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      "type": "GeneticCondition"
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                "id": "SEPIO:0000216",
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              },
              "id": "0039",
              "label": "PS3",
              "type": "Criterion"
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            ],
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        ],
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        "id": "CG-PCER-VARINT:CA000283/MONDO:0017623/003/0/1825",
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      },
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        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA000283/MONDO:0017623/003/el/0/1786",
        "evidenceItem": [
          {
            "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA000283/MONDO:0017623/003/ei/1/1787",
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                "agent": {
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                "type": "Contribution"
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            ],
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              "@id": "https://obofoundry.org/sepio/clingen/0046",
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                "label": "Pathogenic Moderate"
              },
              "id": "0046",
              "label": "PS1",
              "type": "Criterion"
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                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA000283/MONDO:0017623/003/el/0/1786/1788",
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                },
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                  "label": "curator role",
                  "type": "ContributoryRole"
                },
                "type": "Contribution"
              }
            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0061",
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000329",
                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
              },
              "id": "0061",
              "label": "PP2",
              "type": "Criterion"
            },
            "evidenceLine": [
              {
                "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA000283/MONDO:0017623/003/el/0/1837/1839",
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                ],
                "id": "CG-PCER-VARINT:CA000283/MONDO:0017623/003/0/1837/1839",
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              "label": "Met"
            },
            "type": "CriterionAssessment"
          }
        ],
        "evidenceStrength": {
          "@id": "https://obofoundry.org/sepio"
        },
        "id": "CG-PCER-VARINT:CA000283/MONDO:0017623/003/0/1837",
        "type": "EvidenceLine"
      },
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        "@id": "https://erepo.genome.network/evrepo/api/interpretation/CA000283/MONDO:0017623/003/el/0/1747",
        "evidenceItem": [
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                  "label": "curator role",
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                },
                "type": "Contribution"
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            ],
            "criterion": {
              "@id": "https://obofoundry.org/sepio/clingen/0062",
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                "@id": "https://obofoundry.org/sepio/SEPIO:0000329",
                "id": "SEPIO:0000329",
                "label": "Pathogenic Supporting"
              },
              "id": "0062",
              "label": "PP3",
              "type": "Criterion"
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            "evidenceLine": [
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                        "comments": "REVEL score > 0.7 (score of this variant = 0.995)\n[ In addition, SpliceAI shows weak SAS loss score 0.18 and some SAS gain score 0.27]\n",
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                          "date": "2023/10/18",
                          "description": "Date on which this evidence was provided"
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                      }
                    ],
                    "id": "CA000283/MONDO:0017623/003/ci/CA000283/MONDO:0017623/003.002",
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                ],
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            ],
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              "@id": "SEPIO:0000224",
              "label": "Met"
            },
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        ],
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        },
        "id": "CG-PCER-VARINT:CA000283/MONDO:0017623/003/0/1747",
        "type": "EvidenceLine"
      }
    ],
    "id": "CG-PCER-VARINT:CA000283/MONDO:0017623/003",
    "metadata": {
      "created": "2024-09-28T03:07:37.153Z",
      "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": "Sat, 28 Sep 2024 03:07:36 -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": "6978957a-8d30-4cb6-8f2a-f14e69a78254",
    "variant": {
      "@id": "https://reg.genome.network/allele/CA000283",
      "id": "CAR:CA000283",
      "relatedContextualAllele": [
        {
          "alleleName": [
            {
              "name": "NM_000314.8:c.106G>C"
            }
          ],
          "preferred": true
        }
      ],
      "relatedIdentifier": [
        {
          "label": "NM_000314.8(PTEN):c.106G>C (p.Gly36Arg)"
        }
      ],
      "type": "CAR"
    }
  },
  "metadata": {
    "rendered": {
      "by": "https://erepo.genome.network/evrepo/api/summary/srvc",
      "when": "2026-11-04T21:45:38.120Z"
    }
  },
  "status": {
    "code": 200,
    "name": "OK"
  }
}