NM_001048174.2(MUTYH):c.1554T>C (p.Ser518=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 26, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001188981.2
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1554T>C (p.Ser518=)]
NM_001048174.2(MUTYH):c.1554T>C (p.Ser518=)
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
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Last Updated: Feb 20, 2024