NM_001170629.2(CHD8):c.5975G>A (p.Arg1992His) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002697157.2
Allele description [Variation Report for NM_001170629.2(CHD8):c.5975G>A (p.Arg1992His)]
NM_001170629.2(CHD8):c.5975G>A (p.Arg1992His)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
LOC110386946 [Mus musculus]
LOC110386946 [Mus musculus]Gene ID:110386946Gene
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Last Updated: Sep 29, 2024