NM_000530.8(MPZ):c.234G>A (p.Ser78=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 13, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002447158.9
Allele description [Variation Report for NM_000530.8(MPZ):c.234G>A (p.Ser78=)]
NM_000530.8(MPZ):c.234G>A (p.Ser78=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus UTP6 small subunit processome component (Utp6), mRNA
Mus musculus UTP6 small subunit processome component (Utp6), mRNAgi|141803270|ref|NM_144826.3|Nucleotide
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Last Updated: Sep 29, 2024