1 Matching Annotations
  1. Last 7 days
    1. 1 insertion of 2 base pairs

      Case#: One patient from Egypt

      DiseaseAssertion: MPS1-H

      FamilyInfo: Consanguinity present in the family

      CasePresentingHPOs: N/A

      CaseHPOFreeText: N/A

      CaseNotHPOs: N/A

      CaseNotHPOFreeText: N/A

      CaseEnzymeAssay: N/A

      CaseUrineGAGs: N/A

      CaseERT: N/A

      CaseBMT: N/A

      Variant1: c.682insAC in paper but correct nomenclature is c.594_595insAC (p.Leu199ThrfsTer2)

      Variant1ClinVarID: N/A

      Variant1CAID: CA2586973525

      Variant2: c.682insAC in paper but correct nomenclature is c.594_595insAC (p.Leu199ThrfsTer2)

      Variant2ClinVarID: N/A

      Variant2CAID: CA2586973525

      AdditionalVariants: c.346G>A (p.G116R)

      ParentalGenotype: N/A

      PreviouslyPublished N/A