NM_000548.5(TSC2):c.4647T>C (p.Tyr1549=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 19, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001022835.3
Allele description [Variation Report for NM_000548.5(TSC2):c.4647T>C (p.Tyr1549=)]
NM_000548.5(TSC2):c.4647T>C (p.Tyr1549=)
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
-
holin [Bacillus phage PfEFR-5]
holin [Bacillus phage PfEFR-5]gi|1070101311|ref|YP_009285267.1|Protein
-
LOC103489938 [Cucumis melo]
LOC103489938 [Cucumis melo]Gene ID:103489938Gene
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Last Updated: Oct 8, 2024