NM_000268.4(NF2):c.1635A>T (p.Glu545Asp) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002404314.2
Allele description [Variation Report for NM_000268.4(NF2):c.1635A>T (p.Glu545Asp)]
NM_000268.4(NF2):c.1635A>T (p.Glu545Asp)
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
-
DA499080 FCBBF3 Homo sapiens cDNA clone FCBBF3012656 5', mRNA sequence
DA499080 FCBBF3 Homo sapiens cDNA clone FCBBF3012656 5', mRNA sequencegi|80788158|gnl|dbEST|33244395|dbj| 080.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024