"Fulgent Genetics, Fulgent Genetics"[submitter] AND "F5"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 716051	NM_000130.5(F5):c.6554A>G (p.Lys2185Arg)	F5 (K2185R)	Single nucleotide variant (missense variant)	Factor V deficiency +7 more	GBenign/Likely benign
Select item 579171	NM_000130.5(F5):c.5265A>G (p.Ile1755Met)	F5 (I1755M)	Single nucleotide variant (missense variant)	Thrombophilia due to activated protein C resistance +9 more	GConflicting classifications of pathogenicity
Select item 716052	NM_000130.5(F5):c.4923C>T (p.Leu1641=)	F5	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +8 more	GBenign/Likely benign
Select item 875953	NM_000130.5(F5):c.3952C>A (p.Gln1318Lys)	F5 (Q1318K)	Single nucleotide variant (missense variant)	Factor V deficiency +6 more	GLikely benign
Select item 716054	NM_000130.5(F5):c.3162A>C (p.Glu1054Asp)	F5 (E1054D)	Single nucleotide variant (missense variant)	Inborn genetic diseases +7 more	GConflicting classifications of pathogenicity
Select item 716055	NM_000130.5(F5):c.2129A>G (p.His710Arg)	F5 (H710R)	Single nucleotide variant (missense variant)	Factor V deficiency +6 more	GBenign

ClinVar