NM_002691.4(POLD1):c.436C>T (p.Pro146Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003296044.2
Allele description [Variation Report for NM_002691.4(POLD1):c.436C>T (p.Pro146Ser)]
NM_002691.4(POLD1):c.436C>T (p.Pro146Ser)
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
-
90736[uid] AND (alive[prop]) (1)
Gene
-
VCF2 VCP nuclear cofactor family member 2 [Homo sapiens]
VCF2 VCP nuclear cofactor family member 2 [Homo sapiens]Gene ID:90736Gene
-
UI-E-CI1-abb-e-11-0-UI.s1 UI-E-CI1 Homo sapiens cDNA clone UI-E-CI1-abb-e-11-0-U...
UI-E-CI1-abb-e-11-0-UI.s1 UI-E-CI1 Homo sapiens cDNA clone UI-E-CI1-abb-e-11-0-UI 3', mRNA sequencegi|18969031|gnl|dbEST|11244514|gb|B 81.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024