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    Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes
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    1. ClingenBaseline 22 Oct 2026
      c.6113A>G

      Case#: 28

      DiseaseAssertion: Hemophilia A

      FamilyInfo: NA

      ParentalTesting: NA

      CasePresentingHPOs: NA

      CaseHPOFreeText: FVIII:C 5/3% (Moderate Phenotype), No inhibitors present

      CasePreviousTesting: Screened for IVS-22 and IVS-1, sample was blinded for NGS and the sequencing component was validated by comparing results with Sanger Sequencing

      Gene: F8

      Variant: NM_000132.3(F8):c.6113A>G (p.Asn2038Ser)

      ClinVar: 10305 https://www.ncbi.nlm.nih.gov/clinvar/variation/10305/

      CAID: CA255198

      gnomAD: Not reported

      DiseaseEntity:FactorVIIIDeficiency Mutation:Missense FVIIItesting:Partial ParentalTest:Unknown ClinVarID:10305 CAID:CA255198 Zygosity:NoZygosityAssertion InheritancePattern:NoInheritanceAssertion CaseInfo HGNC:3546 Gene:F8 inferred_gene_hgnc:3546 inferred_gene_source:hgnc_tag ClinGen Coag Fac Def VCEP
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    www-thieme-connect-com.libproxy.lib.unc.edu/products/ejournals/pdf/10.1160/TH16-05-0375.pdf