NM_001042492.3(NF1):c.7086A>C (p.Ala2362=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 8, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003987588.1
Allele description [Variation Report for NM_001042492.3(NF1):c.7086A>C (p.Ala2362=)]
NM_001042492.3(NF1):c.7086A>C (p.Ala2362=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024