NM_002522.4(NPTX1):c.170G>A (p.Ser57Asn) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003302388.2
Allele description [Variation Report for NM_002522.4(NPTX1):c.170G>A (p.Ser57Asn)]
NM_002522.4(NPTX1):c.170G>A (p.Ser57Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024