NM_000136.3(FANCC):c.1497T>C (p.Pro499=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002389826.2
Allele description [Variation Report for NM_000136.3(FANCC):c.1497T>C (p.Pro499=)]
NM_000136.3(FANCC):c.1497T>C (p.Pro499=)
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
-
C-X-C chemokine receptor type 5 isoform 2 [Homo sapiens]
C-X-C chemokine receptor type 5 isoform 2 [Homo sapiens]gi|14589869|ref|NP_116743.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024