NM_000143.4(FH):c.486T>C (p.Ile162=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 20, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001023179.3
Allele description [Variation Report for NM_000143.4(FH):c.486T>C (p.Ile162=)]
NM_000143.4(FH):c.486T>C (p.Ile162=)
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
-
pulse width (749)
GEO DataSets
-
Aortic smooth muscle cell disorganization
Aortic smooth muscle cell disorganizationMedGen
-
Anomalous origin of left pulmonary artery from ascending aorta
Anomalous origin of left pulmonary artery from ascending aortaMedGen
-
Aortic rupture
Aortic ruptureMedGen
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See more...Assertion and evidence details
Last Updated: May 1, 2024