NM_000516.7(GNAS):c.366C>T (p.Pro122=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jun 25, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001796813.5
Allele description [Variation Report for NM_000516.7(GNAS):c.366C>T (p.Pro122=)]
NM_000516.7(GNAS):c.366C>T (p.Pro122=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024