NM_006261.5(PROP1):c.423C>T (p.Ala141=) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Jan 3, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000314767.12
Allele description [Variation Report for NM_006261.5(PROP1):c.423C>T (p.Ala141=)]
NM_006261.5(PROP1):c.423C>T (p.Ala141=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024