"premutation" meaning in All languages combined

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "pre",
        "3": "mutation"
      },
      "expansion": "pre- + mutation",
      "name": "prefix"
    }
  ],
  "etymology_text": "From pre- + mutation.",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "premutation (not comparable)",
      "name": "en-adj"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "adj",
  "senses": [
    {
      "categories": [],
      "examples": [
        {
          "ref": "2015 July 30, “Positron Emission Tomography (PET) Quantification of GABA A Receptors in the Brain of Fragile X Patients”, in PLOS ONE, →DOI:",
          "text": "Fragile X syndrome is caused by mutations in the FMR1-gene, which is characterized by an expansion of a CGG triplet in the 5’ UTR. Normal individuals have 6–44 CGG repeats, while carriers of gray zone or premutation alleles have 45–54 and 55–200 repeats, respectively.",
          "type": "quote"
        }
      ],
      "glosses": [
        "Of or relating to a premutation."
      ],
      "id": "en-premutation-en-adj-GW6IWIlC",
      "links": [
        [
          "premutation",
          "#Noun"
        ]
      ],
      "tags": [
        "not-comparable"
      ]
    }
  ],
  "word": "premutation"
}

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "pre",
        "3": "mutation"
      },
      "expansion": "pre- + mutation",
      "name": "prefix"
    }
  ],
  "etymology_text": "From pre- + mutation.",
  "forms": [
    {
      "form": "premutations",
      "tags": [
        "plural"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {},
      "expansion": "premutation (plural premutations)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "_dis": "1 99",
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
            "Entries with incorrect language header",
            "Entry maintenance"
          ],
          "source": "w+disamb"
        },
        {
          "_dis": "9 91",
          "kind": "other",
          "name": "English terms prefixed with pre-",
          "parents": [],
          "source": "w+disamb"
        },
        {
          "_dis": "0 100",
          "kind": "other",
          "name": "Pages with 1 entry",
          "parents": [],
          "source": "w+disamb"
        },
        {
          "_dis": "0 100",
          "kind": "other",
          "name": "Pages with entries",
          "parents": [],
          "source": "w+disamb"
        }
      ],
      "glosses": [
        "A nucleotide sequence variation that is not enough to be classed as a mutation (for example, does not affect protein expression enough to produce clinical symptoms) but nonetheless represents an unusual variant that is predisposed to still greater variation in future cell divisions (that is, predisposed to leading to a mutation)."
      ],
      "id": "en-premutation-en-noun-QYzQRGkK"
    }
  ],
  "word": "premutation"
}

{
  "categories": [
    "English adjectives",
    "English countable nouns",
    "English entries with incorrect language header",
    "English lemmas",
    "English nouns",
    "English terms prefixed with pre-",
    "English uncomparable adjectives",
    "Pages with 1 entry",
    "Pages with entries"
  ],
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "pre",
        "3": "mutation"
      },
      "expansion": "pre- + mutation",
      "name": "prefix"
    }
  ],
  "etymology_text": "From pre- + mutation.",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "premutation (not comparable)",
      "name": "en-adj"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "adj",
  "senses": [
    {
      "categories": [
        "English terms with quotations"
      ],
      "examples": [
        {
          "ref": "2015 July 30, “Positron Emission Tomography (PET) Quantification of GABA A Receptors in the Brain of Fragile X Patients”, in PLOS ONE, →DOI:",
          "text": "Fragile X syndrome is caused by mutations in the FMR1-gene, which is characterized by an expansion of a CGG triplet in the 5’ UTR. Normal individuals have 6–44 CGG repeats, while carriers of gray zone or premutation alleles have 45–54 and 55–200 repeats, respectively.",
          "type": "quote"
        }
      ],
      "glosses": [
        "Of or relating to a premutation."
      ],
      "links": [
        [
          "premutation",
          "#Noun"
        ]
      ],
      "tags": [
        "not-comparable"
      ]
    }
  ],
  "word": "premutation"
}

{
  "categories": [
    "English adjectives",
    "English countable nouns",
    "English entries with incorrect language header",
    "English lemmas",
    "English nouns",
    "English terms prefixed with pre-",
    "English uncomparable adjectives",
    "Pages with 1 entry",
    "Pages with entries"
  ],
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "pre",
        "3": "mutation"
      },
      "expansion": "pre- + mutation",
      "name": "prefix"
    }
  ],
  "etymology_text": "From pre- + mutation.",
  "forms": [
    {
      "form": "premutations",
      "tags": [
        "plural"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {},
      "expansion": "premutation (plural premutations)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "glosses": [
        "A nucleotide sequence variation that is not enough to be classed as a mutation (for example, does not affect protein expression enough to produce clinical symptoms) but nonetheless represents an unusual variant that is predisposed to still greater variation in future cell divisions (that is, predisposed to leading to a mutation)."
      ]
    }
  ],
  "word": "premutation"
}