NM_000268.4(NF2):c.1397G>A (p.Arg466Gln) AND Neurofibromatosis, type 2
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000531371.8
Allele description [Variation Report for NM_000268.4(NF2):c.1397G>A (p.Arg466Gln)]
NM_000268.4(NF2):c.1397G>A (p.Arg466Gln)
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: Aug 4, 2024