NM_000268.4(NF2):c.1248G>A (p.Ala416=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 23, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000570766.3
Allele description [Variation Report for NM_000268.4(NF2):c.1248G>A (p.Ala416=)]
NM_000268.4(NF2):c.1248G>A (p.Ala416=)
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
-
AGENCOURT_26181716 Blumberg_Cho dorsal blastopore lip Xenopus laevis cDNA clone ...
AGENCOURT_26181716 Blumberg_Cho dorsal blastopore lip Xenopus laevis cDNA clone IMAGE:7298469 5', mRNA sequencegi|49494924|gnl|dbEST|23937830|gb|C 33.1|Nucleotide
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Last Updated: Oct 13, 2024