NM_000268.4(NF2):c.1676A>G (p.Asp559Gly) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002405941.2
Allele description [Variation Report for NM_000268.4(NF2):c.1676A>G (p.Asp559Gly)]
NM_000268.4(NF2):c.1676A>G (p.Asp559Gly)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
LOC124453287 [Xenia sp. Carnegie-2017]
LOC124453287 [Xenia sp. Carnegie-2017]Gene ID:124453287Gene
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Last Updated: May 7, 2024