NM_001711.6(BGN):c.357C>T (p.Leu119=) AND not provided
- Germline classification:
- Benign/Likely benign (7 submissions)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000886273.13
Allele description [Variation Report for NM_001711.6(BGN):c.357C>T (p.Leu119=)]
NM_001711.6(BGN):c.357C>T (p.Leu119=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024