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      "type": "VariantPathogenicityInterpretationGuideline",
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            },
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          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA314820/MONDO:0012999/026/0/1645",
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      },
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                },
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                  "date": "2025/3/13",
                  "description": "Date on which this evidence was provided"
                },
                "contributionRole": {
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                  "label": "curator role",
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                "type": "Contribution"
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            ],
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA314820/MONDO:0012999/026/el/0/1780/1782",
                "evidenceItem": [
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                          "date": "2025/3/13",
                          "description": "Date on which this evidence was provided"
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              "label": "Not Met"
            },
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        ],
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        "id": "CG-PCER-VARINT:CA314820/MONDO:0012999/026/0/1780",
        "type": "EvidenceLine"
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                        },
                        "type": "Contribution"
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                    ],
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                    "type": "InfFromBkgrndSciKnow"
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                ],
                "id": "CG-PCER-VARINT:CA314820/MONDO:0012999/026/0/1636/1638",
                "type": "EvidenceLine"
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            ],
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            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
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          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA314820/MONDO:0012999/026/0/1636",
        "type": "EvidenceLine"
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    ],
    "id": "CG-PCER-VARINT:CA314820/MONDO:0012999/026",
    "metadata": {
      "created": "2025-03-13T23:10:05.428Z",
      "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": "Thu, 13 Mar 2025 23:10:05 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "1.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA26334-5",
      "id": "LN:LA26334-5",
      "label": "Likely Benign"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "48f641c9-b475-4f6d-85fc-a2b3a05ba365",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA314820",
      "id": "CAR:CA314820",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000156.6:c.587C>T"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000156.6(GAMT):c.587C>T (p.Ala196Val)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-15T18:16:22.389Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}