NM_006231.4(POLE):c.4341C>T (p.Val1447=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 11, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000561144.3
Allele description [Variation Report for NM_006231.4(POLE):c.4341C>T (p.Val1447=)]
NM_006231.4(POLE):c.4341C>T (p.Val1447=)
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
-
Homo sapiens PAX6 mRNA for paired box protein Pax-6, complete cds, clone: HP0637...
Homo sapiens PAX6 mRNA for paired box protein Pax-6, complete cds, clone: HP06376-ARi61A11gi|326205310|dbj|AB593094.1|Nucleotide
-
DVU0891 [Desulfovibrio vulgaris str. Hildenborough]
DVU0891 [Desulfovibrio vulgaris str. Hildenborough]Gene ID:2794203Gene
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024