NM_000548.5(TSC2):c.552C>T (p.Val184=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Oct 28, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000566695.11
Allele description [Variation Report for NM_000548.5(TSC2):c.552C>T (p.Val184=)]
NM_000548.5(TSC2):c.552C>T (p.Val184=)
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
-
hypothetical protein Syn7803US78_155 [Synechococcus phage ACG-2014d]
hypothetical protein Syn7803US78_155 [Synechococcus phage ACG-2014d]gi|723032731|gb|AIX36574.1|Protein
-
RPL22 AND (alive[prop]) (16123)
Gene
-
LOC121366089 [Homo sapiens]
LOC121366089 [Homo sapiens]Gene ID:121366089Gene
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024