NM_003977.4(AIP):c.756C>T (p.Asp252=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 2, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002396095.2
Allele description [Variation Report for NM_003977.4(AIP):c.756C>T (p.Asp252=)]
NM_003977.4(AIP):c.756C>T (p.Asp252=)
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
-
unnamed protein product [Homo sapiens]
unnamed protein product [Homo sapiens]gi|311821656|emb|CBX85739.1|Protein
-
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024