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    1. F5-P9,10,11PRSS56: c.[1066dupC];[1066dupC],p.[Gln356ProfsX152];[Gln356ProfsX152

      Case#: Gal_2011_Family_5_Proband_P9, female, age 21 years at time of report, family national origin described as Saudi

      CasePresentingHPOs: Hypermetropia HP:0000540, Microphthalmia HP:0000568

      CaseHPOFreeText: The proband received a diagnosis of posterior microphthalmos, with one feature being a moderate papillomacular fold.

      CaseNotHPOs: Ocular hypertension HP:0007906

      CaseNotHPOFreeText: N/A

      CasePreviousTesting: The proband's family may have been previously subjected to linkage mapping, and was also previously genotyped by Sanger sequencing of the MFRP locus.

      CaseMethod1: Sanger sequencing of MFRP

      CaseMethod2: Sanger sequencing of PRSS56

      CaseGenotypingMethod: The proband's family may have been previously subjected to linkage mapping, and was also previously genotyped by Sanger sequencing of the MFRP locus, followed by Sanger sequencing of PRSS56.

      Variant: The individual harbors the NM_001195129.2(PRSS56):c.1066dup (p.Gln356fs) variant in the homozygous state.

      ClinVar: 31077

      gnomAD: This variant is found in gnomAD v4.1.0 at a frequency of 0.0008496 in the Middle Eastern population https://gnomad.broadinstitute.org/variant/2-232523817-A-AC?dataset=gnomad_r4

      VariantEvidence: NM_001195129.2(PRSS56):c.1066dup (p.Gln356fs) is a frameshift variant in exon 9 of 13 and is predicted to trigger nonsense-mediated decay.

      CaseAddInfo: The proband is from a cohort where more than half of the families had known consanguinity.

      CasePMIDs: N/A