NM_000268.4(NF2):c.1746G>A (p.Leu582=) AND Neurofibromatosis, type 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003608089.1
Allele description [Variation Report for NM_000268.4(NF2):c.1746G>A (p.Leu582=)]
NM_000268.4(NF2):c.1746G>A (p.Leu582=)
Condition(s)
- Name:
- Neurofibromatosis, type 2 (SWNV)
- Synonyms:
- NF 2; Neurofibromatosis central type; Acoustic schwannomas bilateral; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007039; MedGen: C0027832; Orphanet: 637; OMIM: 101000
Assertion and evidence details
Last Updated: Feb 28, 2024