443 (P320L)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign

ClinVar