"Revvity Omics, Revvity"[submitter] AND "F5"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689035	NM_000130.5(F5):c.6357_6359del (p.Asn2119del)	F5 (N2119del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2441325	NM_000130.5(F5):c.5788+3A>G	F5	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2441324	NM_000130.5(F5):c.4724A>G (p.Asn1575Ser)	F5 (N1575S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1098457	NM_000130.5(F5):c.3995T>C (p.Leu1332Pro)	F5 (L1332P)	Single nucleotide variant (missense variant)	Factor V deficiency +1 more	GUncertain significance
Select item 2689036	NM_000130.5(F5):c.3679G>A (p.Gly1227Ser)	F5 (G1227S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1084788	NM_000130.5(F5):c.1181T>C (p.Val394Ala)	F5 (V394A)	Single nucleotide variant (missense variant)	Congenital factor V deficiency +1 more	GConflicting classifications of pathogenicity

ClinVar