NM_001711.6(BGN):c.480C>G (p.Ser160=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003331743.1
Allele description [Variation Report for NM_001711.6(BGN):c.480C>G (p.Ser160=)]
NM_001711.6(BGN):c.480C>G (p.Ser160=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 7, 2023