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            },
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        },
        "id": "CG-PCER-VARINT:CA414917660/MONDO:0010602/071/0/1735",
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                  "@id": "https://obofoundry.org/sepio/0000156",
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        "id": "CG-PCER-VARINT:CA414917660/MONDO:0010602/071/0/1831",
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                "id": "CG-PCER-VARINT:CA414917660/MONDO:0010602/071/0/1747/1749",
                "type": "EvidenceLine"
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        ],
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        },
        "id": "CG-PCER-VARINT:CA414917660/MONDO:0010602/071/0/1747",
        "type": "EvidenceLine"
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    ],
    "id": "CG-PCER-VARINT:CA414917660/MONDO:0010602/071",
    "metadata": {
      "created": "2026-05-01T15:22:44.739Z",
      "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, 01 May 2026 15:22:44 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
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      "@id": "https://loinc.org/LA26332-9",
      "id": "LN:LA26332-9",
      "label": "Likely Pathogenic"
    },
    "type": "VariantPathogenicityInterpretation",
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    "variant": {
      "@id": "https://reg.genome.network/allele/CA414917660",
      "id": "CAR:CA414917660",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000132.4:c.984T>G"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000132.4(F8):c.984T>G (p.Phe328Leu)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-27T01:33:30.410Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}