NM_004360.5(CDH1):c.81C>T (p.Pro27=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Mar 21, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001188705.3
Allele description [Variation Report for NM_004360.5(CDH1):c.81C>T (p.Pro27=)]
NM_004360.5(CDH1):c.81C>T (p.Pro27=)
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
-
TSA: Macaca mulatta Mamu_419267 mRNA sequence
TSA: Macaca mulatta Mamu_419267 mRNA sequencegi|384942319|gnl|bpid:PRJNA77627|Ma 9267|gb|JV044694.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024