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      "type": "VariantPathogenicityInterpretationGuideline",
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      "id": "MONDO:0700270",
      "label": "ATM-related cancer predisposition",
      "type": "GeneticCondition"
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            },
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                          "description": "Date on which this evidence was provided"
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              "label": "Met"
            },
            "type": "CriterionAssessment"
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        ],
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          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA287019/MONDO:0700270/020/0/1696",
        "type": "EvidenceLine"
      },
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                  "description": "Date on which this evidence was provided"
                },
                "contributionRole": {
                  "@id": "https://obofoundry.org/sepio/0000156",
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                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA287019/MONDO:0700270/020/el/0/1798/1800",
                "evidenceItem": [
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                        },
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                          "date": "2025/9/15",
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                        "type": "Contribution"
                      }
                    ],
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            ],
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              "label": "Not Met"
            },
            "type": "CriterionAssessment"
          }
        ],
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        },
        "id": "CG-PCER-VARINT:CA287019/MONDO:0700270/020/0/1798",
        "type": "EvidenceLine"
      },
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                  "description": "Date on which this evidence was provided"
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                        },
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                          "description": "Date on which this evidence was provided"
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                ],
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                "type": "EvidenceLine"
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            "statementOutcome": {
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            },
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        ],
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          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA287019/MONDO:0700270/020/0/1747",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA287019/MONDO:0700270/020",
    "metadata": {
      "created": "2025-09-15T21:20:22.828Z",
      "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": "Mon, 15 Sep 2025 21:20:22 -0000",
      "schemaLabel": "Evidence Repository.Beta-1 (Unofficial)",
      "version": "2.0.0"
    },
    "statementOutcome": {
      "@id": "https://loinc.org/LA26332-9",
      "id": "LN:LA26332-9",
      "label": "Likely Pathogenic"
    },
    "type": "VariantPathogenicityInterpretation",
    "uuid": "a1f4fda0-ab77-4c22-a6be-6dc2f95f8e60",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA287019",
      "id": "CAR:CA287019",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000051.4:c.8494C>T"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000051.4(ATM):c.8494C>T (p.Arg2832Cys)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-11-02T03:17:16.919Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}