NM_001711.6(BGN):c.222T>C (p.Val74=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 30, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000913231.5
Allele description [Variation Report for NM_001711.6(BGN):c.222T>C (p.Val74=)]
NM_001711.6(BGN):c.222T>C (p.Val74=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024