NM_000548.5(TSC2):c.2760C>T (p.Val920=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 9, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000163488.3
Allele description [Variation Report for NM_000548.5(TSC2):c.2760C>T (p.Val920=)]
NM_000548.5(TSC2):c.2760C>T (p.Val920=)
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
-
CBWN7610.g1 NICHD_XGC_tropTe1 Xenopus tropicalis cDNA clone IMAGE:8859418 3', mR...
CBWN7610.g1 NICHD_XGC_tropTe1 Xenopus tropicalis cDNA clone IMAGE:8859418 3', mRNA sequencegi|133789551|gnl|dbEST|45219155|gb| 195.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024