Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Versiti Diagnostic Laboratories, |
RCV004595878 | SCV005089671 | pathogenic | Mild hemophilia A | 2024-04-10 | criteria provided, single submitter | clinical testing | The missense variant F8 c.1648C>T, p.Arg550Cys (p.R550C; legacy p.R531C) in exon 11 changes amino acid arginine at codon 550 to cysteine. The arginine at this residue is fairly well conserved among species. This amino acid change occurs at the interface of the A1 and A2 domains. Pathogenic variants in F8 are associated with X-linked hemophilia A characterized by mild to severe bleeding due to a quantitative or qualitative deficiency in factor VIII. This sequence variant has been previously reported in patients with mild to moderate hemophilia A, both with and without the development of inhibitors (PMID:1924291; PMID:8547094; PMID:16769589; PMID:17286776; PMID:20331753; PMID:23926300; PMID:29296726). Patients carrying this variant show discrepancy between 1-stage and 2-stage factor VIII activity assays, with a lower measurement recorded with 2-stage assay (PMID:17286776). This variant was observed in 6 males and 3 females within our laboratory cohort. All 6 males within our laboratory cohort had clot based factor VIII activity levels consistent with moderate or mild hemophilia A; 3 out of 6 males had VWD 2N ruled out by either a 2N binding assay or by negative next generation sequencing. The minor allele frequency of this variant in the general population is 0.000008993 (GnomAD v3). No functional data is available for this variant. In silico computational evidence (REVEL) predicts the variant to be damaging (>=0.644 ); however, computational evidence alone is not sufficient to classify a variant. Different variants causing a change at the same amino acid (c.1648C>G, p.R550G; c.1649G>A, p.R550H; c.1649G>T, p.R550L; c.1649G>C, p.R550P) have also been reported in patients with mild to severe hemophilia A (PMID:1924291; PMID:19473423; PMID:8547094; PMID:11157485; PMID:18179574; PMID:29296726). Functional studies of the alternate p.R550H variant using recombinant protein demonstrated a similar discrepant activity between 1-stage and 2-stage assays and showed an increased rate of A2 subunit dissociation correlating with inactivation of FVIIIa (PMID:11157485). In summary, the collective evidence supports F8 c.1648C>T, p.Arg550Cys as a pathogenic variant for mild to moderate hemophilia A. |
| OMIM | RCV000010936 | SCV000031163 | pathogenic | Hereditary factor VIII deficiency disease | 1992-07-01 | no assertion criteria provided | literature only |