NM_000314.8(PTEN):c.998C>T (p.Ala333Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 26, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000566052.3
Allele description [Variation Report for NM_000314.8(PTEN):c.998C>T (p.Ala333Val)]
NM_000314.8(PTEN):c.998C>T (p.Ala333Val)
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
-
marine metagenome
marine metagenomeThe reconstruction of draft metagenome-assembled genomes from the global oceans.BioProject
-
BioProject Links for BioSample (Select 7618856) (1)
BioProject
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024