NM_001170629.2(CHD8):c.1203A>G (p.Val401=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 23, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002351717.2
Allele description [Variation Report for NM_001170629.2(CHD8):c.1203A>G (p.Val401=)]
NM_001170629.2(CHD8):c.1203A>G (p.Val401=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Rattus norvegicus dynactin subunit 3 (Dctn3), mRNA
Rattus norvegicus dynactin subunit 3 (Dctn3), mRNAgi|157821778|ref|NM_001108659.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024