"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "FA - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 257495	NM_018062.4(FANCL):c.981T>C (p.Ser327=)	FANCL	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group L +3 more	GBenign
Select item 241253	NM_018062.4(FANCL):c.963T>A (p.Asp321Glu)	FANCL (D321E +3 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 241252	NM_018062.4(FANCL):c.670A>G (p.Thr224Ala)	FANCL (T224A +3 more)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign
Select item 257494	NM_018062.4(FANCL):c.375-49C>G	FANCL	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 257493	NM_018062.4(FANCL):c.217-11T>C	FANCL	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 456243	NM_018062.4(FANCL):c.203G>C (p.Arg68Pro)	FANCL (R68P)	Single nucleotide variant (missense variant)	FANCL-related condition +3 more	GConflicting classifications of pathogenicity
Select item 221092	NM_018062.4(FANCL):c.112C>T (p.Leu38Phe)	FANCL (L38F)	Single nucleotide variant (missense variant)	Fanconi anemia +4 more	GConflicting classifications of pathogenicity

ClinVar