NM_001109809.5(ZFP57):c.1426C>T (p.Arg476Trp) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004486062.1
Allele description [Variation Report for NM_001109809.5(ZFP57):c.1426C>T (p.Arg476Trp)]
NM_001109809.5(ZFP57):c.1426C>T (p.Arg476Trp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens dopamine receptor D1 (DRD1), mRNA
Homo sapiens dopamine receptor D1 (DRD1), mRNAgi|1519244884|ref|NM_000794.5|Nucleotide
-
Human mRNA for D-1 dopamine receptor
Human mRNA for D-1 dopamine receptorgi|30398|emb|X58987.1|Nucleotide
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Last Updated: May 7, 2024