NM_017780.4(CHD7):c.5092G>A (p.Val1698Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 1, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002628853.2
Allele description [Variation Report for NM_017780.4(CHD7):c.5092G>A (p.Val1698Met)]
NM_017780.4(CHD7):c.5092G>A (p.Val1698Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Homologene neighbors for GEO Profiles (Select 25676019) (0)
GEO Profiles
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Homologene neighbors for GEO Profiles (Select 7056669) (0)
GEO Profiles
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Profile neighbors for GEO Profiles (Select 7037371) (200)
GEO Profiles
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Related DataSets for GEO Profiles (Select 7043951) (1)
GEO DataSets
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Adult acute myeloid leukemia: bone marrow and peripheral blood expression profil...
Adult acute myeloid leukemia: bone marrow and peripheral blood expression profiles (SHCO)Accession: GDS841GEO DataSets
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Last Updated: Sep 29, 2024