NM_000143.4(FH):c.633A>G (p.Leu211=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002361496.9
Allele description [Variation Report for NM_000143.4(FH):c.633A>G (p.Leu211=)]
NM_000143.4(FH):c.633A>G (p.Leu211=)
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
-
transcriptional repressor CTCFL isoform 11 [Homo sapiens]
transcriptional repressor CTCFL isoform 11 [Homo sapiens]gi|1905532675|ref|NP_001373925.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 8, 2024