ClinVar Miner

Submissions for variant NM_000132.3(F8):c.6245G>A (p.Ser2082Asn) (rs1569559494)

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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 RCV000757252 SCV000885402 uncertain significance not provided 2018-03-01 criteria provided, single submitter clinical testing The F8 c.6245G>A; p.Ser2082Asn variant, also known as Ser2063Asn, is reported in the medical literature in an individual with reportedly severe hemophilia (Cutler 2002). Additionally, another variant in the same codon, p.Ser2082Thr, is reported in the literature in an individual with mild hemophilia (Nair 2014). The c.6245G>A; p.Ser2082Asn variant is not reported in the ClinVar database or in the general population databases (1000 Genomes Project, Exome Variant Server, Genome Aggregation Database), indicating it is not a common polymorphism. The serine at this position is well conserved and computational algorithms (PolyPhen-2, SIFT) predict this variant is deleterious. Considering available information, the clinical significance of this variant cannot be determined with certainty. References: Cutler JA et al. The identification and classification of 41 novel mutations in the factor VIII gene (F8C). Hum Mutat. 2002 Mar;19(3):274-8. Nair PS et al. Mutations in intron 1 and intron 22 inversion negative haemophilia A patients from Western India. PLoS One. 2014 May 20;9(5):e97337.

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