NM_030761.5(WNT4):c.276C>T (p.Leu92=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000951758.6
Allele description [Variation Report for NM_030761.5(WNT4):c.276C>T (p.Leu92=)]
NM_030761.5(WNT4):c.276C>T (p.Leu92=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024