NM_006261.5(PROP1):c.540C>T (p.Ser180=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000931974.8
Allele description [Variation Report for NM_006261.5(PROP1):c.540C>T (p.Ser180=)]
NM_006261.5(PROP1):c.540C>T (p.Ser180=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024