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      "type": "VariantPathogenicityInterpretationGuideline",
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      "@id": "https://api.monarchinitiative.org/api/bioentity/phenotype/MONDO:0010602",
      "id": "MONDO:0010602",
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      "type": "GeneticCondition"
    },
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                          "date": "2025/12/5",
                          "description": "Date on which this evidence was provided"
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                    ],
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            },
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        },
        "id": "CG-PCER-VARINT:CA414919986/MONDO:0010602/071/0/1636",
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                  "date": "2025/12/5",
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                },
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                  "@id": "https://obofoundry.org/sepio/0000156",
                  "id": "SEPIO:0000516",
                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
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            ],
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA414919986/MONDO:0010602/071/el/0/1699/1701",
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                        },
                        "type": "Contribution"
                      }
                    ],
                    "id": "CA414919986/MONDO:0010602/071/ci/CA414919986/MONDO:0010602/071.002",
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                  }
                ],
                "id": "CG-PCER-VARINT:CA414919986/MONDO:0010602/071/0/1774/1776",
                "type": "EvidenceLine"
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            "id": "CG-PCER-VARINT:CA414919986/MONDO:0010602/071/1/1775",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
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          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA414919986/MONDO:0010602/071/0/1774",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA414919986/MONDO:0010602/071",
    "metadata": {
      "created": "2025-12-05T18:05:03.630Z",
      "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, 05 Dec 2025 18:05:03 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA26333-7",
      "id": "LN:LA26333-7",
      "label": "Uncertain Significance"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "d3a7e3f1-03d8-45a1-8c07-de0b02e6ff2c",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA414919986",
      "id": "CAR:CA414919986",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000132.4:c.332C>T"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000132.4(F8):c.332C>T (p.Ala111Val)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-14T14:44:20.376Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}