NM_003924.4(PHOX2B):c.870C>A (p.Pro290=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 23, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000562765.11
Allele description [Variation Report for NM_003924.4(PHOX2B):c.870C>A (p.Pro290=)]
NM_003924.4(PHOX2B):c.870C>A (p.Pro290=)
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
-
Similar Compounds for PubChem Compound (Select 91850823) (526)
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See more...Assertion and evidence details
Last Updated: Jun 9, 2024