ClinVar Miner

Submissions for variant NM_000132.3(F8):c.219C>G (p.Phe73Leu) (rs1603436770)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001056 SCV001158177 likely pathogenic Hereditary factor VIII deficiency disease 2019-02-01 criteria provided, single submitter clinical testing The F8 c.219C>G; p.Phe73Leu variant, to our knowledge, is not reported in the medical literature or gene specific databases. However, two other variants resulting in the same p.Phe73Leu amino acid change (c.217T>C and c.219C>A) have been reported in individuals with moderate to severe hemophilia A and are considered pathogenic or likely pathogenic (Berber 2006, He 2013, Johnsen 2017, Factor VIII database). All forms of the p.Phe73Leu variant are absent from general population databases (Exome Variant Server, Genome Aggregation Database), indicating they are not common polymorphisms. The phenylalanine at codon 73 is moderately conserved, and though computational analyses (SIFT: damaging, PolyPhen-2: benign) predict conflicting effects of this variant on protein structure/function, structural modelling suggests the p.Phe73Leu variant perturbs F8 secondary structure (He 2013). Based on available information, the c.219C>G; p.Phe73Leu variant is considered to be likely pathogenic. References: FVIII Database: http://www.factorviii-db.org Berber E et al. DNA microarray analysis for the detection of mutations in hemophilia A. J Thromb Haemost. 2006 Aug;4(8):1756-62. He Z et al. A strategy for the molecular diagnosis in hemophilia a in Chinese population. Cell Biochem Biophys. 2013 Apr;65(3):463-72. Johnsen JM et al. Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiative. Blood Adv. 2017 May 18;1(13):824-834.

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