NM_144997.7(FLCN):c.42C>T (p.His14=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 13, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000570789.3
Allele description [Variation Report for NM_144997.7(FLCN):c.42C>T (p.His14=)]
NM_144997.7(FLCN):c.42C>T (p.His14=)
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 nucleoporin 88 (NUP88), transcript variant 2, mRNA
Homo sapiens nucleoporin 88 (NUP88), transcript variant 2, mRNAgi|1519316232|ref|NM_002532.6|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024