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                          "id": "CG-PCER-AGENT:CG_50016_EP163553328993009",
                          "type": "Agent"
                        },
                        "comments": "Two other missense variants at the same residue, c.478G>A (p.Asp160Asn) and c.478G>C (p.Asp160His), have been interpreted as pathogenic by the ClinGen MDEP (PM5_Strong).",
                        "contributionDate": {
                          "date": "2026/1/28",
                          "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"
                      }
                    ],
                    "id": "CA367401841/MONDO:0015967/086/ci/CA367401841/MONDO:0015967/086.002",
                    "type": "InfFromBkgrndSciKnow"
                  }
                ],
                "id": "CG-PCER-VARINT:CA367401841/MONDO:0015967/086/0/1621/1623",
                "type": "EvidenceLine"
              }
            ],
            "id": "CG-PCER-VARINT:CA367401841/MONDO:0015967/086/1/1622",
            "statementOutcome": {
              "@id": "SEPIO:0000224",
              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA367401841/MONDO:0015967/086/0/1621",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA367401841/MONDO:0015967/086",
    "metadata": {
      "created": "2026-01-28T21:10:33.554Z",
      "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, 28 Jan 2026 21:10:33 -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": "5ef647b2-9826-4493-a4bf-8bd943827046",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA367401841",
      "id": "CAR:CA367401841",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_033508.3:c.477T>A"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_033508.3:c.477T>A"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-10-28T15:53:28.099Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}