NM_006231.4(POLE):c.94C>T (p.Leu32Phe) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003165639.2
Allele description [Variation Report for NM_006231.4(POLE):c.94C>T (p.Leu32Phe)]
NM_006231.4(POLE):c.94C>T (p.Leu32Phe)
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
-
Tssr30364 AND (alive[prop]) (0)
Gene
-
Pseudocrenilabrinae titin a (ttna) gene, partial sequence.
Pseudocrenilabrinae titin a (ttna) gene, partial sequence.PopSet: 1061341627PopSet
-
RecName: Full=Zinc finger protein 442
RecName: Full=Zinc finger protein 442gi|30580638|sp|Q9H7R0.1|ZN442_HUMANProtein
-
Taxonomy Links for SRA (Select 8013157) (1)
Taxonomy
-
OMIM(Genes) for MedGen (Select 816128) (1)
OMIM
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024