NM_003924.4(PHOX2B):c.621C>T (p.Ser207=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 26, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002366503.2
Allele description [Variation Report for NM_003924.4(PHOX2B):c.621C>T (p.Ser207=)]
NM_003924.4(PHOX2B):c.621C>T (p.Ser207=)
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
-
propionyl-Coenzyme A carboxylase, alpha polypeptide precursor [Homo sapiens]
propionyl-Coenzyme A carboxylase, alpha polypeptide precursor [Homo sapiens]gi|4557833|ref|NP_000273.1|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024