NM_002074.5(GNB1):c.462C>T (p.Asp154=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000955650.9
Allele description [Variation Report for NM_002074.5(GNB1):c.462C>T (p.Asp154=)]
NM_002074.5(GNB1):c.462C>T (p.Asp154=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024