NM_006231.4(POLE):c.755C>T (p.Ala252Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 21, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000492593.3
Allele description [Variation Report for NM_006231.4(POLE):c.755C>T (p.Ala252Val)]
NM_006231.4(POLE):c.755C>T (p.Ala252Val)
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
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Homo sapiens epoxide hydrolase 2 (EPHX2), transcript variant 3, mRNA
Homo sapiens epoxide hydrolase 2 (EPHX2), transcript variant 3, mRNAgi|1675176775|ref|NM_001256483.2|Nucleotide
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TAF10 TATA-box binding protein associated factor 10 [Homo sapiens]
TAF10 TATA-box binding protein associated factor 10 [Homo sapiens]Gene ID:6881Gene
-
Gene Links for GEO Profiles (Select 44336130) (1)
Gene
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See more...Assertion and evidence details
Last Updated: May 1, 2024