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                        "comments": "This variant has not been identified de novo.\n",
                        "contributionDate": {
                          "date": "2026/2/18",
                          "description": "Date on which this evidence was provided"
                        },
                        "contributionRole": {
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                          "id": "SEPIO:0000516",
                          "label": "curator role",
                          "type": "ContributoryRole"
                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA119174/MONDO:0005338/019/ci/CA119174/MONDO:0005338/019.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1663/1665",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/1/1664",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Not Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1663",
        "type": "EvidenceLine"
      },
      {
        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA119174/MONDO:0005338/019/el/0/1735",
        "evidenceItem": [
          {
            "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA119174/MONDO:0005338/019/ei/1/1736",
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              {
                "agent": {
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                },
                "contributionRole": {
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                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA119174/MONDO:0005338/019/el/0/1735/1737",
                "evidenceItem": [
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                          "type": "Agent"
                        },
                        "comments": "Only 1 proband with JOAG had been reported (PMID: 9328473), not meeting the ≥ 2 probands threshold required to meet PS4_Supporting.",
                        "contributionDate": {
                          "date": "2026/2/18",
                          "description": "Date on which this evidence was provided"
                        },
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                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA119174/MONDO:0005338/019/ci/CA119174/MONDO:0005338/019.002",
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                ],
                "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1735/1737",
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              }
            ],
            "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/1/1736",
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        ],
        "evidenceStrength": {
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      },
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        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA119174/MONDO:0005338/019/el/0/1804",
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              {
                "agent": {
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                  "description": "Date on which this evidence was provided"
                },
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                  "label": "curator role",
                  "type": "ContributoryRole"
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                "type": "Contribution"
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            ],
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA119174/MONDO:0005338/019/el/0/1804/1806",
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                ],
                "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1804/1806",
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            ],
            "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/1/1805",
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              "@id": "SEPIO:0000224",
              "label": "Not Met"
            },
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        ],
        "evidenceStrength": {
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        "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1804",
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                          "date": "2026/2/18",
                          "description": "Date on which this evidence was provided"
                        },
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                    ],
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                "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1588/1590",
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            "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/1/1589",
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              "label": "Not Met"
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          }
        ],
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        "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1588",
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      },
      {
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            ],
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                          "type": "Agent"
                        },
                        "comments": "This criterion did not apply to this variant.   \n",
                        "contributionDate": {
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                          "description": "Date on which this evidence was provided"
                        },
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        ],
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                        },
                        "comments": "PM5_Supporting could not be applied to this novel missense variant as although it did meet PP3, the Grantham score was lower (= 142) than the score for the different missense change at the same amino acid residue determined to be likely pathogenic by the ClinGen Glaucoma VCEP (c.1430T>A, p.Ile477Asn, Grantham score = 149, ClinVar ID: 30205).\n\n",
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        ],
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        "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1780",
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        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA119174/MONDO:0005338/019/el/0/1591",
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            ],
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                        "comments": "This criterion did not apply to this variant.   ",
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                "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1591/1593",
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            "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/1/1592",
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        ],
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        "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1591",
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                "type": "Contribution"
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            ],
            "evidenceLine": [
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                          "id": "CG-PCER-AGENT:CG_50053_EP164427275875204",
                          "type": "Agent"
                        },
                        "comments": "20 segregations in 1 family, with juvenile or primary open angle glaucoma (JOAG or POAG), have been reported (PMIDs: 9328473), which fulfilled PP1_Moderate (≥5 meioses in ≥1 family, but not the ≥7 meioses in >1 family for the strong criterion).",
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                          "label": "curator role",
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                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA119174/MONDO:0005338/019/ci/CA119174/MONDO:0005338/019.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1630/1632",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/1/1631",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019/0/1630",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA119174/MONDO:0005338/019",
    "metadata": {
      "created": "2026-02-18T22:18:46.516Z",
      "note": "DISCLAIMER: While the data/content in this document is approved by ClinGen expert panel(s), the SEPIO schema presented here is an initial prototype and has not been reviewed nor finalized by the ClinGen Data Exchange Modeling Team. We expect it to differ significantly from the final schema.",
      "producedAtUTC": "Wed, 18 Feb 2026 22:18:46 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "2.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA26332-9",
      "id": "LN:LA26332-9",
      "label": "Likely Pathogenic"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "6e296ba8-41a9-4f53-b189-0d71102717a4",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA119174",
      "id": "CAR:CA119174",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000261.2:c.1430T>G"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000261.2(MYOC):c.1430T>G (p.Ile477Ser)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-11-02T12:22:34.490Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}