ClinVar Miner

Submissions for variant NM_000132.3(F8):c.606T>G (p.Ser202Arg) (rs1603436217)

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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 RCV001001316 SCV001158501 likely pathogenic Hereditary factor VIII deficiency disease 2019-06-07 criteria provided, single submitter clinical testing The F8 c.606T>G; p.Ser202Arg variant, also reported as Ser183Arg, has been described in at least one individual with mild hemophilia A (HA; see link to F8 database, Moller-Morlang 1999). It is absent from general population databases (Exome Variant Server and Genome Aggregation Database), indicating it is not a common polymorphism. Another variant at this codon (c.605G>A; p.Ser202Asn) as well as several missense variants at surrounding codons (197, 198, 200, 201, 203) have been described in individuals affected with HA (see link to F8 database and references therein, Arruda 1995, Guillet 2006, Lu 2018). Based on available information, the p.Ser202Arg variant is considered likely pathogenic. REFERENCES Link to F8 database: Arruda V et al. Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients. Blood. 1995 Oct 15;86(8):3015-20. Guillet B et al. Detection of 95 novel mutations in coagulation factor VIII gene F8 responsible for hemophilia A: results from a single institution. Hum Mutat. 2006 Jul;27(7):676-85. Lu Y et al. Spectrum and origin of mutations in sporadic cases of haemophilia A in China. Haemophilia. 2018 Mar;24(2):291-298. Moller-Morlang K et al. Mutational-screening in the factor VIII gene resulting in the identification of three novel mutations, one of which is a donor splice mutation. Hum Mutat. 1999;13(6):504.

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