{
  "url": "https://dantelabs.com/genes/myo7a/variants/i134n",
  "gene": {
    "slug": "myo7a",
    "symbol": "MYO7A",
    "hgnc": "HGNC:7606",
    "url": "https://dantelabs.com/genes/myo7a"
  },
  "variant": {
    "bundleId": "2026.10.19-9814e911",
    "bundleDate": "2026-10-19",
    "gene": {
      "slug": "myo7a",
      "symbol": "MYO7A",
      "hgnc": "HGNC:7606"
    },
    "slug": "i134n",
    "name": "I134N",
    "formerSlugs": [],
    "sources": [
      {
        "source": "clinvar",
        "release": "2026-10-12"
      },
      {
        "source": "mondo",
        "release": "2026-10-06"
      },
      {
        "source": "hgnc",
        "release": "2026-10-16"
      },
      {
        "source": "clingen",
        "release": "2026-10-19-c4908f54"
      },
      {
        "source": "dbsnp",
        "release": "b157"
      },
      {
        "source": "genedisease",
        "release": "2026-10-19"
      },
      {
        "source": "giab",
        "release": "v3.6"
      },
      {
        "source": "mane",
        "release": "v1.5"
      },
      {
        "source": "mehari",
        "release": "0.11.0"
      }
    ],
    "status": "active",
    "commonName": null,
    "clinvarName": "NM_000260.4(MYO7A):c.401T>A (p.Ile134Asn)",
    "description": null,
    "classification": "pathogenic",
    "stars": 3,
    "tier": "expert",
    "otherNames": [],
    "aliases": [
      "ile134asn",
      "c-401t-a",
      "rs111033181",
      "ca278663"
    ],
    "changedAt": "2026-10-18",
    "identifiers": {
      "allele": "CA278663",
      "rsIds": [
        "rs111033181"
      ],
      "clinvarVariationId": 43230,
      "vcv": "VCV000043230",
      "clinvarAlleleId": 52400
    },
    "locations": [
      {
        "build": "GRCh38",
        "chrom": "11",
        "pos": 77156022,
        "ref": "T",
        "alt": "A"
      },
      {
        "build": "GRCh37",
        "chrom": "11",
        "pos": 76867068,
        "ref": "T",
        "alt": "A"
      }
    ],
    "consequence": {
      "transcript": "NM_000260.4",
      "maneSelect": true,
      "hgvsC": "c.401T>A",
      "hgvsP": "p.Ile134Asn",
      "consequences": [
        "missense_variant"
      ],
      "impact": "moderate"
    },
    "acmg": {
      "rulesVersion": "4",
      "classification": "uncertain-significance",
      "criteria": [
        {
          "code": "PP5",
          "strength": "supporting",
          "clinvar": {
            "classification": "pathogenic",
            "stars": 3
          }
        }
      ],
      "frequencies": [
        {
          "dataset": "gnomad-exomes",
          "version": "4.1",
          "found": true,
          "filtered": false,
          "frequency": 0.00004241827981560363,
          "alleleCount": 62,
          "alleleNumber": 1461634,
          "homozygotes": 0,
          "groupMax": {
            "group": "nfe",
            "frequency": 0.00005126549876877107
          },
          "filteringMax": {
            "group": "nfe",
            "frequency": 0.00004006000017398037
          }
        },
        {
          "dataset": "gnomad-genomes",
          "version": "4.1",
          "found": true,
          "filtered": false,
          "frequency": 0.0000262829358039293,
          "alleleCount": 4,
          "alleleNumber": 152190,
          "homozygotes": 0,
          "groupMax": {
            "group": "amr",
            "frequency": 0.00006545359792653471
          },
          "filteringMax": {
            "group": "nfe",
            "frequency": 0.00001170999985333765
          }
        }
      ]
    },
    "classifications": [
      {
        "mondoId": "MONDO:0019501",
        "name": "Usher Syndrome",
        "classification": "pathogenic",
        "stars": 3,
        "vcv": "VCV000043230",
        "submissions": 1,
        "lastEvaluated": "2024-09-18",
        "expertPanel": "ClinGen Hearing Loss Variant Curation Expert Panel"
      }
    ],
    "reports": [
      {
        "slug": "usher-syndrome",
        "diseases": [
          {
            "mondoId": "MONDO:0019501",
            "name": "Usher Syndrome",
            "inheritance": "autosomal-recessive"
          }
        ]
      }
    ],
    "difficultRegions": []
  },
  "reports": [
    {
      "slug": "usher-syndrome",
      "name": "Usher Syndrome",
      "diseases": [
        {
          "mondoId": "MONDO:0019501",
          "name": "Usher Syndrome",
          "inheritance": "autosomal-recessive",
          "sameAsReport": true
        }
      ],
      "url": "https://dantelabs.com/conditions/usher-syndrome"
    }
  ]
}