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    "assertionMethod": {
      "type": "VariantPathogenicityInterpretationGuideline"
    },
    "condition": {
      "@id": "https://api.monarchinitiative.org/api/bioentity/phenotype/MONDO:0012589",
      "id": "MONDO:0012589",
      "label": "Pitt-Hopkins syndrome",
      "type": "GeneticCondition"
    },
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        "evidenceItem": [
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                },
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                  "label": "curator role",
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                "type": "Contribution"
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                "id": "SEPIO:0000329",
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              "label": "PP3",
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                      }
                    ],
                    "id": "CA402531414/MONDO:0012589/016/ci/CA402531414/MONDO:0012589/016.002",
                    "type": "InfFromBkgrndSciKnow"
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                ],
                "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016/0/1747/1749",
                "type": "EvidenceLine"
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            ],
            "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016/1/1748",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
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        "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016/0/1747",
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                "contributionDate": {
                  "date": "2021/5/17",
                  "description": "Date on which this evidence was provided"
                },
                "contributionRole": {
                  "@id": "https://obofoundry.org/sepio/0000156",
                  "id": "SEPIO:0000516",
                  "label": "curator role",
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                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0051",
              "defaultStrength": {
                "@id": "https://obofoundry.org/sepio/SEPIO:0000330",
                "id": "SEPIO:0000330",
                "label": "Pathogenic Strong"
              },
              "id": "0051",
              "label": "PS2",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA402531414/MONDO:0012589/016/el/0/1663/1665",
                "evidenceItem": [
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                          "id": "CG-PCER-AGENT:CG_50022_EP161901869799975",
                          "type": "Agent"
                        },
                        "comments": "The p.Gly496Cys variant in TCF4 occurs in the confirmed de novo state in an individual with a neurodevelopmental disorder consistent with TCF4 abnormality",
                        "contributionDate": {
                          "date": "2021/5/17",
                          "description": "Date on which this evidence was provided"
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                      }
                    ],
                    "id": "CA402531414/MONDO:0012589/016/ci/CA402531414/MONDO:0012589/016.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016/0/1663/1665",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016/1/1664",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016/0/1663",
        "type": "EvidenceLine"
      },
      {
        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA402531414/MONDO:0012589/016/el/0/1636",
        "evidenceItem": [
          {
            "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA402531414/MONDO:0012589/016/ei/1/1637",
            "contribution": [
              {
                "agent": {
                  "@id": "https://erepo.genome.network/evrepo/api//agent/CG_50022_EP161901869799975",
                  "id": "CG-PCER-AGENT:CG_50022_EP161901869799975",
                  "type": "Agent"
                },
                "contributionDate": {
                  "date": "2021/5/17",
                  "description": "Date on which this evidence was provided"
                },
                "contributionRole": {
                  "@id": "https://obofoundry.org/sepio/0000156",
                  "id": "SEPIO:0000516",
                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0030",
              "defaultStrength": {
                "@id": "https://obofoundry.org/sepio/SEPIO:0000329",
                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
              },
              "id": "0030",
              "label": "PM2",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA402531414/MONDO:0012589/016/el/0/1636/1638",
                "evidenceItem": [
                  {
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                    "contribution": [
                      {
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                          "type": "Agent"
                        },
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                          "date": "2021/5/17",
                          "description": "Date on which this evidence was provided"
                        },
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                          "@id": "https://obofoundry.org/sepio/0000156",
                          "id": "SEPIO:0000516",
                          "label": "curator role",
                          "type": "ContributoryRole"
                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA402531414/MONDO:0012589/016/ci/CA402531414/MONDO:0012589/016.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016/0/1636/1638",
                "type": "EvidenceLine"
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            ],
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            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016/0/1636",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA402531414/MONDO:0012589/016",
    "metadata": {
      "created": "2024-09-27T21:51:02.225Z",
      "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": "Fri, 27 Sep 2024 21:51:02 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA26332-9",
      "id": "LN:LA26332-9",
      "label": "Likely Pathogenic"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "0a189478-9ece-44c0-87b9-f803923296b4",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA402531414",
      "id": "CAR:CA402531414",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_001348220.1:c.1411G>T"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_001348220.1:c.1411G>T"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-29T15:07:18.969Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}